Does BUMETANIDE Cause Product prescribing issue? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product prescribing issue have been filed in association with BUMETANIDE (Bumetanide). This represents 0.7% of all adverse event reports for BUMETANIDE.
15
Reports of Product prescribing issue with BUMETANIDE
0.7%
of all BUMETANIDE reports
0
Deaths
14
Hospitalizations
How Dangerous Is Product prescribing issue From BUMETANIDE?
Of the 15 reports, 14 (93.3%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUMETANIDE. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does BUMETANIDE Cause?
Acute kidney injury (490)
Drug ineffective (186)
Hypotension (182)
Fatigue (173)
Dehydration (170)
Dyspnoea (147)
Dizziness (129)
Weight increased (113)
Cardiac failure (97)
Renal impairment (89)
What Other Drugs Cause Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which BUMETANIDE Alternatives Have Lower Product prescribing issue Risk?
BUMETANIDE vs BUPIVACAINE
BUMETANIDE vs BUPIVACAINE\BUPIVACAINE ANHYDROUS
BUMETANIDE vs BUPIVACAINE\EPINEPHRINE
BUMETANIDE vs BUPIVACAINE\MELOXICAM
BUMETANIDE vs BUPRENORPHINE