Product image of Milurit (Allopurinol) supplied by GNH India

Milurit

Active Ingredient:
Allopurinol
Origin:
EU

Milurit (Allopurinol)

Allopurinol, the active ingredient in Milurit, is a xanthine oxidase inhibitor presented as a tablet for oral use. It treats gout, hyperuricemia and helps prevent tumor lysis syndrome in appropriate patients.

GNH India supplies Milurit as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Egis Pharmaceuticals Plc

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Indications & Clinical Uses

Allopurinol is a xanthine oxidase inhibitor used in disorders of uric acid metabolism.

  • Gout: reduces serum uric acid levels, decreasing the frequency of acute attacks.
  • Hyperuricemia: lowers elevated uric acid concentrations to target ranges.
  • Tumor lysis syndrome prophylaxis: prevents rapid rise in uric acid during cancer therapy.

How It Works

  • Allopurinol is metabolized to oxypurinol, which competitively inhibits the enzyme xanthine oxidase. By blocking this key step in purine degradation, the conversion of hypoxanthine to xanthine and xanthine to uric acid is reduced, leading to decreased production of uric acid and lower serum urate concentrations. The inhibition is sustained because oxypurinol has a longer half‑life than the parent drug, providing prolonged urate‑lowering effect throughout dosing intervals.

Side Effects

Allopurinol may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Rash: mild skin eruptions or itching.
  • Gastrointestinal upset: nausea, vomiting or abdominal discomfort.
  • Elevated liver enzymes: transient increase in hepatic transaminases.
  • Diarrhea: loose stools, usually self‑limiting.
  • Headache: mild to moderate head pain.

Serious or Rare Side Effects

  • Severe cutaneous adverse reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Aplastic anemia: bone‑marrow failure leading to pancytopenia.
  • Hepatotoxicity: significant liver injury with jaundice.
  • Acute interstitial nephritis: kidney inflammation causing renal impairment.
  • Hypersensitivity syndrome: fever, eosinophilia and organ involvement.

Precautions & Warnings

When prescribing Allopurinol, several safety considerations should be observed.

  • Renal function: adjust dose in patients with impaired kidney function.
  • Hepatic impairment: monitor liver enzymes during therapy.
  • Hypersensitivity risk: discontinue immediately if rash or systemic symptoms develop.
  • Drug interactions: review concomitant medications that may increase toxicity.
  • Pregnancy and lactation: use only if clearly needed, as safety data are limited.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture.

Avoid Interactions

Allopurinol can interact with several medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Azathioprine or mercaptopurine: increased risk of bone‑marrow suppression.
  • Warfarin: enhanced anticoagulant effect, may require INR monitoring.
  • Amoxicillin‑clavulanate: higher incidence of severe skin reactions.

Moderate Interactions (Monitor Closely)

  • Thiazide diuretics: may reduce urate‑lowering effect.
  • ACE inhibitors or ARBs: may increase serum potassium when combined with allopurinol.
  • High‑dose vitamin C: may augment uric acid reduction, monitor for kidney stones.

Frequently Asked Questions

Milurit contains allopurinol, which is prescribed to lower elevated uric acid levels. It is used to manage gout attacks, treat chronic hyperuricemia, and to prevent tumor lysis syndrome in patients undergoing certain cancer therapies.

Allopurinol is converted in the body to oxypurinol, a potent competitive inhibitor of xanthine oxidase. By blocking this enzyme, the conversion of purine metabolites to uric acid is reduced, resulting in lower serum urate concentrations.

The appropriate dose of Milurit is determined by the prescribing clinician based on the patient’s condition, renal function, and response to therapy. Dosage regimens are individualized and should follow the prescriber’s instructions.

Safety data for allopurinol in pregnancy and lactation are limited. It should only be used when clearly needed and after a risk‑benefit assessment by the healthcare provider. Breastfeeding mothers should consult their physician before use.

To order Milurit, submit an enquiry on the product page at gnhindia.com with 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.

Milurit (allopurinol) is a first‑line xanthine oxidase inhibitor, whereas alternatives such as febuxostat also inhibit the same enzyme but have different metabolic profiles. Allopurinol is generally less expensive and has a long history of use, while febuxostat may be preferred in patients with severe renal impairment.

Milurit tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Milurit is taken orally, usually with a full glass of water. It can be taken with or without food, but consistent timing each day helps maintain stable drug levels. Patients should follow the dosing schedule prescribed by their healthcare professional.

Serious adverse reactions include severe skin conditions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, aplastic anemia, and acute interstitial nephritis. Any signs of rash, fever, unexplained bruising or kidney problems require immediate medical attention.

Milurit should be avoided in patients with known hypersensitivity to allopurinol or oxypurinol. Caution is also advised for individuals with severe renal impairment, active liver disease, or those taking medications that markedly increase the risk of bone‑marrow suppression.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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