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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does KETOPROFEN Cause Completed suicide? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Completed suicide have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.

7
Reports of Completed suicide with KETOPROFEN
0.1%
of all KETOPROFEN reports
7
Deaths
5
Hospitalizations

How Dangerous Is Completed suicide From KETOPROFEN?

Of the 7 reports, 7 (100.0%) resulted in death, 5 (71.4%) required hospitalization.

Is Completed suicide Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 7 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 Completed suicide?

ACETAMINOPHEN (6,052) ALCOHOL (5,569) AMLODIPINE (5,267) BUPROPION (5,095) QUETIAPINE (4,997) ALPRAZOLAM (4,873) OXYCODONE (4,330) GABAPENTIN (4,111) ACETAMINOPHEN\HYDROCODONE (3,366) CLONAZEPAM (3,320)

Which KETOPROFEN Alternatives Have Lower Completed suicide Risk?

KETOPROFEN vs KETOPROFEN LYSINE KETOPROFEN vs KETOROLAC TROMETHAMINE KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE KETOPROFEN vs KETOTIFEN KETOPROFEN vs KLONOPIN

Related Pages

KETOPROFEN Full Profile All Completed suicide Reports All Drugs Causing Completed suicide KETOPROFEN Demographics