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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 Foetal death? 231 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 231 reports of Foetal death have been filed in association with KETOPROFEN (Orudis). This represents 4.2% of all adverse event reports for KETOPROFEN.

231
Reports of Foetal death with KETOPROFEN
4.2%
of all KETOPROFEN reports
118
Deaths
6
Hospitalizations

How Dangerous Is Foetal death From KETOPROFEN?

Of the 231 reports, 118 (51.1%) resulted in death, 6 (2.6%) required hospitalization, and 10 (4.3%) were considered life-threatening.

Is Foetal death Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 231 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 Foetal death?

ADALIMUMAB (824) QUETIAPINE (382) VENLAFAXINE (353) ACETAMINOPHEN (327) ALBUTEROL (323) ONDANSETRON (304) FUROSEMIDE (301) BUPROPION (294) FLUCONAZOLE (287) GABAPENTIN (283)

Which KETOPROFEN Alternatives Have Lower Foetal death 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 Foetal death Reports All Drugs Causing Foetal death KETOPROFEN Demographics