Does KETOPROFEN Cause Contraindicated product administered? 345 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 345 reports of Contraindicated product administered have been filed in association with KETOPROFEN (Orudis). This represents 6.2% of all adverse event reports for KETOPROFEN.
345
Reports of Contraindicated product administered with KETOPROFEN
6.2%
of all KETOPROFEN reports
112
Deaths
26
Hospitalizations
How Dangerous Is Contraindicated product administered From KETOPROFEN?
Of the 345 reports, 112 (32.5%) resulted in death, 26 (7.5%) required hospitalization, and 13 (3.8%) were considered life-threatening.
Is Contraindicated product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 345 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 Contraindicated product administered?
ABATACEPT (13,559)
METHOTREXATE (13,121)
ETANERCEPT (12,062)
TOCILIZUMAB (11,547)
ADALIMUMAB (11,270)
LEFLUNOMIDE (11,206)
HYDROXYCHLOROQUINE (10,557)
RITUXIMAB (10,479)
INFLIXIMAB (9,618)
SULFASALAZINE (8,698)
Which KETOPROFEN Alternatives Have Lower Contraindicated product administered Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN