Does DICLOFENAC Cause Condition aggravated? 4,583 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,583 reports of Condition aggravated have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 5.3% of all adverse event reports for DICLOFENAC.
4,583
Reports of Condition aggravated with DICLOFENAC
5.3%
of all DICLOFENAC reports
1,637
Deaths
2,186
Hospitalizations
How Dangerous Is Condition aggravated From DICLOFENAC?
Of the 4,583 reports, 1,637 (35.7%) resulted in death, 2,186 (47.7%) required hospitalization, and 1,851 (40.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 4,583 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DICLOFENAC Alternatives Have Lower Condition aggravated Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN