Does FUROSEMIDE Cause Wrong product administered? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Wrong product administered have been filed in association with FUROSEMIDE (Furosemide). This represents 0.1% of all adverse event reports for FUROSEMIDE.
40
Reports of Wrong product administered with FUROSEMIDE
0.1%
of all FUROSEMIDE reports
6
Deaths
29
Hospitalizations
How Dangerous Is Wrong product administered From FUROSEMIDE?
Of the 40 reports, 6 (15.0%) resulted in death, 29 (72.5%) required hospitalization, and 1 (2.5%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FUROSEMIDE. However, 40 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which FUROSEMIDE Alternatives Have Lower Wrong product administered Risk?
FUROSEMIDE vs FUROSEMIDE\SPIRONOLACTONE
FUROSEMIDE vs FUSIDATE
FUROSEMIDE vs FUSIDIC ACID
FUROSEMIDE vs FUTIBATINIB
FUROSEMIDE vs GABAPENTIN