Does FUROSEMIDE Cause Product prescribing error? 187 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 187 reports of Product prescribing error have been filed in association with FUROSEMIDE (Furosemide). This represents 0.4% of all adverse event reports for FUROSEMIDE.
187
Reports of Product prescribing error with FUROSEMIDE
0.4%
of all FUROSEMIDE reports
8
Deaths
125
Hospitalizations
How Dangerous Is Product prescribing error From FUROSEMIDE?
Of the 187 reports, 8 (4.3%) resulted in death, 125 (66.8%) required hospitalization, and 40 (21.4%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FUROSEMIDE. However, 187 reports have been filed with the FAERS database.
What Other Side Effects Does FUROSEMIDE Cause?
Acute kidney injury (7,984)
Hypotension (4,468)
Dyspnoea (3,559)
Fall (3,410)
Drug ineffective (3,297)
Hyponatraemia (3,127)
Hypokalaemia (2,503)
Dehydration (2,195)
Off label use (2,147)
Fatigue (2,107)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which FUROSEMIDE Alternatives Have Lower Product prescribing error Risk?
FUROSEMIDE vs FUROSEMIDE\SPIRONOLACTONE
FUROSEMIDE vs FUSIDATE
FUROSEMIDE vs FUSIDIC ACID
FUROSEMIDE vs FUTIBATINIB
FUROSEMIDE vs GABAPENTIN