Does KETOPROFEN Cause Cardiogenic shock? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Cardiogenic shock have been filed in association with KETOPROFEN (Orudis). This represents 0.6% of all adverse event reports for KETOPROFEN.
33
Reports of Cardiogenic shock with KETOPROFEN
0.6%
of all KETOPROFEN reports
14
Deaths
10
Hospitalizations
How Dangerous Is Cardiogenic shock From KETOPROFEN?
Of the 33 reports, 14 (42.4%) resulted in death, 10 (30.3%) required hospitalization, and 16 (48.5%) were considered life-threatening.
Is Cardiogenic shock Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 33 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 Cardiogenic shock?
AMLODIPINE (779)
AMIODARONE (595)
BUPROPION (559)
ACETAMINOPHEN (466)
METOPROLOL (454)
BISOPROLOL (413)
VERAPAMIL (412)
NOREPINEPHRINE (381)
HEPARIN (357)
METFORMIN (356)
Which KETOPROFEN Alternatives Have Lower Cardiogenic shock Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN