View Drug - Lasix
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Lasix

Generic: FUROSEMIDE

100%
Basic Information
Manufacturer
Validus Pharmaceuticals LLC
Product Type
HUMAN PRESCRIPTION DRUG
Route of Administration
ORAL
FDA Set ID
2c9b4d8f-0770-482d-a9e6-9c616a440b1a
Indications & Usage
INDICATIONS AND USAGE Edema LASIX is indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome.

LASIX is particularly useful when an agent with greater diuretic potential is desired.

Hypertension Oral LASIX may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents.

Hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with LASIX alone.
Warnings
WARNING LASIX ® (furosemide) is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion.

Therefore, careful medical supervision is required and dose and dose schedule must be adjusted to the individual patient’s needs ( s ee DOSAGE AND ADMINISTRATION ) .

WARNINGS In patients with hepatic cirrhosis and ascites, LASIX therapy is best initiated in the hospital.

In hepatic coma and in states of electrolyte depletion, therapy should not be instituted until the basic condition is improved.

Sudden alterations of fluid and electrolyte balance in patients with cirrhosis may precipitate hepatic coma; therefore, strict observation is necessary during the period of diuresis.

Supplemental potassium chloride and, if required, an aldosterone antagonist are helpful in preventing hypokalemia and metabolic alkalosis.

If increasing azotemia and oliguria occur during treatment of severe progressive renal disease, LASIX should be discontinued.

Cases of tinnitus and reversible or irreversible hearing impairment and deafness have been reported.

Reports usually indicate that LASIX ototoxicity is associated with rapid injection, severe renal impairment, the use of higher than recommended doses, hypoproteinemia or concomitant therapy with aminoglycoside antibiotics, ethacrynic acid, or other ototoxic drugs.

If the physician elects to use high dose parenteral therapy, controlled intravenous infusion is advisable (for adults, an infusion rate not exceeding 4mg LASIX per minute has been used) ( s ee PRECAUTIONS: Drug Interactions ) .
Adverse Reactions
ADVERSE REACTIONS Adverse reactions are categorized below by organ system and listed by decreasing severity.

Gastrointestinal System Reactions 1.

hepatic encephalopathy in patients with hepatocellular insufficiency 6.

oral and gastric irritation 7.

cramping 2.

pancreatitis 8.

diarrhea 3.

jaundice (intrahepatic cholestatic jaundice) 9.

constipation 4.

increased liver enzymes 10.

nausea 5.

anorexia 11.

vomiting Systemic Hypersensitivity Reactions 1.

Severe anaphylactic or anaphylactoid reactions (e.g., with shock) 3.

interstitial nephritis 4.

necrotizing angiitis 2.

systemic vasculitis Central Nervous System Reactions 1.

tinnitus and hearing loss 5.

headache 2.

paresthesias 6.

blurred vision 3.

vertigo 7.

xanthopsia 4.

dizziness Hematologic Reactions 1.

aplastic anemia 5.

leukopenia 2.

thrombocytopenia 6.

anemia 3.

agranulocytosis 7.

eosinophilia 4.

hemolytic anemia Dermatologic-Hypersensitivity Reactions 1.

toxic epidermal necrolysis 7.

bullous pemphigoid 2.

Stevens-Johnson Syndrome 3.

erythema multiforme 8.

purpura 9.

photosensitivity 4.

drug rash with eosinophilia and systemic symptoms 10.

rash 11.

pruritis 5.

acute generalized exanthematous pustulosis 6.

exfoliative dermatitis 12.

urticaria Cardiovascular Reaction 1.

Orthostatic hypotension may occur and be aggravated by alcohol, barbiturates, or narcotics.

2.

Increase in cholesterol and triglyceride serum levels Other Reactions 1.

hyperglycemia 6.

restlessness 2.

glycosuria 7.

urinary bladder spasm 3.

hyperuricemia 8.

thrombophlebitis 4.

muscle spasm 9.

fever 5.

weakness Whenever adverse reactions are moderate or severe, LASIX dosage should be reduced or therapy withdrawn.

To report SUSPECTED ADVERSE REACTIONS, contact Validus Pharmaceuticals LLC at 1-866-982-5438 (1-866-9VALIDUS) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.