GNH USA

Europe — EMA

Lamivudine Aurovitas

GNH USA supplies Lamivudine Aurovitas (Lamivudine), a reverse transcriptase inhibitor for HIV infection and chronic hepatitis B. Request a quote for supply.

Lamivudine

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What is Lamivudine?

Lamivudine, the active ingredient in Lamivudine Aurovitas, is a nucleoside reverse transcriptase inhibitor (NRTI) presented as an oral tablet for oral use. It treats human immunodeficiency virus (HIV) infection and chronic hepatitis B in adult patients.

GNH USA supplies Lamivudine Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support import and distribution across multiple regions. Clients benefit from reliable logistics, batch traceability, and responsive technical support.

What is Lamivudine used for?

Lamivudine is used in antiretroviral therapy and antiviral treatment of hepatitis B, targeting viral replication. - HIV infection: reduces viral load and improves immune function in infected adults. - Chronic hepatitis B infection: suppresses HBV DNA replication and helps prevent disease progression. - Mother-to-child transmission of HIV: lowers the risk of vertical transmission when given to pregnant women. - Combination antiretroviral therapy: contributes to overall regimen efficacy in treatment‑experienced patients.

What are the side effects of Lamivudine?

Lamivudine may cause adverse reactions ranging from mild to serious. Common Side Effects: - Nausea - Headache - Fatigue - Diarrhea Serious or Rare Side Effects: - Lactic acidosis - Severe hepatotoxicity - Pancreatitis - Stevens‑Johnson syndrome or toxic epidermal necrolysis

What precautions apply to Lamivudine?

When prescribing lamivudine, clinicians should observe several precautionary measures to ensure patient safety. - Monitor liver function: assess baseline enzymes and follow up regularly. - Assess renal function: adjust dose in patients with impaired clearance. - Screen for hypersensitivity: discontinue if rash or systemic allergic signs appear. - Avoid use in patients with known mitochondrial toxicity: risk of lactic acidosis. - Use caution during pregnancy: weigh benefits against potential risks. - Store at room temperature: keep in original packaging, protect from moisture and heat.

What does Lamivudine interact with?

Lamivudine can interact with other medicines, influencing efficacy or toxicity. Major Interactions (Avoid): - Didanosine: combined use increases risk of pancreatitis. - Stavudine: concurrent therapy may exacerbate mitochondrial toxicity. - Ribavirin: may enhance hematologic toxicity. Moderate Interactions (Monitor Closely): - Efavirenz: may affect lamivudine plasma levels, requiring monitoring. - Nevirapine: potential for increased liver enzyme elevations. - Warfarin: monitor INR as lamivudine may alter anticoagulant effect. - Oral contraceptives: assess hormonal efficacy, though interaction is limited.

Frequently asked questions

What is Lamivudine Aurovitas used for?+
Lamivudine Aurovitas contains the antiviral agent lamivudine and is indicated for the treatment of human immunodeficiency virus (HIV) infection and for chronic hepatitis B virus infection. It is used as part of combination antiretroviral regimens for HIV and as monotherapy or in combination for hepatitis B management.
How does lamivudine work?+
Lamivudine is a nucleoside analogue that is phosphorylated inside cells to its active triphosphate form. This metabolite competes with natural nucleotides for incorporation by HIV reverse transcriptase and hepatitis B polymerase, causing premature termination of the viral DNA chain and thereby blocking viral replication.
What is the usual dose of lamivudine?+
The prescribing clinician determines the appropriate dose based on the patient’s specific condition, weight, renal function and whether it is used alone or in combination with other antivirals. Dosage may differ between HIV infection, chronic hepatitis B and prophylactic use, and adjustments are made according to clinical guidelines.
Is lamivudine safe in pregnancy or breastfeeding?+
Safety data for lamivudine during pregnancy are limited, and the drug should only be used when the potential benefit to the mother outweighs any possible risk to the fetus. Breastfeeding decisions should follow local guidelines, as lamivudine is excreted in breast milk in small amounts.
How do I order Lamivudine Aurovitas from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com specifying the required quantity of Lamivudine Aurovitas. 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 lamivudine compare with the main alternative drug or class?+
Lamivudine belongs to the nucleoside reverse transcriptase inhibitor (NRTI) class, similar to drugs such as tenofovir and emtricitabine. Compared with tenofovir, lamivudine generally has a lower risk of renal toxicity but may be less potent in some HIV regimens. Choice of agent depends on resistance patterns, patient comorbidities and treatment guidelines.
What are the storage and handling requirements for lamivudine?+
Lamivudine tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and avoid storing in areas with high humidity or direct sunlight.
How is lamivudine administered?+
Lamivudine is administered orally as a tablet. It can be taken with or without food, and the tablet should be swallowed whole with water. Patients should follow the dosing schedule prescribed by their healthcare provider and not alter the regimen without medical advice.
What are the most serious risks to watch for while taking lamivudine?+
Serious adverse events include lactic acidosis, severe hepatotoxicity, pancreatitis and severe skin reactions such as Stevens‑Johnson syndrome. Patients should be instructed to seek immediate medical attention if they experience unexplained fatigue, abdominal pain, rapid breathing, jaundice, severe rash or any signs of hypersensitivity.
Who should not use lamivudine?+
Lamivudine is contraindicated in individuals with known hypersensitivity to the drug or any of its components. It should also be avoided in patients with pre‑existing severe mitochondrial disorders, uncontrolled liver disease, or those who have experienced serious adverse reactions to other nucleoside analogues.
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
Lamivudine
Route
Oral Use
Manufacturer
Aurovitas Pharma Polska Sp. Z O.O
Origin
EU

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