FDA label 2a7d33df-e362-d1e4-e063-6294a90a6d1c

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
fbe70dd9-3e6b-11e8-e053-6394a90a289d
SPL ID
2a7d33df-e362-d1e4-e063-6294a90a6d1c
Version
2
Effective date
2024-12-20
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:33:22

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings and cautions

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 4mg furosemide per minute has been used) (see PRECAUTIONS : Drug Interactions).

Adverse reactions cross-check#

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Adverse reactions sections page 2 of 2 · 7 matching rows.

adverse reactions table

<table ID="ID25" width="555" styleCode="Noautorules"><caption/><col width="312"/><col width="66"/><col width="177"/><tbody><tr><td align="left" valign="top"> 1. aplastic anemia </td><td valign="top"/><td align="left" valign="top"> 5. leukopenia </td></tr><tr><td align="left" valign="top"> 2. thrombocytopenia </td><td valign="top"/><td align="left" valign="top"> 6. anemia </td></tr><tr><td align="left" valign="top"> 3. agranulocytosis </td><td valign="top"/><td align="left" valign="top"> 7.eosinophilia </td></tr><tr><td align="left" valign="top"> 4. hemolytic anemia </td><td valign="top"/><td valign="top"/></tr></tbody></table>

adverse reactions table

<table ID="ID27" width="555" styleCode="Noautorules"><caption/><col width="284"/><col width="65"/><col width="206"/><tbody><tr><td align="left" valign="top"> 1. toxic epidermal necrolysis 2. stevens-johnson syndrome 3. erythema multiforme 4. drug rash with eosinophilia and systemic symptoms 5. acute generalized exanthematous pustulosis 6. exfoliative dermatitis </td><td valign="top"/><td align="left" valign="top"> 7. bullous pemphigoid 8. purpura 9. photosensitivity 10. rash 11. pruritis 12. urticaria </td></tr></tbody></table>

adverse reactions table

<table ID="ID31" width="555" styleCode="Noautorules"><caption/><col width="312"/><col width="66"/><col width="177"/><tbody><tr><td align="left" valign="top"> 1. hyperglycemia </td><td valign="top"/><td align="left" valign="top"> 6. restlessness </td></tr><tr><td align="left" valign="top"> 2. glycosuria </td><td valign="top"/><td align="left" valign="top"> 7. urinary bladder spasm </td></tr><tr><td align="left" valign="top"> 3. hyperuricemia </td><td valign="top"/><td align="left" valign="top"> 8. thrombophlebitis </td></tr><tr><td align="left" valign="top"> 4. muscle spasm 5. weakness </td><td valign="top"/><td align="left" valign="top"> 9. fever </td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.