GNH USA

Europe — EMA

Kivexa

GNH USA supplies Kivexa (Abacavir Sulfate and Lamivudine), a nucleoside reverse transcriptase inhibitor for HIV-1 infection.

Abacavir Sulfate, Lamivudine

Request sourcing

1
Pack/s

What is Abacavir Sulfate, Lamivudine?

Abacavir Sulfate and Lamivudine, the active ingredients in Kivexa, are nucleoside reverse transcriptase inhibitors (NRTIs) presented as oral tablets. They are used in combination therapy to suppress HIV-1 replication in adults and adolescents living with HIV infection. The fixed‑dose combination simplifies treatment regimens and improves adherence for patients.

GNH USA supplies Kivexa as a licensed, GDP‑compliant international pharmaceutical supplier, adhering to EU GMP standards and providing the product to hospitals, pharmacies, and clinics worldwide through validated cold‑chain logistics and regulatory support.

What is Abacavir Sulfate, Lamivudine used for?

Kivexa, a nucleoside reverse transcriptase inhibitor, is used in antiretroviral therapy for HIV-1 infection.

HIV-1 infection (adults): reduces viral load and increases CD4+ cell counts when used as part of combination antiretroviral therapy. HIV-1 infection (adolescents): provides effective viral suppression as part of a regimen approved for patients aged 12 years and older. Co‑infection with hepatitis B: lamivudine component offers activity against HBV, supporting liver health while treating HIV.

What are the side effects of Abacavir Sulfate, Lamivudine?

Common Side Effects: - Nausea: mild to moderate stomach upset. - Headache: transient cranial discomfort. - Fatigue: general tiredness. - Diarrhea: loose stools, usually self‑limiting.

Serious or Rare Side Effects: - Hypersensitivity reaction: potentially life‑threatening, especially with abacavir in HLA‑B*57:01 carriers. - Severe liver injury: elevated transaminases, jaundice. - Lactic acidosis: metabolic disturbance requiring urgent care. - Stevens‑Johnson syndrome: severe skin and mucosal reaction.

What precautions apply to Abacavir Sulfate, Lamivudine?

Before initiating therapy, consider the following precautions.

Screen for HLA‑B*57:01 before starting abacavir: avoid in positive patients. Monitor liver function tests regularly: detect hepatotoxicity early. Assess renal function: dose adjustment may be needed in severe impairment. Educate patients about hypersensitivity signs: stop drug immediately if they occur. Pregnancy and breastfeeding: use only if benefit outweighs risk; limited data available. Store at ambient temperature below 25 °C: keep in original packaging, protect from moisture and light.

What does Abacavir Sulfate, Lamivudine interact with?

Kivexa may interact with several medicines; monitor accordingly.

Major Interactions (Avoid): - Concurrent use with didanosine: increased risk of pancreatitis. - Co‑administration with ribavirin: may increase hemolytic anemia. - Use with other NRTIs that cause mitochondrial toxicity: avoid combined toxicity. - Strong CYP3A4 inducers (e.g., rifampicin) may reduce lamivudine levels.

Moderate Interactions (Monitor Closely): - Protease inhibitors (e.g., lopinavir/ritonavir) may increase abacavir levels; monitor. - Nephrotoxic agents (e.g., tenofovir) require renal monitoring when combined.

Frequently asked questions

What is Kivexa used for?+
Kivexa is a fixed‑dose combination of abacavir sulfate and lamivudine used as part of antiretroviral therapy to treat HIV‑1 infection in adults and adolescents. It helps suppress viral replication and supports immune recovery when prescribed alongside other antiretroviral agents.
How does abacavir sulfate work?+
Abacavir sulfate is a guanosine nucleoside analogue. After intracellular phosphorylation to its active triphosphate, it competes with natural deoxyguanosine triphosphate for incorporation into viral DNA by reverse transcriptase, causing premature chain termination and blocking HIV replication.
What is the usual dose of Kivexa?+
The specific dose of Kivexa is determined by the prescribing clinician based on the patient’s age, weight, renal function, and overall treatment regimen. Dosage decisions follow national HIV treatment guidelines and should be individualized for each patient.
Is Kivexa safe during pregnancy or breastfeeding?+
Safety data for Kivexa in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.
How do I order Kivexa from GNH USA?+
To order Kivexa, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.
How does Kivexa compare with other HIV drugs?+
Kivexa combines two NRTIs in a single tablet, simplifying dosing compared with separate agents. Compared with other fixed‑dose combinations, it offers a well‑studied safety profile and is particularly useful for patients who require both abacavir and lamivudine, though alternative regimens may be preferred based on resistance patterns or tolerability.
What are the storage requirements for Kivexa?+
Kivexa tablets should be stored at ambient temperature below 25 °C. Keep them in the original packaging, protect from moisture and light, and ensure they are out of reach of children.
How is Kivexa administered?+
Kivexa is taken orally, usually once daily with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with water and not crushed or chewed unless specifically advised.
What are the most serious risks associated with Kivexa?+
The most serious risks include a hypersensitivity reaction, especially in patients with the HLA‑B*57:01 allele, severe liver injury, lactic acidosis, and rare skin reactions such as Stevens‑Johnson syndrome. Prompt medical attention is required if any of these symptoms appear.
Who should not use Kivexa?+
Kivexa should not be used in patients known to be positive for the HLA‑B*57:01 allele due to the risk of hypersensitivity. It is also contraindicated in individuals with severe hepatic impairment or those who have previously experienced a severe reaction to either component.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Abacavir Sulfate, Lamivudine
Route
Oral Use
Manufacturer
Viiv Healthcare B.V.
Origin
EU

Related products