Does KETOPROFEN Cause Ventricular hypokinesia? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Ventricular hypokinesia have been filed in association with KETOPROFEN (Orudis). This represents 0.2% of all adverse event reports for KETOPROFEN.
11
Reports of Ventricular hypokinesia with KETOPROFEN
0.2%
of all KETOPROFEN reports
0
Deaths
11
Hospitalizations
How Dangerous Is Ventricular hypokinesia From KETOPROFEN?
Of the 11 reports, 11 (100.0%) required hospitalization, and 7 (63.6%) were considered life-threatening.
Is Ventricular hypokinesia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 11 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 Ventricular hypokinesia?
BISOPROLOL (169)
ASPIRIN (144)
CYCLOPHOSPHAMIDE (140)
SACUBITRIL\VALSARTAN (137)
RAMIPRIL (126)
TRASTUZUMAB (121)
DOXORUBICIN (118)
ATORVASTATIN (108)
FUROSEMIDE (105)
PANTOPRAZOLE (100)
Which KETOPROFEN Alternatives Have Lower Ventricular hypokinesia Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN