Acetazolamide: Difference between revisions

No edit summary
Line 5: Line 5:


==Adult Dosing==
==Adult Dosing==
*[[Glucoma]]
**Closed-angle Glucoma:
***500mg PO/IV, followed by 125-250 mg PO q4h
***500mg PO q12h (sustained release)
**Open-angle Glucoma:
***250mg-1g PO/IV qd
***500mg PO q12h (sustained release)
*Acute Altitude Sickness
**500-1000mg extended release PO qd
**Continue treatment for 48 hours or longer if necessary
*CHF-associated Edema
**250-375mg PO qAM
**5mg/kg
*Drug-induced Edema
**250-375mg PO qAM
*Epilepsy
**8-30 mg/kg/day PO qd
**Do not exceed 30mg/kg/day or 1g/day


==Pediatric Dosing==
==Pediatric Dosing==
*Epilepsy
**<12 years: safety and efficacy not established
**>12 years: 8-30 mg/kg/day PO qd
*Acute Altitude Sickness
**<12 years: safety and efficacy not established
**>12 years: 500-1000 mg PO qd


==Special Populations==
==Special Populations==

Revision as of 04:01, 31 July 2015

General

  • Type: Carbonic anhydrase inhibitor
  • Dosage Forms: PO/IV
  • Common Trade Names: Diamox

Adult Dosing

  • Glucoma
    • Closed-angle Glucoma:
      • 500mg PO/IV, followed by 125-250 mg PO q4h
      • 500mg PO q12h (sustained release)
    • Open-angle Glucoma:
      • 250mg-1g PO/IV qd
      • 500mg PO q12h (sustained release)
  • Acute Altitude Sickness
    • 500-1000mg extended release PO qd
    • Continue treatment for 48 hours or longer if necessary
  • CHF-associated Edema
    • 250-375mg PO qAM
    • 5mg/kg
  • Drug-induced Edema
    • 250-375mg PO qAM
  • Epilepsy
    • 8-30 mg/kg/day PO qd
    • Do not exceed 30mg/kg/day or 1g/day

Pediatric Dosing

  • Epilepsy
    • <12 years: safety and efficacy not established
    • >12 years: 8-30 mg/kg/day PO qd
  • Acute Altitude Sickness
    • <12 years: safety and efficacy not established
    • >12 years: 500-1000 mg PO qd

Special Populations

  • Pregnancy Rating: C
  • Lactation risk: Safe
  • Renal Dosing
    • Adult: CrCl 10-50: give q12h; CrCl<10: avoid use; HD/PD: not defined
    • Pediatric: CrCl 10-50: give q12h; CrCl<10: avoid use, HD/PD: not defined
  • Hepatic Dosing
    • Adult: contraindicated in significant impairment/cirrhosis
    • Pediatric: contraindicated in significant impairment/cirrhosis

Contraindications

  • Allergy to class/drug
  • hypokalemia
  • hyponatremia
  • acidosis, hyperchloremic
  • acidosis, metabolic
  • adrenal insufficiency
  • cirrhosis
  • hepatic disease, severe
  • renal disease, severe
  • glaucoma, angle-closure (long-term use)
  • caution if hypersensitivity to sulfonamides
  • caution if ASA tx, high-dose
  • caution if hepatic impairment
  • caution if pulmonary impairment
  • caution if diabetes mellitus
  • caution if gout
  • caution if elderly pts

Adverse Reactions

Serious

  • metabolic acidosis
  • electrolyte imbalance
  • anaphylaxis
  • erythema multiforme
  • Stevens-Johnson syndrome
  • toxic epidermal necrolysis
  • hepatic necrosis
  • hepatic impairment
  • agranulocytosis
  • anemia, hemolytic
  • myelosuppression
  • leukopenia
  • pancytopenia
  • blood dyscrasias
  • thrombocytopenic purpura
  • seizures
  • paralysis, flaccid
  • crystalluria
  • nephrolithiasis

Common

  • fatigue
  • malaise
  • taste change
  • anorexia
  • nausea/vomiting
  • parethesia
  • diarrhea
  • polyuria
  • electrolyte disorders
  • tinnitus
  • hearing changes
  • myopia
  • drowsiness
  • confusion
  • uticaria
  • rash
  • photosensitivity
  • glucosuria
  • hematuria
  • melena

Pharmacology

  • Half-life: 10-15h
  • Metabolism: CYP450
  • Excretion: urine (100% unchanged)
  • Mechanism of Action: inhibits carbonic anhydrase

Comments

See Also

References