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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 Anuria? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Anuria have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.

14
Reports of Anuria with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
12
Hospitalizations

How Dangerous Is Anuria From KETOPROFEN?

Of the 14 reports, 12 (85.7%) required hospitalization, and 5 (35.7%) were considered life-threatening.

Is Anuria Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 14 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 Anuria?

METFORMIN (705) AMLODIPINE (279) FUROSEMIDE (256) TACROLIMUS (201) PREDNISONE (143) ASPIRIN (135) IBUPROFEN (127) PREDNISOLONE (125) MYCOPHENOLATE MOFETIL (124) BISOPROLOL (123)

Which KETOPROFEN Alternatives Have Lower Anuria 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 Anuria Reports All Drugs Causing Anuria KETOPROFEN Demographics