Does DICLOFENAC Cause Application site erythema? 290 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 290 reports of Application site erythema have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.3% of all adverse event reports for DICLOFENAC.
290
Reports of Application site erythema with DICLOFENAC
0.3%
of all DICLOFENAC reports
0
Deaths
2
Hospitalizations
How Dangerous Is Application site erythema From DICLOFENAC?
Of the 290 reports, 2 (0.7%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Application site erythema Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 290 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 Application site erythema?
NICOTINE (2,004)
SUMATRIPTAN (1,875)
INGENOL MEBUTATE (1,373)
BUPRENORPHINE (1,273)
ESTRADIOL (1,117)
MINOXIDIL (1,061)
METHYLPHENIDATE (543)
ESTRADIOL\NORETHINDRONE (533)
FENTANYL (501)
OXYTROL FOR WOMEN (422)
Which DICLOFENAC Alternatives Have Lower Application site erythema Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN