Warfarin Sodium by REMEDYREPACK INC. WARFARIN SODIUM tablet

Warfarin Sodium by

Drug Labeling and Warnings

Warfarin Sodium by is a Prescription medication manufactured, distributed, or labeled by REMEDYREPACK INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: BLEEDING RISK

    • Warfarin sodium can cause major or fatal bleeding [see Warnings and Precautions ( 5.1)] .
    • Perform regular monitoring of INR in all treated patients [see Dosage and Administration ( 2.1)] .
    • Drugs, dietary changes, and other factors affect INR levels achieved with warfarin sodium therapy [see Drug Interactions ( 7)] .
    • Instruct patients about prevention measures to minimize risk of bleeding and to report signs and symptoms of bleeding [see Patient Counseling Information ( 17)] .
  • 1 INDICATIONS AND USAGE

    Warfarin sodium tablets are indicated for:

    • Prophylaxis and treatment of venous thrombosis and its extension, pulmonary embolism (PE).
    • Prophylaxis and treatment of thromboembolic complications associated with atrial fibrillation (AF) and/or cardiac valve replacement.
    • Reduction in the risk of death, recurrent myocardial infarction (MI), and thromboembolic events such as stroke or systemic embolization after myocardial infarction.

    Limitations of Use

    Warfarin sodium tablets have no direct effect on an established thrombus, nor does it reverse ischemic tissue damage. Once a thrombus has occurred, however, the goals of anticoagulant treatment are to prevent further extension of the formed clot and to prevent secondary thromboembolic complications that may result in serious and possibly fatal sequelae.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Individualized Dosing

    The dosage and administration of warfarin sodium tablets must be individualized for each patient according to the patient’s International Normalized Ratio (INR) response to the drug. Adjust the dose based on the patient’s INR and the condition being treated. Consult the latest evidence-based clinical practice guidelines regarding the duration and intensity of anticoagulation for the indicated conditions.

    2.2 Recommended Target INR Ranges and Durations for Individual Indications

    An INR of greater than 4 appears to provide no additional therapeutic benefit in most patients and is associated with a higher risk of bleeding.

    Venous Thromboembolism (including deep venous thrombosis [DVT] and PE)

    Adjust the warfarin dose to maintain a target INR of 2.5 (INR range, 2 to 3) for all treatment durations. The duration of treatment is based on the indication as follows:

    • For patients with a DVT or PE secondary to a transient (reversible) risk factor, treatment with warfarin for 3 months is recommended.
    • For patients with an unprovoked DVT or PE, treatment with warfarin is recommended for at least 3 months. After 3 months of therapy, evaluate the risk-benefit ratio of long-term treatment for the individual patient.
    • For patients with two episodes of unprovoked DVT or PE, long-term treatment with warfarin is recommended. For a patient receiving long-term anticoagulant treatment, periodically reassess the risk-benefit ratio of continuing such treatment in the individual patient.

    Atrial Fibrillation

    In patients with non-valvular AF, anticoagulate with warfarin to target INR of 2.5 (range, 2 to 3).

    • In patients with non-valvular AF that is persistent or paroxysmal and at high risk of stroke (i.e., having any of the following features: prior ischemic stroke, transient ischemic attack, or systemic embolism, or 2 of the following risk factors: age greater than 75 years, moderately or severely impaired left ventricular systolic function and/or heart failure, history of hypertension, or diabetes mellitus), long-term anticoagulation with warfarin is recommended.
    • In patients with non-valvular AF that is persistent or paroxysmal and at an intermediate risk of ischemic stroke (i.e., having 1 of the following risk factors: age greater than 75 years, moderately or severely impaired left ventricular systolic function and/or heart failure, history of hypertension, or diabetes mellitus), long-term anticoagulation with warfarin is recommended.
    • For patients with AF and mitral stenosis, long-term anticoagulation with warfarin is recommended.
    • For patients with AF and prosthetic heart valves, long-term anticoagulation with warfarin is recommended; the target INR may be increased and aspirin added depending on valve type and position, and on patient factors.

    Mechanical and Bioprosthetic Heart Valves

    • For patients with a bileaflet mechanical valve or a Medtronic Hall (Minneapolis, MN) tilting disk valve in the aortic position who are in sinus rhythm and without left atrial enlargement, therapy with warfarin to a target INR of 2.5 (range, 2 to 3) is recommended.
    • For patients with tilting disk valves and bileaflet mechanical valves in the mitral position, therapy with warfarin to a target INR of 3 (range, 2.5 to 3.5) is recommended.
    • For patients with caged ball or caged disk valves, therapy with warfarin to a target INR of 3 (range, 2.5 to 3.5) is recommended.
    • For patients with a bioprosthetic valve in the mitral position, therapy with warfarin to a target INR of 2.5 (range, 2 to 3) for the first 3 months after valve insertion is recommended. If additional risk factors for thromboembolism are present (AF, previous thromboembolism, left ventricular dysfunction), a target INR of 2.5 (range 2 to 3) is recommended.

    Post-Myocardial Infarction

    • For high-risk patients with MI (e.g., those with a large anterior MI, those with significant heart failure, those with intracardiac thrombus visible on transthoracic echocardiography, those with AF, and those with a history of a thromboembolic event), therapy with combined moderate-intensity (INR, 2 to 3) warfarin plus low-dose aspirin (≤ 100 mg/day) for at least 3 months after the MI is recommended.

    Recurrent Systemic Embolism and Other Indications

    Oral anticoagulation therapy with warfarin has not been fully evaluated by clinical trials in patients with valvular disease associated with AF, patients with mitral stenosis, and patients with recurrent systemic embolism of unknown etiology. However, a moderate dose regimen (INR 2 to 3) may be used for these patients.

    2.3 Initial and Maintenance Dosing

    The appropriate initial dosing of warfarin sodium tablets varies widely for different patients. Not all factors responsible for warfarin dose variability are known, and the initial dose is influenced by:

    • Clinical factors including age, race, body weight, sex, concomitant medications, and comorbidities
    • Genetic factors (CYP2C9 and VKORC1 genotypes) [see Clinical Pharmacology ( 12.5)]

    Select the initial dose based on the expected maintenance dose, taking into account the above factors. Modify this dose based on consideration of patient-specific clinical factors. Consider lower initial and maintenance doses for elderly and/or debilitated patients and in Asian patients [see Use in Specific Populations ( 8.5) and Clinical Pharmacology ( 12.3)] . Routine use of loading doses is not recommended as this practice may increase hemorrhagic and other complications and does not offer more rapid protection against clot formation.

    Individualize the duration of therapy for each patient. In general, anticoagulant therapy should be continued until the danger of thrombosis and embolism has passed [see Dosage and Administration ( 2.2)] .

    Dosing Recommendations without Consideration of Genotype

    If the patient’s CYP2C9 and VKORC1 genotypes are not known, the initial dose of warfarin sodium tablets is usually 2 to 5 mg once daily. Determine each patient’s dosing needs by close monitoring of the INR response and consideration of the indication being treated. Typical maintenance doses are 2 to 10 mg once daily.

    Dosing Recommendations with Consideration of Genotype

    Table 1 displays three ranges of expected maintenance warfarin sodium tablets doses observed in subgroups of patients having different combinations of CYP2C9 and VKORC1 gene variants [see Clinical Pharmacology ( 12.5)] . If the patient’s CYP2C9 and/or VKORC1 genotype are known, consider these ranges in choosing the initial dose. Patients with CYP2C9 *1/*3, *2/*2, *2/*3, and *3/*3 may require more prolonged time (> 2 to 4 weeks) to achieve maximum INR effect for a given dosage regimen than patients without these CYP variants.

    Table 1: Three Ranges of Expected Maintenance Warfarin Sodium Tablets Daily Doses Based on CYP2C9 and VKORC1 Genotypes *
  • * Ranges are derived from multiple published clinical studies. VKORC1−1639G > A (rs9923231) variant is used in this table. Other co-inherited VKORC1 variants may also be important determinants of warfarin dose.
    		•
     

    VKORC1

    		 

    CYP2C9
     

    *1/*1

    		 

    *1/*2

    		 

    *1/*3

    		 

    *2/*2

    		 

    *2/*3

    		 

    *3/*3
     

    GG

    		 

    5 to 7 mg

    		 

    5 to 7 mg

    		 

    3 to 4 mg

    		 

    3 to 4 mg

    		 

    3 to 4 mg

    		 

    0.5 to 2 mg
     

    AG

    		 

    5 to 7 mg

    		 

    3 to 4 mg

    		 

    3 to 4 mg

    		 

    3 to 4 mg

    		 

    0.5 to 2 mg

    		 

    0.5 to 2 mg
     

    AA

    		 

    3 to 4 mg

    		 

    3 to 4 mg

    		 

    0.5 to 2 mg

    		 

    0.5 to 2 mg

    		 

    0.5 to 2 mg

    		 

    0.5 to 2 mg

    2.4 Monitoring to Achieve Optimal Anticoagulation

    Warfarin sodium tablets have a narrow therapeutic range (index), and their action may be affected by factors such as other drugs and dietary vitamin K. Therefore, anticoagulation must be carefully monitored during warfarin sodium tablets therapy. Determine the INR daily after the administration of the initial dose until INR results stabilize in the therapeutic range. After stabilization, maintain dosing within the therapeutic range by performing periodic INRs. The frequency of performing INR should be based on the clinical situation but generally acceptable intervals for INR determinations are 1 to 4 weeks. Perform additional INR tests when other warfarin products are interchanged with warfarin sodium tablets, as well as whenever other medications are initiated, discontinued, or taken irregularly. Heparin, a common concomitant drug, increases the INR [see Dosage and Administration ( 2.8) and Drug Interactions ( 7)] .

    Determinations of whole blood clotting and bleeding times are not effective measures for monitoring of warfarin sodium tablets therapy.

    2.5 Renal Impairment

    No dosage adjustment is necessary for patients with renal failure. Monitor INR more frequently in patients with compromised renal function to maintain INR within the therapeutic range [see Warnings and Precautions ( 5.4) and Use in Specific Populations ( 8.6)].

    2.6 Missed Dose

    The anticoagulant effect of warfarin sodium tablets persists beyond 24 hours. If a patient misses a dose of warfarin sodium tablets at the intended time of day, the patient should take the dose as soon as possible on the same day. The patient should not double the dose the next day to make up for a missed dose.

    2.7 Treatment During Dentistry and Surgery

    Some dental or surgical procedures may necessitate the interruption or change in the dose of warfarin sodium tablets therapy. Consider the benefits and risks when discontinuing warfarin sodium tablets even for a short period of time. Determine the INR immediately prior to any dental or surgical procedure. In patients undergoing minimally invasive procedures who must be anticoagulated prior to, during, or immediately following these procedures, adjusting the dosage of warfarin sodium tablets to maintain the INR at the low end of the therapeutic range may safely allow for continued anticoagulation.

    2.8 Conversion From Other Anticoagulants

    Heparin

    Since the full anticoagulant effect of warfarin sodium tablets is not achieved for several days, heparin is preferred for initial rapid anticoagulation. During initial therapy with warfarin sodium tablets, the interference with heparin anticoagulation is of minimal clinical significance. Conversion to warfarin sodium tablets may begin concomitantly with heparin therapy or may be delayed 3 to 6 days. To ensure therapeutic anticoagulation, continue full dose heparin therapy and overlap warfarin sodium tablets therapy with heparin for 4 to 5 days and until warfarin sodium tablets has produced the desired therapeutic response as determined by INR, at which point heparin may be discontinued.

    As heparin may affect the INR, patients receiving both heparin and warfarin sodium tablets should have INR monitoring at least:

    • 5 hours after the last intravenous bolus dose of heparin, or
    • 4 hours after cessation of a continuous intravenous infusion of heparin, or
    • 24 hours after the last subcutaneous heparin injection.

    Warfarin sodium tablets may increase the activated partial thromboplastin time (aPTT) test, even in the absence of heparin. A severe elevation (> 50 seconds) in aPTT with an INR in the desired range has been identified as an indication of increased risk of postoperative hemorrhage.

    Other Anticoagulants

    Consult the labeling of other anticoagulants for instructions on conversion to warfarin sodium tablets.

  • 3 DOSAGE FORMS AND STRENGTHS

    Warfarin Sodium Tablets USP, 1 mg are available as pink, capsule-shaped, biconvex scored tablets, debossed with TV/1 on the scored side and 1712 on the other side.

    Warfarin Sodium Tablets USP, 2 mg are available as lavender, capsule-shaped, biconvex scored tablets, debossed with TV/2 on the scored side and 1713 on the other side.

    Warfarin Sodium Tablets USP, 2.5 mg are available as green, capsule-shaped, biconvex scored tablets, debossed with TV/2 1/ 2 on the scored side and 1714 on the other side.

    Warfarin Sodium Tablets USP, 3 mg are available as tan, capsule-shaped, biconvex scored tablets, debossed with TV/3 on the scored side and 1715 on the other side.

    Warfarin Sodium Tablets USP, 4 mg are available as blue, capsule-shaped, biconvex scored tablets, debossed with TV/4 on the scored side and 1716 on the other side.

    Warfarin Sodium Tablets USP, 5 mg are available as peach, capsule-shaped, biconvex scored tablets, debossed with TV/5 on the scored side and 1721 on the other side.

    Warfarin Sodium Tablets USP, 6 mg are available as teal, capsule-shaped, biconvex scored tablets, debossed with TV/6 on the scored side and 1718 on the other side.

    Warfarin Sodium Tablets USP, 7.5 mg are available as yellow, capsule-shaped, biconvex scored tablets, debossed with TV/7 1/ 2 on the scored side and 1719 on the other side.

    Warfarin Sodium Tablets USP, 10 mg are available as white, capsule-shaped, biconvex scored tablets, debossed with TV/10 on the scored side and 1720 on the other side.

  • 4 CONTRAINDICATIONS

    Warfarin sodium is contraindicated in:

    • Pregnancy

    Warfarin sodium is contraindicated in women who are pregnant except in pregnant women with mechanical heart valves, who are at high risk of thromboembolism [see Warnings and Precautions ( 5.7) and Use in Specific Populations ( 8.1)] . Warfarin sodium can cause fetal harm when administered to a pregnant woman. Warfarin sodium exposure during pregnancy causes a recognized pattern of major congenital malformations (warfarin embryopathy and fetotoxicity), fatal fetal hemorrhage, and an increased risk of spontaneous abortion and fetal mortality. If warfarin sodium is used during pregnancy or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus [see Use in Specific Populations ( 8.1)] .

    Warfarin sodium is contraindicated in patients with:

    • Hemorrhagic tendencies or blood dyscrasias
    • Recent or contemplated surgery of the central nervous system or eye, or traumatic surgery resulting in large open surfaces [see Warnings and Precautions ( 5.8)]
    • Bleeding tendencies associated with:
    • − Active ulceration or overt bleeding of the gastrointestinal, genitourinary, or respiratory tract
      − Central nervous system hemorrhage
      − Cerebral aneurysms, dissecting aorta
      − Pericarditis and pericardial effusions
      − Bacterial endocarditis
    • Threatened abortion, eclampsia, and preeclampsia
    • Unsupervised patients with conditions associated with potential high level of non-compliance
    • Spinal puncture and other diagnostic or therapeutic procedures with potential for uncontrollable bleeding
    • Hypersensitivity to warfarin or to any other components of this product (e.g., anaphylaxis) [see Adverse Reactions ( 6)]
    • Major regional or lumbar block anesthesia
    • Malignant hypertension
  • 5 WARNINGS AND PRECAUTIONS

    The 7.5 mg tablets contain FD&C Yellow No. 5 (tartrazine), which may cause allergic-type reactions (including bronchial asthma) in certain susceptible individuals. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.

    5.1 Hemorrhage

    Warfarin sodium can cause major or fatal bleeding. Bleeding is more likely to occur within the first month. Risk factors for bleeding include high intensity of anticoagulation (INR > 4), age greater than or equal to 65, history of highly variable INRs, history of gastrointestinal bleeding, hypertension, cerebrovascular disease, anemia, malignancy, trauma, renal impairment, certain genetic factors [see Clinical Pharmacology ( 12.5)] , certain concomitant drugs [see Drug Interactions ( 7)] , and long duration of warfarin therapy.

    Perform regular monitoring of INR in all treated patients. Those at high risk of bleeding may benefit from more frequent INR monitoring, careful dose adjustment to desired INR, and a shortest duration of therapy appropriate for the clinical condition. However, maintenance of INR in the therapeutic range does not eliminate the risk of bleeding.

    Drugs, dietary changes, and other factors affect INR levels achieved with warfarin sodium therapy. Perform more frequent INR monitoring when starting or stopping other drugs, including botanicals, or when changing dosages of other drugs [see Drug Interactions ( 7)] .

    Instruct patients about prevention measures to minimize risk of bleeding and to report signs and symptoms of bleeding [see Patient Counseling Information ( 17)] .

    5.2 Tissue Necrosis

    Warfarin sodium can cause necrosis and/or gangrene of skin and other tissues, which is an uncommon but serious risk (<0.1%). Necrosis may be associated with local thrombosis and usually appears within a few days of the start of warfarin sodium therapy. In severe cases of necrosis, treatment through debridement or amputation of the affected tissue, limb, breast, or penis has been reported.

    Careful clinical evaluation is required to determine whether necrosis is caused by an underlying disease. Although various treatments have been attempted, no treatment for necrosis has been considered uniformly effective. Discontinue warfarin sodium therapy if necrosis occurs. Consider alternative drugs if continued anticoagulation therapy is necessary.

    5.3 Calciphylaxis

    Warfarin sodium can cause fatal and serious calciphylaxis or calcium uremic arteriolopathy, which has been reported in patients with and without end-stage renal disease. When calciphylaxis is diagnosed in these patients, discontinue warfarin sodium and treat calciphylaxis as appropriate. Consider alternative anticoagulation therapy.

    5.4 Acute Kidney Injury

    In patients with altered glomerular integrity or with a history of kidney disease, acute kidney injury may occur with warfarin sodium, possibly in relation to episodes of excessive anticoagulation and hematuria [see Use in Specific Populations ( 8.6)] . More frequent monitoring of anticoagulation is advised in patients with compromised renal function.

    5.5 Systemic Atheroemboli and Cholesterol Microemboli

    Anticoagulation therapy with warfarin sodium may enhance the release of atheromatous plaque emboli. Systemic atheroemboli and cholesterol microemboli can present with a variety of signs and symptoms depending on the site of embolization. The most commonly involved visceral organs are the kidneys followed by the pancreas, spleen, and liver. Some cases have progressed to necrosis or death. A distinct syndrome resulting from microemboli to the feet is known as “purple toes syndrome.” Discontinue warfarin sodium therapy if such phenomena are observed. Consider alternative drugs if continued anticoagulation therapy is necessary.

    5.6 Limb Ischemia, Necrosis, and Gangrene in Patients with HIT and HITTS

    Do not use warfarin sodium as initial therapy in patients with heparin-induced thrombocytopenia (HIT) and with heparin-induced thrombocytopenia with thrombosis syndrome (HITTS). Cases of limb ischemia, necrosis, and gangrene have occurred in patients with HIT and HITTS when heparin treatment was discontinued and warfarin therapy was started or continued. In some patients, sequelae have included amputation of the involved area and/or death. Treatment with warfarin sodium may be considered after the platelet count has normalized.

    5.7 Use in Pregnant Women with Mechanical Heart Valves

    Warfarin sodium can cause fetal harm when administered to a pregnant woman. While warfarin sodium is contraindicated during pregnancy, the potential benefits of using warfarin sodium may outweigh the risks for pregnant women with mechanical heart valves at high risk of thromboembolism. In those individual situations, the decision to initiate or continue warfarin sodium should be reviewed with the patient, taking into consideration the specific risks and benefits pertaining to the individual patient’s medical situation, as well as the most current medical guidelines. Warfarin sodium exposure during pregnancy causes a recognized pattern of major congenital malformations (warfarin embryopathy and fetotoxicity), fatal fetal hemorrhage, and an increased risk of spontaneous abortion and fetal mortality. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus [see Use in Specific Populations ( 8.1)] .

    5.8 Other Clinical Settings with Increased Risks

    In the following clinical settings, the risks of warfarin sodium therapy may be increased:

    • Moderate to severe hepatic impairment
    • Infectious diseases or disturbances of intestinal flora (e.g., sprue, antibiotic therapy)
    • Use of an indwelling catheter
    • Severe to moderate hypertension
    • Deficiency in protein C-mediated anticoagulant response: Warfarin sodium reduces the synthesis of the naturally occurring anticoagulants, protein C and protein S. Hereditary or acquired deficiencies of protein C or its cofactor, protein S, have been associated with tissue necrosis following warfarin administration. Concomitant anticoagulation therapy with heparin for 5 to 7 days during initiation of therapy with warfarin sodium may minimize the incidence of tissue necrosis in these patients.
    • Eye surgery: In cataract surgery, warfarin sodium use was associated with a significant increase in minor complications of sharp needle and local anesthesia block but not associated with potentially sight-threatening operative hemorrhagic complications. As warfarin sodium cessation or reduction may lead to serious thromboembolic complications, the decision to discontinue warfarin sodium before a relatively less invasive and complex eye surgery, such as lens surgery, should be based upon the risks of anticoagulant therapy weighed against the benefits.
    • Polycythemia vera
    • Vasculitis
    • Diabetes mellitus

    5.9 Endogenous Factors Affecting INR

    The following factors may be responsible for increased INR response: diarrhea, hepatic disorders, poor nutritional state, steatorrhea, or vitamin K deficiency.

    The following factors may be responsible for decreased INR response: increased vitamin K intake or hereditary warfarin resistance.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions to warfarin sodium are discussed in greater detail in other sections of the labeling:

    • Hemorrhage [see Boxed Warning, Warnings and Precautions (5.1), and Overdosage ( 10)]
    • Tissue Necrosis [see Warnings and Precautions ( 5.2)]
    • Calciphylaxis [see Warnings and Precautions ( 5.3)]
    • Acute Kidney Injury [see Warnings and Precautions ( 5.4)]
    • Systemic Atheroemboli and Cholesterol Microemboli [see Warnings and Precautions ( 5.5)]
    • Limb Ischemia, Necrosis, and Gangrene in Patients with HIT and HITTS [see Warnings and Precautions ( 5.6)]
    • Other Clinical Settings with Increased Risks [see Warnings and Precautions ( 5.8)]

    Other adverse reactions to warfarin sodium include:

    • Immune system disorders: hypersensitivity/allergic reactions (including urticaria and anaphylactic reactions)
    • Vascular disorders: vasculitis
    • Hepatobiliary disorders: hepatitis, elevated liver enzymes. Cholestatic hepatitis has been associated with concomitant administration of warfarin sodium and ticlopidine.
    • Gastrointestinal disorders: nausea, vomiting, diarrhea, taste perversion, abdominal pain, flatulence, bloating
    • Skin disorders: rash, dermatitis (including bullous eruptions), pruritus, alopecia
    • Respiratory disorders: tracheal or tracheobronchial calcification
    • General disorders: chills
  • 7 DRUG INTERACTIONS

    7.1 General Information

    Drugs may interact with warfarin sodium through pharmacodynamic or pharmacokinetic mechanisms. Pharmacodynamic mechanisms for drug interactions with warfarin sodium are synergism (impaired hemostasis, reduced clotting factor synthesis), competitive antagonism (vitamin K), and alteration of the physiologic control loop for vitamin K metabolism (hereditary resistance). Pharmacokinetic mechanisms for drug interactions with warfarin sodium are mainly enzyme induction, enzyme inhibition, and reduced plasma protein binding. It is important to note that some drugs may interact by more than one mechanism.

    More frequent INR monitoring should be performed when starting or stopping other drugs, including botanicals, or when changing dosages of other drugs, including drugs intended for short-term use (e.g., antibiotics, antifungals, corticosteroids) [ see Boxed Warning].

    Consult the labeling of all concurrently used drugs to obtain further information about interactions with warfarin sodium or adverse reactions pertaining to bleeding.

    7.2 CYP450 Interactions

    CYP450 isozymes involved in the metabolism of warfarin include CYP2C9, 2C19, 2C8, 2C18, 1A2, and 3A4. The more potent warfarin S-enantiomer is metabolized by CYP2C9 while the R-enantiomer is metabolized by CYP1A2 and 3A4.

    • Inhibitors of CYP2C9, 1A2, and/or 3A4 have the potential to increase the effect (increase INR) of warfarin by increasing the exposure of warfarin.
    • Inducers of CYP2C9, 1A2, and/or 3A4 have the potential to decrease the effect (decrease INR) of warfarin by decreasing the exposure of warfarin.

    Examples of inhibitors and inducers of CYP2C9, 1A2, and 3A4 are below in Table 2; however, this list should not be considered all-inclusive. Consult the labeling of all concurrently used drugs to obtain further information about CYP450 interaction potential. The CYP450 inhibition and induction potential should be considered when starting, stopping, or changing dose of concomitant medications. Closely monitor INR if a concomitant drug is a CYP2C9, 1A2, and/or 3A4 inhibitor or inducer.

    Table 2: Examples of CYP450 Interactions with Warfarin

     

    Enzyme

    		 

    Inhibitors

    		 

    Inducers

     

    CYP2C9

    		 

    amiodarone, capecitabine, cotrimoxazole, etravirine, fluconazole, fluvastatin, fluvoxamine, metronidazole, miconazole, oxandrolone, sulfinpyrazone, tigecycline, voriconazole, zafirlukast

    		 

    aprepitant, bosentan, carbamazepine, phenobarbital, rifampin

     

    CYP1A2

    		 

    acyclovir, allopurinol, caffeine, cimetidine, ciprofloxacin, disulfiram, enoxacin, famotidine, fluvoxamine, methoxsalen, mexiletine, norfloxacin, oral contraceptives, phenylpropanolamine, propafenone, propranolol, terbinafine, thiabendazole, ticlopidine, verapamil, zileuton

    		 

    montelukast, moricizine, omeprazole, phenobarbital, phenytoin, cigarette smoking

     

    CYP3A4

    		 

    alprazolam, amiodarone, amlodipine, amprenavir, aprepitant, atorvastatin, atazanavir, bicalutamide, cilostazol, cimetidine, ciprofloxacin, clarithromycin, conivaptan, cyclosporine, darunavir/ritonavir, diltiazem, erythromycin, fluconazole, fluoxetine, fluvoxamine, fosamprenavir, imatinib, indinavir, isoniazid, itraconazole, ketoconazole, lopinavir/ritonavir, nefazodone, nelfinavir, nilotinib, oral contraceptives, posaconazole, ranitidine, ranolazine, ritonavir, saquinavir, telithromycin, tipranavir, voriconazole, zileuton

    		 

    armodafinil, amprenavir, aprepitant, bosentan, carbamazepine, efavirenz, etravirine, modafinil, nafcillin, phenytoin, pioglitazone, prednisone, rifampin, rufinamide

    7.3 Drugs that Increase Bleeding Risk

    Examples of drugs known to increase the risk of bleeding are presented in Table 3. Because bleeding risk is increased when these drugs are used concomitantly with warfarin, closely monitor patients receiving any such drug with warfarin.

    Table 3: Drugs that Can Increase the Risk of Bleeding

     

    Drug Class

    		 

    Specific Drugs

     

    Anticoagulants

    		 

    argatroban, dabigatran, bivalirudin, desirudin, heparin, lepirudin

     

    Antiplatelet Agents

    		 

    aspirin, cilostazol, clopidogrel, dipyridamole, prasugrel, ticlopidine

     

    Non-steroidal Anti-Inflammatory Agents

    		 

    celecoxib, diclofenac, diflunisal, fenoprofen, ibuprofen, indomethacin, ketoprofen, ketorolac, mefenamic acid, naproxen, oxaprozin, piroxicam, sulindac

     

    Serotonin Reuptake Inhibitors

    		 

    citalopram, desvenlafaxine, duloxetine, escitalopram, fluoxetine, fluvoxamine, milnacipran, paroxetine, sertraline, venlafaxine, vilazodone

    7.4 Antibiotics and Antifungals

    There have been reports of changes in INR in patients taking warfarin and antibiotics or antifungals, but clinical pharmacokinetic studies have not shown consistent effects of these agents on plasma concentrations of warfarin.

    Closely monitor INR when starting or stopping any antibiotic or antifungal in patients taking warfarin.

    7.5 Botanical (Herbal) Products and Foods

    More frequent INR monitoring should be performed when starting or stopping botanicals.

    Few adequate, well-controlled studies evaluating the potential for metabolic and/or pharmacologic interactions between botanicals and warfarin sodium exist. Due to a lack of manufacturing standardization with botanical medicinal preparations, the amount of active ingredients may vary. This could further confound the ability to assess potential interactions and effects on anticoagulation.

    Some botanicals may cause bleeding events when taken alone (e.g., garlic and Ginkgo biloba) and may have anticoagulant, antiplatelet, and/or fibrinolytic properties. These effects would be expected to be additive to the anticoagulant effects of warfarin sodium. Conversely, some botanicals may decrease the effects of warfarin sodium (e.g., co-enzyme Q 10, St. John’s wort, ginseng). Some botanicals and foods can interact with warfarin sodium through CYP450 interactions (e.g., echinacea, grapefruit juice, ginkgo, goldenseal, St. John’s wort).

    The amount of vitamin K in food may affect therapy with warfarin sodium. Advise patients taking warfarin sodium to eat a normal, balanced diet maintaining a consistent amount of vitamin K. Patients taking warfarin sodium should avoid drastic changes in dietary habits, such as eating large amounts of green leafy vegetables.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Warfarin sodium is contraindicated in women who are pregnant except in pregnant women with mechanical heart valves, who are at high risk of thromboembolism, and for whom the benefits of warfarin sodium may outweigh the risks [see Warnings and Precautions ( 5.7)] . Warfarin sodium can cause fetal harm. Exposure to warfarin during the first trimester of pregnancy caused a pattern of congenital malformations in about 5% of exposed offspring. Because these data were not collected in adequate and well-controlled studies, this incidence of major birth defects is not an adequate basis for comparison to the estimated incidences in the control group or the U.S. general population and may not reflect the incidences observed in practice. Consider the benefits and risks of warfarin sodium and possible risks to the fetus when prescribing warfarin sodium to a pregnant woman.

    Adverse outcomes in pregnancy occur regardless of the health of the mother or the use of medications. The estimated background risk of major birth defects and 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% to 4% and 15% to 20%, respectively.

    Clinical Considerations

    Fetal/Neonatal Adverse Reactions

    In humans, warfarin crosses the placenta, and concentrations in fetal plasma approach the maternal values. Exposure to warfarin during the first trimester of pregnancy caused a pattern of congenital malformations in about 5% of exposed offspring. Warfarin embryopathy is characterized by nasal hypoplasia with or without stippled epiphyses (chondrodysplasia punctata) and growth retardation (including low birth weight). Central nervous system and eye abnormalities have also been reported, including dorsal midline dysplasia characterized by agenesis of the corpus callosum, Dandy-Walker malformation, midline cerebellar atrophy, and ventral midline dysplasia characterized by optic atrophy. Mental retardation, blindness, schizencephaly, microcephaly, hydrocephalus, and other adverse pregnancy outcomes have been reported following warfarin exposure during the second and third trimesters of pregnancy [see Contraindications ( 4)] .

    8.2 Lactation

    Risk Summary

    Warfarin was not present in human milk from mothers treated with warfarin from a limited published study. Because of the potential for serious adverse reactions, including bleeding in a breastfed infant, consider the developmental and health benefits of breastfeeding along with the mother’s clinical need for warfarin sodium and any potential adverse effects on the breastfed infant from warfarin sodium or from the underlying maternal condition before prescribing warfarin sodium to a lactating woman.

    Clinical Considerations

    Monitor breastfeeding infants for bruising or bleeding.

    Data

    Human Data

    Based on published data in 15 nursing mothers, warfarin was not detected in human milk. Among the 15 full-term newborns, 6 nursing infants had documented prothrombin times within the expected range. Prothrombin times were not obtained for the other 9 nursing infants. Effects in premature infants have not been evaluated.

    8.3 Females and Males of Reproductive Potential

    Pregnancy Testing

    Warfarin sodium can cause fetal harm [see Use in Specific Populations ( 8.1)] .

    Verify the pregnancy status of females of reproductive potential prior to initiating warfarin sodium therapy.

    Contraception

    Females

    Advise females of reproductive potential to use effective contraception during treatment and for at least 1 month after the final dose of warfarin sodium.

    8.4 Pediatric Use

    Adequate and well-controlled studies with warfarin sodium have not been conducted in any pediatric population, and the optimum dosing, safety, and efficacy in pediatric patients is unknown. Pediatric use of warfarin sodium is based on adult data and recommendations, and available limited pediatric data from observational studies and patient registries. Pediatric patients administered warfarin sodium should avoid any activity or sport that may result in traumatic injury.

    The developing hemostatic system in infants and children results in a changing physiology of thrombosis and response to anticoagulants. Dosing of warfarin in the pediatric population varies by patient age, with infants generally having the highest, and adolescents having the lowest milligram per kilogram dose requirements to maintain target INRs. Because of changing warfarin requirements due to age, concomitant medications, diet, and existing medical condition, target INR ranges may be difficult to achieve and maintain in pediatric patients, and more frequent INR determinations are recommended. Bleeding rates varied by patient population and clinical care center in pediatric observational studies and patient registries.

    Infants and children receiving vitamin K-supplemented nutrition, including infant formulas, may be resistant to warfarin therapy, while human milk-fed infants may be sensitive to warfarin therapy.

    8.5 Geriatric Use

    Of the total number of patients receiving warfarin sodium in controlled clinical trials for which data were available for analysis, 1885 patients (24.4%) were 65 years and older, while 185 patients (2.4%) were 75 years and older. No overall differences in effectiveness or safety were observed between these patients and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

    Patients 60 years or older appear to exhibit greater than expected INR response to the anticoagulant effects of warfarin [see Clinical Pharmacology ( 12.3)] . Warfarin sodium is contraindicated in any unsupervised patient with senility. Conduct more frequent monitoring for bleeding with administration of warfarin sodium to elderly patients in any situation or with any physical condition where added risk of hemorrhage is present. Consider lower initiation and maintenance doses of warfarin sodium in elderly patients [see Dosage and Administration ( 2.2, 2.3)] .

    8.6 Renal Impairment

    Renal clearance is considered to be a minor determinant of anticoagulant response to warfarin. No dosage adjustment is necessary for patients with renal impairment. Instruct patients with renal impairment taking warfarin to monitor their INR more frequently [see Warnings and Precautions ( 5.4)] .

    8.7 Hepatic Impairment

    Hepatic impairment can potentiate the response to warfarin through impaired synthesis of clotting factors and decreased metabolism of warfarin. Conduct more frequent monitoring for bleeding when using warfarin sodium in these patients.

  • 10 OVERDOSAGE

    10.1 Signs and Symptoms

    Bleeding (e.g., appearance of blood in stools or urine, hematuria, excessive menstrual bleeding, melena, petechiae, excessive bruising or persistent oozing from superficial injuries, unexplained fall in hemoglobin) is a manifestation of excessive anticoagulation.

    10.2 Treatment

    The treatment of excessive anticoagulation is based on the level of the INR, the presence or absence of bleeding, and clinical circumstances. Reversal of warfarin sodium anticoagulation may be obtained by discontinuing warfarin sodium therapy and, if necessary, by administration of oral or parenteral vitamin K 1.

    The use of vitamin K 1 reduces response to subsequent warfarin sodium therapy and patients may return to a pretreatment thrombotic status following the rapid reversal of a prolonged INR. Resumption of warfarin sodium administration reverses the effect of vitamin K, and a therapeutic INR can again be obtained by careful dosage adjustment. If rapid re-anticoagulation is indicated, heparin may be preferable for initial therapy.

    Prothrombin complex concentrate (PCC), fresh frozen plasma, or activated Factor VII treatment may be considered if the requirement to reverse the effects of warfarin sodium is urgent. A risk of hepatitis and other viral diseases is associated with the use of blood products; PCC and activated Factor VII are also associated with an increased risk of thrombosis. Therefore, these preparations should be used only in exceptional or life-threatening bleeding episodes secondary to warfarin sodium overdosage.

  • 11 DESCRIPTION

    Warfarin sodium tablets USP contain warfarin sodium, an anticoagulant that acts by inhibiting vitamin K-dependent coagulation factors. The chemical name of warfarin sodium is 3-(α-acetonylbenzyl)-4-hydroxycoumarin sodium salt, which is a racemic mixture of the R- and S-enantiomers. Crystalline warfarin sodium is an isopropanol clathrate. Its structural formula may be represented as follows:

    C 19H 15NaO 4 M.W. 330.31

    Crystalline warfarin sodium occurs as a white, odorless, crystalline powder that is discolored by light. It is very soluble in water, freely soluble in alcohol, and very slightly soluble in chloroform and ether.

    Each tablet, for oral administration, contains 1 mg, 2 mg, 2.5 mg, 3 mg, 4 mg, 5 mg, 6 mg, 7.5 mg or 10 mg warfarin sodium, USP. In addition, each tablet contains the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate, magnesium stearate, and microcrystalline cellulose.



    The 1 mg also contains FD&C red no. 40.



    The 2 mg also contains FD&C blue no. 2 aluminum lake and FD&C red no. 40 aluminum lake.



    The 2.5 mg also contains D&C yellow no. 10 aluminum lake and FD&C blue no. 1 aluminum lake.



    The 3 mg also contains FD&C yellow no. 6 aluminum lake, FD&C blue no. 2 aluminum lake, FD&C red no. 40 aluminum lake, and D&C yellow no. 10 aluminum lake.



    The 4 mg also contains FD&C blue no. 1 aluminum lake and FD&C blue no. 2 aluminum lake.



    The 5 mg also contains FD&C yellow no. 6 aluminum lake, FD&C red no. 40 aluminum lake and D&C yellow no. 10 aluminum lake.



    The 6 mg also contains D&C yellow no. 10 aluminum lake and FD&C blue no. 1 aluminum lake.



    The 7.5 mg also contains FD&C yellow no. 5 (tartrazine) aluminum lake and FD&C red no. 40 aluminum lake.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Warfarin acts by inhibiting the synthesis of vitamin K-dependent clotting factors, which include Factors II, VII, IX, and X, and the anticoagulant proteins C and S. Vitamin K is an essential cofactor for the post ribosomal synthesis of the vitamin K-dependent clotting factors. Vitamin K promotes the biosynthesis of γ-carboxyglutamic acid residues in the proteins that are essential for biological activity. Warfarin is thought to interfere with clotting factor synthesis by inhibition of the C1 subunit of vitamin K epoxide reductase (VKORC1) enzyme complex, thereby reducing the regeneration of vitamin K 1 epoxide [see Clinical Pharmacology ( 12.5)] .

    12.2 Pharmacodynamics

    An anticoagulation effect generally occurs within 24 hours after warfarin administration. However, peak anticoagulant effect may be delayed 72 to 96 hours. The duration of action of a single dose of racemic warfarin is 2 to 5 days. The effects of warfarin sodium may become more pronounced as effects of daily maintenance doses overlap. This is consistent with the half-lives of the affected vitamin K-dependent clotting factors and anticoagulation proteins: Factor II - 60 hours, VII - 4 to 6 hours, IX - 24 hours, X - 48 to 72 hours, and proteins C and S are approximately 8 hours and 30 hours, respectively.

    12.3 Pharmacokinetics

    Warfarin sodium is a racemic mixture of the R- and S-enantiomers of warfarin. The S-enantiomer exhibits 2 to 5 times more anticoagulant activity than the R-enantiomer in humans, but generally has a more rapid clearance.

    Absorption

    Warfarin is essentially completely absorbed after oral administration, with peak concentration generally attained within the first 4 hours.

    Distribution

    Warfarin shows a volume of distribution of about 0.14 L/kg. Approximately 99% of the drug is bound to plasma proteins.

    Metabolism

    The elimination of warfarin is almost entirely by metabolism. Warfarin is stereoselectively metabolized by hepatic cytochrome P-450 (CYP450) microsomal enzymes to inactive hydroxylated metabolites (predominant route) and by reductases to reduced metabolites (warfarin alcohols) with minimal anticoagulant activity. Identified metabolites of warfarin include dehydrowarfarin, two diastereoisomer alcohols, and 4′-, 6-, 7-, 8-, and 10- hydroxywarfarin. The CYP450 isozymes involved in the metabolism of warfarin include CYP2C9, 2C19, 2C8, 2C18, 1A2, and 3A4. CYP2C9, a polymorphic enzyme, is likely to be the principal form of human liver CYP450 that modulates the in vivo anticoagulant activity of warfarin. Patients with one or more variant CYP2C9 alleles have decreased S-warfarin clearance [see Clinical Pharmacology ( 12.5)] .

    Excretion

    The terminal half-life of warfarin after a single dose is approximately 1 week; however, the effective half-life ranges from 20 to 60 hours, with a mean of about 40 hours. The clearance of R-warfarin is generally half that of S-warfarin, thus as the volumes of distribution are similar, the half-life of R-warfarin is longer than that of S-warfarin. The half-life of R-warfarin ranges from 37 to 89 hours, while that of S-warfarin ranges from 21 to 43 hours. Studies with radiolabeled drug have demonstrated that up to 92% of the orally administered dose is recovered in urine. Very little warfarin is excreted unchanged in urine. Urinary excretion is in the form of metabolites.

    Geriatric Patients

    Patients 60 years or older appear to exhibit greater than expected INR response to the anticoagulant effects of warfarin. The cause of the increased sensitivity to the anticoagulant effects of warfarin in this age group is unknown but may be due to a combination of pharmacokinetic and pharmacodynamic factors. Limited information suggests there is no difference in the clearance of S-warfarin; however, there may be a slight decrease in the clearance of R-warfarin in the elderly as compared to the young. Therefore, as patient age increases, a lower dose of warfarin is usually required to produce a therapeutic level of anticoagulation [see Dosage and Administration ( 2.3, 2.4)].

    Asian Patients

    Asian patients may require lower initiation and maintenance doses of warfarin. A non-controlled study of 151 Chinese outpatients stabilized on warfarin for various indications reported a mean daily warfarin requirement of 3.3 ± 1.4 mg to achieve an INR of 2 to 2.5. Patient age was the most important determinant of warfarin requirement in these patients, with a progressively lower warfarin requirement with increasing age.

    12.5 Pharmacogenomics

    CYP2C9 and VKORC1 Polymorphisms

    The S-enantiomer of warfarin is mainly metabolized to 7-hydroxywarfarin by CYP2C9, a polymorphic enzyme. The variant alleles, CYP2C9*2 and CYP2C9*3, result in decreased in vitro CYP2C9 enzymatic 7-hydroxylation of S-warfarin. The frequencies of these alleles in Caucasians are approximately 11% and 7% for CYP2C9*2 and CYP2C9*3, respectively.

    Other CYP2C9 alleles associated with reduced enzymatic activity occur at lower frequencies, including *5, *6, and *11 alleles in populations of African ancestry and *5, *9, and *11 alleles in Caucasians.

    Warfarin reduces the regeneration of vitamin K from vitamin K epoxide in the vitamin K cycle through inhibition of VKOR, a multiprotein enzyme complex. Certain single nucleotide polymorphisms in the VKORC1 gene (e.g., –1639G > A) have been associated with variable warfarin dose requirements. VKORC1 and CYP2C9 gene variants generally explain the largest proportion of known variability in warfarin dose requirements.

    CYP2C9 and VKORC1 genotype information, when available, can assist in selection of the initial dose of warfarin [see Dosage and Administration ( 2.3)] .

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenicity, mutagenicity, or fertility studies have not been performed with warfarin.

  • 14 CLINICAL STUDIES

    14.1 Atrial Fibrillation

    In five prospective, randomized, controlled clinical trials involving 3711 patients with non-rheumatic AF, warfarin significantly reduced the risk of systemic thromboembolism including stroke (see Table 4). The risk reduction ranged from 60% to 86% in all except one trial (CAFA: 45%), which was stopped early due to published positive results from two of these trials. The incidence of major bleeding in these trials ranged from 0.6% to 2.7% (see Table 4).

    Table 4: Clinical Studies of Warfarin in Non-Rheumatic AF Patients *
  • * All study results of warfarin vs. control are based on intention-to-treat analysis and include ischemic stroke and systemic thromboembolism, excluding hemorrhagic stroke and transient ischemic attacks.
    		•
      

    N

    		   

    Thromboembolism

    		 

    % Major Bleeding
     

    Study

    		 

    Warfarin-Treated

    Patients

    		 

    Control Patients

    		 

    PT Ratio

    		 

    INR

    		 

    % Risk Reduction

    		 

    p-value

    		 

    Warfarin-Treated

    Patients

    		 

    Control Patients
     

    AFASAK

    		 

    335

    		 

    336

    		 

    1.5 to 2

    		 

    2.8 to 4.2

    		 

    60

    		 

    0.027

    		 

    0.6

    		 

    0
     

    SPAF

    		 

    210

    		 

    211

    		 

    1.3 to 1.8

    		 

    2 to 4.5

    		 

    67

    		 

    0.01

    		 

    1.9

    		 

    1.9
     

    BAATAF

    		 

    212

    		 

    208

    		 

    1.2 to 1.5

    		 

    1.5 to 2.7

    		 

    86

    		 

    < 0.05

    		 

    0.9

    		 

    0.5
     

    CAFA

    		 

    187

    		 

    191

    		 

    1.3 to 1.6

    		 

    2 to 3

    		 

    45

    		 

    0.25

    		 

    2.7

    		 

    0.5
     

    SPINAF

    		 

    260

    		 

    265

    		 

    1.2 to 1.5

    		 

    1.4 to 2.8

    		 

    79

    		 

    0.001

    		 

    2.3

    		 

    1.5

    Trials in patients with both AF and mitral stenosis suggest a benefit from anticoagulation with warfarin sodium [see Dosage and Administration ( 2.2)] .

    14.2 Mechanical and Bioprosthetic Heart Valves

    In a prospective, randomized, open-label, positive-controlled study in 254 patients with mechanical prosthetic heart valves, the thromboembolic-free interval was found to be significantly greater in patients treated with warfarin alone compared with dipyridamole/aspirin-treated patients (p < 0.005) and pentoxifylline/aspirin-treated patients (p < 0.05). The results of this study are presented in Table 5.

    Table 5: Prospective, Randomized, Open-Label, Positive-Controlled Clinical Study of Warfarin in Patients with Mechanical Prosthetic Heart Valves

      

    Patients Treated With

      

    Warfarin

    		 

    Dipyridamole/Aspirin

    		 

    Pentoxifylline/Aspirin
     

    Event

    		   
     

    Thromboembolism

    		 

    2.2/100 py

    		 

    8.6/100 py

    		 

    7.9/100 py

     

    Major Bleeding

    		 

    2.5/100 py

    		 

    0/100 py

    		 

    0.9/100 py

    py = patient years

    In a prospective, open-label, clinical study comparing moderate (INR 2.65) versus high intensity (INR 9) warfarin therapies in 258 patients with mechanical prosthetic heart valves, thromboembolism occurred with similar frequency in the two groups (4 and 3.7 events per 100 patient years, respectively). Major bleeding was more common in the high intensity group. The results of this study are presented in Table 6.

    Table 6: Prospective, Open-Label Clinical Study of Warfarin in Patients with Mechanical Prosthetic Heart Valves

     

    Event

    		 

    Moderate Warfarin Therapy

    INR 2.65

    		 

    High Intensity Warfarin Therapy

    INR 9

     

    Thromboembolism

    		 

    4/100 py

    		 

    3.7/100 py

     

    Major Bleeding

    		 

    0.95/100 py

    		 

    2.1/100 py

    py = patient years

    In a randomized trial in 210 patients comparing two intensities of warfarin therapy (INR 2 to 2.25 vs. INR 2.5 to 4) for a three month period following tissue heart valve replacement, thromboembolism occurred with similar frequency in the two groups (major embolic events 2% vs. 1.9%, respectively, and minor embolic events 10.8% vs. 10.2%, respectively). Major hemorrhages occurred in 4.6% of patients in the higher intensity INR group compared to zero in the lower intensity INR group.

    14.3 Myocardial Infarction

    WARIS (The Warfarin Re-Infarction Study) was a double-blind, randomized study of 1214 patients 2 to 4 weeks post-infarction treated with warfarin to a target INR of 2.8 to 4.8. The primary endpoint was a composite of total mortality and recurrent infarction. A secondary endpoint of cerebrovascular events was assessed. Mean follow-up of the patients was 37 months. The results for each endpoint separately, including an analysis of vascular death, are provided in Table 7.

    Table 7: WARIS – Endpoint Analysis of Separate Events

        

    % Risk
      

    Warfarin

    		 

    Placebo

    		  

    Reduction
     

    Event

    		 

    (N = 607)

    		 

    (N = 607)

    		 

    RR (95% CI)

    		 

    ( p-value)

     

    Total Patient Years of Follow-up

    		 

    2018

    		 

    1944

    		  
     

    Total Mortality

    		 

    94 (4.7/100 py)

    		 

    123 (6.3/100 py)

    		 

    0.76 (0.60, 0.97)

    		 

    24 (p = 0.030)
     

    Vascular Death

    		 

    82 (4.1/100 py)

    		 

    105 (5.4/100 py)

    		 

    0.78 (0.60, 1.02)

    		 

    22 (p = 0.068)
     

    Recurrent MI

    		 

    82 (4.1/100 py)

    		 

    124 (6.4/100 py)

    		 

    0.66 (0.51, 0.85)

    		 

    34 (p = 0.001)
     

    Cerebrovascular Event

    		 

    20 (1/100 py)

    		 

    44 (2.3/100 py)

    		 

    0.46 (0.28, 0.75)

    		 

    54 (p = 0.002)

    RR = Relative risk; Risk reduction = (1 - RR); CI = Confidence interval; MI = Myocardial infarction; py = patient years

    WARIS II (The Warfarin, Aspirin, Re-Infarction Study) was an open-label, randomized study of 3630 patients hospitalized for acute myocardial infarction treated with warfarin to a target INR 2.8 to 4.2, aspirin 160 mg per day, or warfarin to a target INR 2 to 2.5 plus aspirin 75 mg per day prior to hospital discharge. The primary endpoint was a composite of death, nonfatal reinfarction, or thromboembolic stroke. The mean duration of observation was approximately 4 years. The results for WARIS II are provided in Table 8.

    Table 8: WARIS II – Distribution of Events According to Treatment Group

  • * Major bleeding episodes were defined as nonfatal cerebral hemorrhage or bleeding necessitating surgical intervention or blood transfusion.
  • † The rate ratio is for aspirin plus warfarin as compared with aspirin.
  • ‡ The rate ratio is for warfarin as compared with aspirin.
  • § Minor bleeding episodes were defined as non-cerebral hemorrhage not necessitating surgical intervention or blood transfusion.
  • Includes death, nonfatal reinfarction, and thromboembolic cerebral stroke.
    		•
     

    Event

    		 

    Aspirin

    (N = 1206)

    		 

    Warfarin

    (N = 1216)

    		 

    Aspirin plus Warfarin

    (N = 1208)

    		 

    Rate Ratio

    (95% CI)

    		 

    p-value

      

    No. of Events

    		 
     

    Major Bleeding *

    		 

    8

    		 

    33

    		 

    28

    		 

    3.35 † (ND)

    		 

    ND
        

    4 ‡ (ND)

    		 

    ND
     

    Minor Bleeding §

    		 

    39

    		 

    103

    		 

    133

    		 

    3.21 † (ND)

    		 

    ND
        

    2.55 ‡ (ND)

    		 

    ND
     

    Composite Endpoints

    		 

    241

    		 

    203

    		 

    181

    		 

    0.81 (0.69 to 0.95) †

    		 

    0.03
        

    0.71 (0.60 to 0.83) ‡

    		 

    0.001
     

    Reinfarction

    		 

    117

    		 

    90

    		 

    69

    		 

    0.56 (0.41 to 0.78) †

    		 

    < 0.001
        

    0.74 (0.55 to 0.98) ‡

    		 

    0.03
     

    Thromboembolic

    Stroke

    		 

    32

    		 

    17

    		 

    17

    		 

    0.52 (0.28 to 0.98) †

    		 

    0.03
        

    0.52 (0.28 to 0.97) ‡

    		 

    0.03
     

    Death

    		 

    92

    		 

    96

    		 

    95

    		  

    0.82

    CI = confidence interval

    ND = not determined

    There were approximately four times as many major bleeding episodes in the two groups receiving warfarin than in the group receiving aspirin alone. Major bleeding episodes were not more frequent among patients receiving aspirin plus warfarin than among those receiving warfarin alone, but the incidence of minor bleeding episodes was higher in the combined therapy group.

  • 15 REFERENCES

    OSHA Hazardous Drugs. OSHA. http://www.osha.gov/SLTC/hazardousdrugs/index.html.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Warfarin Sodium Tablets USP, 6 mg are available as teal, capsule-shaped, biconvex scored tablets, debossed with TV/6 on the scored side and 1718 on the other side containing 6 mg warfarin sodium, USP, packaged in

    NDC: 70518-0261-0 30 in 1 BLISTER PACK

    Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).

    Protect from light. Keep tightly closed.

    Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

    Special Handling

    Procedures for proper handling and disposal of potentially hazardous drugs should be considered. Guidelines on this subject have been published [see References ( 15)] .

    Pharmacy and clinical personnel who are pregnant should avoid exposure to crushed or broken tablets [see Use in Specific Populations ( 8.1)] .

    KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

    Repackaged and Distributed By:

    Remedy Repack, Inc.

    625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Medication Guide).

    Instructions for Patients

    Advise patients to:

    • Strictly adhere to the prescribed dosage schedule [see Dosage and Administration ( 2.1)] .
    • If the prescribed dose of warfarin sodium is missed, take the dose as soon as possible on the same day but do not take a double dose of warfarin sodium the next day to make up for missed doses [see Dosage and Administration ( 2.6)] .
    • Obtain prothrombin time tests and make regular visits to their physician or clinic to monitor therapy [see Dosage and Administration ( 2.1)] .
    • Be aware that if therapy with warfarin sodium is discontinued, the anticoagulant effects of warfarin sodium may persist for about 2 to 5 days [see Clinical Pharmacology ( 12.2)] .
    • Avoid any activity or sport that may result in traumatic injury [see Use in Specific Populations ( 8.4)] . And to tell their physician if they fall often as this may increase their risk for complications.
    • Eat a normal, balanced diet to maintain a consistent intake of vitamin K. Avoid drastic changes in dietary habits, such as eating large amounts of leafy, green vegetables [see Drug Interactions ( 7.5)] .
    • Contact their physician to report any serious illness, such as severe diarrhea, infection, or fever [see Warnings and Precautions ( 5) and Adverse Reactions ( 6)] .
    • Immediately contact their physician when experiencing pain and discoloration of the skin (a purple bruise like rash) mostly on areas of the body with a high fat content, such as breasts, thighs, buttocks, hips and abdomen [ see Warnings and Precautions ( 5.2) ].
    • Immediately contact their physician when experiencing any unusual symptom or pain since warfarin sodium may cause small cholesterol or athero emboli. On feet it may appear as a sudden cool, painful, purple discoloration of toe(s) or forefoot [ see Warnings and Precautions (5.5) ].
    • Immediately contact their physician when taking warfarin sodium after any heparin formulation therapy and experiencing bloody or black stools or appearence of bruises, or bleeding [ see Warnings and Precautions (5.6) ].
    • To tell all of their healthcare professionals and dentists that they are taking warfarin sodium. This should be done before they have any surgery or dental procedure [ see Dosage and Administration (2.7) ].
    • Carry identification stating that they are taking warfarin sodium.

    Bleeding Risks

    Advise patients to:

    • Notify their physician immediately if any unusual bleeding or symptoms occur. Signs and symptoms of bleeding include: pain, swelling or discomfort, prolonged bleeding from cuts, increased menstrual flow or vaginal bleeding, nosebleeds, bleeding of gums from brushing, unusual bleeding or bruising, red or dark brown urine, red or tar black stools, headache, dizziness, or weakness [see Box Warning and Warnings and Precautions ( 5.1)] .

    Concomitant Medications and Botanicals (Herbals)

    Advise patients to:

    • Not take or discontinue any other drug, including salicylates (e.g., aspirin and topical analgesics), other over-the-counter drugs, and botanical (herbal) products except on advice of your physician [see Drug Interactions ( 7)] .

    Pregnancy and Nursing

    Advise patients to:

    • Notify their physician if they are pregnant or planning to become pregnant or considering breast feeding [ see Use in Specific Populations ( 8.1, 8.2, 8.3) ].
    • Avoid warfarin sodium during pregnancy except in pregnant women with mechanical heart valves, who are at risk of thromboembolism [ see Contraindications ( 4) ]. Use effective measures to avoid pregnancy while taking warfarin sodium. This is very important because their unborn baby could be seriously harmed if they take warfarin sodium while they are pregnant [ see Use in Specific Populations ( 8.1, 8.3) ].

    Manufactured In Croatia By:

    Pliva Hrvatska d.o.o.

    Zagreb, Croatia

    Manufactured For:

    Teva Pharmaceuticals USA, Inc.

    North Wales, PA 19454

    Rev. D 8/2017

    Repackaged and Distributed By:

    Remedy Repack, Inc.

    625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

  • MEDICATION GUIDE

    Warfarin (WAR-far-in) Sodium (SO-dee-um) Tablets

    The 7.5 mg tablets contain FD&C Yellow No. 5 (tartrazine), which may cause allergic-type reactions (including bronchial asthma) in certain susceptible individuals. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.

    What is the most important information I should know about warfarin sodium tablets?

    Warfarin sodium tablets can cause bleeding which can be serious and sometimes lead to death. This is because warfarin sodium tablets are a blood thinner medicine that lowers the chance of blood clots forming in your body.

    • You may have a higher risk of bleeding if you take warfarin sodium tablets and:
      • are 65 years of age or older
      • have a history of stomach or intestinal bleeding
      • have high blood pressure (hypertension)
      • have a history of stroke, or “mini-stroke” (transient ischemic attack or TIA)
      • have serious heart disease
      • have a low blood count or cancer
      • have had trauma, such as an accident or surgery
      • have kidney problems
      • take other medicines that increase your risk of bleeding, including:
        • a medicine that contains heparin
        • other medicines to prevent or treat blood clots
        • non-steroidal anti-inflammatory drugs (NSAIDs)
      • take warfarin sodium for a long time. Warfarin sodium is the active ingredient in warfarin sodium tablets.

    Tell your healthcare provider if you take any of these medicines. Ask your healthcare provider if you are not sure if your medicine is one listed above.

    Many other medicines can interact with warfarin sodium tablets and affect the dose you need or increase warfarin sodium tablets side effects. Do not change or stop any of your medicines or start any new medicines before you talk to your healthcare provider.

    Do not take other medicines that contain warfarin sodium while taking warfarin sodium tablets.

    • Get your regular blood test to check for your response to warfarin sodium tablets. This blood test is called an INR test. The INR test checks to see how fast your blood clots. Your healthcare provider will decide what INR numbers are best for you. Your dose of warfarin sodium tablets will be adjusted to keep your INR in a target range for you.
    • Call your healthcare provider right away if you get any of the following signs or symptoms of bleeding problems:
      • pain, swelling, or discomfort
      • headaches, dizziness, or weakness
      • unusual bruising (bruises that develop without known cause or grow in size)
      • nosebleeds
      • bleeding gums
      • bleeding from cuts takes a long time to stop
      • menstrual bleeding or vaginal bleeding that is heavier than normal
      • pink or brown urine
      • red or black stools
      • coughing up blood
      • vomiting blood or material that looks like coffee grounds
    • Some foods and beverages can interact with warfarin sodium tablets and affect your treatment and dose.
      • Eat a normal, balanced diet. Talk to your healthcare provider before you make any diet changes. Do not eat large amounts of leafy, green vegetables. Leafy, green vegetables contain vitamin K. Certain vegetable oils also contain large amounts of vitamin K. Too much vitamin K can lower the effect of warfarin sodium tablets.
    • Always tell all of your healthcare providers that you take warfarin sodium tablets.
    • Wear or carry information that you take warfarin sodium tablets.

    See “What are the possible side effects of warfarin sodium tablets?” for more information about side effects.

    What are warfarin sodium tablets?

    Warfarin sodium tablets are prescription medicine used to treat blood clots and to lower the chance of blood clots forming in your body. Blood clots can cause a stroke, heart attack, or other serious conditions if they form in the legs or lungs.

    Who should not take warfarin sodium tablets?

    Do not take warfarin sodium tablets if:

    • your risk of having bleeding problems is higher than the possible benefit of treatment. Your healthcare provider will decide if warfarin sodium tablets are right for you.
    • you are pregnant unless you have a mechanical heart valve. Warfarin sodium tablets may cause birth defects, miscarriage, or death of your unborn baby.
    • you are allergic to warfarin or any of the other ingredients in warfarin sodium tablets. See the end of this leaflet for a complete list of ingredients in warfarin sodium tablets.

    Before taking warfarin sodium tablets, tell your healthcare provider about all of your medical conditions, including if you:

    • have bleeding problems
    • fall often
    • have liver problems
    • have kidney problems or are undergoing dialysis
    • have high blood pressure
    • have a heart problem called congestive heart failure
    • have diabetes
    • plan to have any surgery or a dental procedure
    • are pregnant or plan to become pregnant. See “ Who should not take warfarin sodium tablets?”
      • Your healthcare provider will do a pregnancy test before you start treatment with warfarin sodium tablets. Females who can become pregnant should use effective birth control during treatment, and for at least 1 month after the last dose of warfarin sodium tablets.
    • are breastfeeding. You and your healthcare provider should decide if you will take warfarin sodium tablets and breastfeed. Check your baby for bruising or bleeding if you take warfarin sodium tablets and breastfeed.



    Tell all of your healthcare providers and dentists that you are taking warfarin sodium tablets. They should talk to the healthcare provider who prescribed warfarin sodium tablets for you before you have any surgery or dental procedure. Your warfarin sodium tablets may need to be stopped for a short time or you may need your dose adjusted.



    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Some of your other medicines may affect the way warfarin sodium tablets work. Certain medicines may increase your risk of bleeding. See “ What is the most important information I should know about warfarin sodium tablets?”

    How should I take warfarin sodium tablets?

    • Take warfarin sodium tablets exactly as prescribed. Your healthcare provider will adjust your dose from time to time depending on your response to warfarin sodium tablets.
    • You must have regular blood tests and visits with your healthcare provider to monitor your condition.
    • If you miss a dose of warfarin sodium tablets, call your healthcare provider. Take the dose as soon as possible on the same day. Do not take a double dose of warfarin sodium tablets the next day to make up for a missed dose.
    • Call your healthcare provider right away if you:
      • take too much warfarin sodium tablets
      • are sick with diarrhea, an infection, or have a fever
      • fall or injure yourself, especially if you hit your head. Your healthcare provider may need to check you.

    What should I avoid while taking warfarin sodium tablets ?

    • Do not do any activity or sport that may cause a serious injury.

    What are the possible side effects of warfarin sodium tablets?

    Warfarin sodium tablets may cause serious side effects including:

    • See “ What is the most important information I should know about warfarin sodium tablets?”
    • Death of skin tissue (skin necrosis or gangrene). This can happen soon after starting warfarin sodium tablets. It happens because blood clots form and block blood flow to an area of your body. Call your healthcare provider right away if you have pain, color, or temperature change to any area of your body. You may need medical care right away to prevent death or loss (amputation) of your affected body part.
    • Kidney problems. Kidney injury may happen in people who take warfarin sodium tablets. Tell your healthcare provider right away if you develop blood in your urine. Your healthcare provider may do tests more often during treatment with warfarin sodium tablets to check for bleeding if you already have kidney problems.
    • “Purple toes syndrome.” Call your healthcare provider right away if you have pain in your toes and they look purple in color or dark in color.

    These are not all of the side effects of warfarin sodium tablets. For more information, ask your healthcare provider 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 warfarin sodium tablets?

    • Store warfarin sodium tablets at 20° to 25°C (68° to 77°F).
    • Keep warfarin sodium tablets in a tightly closed container.
    • Keep warfarin sodium tablets out of the light.
    • Follow your healthcare provider or pharmacist instructions about the right way to throw away outdated or unused warfarin sodium tablets.
    • Females who are pregnant should not handle crushed or broken warfarin sodium tablets.

    Keep warfarin sodium tablets and all medicines out of the reach of children.

    General information about the safe and effective use of warfarin sodium tablets.

    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use warfarin sodium tablets for a condition for which they were not prescribed. Do not give warfarin sodium tablets to other people, even if they have the same symptoms that you have. They may harm them. You can ask your healthcare provider or pharmacist for information about warfarin sodium tablets that is written for health professionals.

    What are the ingredients in warfarin sodium tablets?

    Active ingredient: warfarin sodium

    Inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate, magnesium stearate, and microcrystalline cellulose. The 1 mg also contains FD&C red no. 40. The 2 mg also contains FD&C blue no. 2 aluminum lake and FD&C red no. 40 aluminum lake. The 2.5 mg also contains D&C yellow no. 10 aluminum lake and FD&C blue no. 1 aluminum lake. The 3 mg also contains FD&C yellow no. 6 aluminum lake, FD&C blue no. 2 aluminum lake, FD&C red no. 40 aluminum lake, and D&C yellow no. 10 aluminum lake. The 4 mg also contains FD&C blue no. 1 aluminum lake and FD&C blue no. 2 aluminum lake. The 5 mg also contains FD&C yellow no. 6 aluminum lake, FD&C red no. 40 aluminum lake and D&C yellow no. 10 aluminum lake. The 6 mg also contains D&C yellow no. 10 aluminum lake and FD&C blue no. 1 aluminum lake. The 7.5 mg also contains FD&C yellow no. 5 (tartrazine) aluminum lake and FD&C red no. 40 aluminum lake.

    For more information, go to www.tevagenerics.com or call 1-888-838-2872.



    Manufactured In Croatia By:

    Pliva Hrvatska d.o.o.

    Zagreb, Croatia

    Manufactured For:

    Teva Pharmaceuticals USA, Inc.

    North Wales, PA 19454

    Repackaged and Distributed By:

    Remedy Repack, Inc.

    625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

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

    Rev. C 5/2017
  • PRINCIPAL DISPLAY PANEL

    DRUG: Warfarin Sodium

    GENERIC: Warfarin Sodium

    DOSAGE: TABLET

    ADMINSTRATION: ORAL

    NDC: 70518-0261-0

    COLOR: turquoise

    SHAPE: OVAL

    SCORE: Two even pieces

    SIZE: 11 mm

    IMPRINT: TV;6;1718

    PACKAGING: 30 in 1 BLISTER PACK

    ACTIVE INGREDIENT(S):

    • WARFARIN SODIUM 6mg in 1

    INACTIVE INGREDIENT(S):

    • D&C YELLOW NO. 10
    • FD&C BLUE NO. 1
    • MICROCRYSTALLINE CELLULOSE
    • MAGNESIUM STEARATE
    • CROSCARMELLOSE SODIUM
    • LACTOSE MONOHYDRATE
    • SILICON DIOXIDE

    Remedy_Label

  • INGREDIENTS AND APPEARANCE
    WARFARIN SODIUM 
    warfarin sodium tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 70518-0261(NDC:0093-1718)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WARFARIN SODIUM (UNII: 6153CWM0CL) (WARFARIN - UNII:5Q7ZVV76EI) WARFARIN SODIUM6 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    Colorturquoise (teal) Score2 pieces
    ShapeOVAL (capsule-shaped) Size11mm
    FlavorImprint Code TV;6;1718
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 70518-0261-030 in 1 BLISTER PACK; Type 0: Not a Combination Product02/23/2017
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA04061602/23/2017
    Labeler - REMEDYREPACK INC. (829572556)
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