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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 Haemorrhage? 18 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Haemorrhage have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.

18
Reports of Haemorrhage with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
10
Hospitalizations

How Dangerous Is Haemorrhage From KETOPROFEN?

Of the 18 reports, 10 (55.6%) required hospitalization, and 3 (16.7%) were considered life-threatening.

Is Haemorrhage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 18 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 Haemorrhage?

RIVAROXABAN (6,571) APIXABAN (4,770) EMICIZUMAB-KXWH (3,612) WARFARIN (2,930) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (2,925) ASPIRIN (2,878) ADALIMUMAB (2,681) IBRUTINIB (1,907) CLOPIDOGREL BISULFATE (1,762) INSULIN LISPRO (1,614)

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