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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 No adverse event? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of No adverse event have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.

17
Reports of No adverse event with KETOPROFEN
0.3%
of all KETOPROFEN reports
1
Deaths
2
Hospitalizations

How Dangerous Is No adverse event From KETOPROFEN?

Of the 17 reports, 1 (5.9%) resulted in death, 2 (11.8%) required hospitalization, and 1 (5.9%) were considered life-threatening.

Is No adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 17 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 No adverse event?

OMALIZUMAB (9,736) ALBUTEROL (8,971) ETONOGESTREL (8,827) TOCILIZUMAB (6,492) RITUXIMAB (5,915) METHYLPHENIDATE (4,197) MOMETASONE FUROATE (3,717) HUMAN IMMUNOGLOBULIN G (3,064) ETHINYL ESTRADIOL\NORELGESTROMIN (3,014) VEDOLIZUMAB (2,477)

Which KETOPROFEN Alternatives Have Lower No adverse event 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 No adverse event Reports All Drugs Causing No adverse event KETOPROFEN Demographics