Does KETOPROFEN Cause Cardiac failure? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Cardiac failure have been filed in association with KETOPROFEN (Orudis). This represents 0.9% of all adverse event reports for KETOPROFEN.
49
Reports of Cardiac failure with KETOPROFEN
0.9%
of all KETOPROFEN reports
16
Deaths
25
Hospitalizations
How Dangerous Is Cardiac failure From KETOPROFEN?
Of the 49 reports, 16 (32.7%) resulted in death, 25 (51.0%) required hospitalization, and 13 (26.5%) were considered life-threatening.
Is Cardiac failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does KETOPROFEN Cause?
Pain (595)
Headache (574)
Hypersensitivity (556)
Erythema (546)
Acute kidney injury (517)
Hyperhidrosis (516)
Hepatic enzyme increased (508)
Asthma (507)
Rheumatoid arthritis (493)
Immunodeficiency (492)
What Other Drugs Cause Cardiac failure?
SACUBITRIL\VALSARTAN (4,504)
FUROSEMIDE (1,841)
APIXABAN (1,575)
CYCLOPHOSPHAMIDE (1,514)
DOXORUBICIN (1,367)
ADALIMUMAB (1,278)
DEXAMETHASONE (1,271)
TREPROSTINIL (1,168)
BISOPROLOL (1,159)
LENALIDOMIDE (1,115)
Which KETOPROFEN Alternatives Have Lower Cardiac failure Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN