Does KETOPROFEN Cause Condition aggravated? 130 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 130 reports of Condition aggravated have been filed in association with KETOPROFEN (Orudis). This represents 2.3% of all adverse event reports for KETOPROFEN.
130
Reports of Condition aggravated with KETOPROFEN
2.3%
of all KETOPROFEN reports
15
Deaths
95
Hospitalizations
How Dangerous Is Condition aggravated From KETOPROFEN?
Of the 130 reports, 15 (11.5%) resulted in death, 95 (73.1%) required hospitalization, and 10 (7.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 130 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which KETOPROFEN Alternatives Have Lower Condition aggravated Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN