Does KETOPROFEN Cause Affective disorder? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Affective disorder have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
14
Reports of Affective disorder with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
14
Hospitalizations
How Dangerous Is Affective disorder From KETOPROFEN?
Of the 14 reports, 14 (100.0%) required hospitalization.
Is Affective disorder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 14 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 Affective disorder?
LEVOTHYROXINE (324)
ARIPIPRAZOLE (273)
LEVETIRACETAM (226)
PREDNISONE (195)
LEVONORGESTREL (185)
RISPERIDONE (178)
DUPILUMAB (175)
OLANZAPINE (165)
DULOXETINE (162)
PREGABALIN (158)
Which KETOPROFEN Alternatives Have Lower Affective disorder Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN