Does DICLOFENAC Cause Haematemesis? 309 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 309 reports of Haematemesis have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.4% of all adverse event reports for DICLOFENAC.
309
Reports of Haematemesis with DICLOFENAC
0.4%
of all DICLOFENAC reports
19
Deaths
220
Hospitalizations
How Dangerous Is Haematemesis From DICLOFENAC?
Of the 309 reports, 19 (6.1%) resulted in death, 220 (71.2%) required hospitalization, and 42 (13.6%) were considered life-threatening.
Is Haematemesis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 309 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 Haematemesis?
ASPIRIN (1,538)
RIVAROXABAN (1,085)
CLOPIDOGREL BISULFATE (954)
IBUPROFEN (836)
APIXABAN (650)
ADALIMUMAB (563)
ACETAMINOPHEN (454)
WARFARIN (426)
SERTRALINE (412)
ENOXAPARIN (404)
Which DICLOFENAC Alternatives Have Lower Haematemesis Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN