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EMA Product

Kivexa

Product approved by European Medicines Agency (EU)

Basic Information

Kivexa

Regulatory Information

EMEA/H/C/000581

Authorised

December 16, 2004

37

November 27, 2023

Company Information

the netherlands

Van Asch van Wijckstraat 55H 3811 LP Amersfoort

ViiV Healthcare BV

Active Substances Detail

abacavirlamivudine

Detailed Information

Therapeutic Indication

### Therapeutic indication Kivexa is indicated in antiretroviral combination therapy for the treatment of Human Immunodeficiency Virus (HIV) infection in adults, adolescents and children weighing at least 25 kg. Before initiating treatment with abacavir, screening for carriage of the HLA-B\*5701 allele should be performed in any HIV-infected patient, irrespective of racial origin. Abacavir should not be used in patients known to carry the HLA-B\*5701 allele.

Overview Summary

Kivexa is used with at least one other antiviral medicine to treat adults and children weighing at least 25 kg who are infected with human immunodeficiency virus (HIV), the virus that causes acquired immune deficiency syndrome (AIDS). Kivexa contains two active substances, abacavir and lamivudine.

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