Does DICLOFENAC Cause Type i hypersensitivity? 111 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 111 reports of Type i hypersensitivity have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.1% of all adverse event reports for DICLOFENAC.
111
Reports of Type i hypersensitivity with DICLOFENAC
0.1%
of all DICLOFENAC reports
0
Deaths
10
Hospitalizations
How Dangerous Is Type i hypersensitivity From DICLOFENAC?
Of the 111 reports, 10 (9.0%) required hospitalization, and 4 (3.6%) were considered life-threatening.
Is Type i hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 111 reports have been filed with the FAERS database.
What Other Side Effects Does DICLOFENAC Cause?
Drug ineffective (24,885)
Product use in unapproved indication (12,197)
Off label use (10,370)
Pain (9,276)
Product use issue (8,009)
Fatigue (7,908)
Rash (7,852)
Rheumatoid arthritis (7,366)
Abdominal discomfort (7,257)
Product administered at inappropriate site (6,919)
What Other Drugs Cause Type i hypersensitivity?
OXALIPLATIN (266)
AMOXICILLIN (260)
LEVOFLOXACIN (180)
ACETAMINOPHEN (129)
CARBOPLATIN (125)
PANTOPRAZOLE (110)
PACLITAXEL (107)
IBUPROFEN (103)
OMEPRAZOLE (98)
PROPOFOL (82)
Which DICLOFENAC Alternatives Have Lower Type i hypersensitivity Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN