Does KETOPROFEN Cause Presyncope? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Presyncope have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
17
Reports of Presyncope with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
10
Hospitalizations
How Dangerous Is Presyncope From KETOPROFEN?
Of the 17 reports, 10 (58.8%) required hospitalization.
Is Presyncope Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 17 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 Presyncope?
TREPROSTINIL (585)
BISOPROLOL (485)
LEVONORGESTREL (429)
ADALIMUMAB (420)
AMBRISENTAN (407)
ASPIRIN (370)
TAMSULOSIN (361)
FUROSEMIDE (348)
SERTRALINE (337)
ETANERCEPT (334)
Which KETOPROFEN Alternatives Have Lower Presyncope Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN