Does DICLOFENAC Cause Intentional product misuse? 729 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 729 reports of Intentional product misuse have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.8% of all adverse event reports for DICLOFENAC.
729
Reports of Intentional product misuse with DICLOFENAC
0.8%
of all DICLOFENAC reports
205
Deaths
187
Hospitalizations
How Dangerous Is Intentional product misuse From DICLOFENAC?
Of the 729 reports, 205 (28.1%) resulted in death, 187 (25.7%) required hospitalization, and 121 (16.6%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 729 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DICLOFENAC Alternatives Have Lower Intentional product misuse Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN