Does BUMETANIDE Cause Product administration error? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product administration error have been filed in association with BUMETANIDE (Bumetanide). This represents 0.5% of all adverse event reports for BUMETANIDE.
10
Reports of Product administration error with BUMETANIDE
0.5%
of all BUMETANIDE reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product administration error From BUMETANIDE?
Of the 10 reports, 7 (70.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUMETANIDE. However, 10 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BUMETANIDE Alternatives Have Lower Product administration error Risk?
BUMETANIDE vs BUPIVACAINE
BUMETANIDE vs BUPIVACAINE\BUPIVACAINE ANHYDROUS
BUMETANIDE vs BUPIVACAINE\EPINEPHRINE
BUMETANIDE vs BUPIVACAINE\MELOXICAM
BUMETANIDE vs BUPRENORPHINE