Does DICLOFENAC Cause Expired product administered? 714 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 714 reports of Expired product administered have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.8% of all adverse event reports for DICLOFENAC.
714
Reports of Expired product administered with DICLOFENAC
0.8%
of all DICLOFENAC reports
0
Deaths
18
Hospitalizations
How Dangerous Is Expired product administered From DICLOFENAC?
Of the 714 reports, 18 (2.5%) required hospitalization, and 3 (0.4%) were considered life-threatening.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 714 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
NICOTINE (704)
Which DICLOFENAC Alternatives Have Lower Expired product administered Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN