VIEKIRA PAK (ombitasvir, paritaprevir, and ritonavir tablets; dasabuvir tablets)

VIEKIRA PAK is a brand-name prescription drug that’s FDA-approved to treat genotype 1 chronic hepatitis C virus (HCV) infection including those with compensated cirrhosis. Brand Name: VIEKIRA PAK (ombitasvir, paritaprevir, and ritonavir tablets; dasabuvir tablets), co-packaged for oral use Initial U.S. Approval: 2014. FDA approved ombitasvir, paritaprevir, and ritonavir (brand name VIEKIRA PAK) is not (yet) registered or available in India but on request Indian patient can buy VIEKIRA PAK at the lowest price.

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VIEKIRA PAK Price In India and Overseas
VIEKIRA PAK (ombitasvir, paritaprevir, and ritonavir tablets

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VIEKIRA PAK (ombitasvir, paritaprevir, and ritonavir tablets

Ombitasvir/paritaprevir/ritonavir is used together with dasabuvir or ribavirin for cases caused by hepatitis C virus genotype 1 or 4. Cure rates are around 95%. Ombitasvir/paritaprevir/ritonavir with dasabuvir was approved for medical use in the United States in 2014, and without dasabuvir in 2015.

VIEKIRA PAK with or without ribavirin is indicated for the treatment of patients with genotype 1 chronic hepatitis C virus (HCV) infection including those with compensated cirrhosis. VIEKIRA PAK includes ombitasvir, a hepatitis C virus NS5A inhibitor, paritaprevir, a hepatitis C virus NS3/4A protease inhibitor, ritonavir, a CYP3A inhibitor and dasabuvir, a hepatitis C virus non-nucleoside NS5B palm polymerase inhibitor.

Ombitasvir/paritaprevir/ritonavir, sold under the brand name Technivie among others, is a medication used to treat hepatitis C. It is a fixed-dose combination of ombitasvir, paritaprevir, and ritonavir. The regimen ombitasvir-paritaprevir-ritonavir plus dasabuvir is FDA-approved for the treatment of chronic hepatitis C genotype 1, including those with compensated cirrhosis. The recommendations for use of the Viekira Pak refer to a dosing regimen of 2 tablets once daily of the fixed-dose combination ombitasvir-paritaprevir-ritonavir plus one tablet twice daily of dasabuvir. The regimen ombitasvir-paritaprevir-ritonavir plus dasabuvir is approved for use in both treatment-naive and treatment-experienced patients.
On December 19, 2014, the United States FDA approved ombitasvir-paritaprevir-ritonavir and dasabuvir for the treatment of genotype 1 chronic hepatitis C infection in adults, including patients with compensated cirrhosis. The medications ombitasvir, paritaprevir, and dasabuvir do not have FDA approval for use as individual drugs outside of use in the Viekira Pak. The drug ritonavir was previously approved by the FDA for use as an HIV protease inhibitor.

Drug (Brand / Generic):VIEKIRA PAK / ombitasvir, paritaprevir, and ritonavir
Current Indications: genotype 1 chronic hepatitis C virus (HCV) infection
Marketed by:: AbbVie Inc.
Approval Date: October 27, 2014

Available as (Form & Strength):
Tablets:
• Ombitasvir, paritaprevir, ritonavir: 12.5/75/50 mg
• Dasabuvir: 250 mg

For more highlights of prescribing information regarding Indications and usage, dosage and administration, dosage forms and strengths, patient counseling information and medication guide. Click Here

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