Does DICLOFENAC Cause Product dose omission issue? 210 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 210 reports of Product dose omission issue have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.2% of all adverse event reports for DICLOFENAC.
210
Reports of Product dose omission issue with DICLOFENAC
0.2%
of all DICLOFENAC reports
3
Deaths
24
Hospitalizations
How Dangerous Is Product dose omission issue From DICLOFENAC?
Of the 210 reports, 3 (1.4%) resulted in death, 24 (11.4%) required hospitalization, and 3 (1.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 210 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which DICLOFENAC Alternatives Have Lower Product dose omission issue Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN