Does KETOPROFEN Cause Temperature regulation disorder? 414 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 414 reports of Temperature regulation disorder have been filed in association with KETOPROFEN (Orudis). This represents 7.5% of all adverse event reports for KETOPROFEN.
414
Reports of Temperature regulation disorder with KETOPROFEN
7.5%
of all KETOPROFEN reports
108
Deaths
6
Hospitalizations
How Dangerous Is Temperature regulation disorder From KETOPROFEN?
Of the 414 reports, 108 (26.1%) resulted in death, 6 (1.4%) required hospitalization, and 8 (1.9%) were considered life-threatening.
Is Temperature regulation disorder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 414 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 Temperature regulation disorder?
CITALOPRAM HYDROBROMIDE (452)
BUPROPION (451)
TOCILIZUMAB (447)
ALBUTEROL (437)
DIPHENHYDRAMINE (437)
ABATACEPT (433)
METHYLPREDNISOLONE (433)
CETIRIZINE (428)
PANTOPRAZOLE (427)
HYDROMORPHONE (424)
Which KETOPROFEN Alternatives Have Lower Temperature regulation disorder Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN