Does KETOPROFEN Cause Intentional product misuse? 341 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 341 reports of Intentional product misuse have been filed in association with KETOPROFEN (Orudis). This represents 6.1% of all adverse event reports for KETOPROFEN.
341
Reports of Intentional product misuse with KETOPROFEN
6.1%
of all KETOPROFEN reports
112
Deaths
35
Hospitalizations
How Dangerous Is Intentional product misuse From KETOPROFEN?
Of the 341 reports, 112 (32.8%) resulted in death, 35 (10.3%) required hospitalization, and 13 (3.8%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 341 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which KETOPROFEN Alternatives Have Lower Intentional product misuse Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN