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

Nevirapină Accord

Active Ingredient:
Nevirapine
Origin:
EU

Nevirapină Accord (Nevirapine)

Nevirapine, the active ingredient in Nevirapină Accord, is a non‑nucleoside reverse transcriptase inhibitor presented as an oral tablet for oral use. It is used in combination antiretroviral therapy to treat HIV‑1 infection in adults and adolescents.
GNH India supplies Nevirapină Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare Polska Sp. Z O.O.

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Indications & Clinical Uses

  • Nevirapină Accord is a non‑nucleoside reverse transcriptase inhibitor indicated for HIV‑1 infection as part of combination antiretroviral therapy.
  • HIV‑1 infection (treatment‑naïve adults): reduces viral load and improves immune function when combined with other antiretrovirals.
  • HIV‑1 infection (treatment‑experienced adults): provides an alternative regimen after failure of other NNRTIs.
  • Pediatric HIV‑1 infection (≥2 years of age): used under specialist supervision as part of a pediatric ART regimen.

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 RNA‑ and DNA‑dependent DNA polymerase activity. This inhibition prevents the synthesis of viral DNA from the RNA template, thereby halting viral replication and reducing plasma HIV levels.

Side Effects

Nevirapină Accord may cause a range of adverse reactions, from mild to severe. Monitoring and prompt reporting of symptoms are recommended.

Common Side Effects

  • Rash: mild to moderate skin eruptions.
  • Nausea: occasional gastrointestinal upset.
  • Fatigue: feeling of tiredness or weakness.
  • Headache: transient cranial discomfort.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe mucocutaneous reaction requiring immediate discontinuation.
  • Hepatic failure: signs of liver injury such as jaundice or elevated enzymes.
  • Severe hypersensitivity: fever, eosinophilia, or organ involvement.
  • Neutropenia: low white‑blood‑cell count increasing infection risk.
  • Lactic acidosis: rare metabolic disturbance with rapid breathing and abdominal pain.

Precautions & Warnings

Before initiating therapy with Nevirapină Accord, clinicians should consider several safety measures.

  • Liver function monitoring: assess baseline enzymes and repeat periodically.
  • Skin reactions: discontinue immediately if a severe rash or mucosal involvement appears.
  • Pregnancy risk assessment: evaluate benefits versus potential fetal risks.
  • Drug interaction review: check all concomitant medications for hepatic enzyme effects.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nevirapină Accord can interact with several medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Ritonavir‑boosted protease inhibitors: may increase nevirapine plasma concentrations.
  • St. John's wort: can markedly reduce nevirapine exposure.
  • Efavirenz: additive hepatotoxic potential when combined.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., carbamazepine, phenytoin): may lower nevirapine levels.
  • Antacids containing aluminum or magnesium: could affect absorption if taken simultaneously.
  • Methadone: may require dose adjustment due to altered metabolism.

Frequently Asked Questions

Nevirapină Accord contains the active ingredient nevirapine, an NNRTI used in combination antiretroviral therapy to treat HIV‑1 infection in adults, adolescents, and children over two years of age. It helps lower viral load and supports immune recovery when taken with other approved HIV medicines.

Nevirapine binds to a specific non‑nucleoside site on the HIV‑1 reverse transcriptase enzyme. This binding causes a structural change that blocks the enzyme’s ability to convert viral RNA into DNA, thereby preventing the virus from replicating and reducing the amount of HIV in the bloodstream.

The dosage of Nevirapină Accord is individualized by a qualified prescriber based on the patient’s clinical status, treatment history, and co‑administered drugs. Only a healthcare professional can determine the appropriate regimen and any necessary dose adjustments.

Safety of nevirapine during pregnancy or lactation is assessed case‑by‑case. Clinicians weigh the potential benefits for the mother against any possible risks to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss treatment options 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 (including any cold‑chain requirements), and necessary import documentation.

Nevirapine is one of several NNRTIs such as efavirenz and rilpivirine. Compared with efavirenz, nevirapine has a lower incidence of central nervous system side effects but a higher risk of skin reactions. Choice of agent depends on individual patient factors, resistance patterns, and tolerability considerations.

Nevirapină Accord should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and store them out of reach of children.

Nevirapină Accord is taken orally, usually with food to improve tolerability. The tablets are swallowed whole with a full glass of water. Patients should follow the dosing schedule prescribed by their clinician and not miss doses.

The most serious risks include severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, and hepatic toxicity that can lead to liver failure. Early signs like rash, fever, jaundice, or unexplained fatigue require immediate medical attention and discontinuation of the drug.

Nevirapină Accord is contraindicated in patients with a known hypersensitivity to nevirapine or any of its excipients. It should also be avoided in individuals with severe pre‑existing liver disease or a history of severe cutaneous adverse reactions to NNRTIs.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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