Does BUMETANIDE Cause Wrong technique in product usage process? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Wrong technique in product usage process have been filed in association with BUMETANIDE (Bumetanide). This represents 1.4% of all adverse event reports for BUMETANIDE.
29
Reports of Wrong technique in product usage process with BUMETANIDE
1.4%
of all BUMETANIDE reports
13
Deaths
22
Hospitalizations
How Dangerous Is Wrong technique in product usage process From BUMETANIDE?
Of the 29 reports, 13 (44.8%) resulted in death, 22 (75.9%) required hospitalization, and 2 (6.9%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUMETANIDE. However, 29 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which BUMETANIDE Alternatives Have Lower Wrong technique in product usage process Risk?
BUMETANIDE vs BUPIVACAINE
BUMETANIDE vs BUPIVACAINE\BUPIVACAINE ANHYDROUS
BUMETANIDE vs BUPIVACAINE\EPINEPHRINE
BUMETANIDE vs BUPIVACAINE\MELOXICAM
BUMETANIDE vs BUPRENORPHINE