TROSPIUM CHLORIDE tablet

TROSPIUM CHLORIDE by

Drug Labeling and Warnings

TROSPIUM CHLORIDE by is a Prescription medication manufactured, distributed, or labeled by Apotex Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    Trospium chloride tablets, USP are a muscarinic antagonist indicated for the treatment of overactive bladder (OAB) with symptoms of urge urinary incontinence, urgency, and urinary frequency.

  • 2 DOSAGE AND ADMINISTRATION

    The recommended dose is 20 mg twice daily. Trospium chloride tablets should be dosed at least one hour before meals or given on an empty stomach. 

    Dosage modification is recommended in the following patient populations:

  • 3 DOSAGE FORMS AND STRENGTHS

    Trospium chloride tablets, USP are supplied as 20 mg (brownish-yellow, round, biconvex, film-coated tablets, engraved “APO” on one side and “TR” over “20” on the other side).

  • 4 CONTRAINDICATIONS

    Trospium chloride tablets are contraindicated in patients with:

    • urinary retention
    • gastric retention
    • uncontrolled narrow-angle glaucoma.
    • known hypersensitivity to the drug or its ingredients. Angioedema, rash and anaphylactic reaction have been reported.
  • 5 WARNINGS AND PRECAUTIONS

    5.1 Risk of Urinary Retention

    Trospium chloride tablets should be administered with caution to patients with clinically significant bladder outflow obstruction because of the risk of urinary retention [see Contraindications (4)].

    5.2 Angioedema

    Angioedema of the face, lips, tongue, and/or larynx has been reported with trospium chloride, the active ingredient in trospium chloride tablets. In one case, angioedema occurred after the first dose of trospium chloride. Angioedema associated with upper airway swelling may be life threatening. If involvement of the tongue, hypopharynx, or larynx occurs, trospium chloride tablets should be promptly discontinued and appropriate therapy and/or measures necessary to ensure a patent airway should be promptly provided.

    5.3 Decreased Gastrointestinal Motility

    Trospium chloride tablets should be administered with caution to patients with gastrointestinal obstructive disorders because of the risk of gastric retention [see Contraindications (4)]. Trospium chloride tablets, like other antimuscarinic agents, may decrease gastrointestinal motility and should be used with caution in patients with conditions such as ulcerative colitis, intestinal atony and myasthenia gravis.

    5.4 Controlled Narrow-angle Glaucoma

    In patients being treated for narrow-angle glaucoma, trospium chloride tablets should only be used if the potential benefits outweigh the risks and in that circumstance only with careful monitoring [see Contraindications (4)].

    5.5 Central Nervous System Effects

    Trospium chloride tablets are associated with anticholinergic central nervous system (CNS) effects [see Adverse Reactions (6.2)]. A variety of CNS anticholinergic effects have been reported, including dizziness, confusion, hallucinations and somnolence. Patients should be monitored for signs of anticholinergic CNS effects, particularly after beginning treatment or increasing the dose. Advise patients not to drive or operate heavy machinery until they know how trospium chloride tablets affect them. If a patient experiences anticholinergic CNS effects, dose reduction or drug discontinuation should be considered.

    5.6 Anticholinergic Adverse Reactions in Patients with Moderate Renal Impairment

    Trospium is substantially excreted by the kidney. The effects of moderate renal impairment on systemic exposure are not known but systemic exposure is likely increased. Therefore, anticholinergic adverse reactions (including dry mouth, constipation, dyspepsia, urinary tract infection, and urinary retention) are expected to be greater in patients with moderate renal impairment [see Dosage and Administration (2), and Use in Specific Populations (8.6)].

  • 6 ADVERSE REACTIONS

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, the 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 clinical practice. 

    The safety of trospium chloride tablets was evaluated in controlled clinical trials in a total of 2975 patients, who were treated with trospium chloride tablets (N=1673), placebo (N=1056) or active control medications (N=246). Of this total, 1181 patients participated in two, 12-week, U.S., efficacy and safety studies and a 9-month open-label extension. Of this total, 591 patients received trospium chloride tablets 20 mg twice daily. In all controlled trials combined, 232 and 208 patients received treatment with trospium chloride tablets for at least 24 and 52 weeks, respectively. 

    In all placebo-controlled trials combined, the incidence of serious adverse events was 2.9% among patients receiving trospium chloride tablets 20 mg twice daily and 1.5% among patients receiving placebo. Table 1 lists adverse reactions from the combined 12-week U.S. safety and efficacy trials were reported by at least 1% of patients, and were reported more frequently in the trospium chloride group than in the placebo group.

    The two most common adverse reactions reported by patients receiving trospium chloride tablets 20 mg twice daily were dry mouth and constipation. The single most frequently reported adverse reaction for trospium chloride tablets, dry mouth, occurred in 20.1% of trospium chloride treated patients and 5.8% of patients receiving placebo. In the two U.S. studies, dry mouth led to discontinuation in 1.9% of patients treated with trospium chloride tablets 20 mg twice daily. For the patients who reported dry mouth, most had their first occurrence of the event within the first month of treatment.

    Table 1. Incidence (%) of adverse reactions with trospium chloride, reported in greater than or equal to 1% of all patients treated with trospium chloride and more frequent with trospium chloride (20 mg twice daily) than placebo in Studies 1 and 2 combined
    Adverse EventPlacebo (N=590)Trospium chloride 20 mg twice daily (N=591)
    Gastrointestinal Disorders
      Dry mouth34 (5.8)119 (20.1)
      Constipation27 (4.6)57 (9.6)
      Abdominal pain upper7 (1.2)9 (1.5)
      Constipation aggravated5 (0.8)8 (1.4)
      Dyspepsia2 (0.3)7 (1.2)
      Flatulence5 (0.8)7 (1.2)
    Nervous System Disorders
      Headache12 (2.0)25 (4.2)
    General Disorders
      Fatigue8 (1.4)11 (1.9)
    Renal and Urinary Disorders
      Urinary retention2 (0.3)7 (1.2)
    Eye Disorders
      Dry eyes NOS2 (0.3)7 (1.2)
    Abbreviations: NOS=not otherwise specified

    Other adverse reactions from the U.S., placebo-controlled trials, occurring in greater than or equal to 0.5% and less than 1.0% of trospium chloride treated patients, and more common with trospium chloride tablets than placebo are: tachycardia, vision blurred, abdominal distension, vomiting, dysgeusia, dry throat, and dry skin.

    During controlled clinical studies, one adverse reaction of angioneurotic edema was reported.

    6.2  Post-marketing Experience

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

    Gastrointestinal – gastritis; Cardiovascular – palpitations, supraventricular tachycardia, chest pain, syncope, “hypertensive crisis”; Immunological – Stevens-Johnson syndrome, anaphylactic reaction, angioedema; Nervous System – dizziness, confusion, vision abnormal, hallucinations, somnolence and delirium; Musculoskeletal – rhabdomyolysis; General – rash. 

  • 7 DRUG INTERACTIONS

    7.1 Digoxin

    Concomitant use of trospium chloride tablets and digoxin did not affect the pharmacokinetics of either drug [see Clinical Pharmacology (12.3)].

    7.2 Drugs Eliminated by Active Tubular Secretion

    Although demonstrated in a drug-drug interaction study not to affect the pharmacokinetics of digoxin, trospium chloride tablets have the potential for pharmacokinetic interactions with other drugs that are eliminated by active tubular secretion (e.g., procainamide, pancuronium, morphine, vancomycin, and tenofovir). Co-administration of trospium chloride tablets with these drugs may increase the serum concentration of trospium chloride tablets and/or the coadministered drug due to competition for this elimination pathway. Careful patient monitoring is recommended in patients receiving such drugs [see Clinical Pharmacology (12.3)].

    7.3 Antimuscarinic Agents

    The concomitant use of trospium chloride tablets with other antimuscarinic agents that produce dry mouth, constipation, and other anticholinergic pharmacological effects may increase the frequency and/or severity of such effects. Trospium chloride tablets may potentially alter the absorption of some concomitantly administered drugs due to anticholinergic effects on gastrointestinal motility.

    7.4 Metformin

    Co-administration of 500 mg metformin immediate release tablets twice daily with trospium chloride 60 mg extended release tablets reduced the steady-state systemic exposure of trospium by approximately 29% for mean AUC0-24 and by 34% for mean Cmax [see Clinical Pharmacology (12.3)].

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Teratogenic Effects

    Pregnancy Category C: There are no adequate and well-controlled studies of trospium chloride tablets in pregnant women. Trospium chloride tablets should be used during pregnancy only if the potential benefit to the patient outweighs the risk to the patient and fetus. Women who become pregnant during trospium chloride treatment are encouraged to contact their physician. 

    Risk Summary

    Based on animal data, trospium chloride tablets are predicted to have a low probability of increased risk of adverse developmental outcomes, above background risk. Adverse developmental findings were not observed to correlate with dose in rats or in rabbits. No increased risk above background was observed in rats and rabbits treated at an exposure approximately equivalent to the maximal recommended human dose (MRHD) of 40 mg.

    Animal Data

    In a rat embryo/fetal development study, pregnant rats received doses of trospium chloride up to 200 mg/kg/day, from implantation to closure of the fetal hard palate, with maternal systemic exposures corresponding to approximately nine times the exposure of women treated at the MRHD of 40 mg, based on AUC. No malformations or fetal toxicity were observed. 

    The offspring of female rats exposed orally, pre- and post-natally, to trospium chloride up to 200 mg/kg/day showed no increased developmental toxicity over background in surviving pups. However, maternal toxicity (death, irregular breathing, increased excitability) was observed at 200 mg/kg/day. A no-effect level for maternal and pup toxicity (survival to Day 4) was 20 mg/kg/day, an exposure approximately equivalent to the maximal recommended human dose (MRHD) of 40 mg. 

    In a rabbit embryo/fetal development study, pregnant rabbits received doses of trospium chloride up to 200 mg/kg/day, from implantation to closure of the fetal hard palate. At 200 mg/kg/day, maternal systemic exposures corresponded to approximately 16 times the exposure of women treated at the MRHD of 40 mg, based on AUC. However, one fetus in each of the three treated dose groups (0.3 to 16 times exposures at the MRHD) demonstrated multiple malformations, including umbilical hernia and skeletal malformations. A maternal no-effect level was set at 20 mg/kg/day, at an exposure approximately equivalent to the maximal recommended human dose (MRHD) of 40 mg, due to clinical signs (reduced feces, hunched posture, diarrhea) observed in a pharmacokinetic study at 200 mg/kg/day.

    8.2 Labor and Delivery

    The effect of trospium chloride tablets on labor and delivery is unknown.

    8.3 Nursing Mothers

    Trospium chloride (2 mg/kg orally and 50 mcg/kg intravenously) was excreted, to a limited extent (less than 1%), into the milk of lactating rats (primarily as parent compound). It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, trospium chloride tablets should be used during lactation only if the potential benefit justifies the potential risk to the newborn.

    8.4 Pediatric Use

    The safety and effectiveness of trospium chloride tablets in pediatric patients have not been established.

    8.5 Geriatric Use

    Of the 591 patients with overactive bladder who received treatment with trospium chloride in the two U.S.,placebo-controlled, efficacy and safety studies, 249 patients (42%) were 65 years of age and older. Eighty-eight trospium chloride tablets treated patients (15%) were greater than or equal to 75 years of age.

    In these 2 studies, the incidence of commonly reported anticholinergic adverse reactions in patients treated with trospium chloride tablets (including dry mouth, constipation, dyspepsia, urinary tract infection, and urinary retention) was higher in patients 75 years of age and older as compared to younger patients. This effect may be related to an enhanced sensitivity to anticholinergic agents in this patient population [see Clinical Pharmacology (12.3)]. Therefore, based upon tolerability, the dose frequency of trospium chloride tablets may be reduced to 20 mg once daily in patients 75 years of age and older.

    8.6 Renal Impairment

    Severe renal impairment (creatinine clearance less than 30 mL/minute) significantly altered the disposition of trospium chloride tablets. A 4.2-fold and 1.8-fold increase in mean AUC(0-∞) and Cmax, respectively, and the appearance of an additional elimination phase with a long half-life (~33 hr) were detected in patients with severe renal impairment compared with nearly age-matched subjects with creatinine clearance equal to or higher than 80 mL/min. The different pharmacokinetic behavior of trospium chloride tablets in patients with severe renal impairment necessitates adjustment of dosage frequency [see Dosage and Administration (2)]. The pharmacokinetics of trospium have not been studied in patients with creatinine clearance ranging from 30 to 80 mL/min.

    Trospium is known to be substantially excreted by the kidney, and the risk of adverse reactions may be greater in patients with impaired renal function.

    8.7 Hepatic Impairment

    There is no information regarding the effect of severe hepatic impairment on exposure to trospium chloride tablets. In a study of patients with mild and with moderate hepatic impairment, given 40 mg of immediate-release trospium chloride, mean Cmax increased 12% and 63%, respectively, and mean AUC(0-∞) decreased 5% and 15%, respectively, compared to healthy subjects. The clinical significance of these findings is unknown. Caution should be used when administering trospium chloride to patients with moderate and severe hepatic impairment.

  • 10 OVERDOSAGE

    Overdosage with antimuscarinic agents, including trospium chloride tablets, can result in severe antimuscarinic effects. Supportive treatment should be provided according to symptoms. In the event of overdosage, electrocardiographic monitoring is recommended.

    A 7-month-old baby experienced tachycardia and mydriasis after administration of a single dose of trospium 10 mg given by a sibling. The baby’s weight was reported as 5 kg. Following admission into the hospital and about 1 hour after ingestion of the trospium, medicinal charcoal was administered for detoxification. While hospitalized, the baby experienced mydriasis and tachycardia up to 230 beats per minute. Therapeutic intervention was not deemed necessary. The baby was discharged as completely recovered the following day.

  • 11 DESCRIPTION

    Trospium chloride tablets, USP are a quaternary ammonium compound with the chemical name of (1α,3β,5α)-3-[(Hydroxydiphenylacetyl)oxy]spiro[8-azoniabicyclo[3.2.1]octane-8,1’-pyrrolidinium] chloride. The molecular formula of trospium chloride is C25H30ClNO3 and its molecular weight is 427.96. The structural formula of trospium chloride is represented below:

    Structure

    Trospium chloride, USP is a white to off-white powder. Very soluble in water. 

    Each trospium chloride tablet, USP contains 20 mg of trospium chloride and is to be given orally. Each tablet also contains the following inactive ingredients: lactose monohydrate, microcrystalline cellulose, croscarmellose sodium, magnesium stearate, colloidal silicon dioxide, hypromellose, hydroxypropylcellulose, polyethylene glycol, titanium dioxide and yellow iron oxide.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Trospium chloride tablets are a muscarinic antagonist. 

    Trospium chloride antagonizes the effect of acetylcholine on muscarinic receptors in cholinergically innervated organs including the bladder. Its parasympatholytic action reduces the tonus of smooth muscle in the bladder. 

    Receptor assays showed that trospium chloride has negligible affinity for nicotinic receptors as compared to muscarinic receptors at concentrations obtained from therapeutic doses.

    12.2 Pharmacodynamics

    Placebo-controlled studies employing urodynamic variables were conducted in patients with conditions characterized by involuntary detrusor contractions. The results demonstrate that trospium chloride tablets increases maximum cystometric bladder capacity and volume at first detrusor contraction.

    Electrophysiology

    The effect of 20 mg twice daily and up to 100 mg twice daily trospium chloride tablets on QT interval was evaluated in a single-blind, randomized, placebo and active (moxifloxacin 400 mg once daily) controlled 5 day parallel trial in 170 male and female healthy volunteer subjects aged 18 to 45 years. The QT interval was measured over a 24-hour period at steady state. The 100 mg twice daily dose of trospium chloride was chosen because this achieves the Cmax expected in severe renal impairment. Trospium chloride tablets were not associated with an increase in individual corrected (QTcI) or Fridericia corrected (QTcF) QT interval at any time during steady state measurement, while moxifloxacin was associated with a 6.4 msec increase in QTcF. 

    In this study, asymptomatic, non-specific T wave inversions were observed more often in subjects receiving trospium chloride tablets than in subjects receiving moxifloxacin or placebo following five days of treatment. This finding was not observed during routine safety monitoring in 2 other placebo-controlled clinical trials in 591 trospium chloride treated overactive bladder patients [see Clinical Studies (14)]. The clinical significance of T wave inversion in this study is unknown. Trospium chloride tablets are associated with an increase in heart rate that correlates with increasing plasma concentrations. In the study described above, trospium chloride demonstrated a mean increase in heart rate compared to placebo of 9.1 bpm for the 20 mg dose and of 18 bpm for the 100 mg dose. In the two U.S. placebo-controlled trials in patients with overactive bladder, the mean increase in heart rate compared to placebo in Study 1 was observed to be 3 bpm and in Study 2 was 4 bpm.

    12.3 Pharmacokinetics

    Absorption

    After oral administration, less than 10% of the dose is absorbed. Mean absolute bioavailability of a 20 mg dose is 9.6% (range: 4 to 16.1%). Peak plasma concentrations (Cmax) occur between 5 to 6 hours post-dose. Mean Cmax increases greater than dose-proportionally; a 3-fold and 4-fold increase in Cmax was observed for dose increases from 20 mg to 40 mg and from 20 mg to 60 mg, respectively. AUC exhibits dose linearity for single doses up to 60 mg. Trospium chloride tablets exhibit diurnal variability in exposure with a decrease in Cmax and AUC of up to 59% and 33%, respectively, for evening relative to morning doses.

    Effect of Food

    Administration with a high (50%) fat-content meal resulted in reduced absorption, with AUC and Cmax values 70 to 80% lower than those obtained when trospium chloride was administered while fasting. Therefore, it is recommended that trospium chloride tablets should be taken at least one hour prior to meals or on an empty stomach [see Dosage and Administration (2)].

    A summary of mean (± standard deviation) pharmacokinetic parameters for a single 20 mg dose of trospium chloride tablets is provided in Table 2.

    Table 2. Mean (±SD) Pharmacokinetic Parameter Estimates for a Single 20 mg Trospium Chloride Tablets Dose in Healthy Volunteers
    CmaxAUC 0-∞Tmaxt1/2
    (ng/mL)(ng/mL · hr)(hr)(hr)
    3.5 ± 4.036.4 ± 21.85.3 ± 1.218.3 ± 3.2

    The mean plasma concentration-time (+ SD) profile for trospium chloride tablets is shown in Figure 1.

    Figure 1 - Mean (+ SD) Concentration-Time Profile for a Single 20 mg Oral Dose of Trospium Chloride Tablets in Healthy Volunteers

    figure-1 

    Distribution

    Protein binding ranged from 50 to 85% when concentration levels of trospium chloride (0.5 to 50 ng/mL) were incubated with human serum in vitro.  

    The 3H-trospium chloride ratio of plasma to whole blood was 1.6:1. This ratio indicates that the majority of 3H-trospium chloride is distributed in plasma. 

    The apparent volume of distribution for a 20 mg oral dose is 395 (± 140) liters. 

    Metabolism

    The metabolic pathway of trospium in humans has not been fully defined. Of the 10% of the dose absorbed, metabolites account for approximately 40% of the excreted dose following oral administration. The major metabolic pathway is hypothesized as ester hydrolysis with subsequent conjugation of benzylic acid to form azoniaspironortropanol with glucuronic acid. Cytochrome P450 (CYP) is not expected to contribute significantly to the elimination of trospium. Data taken from in vitro human liver microsomes investigating the inhibitory effect of trospium on seven CYP isoenzyme substrates (CYP1A2, 2A6, 2C9, 2C19, 2D6, 2E1, and 3A4) suggest a lack of inhibition at clinically relevant concentrations.

    Excretion

    The plasma half-life for trospium chloride tablets following oral administration is approximately 20 hours. After oral administration of an immediate-release formulation of 14C-trospium chloride, the majority of the dose (85.2%) was recovered in feces and a smaller amount (5.8% of the dose) was recovered in urine; 60% of the radioactivity excreted in urine was unchanged trospium. 

    The mean renal clearance for trospium (29.07 L/hour) is 4-fold higher than average glomerular filtration rate, indicating that active tubular secretion is a major route of elimination for trospium. There may be competition for elimination with other compounds that are also renally eliminated [see Drug Interactions (7.2)].

    Drug Interactions

    Digoxin: Concomitant use of 20 mg trospium chloride immediate release tablets twice daily at steady state and a single dose of 0.5 mg digoxin in a crossover study with 40 male and female subjects did not affect the pharmacokinetics of either drug.

    Metformin: A drug interaction study was conducted in which trospium chloride 60 mg extended release tablets once daily was co-administered with Glucophage® (metformin hydrochloride) 500 mg twice daily under steady-state conditions in 44 healthy subjects. Co-administration of 500 mg metformin immediate release tablets twice daily reduced the steady-state systemic exposure of trospium by approximately 29% for mean AUC0-24 and by 34% for mean Cmax. The effect of decrease in trospium exposure on the efficacy of trospium chloride tablets is unknown. The steady-state pharmacokinetics of metformin were comparable when administered with or without 60 mg trospium chloride extended release tablets once daily under fasted condition. The effect of metformin at higher doses on trospium PK is unknown.

    Specific Populations

    Age: Age did not appear to significantly affect the pharmacokinetics of trospium chloride, however, increased anticholinergic side effects unrelated to drug exposure were observed in patients greater than or equal to 75 years of age [see Use in Specific Populations (8.5)]. 

    Pediatric: The pharmacokinetics of trospium chloride tablets were not evaluated in pediatric patients.  

    Race: Pharmacokinetic differences due to race have not been studied. 

    Gender: Studies comparing the pharmacokinetics in different genders had conflicting results. When a single 40 mg trospium chloride tablets dose was administered to 16 elderly subjects, exposure was 45% lower in elderly females compared to elderly males. When 20 mg trospium chloride tablets were dosed twice daily for 4 days to 6 elderly males and 6 elderly females (60 to 75 years), AUC and Cmax were 26% and 68% higher, respectively, in females without hormone replacement therapy than in males. 

    Renal Impairment: In a clinical pharmacokinetic study where a single dose of 40 mg immediate release trospium chloride tablets were administered to 12 healthy males and 12 males with severe renal impairment, severe renal impairment (creatinine clearance less than 30 mL/minute) significantly altered the disposition of trospium chloride tablets. A 4.2-fold and 1.8-fold increase in mean AUC(0-∞) and Cmax, respectively, and the appearance of an additional elimination phase with a long half-life (~33 hours vs. 18 hours) were detected in patients with severe renal impairment compared with nearly age-matched subjects with creatinine clearance equal to or higher than 80 mL/min. The different pharmacokinetic behavior of trospium chloride tablets in patients with severe renal impairment necessitates adjustment of dosage frequency [see Dosage and Administration (2)]. The pharmacokinetics of trospium have not been studied in patients with creatinine clearance ranging from 30 to 80 mL/min. 

    Hepatic Impairment: In a clinical pharmacokinetic study in patients with mild (Child-Pugh score 5 to 6) and with moderate (Child-Pugh score 7 to 8) hepatic impairment, given a single dose of 40 mg immediate-release trospium chloride tablets, mean Cmax increased 12% and 63%, respectively, and mean AUC(0-∞) decreased 5% and 15%, respectively, compared to healthy subjects. There is no information regarding the effect of severe hepatic impairment on exposure to trospium chloride tablets.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenesis

    Carcinogenicity studies with trospium chloride tablets were conducted in mice and rats for 78 weeks and 104 weeks, respectively, at maximally tolerated doses. No evidence of a carcinogenic effect was found in either mice or rats administered up to 200 mg/kg/day, approximately 9 times the expected clinical exposure levels at the maximum recommended human dose (MRHD) of 40 mg.  

    Mutagenesis

    Trospium chloride was not mutagenic nor genotoxic in tests in vitro in bacteria (Ames test) and mammalian cells (L5178Y mouse lymphoma and CHO cells) or in vivo in the rat micronucleus test. 

    Impairment of Fertility

    No evidence of impaired fertility was observed in rats administered doses up to 200 mg/kg/day (about 16 times the expected clinical exposure at the MRHD, based on AUC).

  • 14 CLINICAL STUDIES

    Trospium chloride tablets were evaluated for the treatment of patients with overactive bladder who had symptoms of urinary frequency, urgency, and urge incontinence in two U.S. 12-week, placebo-controlled studies and one 9-month open label extension. 

    Study 1 was a randomized, double-blind, placebo-controlled, parallel-group study in 523 patients. A total of 262 patients received trospium chloride 20 mg twice daily and 261 patients received placebo. The majority of patients were Caucasian (85%) and female (74%) with a mean age of 61 years (range: 21 to 90 years). Entry criteria required that patients have urge or mixed incontinence (with a predominance of urge), urge incontinence episodes of at least 7 per week, and greater than 70 micturitions per week. The patient’s medical history and urinary diary during the treatment-free baseline confirmed the diagnosis. Reductions in urinary frequency, urge incontinence episodes and urinary void volume for placebo and trospium chloride tablets treatment groups are summarized in Table 3 and Figures 2 and 3.

    Table 3. Mean (SE) change from baseline to end of treatment (Week 12 or last observation carried forward) for urinary frequency, urge incontinence episodes, and void volume in Study 1.
    Efficacy endpointPlaceboTrospium chlorideP-value
    N=253N=253
  • * Treatment differences assessed by analysis of variance for ITT:LOCF data set.
  • † Denotes co-primary endpoint
  • ‡ Treatment differences assessed by ranked analysis of variance for ITT: LOCF data set.
  • § Placebo N=253, Trospium chloride N=248
    		•
    Urinary frequency/24hours*†
      Mean baseline12.912.7<0.001
      Mean change from baseline-1.3 (0.2)-2.4 (0.2)
    Urge incontinence episodes/week‡
      Mean baseline30.127.30.012
      Mean change from baseline-13.9 (1.2)-15.4 (1.1)
    Urinary void volume/toilet void (mL)§
      Mean baseline156.6155.1<0.001
      Mean change from baseline7.7 (3.1)32.1 (3.1)

    ITT= intent to treat, LOCF=last observation carried forward.

    figure2

    figure3

    Study 2 was nearly identical in design to Study 1. A total of 329 patients received trospium chloride 20 mg twice daily and 329 patients received placebo. The majority of patients were Caucasian (88%) and female (82%) with a mean age of 61 years (range: 19 to 94 years). Entry criteria were identical to Study 1. Reductions in urinary frequency, urge incontinence episodes, and urinary void volume for placebo and trospium chloride treatment groups are summarized in Table 4 and Figures 4 and 5.

    Table 4. Mean (SE) change from baseline to end of treatment (Week 12 or last observation carried forward) for urinary frequency, urge incontinence episodes, and void volume in Study 2.
    Efficacy endpointPlaceboTrospium chlorideP-value
    N=253N=253
  • * Treatment differences assessed by analysis of variance for ITT:LOCF data set.
  • † Denotes co-primary endpoint
  • ‡ Treatment differences assessed by ranked analysis of variance for ITT: LOCF data set.
  • § Placebo N=320, Trospium chloride N=319
    		•
    Urinary frequency/24hours*†
      Mean baseline13.212.9
      Mean change from baseline-1.8 (0.2)-2.7 (0.2)<0.001
    Urge incontinence episodes/week‡
      Mean baseline27.326.9
      Mean change from baseline-12.1 (1.0)-16.1 (1.0)<0.001
    Urinary void volume/toilet void (mL)§
      Mean baseline154.6154.8
      Mean change from baseline9.4 (2.8)35.6 (2.8)<0.001

    ITT= intent to treat, LOCF=last observation carried forward.

    fig4

    figure5

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Trospium chloride tablets, USP 20 mg (brownish-yellow, round, biconvex, film-coated tablets, engraved “APO” on one side and “TR” over “20” on the other side) are supplied as follows:

    Bottles of 60       NDC: 60505-3454-6

    Bottles of 500     NDC: 60505-3454-5

    Bottles of 1000   NDC: 60505-3454-8

    Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].

  • 17 PATIENT COUNSELING INFORMATION

    “See FDA-approved Patient Labeling (Patient Information)” 

    17.1 Angioedema

    Patients should be informed that trospium chloride, the active ingredient in trospium chloride tablets, may produce angioedema which could result in life-threatening airway obstruction. Patients should be advised to promptly discontinue trospium chloride tablets and seek immediate medical attention if they experience edema of the tongue, edema of the laryngopharynx, or difficulty breathing. 

    17.2 When Not to Use

    Prior to treatment, patients should fully understand the risks and benefits of trospium chloride tablets. In particular, patients should be informed not to take trospium chloride tablets if they:

    • have urinary retention;
    • gastric retention;
    • uncontrolled narrow-angle glaucoma;
    • are allergic to any component of trospium chloride tablets.

    17.3 Administration

     Patients should be instructed regarding the recommended dosing and administration of trospium chloride tablets:

    • Take one trospium chloride tablet twice daily with water.
    • Take trospium chloride tablets on an empty stomach or at least 1 hour before a meal.  

    17.4 Adverse Reactions

    Patients should be informed that the most common side effects with trospium chloride tablets are dry mouth and constipation and that other less common side effects include trouble emptying the bladder, blurred vision, and heat prostration. Because anticholinergics, such as trospium chloride, may produce dizziness or blurred vision, patients should be advised to exercise caution in decisions to engage in potentially dangerous activities until the drug’s effects have been determined. Patients should be informed that alcohol may enhance the drowsiness caused by anticholinergic agents. 

    APOTEX INC.

    Trospium Chloride Tablets, USP

    20 mg

    Manufactured byManufactured for
    Apotex Inc.Apotex Corp.
    Toronto, OntarioWeston, Florida
    Canada M9L 1T933326

    Revision: 7

    Revised: June 2013

  • PATIENT INFORMATION

    Trospium Chloride Tablets, USP

    Read the Patient Information that comes with trospium chloride tablets before you start taking it and each time you get a refill. There may be new information. This leaflet does not take the place of talking with your doctor about your medical condition or your treatment. 

    What are trospium chloride tablets?

    Trospium chloride tablets are a prescription medicine used to treat adults with overactive bladder who have the following symptoms:

    • a strong need to urinate right away;
    • leaking or wetting accidents due to a strong need to urinate right away;
    • a need to urinate often.

    Who should not take trospium chloride tablets?

    Do not take trospium chloride tablets if you:

    • have trouble emptying your bladder;
    • have delayed or slow emptying of your stomach;
    • have an eye problem called “uncontrolled narrow-angle glaucoma”;
    • are allergic to trospium chloride tablets or any of its ingredients. See the end of this leaflet for a complete list of ingredients.

    Trospium chloride tablets have not been studied in children under the age of 18 years.

    What should I tell my doctor before starting trospium chloride tablets?

    Tell your doctor about all of your medical conditions including if you:

    • have any stomach or intestinal problems or problems with constipation;
    • have trouble emptying your bladder or have a weak urine stream;
    • have an eye problem called narrow-angle glaucoma;
    • have kidney problems;
    • have liver problems;
    • are pregnant or planning to become pregnant. It is not known if trospium chloride can harm your  unborn baby.
    • are breastfeeding. It is not known if trospium chloride passes into breast milk and if it can harm  your baby.

    You should talk to your doctor about the best way to feed your baby if you are taking trospium chloride tablets.

    Tell your doctor about all the medicines you take including prescription and nonprescription medicines, vitamins and herbal supplements. Trospium chloride tablets and certain other medicines can interact and make some side effects worse. Trospium chloride tablets can affect how other medicines are handled by the body.

    Know all the medicines you take. Keep a list of them with you to show your doctor and pharmacist each time you get a new medicine.

    How should I take trospium chloride tablets?

    Take trospium chloride tablets exactly as prescribed.

    • Take one trospium chloride tablet twice daily with water.
    • Take trospium chloride tablets on an empty stomach or at least 1 hour before a meal.
    • If you take too much trospium chloride, call your local Poison Control Center or go to an emergency room right away.

    What are the possible side effects of trospium chloride?

    Trospium chloride may cause allergic reactions that may be serious. Symptoms of a serious allergic reaction may include swelling of the face, lips, throat or tongue. If you experience these symptoms, you should stop taking trospium chloride tablets and get emergency medical help right away. 

    The most common side effects with trospium chloride tablets are:

    • dry mouth;
    • constipation;
    • headache.

     Trospium chloride tablets may cause other less common side effects, including:

    • trouble emptying the bladder;
    • blurred vision; and drowsiness. Do not drive or operate heavy machinery until you know how trospium chloride tablets affect you. Alcohol can worsen the drowsiness caused by drugs such as trospium chloride tablets.
    • heat prostration. Due to decreased sweating, heat prostration can occur when drugs such as trospium chloride tablets are used in a hot environment.

    Tell your doctor if you have any side effects that bother you or that do not go away. These are not all possible side effects of trospium chloride tablets. For more information, ask your doctor, healthcare professional or pharmacist.

    How should I store trospium chloride tablets?

    • Keep trospium chloride tablets and all other medicines out of the reach of children.
    • Store trospium chloride tablets at room temperature, 68° to 77°F (20° to 25°C).
    • Safely dispose of trospium chloride tablets that are out of date or that you no longer need.

    General information about trospium chloride tablets

    Medicines are sometimes prescribed for conditions that are not mentioned in patient information leaflets. Do not use trospium chloride tablets for a condition for which it was not prescribed. Do not give trospium chloride tablets to other people, even if they have the same symptoms you have. It may harm them. 

    This leaflet summarizes the most important information about trospium chloride tablets. If you would like more information, talk with your doctor. You can ask your doctor or pharmacist for information about trospium chloride tablets that is written for health professionals.

    What are the ingredients in trospium chloride tablets?

    Each tablet contains the following inactive ingredients: lactose monohydrate, microcrystalline cellulose, croscarmellose sodium, magnesium stearate, colloidal silicon dioxide, hypromellose, hydroxypropylcellulose, polyethylene glycol, titanium dioxide and yellow iron oxide. 

    APOTEX INC.

    Trospium Chloride Tablets, USP

    20 mg

    Manufactured byManufactured for
    Apotex Inc.Apotex Corp.
    Toronto, OntarioWeston, Florida
    Canada M9L 1T933326

    Revision: 7

    Revised: June 2013

  • PRINCIPAL DISPLAY PANEL

    APOTEX CORP. NDC: 60505-3454-6

    Trospium Chloride Tablets

    20 mg

    Rx

    60 bottle tablets

    trospium-chloride-20mg

  • INGREDIENTS AND APPEARANCE
    TROSPIUM CHLORIDE 
    trospium chloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 60505-3454
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Trospium Chloride (UNII: 1E6682427E) (Trospium - UNII:T4Y8ORK057) Trospium Chloride20 mg
    Product Characteristics
    ColorYELLOWScoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code APO;TR;20
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 60505-3454-660 in 1 BOTTLE; Type 0: Not a Combination Product10/15/2012
    2NDC: 60505-3454-5500 in 1 BOTTLE; Type 0: Not a Combination Product10/15/2012
    3NDC: 60505-3454-81000 in 1 BOTTLE; Type 0: Not a Combination Product10/15/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09151310/15/201205/31/2021
    Labeler - Apotex Corp. (845263701)
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