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ethacrynic acid (Edecrin)

 

Classes: Diuretics, Loop

Dosing and uses of Edecrin (ethacrynic acid)

 

Adult dosage forms and strengths

powder for injection

  • 50mg

tablet

  • 25mg

 

Edema

0.5-1 mg/kg up to 100 mg/dose slow IVP, Or

25-100 mg PO qDay or q12hr

May take with food

 

Renal Impairment

Not necessary to supplement dose; not removed by hemo- or peritoneal dialysis

CrCl <10 mL/minute: Not recommended

 

Overdose Management

May use normal saline for volume replacement

May use dopamine or norepinephrine to treat hypotension

If dysrhythmia due to decreased K+ or Mg+ suspected replace aggressively

Discontinue treatment if no symptoms after 6hr

 

Other Indications & Uses

Edema-associated with CHF, hepatic cirrhosis, renal dysfunction, malignancy, & pulmonary edema

Short-term use in children (other than infants) with congenital heart disease or nephrotic syndrome

Use when fluid retention refractory to thiazides, or with impaired renal function

 

Pediatric dosage forms and strengths

powder for injection

  • 50mg

tablet

  • 25mg

 

Congenital Heart Disease, Nephrotic Syndrome

PO: 1 mg/kg/dose qDay; may increase q2-3days to maximum of 3 mg/kg/day

IV: Data limited; 1 mg/kg IV

 

Geriatric dosage forms and strengths

May cause hypertension and fluid imblances in the elderly; use alternatives if available

 

Edema

0.5-1 mg/kg up to 100 mg/dose slow IVP, Or

25-50 mg PO qDay or q12hr

May take with food

 

Edecrin (ethacrynic acid) adverse (side) effects

Frequency not defined

Injection site reaction

Hyperuricemia

Gout

Hypotension

Hypokalemia

Electrolyte abnormalities

Hyperglycemia/hypoglycemia

Hyperlipidemia

Ototoxicity

Tinnitus

Photosensitivity

Muscle cramps

Dizziness

Confusion

Headache

Nausea/vomiting

Anorexia

Dysphagia

Diarrhea

Pancreatitis

Agranulocytosis

Neutropenia

Thrombocytopenia

Hematuria

 

Warnings

Contraindications

Hypersensitivity to ethacrynic acid

Anuria, severe, watery diarrhea

Use in infants

 

Cautions

Avoid concurrent use with lithium or furosemide

Diabetes mellitus, geriatrics, liver disease, renal impairment

Risk of fluid or electrolyte imbalance, hyperglycemia, hyperuricemia, hypotension, metabolic alkalosis

Risk of ototoxicity (tinnitus, reversible/irreversible hearing impairment)

Discontinue use if severe, watery diarrhea occurs

 

Pregnancy and lactation

Pregnancy category: B

Lactation: excretion in milk unknown/not recommended

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Edecrin (ethacrynic acid)

Mechanism of action

Loop diuretic acting at Na/2Cl reabsorptive pump at ascending loop of Henle and distal renal tubule. Intereference with the chloride-binding cotransport system, causes increased excretion of water, sodium, chlorine, magnesium, and calcium.

 

Pharmacokinetics

Half-Life: 2-4 hr

Onset

  • Initial effect: IV: 5-15 min, PO: 30-60 min
  • Max effect: IV: 15 min-3 hr, PO: 2 hr

 

Other Information

Duration: IV: 2-7 hr, PO: 4-8 hr

Bioavailability: 100%

Protein Bound: 90%

Metabolism: conjugation w/ compounds containing sulfhydryl groups, such as cysteine & N-acetylcysteine in liver

Excretion: urine 66%

 

Administration

IV Incompatibilities

Whole blood or its derivatives

Additive: hydralazine, procainamide, ranitidine, tolazoline, triflupromazine

 

IV Compatibilities

Additive: chlorpromazine, cimetidine, prochlorperazine, promazine

Y-site: heparin & hydrocortisone Na-succinate, KCl, vit B/C

 

IV Administration

Do not give SC or IM due to local pain & irritation

Single doses should not exceed 100 mg

Administer IVP at 10 mg/min

If second dose needed, a new injection site is recommended to avoid possible thrombophlebitis