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Intended for UK Healthcare Professionals. This website contains promotional content.
Intended for IE Healthcare Professionals. This website contains promotional content.
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Prescribing information, details of adverse event reporting and indications can be found at the bottom of this page.

The option of one pill, once a day1

VOSEVI® can be taken as one tablet, once daily, with food.1

HCV patients are often feeling tired and worried,2 and may have faced additional challenges, like addiction and comorbidities, on their path to cure.3,*

 

EASL defines cure as SVR, i.e. undetectable viral RNA after treatment completion.3

 

Your patients may face unstable lifestyles, making adherence to complex dosing regimens more difficult.3,4

 

VOSEVI®’s straightforward dosing regimen avoids adding unnecessary complexity to your patients’ lives – keeping your chronic HCV patient on the route to cure, and supporting the ambition to leave no patient behind on the path to HCV elimination.

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Footnotes:

*Concomitant use with medicinal products that are strong P-glycoprotein and/or strong cytochrome P450 inducers, rosuvastin, dabigatran etexilate and ethinylestradiol-containing products are contraindicated with VOSEVI®. VOSEVI® also has multiple interactions with other medicinal products, always refer to the SmPC before prescribing.1

Abbreviations:

EASL = European Association for the Study of the Liver; HCV = hepatitis C virus; RNA = ribonucleic acid; SVR = sustained virologic response.

References:

  1. VOSEVI® Summary of Product Characteristics
  2. Younossi Z et al. Sofosbuvir and velpatasvir with or without voxilaprevir in direct-acting antiviral-naïve chronic hepatitis C: patient-reported outcomes from POLARIS 2 and 3. Aliment Pharmacol Ther. 2018;47:259–267.
  3. European Association for the Study of the Liver (EASL). J Hepatol. 2020;73:1170–1218.
  4. Degenhardt L et al. Estimating the burden of disease attributable to injecting drug use as a risk factor for HIV, hepatitis C, and hepatitis B: findings from the Global Burden of Disease Study 2013. Lancet Infect Dis. 2016;16:1385–1398.

UK-VSV-0090

Date of preparation July 2024