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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 Poisoning deliberate? 139 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Poisoning deliberate have been filed in association with KETOPROFEN (Orudis). This represents 2.5% of all adverse event reports for KETOPROFEN.

139
Reports of Poisoning deliberate with KETOPROFEN
2.5%
of all KETOPROFEN reports
7
Deaths
112
Hospitalizations

How Dangerous Is Poisoning deliberate From KETOPROFEN?

Of the 139 reports, 7 (5.0%) resulted in death, 112 (80.6%) required hospitalization, and 29 (20.9%) were considered life-threatening.

Is Poisoning deliberate Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 139 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 Poisoning deliberate?

ACETAMINOPHEN (2,009) ALPRAZOLAM (1,220) DIAZEPAM (982) TRAMADOL (952) QUETIAPINE (818) OXAZEPAM (691) ZOPICLONE (672) VENLAFAXINE (653) CYAMEMAZINE (637) SERTRALINE (424)

Which KETOPROFEN Alternatives Have Lower Poisoning deliberate 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 Poisoning deliberate Reports All Drugs Causing Poisoning deliberate KETOPROFEN Demographics