Product image of Griseofulvin Brown & Burk Ir (Griseofulvin) supplied by GNH India

Griseofulvin Brown & Burk Ir

Active Ingredient:
Griseofulvin
Origin:
EU

Griseofulvin Brown & Burk Ir (Griseofulvin)

Griseofulvin Brown & Burk Ir, containing the active ingredient griseofulvin, is an oral tablet (strength not specified) marketed in the European Union as a prescription antifungal medication. It belongs to the antifungal drug class and works by disrupting fungal cell mitosis. The product is intended for systemic treatment of dermatophyte infections and is supplied in a sealed container for oral use under appropriate storage conditions.

Manufacturer / TM Owner

Brown & Burk Ir Limited

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Indications & Clinical Uses

Griseofulvin Brown & Burk Ir is prescribed for fungal infections of the skin, hair, and nails caused by dermatophytes.

  • Dermatophytosis of the body (tinea corporis)
  • Scalp infection (tinea capitis)
  • Groin infection (tinea cruris)
  • Foot infection (tinea pedis)
  • Nail infection (tinea unguium)
  • Ringworm infections affecting other body sites

Treatment duration typically extends for several weeks to months, depending on the infection site and clinical response.

Side Effects

Side effects reported with oral griseofulvin vary in frequency and severity.

Common

  • Headache – mild to moderate discomfort that may resolve without treatment.
  • Nausea, vomiting or loss of appetite – gastrointestinal upset common during early therapy.
  • Diarrhea or abdominal cramps – may be transient and improve with continued dosing.
  • Skin rash, pruritus or mild photosensitivity – skin irritation that usually subsides.

Serious

  • Elevated liver enzymes or hepatitis – indicates potential hepatic injury requiring monitoring.
  • Severe allergic reaction, including anaphylaxis or angioedema – requires immediate medical attention.
  • Blood dyscrasias such as neutropenia, thrombocytopenia or anemia – may manifest as fatigue, bruising or infection risk.

Precautions & Warnings

Before initiating Griseofulvin Brown & Burk Ir, certain precautions should be considered to ensure safe use.

  • Assess liver function; avoid use in patients with active hepatic disease.
  • Review pregnancy and lactation status; griseofulvin is generally contraindicated during pregnancy.
  • Evaluate for known hypersensitivity to griseofulvin or other antifungal agents.
  • Monitor complete blood count during prolonged therapy to detect hematologic effects.
  • Advise patients to avoid excessive sunlight exposure due to potential photosensitivity.
  • Consider drug interactions with oral contraceptives, as efficacy may be reduced.
  • Use caution in patients with renal impairment; dosage adjustment may be required.

Avoid Interactions

Griseofulvin can alter the metabolism of several medications; awareness of interactions helps prevent therapeutic failure or toxicity.

Avoid

  • Combined use with warfarin – increased anticoagulant effect.
  • Concurrent administration with oral contraceptives – reduced contraceptive efficacy.
  • Co‑administration with cyclosporine – heightened nephrotoxicity risk.

Use with caution

  • Antiepileptic drugs such as phenobarbital, phenytoin or carbamazepine – may decrease griseofulvin levels.
  • Rifampin or other enzyme‑inducing antibiotics – may lower griseofulvin exposure.
  • Statins (e.g., simvastatin) – monitor for enhanced muscle toxicity.

Frequently Asked Questions

It is used to treat dermatophyte infections such as tinea corporis, tinea capitis, tinea cruris, tinea pedis, and other ringworm‑type skin conditions.

Griseofulvin binds to fungal microtubules, inhibiting mitosis and preventing the fungus from replicating, which allows the immune system to clear the infection.

Griseofulvin is generally contraindicated in pregnancy because it may cause fetal harm; women who are pregnant or planning pregnancy should discuss alternatives with their clinician.

Griseofulvin can reduce the effectiveness of combined oral contraceptives, so an additional non‑hormonal birth control method is recommended during treatment and for a short period after stopping the drug.

Common adverse effects include headache, nausea or vomiting, diarrhea, abdominal cramps, and mild skin rash or itching.

Baseline and periodic liver function tests and a complete blood count are advised to detect hepatic or hematologic abnormalities early.

Treatment duration varies by infection site, ranging from several weeks for skin infections to several months for scalp or nail involvement, as determined by the prescribing physician.

Mild photosensitivity may occur; patients should limit prolonged sun exposure, wear protective clothing, and use sunscreen while taking the medication.

There are no specific food restrictions, but taking the tablet with a full glass of water and a meal can improve absorption and reduce gastrointestinal upset.

Take the missed dose as soon as remembered unless it is close to the time of the next scheduled dose; in that case, skip the missed dose and continue with the regular dosing schedule.

Yes, concurrent use with statins such as simvastatin may increase the risk of muscle toxicity, so clinicians often monitor for symptoms and may adjust the statin dose.

No, it is classified as a prescription‑only medication in the European Union and must be prescribed by a qualified healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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