Does ARIXTRA Cause Incorrect drug administration duration? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Incorrect drug administration duration have been filed in association with ARIXTRA. This represents 6.4% of all adverse event reports for ARIXTRA.
19
Reports of Incorrect drug administration duration with ARIXTRA
6.4%
of all ARIXTRA reports
5
Deaths
19
Hospitalizations
How Dangerous Is Incorrect drug administration duration From ARIXTRA?
Of the 19 reports, 5 (26.3%) resulted in death, 19 (100.0%) required hospitalization.
Is Incorrect drug administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARIXTRA. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does ARIXTRA Cause?
Death (37)
Investigation (33)
Haematoma (27)
Anaemia (20)
Off label use (18)
Thrombosis (17)
Haemorrhage (13)
Cerebral haemorrhage (11)
Gastrointestinal haemorrhage (11)
Neoplasm malignant (11)
What Other Drugs Cause Incorrect drug administration duration?
ETONOGESTREL (1,796)
POLYETHYLENE GLYCOL 3350 (1,722)
NAPROXEN (1,272)
DOCOSANOL (803)
ETHINYL ESTRADIOL\ETONOGESTREL (740)
NICOTINE (561)
RANITIDINE (504)
GUAIFENESIN (490)
INSULIN LISPRO (367)
ACETAMINOPHEN (340)
Which ARIXTRA Alternatives Have Lower Incorrect drug administration duration Risk?
ARIXTRA vs ARMODAFINIL
ARIXTRA vs AROMASIN
ARIXTRA vs ARSENIC TRIOXIDE
ARIXTRA vs ARTEMETHER\LUMEFANTRINE
ARIXTRA vs ARTESUNATE