Does TOCILIZUMAB Cause International normalised ratio increased? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of International normalised ratio increased have been filed in association with TOCILIZUMAB (Tocilizumab-anoh). This represents 0.0% of all adverse event reports for TOCILIZUMAB.
39
Reports of International normalised ratio increased with TOCILIZUMAB
0.0%
of all TOCILIZUMAB reports
8
Deaths
25
Hospitalizations
How Dangerous Is International normalised ratio increased From TOCILIZUMAB?
Of the 39 reports, 8 (20.5%) resulted in death, 25 (64.1%) required hospitalization, and 7 (17.9%) 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 TOCILIZUMAB. However, 39 reports have been filed with the FAERS database.
What Other Side Effects Does TOCILIZUMAB Cause?
Drug ineffective (32,342)
Rheumatoid arthritis (20,652)
Pain (18,384)
Off label use (18,256)
Arthralgia (15,536)
Joint swelling (14,831)
Fatigue (13,802)
Rash (12,327)
Drug intolerance (11,952)
Contraindicated product administered (11,547)
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 TOCILIZUMAB Alternatives Have Lower International normalised ratio increased Risk?
TOCILIZUMAB vs TOCILIZUMAB-AAZG
TOCILIZUMAB vs TOCOPHEROL
TOCILIZUMAB vs TOFACITINIB
TOCILIZUMAB vs TOFERSEN
TOCILIZUMAB vs TOLNAFTATE