FabiFlu Favipiravir 200 mg Tablets

FabiFlu Favipiravir 200 mg Tablets

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उत्पाद विवरण

1. Technical Specifications

Attribute Details
Brand Name FabiFlu 200 mg Tablet
Active Ingredient Favipiravir
Strength 200 mg
Dosage Form Oral Tablet
Packaging Size 34 tablets / 122 tablets (varies by pack)
Packaging Type Strip in carton box
Medicine Type Allopathic, Antiviral
Manufactured By Glenmark Pharmaceuticals Ltd.
Distributed By Authorized pharmaceutical distributors

2. Product Description

FabiFlu 200 mg Tablet contains Favipiravir, an antiviral drug initially developed for influenza. It works by inhibiting the RNA-dependent RNA polymerase (RdRp) enzyme, thereby preventing viral replication inside human cells.

During the COVID-19 pandemic, it was approved under emergency/clinical use authorization in India for the treatment of mild to moderate COVID-19 infections. It may also be investigated for other viral infections.


3. Product Highlights

Attribute Details
Generic Name Favipiravir
Dosage Form Tablet (oral use)
Therapeutic Category Antiviral
Application Area Mild to moderate viral infections, Influenza, COVID-19 (under specific conditions)
Administration Oral, as prescribed by a physician
Storage Conditions Store below 25C, protect from moisture & sunlight
Shelf Life 24 months (as per manufacturer)

4. Therapeutic Uses

  • Treatment of mild to moderate COVID-19 infection (in specific patients as per guidelines)

  • Investigated for influenza and other viral infections


5. Side Effects

Common:

  • Diarrhea

  • Nausea, vomiting

  • Elevated uric acid levels (hyperuricemia)

  • Increased liver enzymes (ALT, AST)

Serious (rare):

  • Liver toxicity

  • Severe allergic reactions (rash, swelling, breathing difficulty)

  • Decreased neutrophil count (neutropenia)

  • Teratogenicity (harmful for fetus if taken during pregnancy)


6. Precautions

  • Should be used only under medical supervision

  • Not recommended in pregnant or breastfeeding women (can cause fetal harm)

  • Men and women should use effective contraception during treatment and after completion (due to teratogenic risk)

  • Dose adjustment may be required in renal and hepatic impairment

  • Avoid alcohol during therapy (can worsen liver side effects)

  • Monitor liver function, uric acid levels, and blood counts during treatment

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