GNH USA

Europe — EMA

Lamivudine Teva Pharma

GNH USA supplies Lamivudine Teva Pharma (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, is a nucleoside reverse transcriptase inhibitor (NRTI) presented as an oral tablet for oral use. It is used to treat human immunodeficiency virus (HIV) infection and chronic hepatitis B infection in adult patients. GNH USA supplies Lamivudine Teva Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Lamivudine used for?

Lamivudine is an antiretroviral medication that targets viral replication in specific infections.

- HIV infection: reduces plasma HIV‑1 RNA levels and helps restore immune function. - Chronic hepatitis B infection: suppresses hepatitis B virus replication and improves liver enzyme profiles. - HIV‑1 infected patients receiving combination antiretroviral therapy: contributes to overall viral suppression as part of a multi‑drug regimen.

What are the side effects of Lamivudine?

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

Common Side Effects: - Headache: mild to moderate intensity. - Nausea: occasional and usually transient. - Fatigue: persistent tiredness reported by some patients. - Diarrhea: loose stools without severe dehydration. - Insomnia: difficulty falling or staying asleep. - Dizziness: sensation of light‑headedness.

Serious or Rare Side Effects: - Lactic acidosis: buildup of lactic acid leading to metabolic disturbances. - Severe hepatotoxicity: marked elevation of liver enzymes or liver failure. - Pancreatitis: inflammation of the pancreas with abdominal pain. - Severe skin reactions: including Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Hypersensitivity: rash, fever, or eosinophilia. - Peripheral neuropathy: tingling or numbness in extremities.

What precautions apply to Lamivudine?

When prescribing lamivudine, clinicians should consider several safety measures.

- Liver function monitoring: assess baseline enzymes and follow periodically. - Renal function assessment: adjust dosing in patients with impaired clearance. - Hepatitis B flare vigilance: watch for reactivation when therapy is stopped. - Pregnancy considerations: evaluate risk‑benefit before use. - Concomitant medication review: avoid drugs that increase mitochondrial toxicity. - Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

What does Lamivudine interact with?

Lamivudine may interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid): - Didanosine: combined use raises risk of pancreatitis and peripheral neuropathy. - Stavudine: concurrent therapy can enhance mitochondrial toxicity.

Moderate Interactions (Monitor Closely): - Protease inhibitors (e.g., ritonavir): may increase lamivudine plasma levels. - Non‑nucleoside reverse transcriptase inhibitors (e.g., efavirenz): may affect viral suppression dynamics. - Nephrotoxic agents (e.g., aminoglycosides): require renal function monitoring. - Alcohol: can exacerbate liver toxicity. - Herbal supplements (e.g., St. John’s wort): may alter drug metabolism.

Frequently asked questions

What conditions is Lamivudine Teva Pharma used to treat?+
Lamivudine Teva Pharma is prescribed for the treatment of human immunodeficiency virus (HIV) infection and chronic hepatitis B infection. In HIV, it helps lower viral load and improve immune function, while in hepatitis B it suppresses viral replication and supports liver health.
How does lamivudine work in the body?+
Lamivudine is converted inside cells to its active triphosphate form, which mimics natural nucleotides. When incorporated into viral DNA by reverse transcriptase or hepatitis B polymerase, it terminates the DNA chain, preventing the virus from completing replication and thereby reducing viral load.
What is the usual dose of lamivudine?+
The specific dose of lamivudine is determined by the prescribing clinician based on the patient’s condition, weight, renal function, and other individual factors. Healthcare professionals follow approved guidelines and adjust the regimen as needed for optimal therapeutic effect.
Is lamivudine safe to use during pregnancy or breastfeeding?+
Safety data for lamivudine in pregnancy and lactation are limited, and the drug should only be used if the potential benefits outweigh any possible risks. Clinicians evaluate each case individually, and breastfeeding mothers should discuss potential exposure with their healthcare provider.
How do I order Lamivudine Teva Pharma 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, and any necessary import documentation.
How does lamivudine compare with other antiretroviral drugs?+
Lamivudine belongs to the nucleoside reverse transcriptase inhibitor (NRTI) class, offering a favorable safety profile and convenient oral dosing. Compared with some older NRTIs, it has lower mitochondrial toxicity and is often combined with other agents to form a potent, well‑tolerated regimen.
What are the recommended storage conditions for lamivudine tablets?+
Lamivudine tablets should be stored at room temperature, below 25 °C, in their original packaging. Keep them away from excess moisture, direct sunlight, and heat sources to maintain potency throughout the shelf life.
How is lamivudine administered to patients?+
Lamivudine is taken orally, usually with or without food, as a tablet swallowed whole with water. The exact timing and frequency are set by the prescriber, who may align dosing with other antiretroviral agents for convenience.
What are the most serious risks associated with lamivudine therapy?+
Serious risks include lactic acidosis, severe liver injury, pancreatitis, and rare hypersensitivity reactions such as Stevens‑Johnson syndrome. Patients should be monitored for symptoms like unexplained fatigue, abdominal pain, jaundice, or skin rash and seek medical attention promptly if they occur.
Who should not use lamivudine?+
Lamivudine is contraindicated in patients with known hypersensitivity to the drug or any of its components. Caution is also advised for individuals with severe hepatic or renal impairment, and it should be avoided in combination with certain NRTIs that increase toxicity risk.
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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