Does DICLOFENAC Cause Adulterated product? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Adulterated product have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.0% of all adverse event reports for DICLOFENAC.
7
Reports of Adulterated product with DICLOFENAC
0.0%
of all DICLOFENAC reports
0
Deaths
5
Hospitalizations
How Dangerous Is Adulterated product From DICLOFENAC?
Of the 7 reports, 5 (71.4%) required hospitalization, and 3 (42.9%) were considered life-threatening.
Is Adulterated product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 7 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 Adulterated product?
LISDEXAMFETAMINE DIMESYLATE (31)
THEOBROMINE (29)
ACETAMINOPHEN (28)
LIDOCAINE (28)
COCAINE (27)
CAFFEINE (24)
CODEINE (23)
THEOPHYLLINE (23)
FENTANYL (22)
MORPHINE (22)
Which DICLOFENAC Alternatives Have Lower Adulterated product Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN