Does DICLOFENAC Cause Incorrect product administration duration? 362 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 362 reports of Incorrect product administration duration have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.4% of all adverse event reports for DICLOFENAC.
362
Reports of Incorrect product administration duration with DICLOFENAC
0.4%
of all DICLOFENAC reports
67
Deaths
83
Hospitalizations
How Dangerous Is Incorrect product administration duration From DICLOFENAC?
Of the 362 reports, 67 (18.5%) resulted in death, 83 (22.9%) required hospitalization, and 68 (18.8%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 362 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
OMEPRAZOLE (302)
ALENDRONATE (287)
Which DICLOFENAC Alternatives Have Lower Incorrect product administration duration Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN