Product image of Lamivudine Teva Pharma (Lamivudine) supplied by GNH India

Lamivudine Teva Pharma

Active Ingredient:
Lamivudine
Origin:
EU

Lamivudine Teva Pharma (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 India supplies Lamivudine Teva Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

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.

How It Works

  • Lamivudine is phosphorylated intracellularly to its active triphosphate form, which competes with natural deoxycytidine nucleotides for incorporation into viral DNA. By acting as a chain terminator, it inhibits HIV reverse transcriptase and also blocks hepatitis B virus polymerase, preventing elongation of the viral genome and halting replication.

Side Effects

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.

Precautions & Warnings

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.

Avoid Interactions

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

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.

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.

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.

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.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India 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.

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.

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.

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.

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.

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.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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