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

Lamivudine Teva Pharma B.V

Active Ingredient:
Lamivudine
Origin:
EU

Lamivudine Teva Pharma B.V (Lamivudine)

Lamivudine, the active ingredient in Lamivudine Teva Pharma B.V., is a nucleoside reverse transcriptase inhibitor presented as an oral tablet for oral use. It treats HIV-1 infection and chronic hepatitis B in adults.
GNH India supplies Lamivudine Teva Pharma B.V. as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

1
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Indications & Clinical Uses

Lamivudine is used in antiretroviral and antiviral therapy for viral infections affecting the immune and hepatic systems.

  • HIV-1 infection: reduces viral load and improves immune function when used in combination regimens.
  • HIV-2 infection: contributes to viral suppression as part of combination therapy.
  • Chronic hepatitis B infection: suppresses HBV replication and helps prevent liver disease progression.

How It Works

  • Lamivudine is phosphorylated intracellularly to its active triphosphate form, which competes with natural deoxycytidine triphosphate for incorporation into viral DNA. Incorporation leads to premature chain termination, thereby inhibiting HIV reverse transcriptase and hepatitis B virus DNA polymerase, preventing viral replication.

Side Effects

Lamivudine may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal discomfort.
  • Headache: transient cranial pain.
  • Fatigue: general feeling of tiredness.
  • Diarrhea: loose stools, usually self‑limiting.
  • Insomnia: difficulty falling or staying asleep.
  • Rash: mild skin eruptions.

Serious or Rare Side Effects

  • Lactic acidosis: metabolic disturbance requiring urgent care.
  • Severe hepatomegaly with steatosis: significant liver enlargement.
  • Pancreatitis: inflammation of the pancreas.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hypersensitivity: systemic allergic response.
  • Bone marrow suppression: anemia, neutropenia, or thrombocytopenia.

Precautions & Warnings

Before initiating lamivudine therapy, several safety considerations should be addressed.

  • Liver function monitoring: assess baseline enzymes and watch for hepatitis flare.
  • Renal function assessment: adjust dosing in impaired clearance.
  • Pregnancy counseling: discuss potential risks and benefits with a healthcare provider.
  • Adherence reinforcement: emphasize importance of consistent dosing to prevent resistance.
  • Hypersensitivity screening: avoid in patients with known allergic reactions to lamivudine.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lamivudine can interact with other medications, influencing efficacy or toxicity.

Major Interactions (Avoid)

  • Didanosine: concurrent use increases risk of pancreatitis.
  • Stavudine: combined therapy may enhance mitochondrial toxicity.
  • Other NRTIs: may lead to additive bone marrow suppression.

Moderate Interactions (Monitor Closely)

  • Tenofovir: monitor renal function due to combined nephrotoxic potential.
  • Efavirenz: observe for central nervous system side effects.
  • Protease inhibitors (e.g., ritonavir): may alter lamivudine plasma levels.
  • Alcohol: increased hepatic strain warrants caution.

Frequently Asked Questions

Lamivudine Teva Pharma B.V is indicated for the treatment of HIV-1 infection and chronic hepatitis B infection. It is used as part of combination antiretroviral therapy for HIV and as monotherapy or in combination for hepatitis B to suppress viral replication.

Lamivudine is converted inside cells to its active triphosphate form, which mimics the natural nucleoside deoxycytidine. When incorporated into viral DNA by reverse transcriptase or HBV polymerase, it causes premature chain termination, halting viral replication.

The specific dose of lamivudine is determined by the prescribing healthcare professional based on the patient’s condition, weight, renal function, and other clinical factors. Patients should follow the exact regimen provided by their prescriber.

Safety of lamivudine in pregnancy and lactation should be evaluated by a qualified clinician. While some data suggest it can be used when benefits outweigh risks, the decision must be individualized and discussed with a 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 and is often combined with other NRTIs or agents from different classes. Compared with some newer NRTIs, lamivudine has a well‑established safety profile but may require combination with additional drugs to achieve optimal viral suppression.

Lamivudine tablets should be stored at room temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Lamivudine is taken orally, usually with or without food, as directed by the prescriber. The tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include lactic acidosis, severe hepatomegaly with steatosis, pancreatitis, severe skin reactions such as Stevens‑Johnson syndrome, and bone marrow suppression. Patients should seek immediate medical attention if they experience symptoms like unexplained fatigue, abdominal pain, rash, or unusual bruising.

Lamivudine should be avoided in individuals with known hypersensitivity to the drug or any of its components. Caution is also advised for patients with severe hepatic impairment, mitochondrial disorders, or those taking contraindicated medications such as didanosine.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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