Does ANDEXANET ALFA Cause Off label use? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Off label use have been filed in association with ANDEXANET ALFA (ANDEXXA). This represents 6.0% of all adverse event reports for ANDEXANET ALFA.
64
Reports of Off label use with ANDEXANET ALFA
6.0%
of all ANDEXANET ALFA reports
41
Deaths
6
Hospitalizations
How Dangerous Is Off label use From ANDEXANET ALFA?
Of the 64 reports, 41 (64.1%) resulted in death, 6 (9.4%) required hospitalization, and 6 (9.4%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANDEXANET ALFA. However, 64 reports have been filed with the FAERS database.
What Other Side Effects Does ANDEXANET ALFA Cause?
Death (175)
Cerebral infarction (139)
Cerebral haemorrhage (50)
Thrombosis (43)
Acute myocardial infarction (42)
Myocardial infarction (42)
Cerebrovascular accident (40)
Ischaemic stroke (38)
Pulmonary embolism (38)
Heparin resistance (37)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which ANDEXANET ALFA Alternatives Have Lower Off label use Risk?
ANDEXANET ALFA vs ANDROGEL
ANDEXANET ALFA vs ANETHOLTRITHION
ANDEXANET ALFA vs ANGIOTENSIN II
ANDEXANET ALFA vs ANHYDROUS CITRIC ACID\ASPIRIN\SODIUM BICARBONATE
ANDEXANET ALFA vs ANHYDROUS CITRIC ACID\MAGNESIUM\SODIUM PICOSULFATE