Does FUROSEMIDE Cause Product dose omission in error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product dose omission in error have been filed in association with FUROSEMIDE (Furosemide). This represents 0.0% of all adverse event reports for FUROSEMIDE.
14
Reports of Product dose omission in error with FUROSEMIDE
0.0%
of all FUROSEMIDE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission in error From FUROSEMIDE?
Of the 14 reports, 4 (28.6%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FUROSEMIDE. However, 14 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 dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which FUROSEMIDE Alternatives Have Lower Product dose omission in error Risk?
FUROSEMIDE vs FUROSEMIDE\SPIRONOLACTONE
FUROSEMIDE vs FUSIDATE
FUROSEMIDE vs FUSIDIC ACID
FUROSEMIDE vs FUTIBATINIB
FUROSEMIDE vs GABAPENTIN