Does KETOPROFEN Cause Syncope? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Syncope have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
19
Reports of Syncope with KETOPROFEN
0.3%
of all KETOPROFEN reports
1
Deaths
12
Hospitalizations
How Dangerous Is Syncope From KETOPROFEN?
Of the 19 reports, 1 (5.3%) resulted in death, 12 (63.2%) required hospitalization, and 3 (15.8%) were considered life-threatening.
Is Syncope Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 19 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 Syncope?
AMBRISENTAN (2,140)
TREPROSTINIL (1,908)
ADALIMUMAB (1,795)
FUROSEMIDE (1,431)
LENALIDOMIDE (1,280)
BISOPROLOL (1,279)
METOPROLOL (1,251)
AMLODIPINE (1,224)
ASPIRIN (1,193)
SACUBITRIL\VALSARTAN (1,163)
Which KETOPROFEN Alternatives Have Lower Syncope Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN