DRUGS & SUPPLEMENTS

Ribavarin

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Ribavarin uses


WARNING: RISK OF SERIOUS DISORDERS AND RIBAVIRIN-ASSOCIATED EFFECTS

WARNING: RISK OF SERIOUS DISORDERS AND RIBAVIRINASSOCIATED EFFECTS

See full prescribing information for complete boxed warning.

  • Ribavarin monotherapy, including Ribavarin, is not effective for the treatment of chronic hepatitis C virus infection (Boxed Warning).
  • The hemolytic anemia associated with Ribavarin therapy may result in worsening of cardiac disease and lead to fatal and nonfatal myocardial infarctions. Patients with a history of significant or unstable cardiac disease should not be treated with Ribavarin (2.3, 5.2, 6.1).
  • Significant teratogenic and embryocidal effects have been demonstrated in all animal species exposed to Ribavarin. Therefore, Ribavarin is contraindicated in women who are pregnant and in the male partners of women who are pregnant. Extreme care must be taken to avoid pregnancy during therapy and for 6 months after completion of treatment in both female patients and in female partners of male patients who are taking Ribavarin therapy (4, 5.1, 8.1).
Ribavarin monotherapy is not effective for the treatment of chronic hepatitis C virus infection and should not be used alone for this indication.

The primary clinical toxicity of Ribavarin is hemolytic anemia. The anemia associated with Ribavarin therapy may result in worsening of cardiac disease and lead to fatal and nonfatal myocardial infarctions. Patients with a history of significant or unstable cardiac disease should not be treated with Ribavarin.

Significant teratogenic and/or embryocidal effects have been demonstrated in all animal species exposed to Ribavarin. In addition, Ribavarin has a multiple dose half-life of 12 days, and it may persist in non-plasma compartments for as long as 6 months. Therefore, Ribavarin, including Ribavarin, is contraindicated in women who are pregnant and in the male partners of women who are pregnant. Extreme care must be taken to avoid pregnancy during therapy and for 6 months after completion of therapy in both female patients and in female partners of male patients who are taking Ribavarin therapy. At least two reliable forms of effective contraception must be utilized during treatment and during the 6month post treatment follow-up period.

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RECENT MAJOR CHANGES

 Warnings and Precautions (5.8)                                                                08/2015

1 INDICATIONS AND USAGE

Ribavarin is a nucleoside analogue indicated for the treatment of chronic hepatitis C (CHC) virus infection in combination with peginterferon alfa-2a in patients 5 years of age and older with compensated liver disease not previously treated with interferon alpha, and in adult CHC patients coinfected with HIV (1)

Ribavarin tablets in combination with peginterferon alfa-2a are indicated for the treatment of patients 5 years of age and older with chronic hepatitis C (CHC) virus infection who have compensated liver disease and have not been previously treated with interferon alpha.

The following points should be considered when initiating Ribavarin tablets combination therapy with peginterferon alfa-2a:

  • This indication is based on clinical trials of combination therapy in patients with CHC and compensated liver disease, some of whom had histological evidence of cirrhosis (Child-Pugh class A), and in adult patients with clinically stable HIV disease and CD4 count greater than 100 cells/mm3.
  • This indication is based on achieving undetectable HCV RNA after treatment for 24 or 48 weeks, based on HCV genotype, and maintaining a Sustained Virologic Response (SVR) 24 weeks after the last dose.
  • Safety and efficacy data are not available for treatment longer than 48 weeks.
  • The safety and efficacy of Ribavarin tablets and peginterferon alfa-2a therapy have not been established in liver or other organ transplant recipients, patients with decompensated liver disease, or previous non-responders to interferon therapy.
  • The safety and efficacy of Ribavarin tablets therapy for the treatment of adenovirus, RSV, parainfluenza or influenza infections have not been established. Ribavarin tablets should not be used for these indications. Ribavarin for inhalation has a separate package insert, which should be consulted if Ribavarin inhalation therapy is being considered.
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2 DOSAGE AND ADMINISTRATION

  • CHC: Ribavarin is administered according to body weight and genotype
  • CHC with HIV coinfection: 800 mg by mouth daily for a total of 48 weeks, regardless of genotype (2.2)
  • Dose reduction or discontinuation is recommended in patients experiencing certain adverse reactions or renal impairment (2.3, 2.4)
Ribavarin should be taken with food. Ribavarin should be given in combination with peginterferon alfa-2a; it is important to note that Ribavarin should never be given as monotherapy. See peginterferon alfa-2a Package Insert for all instructions regarding peginterferon alfa-2a dosing and administration.

2.1 Chronic Hepatitis C Monoinfection

Adult Patients

The recommended dose of Ribavarin tablets is provided in Table 1. The recommended duration of treatment for patients previously untreated with Ribavarin and interferon is 24 to 48 weeks.

The daily dose of Ribavarin is 800 mg to 1200 mg administered orally in two divided doses. The dose should be individualized to the patient depending on baseline disease characteristics (e.g., genotype), response to therapy, and tolerability of the regimen (see Table 1).

Hepatitis  Virus  ( HCV Genotype 

Peginterferon  Alfa - 2a  Dose *

( once  weekly )

Ribavirin  Dose

( daily )

Duration

Genotypes 2 and 3 showed no increased response to treatment beyond 24 weeks (see Table 10).

Data on genotypes 5 and 6 are insufficient for dosing recommendations.

*See Peginterferon alfa-2a Package Insert for further details on peginterferon alfa-2a dosing and administration, including dose modification in patients with renal impairment.

Genotypes 1, 4 

180 mcg

< 75 kg = 1000 mg 

≥ 75 kg = 1200 mg

48 weeks

48 weeks

Genotypes 2, 3 

180 mcg

800 mg

24 weeks

Pediatric Patients

Peginterferon alfa-2a is administered as 180 mcg/1.73m2 x BSA once weekly subcutaneously, to a maximum dose of 180 mcg, and should be given in combination with Ribavarin. The recommended treatment duration for patients with genotype 2 or 3 is 24 weeks and for other genotypes is 48 weeks.

Ribavarin should be given in combination with peginterferon alfa-2a. Ribavarin is available only as a 200 mg tablet and therefore the healthcare provider should determine if this sized tablet can be swallowed by the pediatric patient. The recommended doses for Ribavarin are provided in Table 2. Patients who initiate treatment prior to their 18th birthday should maintain pediatric dosing through the completion of therapy

*approximately 15 mg/kg/day

Body  Weight  in  kilograms  ( kg

Ribavirin  Daily  Dose

Ribavirin  Number  of  Tablets 

23 to 33 

400 mg/day 

1 x 200 mg tablet A.M. 

1 x 200 mg tablet P.M. 

34 to 46 

600 mg/day 

1 x 200 mg tablet A.M. 

2 x 200 mg tablets P.M. 

47 to 59 

800 mg/day 

2 x 200 mg tablets A.M. 

2 x 200 mg tablets P.M. 

60 to 74 

1000 mg/day 

2 x 200 mg tablets A.M. 

3 x 200 mg tablets P.M. 

≥ 75 

1200 mg/day 

3 x 200 mg tablets A.M. 

3 x 200 mg tablets P.M. 

2.2 Chronic Hepatitis C with HIV Coinfection

Adult Patients

The recommended dose for treatment of chronic hepatitis C in patients coinfected with HIV is peginterferon alfa-2a 180 mcg subcutaneous once weekly and Ribavarin 800 mg by mouth daily for a total duration of 48 weeks, regardless of HCV genotype.

2.3 Dose Modifications

Adult and Pediatric Patients

If severe adverse reactions or laboratory abnormalities develop during combination ribavirin/peginterferon alfa-2a therapy, the dose should be modified or discontinued, if appropriate, until the adverse reactions abate or decrease in severity. If intolerance persists after dose adjustment, ribavirin/peginterferon alfa-2a therapy should be discontinued. Table 3 provides guidelines for dose modifications and discontinuation based on the patient's hemoglobin concentration and cardiac status.

Ribavarin should be administered with caution to patients with pre-existing cardiac disease. Patients should be assessed before commencement of therapy and should be appropriately monitored during therapy. If there is any deterioration of cardiovascular status, therapy should be stopped [see WARNINGS AND PRECAUTIONS ].

Body  weight  in  kilograms  ( kg

Laboratory  Values



Hemoglobin <10 g/dL in patients with no cardiac disease, or Decrease in hemoglobin of ≥2 g/dL during any 4 week period in patients with history of stable cardiac disease 

Hemoglobin <8.5 g/dL in patients with no cardiac disease, or Hemoglobin <12 g/dL despite 4 weeks at reduced dose in patients with history of stable cardiac disease

Adult  Patients  older  than  18  years  of  age



Any weight 

1 x 200 mg tablet A.M.

 2 x 200 mg tablets P.M.

Discontinue Ribavirin

Pediatric  Patients  to  18  years  of  age 



23 to 33 kg 

1 x 200 mg tablet A.M. 


34 to 46 kg 

1 x 200 mg tablet A.M. 

1 x 200 mg tablet P.M.


47 to 59 kg 

1 x 200 mg tablet A.M. 

1 x 200 mg tablet P.M.

Discontinue Ribavirin 

60 to 74 kg 

1 x 200 mg tablet A.M. 

2 x 200 mg tablets P.M.


≥ 75kg 

1 x 200 mg tablet A.M. 

2 x 200 mg tablets P.M.


The guidelines for Ribavarin dose modifications outlined in this table also apply to laboratory abnormalities or adverse reactions other than decreases in hemoglobin values.

Adult Patients

Once Ribavarin has been withheld due to either a laboratory abnormality or clinical adverse reaction, an attempt may be made to restart Ribavarin at 600 mg daily and further increase the dose to 800 mg daily. However, it is not recommended that Ribavarin be increased to the original assigned dose (1000 mg to 1200 mg).

Pediatric Patients

Upon resolution of a laboratory abnormality or clinical adverse reaction, an increase in Ribavarin dose to the original dose may be attempted depending upon the physician's judgment. If Ribavarin has been withheld due to a laboratory abnormality or clinical adverse reaction, an attempt may be made to restart Ribavarin at one-half the full dose.

2.4 Renal Impairment

The total daily dose of Ribavarin should be reduced for patients with creatinine clearance less than or equal to 50 mL/min; and the weekly dose of peginterferon alfa-2a should be reduced for creatinine clearance less than 30 mL/min as follows in Table 4 [see USE IN SPECIFIC POPULATIONS (8.7), PHARMACOKINETICS (12.3), and Peginterferon Alfa-2a PACKAGE INSERT].

Creatinine  Clearance 

Peginterferon  Alfa - 2a  Dose  ( once  weekly )

Ribavirin  Dose

( daily )

30 to 50 mL/min 

180 mcg

Alternating doses, 200 mg and 400 mg every other day

Less than 30 mL/min 

135 mcg

200 mg daily

Hemodialysis 

135 mcg

200 mg daily

The dose of Ribavarin should not be further modified in patients with renal impairment. If severe adverse reactions or laboratory abnormalities develop, Ribavarin should be discontinued, if appropriate, until the adverse reactions abate or decrease in severity. If intolerance persists after restarting Ribavarin, Ribavarin /peginterferon alfa-2a therapy should be discontinued.

No data are available for pediatric subjects with renal impairment.

2.5 Discontinuation of Dosing

Discontinuation of peginterferon alfa-2a /ribavirin therapy should be considered if the patient has failed to demonstrate at least a 2 log10 reduction from baseline in HCV RNA by 12 weeks of therapy, or undetectable HCV RNA levels after 24 weeks of therapy.

Peginterferon alfa-2a/ribavirin therapy should be discontinued in patients who develop hepatic decompensation during treatment [see WARNINGS AND PRECAUTIONS (5.3)].

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3 DOSAGE FORMS AND STRENGTHS

  • Ribavarin tablets 200 mg or 400 mg or 500 mg or 600 mg (3)
Ribavarin tablets for oral administration are available as:

200 mg - light pink to pink, round, biconvex, beveled, film-coated tablets;

400 mg - light pink to pink, capsule shaped, biconvex, film-coated tablets;

500 mg - light pink to pink, modified capsule shaped, biconvex, film-coated tablets;

600 mg - light pink to pink, modified capsule shaped, biconvex, film-coated tablets

4 CONTRAINDICATIONS

  • Pregnant women and men whose female partners are pregnant (4, 5.1, 8.1)
  • Hemoglobinopathies (4)
  • Coadministration with didanosine (4, 7.1)
Ribavarin in combination with peginterferon alfa-2a is contraindicated in patients with:

  • Autoimmune hepatitis (4)
  • Hepatic decompensation in cirrhotic patients (4, 5.3)
Ribavarin is contraindicated in:

  • Women who are pregnant. Ribavarin may cause fetal harm when administered to a pregnant woman. Ribavarin is contraindicated in women who are or may become pregnant. 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 the fetus [see WARNINGS AND PRECAUTIONS (5.1), USE IN SPECIFIC POPULATIONS (8.1), and PATIENT COUNSELING INFORMATION (17)].
  • Men whose female partners are pregnant.
  • Patients with hemoglobinopathies (e.g., thalassemia major or sickle-cell anemia).
  • In combination with didanosine. Reports of fatal hepatic failure, as well as peripheral neuropathy, pancreatitis, and symptomatic hyperlactatemia/lactic acidosis have been reported in clinical trials.
Ribavarin and peginterferon alfa-2a combination therapy is contraindicated in patients with:

  • Autoimmune hepatitis.
  • Hepatic decompensation (Child-Pugh score greater than 6; class B and C) in cirrhotic CHC monoinfected patients before treatment [see WARNINGS AND PRECAUTIONS (5.3)].
  • Hepatic decompensation (Child-Pugh score greater than or equal to 6) in cirrhotic CHC patients coinfected with HIV before treatment.
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5 WARNINGS AND PRECAUTIONS

  • Birth defects and fetal death with Ribavarin: Do not use in pregnancy and for 6 months after treatment. Patients must have a negative pregnancy test prior to therapy, use at least 2 forms of contraception and undergo monthly pregnancy tests
Peginterferon alfa-2a/Ribavirin: Patients exhibiting the following conditions should be closely monitored and may require dose reduction or discontinuation of therapy:

  • Hemolytic anemia may occur with a significant initial drop in hemoglobin. This may result in worsening cardiac disease leading to fatal or nonfatal myocardial infarctions (5.2, 6.1)
  • Risk of hepatic failure and death: Monitor hepatic function during treatment and discontinue treatment for hepatic decompensation (5.3)
  • Severe hypersensitivity reactions including urticaria, angioedema, bronchoconstriction, and anaphylaxis, and serious skin reactions such as Stevens-Johnson Syndrome (5.4)
  • Pulmonary disorders, including pulmonary function impairment and pneumonitis, including fatal cases of pneumonia (5.5)
  • Severe depression and suicidal ideation, autoimmune and infectious disorders, suppression of bone marrow function, pancreatitis, and diabetes (5)
  • Bone marrow suppression with azathioprine coadministration (5.6)
  • Growth impairment with combination therapy in pediatric patients (5.8)
Significant adverse reactions associated with ribavirin/peginterferon alfa-2a combination therapy include severe depression and suicidal ideation, hemolytic anemia, suppression of bone marrow function, autoimmune and infectious disorders, ophthalmologic disorders, cerebrovascular disorders, pulmonary dysfunction, colitis, pancreatitis, and diabetes.

The Peginterferon alfa-2a Package Insert should be reviewed in its entirety for additional safety information prior to initiation of combination treatment.

5.1 Pregnancy

Ribavarin may cause birth defects and/or death of the exposed fetus. Ribavarin has demonstrated significant teratogenic and/or embryocidal effects in all animal species in which adequate studies have been conducted. These effects occurred at doses as low as one twentieth of the recommended human dose of Ribavarin.

Ribavarin therapy should not be started unless a report of a negative pregnancy test has been obtained immediately prior to planned initiation of therapy. Extreme care must be taken to avoid pregnancy in female patients and in female partners of male patients. Patients should be instructed to use at least two forms of effective contraception during treatment and for 6 months after treatment has been stopped. Pregnancy testing should occur monthly during Ribavarin therapy and for 6 months after therapy has stopped [see BOXED WARNING, CONTRAINDICATIONS (4), USE IN SPECIFIC POPULATIONS (8.1), and PATIENT COUNSELING INFORMATION (17)].

5.2 Anemia

The primary toxicity of Ribavarin is hemolytic anemia, which was observed in approximately 13% of all ribavirin/peginterferon alfa-2a- treated subjects in clinical trials. Anemia associated with Ribavarin occurs within 1 to 2 weeks of initiation of therapy. Because the initial drop in hemoglobin may be significant, it is advised that hemoglobin or hematocrit be obtained pretreatment and at week 2 and week 4 of therapy or more frequently if clinically indicated. Patients should then be followed as clinically appropriate. Caution should be exercised in initiating treatment in any patient with baseline risk of severe anemia [see DOSAGE AND ADMINISTRATION (2.3)].

Fatal and nonfatal myocardial infarctions have been reported in patients with anemia caused by Ribavarin. Patients should be assessed for underlying cardiac disease before initiation of Ribavarin therapy. Patients with pre-existing cardiac disease should have electrocardiograms administered before treatment, and should be appropriately monitored during therapy. If there is any deterioration of cardiovascular status, therapy should be suspended or discontinued [see DOSAGE AND ADMINISTRATION (2.3)]. Because cardiac disease may be worsened by drug-induced anemia, patients with a history of significant or unstable cardiac disease should not use Ribavarin [see BOXED WARNING, and DOSAGE AND ADMINISTRATION (2.3)].

5.3 Hepatic Failure

Chronic hepatitis C (CHC) patients with cirrhosis may be at risk of hepatic decompensation and death when treated with alpha interferons, including peginterferon alfa-2a. Cirrhotic CHC patients coinfected with HIV receiving highly active antiretroviral therapy (HAART) and interferon alfa-2a with or without Ribavarin appear to be at increased risk for the development of hepatic decompensation compared to patients not receiving HAART. In Study NR15961 [see CLINICAL STUDIES (14.3)], among 129 CHC/HIV cirrhotic patients receiving HAART, 14 (11%) of these patients across all treatment arms developed hepatic decompensation resulting in 6 deaths. All 14 patients were on NRTIs, including stavudine, didanosine, abacavir, zidovudine, and lamivudine. These small numbers of patients do not permit discrimination between specific NRTIs or the associated risk. During treatment, patients’ clinical status and hepatic function should be closely monitored for signs and symptoms of hepatic decompensation. Treatment with peginterferon alfa-2a/ Ribavarin should be discontinued immediately in patients with hepatic decompensation [see CONTRAINDICATIONS (4)]

5.4 Hypersensitivity

Severe acute hypersensitivity reactions have been observed during alpha interferon and Ribavarin therapy. If such a reaction occurs, therapy with peginterferon alfa-2a and Ribavarin should be discontinued immediately and appropriate medical therapy instituted. Serious skin reactions including vesiculobullous eruptions, reactions in the spectrum of Stevens-Johnson Syndrome (erythema multiforme major) with varying degrees of skin and mucosal involvement and exfoliative dermatitis (erythroderma) have been reported in patients receiving peginterferon alfa-2a with and without Ribavarin. Patients developing signs or symptoms of severe skin reactions must discontinue therapy [see ADVERSE REACTIONS (6.2)].

5.5 Pulmonary Disorders

Dyspnea, pulmonary infiltrates, pneumonitis, pulmonary hypertension, and pneumonia have been reported during therapy with Ribavarin and interferon. Occasional cases of fatal pneumonia have occurred. In addition, sarcoidosis or the exacerbation of sarcoidosis has been reported. If there is evidence of pulmonary infiltrates or pulmonary function impairment, patients should be closely monitored and, if appropriate, combination ribavirin/peginterferon alfa-2a treatment should be discontinued.

5.6 Bone Marrow Suppression

Pancytopenia and bone marrow suppression have been reported in the literature to occur within 3 to 7 weeks after the concomitant administration of pegylated interferon/ribavirin and azathioprine. In this limited number of patients (n=8), myelotoxicity was reversible within 4 to 6 weeks upon withdrawal of both HCV antiviral therapy and concomitant azathioprine and did not recur upon reintroduction of either treatment alone. peginterferon alfa-2a, Ribavarin, and azathioprine should be discontinued for pancytopenia, and pegylated interferon/ribavirin should not be re-introduced with concomitant azathioprine [see Drug Interactions (7.3)].

5.7 Pancreatitis

Ribavarin and peginterferon alfa-2a therapy should be suspended in patients with signs and symptoms of pancreatitis, and discontinued in patients with confirmed pancreatitis.

5.8 Impact on Growth in Pediatric Patients

During combination therapy for up to 48 weeks with peginterferon alfa-2a  plus Ribavarin, growth inhibition was observed in pediatric subjects 5 to 17 years of age. Decreases in weight for age z-score and height for age z-score up to 48 weeks of therapy compared with baseline were observed. At 2 years post-treatment, 16% of pediatric subjects were more than 15 percentiles below their baseline weight curve and 11% were more than 15 percentiles below their baseline height curve.

The available longer term data on subjects who were followed up to 6 years post-treatment are too limited to determine the risk of reduced adult height in some patients .

5.9 Laboratory Tests

Before beginning ribavirin/peginterferon alfa-2a combination therapy, standard hematological and biochemical laboratory tests are recommended for all patients. Pregnancy screening for women of childbearing potential must be performed. Patients who have pre-existing cardiac abnormalities should have electrocardiograms administered before treatment with ribavirin/peginterferon alfa-2a.

 

After initiation of therapy, hematological tests should be performed at 2 weeks and 4 weeks and biochemical tests should be performed at 4 weeks. Additional testing should be performed periodically during therapy. In adult clinical studies, the CBC (including hemoglobin level and white blood cell and platelet counts) and chemistries (including liver function tests and uric acid) were measured at 1, 2, 4, 6, and 8 weeks, and then every 4 to 6 weeks or more frequently if abnormalities were found. In the pediatric clinical trial, hematological and chemistry assessments were at 1, 3, 5, and 8 weeks, then every 4 weeks. Thyroid stimulating hormone (TSH) was measured every 12 weeks. Monthly pregnancy testing should be performed during combination therapy and for 6 months after discontinuing therapy.

The entrance criteria used for the clinical studies of Ribavarin and peginterferon alfa-2a may be considered as a guideline to acceptable baseline values for initiation of treatment:

  • Platelet count greater than or equal to 90,000 cells/mm3 (as low as 75,000 cells/mm3 in HCV patients with cirrhosis or 70,000 cells/mm3 in patients with CHC and HIV)
  • Absolute neutrophil count (ANC) greater than or equal to 1500 cells/mm3
  • TSH and T4 within normal limits or adequately controlled thyroid function
  • CD4+ cell count greater than or equal to 200 cells/mm3or CD4+ cell count greater than or equal to 100 cells/mm3 but less than 200 cells/mm3 and HIV-1 RNA less than 5,000 copies/mL in patients coinfected with HIV
  • Hemoglobin greater than or equal to 12 g/dL for women and greater than or equal to 13 g/dL for men in CHC monoinfected patients
  • Hemoglobin greater than or equal to 11 g/dL for women and greater than or equal to 12 g/dL for men in patients with CHC and HIV

6 ADVERSE REACTIONS

The most common adverse reactions in adults receiving combination therapy are fatigue/asthenia, pyrexia, myalgia, and headache. (6.1)

The most common adverse reactions in pediatric subjects were similar to those seen in adults. (6.1)

To report SUSPECTED ADVERSE REACTIONS, contact Zydus Pharmaceuticals USA Inc. at 1-877-993-8779 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Peginterferon alfa-2a in combination with Ribavarin causes a broad variety of serious adverse reactions [see BOXED WARNING and WARNINGS AND PRECAUTIONS (5)]. The most common serious or life-threatening adverse reactions induced or aggravated by ribavirin/peginterferon alfa-2a include depression, suicide, relapse of drug abuse/overdose, and bacterial infections each occurring at a frequency of less than 1%. Hepatic decompensation occurred in 2% (10/574) CHC/HIV patients [see WARNINGS AND PRECAUTIONS (5.3)].

6.1 Clinical Studies Experience

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

Adult Patients

In the pivotal registration trials NV15801 and NV15942, 886 patients received Ribavarin for 48 weeks at doses of 1000/1200 mg based on body weight. In these trials, one or more serious adverse reactions occurred in 10% of CHC monoinfected subjects and in 19% of CHC/HIV subjects receiving peginterferon alfa-2a alone or in combination with Ribavarin. The most common serious adverse event (3% in CHC and 5% in CHC/HIV) was bacterial infection (e.g., sepsis, osteomyelitis, endocarditis, pyelonephritis, pneumonia).

Other serious adverse reactions occurred at a frequency of less than 1% and included: suicide, suicidal ideation, psychosis, aggression, anxiety, drug abuse and drug overdose, angina, hepatic dysfunction, fatty liver, cholangitis, arrhythmia, diabetes mellitus, autoimmune phenomena (e.g., hyperthyroidism, hypothyroidism, sarcoidosis, systemic lupus erythematosus, rheumatoid arthritis), peripheral neuropathy, aplastic anemia, peptic ulcer, gastrointestinal bleeding, pancreatitis, colitis, corneal ulcer, pulmonary embolism, coma, myositis, cerebral hemorrhage, thrombotic thrombocytopenic purpura, psychotic disorder, and hallucination.

The percentage of patients in clinical trials who experienced one or more adverse events was 98%. The most commonly reported adverse reactions were psychiatric reactions, including depression, insomnia, irritability, anxiety, and flu-like symptoms such as fatigue, pyrexia, myalgia, headache and rigors. Other common reactions were anorexia, nausea and vomiting, diarrhea, arthralgias, injection site reactions, alopecia, and pruritus. Table 5 shows rates of adverse events occurring in greater than or equal to 5% of subjects receiving pegylated interferon and Ribavarin combination therapy in the CHC Clinical Trial, NV15801.

Ten percent of CHC monoinfected patients receiving 48 weeks of therapy with peginterferon alfa-2a in combination with Ribavarin discontinued therapy; 16% of CHC/HIV coinfected patients discontinued therapy. The most common reasons for discontinuation of therapy were psychiatric, flu-like syndrome (e.g., lethargy, fatigue, headache), dermatologic and gastrointestinal disorders, and laboratory abnormalities (thrombocytopenia, neutropenia, and anemia).

Overall 39% of patients with CHC or CHC/HIV required modification of peginterferon alfa-2a and/or Ribavarin therapy. The most common reason for dose modification of peginterferon alfa-2a in CHC and CHC/HIV patients was for laboratory abnormalities; neutropenia (20% and 27%, respectively) and thrombocytopenia (4% and 6%, respectively). The most common reason for dose modification of Ribavarin in CHC and CHC/HIV patients was anemia (22% and 16%, respectively).

Peginterferon alfa-2a dose was reduced in 12% of patients receiving 1000 mg to 1200 mg Ribavarin for 48 weeks and in 7% of patients receiving 800 mg Ribavarin for 24 weeks. Ribavarin dose was reduced in 21% of patients receiving 1000 mg to 1200 mg Ribavarin for 48 weeks and in 12% of patients receiving 800 mg Ribavarin for 24 weeks.

Chronic hepatitis C monoinfected patients treated for 24 weeks with peginterferon alfa-2a and 800 mg Ribavarin were observed to have lower incidence of serious adverse events (3% vs. 10%), hemoglobin less than 10g/dL (3% vs. 15%), dose modification of peginterferon alfa-2a (30% vs. 36%) and Ribavarin (19% vs. 38%), and of withdrawal from treatment (5% vs. 15%) compared to patients treated for 48 weeks with peginterferon alfa-2a and 1000 mg or 1200 mg Ribavarin. On the other hand, the overall incidence of adverse events appeared to be similar in the two treatment groups.


CHC  Combination  Therapy  Study  NV15801


*Severe hematologic abnormalities (lymphocyte less than 500 cells/mm3; hemoglobin less than 10 g/dL; neutrophil less than 750 cells/mm3; platelet less than 50,000 cells/mm3).

Body  System

Peginterferon  Alfa - 2a  180  mcg  1000  mg  or  1200  mg  Ribavirin  Tablets

48  weeks

Interferon  alfa - 2b  1000  mg  or  1200  mg  Ribavirin  Capsules

48  weeks


N = 451

N = 443


%

%

Application  Site  Disorders



Injection site reaction 

23

16

Endocrine  Disorders



Hypothyroidism

4

5

Flu - like  Symptoms  and  Signs 



Fatigue/Asthenia

65

68

Pyrexia

41

55

Rigors

25

37

Pain

10

9

Gastrointestinal 



Nausea/Vomiting

25

29

Diarrhea

11

10

Abdominal pain

8

9

Dry mouth

4

7

Dyspepsia 

6

5

Hematologic



Lymphopenia 

14

12

Anemia

11

11

Neutropenia

27

8

Thrombocytopenia 

5

< 1

Metabolic  and  Nutritional 



Anorexia 

24

26

Weight decrease 

10

10

Musculoskeletal Connective  Tissue  and  Bone 



Myalgia 

40

49

Arthralgia 

22

23

Back pain 

5

5

Neurological 



Headache 

43

49

Dizziness (excluding vertigo) 

14

14

Memory impairment 

6

5

Psychiatric 



Irritability/Anxiety/Nervousness 

33

38

Insomnia 

30

37

Depression 

20

28

Concentration impairment 

10

13

Mood alteration 

5

6

Resistance  Mechanism  Disorders 



Overall

12

10

Respiratory Thoracic  and  Mediastinal 



Dyspnea 

13

14

Cough 

10

7

Dyspnea exertional 

4

7

Skin  and  Subcutaneous  Tissue 



Alopecia 

28

33

Pruritus 

19

18

Dermatitis 

16

13

Dry skin 

10

13

Rash 

8

5

Sweating increased 

6

5

Eczema 

5

4

Visual  Disorders 



Vision blurred 

5

2

Pediatric Patients

In a clinical trial with 114 pediatric subjects (5 to 17 years of age) treated with peginterferon alfa-2a alone or in combination with Ribavarin, dose modifications were required in approximately one-third of subjects, most commonly for neutropenia and anemia. In general, the safety profile observed in pediatric subjects was similar to that seen in adults. In the pediatric study, the most common adverse events in subjects treated with combination therapy peginterferon alfa-2a and Ribavarin for up to 48 weeks were influenza-like illness (91%), upper respiratory tract infection (60%), headache (64%), gastrointestinal disorder (56%), skin disorder (47%), and injection-site reaction (45%). Seven subjects receiving combination peginterferon alfa-2a and Ribavarin treatment for 48 weeks discontinued therapy for safety reasons (depression, psychiatric evaluation abnormal, transient blindness, retinal exudates, hyperglycemia, type 1 diabetes mellitus, and anemia). Severe adverse events were reported in 2 subjects in the peginterferon alfa-2a plus Ribavarin combination therapy group (hyperglycemia and cholecystectomy).

* Displayed adverse drug reactions include all grades of reported adverse clinical events considered possibly, probably, or definitely related to study drug.

**Subjects in the peginterferon alfa-2a plus placebo arm who did not achieve undetectable viral load at week 24 switched to combination treatment thereafter. Therefore, only the first 24 weeks are presented for the comparison of combination therapy with monotherapy.


Study  NV17424




System  Organ  Class

Peginterferon  Alfa - 2a

180  mcg / 1 . 73  m ²  BSA  Ribavarin

15  mg / kg 

( N = 55 )

Peginterferon  Alfa - 2a

180  mcg / 1 . 73  m ²  BSA  Placebo ** 

( N = 59 )


%

%

General  disorders  and  administration  site  conditions



Influenza like illness

91

81

Injection site reaction

44

42

Fatigue

25

20

Irritability

24

14

Gastrointestinal  disorders



Gastrointestinal disorder

49

44

Nervous  system  disorders



Headache

51

39

Skin  and  subcutaneous  tissue  disorders



Rash

15

10

Pruritus

11

12

Musculoskeletal connective  tissue  and  bone  disorders



Musculoskeletal pain

35

29

Psychiatric  disorders



Insomnia

9

12

Metabolism  and  nutrition  disorders



Decreased appetite

11

14

In pediatric subjects randomized to combination therapy, the incidence of most adverse reactions was similar for the entire treatment period (up to 48 weeks plus 24 weeks follow-up) in comparison to the first 24 weeks, and increased only slightly for headache, gastrointestinal disorder, irritability and rash. The majority of adverse reactions occurred in the first 24 weeks of treatment.

Growth Inhibition in Pediatric Subjects .

Pediatric subjects treated with PEGASYS plus Ribavarin combination therapy showed a delay in weight and height increases with up to 48 weeks of therapy compared with baseline. Both weight for age and height for age z-scores as well as the percentiles of the normative population for subject weight and height decreased during treatment. At the end of 2 years follow-up after treatment, most subjects had returned to baseline normative curve percentiles for weight (64th mean percentile at baseline, 60th mean percentile at 2 years post-treatment) and height (54th mean percentile at baseline, 56th mean percentile at 2 years post-treatment). At the end of treatment, 43% (23 of 53) of subjects experienced a weight percentile decrease of more than 15 percentiles, and 25% (13 of 53) experienced a height percentile decrease of more than 15 percentiles on the normative growth curves. At 2 years post-treatment, 16% (6 of 38) of subjects were more than 15 percentiles below their baseline weight curve and 11% (4 of 38) were more than 15 percentiles below their baseline height curve.

Thirty-eight of the 114 subjects enrolled in the long-term follow-up study, extending up to 6 years posttreatment. For most subjects, post-treatment recovery in growth at 2 years post-treatment was maintained to 6 years post-treatment.

Common Adverse Reactions in CHC with HIV Coinfection (Adults)

The adverse event profile of coinfected patients treated with peginterferon alfa-2a/ribavirin in Study NR15961 was generally similar to that shown for monoinfected patients in Study NV15801 (Table 5). Events occurring more frequently in coinfected patients were neutropenia (40%), anemia (14%), thrombocytopenia (8%), weight decrease (16%), and mood alteration (9%).

Laboratory Test Abnormalities

Adult Patients  

Anemia due to hemolysis is the most significant toxicity of Ribavarin therapy. Anemia (hemoglobin less than 10 g/dL) was observed in 13% of all Ribavarin and peginterferon alfa-2a combination-treated patients in clinical trials. The maximum drop in hemoglobin occurred during the first 8 weeks of initiation of Ribavarin therapy [see DOSAGE AND ADMINISTRATION (2.3)].

Laboratory  Parameter

Peginterferon  Alfa - 2a  

Ribavirin 

1000 / 1200  mg 

48  wks

Interferon  alfa - 2b 


Ribavirin 

1000 / 1200  mg 

48  wks


( N = 887 )

( N = 443 )

Neutrophils  ( cells / mm3 )



1,000 <1,500

34%

38%

500 <1,000

49%

21%

<500

5%

1%

Platelets  ( cells / mm3 )



50,000 - <75,000

11%

4%

20,000 - <50,000

5%

< 1%

<20,000

0

0

Hemoglobin  ( g / dL )



8.5 - 9.9

11%

11%

<8.5

2%

< 1%

Pediatric Patients

Decreases in hemoglobin, neutrophils and platelets may require dose reduction or permanent discontinuation from treatment [see DOSAGE AND ADMINISTRATION (2.4)]. Most laboratory abnormalities noted during the clinical trial returned to baseline levels shortly after discontinuation of treatment.

* Subjects in the peginterferon alfa-2a plus placebo arm who did not achieve undetectable viral load at week 24 switched to combination treatment thereafter. Therefore, only the first 24 weeks are presented for the comparison of combination therapy with monotherapy.

Laboratory  Parameter 

Peginterferon  Alfa - 2a  180  mcg / 1 . 73  m ²  BSA  Ribavirin  15  mg / kg 

( N = 55 )

Peginterferon  Alfa - 2a  180  mcg / 1 . 73  m ²  BSA  Placebo *

( N = 59 )

Neutrophils  ( cells / mm3 )



1,000 to < 1,500 

31%

39%

750 to < 1,000 

27%

17%

500 to < 750 

25%

15%

< 500 

7%

5%

Platelets  ( cells / mm3 )



75,000 to < 100,000 

4%

2%

50,000 to < 75,000 

0%

2%

< 50,000 

0%

0%

Hemoglobin  ( g / dL )



8.5 to < 10 

7%

3%

< 8.5 

0%

0%

In patients randomized to combination therapy, the incidence of abnormalities during the entire treatment phase (up to 48 weeks plus 24 weeks follow-up) in comparison to the first 24 weeks increased slightly for neutrophils between 500 and 1,000 cells/mm  and hemoglobin values between 8.5 and 10 g/dL. The majority of hematologic abnormalities occurred in the first 24 weeks of treatment.

6.2 Postmarketing Experience

The following adverse reactions have been identified and reported during post-approval use of peginterferon alfa-2a/ribavirin combination therapy. 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.

Blood and Lymphatic System disorders

Pure red cell aplasia

Ear and Labyrinth disorders

Hearing impairment, hearing loss

Eye disorders

Serous retinal detachment

Immune disorders

Liver and renal graft rejection

Metabolism and Nutrition disorders

Dehydration

Skin and Subcutaneous Tissue disorders

Stevens-Johnson Syndrome (SJS)

Toxic epidermal necrolysis (TEN)

7 DRUG INTERACTIONS

  • Nucleoside analogues: Closely monitor for toxicities. Discontinue nucleoside reverse transcriptase inhibitors or reduce dose or discontinue interferon, Ribavarin or both with worsening toxicities
  • Azathioprine: Concomitant use of azathioprine with Ribavarin has been reported to induce severe pancytopenia and may increase the risk of azathioprine-related myelotoxicity (7.3)
Results from a pharmacokinetic sub-study demonstrated no pharmacokinetic interaction between peginterferon alfa-2a and Ribavarin.

7.1 Nucleoside Reverse Transcriptase Inhibitors (NRTIs)

In vitro data indicate Ribavarin reduces phosphorylation of lamivudine, stavudine, and zidovudine. However, no pharmacokinetic (e.g., plasma concentrations or intracellular triphosphorylated active metabolite concentrations) or pharmacodynamic (e.g., loss of HIV/HCV virologic suppression) interaction was observed when Ribavarin and lamivudine (n=18), stavudine (n=10), or zidovudine (n=6) were co-administered as part of a multi-drug regimen to HCV/HIV coinfected patients.

In Study NR15961 among the CHC/HIV coinfected cirrhotic patients receiving NRTIs, cases of hepatic decompensation (some fatal) were observed [see WARNINGS AND PRECAUTIONS (5.3)].

Patients receiving peginterferon alfa-2a/ribavirin and NRTIs should be closely monitored for treatment-associated toxicities. Physicians should refer to prescribing information for the respective NRTIs for guidance regarding toxicity management. In addition, dose reduction or discontinuation of peginterferon alfa-2a, Ribavarin or both should also be considered if worsening toxicities are observed, including hepatic decompensation (e.g., Child-Pugh greater than or equal to 6) [see WARNINGS AND PRECAUTIONS (5.3) and DOSAGE AND ADMINISTRATION (2.3)].

Didanosine

Co-administration of Ribavarin and didanosine is contraindicated. Didanosine or its active metabolite (dideoxyadenosine 5'-triphosphate) concentrations are increased when didanosine is co-administered with Ribavarin, which could cause or worsen clinical toxicities. Reports of fatal hepatic failure as well as peripheral neuropathy, pancreatitis, and symptomatic hyperlactatemia/lactic acidosis have been reported in clinical trials [see CONTRAINDICATIONS (4)].

Zidovudine

In Study NR15961, patients who were administered zidovudine in combination with peginterferon alfa-2a/ribavirin developed severe neutropenia (ANC less than 500) and severe anemia (hemoglobin less than 8 g/dL) more frequently than similar patients not receiving zidovudine (neutropenia 15% vs. 9%) (anemia 5% vs. 1%). Discontinuation of zidovudine should be considered as medically appropriate.

7.2 Drugs Metabolized by Cytochrome P450

In vitro studies indicate that Ribavarin does not inhibit CYP 2C9, CYP 2C19, CYP 2D6 or CYP 3A4.

7.3 Azathioprine

The use of Ribavarin to treat chronic hepatitis C in patients receiving azathioprine has been reported to induce severe pancytopenia and may increase the risk of azathioprine-related myelotoxicity. Inosine monophosphate dehydrogenase (IMDH) is required for one of the metabolic pathways of azathioprine. Ribavarin is known to inhibit IMDH, thereby leading to accumulation of an azathioprine metabolite, 6-methylthioinosine monophosphate (6-MTITP), which is associated with myelotoxicity (neutropenia, thrombocytopenia, and anemia). Patients receiving azathioprine with Ribavarin should have complete blood counts, including platelet counts, monitored weekly for the first month, twice monthly for the second and third months of treatment, then monthly or more frequently if dosage or other therapy changes are necessary [see WARNINGS AND PRECAUTIONS (5.6)].

8 USE IN SPECIFIC POPULATIONS

  • Ribavarin Pregnancy Registry
  • Pediatrics: Safety and efficacy in pediatric patients less than 5 years old have not been established (8.4)
  • Renal Impairment: Dose should be reduced in patients with creatinine clearance less than or equal to 50 mL/min (8.7)
  • Organ Transplant: Safety and efficacy have not been studied (8.10)

8.1 Pregnancy

Teratogenic Effects

Pregnancy: Category X.

Ribavarin produced significant embryocidal and/or teratogenic effects in all animal species in which adequate studies have been conducted. Malformations of the skull, palate, eye, jaw, limbs, skeleton, and gastrointestinal tract were noted. The incidence and severity of teratogenic effects increased with escalation of the drug dose. Survival of fetuses and offspring was reduced [see CONTRAINDICATIONS (4) and WARNINGS AND PRECAUTIONS (5.1)].

In conventional embryotoxicity/teratogenicity studies in rats and rabbits, observed no-effect dose levels were well below those for proposed clinical use (0.3 mg/kg/day for both the rat and rabbit; approximately 0.06 times the recommended daily human dose of Ribavarin). No maternal toxicity or effects on offspring were observed in a peri/postnatal toxicity study in rats dosed orally at up to 1 mg/kg/day (approximately 0.01 times the maximum recommended daily human dose of Ribavarin).

Treatment and Post-treatment: Potential Risk to the Fetus

Ribavarin is known to accumulate in intracellular components from where it is cleared very slowly. It is not known whether Ribavarin is contained in sperm, and if so, will exert a potential teratogenic effect upon fertilization of the ova. However, because of the potential human teratogenic effects of Ribavarin, male patients should be advised to take every precaution to avoid risk of pregnancy for their female partners.

Ribavarin should not be used by pregnant women or by men whose female partners are pregnant. Female patients of childbearing potential and male patients with female partners of childbearing potential should not receive Ribavarin unless the patient and his/her partner are using effective contraception (two reliable forms) during therapy and for 6 months post therapy [see CONTRAINDICATIONS (4)].

Ribavarin Pregnancy Registry

A Ribavarin Pregnancy Registry has been established to monitor maternal-fetal outcomes of pregnancies of female patients and female partners of male patients exposed to Ribavarin during treatment and for 6 months following cessation of treatment. Healthcare providers and patients are encouraged to report such cases by calling 1-800-593-2214.

8.3 Nursing Mothers

It is not known whether Ribavarin is excreted in human milk. Because many drugs are excreted in human milk and to avoid any potential for serious adverse reactions in nursing infants from Ribavarin, a decision should be made either to discontinue nursing or therapy with Ribavarin, based on the importance of the therapy to the mother.

8.4 Pediatric Use

Pharmacokinetic evaluations in pediatric patients have not been performed.

Safety and effectiveness of Ribavarin have not been established in patients below the age of 5 years.

8.5 Geriatric Use

Clinical studies of Ribavarin and peginterferon alfa-2a did not include sufficient numbers of subjects aged 65 or over to determine whether they respond differently from younger subjects. Specific pharmacokinetic evaluations for Ribavarin in the elderly have not been performed. The risk of toxic reactions to this drug may be greater in patients with impaired renal function. The dose of Ribavarin should be reduced in patients with creatinine clearance less than or equal to 50 mL/min; and the dose of peginterferon alfa-2a should be reduced in patients with creatinine clearance less than 30 mL/min [see DOSAGE AND ADMINISTRATION ; USE IN SPECIFIC POPULATIONS (8.7)].

8.6 Race

A pharmacokinetic study in 42 subjects demonstrated there is no clinically significant difference in Ribavarin pharmacokinetics among Black (n=14), Hispanic (n=13) and Caucasian (n=15) subjects.

8.7 Renal Impairment

Renal function should be evaluated in all patients prior to initiation of Ribavarin by estimating the patient's creatinine clearance.

A clinical trial evaluated treatment with Ribavarin and peginterferon alfa-2a in 50 CHC subjects with moderate or severe (creatinine clearance less than 30 mL/min) renal impairment or end stage renal disease (ESRD) requiring chronic hemodialysis (HD). In 18 subjects with ESRD receiving chronic HD, Ribavarin was administered at a dose of 200 mg daily with no apparent difference in the adverse event profile in comparison to subjects with normal renal function. Dose reductions and temporary interruptions of Ribavarin (due to ribavirin-related adverse reactions, mainly anemia) were observed in up to one-third ESRD/HD subjects during treatment; and only one-third of these subjects received Ribavarin for 48 weeks. Ribavarin plasma exposures were approximately 20% lower in subjects with ESRD on HD compared to subjects with normal renal function receiving the standard 1000/1200 mg Ribavarin daily dose.

Subjects with moderate (n=17) or severe (n=14) renal impairment did not tolerate 600 mg or 400 mg daily doses of Ribavarin, respectively, due to ribavirin-related adverse reactions, mainly anemia, and exhibited 20% to 30% higher Ribavarin plasma exposures (despite frequent dose modifications) compared to subjects with normal renal function (creatinine clearance greater than 80 mL/min) receiving the standard dose of Ribavarin. Discontinuation rates were higher in subjects with severe renal impairment compared to that observed in subjects with moderate renal impairment or normal renal function. Pharmacokinetic modeling and simulation indicate that a dose of 200 mg daily in patients with severe renal impairment and a dose of 200 mg daily alternating with 400 mg the following day in patients with moderate renal impairment will provide plasma Ribavarin exposure similar to patients with normal renal function receiving the approved regimen of Ribavarin. These doses have not been studied in patients [see DOSAGE AND ADMINISTRATION (2.4), and CLINICAL PHARMACOLOGY (12.3)].

Based on the pharmacokinetic and safety results from this trial, patients with creatinine clearance less than or equal to 50 mL/min should receive a reduced dose of Ribavarin; and patients with creatinine clearance less than 30 mL/min should receive a reduced dose of peginterferon alfa-2a. The clinical and hematologic status of patients with creatinine clearance less than or equal to 50 mL/min receiving Ribavarin should be carefully monitored. Patients with clinically significant laboratory abnormalities or adverse reactions which are persistently severe or worsening should have therapy withdrawn [see DOSAGE AND ADMINISTRATION (2.4), CLINICAL PHARMACOLOGY (12.3), and PEGINTERFERON ALFA-2A PACKAGE INSERT].

8.8 Hepatic Impairment

The effect of hepatic impairment on the pharmacokinetics of Ribavarin following administration of Ribavarin has not been evaluated. The clinical trials of Ribavarin were restricted to patients with Child-Pugh class A disease.

8.9 Gender

No clinically significant differences in the pharmacokinetics of Ribavarin were observed between male and female subjects.

Ribavarin pharmacokinetics, when corrected for weight, are similar in male and female patients.

8.10 Organ Transplant Recipients

The safety and efficacy of peginterferon alfa-2a and Ribavarin treatment have not been established in patients with liver and other transplantations. As with other alpha interferons, liver and renal graft rejections have been reported on peginterferon alfa-2a, alone or in combination with Ribavarin [see ADVERSE REACTIONS (6.2)].

10 OVERDOSAGE

No cases of overdose with Ribavarin have been reported in clinical trials. Hypocalcemia and hypomagnesemia have been observed in persons administered greater than the recommended dosage of Ribavarin. In most of these cases, Ribavarin was administered intravenously at dosages up to and in some cases exceeding four times the recommended maximum oral daily dose.

11 DESCRIPTION

Ribavarin is a nucleoside analogue with antiviral activity. The chemical name of Ribavarin is 1-β-D-ribofuranosyl-1H-1,2,4-triazole-3-carboxamide and has the following structural formula:

The molecular formula of Ribavarin is C8H12N4O5 and the molecular weight is 244.2.

Ribavarin, USP is white, crystalline powder. It is freely soluble in water and slightly soluble in dehydrated alcohol.

Each film-coated Ribavarin tablet intended for oral administration contains 200 mg or 400 mg or 500 mg or 600 mg of Ribavarin. In addition, each tablet contains the following inactive ingredients: crospovidone, hypromellose, iron oxide red, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, silicon dioxide, talc and titanium dioxide.

Organic test number pending in the USP.

structured formula for Ribavarin

12 CLINICAL PHARMACOLOGY

12.1 Mechanism of Action

Ribavarin is an antiviral drug [see MICROBIOLOGY ].

12.3 Pharmacokinetics

Multiple dose Ribavarin pharmacokinetic data are available for HCV patients who received Ribavarin in combination with peginterferon alfa-2a. Following administration of 1200 mg/day with food for 12 weeks mean±SD (n=39; body weight greater than 75 kg) AUC0-12hr was 25,361±7110 ng·hr/mL and Cmax was 2748±818 ng/mL. The average time to reach Cmax was 2 hours. Trough Ribavarin plasma concentrations following 12 weeks of dosing with food were 1662±545 ng/mL in HCV infected patients who received 800 mg/day (n=89), and 2112±810 ng/mL in patients who received 1200 mg/day (n=75; body weight greater than 75 kg).

The terminal half-life of Ribavarin following administration of a single oral dose of Ribavarin is about 120 to 170 hours. The total apparent clearance following administration of a single oral dose of Ribavarin is about 26 L/h. There is extensive accumulation of Ribavarin after multiple dosing (twice daily) such that the Cmax at steady state was four-fold higher than that of a single dose.

Effect of Food on Absorption of Ribavarin

Bioavailability of a single oral dose of Ribavarin was increased by co-administration with a high-fat meal. The absorption was slowed (Tmax was doubled) and the AUC0-192h and Cmax increased by 42% and 66%, respectively, when Ribavarin was taken with a high-fat meal compared with fasting conditions [see DOSAGE AND ADMINISTRATION (2) and PATIENT COUNSELING INFORMATION (17)].

Elimination and Metabolism

The contribution of renal and hepatic pathways to Ribavarin elimination after administration of Ribavarin is not known. In vitro studies indicate that Ribavarin is not a substrate of CYP450 enzymes.

Renal Impairment

A clinical trial evaluated 50 CHC subjects with either moderate (creatinine clearance 30 to 50 mL/min) or severe (creatinine clearance less than 30 mL/min) renal impairment or end stage renal disease (ESRD) requiring chronic hemodialysis (HD). The apparent clearance of Ribavarin was reduced in subjects with creatinine clearance less than or equal to 50 mL/min, including subjects with ESRD on HD, exhibiting approximately 30% of the value found in subjects with normal renal function. Pharmacokinetic modeling and simulation indicates that a dose of 200 mg daily in patients with severe renal impairment and a dose of 200 mg daily alternating with 400 mg the following day in patients with moderate renal impairment will provide plasma Ribavarin exposures similar to that observed in patients with normal renal function receiving the standard 1000/1200 mg Ribavarin daily dose. These doses have not been studied in patients.

In 18 subjects with ESRD receiving chronic HD, Ribavarin was administered at a dose of 200 mg daily. Ribavarin plasma exposures in these subjects were approximately 20% lower compared to subjects with normal renal function receiving the standard 1000/1200 mg Ribavarin daily dose [see DOSAGE AND ADMINISTRATION (2.4), USE IN SPECIFIC POPULATIONS (8.7)].

Plasma Ribavarin is removed by hemodialysis with an extraction ratio of approximately 50%; however, due to the large volume of distribution of Ribavarin, plasma exposure is not expected to change with hemodialysis.

12.4 Microbiology

Mechanism of Action

The mechanism by which Ribavarin contributes to its antiviral efficacy in the clinic is not fully understood. Ribavarin has direct antiviral activity in tissue culture against many RNA viruses. Ribavarin increases the mutation frequency in the genomes of several RNA viruses and Ribavarin triphosphate inhibits HCV polymerase in a biochemical reaction.

Antiviral Activity in Cell Culture

In the stable HCV cell culture model system (HCV replicon), Ribavarin inhibited autonomous HCV RNA replication with a 50% effective concentration (EC50) value of 11 to 21 mcM. In the same model, PEG-IFN α-2a also inhibited HCV RNA replication, with an EC50 value of 0.1 to 3 ng/mL. The combination of PEG-IFN α-2a and Ribavarin was more effective at inhibiting HCV RNA replication than either agent alone.

Resistance

Different HCV genotypes display considerable clinical variability in their response to PEG-IFN-α and Ribavarin therapy. Viral genetic determinants associated with the variable response have not been definitively identified.

Cross-resistance

Cross-resistance between IFN α and Ribavarin has not been observed.

13 NONCLINICAL TOXICOLOGY

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

Carcinogenesis

In a p53 mouse carcinogenicity study up to the maximum tolerated dose of 100 mg/kg/day, Ribavarin was not oncogenic. Ribavarin was also not oncogenic in a rat 2 year carcinogenicity study at doses up to the maximum tolerated dose of 60 mg/kg/day. On a body surface area basis, these doses are approximately 0.5 and 0.6 times the maximum recommended daily human dose of Ribavarin, respectively.

 

Mutagenesis

Ribavarin demonstrated mutagenic activity in the in vitro mouse lymphoma assay. No clastogenic activity was observed in an in vivo mouse micronucleus assay at doses up to 2000 mg/kg. However, results from studies published in the literature show clastogenic activity in the in vivo mouse micronucleus assay at oral doses up to 2000 mg/kg. A dominant lethal assay in rats was negative, indicating that if mutations occurred in rats they were not transmitted through male gametes.

 

Impairment of Fertility

In a fertility study in rats, Ribavarin showed a marginal reduction in sperm counts at the dose of 100 mg/kg/day with no effect on fertility. Upon cessation of treatment, total recovery occurred after 1 spermatogenesis cycle. Abnormalities in sperm were observed in studies in mice designed to evaluate the time course and reversibility of ribavirin-induced testicular degeneration at doses of 15 to 150 mg/kg/day (approximately 0.1 to 0.8 times the maximum recommended daily human dose of Ribavarin) administered for 3 to 6 months. Upon cessation of treatment, essentially total recovery from ribavirin-induced testicular toxicity was apparent within 1 or 2 spermatogenic cycles.

Female patients of childbearing potential and male patients with female partners of childbearing potential should not receive Ribavarin unless the patient and his/her partner are using effective contraception (two reliable forms). Based on a multiple dose half-life (t1/2) of Ribavarin of 12 days, effective contraception must be utilized for 6 months post therapy (i.e., 15 half-lives of clearance for Ribavarin).

 

No reproductive toxicology studies have been performed using peginterferon alfa-2a in combination with Ribavarin. However, peginterferon alfa-2a and Ribavarin when administered separately, each has adverse effects on reproduction. It should be assumed that the effects produced by either agent alone would also be caused by the combination of the two agents.

13.2 ANIMAL PHARMACOLOGY AND OR TOXICOLOGY

In a study in rats, it was concluded that dominant lethality was not induced by Ribavarin at doses up to 200 mg/kg for 5 days (up to 1.7 times the maximum recommended human dose of Ribavarin).

Long-term studies in the mouse and rat (18 to 24 months; dose 20 to 75, and 10 to 40 mg/kg/day, respectively, approximately 0.1 to 0.4 times the maximum daily human dose of Ribavarin) have demonstrated a relationship between chronic Ribavarin exposure and an increased incidence of vascular lesions (microscopic hemorrhages) in mice. In rats, retinal degeneration occurred in controls, but the incidence was increased in ribavirin-treated rats.

14 CLINICAL STUDIES

14.1 Chronic Hepatitis C Patients

Adult Patients

The safety and effectiveness of peginterferon alfa-2a in combination with Ribavarin for the treatment of hepatitis C virus infection were assessed in two randomized controlled clinical trials. All patients were adults, had compensated liver disease, detectable hepatitis C virus, liver biopsy diagnosis of chronic hepatitis, and were previously untreated with interferon. Approximately 20% of patients in both studies had compensated cirrhosis. Patients coinfected with HIV were excluded from these studies.

In Study NV15801, patients were randomized to receive either peginterferon alfa-2a 180 mcg subcutaneous once weekly with an oral placebo, peginterferon alfa-2a 180 mcg once weekly with Ribavarin 1000 mg by mouth (body weight less than 75 kg) or 1200 mg by mouth (body weight greater than or equal to 75 kg) or interferon alfa-2b 3 MIU subcutaneous three times a week plus Ribavarin 1000 mg or 1200 mg by mouth. All patients received 48 weeks of therapy followed by 24 weeks of treatment-free follow-up. Ribavarin or placebo treatment assignment was blinded. Sustained virological response was defined as undetectable (less than 50 IU/mL) HCV RNA on or after study week 68. Peginterferon alfa-2a in combination with Ribavarin resulted in a higher SVR compared to peginterferon alfa-2a alone or interferon alfa-2b and Ribavarin (Table 9). In all treatment arms, patients with viral genotype 1, regardless of viral load, had a lower response rate to peginterferon alfa-2a in combination with Ribavarin compared to patients with other viral genotypes.


Interferon  alfa - 2b  Ribavirin  1000  mg  or  1200  mg

Peginterferon  Alfa - 2a  Placebo

Peginterferon  Alfa - 2a  Ribavirin  1000  mg  or  1200  mg

All patients 

197/444 (44%)

65/224 (29%)

241/453 (53%)

Genotype 1 

103/285 (36%)

29/145 (20%)

132/298 (44%)

Genotypes 2 to 6 

94/159 (59%)

36/79 (46%)

109/155 (70%)

Difference in overall treatment response (Peginterferon alfa-2a/ribavirin – Interferon alfa-2b/ribavirin) was 9% (95% CI 2.3, 15.3).

In Study NV15942, all patients received peginterferon alfa-2a 180 mcg subcutaneous once weekly and were randomized to treatment for either 24 or 48 weeks and to a Ribavarin dose of either 800 mg or 1000 mg/1200 mg (for body weight less than 75 kg/ greater than or equal to 75 kg). Assignment to the four treatment arms was stratified by viral genotype and baseline HCV viral titer. Patients with genotype 1 and high viral titer (defined as greater than 2 x 106HCV RNA copies/mL serum) were preferentially assigned to treatment for 48 weeks.

Sustained Virologic Response (SVR) and HCV Genotype

HCV 1 and 4–Irrespective of baseline viral titer, treatment for 48 weeks with peginterferon alfa-2a and 1000 mg or 1200 mg of Ribavarin resulted in higher SVR (defined as undetectable HCV RNA at the end of the 24 week treatment-free follow-up period) compared to shorter treatment (24 weeks) and/or 800 mg Ribavarin.

HCV 2 and 3– Irrespective of baseline viral titer, treatment for 24 weeks with peginterferon alfa-2a and 800 mg of Ribavarin resulted in a similar SVR compared to longer treatment (48 weeks) and/or 1000 mg or 1200 mg of Ribavarin (see Table 10).

The numbers of patients with genotype 5 and 6 were too few to allow for meaningful assessment.


24  Weeks  Treatment


48  Weeks  Treatment


*1000 mg for body weight less than 75 kg; 1200 mg for body weight greater than or equal to 75 kg.


Peginterferon  Alfa - 2a  Ribavirin  800  mg

( N = 207 )

Peginterferon  Alfa - 2a  Ribavirin  1000  mg  or  1200  mg *

( N = 280 )

Peginterferon  Alfa - 2a  Ribavirin  800  mg

( N = 361 )

Peginterferon  Alfa - 2a  Ribavirin  1000  mg  or  1200  mg *

( N = 436 )

Genotype 1 

29/101 (29%)

48/118 (41%)

99/250 (40%)

138/271 (51%)

Genotypes 2, 3 

79/96 (82%)

116/144 (81%)

75/99 (76%)

117/153 (76%)

Genotype 4 

0/5 (0%)

7/12 (58%)

5/8 (63%)

9/11 (82%)

Pediatric Patients

Previously untreated pediatric subjects 5 through 17 years of age (55% less than 12 years old) with chronic hepatitis C, compensated liver disease and detectable HCV RNA were treated with Ribavarin approximately 15 mg/kg/day plus peginterferon alfa-2a 180 mcg/1.73 m2 x body surface area once weekly for 48 weeks. All subjects were followed for 24 weeks post-treatment. Sustained virological response (SVR) was defined as undetectable (less than 50 IU/mL) HCV RNA on or after study week 68. A total of 114 subjects were randomized to receive either combination treatment of Ribavarin plus peginterferon alfa-2a or peginterferon alfa-2a monotherapy; subjects failing peginterferon alfa-2a monotherapy at 24 weeks or later could receive open-label Ribavarin plus peginterferon alfa-2a. The initial randomized arms were balanced for demographic factors; 55 subjects received initial combination treatment of Ribavarin plus peginterferon alfa-2a and 59 received peginterferon alfa-2a plus placebo; in the overall intent-to-treat population, 45% were female, 80% were Caucasian, and 81% were infected with HCV genotype 1. The SVR results are summarized in Table 11.

*Results indicate undetectable HCV RNA defined as HCV RNA less than 50 IU/mL at 24 weeks post-treatment using the AMPLICOR HCV test v2

**Scheduled treatment duration was 48 weeks regardless of the genotype

***Includes HCV genotypes 2,3 and others


Peginterferon  alfa - 2a  180  mcg / 1 . 73  m ²  BSA  Ribavirin  15  mg / kg *

( N = 55 )

Peginterferon  alfa - 2a  180  mcg / 1 . 73  m ²  BSA  + Placebo *

( N = 59 )

All  HCV  genotypes ** 

29 (53%)

12 (20%)

HCV  genotype 

21/45 (47%)

8/47 (17%)

HCV  non - genotype  1 *** 

8/10 (80%)

4/12 (33%)

14.2 Other Treatment Response Predictors

Treatment response rates are lower in patients with poor prognostic factors receiving pegylated interferon alpha therapy. In studies NV15801 and NV15942, treatment response rates were lower in patients older than 40 years (50% vs. 66%), in patients with cirrhosis (47% vs. 59%), in patients weighing over 85 kg (49% vs. 60%), and in patients with genotype 1 with high vs. low viral load (43% vs. 56%). African-American patients had lower response rates compared to Caucasians.

In studies NV15801 and NV15942, lack of early virologic response by 12 weeks (defined as HCV RNA undetectable or greater than 2 log10 lower than baseline) was grounds for discontinuation of treatment. Of patients who lacked an early viral response by 12 weeks and completed a recommended course of therapy despite a protocol-defined option to discontinue therapy, 5/39 (13%) achieved an SVR. Of patients who lacked an early viral response by 24 weeks, 19 completed a full course of therapy and none achieved an SVR.

14.3 Chronic Hepatitis C/HIV Coinfected Patients

In Study NR15961, patients with CHC/HIV were randomized to receive either peginterferon alfa-2a 180 mcg subcutaneous once weekly plus an oral placebo, peginterferon alfa-2a 180 mcg once weekly plus Ribavarin 800 mg by mouth daily or interferon alfa-2a, 3 MIU subcutaneous three times a week plus Ribavarin 800 mg by mouth daily. All patients received 48 weeks of therapy and sustained virologic response (SVR) was assessed at 24 weeks of treatment-free follow-up. Ribavarin or placebo treatment assignment was blinded in the peginterferon alfa-2a treatment arms. All patients were adults, had compensated liver disease, detectable hepatitis C virus, liver biopsy diagnosis of chronic hepatitis C, and were previously untreated with interferon. Patients also had CD4+ cell count greater than or equal to 200 cells/mm3 or CD4+ cell count greater than or equal to 100 cells/mm3 but less than 200 cells/mm3 and HIV-1 RNA less than 5000 copies/mL, and stable status of HIV. Approximately 15% of patients in the study had cirrhosis. Results are shown in Table 12.


Interferon  Alfa - 2a  Ribavirin  800  mg

( N = 289 )

Peginterferon  Alfa - 2a  Placebo

( N = 289 )

Peginterferon  Alfa - 2a  Ribavirin  800  mg

( N = 290 )

All patients 

33 (11%)

58 (20%)

116 (40%)

Genotype 1 

12/171 (7%)

24/175 (14%)

51/176 (29%)

Genotypes 2, 3 

18/89 (20%)

32/90 (36%)

59/95 (62%)

Treatment response rates were lower in CHC/HIV patients with poor prognostic factors (including HCV genotype 1, HCV RNA greater than 800,000 IU/mL, and cirrhosis) receiving pegylated interferon alpha therapy.

Of the patients who did not demonstrate either undetectable HCV RNA or at least a 2 log10 reduction from baseline in HCV RNA titer by 12 weeks of peginterferon alfa-2a and Ribavarin combination therapy, 2% (2/85) achieved an SVR.

In CHC patients with HIV coinfection who received 48 weeks of peginterferon alfa-2a alone or in combination with Ribavarin treatment, mean and median HIV RNA titers did not increase above baseline during treatment or 24 weeks post-treatment.

16 HOW SUPPLIED/STORAGE AND HANDLING

Ribavarin Tablets, 200 mg are light pink to pink, round, biconvex, beveled, film-coated tablets debossed with the logo of 'ZC19' on one side, other side plain and supplied as follows:

NDC 68382-046-03 in bottle of 168 tablets

NDC 68382-046-28 in bottle of 180 tablets

NDC 68382-046-10 in bottle of 1000 tablets

NDC 68382-046-77 in unit-dose blister cartons of 100 (10 x 10) unit-dose tablets

Ribavarin Tablets, 400 mg are light pink to pink, capsule shaped, biconvex, film-coated tablets debossed with 'ZD' and '07' on one side and plain on other side and supplied as follows:

NDC 68382-127-17 in bottle of 28 tablets

NDC 68382-127-07 in bottle of 56 tablets

NDC 68382-127-14 in bottle of 60 tablets

Ribavarin Tablets, 500 mg are light pink to pink, modified capsule shaped, biconvex, film-coated tablets debossed with 'ZC56' on one side and plain on the other side and supplied as follows:

NDC 68382-128-17 in bottle of 28 tablets

NDC 68382-128-07 in bottle of 56 tablets

NDC 68382-128-14 in bottle of 60 tablets

Ribavarin Tablets, 600 mg are light pink to pink, modified capsule shaped, biconvex, film-coated tablets debossed with 'ZD' and '08' on one side and plain on other side and supplied as follows:

NDC 68382-129-17 in bottle of 28 tablets

NDC 68382-129-07 in bottle of 56 tablets

NDC 68382-129-14 in bottle of 60 tablets

Storage and Handling

Store at 20° to 25°C (68° to 77°F).

Keep bottle tightly closed.

17 PATIENT COUNSELING INFORMATION

  • See FDA-approved patient labeling (Medication Guide)
     Pregnancy

Patients must be informed that Ribavarin may cause birth defects and/or death of the exposed fetus. Ribavarin therapy must not be used by women who are pregnant or by men whose female partners are pregnant. Extreme care must be taken to avoid pregnancy in female patients and in female partners of male patients taking Ribavarin therapy and for 6 months post therapy. Patients should use two reliable methods of birth control while taking Ribavarin therapy and for 6 months post therapy. Ribavarin therapy should not be initiated until a report of a negative pregnancy test has been obtained immediately prior to initiation of therapy. Patients must perform a pregnancy test monthly during therapy and for 6 months post therapy.

Female patients of childbearing potential and male patients with female partners of childbearing potential must be advised of the teratogenic/embryocidal risks and must be instructed to practice effective contraception during Ribavarin therapy and for 6 months post therapy. Patients should be advised to notify the healthcare provider immediately in the event of a pregnancy [see CONTRAINDICATIONS (4) and WARNINGS AND PRECAUTIONS (5.1)].

Anemia

The most common adverse event associated with Ribavarin is anemia, which may be severe [see BOXED WARNING, WARNINGS AND PRECAUTIONS (5.2) and ADVERSE REACTIONS (6.1)]. Patients should be advised that laboratory evaluations are required prior to starting Ribavarin therapy and periodically thereafter [see WARNINGS AND PRECAUTIONS (5.9)]. It is advised that patients be well hydrated, especially during the initial stages of treatment.

Patients who develop dizziness, confusion, somnolence, and fatigue should be cautioned to avoid driving or operating machinery.

Patients should be advised to take Ribavarin with food.

Patients should be questioned about prior history of drug abuse before initiating ribavirin/peginterferon alfa-2a, as relapse of drug addiction and drug overdoses have been reported in patients treated with interferons.

Patients should be advised not to drink alcohol, as alcohol may exacerbate chronic hepatitis C infection.

Patients should be informed about what to do in the event they miss a dose of Ribavarin. The missed doses should be taken as soon as possible during the same day. Patients should not double the next dose. Patients should be advised to call their healthcare provider if they have questions.

Patients should be informed that the effect of peginterferon alfa-2a/ribavirin treatment of hepatitis C infection on transmission is not known, and that appropriate precautions to prevent transmission of hepatitis C virus during treatment or in the event of treatment failure should be taken.

Patients should be informed regarding the potential benefits and risks attendant to the use of Ribavarin. Instructions on appropriate use should be given, including review of the contents of the enclosed MEDICATION GUIDE, which is not a disclosure of all or possible adverse effects.

Manufactured by:

Cadila Healthcare Ltd.

Ahmedabad, India

Distributed by:

Zydus Pharmaceuticals USA Inc.

Pennington, NJ 08534

Rev.: 10/15

MEDICATION GUIDE

Ribavarin

(rye-ba-VYE-rin)

Tablets

Read this Medication Guide carefully before you start taking Ribavarin and read the Medication Guide each time you get more Ribavarin. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or your treatment.

Also read the Medication Guide for peginterferon alfa-2a.

What is the most important information I should know about Ribavarin?

  • You should not take Ribavarin alone to treat chronic hepatitis C infection. Ribavarin should be used with peginterferon alfa-2a to treat chronic hepatitis C infection.
  • Ribavarin may cause you to have a blood problem (hemolytic anemia) that can worsen any heart problems you have, and cause you to have a heart attack or die. Tell your healthcare provider if you have ever had any heart problems. Ribavarin may not be right for you. If you have chest pain while you take Ribavarin, get emergency medical attention right away.
  • Ribavarin may cause birth defects or death of your unborn baby. If you are pregnant or your sexual partner is pregnant, do not take Ribavarin. You or your sexual partner should not become pregnant while you take Ribavarin and for 6 months after treatment is over. You must use two forms of birth control when you take Ribavarin and for the 6 months after treatment.
  • Females must have a pregnancy test before starting Ribavarin, every month while treated with Ribavarin, and every month for the 6 months after treatment with Ribavarin.
  • If you or your female sexual partner becomes pregnant while taking Ribavarin or within 6 months after you stop taking Ribavarin, tell your healthcare provider right away. You or your healthcare provider should contact the Ribavarin Pregnancy Registry by calling 1-800-593-2214. The Ribavarin Pregnancy Registry collects information about what happens to mothers and their babies if the mother takes Ribavarin while she is pregnant.
What is R ibavirin?

Ribavarin is a prescription medicine used with another medicine called peginterferon alfa-2a to treat chronic (lasting a long time) hepatitis C infection in people 5 years and older whose liver still works normally, and who have not been treated before with a medicine called an interferon alpha. It is not known if Ribavarin is safe and will work in children under 5 years of age.

Who should not take Ribavarin?

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

Do not take Ribavarin if you:

  • have certain types of hepatitis caused by your immune system attacking your liver (autoimmune hepatitis)
  • have certain blood disorders, such as thalassemia major or sickle-cell anemia (hemoglobinopathies)
  • take didanosine (Videx or Videx EC)
Talk to your healthcare provider before starting treatment with Ribavarin if you have any of these medical conditions.

What should I tell my healthcare provider before taking Ribavarin?

Before you take Ribavarin, tell your healthcare provider if you have or have had:

  • treatment for hepatitis C that did not work for you
  • serious allergic reactions to Ribavarin or to any of the ingredients in Ribavarin. See the end of this Medication Guide for a list of ingredients.
  • breathing problems. Ribavarin may cause or worsen your breathing problems you already have.
  • vision problems. Ribavarin may cause eye problems or worsen eye problems you already have. You should have an eye exam before you start treatment with Ribavarin.
  • certain blood disorders such as anemia
  • high blood pressure, heart problems or have had a heart attack. Your healthcare provider should test your blood and heart before you start treatment with Ribavarin.
  • thyroid problems
  • diabetes. Ribavarin and peginterferon alfa-2a combination therapy may make your diabetes worse or harder to treat.
  • liver problems other than hepatitis C virus infection
  • human immunodeficiency virus (HIV) or other immunity problems
  • mental health problems, including depression or thoughts of suicide
  • kidney problems
  • an organ transplant
  • drug addiction or abuse
  • infection with hepatitis B virus
  • any other medical condition
  • are breastfeeding. It is not known if Ribavarin passes into your breastmilk. You and your healthcare provider should decide if you will take Ribavarin or breastfeed.
Tell your healthcare provider about all the medicines you take, including prescription and non-prescription medicines, vitamins and herbal supplements. Some medicines can cause serious side effects if taken while you also take Ribavarin. Some medicines may affect how Ribavarin works or Ribavarin may affect how your other medicines work.

Especially tell your healthcare provider if you take any medicines to treat HIV, including didanosine (Videx or Videx EC), or if you take azathioprine (Imuran or Azasan).

Know the medicines you take. Keep a list of them to show your healthcare provider or pharmacist when you get a new medicine.

How should I take Ribavarin?

  • Take Ribavarin exactly as your healthcare provider tells you. Your healthcare provider will tell you how much Ribavarin to take and when to take it. For children 5 years of age and older your healthcare provider will prescribe the dose of Ribavarin based on weight.
  • Take Ribavarin with food.
  • If you miss a dose of Ribavarin, take the missed dose as soon as possible during the same day. Do not double the next dose. If you have questions about what to do, call your healthcare provider.
  • If you take too much Ribavarin, call your healthcare provider or local Poison Control Center right away, or go the nearest hospital emergency room right away.
  • Your healthcare provider should do blood tests before you start treatment with Ribavarin, at weeks 2 and 4 of treatment, and then as needed to see how well you are tolerating treatment and to check for side effects. Your healthcare provider may change your dose of Ribavarin based on blood test results or side effects you may have.
  • If you have heart problems, your healthcare provider should check your heart by doing an electrocardiogram before you start treatment with Ribavarin, and if needed during treatment.
What should I avoid while taking Ribavarin?

  • Ribavarin can make you feel tired, dizzy, or confused. You should not drive or operate machinery if you have any of these symptoms.
  • Do not drink alcohol, including beer, wine, and liquor. This may make your liver disease worse.
What are the possible side effects of Ribavarin?

Ribavarin may cause serious side effects including:

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

  • Swelling and irritation of your pancreas (pancreatitis). You may have stomach pain, nausea, vomiting or diarrhea.
  • Severe allergic reactions. Symptoms may include hives, wheezing, trouble breathing, chest pain, swelling of your mouth, tongue, or lips, or severe rash.
  • Serious breathing problems. Difficulty breathing may be a sign of a serious lung infection (pneumonia) that can lead to death.
  • Serious eye problems that may lead to vision loss or blindness.
  • Liver problems. Some people may get worsening of liver function. Tell your healthcare provider right away if you have any of these symptoms: stomach bloating, confusion, brown urine, and yellow eyes.
  • Severe depression
  • Suicidal thoughts and attempts
  • Effect on growth in children. Children can experience a delay in weight gain and height increase while being treated with peginterferon alfa-2a and Ribavarin. Catch-up in growth happens after treatment stops, but some children may not reach the height that they were expected to have before treatment. Talk to your healthcare provider if you are concerned about your child's growth during treatment with peginterferon alfa-2a and Ribavarin.
Call your healthcare provider or get medical help right away if you have any of the symptoms listed above. These may be signs of a serious side effect of Ribavarin treatment.

Common side effects of Ribavarin taken with peginterferon alfa-2a include:

  • flu-like symptoms-feeling tired, headache, shaking along with high temperature (fever), and muscle or joint aches
  • mood changes, feeling irritable, anxiety, and difficulty sleeping
  • loss of appetite, nausea, vomiting, and diarrhea
  • hair loss
  • itching
Tell your healthcare provider about any side effect that bothers you or that does not go away.

These are not all the possible side effects of Ribavarin treatment. 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.

Please address medical inquiries to, (MedicalAffairsRibavarinzydususa.com) Tel.: 1-877-993-8779.

How should I store Ribavarin?

  • Store Ribavarin tablets between 20° to 25°C (68° to 77°F).59°F.
  • Keep the bottle tightly closed.
Keep Ribavarin and all medicines out of the reach of children.

General information about the safe and effective use of Ribavarin

It is not known if treatment with Ribavarin in combination with peginterferon alfa-2a will prevent an infected person from spreading the hepatitis C virus to another person while on treatment.

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

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

What are the ingredients in Ribavarin Tablets?

Active Ingredient: Ribavarin, USP

Inactive Ingredients: crospovidone, hypromellose, iron oxide red, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, silicon dioxide, talc and titanium dioxide.

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

This product's label may have been updated. For current full prescribing information, please visit www.zydususa.com.

Manufactured by:

Cadila Healthcare Ltd.

Ahmedabad, India

Distributed by:

Zydus Pharmaceuticals USA Inc.

Pennington, NJ 08534

Rev.: 02/15

NDC 68382-046-03 in bottle of 168 tablets

Ribavarin  Tablets, 200 mg

Rx only

168 tablets

ZYDUS

NDC 68382-127-07 in bottle of 56 tablets

Ribavarin  Tablets, 400 mg

Rx only

56 tablets

ZYDUS

NDC 68382-128-07 in bottle of 56 tablets

Ribavarin  Tablets, 500 mg

Rx only

56 tablets

ZYDUS

NDC 68382-129-07 in bottle of 56 tablets

Ribavarin Tablets, 600 mg

Rx only

56 tablets

ZYDUS

Ribavarin tablets, 200 mg Ribavarin tablet,400 mg Ribavarin Tablet 500 mg Ribavarin tablet 600 mg

Ribavarin pharmaceutical active ingredients containing related brand and generic drugs:

infoActive ingredient is the part of the drug or medicine which is biologically active. This portion of the drug is responsible for the main action of the drug which is intended to cure or reduce the symptom or disease. The other portions of the drug which are inactive are called excipients; there role is to act as vehicle or binder. In contrast to active ingredient, the inactive ingredient's role is not significant in the cure or treatment of the disease. There can be one or more active ingredients in a drug.


Ribavarin available forms, composition, doses:

infoForm of the medicine is the form in which the medicine is marketed in the market, for example, a medicine X can be in the form of capsule or the form of chewable tablet or the form of tablet. Sometimes same medicine can be available as injection form. Each medicine cannot be in all forms but can be marketed in 1, 2, or 3 forms which the pharmaceutical company decided based on various background research results.
Composition is the list of ingredients which combinedly form a medicine. Both active ingredients and inactive ingredients form the composition. The active ingredient gives the desired therapeutic effect whereas the inactive ingredient helps in making the medicine stable.
Doses are various strengths of the medicine like 10mg, 20mg, 30mg and so on. Each medicine comes in various doses which is decided by the manufacturer, that is, pharmaceutical company. The dose is decided on the severity of the symptom or disease.


Ribavarin destination | category:

infoDestination is defined as the organism to which the drug or medicine is targeted. For most of the drugs what we discuss, human is the drug destination.
Drug category can be defined as major classification of the drug. For example, an antihistaminic or an antipyretic or anti anginal or pain killer, anti-inflammatory or so.


Ribavarin Anatomical Therapeutic Chemical codes:

infoA medicine is classified depending on the organ or system it acts [Anatomical], based on what result it gives on what disease, symptom [Therapeutical], based on chemical composition [Chemical]. It is called as ATC code. The code is based on Active ingredients of the medicine. A medicine can have different codes as sometimes it acts on different organs for different indications. Same way, different brands with same active ingredients and same indications can have same ATC code.


Ribavarin pharmaceutical companies:

infoPharmaceutical companies are drug manufacturing companies that help in complete development of the drug from the background research to formation, clinical trials, release of the drug into the market and marketing of the drug.
Researchers are the persons who are responsible for the scientific research and is responsible for all the background clinical trials that resulted in the development of the drug.


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References

  1. Dailymed."RIBAVIRIN TABLET, FILM COATED [ZYDUS PHARMACEUTICALS (USA) INC.]". https://dailymed.nlm.nih.gov/dailym... (accessed August 28, 2018).
  2. Dailymed."RIBAVIRIN: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailym... (accessed August 28, 2018).
  3. "ribavirin". https://pubchem.ncbi.nlm.nih.gov/co... (accessed August 28, 2018).

Frequently asked Questions

Can i drive or operate heavy machine after consuming Ribavarin?

Depending on the reaction of the Ribavarin after taken, if you are feeling dizziness, drowsiness or any weakness as a reaction on your body, Then consider Ribavarin not safe to drive or operate heavy machine after consumption. Meaning that, do not drive or operate heavy duty machines after taking the capsule if the capsule has a strange reaction on your body like dizziness, drowsiness. As prescribed by a pharmacist, it is dangerous to take alcohol while taking medicines as it exposed patients to drowsiness and health risk. Please take note of such effect most especially when taking Primosa capsule. It's advisable to consult your doctor on time for a proper recommendation and medical consultations.

Is Ribavarin addictive or habit forming?

Medicines are not designed with the mind of creating an addiction or abuse on the health of the users. Addictive Medicine is categorically called Controlled substances by the government. For instance, Schedule H or X in India and schedule II-V in the US are controlled substances.

Please consult the medicine instruction manual on how to use and ensure it is not a controlled substance.In conclusion, self medication is a killer to your health. Consult your doctor for a proper prescription, recommendation, and guidiance.

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Review

sDrugs.com conducted a study on Ribavarin, and the result of the survey is set out below. It is noteworthy that the product of the survey is based on the perception and impressions of the visitors of the website as well as the views of Ribavarin consumers. We, as a result of this, advice that you do not base your therapeutic or medical decisions on this result, but rather consult your certified medical experts for their recommendations.

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The information was verified by Dr. Arunabha Ray, MD Pharmacology

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