Does KETOPROFEN Cause Suicidal ideation? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Suicidal ideation have been filed in association with KETOPROFEN (Orudis). This represents 0.5% of all adverse event reports for KETOPROFEN.
28
Reports of Suicidal ideation with KETOPROFEN
0.5%
of all KETOPROFEN reports
0
Deaths
20
Hospitalizations
How Dangerous Is Suicidal ideation From KETOPROFEN?
Of the 28 reports, 20 (71.4%) required hospitalization, and 2 (7.1%) were considered life-threatening.
Is Suicidal ideation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 28 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 Suicidal ideation?
DULOXETINE (4,014)
ARIPIPRAZOLE (2,618)
SERTRALINE (2,168)
QUETIAPINE (2,072)
PREGABALIN (1,718)
VENLAFAXINE (1,699)
OXYCODONE (1,654)
SODIUM OXYBATE (1,403)
MONTELUKAST (1,375)
FINASTERIDE (1,301)
Which KETOPROFEN Alternatives Have Lower Suicidal ideation Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN