Does DICLOFENAC Cause Product prescribing error? 296 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 296 reports of Product prescribing error have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.3% of all adverse event reports for DICLOFENAC.
296
Reports of Product prescribing error with DICLOFENAC
0.3%
of all DICLOFENAC reports
3
Deaths
134
Hospitalizations
How Dangerous Is Product prescribing error From DICLOFENAC?
Of the 296 reports, 3 (1.0%) resulted in death, 134 (45.3%) required hospitalization, and 15 (5.1%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 296 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which DICLOFENAC Alternatives Have Lower Product prescribing error Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN