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

Nevirapine Accord

Active Ingredient:
Nevirapine
Origin:
EU

Nevirapine Accord (Nevirapine)

Nevirapine, the active ingredient in Nevirapine Accord, is a Non-nucleoside reverse transcriptase inhibitor (NNRTI) presented as an oral tablet for oral use. It is employed in combination regimens to treat HIV-1 infection in adults and adolescents, helping to suppress viral replication and improve immune function.

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

Manufacturer / TM Owner

Accord Healthcare Limited

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Indications & Clinical Uses

Nevirapine is an antiretroviral medication used in the management of HIV‑1 infection as part of combination therapy.

  • HIV‑1 infection (treatment): Reduces viral load when used with other antiretroviral agents.
  • Treatment‑experienced HIV‑1 patients: Provides an alternative option for those with resistance to other drugs.
  • Pediatric HIV‑1 infection (≥2 kg): Used under specialist supervision as part of a regimen for children.

How It Works

  • Nevirapine binds to a hydrophobic pocket of the HIV‑1 reverse transcriptase enzyme, inducing a conformational change that inhibits both RNA‑dependent and DNA‑dependent DNA polymerase activities. This blockade prevents the synthesis of viral DNA from the RNA template, thereby halting replication of the virus within infected cells.

Side Effects

Nevirapine may cause a range of adverse reactions, from mild to severe. Monitoring for side effects is essential during therapy.

Common Side Effects

  • Rash: Often mild, may appear on trunk or limbs.
  • Headache: Transient, usually resolves without intervention.
  • Nausea: May be accompanied by mild abdominal discomfort.
  • Fatigue: Generalized tiredness reported by some patients.
  • Diarrhea: Loose stools occurring early in treatment.
  • Elevated liver enzymes: Detected in routine blood tests.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: Severe skin reaction requiring immediate medical attention.
  • Hepatotoxicity: Significant liver injury, presenting with jaundice or elevated bilirubin.
  • Severe hypersensitivity: Includes fever, eosinophilia, and organ involvement.
  • Hematologic abnormalities: Such as anemia or neutropenia.
  • Immune reconstitution syndrome: Worsening of opportunistic infections after immune recovery.

Precautions & Warnings

Before initiating Nevirapine, clinicians should assess patient history and monitor for potential risks.

  • Liver function: Evaluate baseline hepatic enzymes and monitor regularly.
  • Skin reactions: Inspect for rash; discontinue if severe or progressing.
  • Pregnancy: Use only if benefits outweigh risks; consult specialist.
  • Drug resistance: Perform resistance testing when possible.
  • Concomitant medications: Review for interactions that affect metabolism.
  • Store at ambient temperature: Keep below 25 °C, in original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Nevirapine interacts with several drug classes, influencing efficacy and safety.

Major Interactions (Avoid)

  • Rifampicin: Reduces nevirapine plasma levels, compromising antiviral effect.
  • Carbamazepine: Induces metabolism, leading to subtherapeutic concentrations.
  • St. John's wort: Potent CYP3A4 inducer, markedly decreasing nevirapine exposure.

Moderate Interactions (Monitor Closely)

  • Protease inhibitors (e.g., ritonavir): May increase nevirapine levels, requiring dose adjustment.
  • Hormonal contraceptives: Potential reduction in contraceptive efficacy.
  • Warfarin: May alter anticoagulant effect; monitor INR closely.

Frequently Asked Questions

Nevirapine Accord contains the active ingredient nevirapine, an NNRTI used in combination with other antiretroviral agents to treat HIV‑1 infection in adults, adolescents, and selected pediatric patients. It helps lower viral load and supports immune recovery when part of a prescribed regimen.

Nevirapine binds to a specific hydrophobic pocket on the HIV‑1 reverse transcriptase enzyme, causing a conformational change that blocks both RNA‑dependent and DNA‑dependent DNA polymerase activities. This inhibition prevents the virus from converting its RNA into DNA, thereby stopping replication within host cells.

The dosing of Nevirapine Accord is determined by the prescribing clinician based on the patient’s age, weight, treatment history, and co‑administered medications. Healthcare providers follow established guidelines and adjust the regimen according to clinical response and laboratory monitoring.

Nevirapine may be used in pregnancy only when the potential benefits justify the potential risks to the fetus. It crosses the placenta and is excreted in breast milk, so clinicians must evaluate maternal health, viral load, and alternative options before prescribing to pregnant or nursing individuals.

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.

Nevirapine belongs to the NNRTI class, offering a distinct mechanism from nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitors. Compared with efavirenz, another NNRTI, nevirapine has a different side‑effect profile, with a higher risk of rash and hepatotoxicity but lower central nervous system effects.

Nevirapine Accord should be stored at ambient temperature, below 25 °C, in its original packaging to protect from moisture and light. Keep the product out of reach of children and avoid storing in humid or excessively hot environments.

Nevirapine Accord is taken orally, usually with food to reduce gastrointestinal discomfort. The tablet is swallowed whole with a full glass of water, and dosing intervals are defined by the prescribing clinician as part of the overall antiretroviral regimen.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and potentially life‑threatening hepatotoxicity. Early signs such as rash, fever, jaundice, or elevated liver enzymes require immediate medical evaluation and possible discontinuation of therapy.

Nevirapine is contraindicated in patients with a known hypersensitivity to nevirapine or any component of the formulation, and in individuals with moderate to severe hepatic impairment. Caution is also advised for patients with pre‑existing skin disorders or those receiving interacting medications that may increase toxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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