Does DICLOFENAC Cause International normalised ratio increased? 97 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 97 reports of International normalised ratio increased have been filed in association with DICLOFENAC (Diclofenac Sodium Delayed Release). This represents 0.1% of all adverse event reports for DICLOFENAC.
97
Reports of International normalised ratio increased with DICLOFENAC
0.1%
of all DICLOFENAC reports
8
Deaths
59
Hospitalizations
How Dangerous Is International normalised ratio increased From DICLOFENAC?
Of the 97 reports, 8 (8.2%) resulted in death, 59 (60.8%) required hospitalization, and 24 (24.7%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DICLOFENAC. However, 97 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 International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which DICLOFENAC Alternatives Have Lower International normalised ratio increased Risk?
DICLOFENAC vs DICLOFENAC DIETHYLAMINE
DICLOFENAC vs DICLOFENAC EPOLAMINE
DICLOFENAC vs DICLOFENAC\DICLOFENAC
DICLOFENAC vs DICLOFENAC\MISOPROSTOL
DICLOFENAC vs DICLOXACILLIN