Acetazolamide Dosing in Adults
For most adult indications, acetazolamide dosing ranges from 250 mg to 1000 mg daily in divided doses, with the specific regimen determined by the clinical indication—glaucoma typically requires 250-1000 mg/24 hours in divided doses, epilepsy 375-1000 mg daily, and acute mountain sickness prophylaxis 500-750 mg daily for rapid ascents above 3500 meters. 1, 2
Indication-Specific Dosing
Glaucoma
- Chronic open-angle glaucoma: 250 mg to 1 g per 24 hours, usually in divided doses for amounts over 250 mg 1
- Doses exceeding 1 g per 24 hours typically do not produce increased therapeutic effect 1
- Acute closed-angle glaucoma: 250 mg every 4 hours, though some cases respond to 250 mg twice daily 1
- For acute cases, consider an initial 500 mg dose followed by 125-250 mg every 4 hours 1
- IV therapy may be used for rapid relief of ocular tension in acute situations 1
Epilepsy
- Optimal dosing range: 375-1000 mg daily in divided doses 1
- Total daily dose suggestion: 8-30 mg/kg in divided doses 1
- When adding to existing anticonvulsants, start with 250 mg once daily and titrate upward 1
- Doses exceeding 1 g daily may not provide additional benefit 1
Congestive Heart Failure (Diuresis)
- Starting dose: 250-375 mg once daily in the morning 1
- Best results occur with alternate-day dosing or 2 days on/1 day off to allow kidney recovery 1
- Do not increase dose if edema persists; instead skip a day to allow renal recovery 1
Drug-Induced Edema
- Recommended dose: 250-375 mg once daily for 1-2 days, alternating with a day of rest 1
Acute Mountain Sickness (AMS)
- For rapid ascents above 3500 m: 500-750 mg/day within 24 hours of altitude exposure appears most effective 2
- Lower doses (125 mg twice daily) are recommended in North American guidelines for standard prophylaxis 3
- Evidence suggests 62.5 mg twice daily may be noninferior to 125 mg twice daily, though this requires further validation 3
Idiopathic Intracranial Hypertension
- Initial dose: 25 mg/kg/day, titrated upward until clinical response (maximum 100 mg/kg/day) 4
- Important contraindication: Do NOT use acetazolamide for elevated intracranial pressure in cryptococcal meningitis due to risk of severe acidosis and hypokalemia 5
Administration Considerations
Route of Administration
- Oral route is standard for most indications 1
- IV administration: Preferred for parenteral use when needed; intramuscular route is NOT recommended 1
- For pediatric cerebral edema (CAR T complications): 15 mg/kg IV initially (max 1000 mg), then 8-12 mg/kg every 12 hours (max 1000 mg) 5
Dosing Frequency
- Standard interval: Every 6-12 hours depending on indication 6
- Plasma half-life is 4-8 hours, though pharmacologic effects last longer 6
- Renal impairment: Do not dose more frequently than every 12 hours if creatinine clearance <50 mL/min 6
- In ESRD/dialysis patients, marked dose reduction is required (e.g., 125 mg/day) due to prolonged half-life (28.5 hours vs 5-10 hours in normal renal function) 7
Critical Safety Considerations
Common Side Effects (Dose-Dependent)
- Paresthesias: Occur in approximately 50% of patients, increasing with higher doses 4
- Dysgeusia: Affects approximately 1 in 18 patients 4
- Fatigue: Occurs in approximately 1 in 11 patients 4
- Other common effects include polyuria, nausea, tinnitus, and cognitive slowing 4
Serious Adverse Effects
- Electrolyte imbalances: Particularly hypokalemia and metabolic acidosis 4, 5
- Renal stones: Rare but recognized complication 4
- In clinical practice, 48% of patients discontinue at mean doses of 1.5 g/day due to side effects 4
Contraindications
- Pregnancy: Contraindicated due to teratogenic risks 4
- Cryptococcal meningitis with elevated ICP: Specifically contraindicated per CDC guidelines 5
Monitoring Requirements
- Electrolytes (particularly potassium and bicarbonate) should be monitored during therapy 4
- Therapeutic serum range: 5-10 mcg/mL 7
Practical Dosing Strategy
Start low and titrate gradually: Begin with 250-500 mg twice daily and increase as needed to minimize initial side effect burden 4. This approach balances efficacy with tolerability, particularly given the high discontinuation rates at higher doses.