GNH USA

Europe — EMA

Lamivudine Teva Pharma B.V.

GNH USA supplies Lamivudine Teva Pharma B.V. (Lamivudine), a nucleoside reverse transcriptase inhibitor for HIV infection and chronic hepatitis B.

Lamivudine

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What is Lamivudine?

Lamivudine, the active ingredient in Lamivudine Teva Pharma B.V., is a nucleoside reverse transcriptase inhibitor (NRTI) presented as an oral tablet for oral use. It is used to treat HIV infection and chronic hepatitis B in adults and children as prescribed by a healthcare professional.

GNH USA supplies Lamivudine Teva Pharma B.V. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Lamivudine used for?

Lamivudine is an antiretroviral nucleoside analogue that targets viral replication in specific infections. - HIV infection: reduces plasma HIV‑1 RNA levels and helps restore immune function. - Chronic hepatitis B: suppresses HBV DNA replication, decreasing liver inflammation and disease progression. - HIV/HBV co‑infection: controls both viruses simultaneously, improving overall clinical outcomes.

What are the side effects of Lamivudine?

Lamivudine is generally well tolerated, but adverse reactions can occur.

Common Side Effects: - Nausea: mild to moderate stomach upset. - Headache: transient cranial discomfort. - Fatigue: reduced energy levels. - Diarrhea: loose stools. - Insomnia: difficulty sleeping. - Dizziness: light‑headed sensation.

Serious or Rare Side Effects: - Lactic acidosis: severe metabolic disturbance requiring immediate care. - Hepatotoxicity: significant liver enzyme elevation or failure. - Pancreatitis: inflammation of the pancreas with abdominal pain. - Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Hypersensitivity: rash, fever, eosinophilia. - Anemia: marked reduction in red blood cells.

What precautions apply to Lamivudine?

Before initiating lamivudine therapy, consider the following safety measures. - Renal impairment: assess kidney function and adjust dose if necessary. - Hepatic disease: monitor liver enzymes regularly. - Pregnancy: risk category unknown; discuss potential benefits and risks with a physician. - Lactation: unknown excretion in breast milk; weigh maternal benefit against infant risk. - Drug resistance: perform virologic monitoring to detect resistance development. - Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

What does Lamivudine interact with?

Lamivudine may interact with other medicines; review the following categories.

Major Interactions (Avoid): - Didanosine: concurrent use increases risk of pancreatitis. - Stavudine: combined therapy may heighten mitochondrial toxicity.

Moderate Interactions (Monitor Closely): - Tenofovir: additive renal toxicity; monitor kidney function. - Nevirapine: hepatic enzyme induction may alter lamivudine levels. - Efavirenz: overlapping central nervous system effects; observe for increased neuropsychiatric symptoms.

Frequently asked questions

What conditions is Lamivudine Teva Pharma B.V. used for?+
Lamivudine Teva Pharma B.V. is indicated for the treatment of HIV infection and chronic hepatitis B. In patients co‑infected with both viruses, it helps control viral replication of each, improving immune status and reducing liver disease progression when prescribed by a qualified clinician.
How does lamivudine work in the body?+
Lamivudine is taken up by cells and converted to its active triphosphate form. This analogue competes with natural nucleotides for incorporation into viral DNA by HIV reverse transcriptase and hepatitis B polymerase. Once incorporated, it terminates the DNA chain, halting viral replication and limiting disease spread.
What is the usual dose of lamivudine?+
The specific dose of lamivudine is determined by the prescribing healthcare professional based on the patient’s age, weight, renal function, and the condition being treated. Dosage regimens may differ for HIV versus hepatitis B, and adjustments are made according to clinical response and laboratory monitoring.
Is lamivudine safe during pregnancy or breastfeeding?+
Lamivudine’s pregnancy category is not definitively established. It may be used during pregnancy only if the potential benefits outweigh the risks, and this decision should be made by a qualified obstetrician. Information on excretion in breast milk is limited; breastfeeding mothers should consult their physician to assess safety.
How do I order Lamivudine Teva Pharma B.V. from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.
How does lamivudine compare with other antiretroviral drugs?+
Lamivudine belongs to the nucleoside reverse transcriptase inhibitor (NRTI) class and is often combined with other antiretrovirals for a synergistic effect. Compared with older NRTIs, lamivudine generally has a more favorable safety profile and lower mitochondrial toxicity, but resistance can develop if used as monotherapy, making combination regimens preferred.
What are the recommended storage conditions for lamivudine tablets?+
Lamivudine tablets should be stored at ambient temperature, below 25 °C, in their original container. Protect them from moisture, excessive heat and direct sunlight. Do not store in bathrooms or near kitchen appliances that generate steam, as humidity can affect tablet integrity.
How is lamivudine administered to patients?+
Lamivudine is administered orally, usually as a tablet taken with or without food. The exact timing and frequency are prescribed by the treating physician, who will also advise whether the medication should be taken once daily or divided into multiple doses based on the therapeutic regimen.
What are the most serious risks associated with lamivudine therapy?+
Serious risks, though uncommon, include lactic acidosis, severe hepatotoxicity, pancreatitis, hypersensitivity reactions such as Stevens‑Johnson syndrome, and significant anemia. Patients should be monitored regularly for signs of metabolic disturbances, liver dysfunction, pancreatic pain, skin eruptions, or unexplained fatigue.
Who should not use lamivudine?+
Lamivudine is contraindicated in patients with known hypersensitivity to the drug or any of its excipients. Individuals with severe renal impairment may require dose adjustment, and those with active, uncontrolled liver disease should be evaluated carefully before initiation. Pregnant or breastfeeding women should discuss potential risks with their healthcare provider.
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
Teva B.V
Origin
EU

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