Category:
Description:
Indications:
Contraindications:
Precautions:
-
Pregnancy
category C; excreted into breast milk
-
Diabetes
mellitus, dehydration, severe renal disease, cirrhosis ascites
-
System
lupus erythematosis
-
Gout
-
Take
with food or milk to reduce GI upset; avoid prolonged exposure to
sunlight
Adverse
Reactions (Side Effects):
-
CNS:
dizziness, fever, headache, paresthesia, restlessness, vertigo
-
CV:
chest pain, cardiovascular collapse, ECG changes, orthostatic
hypotension
-
EENT:
blurred vision, ototoxicity
-
GI:
anorexia, constipation, cramping, diarrhea, ischemic hepatitis,
jaundice, nausea, vomiting, oral and gastric irritation
-
GU:
glycosuria, hyperuricemia, urinary bladder spasm
-
HEME:
agranulocytosis, anemia, aplastic anemia, leukopenia, purpura,
thrombocytopenia
-
METAB:
hyperglycemia
-
SKIN:
erythema multiforme, exfoliative dermatitis, interstitial nephritis,
necrotizing angiitis, photosensitivity, pruritis, rash urticaria
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Dosage:
Administered
orally (tablets, solution), intravenously, and intramuscularly
-
Adult:
-
PO
20-80 mg daily in the morning; may give another dose in 6 hours;
increase in increments of 20-40mg up to 400mg daily if response
not satisfactory:
-
IM/IV
20-40mg, increased by 20mg every 2 hours until desired response
(rule of thumb: IV dose = ½ oral dose).
-
Pulmonary
edema:
-
Child:
Drug
Interactions:
-
Additive/increased
ototoxicity: aminoglycosides
-
Enhanced
nephrotoxicity: cephalosporins
-
Diuretic
induced hypokalemia may increase risk of digitalis toxicity: digoxin,
digitoxin
-
Reduced
diuretic response: barbiturates,
phenytoin
-
Case
reports of sudden death hyponatremia proposed; causal relationships
not established: seratonin-reuptake
inhibitors
-
Additive
hypokalemia: terbutaline
|
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
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