Does DICLOFENAC Cause Product complaint? 511 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 511 reports of Product complaint have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.6% of all adverse event reports for DICLOFENAC.
511
Reports of Product complaint with DICLOFENAC
0.6%
of all DICLOFENAC reports
4
Deaths
8
Hospitalizations
How Dangerous Is Product complaint From DICLOFENAC?
Of the 511 reports, 4 (0.8%) resulted in death, 8 (1.6%) required hospitalization, and 6 (1.2%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 511 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 Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which DICLOFENAC Alternatives Have Lower Product complaint Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN