Does KETOPROFEN Cause Dyschezia? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Dyschezia have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
14
Reports of Dyschezia with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
12
Hospitalizations
How Dangerous Is Dyschezia From KETOPROFEN?
Of the 14 reports, 12 (85.7%) required hospitalization.
Is Dyschezia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 14 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 Dyschezia?
ADALIMUMAB (262)
VEDOLIZUMAB (225)
CARBIDOPA\LEVODOPA (194)
POLYETHYLENE GLYCOL 3350 (82)
INFLIXIMAB (67)
LINACLOTIDE (56)
INFLIXIMAB-DYYB (53)
CAPECITABINE (51)
RUXOLITINIB (45)
NIRMATRELVIR\RITONAVIR (43)
Which KETOPROFEN Alternatives Have Lower Dyschezia Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN