Does TOCILIZUMAB Cause Haemoglobin increased? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Haemoglobin increased have been filed in association with TOCILIZUMAB (Tocilizumab-anoh). This represents 0.0% of all adverse event reports for TOCILIZUMAB.
43
Reports of Haemoglobin increased with TOCILIZUMAB
0.0%
of all TOCILIZUMAB reports
12
Deaths
17
Hospitalizations
How Dangerous Is Haemoglobin increased From TOCILIZUMAB?
Of the 43 reports, 12 (27.9%) resulted in death, 17 (39.5%) required hospitalization, and 14 (32.6%) were considered life-threatening.
Is Haemoglobin increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOCILIZUMAB. However, 43 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 Haemoglobin increased?
RUXOLITINIB (332)
TREPROSTINIL (245)
SOTATERCEPT (151)
CLOZAPINE (142)
SOTATERCEPT-CSRK (100)
DARBEPOETIN ALFA (99)
TESTOSTERONE (96)
METFORMIN (93)
VOXELOTOR (86)
ROSUVASTATIN (85)
Which TOCILIZUMAB Alternatives Have Lower Haemoglobin increased Risk?
TOCILIZUMAB vs TOCILIZUMAB-AAZG
TOCILIZUMAB vs TOCOPHEROL
TOCILIZUMAB vs TOFACITINIB
TOCILIZUMAB vs TOFERSEN
TOCILIZUMAB vs TOLNAFTATE