Does KETOPROFEN Cause Stevens-johnson syndrome? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Stevens-johnson syndrome have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
14
Reports of Stevens-johnson syndrome with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
12
Hospitalizations
How Dangerous Is Stevens-johnson syndrome From KETOPROFEN?
Of the 14 reports, 12 (85.7%) required hospitalization, and 5 (35.7%) were considered life-threatening.
Is Stevens-johnson syndrome Listed in the Official Label?
Yes, Stevens-johnson syndrome is listed as a known adverse reaction in the official FDA drug label for KETOPROFEN.
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 Stevens-johnson syndrome?
LAMOTRIGINE (1,384)
ALLOPURINOL (715)
IBUPROFEN (711)
SULFAMETHOXAZOLE\TRIMETHOPRIM (665)
ACETAMINOPHEN (649)
CARBAMAZEPINE (440)
PEMBROLIZUMAB (395)
LEVETIRACETAM (374)
CIPROFLOXACIN (349)
VANCOMYCIN (313)
Which KETOPROFEN Alternatives Have Lower Stevens-johnson syndrome Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN