Does KETOPROFEN Cause Anaemia? 118 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 118 reports of Anaemia have been filed in association with KETOPROFEN (Orudis). This represents 2.1% of all adverse event reports for KETOPROFEN.
118
Reports of Anaemia with KETOPROFEN
2.1%
of all KETOPROFEN reports
16
Deaths
83
Hospitalizations
How Dangerous Is Anaemia From KETOPROFEN?
Of the 118 reports, 16 (13.6%) resulted in death, 83 (70.3%) required hospitalization, and 24 (20.3%) were considered life-threatening.
Is Anaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 118 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 Anaemia?
LENALIDOMIDE (5,322)
CARBOPLATIN (5,312)
RIBAVIRIN (5,130)
ASPIRIN (4,568)
CYCLOPHOSPHAMIDE (4,486)
RITUXIMAB (4,399)
DEXAMETHASONE (4,352)
ADALIMUMAB (3,994)
PACLITAXEL (3,949)
METHOTREXATE (3,913)
Which KETOPROFEN Alternatives Have Lower Anaemia Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN