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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 Dyspnoea? 147 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 147 reports of Dyspnoea have been filed in association with BUMETANIDE (Bumetanide). This represents 6.9% of all adverse event reports for BUMETANIDE.

147
Reports of Dyspnoea with BUMETANIDE
6.9%
of all BUMETANIDE reports
13
Deaths
80
Hospitalizations

How Dangerous Is Dyspnoea From BUMETANIDE?

Of the 147 reports, 13 (8.8%) resulted in death, 80 (54.4%) required hospitalization, and 4 (2.7%) were considered life-threatening.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BUMETANIDE. However, 147 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) Dizziness (129) Weight increased (113) Cardiac failure (97) Renal impairment (89) Hypokalaemia (80)

What Other Drugs Cause Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

Which BUMETANIDE Alternatives Have Lower Dyspnoea 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 Dyspnoea Reports All Drugs Causing Dyspnoea BUMETANIDE Demographics