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Other · Xanthine Oxidase Inhibitor — Urate-Lowering Agent

Allopurinol (allopurinol)

Also sold as: Zyloric, Allorin, Algout, Alopur

Pregnancy

Cat C

Lactation

Caution

Schedule

H

Forms

Tablets 100 mg +1

Indications

Adult Dosing

Gout — initiation and titration

50–100 mg orally once daily (starting dose); increase by 100 mg every 2–4 weeks

Ongoing; titrate to target serum uric acid <6 mg/dL (or <5 mg/dL in tophaceous gout); maximum 900 mg/day

CRITICAL: Never initiate allopurinol during an acute gout attack — wait until the attack has fully resolved (at least 2–4 weeks). Starting allopurinol during an attack prolongs and worsens the attack. Continue colchicine or NSAID prophylaxis for 3–6 months after initiating allopurinol to prevent mobilisation flares.

Chemotherapy-induced hyperuricaemia (tumour lysis syndrome prophylaxis)

300–600 mg orally once daily

Start 1–2 days before chemotherapy; continue for 3–7 days post-chemotherapy

IV allopurinol available for patients unable to take orally. Rasburicase preferred for high-risk tumour lysis syndrome. Allopurinol 300 mg OD is standard; increase to 600 mg/day for high tumour burden.

Uric acid nephrolithiasis

200–300 mg orally once to twice daily

Long-term; combine with adequate hydration and urinary alkalinisation (sodium bicarbonate)

Target urinary uric acid excretion <600 mg/day. Alkalinise urine to pH 6.0–6.5 with potassium citrate or sodium bicarbonate to improve uric acid solubility.

Maximum daily dose: 900 mg/day (in divided doses if >300 mg/day)

Renal Dose Adjustment

CrCl / eGFRDose Adjustment
CrCl 60–90 mL/min200 mg/day
CrCl 20–59 mL/min100–200 mg/day
CrCl <20 mL/min100 mg/day or every 2 days
Dialysis100 mg after each dialysis session. Oxypurinol (active metabolite) accumulates in renal impairment — dose reduction mandatory.
Calculate eGFR / CrCl →

Hepatic Adjustment

Reduce dose in severe hepatic impairment — monitor liver function tests. Mild-to-moderate impairment: use with caution; no specific dose established.

Pregnancy & Lactation

Pregnancy: Category C

Limited human data. Animal studies show no teratogenicity. Gout in pregnancy is rare — if urate-lowering therapy is essential, use with caution and only after risk-benefit discussion. Avoid if possible, especially in first trimester.

Lactation: Caution

Allopurinol and its active metabolite oxypurinol are excreted in breast milk. Reports of maculopapular rash in breastfed infants. Avoid use during breastfeeding if possible; if essential, monitor infant for rash and haematological abnormalities.

Top Drug Interactions

Interacting DrugEffectSeverity
Azathioprine and 6-mercaptopurine (6-MP)Allopurinol inhibits xanthine oxidase which is the primary enzyme metabolising azathioprine and 6-MP — results in 3–4-fold increase in plasma levels causing severe myelosuppression, bone marrow failure. If combination is unavoidable, reduce azathioprine/6-MP dose by 75% and monitor FBC closelyMajor
Ampicillin and amoxicillinIncreased incidence of skin rash (maculopapular) — approximately 3-fold increase; mechanism unclear. Avoid combination if possible; use alternative antibioticsModerate
WarfarinAllopurinol inhibits hepatic metabolism of warfarin — increased anticoagulant effect and raised INR; monitor INR closely when starting, stopping, or dose-changing allopurinolModerate
Diuretics (thiazides, loop diuretics) and ACE inhibitorsDiuretics raise serum uric acid (reducing allopurinol efficacy) and increase risk of allopurinol hypersensitivity reactions (DRESS, SJS); ACEIs also increase hypersensitivity risk — monitor closely in patients on these combinationsModerate

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Side Effects

Common

  • Nausea and gastrointestinal upset
  • Skin rash — maculopapular (most common; STOP if any rash occurs and do not rechallenge without specialist review)
  • Headache
  • Drowsiness
  • Acute gout flare on initiation (mobilisation flare — give colchicine prophylaxis)

Serious / Discontinue If

  • Allopurinol hypersensitivity syndrome (AHS) — fever, rash, hepatitis, eosinophilia, renal failure; mortality up to 25% — immediate discontinuation required
  • Severe cutaneous adverse reactions (SCAR) — Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), DRESS (drug rash with eosinophilia and systemic symptoms) — strongly associated with HLA-B*5801 allele
  • Agranulocytosis and aplastic anaemia (rare)
  • Hepatotoxicity — elevated liver enzymes, hepatic necrosis (rare)
  • Vasculitis

Contraindications

Available Indian Brands

BrandManufacturerPrice (approx)
Zyloric 100 mg TabletsGSK India₹28/10 tablets
Allorin 100 mg TabletsCipla₹22/10 tablets
Algout 100 mg TabletsMankind Pharma₹18/10 tablets

Monitoring Required

Patient Counseling Points

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Clinically reviewed by: Dr. Sanjay Kulkarni, MD (Medicine), DM (Clinical Immunology & Rheumatology)

Last reviewed: 2026-04-15

References

  • Khanna D, et al. 2012 American College of Rheumatology guidelines for management of gout. Part 1: Systematic nonpharmacologic and pharmacologic therapeutic approaches to hyperuricemia. Arthritis Care Res (Hoboken). 2012;64(10):1431–1446.
  • FitzGerald JD, et al. 2020 American College of Rheumatology Guideline for the Management of Gout. Arthritis Care Res (Hoboken). 2020;72(6):744–760.
  • Hershfield MS, et al. Clinical pharmacogenomics: HLA genotyping for allopurinol in Asian patients. Arthritis Rheumatol. 2013;65(10):2566–2577.
  • GSK India. Zyloric prescribing information. 2024.
Disclaimer: This information is for clinical reference only. It is not exhaustive and does not substitute clinical judgement. Always verify current dosing against the manufacturer's prescribing information and current treatment guidelines. Drug prices are approximate and may vary.