Does DICLOFENAC Cause Adverse event? 871 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 871 reports of Adverse event have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 1.0% of all adverse event reports for DICLOFENAC.
871
Reports of Adverse event with DICLOFENAC
1.0%
of all DICLOFENAC reports
422
Deaths
445
Hospitalizations
How Dangerous Is Adverse event From DICLOFENAC?
Of the 871 reports, 422 (48.5%) resulted in death, 445 (51.1%) required hospitalization, and 522 (59.9%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for DICLOFENAC.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which DICLOFENAC Alternatives Have Lower Adverse event Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN