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fenoldopam (Corlopam)

 

Classes: Vasodilators; Endocrine, Dopamine Agonists

Dosing and uses of Corlopam (fenoldopam)

 

Adult dosage forms and strengths

injectable solution

  • 10mg/mL

 

Severe/Malignant Hypertension, Hypertensive Emergencies

Initiate dosing at 0.01 to 0.3 mcg/kg/min by continuous IV infusion

Titrate by 0.05-0.1 mcg/kg/min q15min or longer until target blood pressure reached; up to 1.6 mcg/kg/min used in clinical trials; may continue maintenance infusion for up to 48 hr

In hospital use only

 

Monitor

Continuously monitor BP (usually by means of an intra-arterial line) & heart rate

 

Other Indications & Uses

Short-term (No more than 48 hr adult, 4 hr Peds), in-hospital treatment of

  • Severe or malignant hypertension
  • Hypertensive emergencies

 

Pediatric dosage forms and strengths

injectable solution

  • 10mg/mL

 

Severe/Malignant HTN, Hypertensive Emergencies

Initial 0.2 mcg/kg/min continuous IV infusion pump for <4 hr

Titrate q20-30min up to 0.3-0.5 mcg/kg/min; not to exceed 0.8 mcg/kg/min

In hospital use only

 

Monitor

Continuously monitor BP (usually by means of an intra-arterial line) & heart rate

 

Corlopam (fenoldopam) adverse (side) effects

Frequency not defined

Angina

Cardiac dysrhythmia

Dizziness

Flushing

Heart failure

Hypotension

Myocardial infarction

Tachycardia

Headache

Nausea

Vomiting

Serum creatinine raised

 

Warnings

Contraindications

Hypersensitivity to fenoldopam and sulfite

 

Cautions

Causes a dose-related tachycardia, particularly with infusion rates above 0.1 mcg/kg/min

Monitor potassium levels

Increased intraocular pressure in patients with glaucoma or intraocular hypertension

Contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms in susceptible patients

 

Pregnancy and lactation

Pregnancy category: B

Lactation: Excretion in milk unknown; use with caution

 

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 Corlopam (fenoldopam)

Mechanism of action

D1-dopamine receptor agonist: rapid-acting vasodilator; decreases peripheral resistance and increases renal blood flow; has minimal adrenergic effects

Also diuretic, natriuretic

 

Pharmacokinetics

Half-Life: 5 min

Duration: 1-4 hr post infusion

Onset: initial effect: 10 min, max effect: 30-120 min

Vd: 0.6 L/kg

Metabolism: in the liver to a variety of sulfate, glucuronide, & methoxy metabolites

Metabolite: fenoldopam-8-sulfate, fenoldopam-7-sulfate, fenoldopam glucuronide conjugates, and other minor metabolites

Excretion: Urine (90%), feces (10%)

 

Administration

IV Incompatibilities

Y-site: aminophylline, amphotericin B, ampicillin, bumetanide, cefoxitin, dexamethasone sodium PO4, diazepam, fosphenytoin, furosemide, ketorolac, methohexital, methylprednisolone Na-succinate, pentobarbital, phenytoin, prochlorperazine, Na-bicarb, thiopentaL

 

IV Compatibilities

Solution: D5W, Ns

Y-site (partial list): alfentanil, atropine, cefazolin, cefepime, ciprofloxacin, cisatracurium, clindamycin, dalfopristin-quinupristin, digoxin, diltiazem, dobutamine, dopamine, epinephrine, erythromycin, esmolol, heparin, hydromorphone, hydroxyzine, linezolid, lorazepam, MgSO4, morphine SO4, mannitol, midazolam, nitroglycerin, KCl, propofol, propranolol, TMP-SMX, vancomycin, verapamiL

 

IV Preparation

Adult Infusion: dilute in NS or D5W to a final concentration of 40 mcg/mL; for each 1 mL (=10 mg) of drug use 250 mL diluent

Pediatric Infusion: dilute in NS or D5W to a final concentration of 60 mcg/mL; for each 1.5 mL (=15 mg) of drug use 250 mL diluent

 

IV Administration

Use diluted solution within 24 hr

Use continuous infusion pump