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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 Status epilepticus? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Status epilepticus have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.

5
Reports of Status epilepticus with KETOPROFEN
0.1%
of all KETOPROFEN reports
0
Deaths
5
Hospitalizations

How Dangerous Is Status epilepticus From KETOPROFEN?

Of the 5 reports, 5 (100.0%) required hospitalization, and 5 (100.0%) were considered life-threatening.

Is Status epilepticus Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 5 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 Status epilepticus?

LEVETIRACETAM (1,883) LACOSAMIDE (874) VALPROIC ACID (587) PHENYTOIN (544) BUPROPION (490) LAMOTRIGINE (438) MIDAZOLAM (369) CLOBAZAM (366) PHENOBARBITAL (317) TOPIRAMATE (315)

Which KETOPROFEN Alternatives Have Lower Status epilepticus 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 Status epilepticus Reports All Drugs Causing Status epilepticus KETOPROFEN Demographics