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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 Intentional overdose? 175 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 175 reports of Intentional overdose have been filed in association with KETOPROFEN (Orudis). This represents 3.2% of all adverse event reports for KETOPROFEN.

175
Reports of Intentional overdose with KETOPROFEN
3.2%
of all KETOPROFEN reports
3
Deaths
115
Hospitalizations

How Dangerous Is Intentional overdose From KETOPROFEN?

Of the 175 reports, 3 (1.7%) resulted in death, 115 (65.7%) required hospitalization, and 45 (25.7%) were considered life-threatening.

Is Intentional overdose Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 175 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 Intentional overdose?

ACETAMINOPHEN (6,869) QUETIAPINE (3,926) AMLODIPINE (3,427) PROMETHAZINE (3,193) IBUPROFEN (3,185) SERTRALINE (2,540) ALPRAZOLAM (2,389) DIAZEPAM (2,260) VENLAFAXINE (2,187) BUPROPION (2,103)

Which KETOPROFEN Alternatives Have Lower Intentional overdose 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 Intentional overdose Reports All Drugs Causing Intentional overdose KETOPROFEN Demographics