Does DICLOFENAC Cause Product quality issue? 926 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 926 reports of Product quality issue have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 1.1% of all adverse event reports for DICLOFENAC.
926
Reports of Product quality issue with DICLOFENAC
1.1%
of all DICLOFENAC reports
569
Deaths
502
Hospitalizations
How Dangerous Is Product quality issue From DICLOFENAC?
Of the 926 reports, 569 (61.4%) resulted in death, 502 (54.2%) required hospitalization, and 527 (56.9%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 926 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which DICLOFENAC Alternatives Have Lower Product quality issue Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN