FUROSEMIDE FUROSEMIDE HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Approved Furosemide is a diuretic which is an anthranilic acid derivative. Chemically, it is 4-chloro-N-furfuryl-5-sulfamoylanthranilic acid. Furosemide is a white to slightly yellow, odorless, crystalline powder. Practically insoluble in water; freely soluble in acetone, in dimethylformamide, and in solutions of alkali hydroxides; soluble in methanol; sparingly soluble in alcohol; slightly soluble in ether; very slightly soluble in chloroform. The structural formula is as follows: Furosemide Injection, USP is a sterile, nonpyrogenic solution of furosemide in Water for Injection prepared with the aid of sodium hydroxide for intramuscular (IM) or intravenous (IV) use. Each mL contains: Furosemide 10 mg; Water for Injection q.s.; sodium chloride to adjust isotonicity; sodium hydroxide and if necessary hydrochloric acid to adjust pH between 8.0 and 9.3. DESCRIPTION
FunFoxMeds bottle
Substance Furosemide
Route
INTRAMUSCULAR INTRAVENOUS
Applications
NDA018902

Drug Facts

Composition & Profile

Strengths
20 mg/2 ml 10 mg/ml 2 ml 4 ml 10 ml
Quantities
2 ml 4 ml 10 ml 25 vial
Treats Conditions
Indications Usage Parenteral Therapy Should Be Reserved For Patients Unable To Take Oral Medication Or For Patients In Emergency Clinical Situations Edema Furosemide 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 Furosemide Is Particularly Useful When An Agent With Greater Diuretic Potential Is Desired Furosemide Is Indicated As Adjunctive Therapy In Acute Pulmonary Edema The Iv Administration Of Furosemide Is Indicated When A Rapid Onset Of Diuresis Is Desired E G In Acute Pulmonary Edema If Gastrointestinal Absorption Is Impaired Or Oral Medication Is Not Practical For Any Reason Furosemide Is Indicated By The Im Or Iv Route Parenteral Use Should Be Replaced With Oral Furosemide As Soon As Practical

Identifiers & Packaging

Container Type BOTTLE
UPC
0363323280017
UNII
7LXU5N7ZO5
Packaging

HOW SUPPLIED NDC 51662-1572-1 FUROSEMIDE INJECTION, USP 20mg PER 2mL (10mg PER mL) 2mL VIAL NDC 51662-1572-2 FUROSEMIDE INJECTION, USP 20mg PER 2mL (10mg PER mL) 2mL VIAL IN A POUCH NDC 51662-1572-3 CASE OF 25 FUROSEMIDE INJECTION, USP 20mg PER 2mL (10mg PER mL) 2mL VIALS HF Acquisition Co LLC, DBA HealthFirst Mukilteo, WA 98275 Also supplied in the following manufacture supplied dosage forms Furosemide injection, USP 2 mL, 4 mL and 10 mL sizes are single dose vials, packaged 25 vials per tray. Preservative Free. Discard unused portion. Use only if solution is clear and seal intact. PROTECT FROM LIGHT. Do not use if solution is discolored. Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. HS; PRINCIPAL DISPLAY PANEL - 51662-1572-1 2mL mL VIAL AND SERIALIZED LABEL VIAL SERIALIZED; PRINCIPAL DISPLAY PANEL 51662-1572-2 POUCH LABELING 51662-1572-2 POUCH LABELING POUCH LABELING VIAL LABEL; PRINCIPAL DISPLAY PANEL 51662-1572-3 CASE LABELING 51662-1572-2 CASE LABELING Case Labeling RFID Label

Package Descriptions
  • HOW SUPPLIED NDC 51662-1572-1 FUROSEMIDE INJECTION, USP 20mg PER 2mL (10mg PER mL) 2mL VIAL NDC 51662-1572-2 FUROSEMIDE INJECTION, USP 20mg PER 2mL (10mg PER mL) 2mL VIAL IN A POUCH NDC 51662-1572-3 CASE OF 25 FUROSEMIDE INJECTION, USP 20mg PER 2mL (10mg PER mL) 2mL VIALS HF Acquisition Co LLC, DBA HealthFirst Mukilteo, WA 98275 Also supplied in the following manufacture supplied dosage forms Furosemide injection, USP 2 mL, 4 mL and 10 mL sizes are single dose vials, packaged 25 vials per tray. Preservative Free. Discard unused portion. Use only if solution is clear and seal intact. PROTECT FROM LIGHT. Do not use if solution is discolored. Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. HS
  • PRINCIPAL DISPLAY PANEL - 51662-1572-1 2mL mL VIAL AND SERIALIZED LABEL VIAL SERIALIZED
  • PRINCIPAL DISPLAY PANEL 51662-1572-2 POUCH LABELING 51662-1572-2 POUCH LABELING POUCH LABELING VIAL LABEL
  • PRINCIPAL DISPLAY PANEL 51662-1572-3 CASE LABELING 51662-1572-2 CASE LABELING Case Labeling RFID Label

Overview

Furosemide is a diuretic which is an anthranilic acid derivative. Chemically, it is 4-chloro-N-furfuryl-5-sulfamoylanthranilic acid. Furosemide is a white to slightly yellow, odorless, crystalline powder. Practically insoluble in water; freely soluble in acetone, in dimethylformamide, and in solutions of alkali hydroxides; soluble in methanol; sparingly soluble in alcohol; slightly soluble in ether; very slightly soluble in chloroform. The structural formula is as follows: Furosemide Injection, USP is a sterile, nonpyrogenic solution of furosemide in Water for Injection prepared with the aid of sodium hydroxide for intramuscular (IM) or intravenous (IV) use. Each mL contains: Furosemide 10 mg; Water for Injection q.s.; sodium chloride to adjust isotonicity; sodium hydroxide and if necessary hydrochloric acid to adjust pH between 8.0 and 9.3. DESCRIPTION

Indications & Usage

INDICATIONS & USAGE Parenteral therapy should be reserved for patients unable to take oral medication or for patients in emergency clinical situations. Edema Furosemide 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. Furosemide is particularly useful when an agent with greater diuretic potential is desired. Furosemide is indicated as adjunctive therapy in acute pulmonary edema. The IV administration of furosemide is indicated when a rapid onset of diuresis is desired, e.g., in acute pulmonary edema. If gastrointestinal absorption is impaired or oral medication is not practical for any reason, furosemide is indicated by the IM or IV route. Parenteral use should be replaced with oral furosemide as soon as practical.

Dosage & Administration

DOSAGE & ADMINISTRATION Adults Parenteral therapy with furosemide injection should be used only in patients unable to take oral medication or in emergency situations and should be replaced with oral therapy as soon as practical. Edema- The usual initial dose of furosemide is 20 to 40 mg given as a single dose, injected IM or IV. The IV dose should be given slowly (one to two minutes). Ordinarily a prompt diuresis ensues. If needed, another dose may be administered in the same manner two hours later or the dose may be increased. The dose may be raised by 20 mg and given not sooner than two hours after the previous dose until the desired diuretic effect has been obtained. This individually determined single dose should then be given once or twice daily. Therapy should be individualized according to patient response to gain maximal therapeutic response and to determine the minimal dose needed to maintain that response. Close medical supervision is necessary. If the physician elects to use high dose parenteral therapy, add the furosemide to either Sodium Chloride Injection USP, Lactated Ringer’s Injection USP, or Dextrose Injection 5% USP, after pH has been adjusted to above 5.5, and administer as a controlled IV infusion at a rate not greater than 4 mg/min. Furosemide injection is a buffered alkaline solution with a pH of about 9 and the drug may precipitate at pH values below 7. Care must be taken to ensure that the pH of the prepared infusion solution is in the weakly alkaline to neutral range. Acid solutions, including other parenteral medications (e.g., labetalol, ciprofloxacin, amrinone, milrinone) must not be administered concurrently in the same infusion because they may cause precipitation of the furosemide. In addition, furosemide injection should not be added to a running intravenous line containing any of these acidic products. Acute Pulmonary Edema- The usual initial dose of furosemide is 40 mg injected slowly IV (over one to two minutes). If a satisfactory response does not occur within one hour, the dose may be increased to 80 mg injected slowly IV (over one to two minutes). If necessary, additional therapy (e.g., digitalis, oxygen) may be administered concomitantly. Geriatric Patients In general, dose selection for the elderly patient should be cautious, usually starting at the low end of the dosing range (see PRECAUTIONS, GERIATRIC USE ). Pediatric Patients Parenteral therapy should be used only in patients unable to take oral medication or in emergency situations and should be replaced with oral therapy as soon as practical. The usual initial dose of furosemide injection (IM or IV) in pediatric patients is 1 mg/kg body weight and should be given slowly under close medical supervision. If the diuretic response to the initial dose is not satisfactory, dosage may be increased by 1 mg/kg not sooner than two hours after the previous dose, until the desired diuretic effect has been obtained. Doses greater than 6 mg/kg body weight are not recommended. Literature reports suggest that the maximum dose for premature infants should not exceed 1 mg/kg/day (see WARNINGS, PEDIATRIC USE ). Furosemide injection should be inspected visually for particulate matter and discoloration before administration. Do not use if solution is discolored.

Warnings & Precautions
WARNINGS In patients with hepatic cirrhosis and ascites, furosemide 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, furosemide should be discontinued. Cases of tinnitus and reversible or irreversible hearing impairment and deafness have been reported. Reports usually indicate that furosemide 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 4 mg furosemide per minute has been used) (see PRECAUTIONS, DRUG INTERACTIONS) . Pediatric Use In premature neonates with respiratory distress syndrome, diuretic treatment with furosemide in the first few weeks of life may increase the risk of persistent patent ductus arteriosus (PDA), possibly through a prostaglandin-E-mediated process. Literature reports indicate that premature infants with post conceptual age (gestational plus postnatal) less than 31 weeks receiving doses exceeding 1 mg/kg/24 hours may develop plasma levels which could be associated with potential toxic effects including ototoxicity. Hearing loss in neonates has been associated with the use of furosemide injection (see WARNINGS , above).
Contraindications

Furosemide is contraindicated in patients with anuria and in patients with a history of hypersensitivity to furosemide.

Adverse Reactions

Adverse reactions are categorized below by organ system and listed by decreasing severity. Gastrointestinal System Reactions Hepatic encephalopathy in patients with hepatocellular insufficiency Pancreatitis Jaundice (intrahepatic cholestatic jaundice) Increased liver enzymes Anorexia Oral and gastric irritation Cramping Diarrhea Constipation Nausea Vomiting Systemic Hypersensitivity Reactions Severe anaphylactic or anaphylactoid reactions (e.g., with shock) Systemic vasculitis Interstitial nephritis Necrotizing angiitis Central Nervous System Reactions Tinnitus and hearing loss Paresthesias Vertigo Dizziness Headache Blurred vision Xanthopsia Hematologic Reactions Aplastic anemia Thrombocytopenia Agranulocytosis Hemolytic anemia Leukopenia Anemia Eosinophilia Dermatologic-Hypersensitivity Reactions Toxic epidermal necrolysis Stevens-Johnson Syndrome Erythema multiforme Drug rash with eosinophila and systemic symptoms Acute generalized exanthematous pustulosis Exfoliative dermatitis Bullous pemphigoid Purpura Photosensitivity Rash Pruritus Urticaria Cardiovascular Reactions Orthostatic hypotension may occur and be aggravated by alcohol, barbiturates or narcotics Increase in cholesterol and triglyceride serum levels Other Reactions Hyperglycemia Glycosuria Hyperuricemia Muscle spasm Weakness Restlessness Urinary bladder spasm Thrombophlebitis Transient injection site pain following intramuscular injection Fever Whenever adverse reactions are moderate or severe, furosemide dosage should be reduced or therapy withdrawn.


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