Does KETOPROFEN Cause Oedema peripheral? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Oedema peripheral have been filed in association with KETOPROFEN (Orudis). This represents 0.8% of all adverse event reports for KETOPROFEN.
42
Reports of Oedema peripheral with KETOPROFEN
0.8%
of all KETOPROFEN reports
2
Deaths
18
Hospitalizations
How Dangerous Is Oedema peripheral From KETOPROFEN?
Of the 42 reports, 2 (4.8%) resulted in death, 18 (42.9%) required hospitalization, and 2 (4.8%) were considered life-threatening.
Is Oedema peripheral Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 42 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 Oedema peripheral?
AMBRISENTAN (2,959)
TREPROSTINIL (2,816)
ADALIMUMAB (2,356)
LENALIDOMIDE (2,298)
AMLODIPINE (2,076)
PREDNISONE (2,029)
METHOTREXATE (1,939)
MACITENTAN (1,932)
RITUXIMAB (1,698)
TOCILIZUMAB (1,574)
Which KETOPROFEN Alternatives Have Lower Oedema peripheral Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN