Does KETOPROFEN Cause Haematemesis? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Haematemesis have been filed in association with KETOPROFEN (Orudis). This represents 0.4% of all adverse event reports for KETOPROFEN.
23
Reports of Haematemesis with KETOPROFEN
0.4%
of all KETOPROFEN reports
0
Deaths
15
Hospitalizations
How Dangerous Is Haematemesis From KETOPROFEN?
Of the 23 reports, 15 (65.2%) required hospitalization, and 7 (30.4%) were considered life-threatening.
Is Haematemesis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 23 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 Haematemesis?
ASPIRIN (1,538)
RIVAROXABAN (1,085)
CLOPIDOGREL BISULFATE (954)
IBUPROFEN (836)
APIXABAN (650)
ADALIMUMAB (563)
ACETAMINOPHEN (454)
WARFARIN (426)
SERTRALINE (412)
ENOXAPARIN (404)
Which KETOPROFEN Alternatives Have Lower Haematemesis Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN