Allopurinol: Uses, Dosage, Side Effects & Brands | MedexInfo
Allopurinol
Rx / Oral
Therapeutic ClassXanthine Oxidase Inhibitor / Antigout
Common Dose100–300 mg daily; up to 800 mg in divided doses
RouteOral
PregnancyCategory C – Use only if clearly needed
Indications ▼
Chronic gout and hyperuricemia
Prevention of uric acid nephrolithiasis (kidney stones)
Management of hyperuricemia associated with malignancy (tumor lysis syndrome)
Mechanism & Pharmacokinetics ▼
Mechanism: Inhibits xanthine oxidase enzyme, reducing conversion of hypoxanthine and xanthine to uric acid, thereby lowering serum and urinary uric acid levels.
Pharmacokinetics: Well absorbed orally; metabolized in liver to oxypurinol (active metabolite). Excreted via kidneys; half-life ~1–2 hours (parent) and ~15 hours (oxypurinol).
Dosage & Administration ▼
| Patient Group | Dose / Strength | Frequency |
|---|---|---|
| Adults (Gout) | 100–300 mg orally | Once daily; may titrate up to 800 mg/day in divided doses |
| Renal Impairment | Reduce dose based on creatinine clearance | As per guidelines |
| Tumor Lysis Syndrome | 600–800 mg/day in divided doses | Adjust per uric acid levels |
| Children | Use only if prescribed by pediatrician | Individualized |
Side Effects ▼
Rash, pruritus, nausea, diarrhea
Headache, drowsiness
Rare: Stevens-Johnson syndrome, toxic epidermal necrolysis, hepatotoxicity
Gastrointestinal upset (take with food to reduce)
Contraindications ▼
Hypersensitivity to allopurinol
Previous severe cutaneous adverse reactions to allopurinol
Use caution in severe renal or hepatic impairment
Drug Interaction ▼
Azathioprine or mercaptopurine – increased toxicity risk
Warfarin – may alter anticoagulant effect
Theophylline – may increase serum levels
Concomitant renal-toxic drugs – monitor kidney function
Pregnancy & Lactation ▼
Category C – use only if potential benefit outweighs risk
Use caution during breastfeeding; minimal excretion in milk
Clinical / Research Summary ▼
Therapeutic Role: Allopurinol is a xanthine oxidase inhibitor primarily used for the prevention and long-term management of hyperuricemia and gout. It is also used to prevent uric acid nephropathy in patients receiving chemotherapy.
Mechanism-Based Evidence: Allopurinol inhibits xanthine oxidase, reducing the conversion of hypoxanthine and xanthine to uric acid. This lowers serum uric acid levels and prevents urate crystal deposition in joints and tissues.
Clinical Effectiveness: Clinical trials show that allopurinol effectively reduces serum uric acid concentrations, decreases the frequency of gout attacks, and prevents complications such as tophi formation and kidney stones. Dose titration is guided by serum urate levels and renal function.
Safety Profile: Allopurinol is generally well tolerated. Common adverse effects include rash, gastrointestinal discomfort, and transient liver enzyme elevation. Rare but severe hypersensitivity reactions (e.g., allopurinol hypersensitivity syndrome) can occur, especially in patients with renal impairment or certain HLA genotypes.
Research Directions: Ongoing research explores genetic predictors of hypersensitivity, the role of allopurinol in cardiovascular and renal protection, and combination therapies for refractory hyperuricemia.
Patient Counseling Points ▼
Take after meals to reduce gastrointestinal upset
Maintain adequate hydration to prevent kidney stones
Do not discontinue therapy abruptly
Report rash, fever, jaundice, or unusual bleeding immediately
Storage & Handling ▼
Store at 20–25°C, protect from light and moisture
Keep container tightly closed
Keep out of reach of children
Brand Names (Bangladesh & Global) ▼
Bangladesh (Local Brands):
Global / International Brands:
Medical Disclaimer: This clinical summary is for educational purposes only. Always consult a qualified healthcare provider before use.