Enalapril/Enalaprilat
(Vasotec)
|
Category:
Description:
Indications:
Precautions:
-
Pregnancy
category C (1st trimester), category D (2nd and
3rd trimesters); ACE inhibitors can cause fetal and
neonatal morbidity and death when administered to pregnant women
-
Impaired
renal function, dialysis patients, hypovolemia, diuretic therapy
-
Collagen-vascular
diseases, CHF, elderly, bilateral renal artery stenosis
Adverse
Reactions (Side Effects):
-
CNS:
anxiety, dizziness, fatigue, headache, insomnia, paresthesia
-
CV:
angina, hypotension, palpitations, postural hypotension, syncope
-
GI:
abdominal pain, constipation, melena, nausea, vomiting
-
GU:
decreased libido, impotence, increased BUN/creatinine, UTI
-
METAB:
hyperkalemia, hyponatremia
-
MS:
arthralgia, arthritis, myalgia
-
RESP:
asthma, bronchitis, cough, dyspnea, sinusitis
-
SKIN:
angioedema, flushing, rash, sweating
|
Dosage:
Administered
orally, intravenously
-
Adult:
PO 2.5-5mg daily, increase as needed, usually 10-40mg daily
divided 1-2 times; IV (enalaprilat) 0.625-1.25 mg/dose given over 5
minutes every 6 hours; dosing adjustment in renal impairment: CrCl
10-50 ml/min, 75%-100% of normal dose; CrCl <10 ml/min, 50% of
normal dose
-
Child:
PO 0.1 mg/kg/day initially, increase as needed over 2 weeks to
max of 0.5 mg/kg/day; IV (enalaprilat) 5-10 mcg/kg/dose every 8-24
hours
Drug
interactions:
-
Allopurinal:
predisposition to hypersensitivity reactions to ACE inhibitors
-
Aspirin,
NSAIDS: inhibition of the antihypertensive response to Ace inhibitors
-
Prazosin,
terazosin, doxazosin: exaggerated first-dose hypotensive response to a-blockers
|
Source:
Operational Medicine 2001, Health
Care in Military Settings, NAVMED P-5139, May 1, 2001, Bureau
of Medicine and Surgery, Department of the Navy, 2300 E Street NW, Washington,
D.C., 20372-5300
|