Does ARIXTRA Cause Condition aggravated? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with ARIXTRA. This represents 1.7% of all adverse event reports for ARIXTRA.
5
Reports of Condition aggravated with ARIXTRA
1.7%
of all ARIXTRA reports
3
Deaths
4
Hospitalizations
How Dangerous Is Condition aggravated From ARIXTRA?
Of the 5 reports, 3 (60.0%) resulted in death, 4 (80.0%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARIXTRA. However, 5 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ARIXTRA Alternatives Have Lower Condition aggravated Risk?
ARIXTRA vs ARMODAFINIL
ARIXTRA vs AROMASIN
ARIXTRA vs ARSENIC TRIOXIDE
ARIXTRA vs ARTEMETHER\LUMEFANTRINE
ARIXTRA vs ARTESUNATE