Does KETOPROFEN Cause Cardiomyopathy? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Cardiomyopathy have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.
5
Reports of Cardiomyopathy with KETOPROFEN
0.1%
of all KETOPROFEN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Cardiomyopathy From KETOPROFEN?
Of the 5 reports, 3 (60.0%) required hospitalization, and 3 (60.0%) were considered life-threatening.
Is Cardiomyopathy Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 5 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 Cardiomyopathy?
DOXORUBICIN (820)
CYCLOPHOSPHAMIDE (581)
SACUBITRIL\VALSARTAN (444)
CLOZAPINE (404)
PREDNISONE (379)
RITUXIMAB (379)
ROSIGLITAZONE (374)
VINCRISTINE (326)
TRASTUZUMAB (292)
HYDROXYCHLOROQUINE (231)
Which KETOPROFEN Alternatives Have Lower Cardiomyopathy Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN