• API - Abacavir Lamivudine
  • Packaging - Tablets
  • Strength - 600mg/300mg

What is Abacavir Lamivudine, and what it is used for?

Abacavir Lamivudine, a combination of abacavir and lamivudine, both nucleoside analogue HIV-1 reverse transcriptase inhibitors, is used in combination with other antiretroviral agents for the treatment of HIV-1 infection.


The recommended dosage of Abacavir Lamivudine for adults and pediatric patients weighing at least 25 kg is one tablet (600mg/300mg) taken orally once daily, along with other antiretroviral agents, with or without food. Prior to prescribing these tablets, assess pediatric patients for the ability to swallow tablets.

Side effects

The most commonly reported side effects due to Abacavir Lamivudine include: insomnia, drug hypersensitivity, depression/depressed mood, nausea, headache/migraine, fatigue/malaise, dizziness/vertigo, and diarrhea.

Warnings And Precautions
  • Prior to initiating treatment with abacavir lamivudine combination medicine, screen for the HLA-B*5701 allele because of abacavir.
  • Use of Abacavir Lamivudine is restricted in patients who have the HLA-B*5701 allele, with prior hypersensitivity reaction to abacavir or lamivudine, with moderate or severe hepatic impairment.
  • Serious and sometimes fatal hypersensitivity reactions may occur. These reactions included multi-organ failure and anaphylaxis and typically occur within the first 6 weeks of treatment with abacavir; although abacavir hypersensitivity reactions may occur any time during treatment.
  • Clinical and laboratory evidence of exacerbations of hepatitis may occur after discontinuation of lamivudine. Patients should be precisely monitored with both clinical and laboratory follow-up for at least some months after stopping treatment.
  • Suspend treatment with Abacavir Lamivudine in any patient who develops clinical or laboratory findings suggestive of lactic acidosis or pronounced hepatotoxicity, which may include hepatomegaly and steatosis even in the absence of marked transaminase elevations.
  • Instruct women with HIV-1 infection not to breastfeed while taking treatment with abacavir lamivudine 600 mg / 300 mg because HIV-1 can be passed to the baby in breast milk.
Storage and Handling

Store tablets at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F). Store the tablets in a closed container, away from the heat, moisture, and direct light. Keep from freezing.

Drug Interactions of Abacavir Lamivudine
  • Use of single doses of lamivudine and sorbitol simultaneously resulted in a sorbitol dose-dependent reduction in the exposure of lamivudine. When possible, avoid administration of sorbitol-containing drugs with lamivudine-containing medications.
  • Co-administration with abacavir/dolutegravir/lamivudine resulted in increased riociguat exposure, which may increase the probability of riociguat adverse reactions. Reduction in the dose of riociguat may be needed.

Commonly asked questions:

Abacavir lamivudine (Kivexa 600 mg), is a fixed-dose combination antiretroviral medication authorized for the treatment of HIV/AIDS.

Abacavir Lamivudine is supplied in 600mg/300mg dosage strengths.

Abacavir Lamivudine is a kind of fixed-dose combination medicine that typically comes in the form of a tablet for oral administration.

Abacavir Lamivudine specifically is a type of drug called nucleoside reverse transcriptase inhibitors (NRTIs).

You can buy Abacavir Lamivudine from any authorized wholesaler after getting a prescription from a qualified doctor. It is always better to check the credential of the wholesaler/supplier/exporter before buying the product.
The buyer should check the existing law in their home country before importing the product.

Patients can simply fill the order form or can send mail at info@ikrispharmanetwork.com. Patients can also send WhatsApp messages to +91 8130290915 or can dial Toll-Free number: 18008891064. We will reply ASAP with the details of the abacavir lamivudine price in India and procurement procedure.
Note:- The order will be confirmed only after the receipt of the Valid prescription of the Clinician.


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