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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BUMETANIDE Cause Ejection fraction decreased? 32 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Ejection fraction decreased have been filed in association with BUMETANIDE (Bumetanide). This represents 1.5% of all adverse event reports for BUMETANIDE.

32
Reports of Ejection fraction decreased with BUMETANIDE
1.5%
of all BUMETANIDE reports
11
Deaths
23
Hospitalizations

How Dangerous Is Ejection fraction decreased From BUMETANIDE?

Of the 32 reports, 11 (34.4%) resulted in death, 23 (71.9%) required hospitalization, and 1 (3.1%) were considered life-threatening.

Is Ejection fraction decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BUMETANIDE. However, 32 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 Ejection fraction decreased?

SACUBITRIL\VALSARTAN (2,551) TRASTUZUMAB (1,579) DOXORUBICIN (834) CYCLOPHOSPHAMIDE (754) PERTUZUMAB (644) DOCETAXEL (520) PACLITAXEL (466) BISOPROLOL (314) RITUXIMAB (296) CARVEDILOL (284)

Which BUMETANIDE Alternatives Have Lower Ejection fraction decreased Risk?

BUMETANIDE vs BUPIVACAINE BUMETANIDE vs BUPIVACAINE\BUPIVACAINE ANHYDROUS BUMETANIDE vs BUPIVACAINE\EPINEPHRINE BUMETANIDE vs BUPIVACAINE\MELOXICAM BUMETANIDE vs BUPRENORPHINE

Related Pages

BUMETANIDE Full Profile All Ejection fraction decreased Reports All Drugs Causing Ejection fraction decreased BUMETANIDE Demographics