Does ARIXTRA Cause Subdural haematoma? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Subdural haematoma have been filed in association with ARIXTRA. This represents 2.0% of all adverse event reports for ARIXTRA.
6
Reports of Subdural haematoma with ARIXTRA
2.0%
of all ARIXTRA reports
2
Deaths
4
Hospitalizations
How Dangerous Is Subdural haematoma From ARIXTRA?
Of the 6 reports, 2 (33.3%) resulted in death, 4 (66.7%) required hospitalization, and 2 (33.3%) were considered life-threatening.
Is Subdural haematoma Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARIXTRA. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does ARIXTRA Cause?
Death (37)
Investigation (33)
Haematoma (27)
Anaemia (20)
Incorrect drug administration duration (19)
Off label use (18)
Thrombosis (17)
Haemorrhage (13)
Cerebral haemorrhage (11)
Gastrointestinal haemorrhage (11)
What Other Drugs Cause Subdural haematoma?
RIVAROXABAN (1,423)
ASPIRIN (1,181)
APIXABAN (1,025)
WARFARIN (1,012)
CLOPIDOGREL BISULFATE (809)
DABIGATRAN ETEXILATE (648)
IBRUTINIB (342)
HEPARIN (201)
ENOXAPARIN (156)
CYCLOPHOSPHAMIDE (146)
Which ARIXTRA Alternatives Have Lower Subdural haematoma Risk?
ARIXTRA vs ARMODAFINIL
ARIXTRA vs AROMASIN
ARIXTRA vs ARSENIC TRIOXIDE
ARIXTRA vs ARTEMETHER\LUMEFANTRINE
ARIXTRA vs ARTESUNATE