Does ARIXTRA Cause Gastrointestinal haemorrhage? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Gastrointestinal haemorrhage have been filed in association with ARIXTRA. This represents 3.7% of all adverse event reports for ARIXTRA.
11
Reports of Gastrointestinal haemorrhage with ARIXTRA
3.7%
of all ARIXTRA reports
1
Deaths
10
Hospitalizations
How Dangerous Is Gastrointestinal haemorrhage From ARIXTRA?
Of the 11 reports, 1 (9.1%) resulted in death, 10 (90.9%) required hospitalization, and 4 (36.4%) were considered life-threatening.
Is Gastrointestinal haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARIXTRA. However, 11 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)
Neoplasm malignant (11)
What Other Drugs Cause Gastrointestinal haemorrhage?
RIVAROXABAN (20,041)
ASPIRIN (13,172)
CLOPIDOGREL BISULFATE (5,513)
DABIGATRAN ETEXILATE (4,081)
APIXABAN (4,030)
WARFARIN (2,469)
IBUPROFEN (1,496)
ADALIMUMAB (943)
PRADAXA (907)
NAPROXEN (770)
Which ARIXTRA Alternatives Have Lower Gastrointestinal haemorrhage Risk?
ARIXTRA vs ARMODAFINIL
ARIXTRA vs AROMASIN
ARIXTRA vs ARSENIC TRIOXIDE
ARIXTRA vs ARTEMETHER\LUMEFANTRINE
ARIXTRA vs ARTESUNATE