ACTOPLUS MET- pioglitazone and metformin hydrochloride tablet, film coated

Actoplus Met by

Drug Labeling and Warnings

Actoplus Met by is a Prescription medication manufactured, distributed, or labeled by Takeda Pharmaceuticals America, Inc., Sumika Chemical Analysis Service, Ltd. (SCAS), Takeda Ireland Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: CONGESTIVE HEART FAILURE AND LACTIC ACIDOSIS

    Congestive Heart Failure

    • Thiazolidinediones, including pioglitazone, which is a component of ACTOPLUS MET, cause or exacerbate congestive heart failure in some patients [see Warnings and Precautions (5.1)].
    • After initiation of ACTOPLUS MET, and after dose increases, monitor patients carefully for signs and symptoms of heart failure (e.g., excessive, rapid weight gain, dyspnea, and/or edema). If heart failure develops, it should be managed according to current standards of care and discontinuation or dose reduction of ACTOPLUS MET must be considered [see Warnings and Precautions (5.1)].
    • ACTOPLUS MET is not recommended in patients with symptomatic heart failure [see Warnings and Precautions (5.1)].
    • Initiation of ACTOPLUS MET in patients with established New York Heart Association (NYHA) Class III or IV heart failure is contraindicated [see Contraindications (4) and Warnings and Precautions (5.1)].

    Lactic Acidosis

    • Post-marketing cases of metformin-associated lactic acidosis have resulted in death, hypothermia, hypotension, and resistant bradyarrhythmias. The onset of metformin-associated lactic acidosis is often subtle, accompanied only by nonspecific symptoms such as malaise, myalgias, respiratory distress, somnolence, and abdominal pain. Metformin-associated lactic acidosis was characterized by elevated blood lactate levels (greater than 5 mmol/L), anion gap acidosis (without evidence of ketonuria or ketonemia), an increased lactate:pyruvate ratio; and metformin plasma levels generally greater than 5 mcg/mL [see Warnings and Precautions (5.2)].
    • Risk factors for metformin-associated lactic acidosis include renal impairment, concomitant use of certain drugs (e.g., carbonic anhydrase inhibitors such as topiramate), age 65 years old or greater, having a radiological study with contrast, surgery and other procedures, hypoxic states (e.g., acute congestive heart failure), excessive alcohol intake, and hepatic impairment.
    • Steps to reduce the risk of and manage metformin-associated lactic acidosis in these high risk groups are provided in the Full Prescribing Information [see Dosage and Administration (2.2), Contraindications (4), Warnings and Precautions (5.2), Drug Interactions (7), and Use in Specific Populations (8.6, 8.7)].
    • If metformin-associated lactic acidosis is suspected, immediately discontinue ACTOPLUS MET and institute general supportive measures in a hospital setting. Prompt hemodialysis is recommended [see Warnings and Precautions (5.2)].
  • 1 INDICATIONS AND USAGE

    ACTOPLUS MET is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus when treatment with both pioglitazone and metformin is appropriate [see Clinical Studies (14)].

    Important Limitations of Use

    Pioglitazone exerts its antihyperglycemic effect only in the presence of endogenous insulin. ACTOPLUS MET should not be used to treat type 1 diabetes or diabetic ketoacidosis, as it would not be effective in these settings.

    Use caution in patients with liver disease [see Warnings and Precautions (5.5)].

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Recommendations for All Patients

    ACTOPLUS MET should be taken with meals to reduce the gastrointestinal side effects associated with metformin.

    If therapy with a combination tablet containing pioglitazone and metformin is considered appropriate the recommended starting dose is:

    • 15 mg/500 mg twice daily or 15 mg/850 mg once daily and gradually titrated, as needed, after assessing adequacy of therapeutic response and tolerability,
    • for patients with New York Heart Association (NYHA) Class I or Class II congestive heart failure: 15 mg/500 mg or 15 mg/850 mg once daily and gradually titrated, as needed, after assessing adequacy of therapeutic response and tolerability,
    • for patients inadequately controlled on metformin monotherapy: 15 mg/500 mg twice daily or 15 mg/850 mg once or twice daily (depending on the dose of metformin already being taken) and gradually titrated, as needed, after assessing adequacy of therapeutic response and tolerability,
    • for patients inadequately controlled on pioglitazone monotherapy: 15 mg/500 mg twice daily or 15 mg/850 mg once daily and gradually titrated, as needed, after assessing adequacy of therapeutic response and tolerability,
    • for patients who are changing from combination therapy of pioglitazone plus metformin as separate tablets: ACTOPLUS MET should be taken at doses that are as close as possible to the dose of pioglitazone and metformin already being taken.

    ACTOPLUS MET may be titrated up to a maximum daily dose of 45 mg of pioglitazone and 2550 mg of metformin.

    Metformin doses above 2000 mg may be better tolerated given three times a day.

    After initiation of ACTOPLUS MET or with dose increase, monitor patients carefully for adverse reactions related to fluid retention such as weight gain, edema, and signs and symptoms of congestive heart failure [see Boxed Warning and Warnings and Precautions (5.1)]. Liver tests (serum alanine and aspartate aminotransferases, alkaline phosphatase, and total bilirubin) should be obtained prior to initiating ACTOPLUS MET. Routine periodic monitoring of liver tests during treatment with ACTOPLUS MET is not recommended in patients without liver disease. Patients who have liver test abnormalities prior to initiation of ACTOPLUS MET or who are found to have abnormal liver tests while taking ACTOPLUS MET should be managed as described under Warnings and Precautions [see Warnings and Precautions (5.5) and Clinical Pharmacology (12.3)].

    2.2 Recommendations for Use in Renal Impairment

    Assess renal function prior to initiation of ACTOPLUS MET and periodically thereafter.

    ACTOPLUS MET is contraindicated in patients with an estimated glomerular filtration rate (eGFR) below 30 mL/min/1.73 m2.

    Initiation of ACTOPLUS MET in patients with an eGFR between 30 – 45 mL/min/1.73 m2 is not recommended.

    In patients taking ACTOPLUS MET whose eGFR later falls below 45 mL/min/1.73 m2, assess the benefit risk of continuing therapy.

    Discontinue ACTOPLUS MET if the patient's eGFR later falls below 30 mL/min/1.73 m2 [see Contraindications (4) and Warnings and Precautions (5.2)].

    2.3 Concomitant Use with Strong CYP2C8 Inhibitors

    Coadministration of pioglitazone (one of the ingredients in ACTOPLUS MET) and gemfibrozil, a strong CYP2C8 inhibitor, increases pioglitazone exposure approximately 3-fold. Therefore, the maximum recommended dose of ACTOPLUS MET is 15 mg/850 mg daily when used in combination with gemfibrozil or other strong CYP2C8 inhibitors [see Drug Interactions (7.1) and Clinical Pharmacology (12.3)].

    2.4 Discontinuation for Iodinated Contrast Imaging Procedures

    Discontinue ACTOPLUS MET at the time of, or prior to, an iodinated contrast imaging procedure in patients with an eGFR between 30 and 60 mL/min/1.73 m2; in patients with a history of liver disease, alcoholism or heart failure; or in patients who will be administered intra-arterial iodinated contrast. Re-evaluate eGFR 48 hours after the imaging procedure; restart ACTOPLUS MET if renal function is stable [see Warnings and Precautions (5.2)].

  • 3 DOSAGE FORMS AND STRENGTHS

    • 15 mg/500 mg tablets: White to off-white, oblong, film-coated tablets debossed with "4833M" on one side and "15/500" on the other
    • 15 mg/850 mg tablets: White to off-white, oblong, film-coated tablets debossed with "4833M" on one side and "15/850" on the other
  • 4 CONTRAINDICATIONS

    • Initiation in patients with established NYHA Class III or IV heart failure [see Boxed Warning].
    • Severe renal impairment (eGFR below 30 mL/min/1.73 m2) [see Warnings and Precautions (5.2)].
    • Use in patients with known hypersensitivity to pioglitazone, metformin, or any other component of ACTOPLUS MET.
    • Metabolic acidosis, including diabetic ketoacidosis. Diabetic ketoacidosis should be treated with insulin.
  • 5 WARNINGS AND PRECAUTIONS

    5.1 Congestive Heart Failure

    Pioglitazone

    Pioglitazone, like other thiazolidinediones, can cause dose-related fluid retention when used alone or in combination with other antidiabetic medications and is most common when pioglitazone is used in combination with insulin. Fluid retention may lead to or exacerbate congestive heart failure. Patients treated with ACTOPLUS MET should be observed for signs and symptoms of congestive heart failure. If congestive heart failure develops, it should be managed according to current standards of care and discontinuation or dose reduction of ACTOPLUS MET must be considered [see Boxed Warning, Contraindications (4), and Adverse Reactions (6.1)].

    5.2 Lactic Acidosis

    Metformin hydrochloride

    Lactic Acidosis

    There have been post-marketing cases of metformin-associated lactic acidosis, including fatal cases. These cases had a subtle onset and were accompanied by nonspecific symptoms such as malaise, myalgias, abdominal pain, respiratory distress, or increased somnolence; however, hypothermia, hypotension and resistant bradyarrhythmias have occurred with severe acidosis. Metformin-associated lactic acidosis was characterized by elevated blood lactate concentrations (greater than 5 mmol/L), anion gap acidosis (without evidence of ketonuria or ketonemia), and an increased lactate:pyruvate ratio;metformin plasma levels generally greater than 5 mcg/mL. Metformin decreases liver uptake of lactate increasing lactate blood levels which may increase the risk of lactic acidosis, especially in patients at risk.

    If metformin-associated lactic acidosis is suspected, general supportive measures should be instituted promptly in a hospital setting, along with immediate discontinuation of ACTOPLUS MET. In ACTOPLUS MET-treated patients with a diagnosis or strong suspicion of lactic acidosis, prompt hemodialysis is recommended to correct the acidosis and remove accumulated metformin (metformin hydrochloride is dialyzable, with a clearance of up to 170 mL/min under good hemodynamic conditions). Hemodialysis has often resulted in reversal of symptoms and recovery.

    Educate patients and their families about the symptoms of lactic acidosis and if these symptoms occur instruct them to discontinue ACTOPLUS MET and report these symptoms to their healthcare provider.

    For each of the known and possible risk factors for metformin-associated lactic acidosis, recommendations to reduce the risk of and manage metformin-associated lactic acidosis are provided below:

    Renal Impairment

    The postmarketing metformin-associated lactic acidosis cases primarily occurred in patients with significant renal impairment. The risk of metformin accumulation and metformin-associated lactic acidosis increases with the severity of renal impairment because metformin is substantially excreted by the kidney. Clinical recommendations based upon the patient's renal function include [see Dosage and Administration (2.2), Clinical Pharmacology (12.3)].

    • Before initiating ACTOPLUS MET, obtain an eGFR.
    • ACTOPLUS MET is contraindicated in patients with an eGFR less than 30mL/min /1.73 m2. Initiation of ACTOPLUS MET is not recommended in patients with eGFR between 30 – 45 mL/min/1.73 m2 [see Contraindications (4)].
    • Obtain an eGFR at least annually in all patients taking ACTOPLUS MET. In patients at increased risk for the development of renal impairment (e.g., the elderly), renal function should be assessed more frequently.
    • In patients taking ACTOPLUS MET whose eGFR later falls below 45 mL/min/1.73 m2, assess the benefit and risk of continuing therapy.

    Drug Interactions

    The concomitant use of ACTOPLUS MET with specific drugs may increase the risk of metformin-associated lactic acidosis: those that impair renal function, result in significant hemodynamic change, interfere with acid-base balance or increase metformin accumulation (e.g. cationic drugs) [see Drug Interactions (7)]. Therefore, consider more frequent monitoring of patients.

    Age 65 or Greater

    The risk of metformin-associated lactic acidosis increases with the patient's age because elderly patients have a greater likelihood of having hepatic, renal, or cardiac impairment than younger patients. Assess renal function more frequently in elderly patients [see Use in Specific Populations (8.5)].

    Radiological Studies with Contrast

    Administration of intravascular iodinated contrast agents in metformin-treated patients has led to an acute decrease in renal function and the occurrence of lactic acidosis. Stop ACTOPLUS MET at the time of, or prior to, an iodinated contrast imaging procedure in patients with an eGFR between 30 and 60 mL/min/1.73 m2; in patients with a history of hepatic impairment, alcoholism, or heart failure; or in patients who will be administered intra-arterial iodinated contrast. Re-evaluate eGFR 48 hours after the imaging procedure, and restart ACTOPLUS MET if renal function is stable.

    Surgery and Other Procedures

    Withholding of food and fluids during surgical or other procedures may increase the risk for volume depletion, hypotension and renal impairment. ACTOPLUS MET should be temporarily discontinued while patients have restricted food and fluid intake.

    Hypoxic States

    Several of the postmarketing cases of metformin-associated lactic acidosis occurred in the setting of acute congestive heart failure (particularly when accompanied by hypoperfusion and hypoxemia). Cardiovascular collapse (shock), acute myocardial infarction, sepsis, and other conditions associated with hypoxemia have been associated with lactic acidosis and may also cause prerenal azotemia. When such events occur, discontinue ACTOPLUS MET.

    Excessive Alcohol Intake

    Alcohol potentiates the effect of metformin on lactate metabolism and this may increase the risk of metformin-associated lactic acidosis. Warn patients against excessive alcohol intake while receiving ACTOPLUS MET.

    Hepatic Impairment

    Patients with hepatic impairment have developed with cases of metformin-associated lactic acidosis. This may be due to impaired lactate clearance resulting in higher lactate blood levels. Therefore, avoid use of ACTOPLUS MET in patients with clinical or laboratory evidence of hepatic disease.

    5.3 Edema

    In controlled clinical trials with pioglitazone, edema was reported more frequently in patients treated with pioglitazone than in placebo-treated patients and is dose related [see Adverse Reactions (6.1)]. In postmarketing experience, reports of new onset or worsening of edema have been received.

    ACTOPLUS MET should be used with caution in patients with edema. Because thiazolidinediones, including pioglitazone, can cause fluid retention, which can exacerbate or lead to congestive heart failure, ACTOPLUS MET should be used with caution in patients at risk for congestive heart failure. Patients treated with ACTOPLUS MET should be monitored for signs and symptoms of congestive heart failure [see Boxed Warning, Warnings and Precautions (5.1), and Patient Counseling Information (17.1)].

    5.4 Hypoglycemia

    Patients receiving ACTOPLUS MET in combination with insulin or other antidiabetic medications (particularly insulin secretagogues such as sulfonylureas) may be at risk for hypoglycemia. A reduction in the dose of the concomitant antidiabetic medication may be necessary to reduce the risk of hypoglycemia [see Drug Interactions (7.7)].

    Hypoglycemia can also occur when caloric intake is deficient or when strenuous exercise is not compensated by caloric supplement. Elderly, debilitated, or malnourished patients, and those with adrenal or pituitary insufficiency or alcohol intoxication are particularly susceptible to hypoglycemic effects. Hypoglycemia may be difficult to recognize in the elderly, and in people who are taking beta-adrenergic blocking drugs.

    5.5 Hepatic Effects

    There have been postmarketing reports of fatal and nonfatal hepatic failure in patients taking pioglitazone, although the reports contain insufficient information necessary to establish the probable cause. There has been no evidence of drug-induced hepatotoxicity in the pioglitazone controlled clinical trial database to date [see Adverse Reactions (6.1)].

    Patients with type 2 diabetes may have fatty liver disease or cardiac disease with episodic congestive heart failure, both of which may cause liver test abnormalities, and they may also have other forms of liver disease, many of which can be treated or managed. Therefore, obtaining a liver test panel (serum alanine aminotransferase [ALT], aspartate aminotransferase [AST], alkaline phosphatase, and total bilirubin) and assessing the patient is recommended before initiating ACTOPLUS MET therapy.

    In patients with abnormal liver tests, ACTOPLUS MET should be initiated with caution.

    Measure liver tests promptly in patients who report symptoms that may indicate liver injury, including fatigue, anorexia, right upper abdominal discomfort, dark urine or jaundice. In this clinical context, if the patient is found to have abnormal liver tests (ALT greater than three times the upper limit of the reference range), ACTOPLUS MET treatment should be interrupted and investigation done to establish the probable cause. ACTOPLUS MET should not be restarted in these patients without another explanation for the liver test abnormalities.

    Patients who have serum ALT greater than three times the reference range with serum total bilirubin greater than two times the reference range without alternative etiologies are at risk for severe drug-induced liver injury, and should not be restarted on ACTOPLUS MET. For patients with lesser elevations of serum ALT or bilirubin and with an alternate probable cause, treatment with ACTOPLUS MET can be used with caution.

    5.6 Urinary Bladder Tumors

    Tumors were observed in the urinary bladder of male rats in the two-year carcinogenicity study [see Nonclinical Toxicology (13.1)]. In addition, during the three year PROactive clinical trial, 14 patients out of 2605 (0.54%) randomized to pioglitazone and 5 out of 2633 (0.19%) randomized to placebo were diagnosed with bladder cancer. After excluding patients in whom exposure to study drug was less than one year at the time of diagnosis of bladder cancer, there were 6 (0.23%) cases on pioglitazone and two (0.08%) cases on placebo. After completion of the trial, a large subset of patients was observed for up to 10 additional years, with little additional exposure to pioglitazone. During the 13 years of both PROactive and observational follow-up, the occurrence of bladder cancer did not differ between patients randomized to pioglitazone or placebo (HR =1.00; [95% CI: 0.59–1.72]).

    Findings regarding the risk of bladder cancer in patients exposed to pioglitazone vary among observational studies; some did not find an increased risk of bladder cancer associated with pioglitazone, while others did.

    A large prospective10-year observational cohort study conducted in the United States found no statistically significant increase in the risk of bladder cancer in diabetic patients ever exposed to pioglitazone, compared to those never exposed to pioglitazone (HR =1.06 [95% CI 0.89–1.26]).

    A retrospective cohort study conducted with data from the United Kingdom found a statistically significant association between ever exposure to pioglitazone and bladder cancer (HR: 1.63; [95% CI: 1.22–2.19]).

    Associations between cumulative dose or cumulative duration of exposure to pioglitazone and bladder cancer were not detected in some studies including the 10-year observational study in the U.S., but were in others. Inconsistent findings and limitations inherent in these and other studies preclude conclusive interpretations of the observational data.

    Pioglitazone may be associated with an increase in the risk of urinary bladder tumors. There are insufficient data to determine whether pioglitazone is a tumor promoter for urinary bladder tumors.

    Consequently, ACTOPLUS MET should not be used in patients with active bladder cancer and the benefits of glycemic control versus unknown risks for cancer recurrence with ACTOPLUS MET should be considered in patients with a prior history of bladder cancer.

    5.7 Fractures

    In PROactive (the Prospective Pioglitazone Clinical Trial in Macrovascular Events), 5238 patients with type 2 diabetes and a history of macrovascular disease were randomized to pioglitazone (N=2605), force-titrated up to 45 mg daily or placebo (N=2633) in addition to standard of care. During a mean follow-up of 34.5 months, the incidence of bone fracture in females was 5.1% (44/870) for pioglitazone versus 2.5% (23/905) for placebo. This difference was noted after the first year of treatment and persisted during the course of the study. The majority of fractures observed in female patients were nonvertebral fractures including lower limb and distal upper limb. No increase in the incidence of fracture was observed in men treated with pioglitazone (1.7%) versus placebo (2.1%). The risk of fracture should be considered in the care of patients, especially female patients, treated with ACTOPLUS MET and attention should be given to assessing and maintaining bone health according to current standards of care.

    5.8 Macular Edema

    Macular edema has been reported in postmarketing experience in diabetic patients who were taking pioglitazone or another thiazolidinedione. Some patients presented with blurred vision or decreased visual acuity, but others were diagnosed on routine ophthalmologic examination.

    Most patients had peripheral edema at the time macular edema was diagnosed. Some patients had improvement in their macular edema after discontinuation of the thiazolidinedione.

    Patients with diabetes should have regular eye exams by an ophthalmologist according to current standards of care. Patients with diabetes who report any visual symptoms should be promptly referred to an ophthalmologist, regardless of the patient's underlying medications or other physical findings [see Adverse Reactions (6.1)].

    5.9 Vitamin B12 Levels

    In controlled clinical trials of metformin of 29 weeks' duration, a decrease to subnormal levels of previously normal serum vitamin B12 levels, without clinical manifestations, was observed in approximately 7% of patients. Such decrease, possibly due to interference with B12 absorption from the B12-intrinsic factor complex, is, however, very rarely associated with anemia and appears to be rapidly reversible with discontinuation of metformin or vitamin B12 supplementation. Measurement of hematologic parameters on an annual basis is advised in patients on ACTOPLUS MET and any apparent abnormalities should be appropriately investigated and managed. Certain individuals (those with inadequate vitamin B12 or calcium intake or absorption) appear to be predisposed to developing subnormal vitamin B12 levels. In these patients, routine serum vitamin B12 measurements at two- to three-year intervals may be useful.

    5.10 Macrovascular Outcomes

    There have been no clinical studies establishing conclusive evidence of macrovascular risk reduction with ACTOPLUS MET.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions are discussed elsewhere in the labeling:

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    Pioglitazone

    Over 8500 patients with type 2 diabetes have been treated with pioglitazone in randomized, double-blind, controlled clinical trials, including 2605 patients with type 2 diabetes and macrovascular disease treated with pioglitazone from the PROactive clinical trial. In these trials, over 6000 patients have been treated with pioglitazone for six months or longer, over 4500 patients have been treated with pioglitazone for one year or longer, and over 3000 patients have been treated with pioglitazone for at least two years.

    In six pooled 16- to 26-week placebo-controlled monotherapy and 16- to 24-week add-on combination therapy trials, the incidence of withdrawals due to adverse events was 4.5% for patients treated with pioglitazone and 5.8% for comparator-treated patients.

    The most common adverse events leading to withdrawal were related to inadequate glycemic control, although the incidence of these events was lower (1.5%) with pioglitazone than with placebo (3.0%).

    In the PROactive trial, the incidence of withdrawals due to adverse events was 9.0% for patients treated with pioglitazone and 7.7% for placebo-treated patients. Congestive heart failure was the most common serious adverse event leading to withdrawal occurring in 1.3% of patients treated with pioglitazone and 0.6% of patients treated with placebo.

    Common Adverse Events: 16- to 26-Week Monotherapy Trials

    A summary of the incidence and type of common adverse events reported in three pooled 16- to 26-week placebo-controlled monotherapy trials of pioglitazone is provided in Table 1. Terms that are reported represent those that occurred at an incidence of >5% and more commonly in patients treated with pioglitazone than in patients who received placebo. None of these adverse events were related to the pioglitazone dose.

    Table 1. Three Pooled 16- to 26-Week Placebo-Controlled Clinical Trials of Pioglitazone Monotherapy: Adverse Events Reported at an Incidence >5% and More Commonly in Patients Treated with Pioglitazone than in Patients Treated with Placebo

    % of Patients

    Placebo
    N=259

    Pioglitazone
    N=606

    Upper Respiratory Tract Infection

    8.5

    13.2

    Headache

    6.9

    9.1

    Sinusitis

    4.6

    6.3

    Myalgia

    2.7

    5.4

    Pharyngitis

    0.8

    5.1

    Common Adverse Events: 16- to 24-Week Add-on Combination Therapy Trials

    A summary of the overall incidence and types of common adverse events reported in trials of pioglitazone add-on to metformin is provided in Table 2. Terms that are reported represent those that occurred at an incidence of >5% and more commonly with the highest tested dose of pioglitazone.

    Table 2. 16- to 24-Week Clinical Trials of Pioglitazone Add-on to Metformin

    16-Week Placebo-Controlled Trial
    Adverse Events Reported in >5% of Patients and More Commonly in Patients Treated with Pioglitazone + Metformin than in Patients Treated with Placebo + Metformin

    % of Patients

    Placebo + Metformin
    N=160

    Pioglitazone 30 mg + Metformin
    N=168

    Edema

    2.5

    6.0

    Headache

    1.9

    6.0

    24-Week Non-Controlled Double-Blind Trial
    Adverse Events Reported in >5% of Patients and More Commonly in Patients Treated with Pioglitazone 45 mg + Metformin than in Patients Treated with Pioglitazone 30 mg + Metformin

    % of Patients

    Pioglitazone 30 mg + Metformin
    N=411

    Pioglitazone 45 mg + Metformin
    N=416

    Upper Respiratory Tract Infection

    12.4

    13.5

    Edema

    5.8

    13.9

    Headache

    5.4

    5.8

    Weight Increased

    2.9

    6.7

    Note: The preferred terms of edema peripheral, generalized edema, pitting edema, and fluid retention were combined to form the aggregate term of "edema."

    Common Adverse Events: 24-Week ACTOPLUS MET Clinical Trial

    Table 3 summarizes the incidence and types of adverse reactions reported in a controlled, 24-week double-blind clinical trial of ACTOPLUS MET dosed twice daily in patients with inadequate glycemic control on diet and exercise (N=600).

    Table 3. Adverse Events (≥5% for ACTOPLUS MET) Reported by Patients with Inadequate Glycemic Control on Diet and Exercise in a 24-Week Double-Blind Clinical Trial of ACTOPLUS MET Administered Twice Daily

    % of Patients

    ACTOPLUS MET
    15/850 mg
    Twice Daily
    N=201

    Pioglitazone
    15 mg
    Twice Daily
    N=190

    Metformin
    850 mg
    Twice Daily
    N=209

    Diarrhea

    9.0

    2.6

    15.3

    Headache

    5.5

    2.6

    4.8

    In this 24-week trial, abdominal pain was reported in 2.0% of patients in the ACTOPLUS MET group, 1.6% in the pioglitazone monotherapy group and 3.3% in the metformin monotherapy group.

    Common Adverse Events: PROactive Trial

    A summary of the overall incidence and types of common adverse events reported in the PROactive trial is provided in Table 4. Terms that are reported represent those that occurred at an incidence of >5% and more commonly in patients treated with pioglitazone than in patients who received placebo.

    Table 4. PROactive Trial: Incidence and Types of Adverse Events Reported in >5% of Patients Treated with Pioglitazone and More Commonly than Placebo

    % of Patients

    Placebo
    N=2633

    Pioglitazone
    N=2605

    Hypoglycemia

    18.8

    27.3

    Edema

    15.3

    26.7

    Cardiac Failure

    6.1

    8.1

    Pain in Extremity

    5.7

    6.4

    Back Pain

    5.1

    5.5

    Chest Pain

    5.0

    5.1

    Mean duration of patient follow-up was 34.5 months.

    Congestive Heart Failure

    A summary of the incidence of adverse events related to congestive heart failure is provided in Table 5 for the 16- to 24-week add-on to metformin trials. None of the events were fatal.

    Table 5. Treatment-Emergent Adverse Events of Congestive Heart Failure (CHF) Patients Treated with Pioglitazone or Placebo Added on to Metformin

    Number (%) of Patients

    Placebo-Controlled Trial
    (16 weeks)

    Non-Controlled Double-Blind Trial
    (24 weeks)

    Placebo + Metformin
    N=160

    Pioglitazone
    30 mg + Metformin
    N=168

    Pioglitazone
    30 mg + Metformin
    N=411

    Pioglitazone
    45 mg + Metformin
    N=416

    At least one congestive heart failure event

    0

    1 (0.6%)

    0

    1 (0.2%)

    Hospitalized

    0

    1 (0.6%)

    0

    1 (0.2%)

    Table 6. Treatment-Emergent Adverse Events of Congestive Heart Failure (CHF)

    Patients Treated with Pioglitazone or Placebo Added on to a Sulfonylurea

    Number (%) of Patients

    Placebo-Controlled Trial
    (16 weeks)

    Non-Controlled Double-Blind Trial
    (24 weeks)

    Placebo + Sulfonylurea
    N=187

    Pioglitazone
    15 mg + Sulfonylurea
    N=184

    Pioglitazone
    30 mg + Sulfonylurea
    N=189

    Pioglitazone
    30 mg + Sulfonylurea
    N=351

    Pioglitazone
    45 mg + Sulfonylurea
    N=351

    At least one congestive heart failure event

    2 (1.1%)

    0

    0

    1 (0.3%)

    6 (1.7%)

    Hospitalized

    2 (1.1%)

    0

    0

    0

    2 (0.6%)

    Patients Treated with Pioglitazone or Placebo Added on to Insulin

    Number (%) of Patients

    Placebo-Controlled Trial
    (16 weeks)

    Non-Controlled Double-Blind Trial
    (24 weeks)

    Placebo + Insulin
    N=187

    Pioglitazone
    15 mg + Insulin
    N=191

    Pioglitazone
    30 mg + Insulin
    N=188

    Pioglitazone
    30 mg + Insulin
    N=345

    Pioglitazone
    45 mg + Insulin
    N=345

    At least one congestive heart failure event

    0

    2 (1.0%)

    2 (1.1%)

    3 (0.9%)

    5 (1.4%)

    Hospitalized

    0

    2 (1.0%)

    1 (0.5%)

    1 (0.3%)

    3 (0.9%)

    Patients Treated with Pioglitazone or Placebo Added on to Metformin

    Number (%) of Patients

    Placebo-Controlled Trial
    (16 weeks)

    Non-Controlled Double-Blind Trial
    (24 weeks)

    Placebo + Metformin
    N=160

    Pioglitazone
    30 mg + Metformin
    N=168

    Pioglitazone
    30 mg + Metformin
    N=411

    Pioglitazone
    45 mg + Metformin
    N=416

    At least one congestive heart failure event

    0

    1 (0.6%)

    0

    1 (0.2%)

    Hospitalized

    0

    1 (0.6%)

    0

    1 (0.2%)

    Table 7. Treatment-Emergent Adverse Events of Congestive Heart Failure (CHF) in Patients with NYHA Class II or III Congestive Heart Failure Treated with Pioglitazone or Glyburide

    Number (%) of Subjects

    Pioglitazone
    N=262

    Glyburide
    N=256

    Death due to cardiovascular causes (adjudicated)

    5 (1.9%)

    6 (2.3%)

    Overnight hospitalization for worsening CHF (adjudicated)

    26 (9.9%)

    12 (4.7%)

    Emergency room visit for CHF (adjudicated)

    4 (1.5%)

    3 (1.2%)

    Patients experiencing CHF progression during study

    35 (13.4%)

    21 (8.2%)

    Congestive heart failure events leading to hospitalization that occurred during the PROactive trial are summarized in Table 8.

    Table 8. Treatment-Emergent Adverse Events of Congestive Heart Failure (CHF) in PROactive Trial

    Number (%) of Patients

    Placebo
    N=2633

    Pioglitazone
    N=2605

    At least one hospitalized congestive heart failure event

    108 (4.1%)

    149 (5.7%)

    Fatal

    22 (0.8%)

    25 (1.0%)

    Hospitalized, nonfatal

    86 (3.3%)

    124 (4.7%)

    Cardiovascular Safety

    In the PROactive trial, 5238 patients with type 2 diabetes and a history of macrovascular disease were randomized to pioglitazone (N=2605), force-titrated up to 45 mg daily or placebo (N=2633) in addition to standard of care. Almost all patients (95%) were receiving cardiovascular medications (beta blockers, ACE inhibitors, angiotensin II receptor blockers, calcium channel blockers, nitrates, diuretics, aspirin, statins, and fibrates). At baseline, patients had a mean age of 62 years, mean duration of diabetes of 9.5 years, and mean HbA1c of 8.1%. Mean duration of follow-up was 34.5 months.

    The primary objective of this trial was to examine the effect of pioglitazone on mortality and macrovascular morbidity in patients with type 2 diabetes mellitus who were at high risk for macrovascular events. The primary efficacy variable was the time to the first occurrence of any event in a cardiovascular composite endpoint that included all-cause mortality, nonfatal myocardial infarction (MI) including silent MI, stroke, acute coronary syndrome, cardiac intervention including coronary artery bypass grafting or percutaneous intervention, major leg amputation above the ankle, and bypass surgery or revascularization in the leg. A total of 514 (19.7%) patients treated with pioglitazone and 572 (21.7%) placebo-treated patients experienced at least one event from the primary composite endpoint (HR 0.90; 95% CI: 0.80, 1.02; p=0.10).

    Although there was no statistically significant difference between pioglitazone and placebo for the three-year incidence of a first event within this composite, there was no increase in mortality or in total macrovascular events with pioglitazone. The number of first occurrences and total individual events contributing to the primary composite endpoint is shown in Table 9.

    Table 9. PROactive Trial: Number of First and Total Events for Each Component Within the Cardiovascular Composite Endpoint

    Cardiovascular Events

    Placebo
    N=2633

    Pioglitazone
    N=2605

    First Events
    n (%)

    Total events
    n

    First Events
    n (%)

    Total events
    n

    Any event

    572 (21.7)

    900

    514 (19.7)

    803

      All-cause mortality

    122 (4.6)

    186

    110 (4.2)

    177

      Nonfatal myocardial infarction (MI)

    118 (4.5)

    157

    105 (4.0)

    131

      Stroke

    96 (3.6)

    119

    76 (2.9)

    92

      Acute coronary syndrome

    63 (2.4)

    78

    42 (1.6)

    65

      Cardiac intervention (CABG/PCI)

    101 (3.8)

    240

    101 (3.9)

    195

      Major leg amputation

    15 (0.6)

    28

    9 (0.3)

    28

      Leg revascularization

    57 (2.2)

    92

    71 (2.7)

    115

    CABG = coronary artery bypass grafting; PCI = percutaneous intervention

    Weight Gain

    Dose-related weight gain occurs when pioglitazone is used alone or in combination with other antidiabetic medications. The mechanism of weight gain is unclear but probably involves a combination of fluid retention and fat accumulation.

    Tables 10, 11, and 12 summarize the changes in body weight with pioglitazone and placebo in the 16- to 26-week randomized, double-blind monotherapy and 16- to 24-week combination add-on therapy trials, the PROactive trial, and the 24-week ACTOPLUS MET trial.

    Table 10. Weight Changes (kg) from Baseline During Randomized, Double-Blind Clinical Trials

    Control Group
    (Placebo)

    Pioglitazone
    15 mg

    Pioglitazone
    30 mg

    Pioglitazone
    45 mg

    Median
    (25th, 75th percentile)

    Median
    (25th, 75th percentile)

    Median
    (25th, 75th percentile)

    Median
    (25th, 75th percentile)

    Monotherapy
    (16 to 26 weeks)

    -1.4 (-2.7, 0.0)
    N=256

    0.9 (-0.5, 3.4)
    N=79

    1.0 (-0.9, 3.4)
    N=188

    2.6 (0.2, 5.4)
    N=79


    Combination Therapy
    (16 to 24 weeks)

    Sulfonylurea

    -0.5 (-1.8, 0.7)
    N=187

    2.0 (0.2, 3.2)
    N=183

    3.1 (1.1, 5.4)
    N=528

    4.1 (1.8, 7.3)
    N=333

    Metformin

    -1.4 (-3.2, 0.3)
    N=160

    N/A

    0.9 (-1.3, 3.2)
    N=567

    1.8 (-0.9, 5.0)
    N=407

    Insulin

    0.2 (-1.4, 1.4)
    N=182

    2.3 (0.5, 4.3)
    N=190

    3.3 (0.9, 6.3)
    N=522

    4.1 (1.4, 6.8)
    N=338

    Table 11. Median Change in Body Weight in Patients Treated with Pioglitazone Versus Patients Treated with Placebo During the Double-Blind Treatment Period in the PROactive Trial

    Placebo

    Pioglitazone

    Median
    (25th, 75th percentile)

    Median
    (25th, 75th percentile)

    Change from baseline to final visit (kg)

    -0.5 (-3.3, 2.0)
    N=2581

    +3.6 (0.0, 7.5)
    N=2560

    Note: Median exposure for both pioglitazone and placebo was 2.7 years.

    Table 12. Weight Changes (kg) from Baseline During Double-Blind Clinical Trial with ACTOPLUS MET in Patients with Inadequate Glycemic Control on Diet and Exercise

    ACTOPLUS MET
    15/850 mg
    Twice Daily

    Pioglitazone
    15 mg
    Twice Daily

    Metformin
    850 mg
    Twice Daily

    Median
    (25th , 75th percentile)

    Median
    (25th , 75th percentile)

    Median
    (25th , 75th percentile)

    Change from baseline to final visit (kg)

    1.00 (-1.0, 3.0)
    N=198

    1.35 (-0.7, 4.1)
    N=178

    -1.00 (-2.6, 0.4)
    N=203

    Note: Trial duration of 24 weeks.

    Edema

    Edema induced from taking pioglitazone is reversible when pioglitazone is discontinued. The edema usually does not require hospitalization unless there is coexisting congestive heart failure.

    In the 24-week ACTOPLUS MET trial, edema was reported in 3.0% of patients in the ACTOPLUS MET group, 4.2% in the pioglitazone monotherapy group, and 1.4% in the metformin monotherapy group.

    A summary of the frequency and types of edema adverse events occurring in clinical investigations of pioglitazone is provided in Table 13.

    Table 13. Adverse Events of Edema in Patients Treated with Pioglitazone

    Number (%) of Patients

    Placebo

    Pioglitazone
    15 mg

    Pioglitazone
    30 mg

    Pioglitazone
    45 mg

    Monotherapy
    (16 to 26 weeks)

    3 (1.2%)
    N=259

    2 (2.5%)
    N= 81

    13 (4.7%)
    N= 275

    11 (6.5%)
    N=169

    Combined Therapy
    (16 to 24 weeks)

    Sulfonylurea

    4 (2.1%)
    N=187

    3 (1.6%)
    N=184

    61 (11.3%)
    N=540

    81 (23.1%)
    N=351

    Metformin

    4 (2.5%)
    N=160

    N/A

    34 (5.9%)
    N=579

    58 (13.9%)
    N=416

    Insulin

    13 (7.0%)
    N=187

    24 (12.6%)
    N=191

    109 (20.5%)
    N=533

    90 (26.1%)
    N=345

    Note: The preferred terms of edema peripheral, generalized edema, pitting edema, and fluid retention were combined to form the aggregate term of "edema."

    Table 14. Adverse Events of Edema in Patients in the PROactive Trial

    Number (%) of Patients

    Placebo
    N=2633

    Pioglitazone
    N=2605

    419 (15.9%)

    712 (27.3%)

    Note: The preferred terms of edema peripheral, generalized edema, pitting edema, and fluid retention were combined to form the aggregate term of "edema."

    Hepatic Effects

    There has been no evidence of pioglitazone-induced hepatotoxicity in the pioglitazone controlled clinical trial database to date. One randomized, double-blind, three-year trial comparing pioglitazone to glyburide as add-on to metformin and insulin therapy was specifically designed to evaluate the incidence of serum ALT elevation to greater than three times the upper limit of the reference range, measured every eight weeks for the first 48 weeks of the trial then every 12 weeks thereafter. A total of 3/1051 (0.3%) patients treated with pioglitazone and 9/1046 (0.9%) patients treated with glyburide developed ALT values greater than three times the upper limit of the reference range. None of the patients treated with pioglitazone in the pioglitazone controlled clinical trial database to date have had a serum ALT greater than three times the upper limit of the reference range and a corresponding total bilirubin greater than two times the upper limit of the reference range, a combination predictive of the potential for severe drug-induced liver injury.

    Hypoglycemia

    In the pioglitazone clinical trials, adverse events of hypoglycemia were reported based on clinical judgment of the investigators and did not require confirmation with fingerstick glucose testing.

    In the 16-week add-on to sulfonylurea trial, the incidence of reported hypoglycemia was 3.7% with pioglitazone 30 mg and 0.5% with placebo. In the 16-week add-on to insulin trial, the incidence of reported hypoglycemia was 7.9% with pioglitazone 15 mg, 15.4% with pioglitazone 30 mg, and 4.8% with placebo.

    The incidence of reported hypoglycemia was higher with pioglitazone 45 mg compared to pioglitazone 30 mg in both the 24-week add-on to sulfonylurea trial (15.7% versus 13.4%) and in the 24-week add-on to insulin trial (47.8% versus 43.5%).

    Three patients in these four trials were hospitalized due to hypoglycemia. All three patients were receiving pioglitazone 30 mg (0.9%) in the 24-week add-on to insulin trial. An additional 14 patients reported severe hypoglycemia (defined as causing considerable interference with patient's usual activities) that did not require hospitalization. These patients were receiving pioglitazone 45 mg in combination with sulfonylurea (n=2) or pioglitazone 30 mg or 45 mg in combination with insulin (n=12).

    Urinary Bladder Tumors

    Tumors were observed in the urinary bladder of male rats in the two-year carcinogenicity study [see Nonclinical Toxicology (13.1)]. During the three year PROactive clinical trial, 14 patients out of 2605 (0.54%) randomized to pioglitazone and 5 out of 2633 (0.19%) randomized to placebo were diagnosed with bladder cancer. After excluding patients in whom exposure to study drug was less than one year at the time of diagnosis of bladder cancer, there were 6 (0.23%) cases on pioglitazone and two (0.08%) cases on placebo. After completion of the trial, a large subset of patients was observed for up to 10 additional years, with little additional exposure to pioglitazone. During the 13 years of both PROactive and observational follow-up, the occurrence of bladder cancer did not differ between patients randomized to pioglitazone or placebo (HR =1.00; 95% CI: 0.59-1.72) [see Warnings and Precautions (5.6)].

    Metformin hydrochloride

    In a double-blind clinical study of metformin in patients with type 2 diabetes, a total of 141 patients received metformin therapy (up to 2550 mg per day) and 145 patients received placebo. Adverse reactions reported in greater than 5% of the metformin patients, and that were more common in metformin than placebo-treated patients, are listed in Table 15. In this trial, diarrhea led to discontinuation of study medication in 6% of patients treated with metformin.

  • * Reactions that were more common in metformin than placebo-treated patients.
    		•

    Table 15. Most Common Adverse Reactions (>5.0%) in a Placebo-Controlled Clinical Study of Metformin Monotherapy*

    Adverse Reaction

    Metformin Monotherapy
    (n=141)

    Placebo
    (n=145)

    % of Patients

    Diarrhea

    53.2

    11.7

    Nausea/Vomiting

    25.5

    8.3

    Flatulence

    12.1

    5.5

    Asthenia

    9.2

    5.5

    Indigestion

    7.1

    4.1

    Abdominal Discomfort

    6.4

    4.8

    Headache

    5.7

    4.8

    Laboratory Abnormalities

    Hematologic Effects

    Pioglitazone may cause decreases in hemoglobin and hematocrit. In placebo-controlled monotherapy trials, mean hemoglobin values declined by 2% to 4% in patients treated with pioglitazone compared with a mean change in hemoglobin of -1% to +1% in placebo-treated patients. These changes primarily occurred within the first four to 12 weeks of therapy and remained relatively constant thereafter. These changes may be related to increased plasma volume associated with pioglitazone therapy and are not likely to be associated with any clinically significant hematologic effects.

    Vitamin B12 Concentrations

    Metformin may lower serum vitamin B12 concentrations. Measurement of hematologic parameters on an annual basis is advised in patients on ACTOPLUS MET and any apparent abnormalities should be appropriately investigated and managed [see Warnings and Precautions (5.9)].

    Creatine Phosphokinase

    During protocol-specified measurement of serum creatine phosphokinase (CPK) in pioglitazone clinical trials, an isolated elevation in CPK to greater than 10 times the upper limit of the reference range was noted in nine (0.2%) patients treated with pioglitazone (values of 2150 to 11400 IU/L) and in no comparator-treated patients. Six of these nine patients continued to receive pioglitazone, two patients were noted to have the CPK elevation on the last day of dosing, and one patient discontinued pioglitazone due to the elevation. These elevations resolved without any apparent clinical sequelae. The relationship of these events to pioglitazone therapy is unknown.

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of pioglitazone. Because these reactions are reported voluntarily from a population of uncertain size, it is generally not possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    Pioglitazone

    Postmarketing reports of congestive heart failure have been reported in patients treated with pioglitazone, both with and without previously known heart disease and both with and without concomitant insulin administration.

    In postmarketing experience, there have been reports of unusually rapid increases in weight and increases in excess of that generally observed in clinical trials. Patients who experience such increases should be assessed for fluid accumulation and volume-related events such as excessive edema and congestive heart failure [see Boxed Warning and Warnings and Precautions (5.1)].

    Metformin

    Cholestatic, hepatocellular, and mixed hepatocellular liver injury.

  • 7 DRUG INTERACTIONS

    7.1 Strong CYP2C8 Inhibitors

    An inhibitor of CYP2C8 (e.g., gemfibrozil) significantly increases the exposure (area under the serum concentration-time curve or AUC) and half-life (t½) of pioglitazone. Therefore, the maximum recommended dose of pioglitazone is 15 mg daily if used in combination with gemfibrozil or other strong CYP2C8 inhibitors [see Dosage and Administration (2.3) and Clinical Pharmacology (12.3)].

    7.2 CYP2C8 Inducers

    An inducer of CYP2C8 (e.g., rifampin) may significantly decrease the exposure (AUC) of pioglitazone. Therefore, if an inducer of CYP2C8 is started or stopped during treatment with pioglitazone, changes in diabetes treatment may be needed based on clinical response without exceeding the maximum recommended daily dose of 45 mg for pioglitazone [see Clinical Pharmacology (12.3)].

    7.3 Carbonic Anhydrase Inhibitors

    Topiramate or other carbonic anhydrase inhibitors (e.g., zonisamide, acetazolamide or dichlorphenamide) frequently causes a decrease in serum bicarbonate and induce non-anion gap, hyperchloremic metabolic acidosis. Concomitant use of these drugs with ACTOPLUS MET may increase the risk for lactic acidosis. Consider more frequent monitoring of these patients.

    7.4 Drugs that Reduce Metformin Clearance

    Concomitant use of drugs that interfere with common renal tubular transport systems involved in the renal elimination of metformin (e.g., organic cationic transporter-2 [OCT2]/multidrug and toxin extrusion [MATE] inhibitors such as ranolazine, vandetanib, dolutegravir, and cimetidine) could increase systemic exposure to metformin and may increase the risk for lactic acidosis [see Clinical Pharmacology (12.3)]. Consider the benefits and risks of concomitant use.

    7.5 Alcohol

    Alcohol is known to potentiate the effect of metformin on lactate metabolism. Warn patients against excessive alcohol intake while receiving ACTOPLUS MET.

    7.6 Insulin Secretagogues or Insulin

    If hypoglycemia occurs in a patient coadministered ACTOPLUS MET and an insulin secretagogue (e.g., sulfonylurea), the dose of the insulin secretagogue should be reduced.

    If hypoglycemia occurs in a patient coadministered ACTOPLUS MET and insulin, the dose of insulin should be decreased by 10% to 25%. Further adjustments to the insulin dose should be individualized based on glycemic response.

    7.7 Drugs Affecting Glycemic Control

    Certain drugs tend to produce hyperglycemia and may lead to loss of glycemic control. These drugs include the thiazides and other diuretics, corticosteroids, phenothiazines, thyroid products, estrogens, oral contraceptives, phenytoin, nicotinic acid, sympathomimetics, calcium channel blockers, and isoniazid. When such drugs are administered to a patient receiving ACTOPLUS MET, the patient should be closely observed for loss of blood glucose control. When such drugs are withdrawn from a patient receiving ACTOPLUS MET, the patient should be observed closely for hypoglycemia.

    7.8 Topiramate

    A decrease in the exposure of pioglitazone and its active metabolites were noted with concomitant administration of pioglitazone and topiramate [see Clinical Pharmacology (12.3)]. The clinical relevance of this decrease is unknown; however, when ACTOPLUS MET and topiramate are used concomitantly, monitor patients for adequate glycemic control.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Limited data with ACTOPLUS MET or pioglitazone in pregnant women are not sufficient to determine a drug-associated risk for major birth defects or miscarriage. Published studies with metformin use during pregnancy have not reported a clear association with metformin and major birth defect or miscarriage risk [see Data]. There are risks to the mother and fetus associated with poorly controlled diabetes in pregnancy [see Clinical Considerations].

    In animal reproduction studies, no adverse developmental effects were observed when pioglitazone was administered to pregnant rats and rabbits during organogenesis at exposures up to 5- and 35-times the 45 mg clinical dose, respectively, based on body surface area. No adverse developmental effects were observed when metformin was administered to pregnant Sprague Dawley rats and rabbits during the period of organogenesis at doses up to 2- to 6-times, respectively, a 2000 mg clinical dose, based on body surface area [see Data].

    The estimated background risk of major birth defects is 6-10% in women with pre-gestational diabetes with a HbA1c >7 and has been reported to be as high as 20-25% in women with a HbA1c >10. The estimated background risk of miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively.

    Clinical Considerations

    Disease-associated maternal and/or embryo/fetal risk

    Poorly controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, spontaneous abortions, preterm delivery, still birth and delivery complications. Poorly controlled diabetes increases the fetal risk for major birth defects, still birth, and macrosomia related morbidity.

    Data

    Human Data

    Published data from post-marketing studies have not reported a clear association with metformin and major birth defects, miscarriage, or adverse maternal or fetal outcomes when metformin was used during pregnancy. However, these studies cannot definitely establish the absence of any metformin-associated risk because of methodological limitations, including small sample size and inconsistent comparator groups.

    Animal Data

    Pioglitazone and Metformin hydrochloride

    Animal reproduction studies were not conducted with the combined products in ACTOPLUS MET. The following data are based on studies conducted with the individual components of ACTOPLUS MET.

    Pioglitazone

    Pioglitazone administered to pregnant rats during organogenesis did not cause adverse developmental effects at a dose of 20 mg/kg (~5-times the 45 mg clinical dose), but delayed parturition and reduced embryofetal viability at 40 and 80 mg/kg, or ≥9-times the 45 mg clinical dose, by body surface area. In pregnant rabbits administered pioglitazone during organogenesis, no adverse developmental effects were observed at 80 mg/kg (~35-times the 45 mg clinical dose), but reduced embryofetal viability at 160 mg/kg, or ~69-times the 45 mg clinical dose, by body surface area. When pregnant rats received pioglitazone during late gestation and lactation, delayed postnatal development, attributed to decreased body weight, occurred in offspring at maternal doses of 10 mg/kg and above or ≥2-times the 45 mg clinical dose, by body surface area.

    Metformin hydrochloride

    Metformin hydrochloride did not cause adverse developmental effects when administered to pregnant Sprague Dawley rats and rabbits up to 600 mg/kg/day during the period of organogenesis. This represents an exposure of about 2- to 6-times a 2000 mg clinical dose based on body surface area (mg/m2) for rats and rabbits, respectively.

    8.2 Lactation

    Risk Summary

    There is no information regarding the presence of ACTOPLUS MET or pioglitazone in human milk, the effects on the breastfed infant, or the effects on milk production. Pioglitazone is present in rat milk; however, due to species-specific differences in lactation physiology, animal data may not reliably predict drug levels in human milk. Limited published studies report that metformin is present in human milk [see Data]. However, there is insufficient information on the effects of metformin on the breastfed infant and no available information on the effects of metformin on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for ACTOPLUS MET and any potential adverse effects on the breastfed infant from ACTOPLUS MET or from the underlying maternal condition.

    Data

    Published clinical lactation studies report that metformin is present in human milk which resulted in infant doses approximately 0.11% to 1% of the maternal weight-adjusted dosage and a milk/plasma ratio ranging between 0.13 and 1. However, the studies were not designed to definitely establish the risk of use of metformin during lactation because of small sample size and limited adverse event data collected in infants.

    8.3 Females and Males of Reproductive Potential

    Discuss the potential for unintended pregnancy with premenopausal women as therapy with ACTOPLUS MET, may result in ovulation in some anovulatory women.

    8.4 Pediatric Use

    Safety and effectiveness of ACTOPLUS MET in pediatric patients have not been established.

    ACTOPLUS MET is not recommended for use in pediatric patients based on adverse effects observed in adults, including fluid retention and congestive heart failure, fractures, and urinary bladder tumors [see Warnings and Precautions (5.1, 5.3, 5.6, 5.7)].

    8.5 Geriatric Use

    Pioglitazone

    A total of 92 patients (15.2%) treated with pioglitazone in the three pooled 16- to 26-week double-blind, placebo-controlled, monotherapy trials were ≥65 years old and two patients (0.3%) were ≥75 years old. In the two pooled 16- to 24-week add-on to sulfonylurea trials, 201 patients (18.7%) treated with pioglitazone were ≥65 years old and 19 (1.8%) were ≥75 years old. In the two pooled 16- to 24-week add-on to metformin trials, 155 patients (15.5%) treated with pioglitazone were ≥65 years old and 19 (1.9%) were ≥75 years old. In the two pooled 16- to 24-week add-on to insulin trials, 272 patients (25.4%) treated with pioglitazone were ≥65 years old and 22 (2.1%) were ≥75 years old.

    In PROactive Trial, 1068 patients (41.0%) treated with pioglitazone were ≥65 years old and 42 (1.6%) were ≥75 years old.

    In pharmacokinetic studies with pioglitazone, no significant differences were observed in pharmacokinetic parameters between elderly and younger patients [see Clinical Pharmacology (12.3)].

    Although clinical experiences have not identified differences in effectiveness and safety between the elderly (≥65 years) and younger patients, these conclusions are limited by small sample sizes for patients ≥75 years old.

    Metformin hydrochloride

    Controlled clinical studies of metformin did not include sufficient numbers of elderly patients to determine whether they respond differently from younger patients, although other reported clinical experience has not identified differences in responses between the elderly and young patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy and the higher risk of lactic acidosis. Assess renal function more frequently in elderly patients [see Warnings and Precautions (5.2) and Dosage and Administration (2.2)].

    8.6 Renal Impairment

    Metformin is substantially excreted by the kidney, and the risk of metformin accumulation and lactic acidosis increases with the degree of renal impairment. ACTOPLUS MET is contraindicated in severe renal impairment, patients with an eGFR below 30 mL/min/1.73 m2 [see Dosage and Administration (2.2), Contraindications (4), Warnings and Precautions (5.2) and Clinical Pharmacology (12.3)].

    8.7 Hepatic Impairment

    Use of metformin in patients with hepatic impairment has been associated with some cases of lactic acidosis. ACTOPLUS MET is not recommended in patients with hepatic impairment [see Warnings and Precautions (5.2)].

  • 10 OVERDOSAGE

    Pioglitazone

    During controlled clinical trials, one case of overdose with pioglitazone was reported. A male patient took 120 mg per day for four days, then 180 mg per day for seven days. The patient denied any clinical symptoms during this period.

    In the event of overdosage, appropriate supportive treatment should be initiated according to the patient's clinical signs and symptoms.

    Metformin hydrochloride

    Overdose of metformin hydrochloride has occurred, including ingestion of amounts greater than 50 grams. Hypoglycemia was reported in approximately 10% of cases, but no causal association with metformin hydrochloride has been established. Lactic acidosis has been reported in approximately 32% of metformin overdose cases [see Warnings and Precautions (5.2)]. Metformin is dialyzable with a clearance of up to 170 mL/min under good hemodynamic conditions. Therefore, hemodialysis may be useful for removal of accumulated metformin from patients in whom metformin overdosage is suspected.

  • 11 DESCRIPTION

    ACTOPLUS MET tablets are a thiazolidinediones and biguanide combination product that contains two oral antidiabetic medications: pioglitazone hydrochloride and metformin hydrochloride.

    Pioglitazone [(±)-5-[[4-[2-(5-ethyl-2-pyridinyl) ethoxy]phenyl]methyl]-2,4-] thiazolidinedione monohydrochloride contains one asymmetric carbon, and the compound is synthesized and used as the racemic mixture. The two enantiomers of pioglitazone interconvert in vivo. No differences were found in the pharmacologic activity between the two enantiomers. The structural formula is as shown:

    Chemical Structure

    pioglitazone hydrochloride

    Pioglitazone hydrochloride is an odorless white crystalline powder that has a molecular formula of C19H20N2O3SHCl and a molecular weight of 392.90 daltons. It is soluble in N,N-dimethylformamide, slightly soluble in anhydrous ethanol, very slightly soluble in acetone and acetonitrile, practically insoluble in water, and insoluble in ether.

    Metformin hydrochloride (N,N-dimethylimidodicarbonimidic diamide hydrochloride) is a white crystalline powder with a molecular formula of C4H11N5HCl and a molecular weight of 165.62. Metformin hydrochloride is freely soluble in water and is practically insoluble in acetone, ether, and chloroform. The pKa of metformin is 12.4. The pH of a 1% aqueous solution of metformin hydrochloride is 6.68. The structural formula is as shown:

    Chemical Structure

    metformin hydrochloride

    ACTOPLUS MET is available as a tablet for oral administration containing 15 mg pioglitazone (as the base) with 500 mg metformin hydrochloride (15 mg/500 mg) or 15 mg pioglitazone (as the base) with 850 mg metformin hydrochloride (15 mg/850 mg) formulated with the following excipients: povidone USP, microcrystalline cellulose NF, croscarmellose sodium NF, magnesium stearate NF, hypromellose 2910 USP, polyethylene glycol 8000 NF, titanium dioxide USP, and talc USP.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    ACTOPLUS MET combines two antidiabetic medications with different mechanisms of action to improve glycemic control in adults with type 2 diabetes: pioglitazone, a thiazolidinedione, and metformin hydrochloride, a biguanide. Thiazolidinediones are insulin-sensitizing agents that act primarily by enhancing peripheral glucose utilization, whereas biguanides act primarily by decreasing endogenous hepatic glucose production.

    Pioglitazone

    Pioglitazone is a thiazolidinedione that depends on the presence of insulin for its mechanism of action. Pioglitazone decreases insulin resistance in the periphery and in the liver resulting in increased insulin-dependent glucose disposal and decreased hepatic glucose output. Pioglitazone is not an insulin secretagogue. Pioglitazone is an agonist for peroxisome proliferator-activated receptor-gamma (PPARγ). PPAR receptors are found in tissues important for insulin action such as adipose tissue, skeletal muscle, and liver. Activation of PPARγ nuclear receptors modulates the transcription of a number of insulin responsive genes involved in the control of glucose and lipid metabolism.

    In animal models of diabetes, pioglitazone reduces the hyperglycemia, hyperinsulinemia, and hypertriglyceridemia characteristic of insulin-resistant states such as type 2 diabetes. The metabolic changes produced by pioglitazone result in increased responsiveness of insulin-dependent tissues and are observed in numerous animal models of insulin resistance.

    Because pioglitazone enhances the effects of circulating insulin (by decreasing insulin resistance), it does not lower blood glucose in animal models that lack endogenous insulin.

    Metformin hydrochloride

    Metformin hydrochloride improves glucose tolerance in patients with type 2 diabetes, lowering both basal and postprandial plasma glucose. Metformin decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. Metformin does not produce hypoglycemia in either patients with type 2 diabetes or healthy subjects [except in specific circumstances, see Warnings and Precautions (5.4)] and does not cause hyperinsulinemia. With metformin therapy, insulin secretion remains unchanged while fasting insulin levels and day-long plasma insulin response may actually decrease.

    12.2 Pharmacodynamics

    Pioglitazone

    Clinical studies demonstrate that pioglitazone improves insulin sensitivity in insulin-resistant patients. Pioglitazone enhances cellular responsiveness to insulin, increases insulin-dependent glucose disposal and improves hepatic sensitivity to insulin. In patients with type 2 diabetes, the decreased insulin resistance produced by pioglitazone results in lower plasma glucose concentrations, lower plasma insulin concentrations, and lower HbA1c values. In controlled clinical trials, pioglitazone had an additive effect on glycemic control when used in combination with a sulfonylurea, metformin, or insulin [see Clinical Studies (14)].

    Patients with lipid abnormalities were included in clinical trials with pioglitazone. Overall, patients treated with pioglitazone had mean decreases in serum triglycerides, mean increases in HDL cholesterol, and no consistent mean changes in LDL and total cholesterol. There is no conclusive evidence of macrovascular benefit with pioglitazone [see Warnings and Precautions (5.10) and Adverse Reactions (6.1)].

    In a 26-week, placebo-controlled, dose-ranging monotherapy study, mean serum triglycerides decreased in the 15-mg, 30-mg, and 45-mg pioglitazone dose groups compared to a mean increase in the placebo group. Mean HDL cholesterol increased to a greater extent in patients treated with pioglitazone than in the placebo-treated patients. There were no consistent differences for LDL and total cholesterol in patients treated with pioglitazone compared to placebo (see Table 16).

  • * Adjusted for baseline, pooled center, and pooled center by treatment interaction
  • † p <0.05 versus placebo

    • Table 16. Lipids in a 26-Week Placebo-Controlled Monotherapy Dose-Ranging Study

    Placebo

    Pioglitazone
    15 mg
    Once Daily

    Pioglitazone
    30 mg
    Once Daily

    Pioglitazone
    45 mg
    Once Daily

    Triglycerides (mg/dL)

    N=79

    N=79

    N=84

    N=77

    Baseline (mean)

    263

    284

    261

    260

    Percent change from baseline (adjusted mean*)

    4.8%

    -9.0%†

    -9.6%†

    -9.3%†

    HDL Cholesterol (mg/dL)

    N=79

    N=79

    N=83

    N=77

    Baseline (mean)

    42

    40

    41

    41

    Percent change from baseline (adjusted mean*)

    8.1%

    14.1%†

    12.2%

    19.1%†

    LDL Cholesterol (mg/dL)

    N=65

    N=63

    N=74

    N=62

    Baseline (mean)

    139

    132

    136

    127

    Percent change from baseline (adjusted mean*)

    4.8%

    7.2%

    5.2%

    6.0%

    Total Cholesterol (mg/dL)

    N=79

    N=79

    N=84

    N=77

    Baseline (mean)

    225

    220

    223

    214

    Percent change from baseline (adjusted mean*)

    4.4%

    4.6%

    3.3%

    6.4%

    In the two other monotherapy studies (16 weeks and 24 weeks) and in combination therapy studies with metformin (16 weeks and 24 weeks), the results were generally consistent with the data above.

    12.3 Pharmacokinetics

    Absorption

    ACTOPLUS MET

    In bioequivalence studies of ACTOPLUS MET 15 mg/500 mg and 15 mg/850 mg, the area under the curve (AUC) and maximum concentration (Cmax) of both the pioglitazone and the metformin component following a single dose of the combination tablet were bioequivalent to ACTOS 15 mg concomitantly administered with Glucophage (500 mg or 850 mg respectively) tablets under fasted conditions in healthy subjects.

    Administration of ACTOPLUS MET 15 mg/850 mg with food resulted in no change in overall exposure of pioglitazone. With metformin there was no change in AUC; however, mean peak serum concentration of metformin was decreased by 28% when administered with food. A delayed time to peak serum concentration was observed for both components (1.9 hours for pioglitazone and 0.8 hours for metformin) under fed conditions. These changes are not likely to be clinically significant.

    Pioglitazone

    Following once-daily administration of pioglitazone, steady-state serum concentrations of both pioglitazone and its major active metabolites, M-III (keto derivative of pioglitazone) and M-IV (hydroxyl derivative of pioglitazone), are achieved within seven days. At steady-state, M-III and M-IV reach serum concentrations equal to or greater than that of pioglitazone. At steady-state, in both healthy volunteers and patients with type 2 diabetes, pioglitazone comprises approximately 30% to 50% of the peak total pioglitazone serum concentrations (pioglitazone plus active metabolites) and 20% to 25% of the total AUC.

    Cmax, AUC, and trough serum concentrations (Cmin) for pioglitazone and M-III and M-IV, increased proportionally with administered doses of 15 mg and 30 mg per day.

    Following oral administration of pioglitazone, Tmax of pioglitazone was within two hours. Food delays the Tmax to three to four hours, but does not alter the extent of absorption (AUC).

    Metformin hydrochloride

    The absolute bioavailability of a 500 mg metformin tablet given under fasting conditions is approximately 50% - 60%. Studies using single oral doses of metformin tablets of 500 mg to 1500 mg, and 850 mg to 2550 mg, indicate that there is a lack of dose proportionality with increasing doses, which is due to decreased absorption rather than an alteration in elimination. At usual clinical doses and dosing schedules of metformin, steady-state plasma concentrations of metformin are reached within 24 to 48 hours and are generally <1 mcg/mL. During controlled clinical trials, maximum metformin plasma levels did not exceed 5 mcg/mL, even at maximum doses.

    Food decreases the rate and extent of metformin absorption, as shown by a 40% lower mean Cmax, a 25% lower AUC, and a 35-minute prolongation of Tmax following administration of a single 850 mg tablet of metformin with food, compared to the same tablet strength administered fasting. The clinical relevance of these decreases is unknown.

    Distribution

    Pioglitazone

    The mean apparent volume of distribution (Vd/F) of pioglitazone following single-dose administration is 0.63 ± 0.41 (mean ± SD) L/kg of body weight. Pioglitazone is extensively protein bound (>99%) in human serum, principally to serum albumin. Pioglitazone also binds to other serum proteins, but with lower affinity. M-III and M-IV are also extensively bound (>98%) to serum albumin.

    Metformin hydrochloride

    The Vd/F of metformin following single oral doses of 850 mg immediate-release metformin averaged 654 ± 358 L. Metformin is negligibly bound to plasma proteins. Metformin partitions into erythrocytes, most likely as a function of time.

    Metabolism

    Pioglitazone

    Pioglitazone is extensively metabolized by hydroxylation and oxidation; the metabolites also partly convert to glucuronide or sulfate conjugates. Metabolites M-III and M-IV are the major circulating active metabolites in humans.

    In vitro data demonstrate that multiple CYP isoforms are involved in the metabolism of pioglitazone which include CYP2C8 and, to a lesser degree, CYP3A4 with additional contributions from a variety of other isoforms, including the mainly extrahepatic CYP1A1. In vivo study of pioglitazone in combination with gemfibrozil, a strong CYP2C8 inhibitor, showed that pioglitazone is a CYP2C8 substrate [see Dosage and Administration (2.3) and Drug Interactions (7.1)]. Urinary 6ß-hydroxycortisol/cortisol ratios measured in patients treated with pioglitazone showed that pioglitazone is not a strong CYP3A4 enzyme inducer.

    Metformin hydrochloride

    Intravenous single-dose studies in healthy subjects demonstrate that metformin is excreted unchanged in the urine and does not undergo hepatic metabolism (no metabolites have been identified in humans) nor biliary excretion.

    Excretion and Elimination

    Pioglitazone

    Following oral administration, approximately 15% to 30% of the pioglitazone dose is recovered in the urine. Renal elimination of pioglitazone is negligible and the drug is excreted primarily as metabolites and their conjugates. It is presumed that most of the oral dose is excreted into the bile either unchanged or as metabolites and eliminated in the feces.

    The mean serum half-life (t½) of pioglitazone and its metabolites (M-III and M-IV) range from three to seven hours and 16 to 24 hours, respectively. Pioglitazone has an apparent clearance, CL/F, calculated to be five to seven L/hr.

    Metformin hydrochloride

    Renal clearance is approximately 3.5 times greater than creatinine clearance (CLcr), which indicates that tubular secretion is the major route of metformin elimination. Following oral administration, approximately 90% of the absorbed drug is eliminated via the renal route within the first 24 hours, with a plasma elimination t½ of approximately 6.2 hours. In blood, the elimination t½ is approximately 17.6 hours, suggesting that the erythrocyte mass may be a compartment of distribution.

    Specific Populations

    Renal Impairment

    Pioglitazone

    The serum elimination half-life of pioglitazone, M-III and M-IV remains unchanged in patients with moderate (CLcr 30 to 50 mL/min) and severe (CLcr <30 mL/min) renal impairment when compared to subjects with normal renal function. Therefore, no dose adjustment in patients with renal impairment is required.

    Metformin hydrochloride

    In patients with decreased renal function, the plasma and blood t1/2 of metformin is prolonged and the renal clearance is decreased [see Dosage and Administration (2.2), Contraindications (4) and Warnings and Precautions (5.2)].

    Hepatic Impairment

    Pioglitazone

    Compared with healthy controls, subjects with impaired hepatic function (Child-Turcotte-Pugh Grade B/C) have an approximate 45% reduction in pioglitazone and total pioglitazone (pioglitazone, M-III, and M-IV) mean Cmax but no change in the mean AUC values. Therefore, no dose adjustment in patients with hepatic impairment is required.

    There are postmarketing reports of liver failure with pioglitazone and clinical trials have generally excluded patients with serum ALT >2.5 times the upper limit of the reference range. Use ACTOPLUS MET with caution in patients with liver disease [see Warnings and Precautions (5.5)].

    Metformin hydrochloride

    No pharmacokinetic studies of metformin have been conducted in subjects with hepatic impairment [see Warnings and Precautions (5.5)].

    Geriatric Patients

    Pioglitazone

    In healthy elderly subjects, Cmax of pioglitazone was not significantly different, but AUC values were approximately 21% higher than those achieved in younger subjects. The mean t½ of pioglitazone was also prolonged in elderly subjects (about ten hours) as compared to younger subjects (about seven hours). These changes were not of a magnitude that would be considered clinically relevant.

    Metformin hydrochloride

    Limited data from controlled pharmacokinetic studies of metformin in healthy elderly subjects suggest that total CL/F is decreased, the t½ is prolonged, and Cmax is increased, compared to healthy young subjects. From these data, it appears that the change in metformin pharmacokinetics with aging is primarily accounted for by a change in renal function.

    Pediatrics

    Pioglitazone

    Safety and efficacy of pioglitazone in pediatric patients have not been established. ACTOPLUS MET is not recommended for use in pediatric patients [see Use in Specific Populations (8.4)].

    Metformin hydrochloride

    After administration of a single oral metformin 500 mg tablet with food, geometric mean metformin Cmax and AUC differed less than 5% between pediatric type 2 diabetic patients (12 to 16 years of age) and gender- and weight-matched healthy adults (20 to 45 years of age), and all with normal renal function.

    Gender

    Pioglitazone

    The mean Cmax and AUC values of pioglitazone were increased 20% to 60% in women compared to men. In controlled clinical trials, HbA1c decreases from baseline were generally greater for females than for males (average mean difference in HbA1c 0.5%). Because therapy should be individualized for each patient to achieve glycemic control, no dose adjustment is recommended based on gender alone.

    Metformin hydrochloride

    Metformin pharmacokinetic parameters did not differ significantly between normal subjects and patients with type 2 diabetes when analyzed according to gender (males=19, females=16). Similarly, in controlled clinical studies in patients with type 2 diabetes, the antihyperglycemic effect of metformin was comparable in males and females.

    Ethnicity

    Pioglitazone

    Pharmacokinetic data among various ethnic groups are not available.

    Metformin hydrochloride

    No studies of metformin pharmacokinetic parameters according to race have been performed. In controlled clinical studies of metformin in patients with type 2 diabetes, the antihyperglycemic effect was comparable in whites (n=249), blacks (n=51), and Hispanics (n=24).

    Drug-Drug Interactions

    Specific pharmacokinetic drug interaction studies with ACTOPLUS MET have not been performed, although such studies have been conducted with the individual pioglitazone and metformin components.

    Pioglitazone

  • * Daily for 7 days unless otherwise noted
  • † % change (with/without coadministered drug and no change = 0%); symbols of ↑ and ↓ indicate the exposure increase and decrease, respectively
  • ‡ Pioglitazone had no clinically significant effect on prothrombin time
    		•

    Table 17. Effect of Pioglitazone Coadministration on Systemic Exposure of Other Drugs

    Coadministered Drug

    Pioglitazone Dosage
    Regimen (mg)*

    Name and Dose Regimens

    Change in AUC†

    Change in Cmax†

    45 mg
    (N = 12)

    Warfarin‡

    Daily loading then maintenance doses
    based PT and INR values
    Quick's Value = 35 ± 5%

    R-Warfarin

    ↓3%

    R-Warfarin

    ↓2%

    S-Warfarin

    ↓1%

    S-Warfarin

    ↑1%

    45 mg
    (N = 12)

    Digoxin

    0.200 mg twice daily (loading dose) then 0.250 mg daily (maintenance dose, 7 days)

    ↑15%

    ↑17%

    45 mg daily for 21 days
    (N = 35)

    Oral Contraceptive

    [Ethinyl Estradiol (EE) 0.035 mg plus
    Norethindrone (NE) 1 mg] for 21 days

    EE

    ↓11%

    EE

    ↓13%

    NE

    ↑3%

    NE

    ↓7%

    45 mg
    (N = 23)

    Fexofenadine

    60 mg twice daily for 7 days

    ↑30%

    ↑37%

    45 mg
    (N = 14)

    Glipizide

    5 mg daily for 7 days

    ↓3%

    ↓8%

    45 mg daily for 8 days
    (N = 16)

    Metformin

    1000 mg single dose on Day 8

    ↓3%

    ↓5%

    45 mg
    (N = 21)

    Midazolam

    7.5 mg single dose on Day 15

    ↓26%

    ↓26%

    45 mg
    (N = 24)

    Ranitidine

    150 mg twice daily for 7 days

    ↑1%

    ↓1%

    45 mg daily for 4 days
    (N = 24)

    Nifedipine ER

    30 mg daily for 4 days

    ↓13%

    ↓17%

    45 mg
    (N = 25)

    Atorvastatin Ca

    80 mg daily for 7 days

    ↓14%

    ↓23%

    45 mg
    (N = 22)

    Theophylline

    400 mg twice daily for 7 days

    ↑2%

    ↑5%
  • * Daily for 7 days unless otherwise noted
  • † Mean ratio (with/without coadministered drug and no change = 1-fold) % change (with/without coadministered drug and no change = 0%); symbols of ↑ and ↓ indicate the exposure increase and decrease, respectively
  • ‡ The half-life of pioglitazone increased from 8.3 hours to 22.7 hours in the presence of gemfibrozil [see Dosage and Administration (2.3) and Drug Interactions (7.1)]
  • § Indicates duration of concomitant administration with highest twice-daily dose of topiramate from Day 14 onwards over the 22 days of study
  • Additional decrease in active metabolites; 60% for M-III and 16% for M-IV
    		•

    Table 18. Effect of Coadministered Drugs on Pioglitazone Systemic Exposure

    Coadministered Drug and Dosage Regimen

    Pioglitazone

    Dose Regimen
    (mg)*

    Change in AUC†

    Change in Cmax†

    Gemfibrozil 600 mg
    twice daily for 2 days
    (N = 12)

    15-mg
    single dose

    ↑3.2-fold‡

    ↑6%

    Ketoconazole 200 mg
    twice daily for 7 days
    (N = 28)

    45 mg

    ↑34%

    ↑14%

    Rifampin 600 mg
    daily for 5 days
    (N = 10)

    30-mg
    single dose

    ↓54%

    ↓5%

    Fexofenadine 60 mg
    twice daily for 7 days
    (N = 23)

    45 mg

    ↑1%

    0%

    Ranitidine 150 mg
    twice daily for 4 days
    (N = 23)

    45 mg

    ↓13%

    ↓16%

    Nifedipine ER 30 mg
    daily for 7 days
    (N = 23)

    45 mg

    ↑5%

    ↑4%

    Atorvastatin Ca 80 mg
    daily for 7 days
    (N = 24)

    45 mg

    ↓24%

    ↓31%

    Theophylline 400 mg
    twice daily for 7 days
    (N = 22)

    45 mg

    ↓4%

    ↓2%

    Topiramate 96 mg
    twice daily for 7 days§

    30 mg§

    ↓15%

    0%
    (N = 26)   

    Metformin hydrochloride

  • * All metformin and coadministered drugs were given as single doses
  • † AUC = AUC0–∞
  • ‡ Metformin hydrochloride extended-release tablets, 500 mg
  • § Ratio of arithmetic means
  • At steady-state with topiramate 100 mg every 12 hours and metformin 500 mg every 12 hours; AUC = AUC0-12h

    • Table 19. Effect of Coadministered Drug on Plasma Metformin Systemic Exposure

    Coadministered Drug

    Dose of Coadministered Drug*

    Dose of Metformin*

    Geometric Mean Ratio
    (ratio with/without coadministered drug)
    No effect = 1.00

    AUC†

    Cmax

    No dosing adjustments required for the following:

    Glyburide

    5 mg

    500 mg‡

    0.98§

    0.99§

    Furosemide

    40 mg

    850 mg

    1.09§

    1.22§

    Nifedipine

    10 mg

    850 mg

    1.16

    1.21

    Propranolol

    40 mg

    850 mg

    0.90

    0.94

    Ibuprofen

    400 mg

    850 mg

    1.05§

    1.07§

    Drugs that are eliminated by renal tubular secretion may increase the accumulation of metformin [see Warnings and Precautions (5) and Drug Interactions (7)].

    Cimetidine

    400 mg

    850 mg

    1.40

    1.61

    Carbonic anhydrase inhibitors may cause metabolic acidosis [see Warnings and Precautions (5) and Drug Interactions (7)].

    Topiramate

    100 mg

    500 mg

    1.25

    1.17
  • * All metformin and coadministered drugs were given as single doses
  • † AUC = AUC0–∞
  • ‡ AUC0-24 hr reported
  • § Ratio of arithmetic means, p-value of difference <0.05
  • Ratio of arithmetic means
    		•

    Table 20. Effect of Metformin on Coadministered Drug Systemic Exposure

    Coadministered Drug

    Dose of Coadministered Drug*

    Dose of Metformin*

    Geometric Mean Ratio
    (ratio with/without coadministered drug)
    No effect = 1.00

    AUC†

    Cmax

    No dosing adjustments required for the following:

    Glyburide

    5 mg

    500 mg‡

    0.78§

    0.63§

    Furosemide

    40 mg

    850 mg

    0.87§

    0.69§

    Nifedipine

    10 mg

    850 mg

    1.10‡

    1.08

    Propranolol

    40 mg

    850 mg

    1.01‡

    0.94

    Ibuprofen

    400 mg

    850 mg

    0.97

    1.01

    Cimetidine

    400 mg

    850 mg

    0.95‡

    1.01
  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    ACTOPLUS MET

    No animal studies have been conducted with ACTOPLUS MET. The following data are based on findings in studies performed with pioglitazone or metformin individually.

    Pioglitazone

    A two-year carcinogenicity study was conducted in male and female rats at oral doses up to 63 mg/kg (approximately 14 times the maximum recommended human oral dose of 45 mg based on mg/m2). Drug-induced tumors were not observed in any organ except for the urinary bladder of male rats. Benign and/or malignant transitional cell neoplasms were observed in male rats at 4 mg/kg/day and above (approximately equal to the maximum recommended human oral dose based on mg/m2). Urinary calculi with subsequent irritation and hyperplasia were postulated as the mechanism for bladder tumors observed in male rats. A two-year mechanistic study in male rats utilizing dietary acidification to reduce calculi formation was completed in 2009. Dietary acidification decreased but did not abolish the hyperplastic changes in the bladder. The presence of calculi exacerbated the hyperplastic response to pioglitazone but was not considered the primary cause of the hyperplastic changes.

    The relevance to humans of the bladder findings in the male rat cannot be excluded.

    A two-year carcinogenicity study was also conducted in male and female mice at oral doses up to 100 mg/kg/day (approximately 11 times the maximum recommended human oral dose based on mg/m2). No drug-induced tumors were observed in any organ.

    Pioglitazone hydrochloride was not mutagenic in a battery of genetic toxicology studies, including the Ames bacterial assay, a mammalian cell forward gene mutation assay (CHO/HPRT and AS52/XPRT), an in vitro cytogenetics assay using CHL cells, an unscheduled DNA synthesis assay, and an in vivo micronucleus assay.

    No adverse effects upon fertility were observed in male and female rats at oral doses up to 40 mg/kg pioglitazone hydrochloride daily prior to and throughout mating and gestation (approximately nine times the maximum recommended human oral dose based on mg/m2).

    Metformin hydrochloride

    Long-term carcinogenicity studies have been performed in rats (dosing duration of 104 weeks) and mice (dosing duration of 91 weeks) at doses up to and including 900 mg/kg/day and 1500 mg/kg/day, respectively. These doses are both approximately four times a human daily dose of 2000 mg of the metformin component of ACTOPLUS MET based on body surface area comparisons. No evidence of carcinogenicity with metformin was found in either male or female mice. Similarly, there was no tumorigenic potential observed with metformin in male rats. There was, however, an increased incidence of benign stromal uterine polyps in female rats treated with 900 mg/kg/day.

    There was no evidence of mutagenic potential of metformin in the following in vitro tests: Ames test (S. typhimurium), gene mutation test (mouse lymphoma cells), or chromosomal aberrations test (human lymphocytes). Results in the in vivo mouse micronucleus test were also negative.

    Fertility of male or female rats was unaffected by metformin when administered at doses as high as 600 mg/kg/day, which is approximately three times the maximum recommended human daily dose of the metformin component of ACTOPLUS MET based on body surface area comparisons.

    13.2 Animal Toxicology and/or Pharmacology

    Heart enlargement has been observed in mice (100 mg/kg), rats (4 mg/kg and above) and dogs (3 mg/kg) treated orally with pioglitazone hydrochloride (approximately 11, one, and two times the maximum recommended human oral dose for mice, rats, and dogs, respectively, based on mg/m2). In a one-year rat study, drug-related early death due to apparent heart dysfunction occurred at an oral dose of 160 mg/kg/day (approximately 35 times the maximum recommended human oral dose based on mg/m2). Heart enlargement was seen in a 13-week study in monkeys at oral doses of 8.9 mg/kg and above (approximately four times the maximum recommended human oral dose based on mg/m2), but not in a 52-week study at oral doses up to 32 mg/kg (approximately 13 times the maximum recommended human oral dose based on mg/m2).

  • 14 CLINICAL STUDIES

    14.1 Patients Who Have Inadequate Glycemic Control with Diet and Exercise Alone

    In a 24-week, randomized, double-blind clinical trial, 600 patients with type 2 diabetes mellitus inadequately controlled with diet and exercise alone (mean baseline HbA1c 8.7%) were randomized to ACTOPLUS MET 15/850 mg, pioglitazone 15 mg, or metformin 850 mg twice daily. Statistically significant improvements in HbA1c and fasting plasma glucose (FPG) were observed in patients treated with ACTOPLUS MET compared to either pioglitazone or metformin alone (see Table 21).

  • * Adjusted for baseline
  • † p ≤0.05 versus ACTOPLUS MET
    		•

    Table 21. Glycemic Parameters in 24-Week Study of ACTOPLUS MET in Patients with Type 2 Diabetes Mellitus Inadequately Controlled with Diet and Exercise

    Parameter

    Treatment Group

    ACTOPLUS MET 15/850 mg
    Twice Daily

    Pioglitazone
    15 mg
    Twice Daily

    Metformin
    850 mg
    Twice Daily

    HbA1c (%)

    N=188

    N=162

    N=193

      Baseline (mean)

    8.9

    8.7

    8.7

      Change from Baseline (adjusted mean*)

    -1.8

    -1.0

    -1.0

      Difference between ACTOPLUS MET (adjusted mean*)
      95% Confidence Interval

    0.9†
    (0.5, 1.2)

    0.8†
    (0.5, 1.2)

      % of patients with HbA1c ≤7%

    64

    47

    39

    Fasting Plasma Glucose (mg/dL)

    N=196

    N=176

    N=202

      Baseline (mean)

    177

    171

    171

      Change from Baseline (adjusted mean*)

    -40

    -22

    -25

      Difference between ACTOPLUS MET (adjusted mean*)
      95% Confidence Interval

    18†
    (8, 28)

    15†
    (6, 25)

    14.2 Patients Previously Treated with Metformin

    The efficacy and safety of pioglitazone as add-on to metformin therapy have been established in two clinical studies. Bioequivalence of ACTOPLUS MET with coadministered pioglitazone and metformin tablets was demonstrated for both ACTOPLUS MET strengths [see Clinical Pharmacology (12.3)].

    The two clinical trials testing pioglitazone as add-on to metformin therapy included patients with type 2 diabetes on any dose of metformin, either alone or in combination with another antidiabetic agent. All other antidiabetic agents were withdrawn at least three weeks prior to starting study treatment.

    In the first trial, 328 patients were randomized to receive either 30 mg of pioglitazone or placebo once daily for 16 weeks in addition to their current metformin regimen. Treatment with pioglitazone as add-on to metformin produced statistically significant improvements in HbA1c and FPG at endpoint compared to placebo add-on to metformin (see Table 22).

  • * Adjusted for baseline, pooled center, and pooled center by treatment interaction
  • † p ≤0.05 vs. placebo + metformin
    		•

    Table 22. Glycemic Parameters in a 16-Week Placebo-Controlled, Add-on to Metformin Trial

    Placebo + Metformin

    Pioglitazone
    30 mg + Metformin

    Total Population

    HbA1c (%)

    N=153

    N=161

    Baseline (mean)

    9.8

    9.9

    Change from baseline (adjusted mean*)

    0.2

    -0.6

    Difference from placebo + metformin (adjusted mean*)
    95% Confidence Interval

    -0.8†
    (-1.2, -0.5)

    Fasting Plasma Glucose (mg/dL)

    N=157

    N=165

    Baseline (mean)

    260

    254

    Change from baseline (adjusted mean*)

    -5

    -43

    Difference from placebo + metformin (adjusted mean*)
    95% Confidence Interval

    -38†
    (-49, -26)

    In the second trial, 827 patients were randomized to receive either 30 mg or 45 mg of pioglitazone once daily for 24 weeks in addition to their current metformin regimen. The mean reduction from baseline at Week 24 in HbA1c was 0.8% for the 30 mg dose and 1.0% for the 45 mg dose (see Table 23). The mean reduction from baseline at Week 24 in FPG was 38 mg/dL for the 30 mg dose and 51 mg/dL for the 45 mg dose.

  • * Adjusted for baseline, pooled center, and pooled center by treatment interaction
  • † p ≤0.05 vs. 30 mg daily pioglitazone + metformin
    		•

    Table 23. Glycemic Parameters in a 24-Week Add-on to Metformin Study

    Pioglitazone
    30 mg + Metformin

    Pioglitazone
    45 mg + Metformin

    Total Population

    HbA1c (%)

    N=400

    N=398

    Baseline (mean)

    9.9

    9.8

    Change from baseline (adjusted mean*)

    -0.8

    -1.0

    Difference from 30 mg daily pioglitazone + metformin (adjusted mean*) (95% CI)

    -0.2
    (-0.5, 0.1)

    Fasting Plasma Glucose (mg/dL)

    N=398

    N=399

    Baseline (mean)

    233

    232

    Change from baseline (adjusted mean*)

    -38

    -51

    Difference from 30 mg daily pioglitazone + metformin (adjusted mean*) (95% CI)

    -12†
    (-21, -4)

    95% CI = 95% confidence interval

    The therapeutic effect of pioglitazone in combination with metformin was observed in patients regardless of the metformin dose.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    ACTOPLUS MET is available in 15 mg pioglitazone (as the base)/500 mg metformin hydrochloride and 15 mg pioglitazone (as the base)/850 mg metformin hydrochloride tablets as follows:

    15 mg/500 mg tablet: white to off-white, oblong, film-coated tablet with "4833M" on one side and "15/500" on the other, available in:

    Bottles of 60

    NDC: 64764-155-60

    Bottles of 180

    NDC: 64764-155-18

    15 mg/850 mg tablet: white to off-white, oblong, film-coated tablet with "4833M" on one side and "15/850" on the other, available in:

    Bottles of 60

    NDC: 64764-158-60

    Bottles of 180

    NDC: 64764-158-18

    Storage: Store at 25°C (77°F); excursions permitted to 15°-30°C (59°-86°F) [see USP Controlled Room Temperature]. Keep container tightly closed, and protect from moisture and humidity.

  • 17 PATIENT COUNSELING INFORMATION

    See FDA-Approved Patient Labeling (Medication Guide).

    • It is important to instruct patients to adhere to dietary instructions and to have blood glucose and glycosylated hemoglobin tested regularly. During periods of stress such as fever, trauma, infection, or surgery, medication requirements may change and patients should be reminded to seek medical advice promptly.
    • Tell patients to promptly report any sign of macroscopic hematuria or other symptoms such as dysuria or urinary urgency that develop or increase during treatment as these may be due to bladder cancer.
    • Explain to patients the risks of lactic acidosis, its symptoms and conditions that predispose to its development, as noted in the Warnings and Precautions (5.2) section. Advise patients to discontinue ACTOPLUS MET immediately and to promptly notify their healthcare professional if unexplained hyperventilation, myalgia, gastrointestinal symptoms, malaise, unusual somnolence, or other nonspecific symptoms occur. Instruct patients to inform their doctor that they are taking ACTOPLUS MET prior to any surgical or radiological procedure, as temporary discontinuation of ACTOPLUS MET may be required until renal function has been confirmed to be normal.
    • Counsel patients against excessive alcohol intake while receiving ACTOPLUS MET.
    • Inform patients to immediately report symptoms of an unusually rapid increase in weight or edema, shortness of breath, or other symptoms of heart failure while receiving ACTOPLUS MET.
    • Tell patients to promptly stop taking ACTOPLUS MET and seek immediate medical advice if there is unexplained nausea, vomiting, abdominal pain, fatigue, anorexia, or dark urine as these symptoms may be due to hepatotoxicity.
    • Inform patients about the importance of regular testing of renal function and hematologic parameters when receiving treatment with ACTOPLUS MET.
    • Inform female patients that treatment with ACTOPLUS MET may result in an unintended pregnancy in some premenopausal anovulatory females due to its effect on ovulation [see Use in Specific Populations (8.3)].
    • Patients should be advised to notify their health practitioner or call the Poison Control Center immediately in case of ACTOPLUS MET overdose.
    • Combination antihyperglycemic therapy may cause hypoglycemia. When initiating ACTOPLUS MET, the risks of hypoglycemia, its symptoms and treatment, and conditions that predispose to its development should be explained to patients and their family members.
    • Patients should be told to take ACTOPLUS MET as prescribed and instructed that any change in dosing should only be done if directed by their physician. If a dose is missed on one day, the dose should not be doubled the following day.
  • SPL UNCLASSIFIED SECTION

    Distributed by:
    Takeda Pharmaceuticals America, Inc.
    Deerfield, IL 60015

    ACTOS and ACTOPLUS MET are trademarks of Takeda Pharmaceutical Company Limited registered with the U.S. Patent and Trademark Office and used under license by Takeda Pharmaceuticals America, Inc.

    All other trademarks are the property of their respective owners.

    ©2009 - 2017 Takeda Pharmaceuticals America, Inc.

    APM001 R15

  • MEDICATION GUIDE

    MEDICATION GUIDE
    ACTOPLUS MET (ak-TŌ-plus-met)
    (pioglitazone and metformin hydrochloride) tablets

    Read this Medication Guide carefully before you start taking ACTOPLUS MET and each time you get a refill. There may be new information. This information does not take the place of talking with your doctor about your medical condition or your treatment. If you have any questions about ACTOPLUS MET, ask your doctor or pharmacist.

    What is the most important information I should know about ACTOPLUS MET?

    ACTOPLUS MET can cause serious side effects, including:

    • new or worse heart failure. Pioglitazone, one of the medicines in ACTOPLUS MET, can cause your body to keep extra fluid (fluid retention), which leads to swelling (edema) and weight gain. Extra body fluid can make some heart problems worse or lead to heart failure. Heart failure means your heart does not pump blood well enough.
      • Do not take ACTOPLUS MET if you have severe heart failure
      • If you have heart failure with symptoms (such as shortness of breath or swelling), even if these symptoms are not severe, ACTOPLUS MET may not be right for you.
        Call your doctor right away if you have any of the following:
      • swelling or fluid retention, especially in the ankles or legs
      • shortness of breath or trouble breathing, especially when you lie down
      • an unusually fast increase in weight
      • unusual tiredness
    • lactic acidosis. Metformin, one of the medicines in ACTOPLUS MET, can cause a rare but serious condition called lactic acidosis (a buildup of an acid in the blood) that can cause death. Lactic acidosis is a medical emergency and must be treated in the hospital.

    Call your doctor right away if you have any of the following symptoms, which could be signs of lactic acidosis:

    • you feel cold in your hands or feet
    • you feel dizzy or lightheaded
    • you have a slow or irregular heartbeat
    • you feel very weak or tired
    • you have unusual (not normal) muscle pain
    • you have trouble breathing
    • you feel sleepy or drowsy
    • you have stomach pains, nausea, or vomiting

    Most people who have had lactic acidosis with metformin have other things that, combined with the metformin, led to the lactic acidosis. Tell your doctor if you have any of the following, because you have a higher chance for getting lactic acidosis with ACTOPLUS MET if you:

    • have severe kidney problems or your kidneys are affected by certain x-ray tests that use injectable dye. have liver problems
    • drink alcohol very often, or drink a lot of alcohol in short-term "binge" drinking
    • get dehydrated (lose a large amount of body fluids). This can happen if you are sick with a fever, vomiting, or diarrhea. Dehydration can also happen when you sweat a lot with activity or exercise and do not drink enough fluids
    • have surgery
    • have a heart attack, severe infection, or stroke

    The best way to keep from having a problem with lactic acidosis from metformin is to tell your doctor if you have any of the problems in the list above. Your doctor may decide to stop your ACTOPLUS MET for a while if you have any of these things.

    ACTOPLUS MET can have other serious side effects. See "What are the possible side effects of ACTOPLUS MET?"

    What is ACTOPLUS MET?

    ACTOPLUS MET contains two prescription diabetes medicines called pioglitazone (ACTOS) and metformin hydrochloride (GLUCOPHAGE). ACTOPLUS MET can be used with diet and exercise to improve blood sugar (glucose) control in adults with type 2 diabetes.

    ACTOPLUS MET is not for people with type 1 diabetes.

    ACTOPLUS MET is not for people with diabetic ketoacidosis (increased ketones in your blood or urine).

    It is not known if ACTOPLUS MET is safe and effective in children under the age of 18. ACTOPLUS MET is not recommended for use in children.

    Who should not take ACTOPLUS MET?

    See "What is the most important information I should know about ACTOPLUS MET?"

    Do not take ACTOPLUS MET if you:

    • have severe heart failure
    • are allergic to pioglitazone, metformin, or any of the ingredients in ACTOPLUS MET. See the end of this Medication Guide for a complete list of ingredients in ACTOPLUS MET
    • have severe kidney problems
    • have a condition called metabolic acidosis, including diabetic ketoacidosis. Diabetic ketoacidosis should be treated with insulin

    Tell your doctor before taking ACTOPLUS MET if you have any of these conditions.

    What should I tell my doctor before taking ACTOPLUS MET?

    Before you take ACTOPLUS MET, tell your doctor if you:

    • have heart failure
    • have severe kidney problems
    • are going to have dye injected into a vein for an x-ray, CAT scan, heart study, or other type of scanning
    • will be undergoing a surgical procedure
    • drink a lot of alcohol (all the time or short binge drinking)
    • have type 1 ("juvenile") diabetes or had diabetic ketoacidosis
    • have a type of diabetic eye disease that causes swelling in the back of the eye (macular edema)
    • have liver problems
    • have or have had cancer of the bladder
    • are pregnant or plan to become pregnant. It is not known if ACTOPLUS MET can harm your unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant about the best way to control your blood glucose levels while pregnant
    • are a premenopausal woman (before the "change of life") who does not have periods regularly or at all. ACTOPLUS MET may increase your chance of becoming pregnant. Talk to your doctor about birth control choices while taking ACTOPLUS MET. Tell your doctor right away if you become pregnant while taking ACTOPLUS MET
    • are breastfeeding or plan to breastfeed. It is not known if ACTOPLUS MET passes into your milk and if it can harm your baby. Talk to your doctor about the best way to control your blood glucose levels while breastfeeding

    Tell your doctor about all the medicines you take, including prescription and over the counter medicines, vitamins, and herbal supplements.

    ACTOPLUS MET and some of your other medicines can affect each other. You may need to have your dose of ACTOPLUS MET or certain other medicines changed.

    Know the medicines you take. Keep a list of your medicines and show it to your doctor and pharmacist before you start a new medicine. They will tell you if it is okay to take ACTOPLUS MET with other medicines.

    How should I take ACTOPLUS MET?

    • Take ACTOPLUS MET exactly as your doctor tells you to take it
    • Your doctor may need to change your dose of ACTOPLUS MET. Do not change your ACTOPLUS MET dose unless your doctor tells you to
    • ACTOPLUS MET may be prescribed alone or with other diabetes medicines. This will depend on how well your blood sugar is controlled
    • Take ACTOPLUS MET with meals to lower your chance of an upset stomach
    • If you miss a dose of ACTOPLUS MET, take your next dose as prescribed unless your doctor tells you differently. Do not take two doses at one time the next day
    • If you take too much ACTOPLUS MET, call your doctor or go to the nearest hospital emergency room right away
    • If your body is under stress such as from a fever, infection, accident, or surgery, the dose of your diabetes medicines may need to be changed. Call your doctor right away
    • Stay on your diet and exercise programs and test your blood sugar regularly while taking ACTOPLUS MET
    • Your doctor should do certain blood tests before you start and while you take ACTOPLUS MET
    • Your doctor should also do hemoglobin A1C testing to check how well your blood sugar is controlled with ACTOPLUS MET
    • Your doctor should check your eyes regularly while you take ACTOPLUS MET

    What are the possible side effects of ACTOPLUS MET?

    ACTOPLUS MET may cause serious side effects, including:

    • See "What is the most important information I should know about ACTOPLUS MET?"
    • low blood sugar (hypoglycemia). This can happen if you skip meals, if you also use another medicine that lowers blood sugar, or if you have certain medical problems. Lightheadedness, dizziness, shakiness, or hunger may happen if your blood sugar is too low. Call your doctor if low blood sugar levels are a problem for you
    • liver problems. Call your doctor right away if you have:
      • nausea or vomiting
      • stomach pain
      • unusual or unexplained tiredness
      • loss of appetite
      • dark urine
      • yellowing of your skin or the whites of your eyes
    • bladder cancer. There may be an increased chance of having bladder cancer when you take ACTOPLUS MET. You should not take ACTOPLUS MET if you are receiving treatment for bladder cancer. Tell your doctor right away if you have any of the following symptoms of bladder cancer:
      • blood or a red color in your urine
      • an increased need to urinate
      • pain while you urinate
    • broken bones (fractures). Usually in the hand, upper arm, or foot in women. Talk to your doctor for advice on how to keep your bones healthy
    • diabetic eye disease with swelling in the back of the eye (macular edema). Tell your doctor right away if you have any changes in your vision. Your doctor should check your eyes regularly
    • release of an egg from an ovary in a woman (ovulation) leading to pregnancy. Ovulation may happen when premenopausal women who do not have regular monthly periods take ACTOPLUS MET. This can increase your chance of getting pregnant.
    • low red blood cell count (anemia).

    The most common side effects of ACTOPLUS MET include:

    • cold-like symptoms (upper respiratory tract infection)
    • swelling (edema)
    • diarrhea
    • headache
    • increased weight

    Tell your doctor if you have any side effect that bothers you or that does not go away. These are not all the side effects of ACTOPLUS MET. For more information, ask your doctor or pharmacist.

    Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

    How should I store ACTOPLUS MET?

    • Store ACTOPLUS MET at 68°F to 77°F (20°C to 25°C). Keep ACTOPLUS MET in the original container and protect from light

    Keep the ACTOPLUS MET bottle tightly closed and keep tablets dry

    Keep ACTOPLUS MET and all medicines out of the reach of children.

    General information about the safe and effective use of ACTOPLUS MET

    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use ACTOPLUS MET for a condition for which it was not prescribed. Do not give ACTOPLUS MET to other people, even if they have the same symptoms you have. It may harm them.

    This Medication Guide summarizes the most important information about ACTOPLUS MET. If you would like more information, talk with your doctor. You can ask your doctor or pharmacist for information about ACTOPLUS MET that is written for healthcare professionals.

    For more information, go to www.actoplusmet.com or call 1-877-825-3327.

    What are the ingredients in ACTOPLUS MET?

    Active Ingredients: pioglitazone hydrochloride and metformin hydrochloride

    Inactive Ingredients: povidone, microcrystalline cellulose, croscarmellose sodium, magnesium stearate, hypromellose 2910, polyethylene glycol 8000, titanium dioxide, and talc

    ACTOS and ACTOPLUS MET are trademarks of Takeda Pharmaceutical Company Limited registered with the U.S. Patent and Trademark Office and used under license by Takeda Pharmaceuticals America, Inc.

    This Medication Guide has been approved by the U.S. Food and Drug Administration.

    Distributed by:
    Takeda Pharmaceuticals America, Inc.
    Deerfield, IL 60015

    Revised: December 2016

    ©2009 - 2017 Takeda Pharmaceuticals America, Inc.

    APM001 R15

  • PRINCIPAL DISPLAY PANEL - 15 mg/500 mg Tablet Bottle Label

    NDC: 64764-155-60
    60 Tablets

    actoplus met

    pioglitazone 15 mg and
    metformin HCl 500 mg tablets

    Each film-coated tablet contains
    pioglitazone hydrochloride
    equivalent to 15 mg pioglitazone
    and 500 mg metformin HCl.

    Dispense with Medication Guide
    available in package insert or at
    www.actoplusmet.com

    Takeda

    Rx Only

    PRINCIPAL DISPLAY PANEL - 15 mg/500 mg Tablet Bottle Label
  • PRINCIPAL DISPLAY PANEL - 15 mg/850 mg Tablet Bottle Label

    NDC: 64764-158-60
    60 Tablets

    actoplus met

    pioglitazone 15 mg and
    metformin HCl 850 mg tablets

    Each film-coated tablet contains
    pioglitazone hydrochloride
    equivalent to 15 mg pioglitazone
    and 850 mg metformin HCl.

    Dispense with Medication Guide
    available in package insert or at
    www.actoplusmet.com

    Takeda

    Rx Only

    PRINCIPAL DISPLAY PANEL - 15 mg/850 mg Tablet Bottle Label
  • INGREDIENTS AND APPEARANCE
    ACTOPLUS MET 
    pioglitazone and metformin hydrochloride tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 64764-155
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PIOGLITAZONE HYDROCHLORIDE (UNII: JQT35NPK6C) (pioglitazone - UNII:X4OV71U42S) pioglitazone15 mg
    metformin hydrochloride (UNII: 786Z46389E) (metformin - UNII:9100L32L2N) metformin hydrochloride500 mg
    Inactive Ingredients
    Ingredient NameStrength
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    microcrystalline cellulose (UNII: OP1R32D61U)  
    croscarmellose sodium (UNII: M28OL1HH48)  
    magnesium stearate (UNII: 70097M6I30)  
    hypromellose 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
    polyethylene glycol 8000 (UNII: Q662QK8M3B)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    talc (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorWHITE (white to off-white) Scoreno score
    ShapeOVAL (oblong) Size14mm
    FlavorImprint Code 4833M;15;500
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 64764-155-6060 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/29/2005
    2NDC: 64764-155-18180 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/29/2005
    3NDC: 64764-155-414 in 1 TRAY08/29/2005
    31 in 1 CARTON
    37 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02184208/29/2005
    ACTOPLUS MET 
    pioglitazone and metformin hydrochloride tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 64764-158
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PIOGLITAZONE HYDROCHLORIDE (UNII: JQT35NPK6C) (pioglitazone - UNII:X4OV71U42S) pioglitazone15 mg
    metformin hydrochloride (UNII: 786Z46389E) (metformin - UNII:9100L32L2N) metformin hydrochloride850 mg
    Inactive Ingredients
    Ingredient NameStrength
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    microcrystalline cellulose (UNII: OP1R32D61U)  
    croscarmellose sodium (UNII: M28OL1HH48)  
    magnesium stearate (UNII: 70097M6I30)  
    hypromellose 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
    polyethylene glycol 8000 (UNII: Q662QK8M3B)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    talc (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorWHITE (white to off-white) Scoreno score
    ShapeOVAL (oblong) Size18mm
    FlavorImprint Code 4833M;15;850
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 64764-158-6060 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/29/2005
    2NDC: 64764-158-18180 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/29/2005
    3NDC: 64764-158-414 in 1 TRAY08/29/2005
    31 in 1 CARTON
    37 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02184208/29/2005
    Labeler - Takeda Pharmaceuticals America, Inc. (830134016)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sumika Chemical Analysis Service, Ltd. (SCAS)692370635ANALYSIS(64764-155, 64764-158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Takeda Ireland Ltd.986017670MANUFACTURE(64764-158)

    • Trademark Results [Actoplus Met]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ACTOPLUS MET
    ACTOPLUS MET
    78218773 3149378 Live/Registered
    TAKEDA PHARMACEUTICAL COMPANY LIMITED
    2003-02-25
    ACTOPLUS MET
    ACTOPLUS MET
    78174989 not registered Dead/Abandoned
    Takeda Chemical Industries, Ltd.
    2002-10-16
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.