Product image of Nevirapine Wockhardt (Nevirapine) supplied by GNH India

Nevirapine Wockhardt

Active Ingredient:
Nevirapine
Origin:
EU

Nevirapine Wockhardt (Nevirapine)

Nevirapine, the active ingredient in Nevirapine Wockhardt, is a non‑nucleoside reverse transcriptase inhibitor presented as an oral tablet for oral use. It is employed in the treatment of HIV‑1 infection, typically as part of combination antiretroviral therapy for adults and children.

GNH India supplies Nevirapine Wockhardt as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Wockhardt Uk Ltd

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Indications & Clinical Uses

Nevirapine is used to manage HIV‑1 infection and is incorporated into combination antiretroviral regimens.

  • HIV‑1 infection (adults): reduces viral replication and improves immune function.
  • HIV‑1 infection (children): provides viral suppression as part of pediatric treatment protocols.
  • Combination antiretroviral therapy: contributes to multi‑drug regimens to achieve durable viral load suppression.

How It Works

  • Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, inducing a conformational change that blocks the enzyme’s activity. This inhibition prevents the transcription of viral RNA into DNA, thereby halting the replication cycle of HIV and reducing viral load in the patient.

Side Effects

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

Common Side Effects

  • Rash: mild to moderate skin eruptions.
  • Nausea: occasional gastrointestinal discomfort.
  • Fatigue: general tiredness.
  • Headache: transient cranial pain.
  • Dizziness: occasional light‑headedness.
  • Diarrhoea: loose stools.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate medical attention.
  • Hepatic failure: signs of liver dysfunction such as jaundice.
  • Severe hypersensitivity: fever, eosinophilia, or organ involvement.
  • Neutropenia: marked reduction in white blood cells.
  • Anemia: decreased red blood cell count.
  • Hepatotoxicity: elevated liver enzymes or hepatitis.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient history and monitor for specific risks.

  • Liver function monitoring: perform baseline and periodic liver enzyme tests.
  • Rash assessment: evaluate any skin changes promptly.
  • Hypersensitivity vigilance: watch for fever, eosinophilia, or organ involvement.
  • Hepatic impairment avoidance: avoid in patients with severe liver disease.
  • Pregnancy counseling: discuss unknown fetal risk and consider alternatives.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nevirapine interacts with several medicines that can alter its efficacy or safety.

Major Interactions (Avoid)

  • Rifampin: induces metabolism, reducing nevirapine levels.
  • St. John’s wort: strong enzyme inducer, decreasing drug exposure.
  • Protease inhibitors (e.g., ritonavir): can increase nevirapine concentrations and toxicity.

Moderate Interactions (Monitor Closely)

  • Azole antifungals: may raise nevirapine levels; monitor liver function.
  • Warfarin: potential alteration of anticoagulant effect; check INR regularly.

Frequently Asked Questions

Nevirapine Wockhardt contains the active ingredient nevirapine, an NNRTI used to treat HIV‑1 infection. It is prescribed as part of combination antiretroviral therapy to suppress viral replication and improve immune function in both adult and pediatric patients.

Nevirapine binds to a non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme, causing a conformational change that blocks the enzyme’s activity. This prevents the conversion of viral RNA into DNA, halting the HIV replication cycle and reducing viral load.

The specific dose of Nevirapine Wockhardt is determined by the prescribing clinician based on the patient’s age, weight, treatment history, and co‑administered medications. Only a qualified healthcare professional should set the dosing regimen.

Nevirapine’s pregnancy category is listed as unknown, and safety data are limited. Clinicians must weigh potential benefits against risks and consider alternative therapies. Breastfeeding while on nevirapine should be 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 necessary import documentation.

Nevirapine belongs to the NNRTI class, offering a distinct mechanism from nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitors. Compared with some NNRTIs, nevirapine has a longer half‑life but may carry a higher risk of rash and hepatic toxicity, requiring careful monitoring.

Nevirapine Wockhardt tablets should be stored at room temperature, below 25 °C, in the original packaging. Protect them from moisture, excessive heat, and direct sunlight to maintain product stability.

Nevirapine Wockhardt is taken orally, usually with food to reduce gastrointestinal discomfort. The tablets are swallowed whole with a full glass of water, and the dosing schedule is set by the prescribing clinician.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, hepatic failure, hypersensitivity syndrome, and significant neutropenia or anemia. Patients should be educated to report any rash, jaundice, fever, or unexplained fatigue immediately.

Nevirapine Wockhardt should be avoided in patients with known hypersensitivity to nevirapine or other NNRTIs, those with severe hepatic impairment, and individuals with a history of severe rash or Stevens‑Johnson syndrome related to antiretroviral therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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