Does BUMETANIDE Cause Eosinophilia? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Eosinophilia have been filed in association with BUMETANIDE (Bumetanide). This represents 1.6% of all adverse event reports for BUMETANIDE.
35
Reports of Eosinophilia with BUMETANIDE
1.6%
of all BUMETANIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Eosinophilia From BUMETANIDE?
Of the 35 reports, 2 (5.7%) required hospitalization, and 1 (2.9%) were considered life-threatening.
Is Eosinophilia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUMETANIDE. However, 35 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 Eosinophilia?
ALBUTEROL (1,054)
PREDNISONE (815)
CLOZAPINE (806)
MONTELUKAST (741)
PANTOPRAZOLE (709)
VANCOMYCIN (695)
MEPOLIZUMAB (606)
ALLOPURINOL (554)
BUDESONIDE\FORMOTEROL (553)
PIPERACILLIN\TAZOBACTAM (530)
Which BUMETANIDE Alternatives Have Lower Eosinophilia Risk?
BUMETANIDE vs BUPIVACAINE
BUMETANIDE vs BUPIVACAINE\BUPIVACAINE ANHYDROUS
BUMETANIDE vs BUPIVACAINE\EPINEPHRINE
BUMETANIDE vs BUPIVACAINE\MELOXICAM
BUMETANIDE vs BUPRENORPHINE