Following a limited submission
AWMSG advice |
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Status: Recommended | |||
Nevirapine (Viramune®) prolonged release tablets are recommended as an option for use within NHS Wales in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus type 1 (HIV-1) infected adults, adolescents, and children three years and above and able to swallow tablets. Prolonged release tablets are not suitable for the 14-day lead-in phase for patients starting nevirapine. Other nevirapine formulations, such as immediate release tablets or oral suspension should be used. Most of the experience with Viramune® is in combination with nucleoside reverse transcriptase inhibitors (NRTIs). The choice of a subsequent therapy after Viramune® should be based on clinical experience and resistance testing. |
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Medicine details |
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Medicine name | nevirapine (Viramune®) | ||
Formulation | 400 mg prolonged-release tablet | ||
Reference number | 1430 | ||
Indication | In combination with other anti-retroviral medicinal products for the treatment of HIV-1 infected adults. Prolonged-release tablets are not suitable for the 14-day lead-in phase for patients starting nevirapine. Other nevirapine formulations, such as immediate-release tablets or oral suspension should be used. Most of the experience with Viramune is in combination with nucleoside reverse transcriptase inhibitors (NRTIs). The choice of a subsequent therapy after Viramune should be based on clinical experience and resistance testing |
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Company | Boehringer Ingelheim Ltd | ||
BNF chapter | Infections | ||
Submission type | Limited | ||
Status | Recommended | ||
Advice number | 1512 | ||
NMG meeting date | 15/05/2012 | ||
AWMSG meeting date | 20/06/2012 | ||
Ratification by Welsh Government | 23/07/2012 | ||
Date of issue | 27/07/2012 | ||
Date of last review | 30/08/2016 |