Does ARIXTRA Cause Investigation? 33 Reports in FDA Database

Q: Does ARIXTRA cause Investigation?

33 reports of Investigation have been filed with the FDA for ARIXTRA, representing 11.1% of all ARIXTRA adverse event reports.

Q: How dangerous is Investigation from ARIXTRA?

Of 33 reports, 3 (9.1%) resulted in death and 32 required hospitalization.

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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Investigation have been filed in association with ARIXTRA. This represents 11.1% of all adverse event reports for ARIXTRA.

Reports of Investigation with ARIXTRA

11.1%

of all ARIXTRA reports

Deaths

Hospitalizations

How Dangerous Is Investigation From ARIXTRA?

Of the 33 reports, 3 (9.1%) resulted in death, 32 (97.0%) required hospitalization.

Is Investigation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ARIXTRA. However, 33 reports have been filed with the FAERS database.

What Other Side Effects Does ARIXTRA Cause?

Death (37) Haematoma (27) Anaemia (20) Incorrect drug administration duration (19) Off label use (18) Thrombosis (17) Haemorrhage (13) Cerebral haemorrhage (11) Gastrointestinal haemorrhage (11) Neoplasm malignant (11)

What Other Drugs Cause Investigation?

ARANESP (403) NEULASTA (371) XGEVA (115) FLUTICASONE\SALMETEROL (96) DARBEPOETIN ALFA (86) ADVAIR (77) DENOSUMAB (65) ADVAIR HFA (51) ALBUTEROL (51) VENTOLIN (47)

Which ARIXTRA Alternatives Have Lower Investigation Risk?

ARIXTRA vs ARMODAFINIL ARIXTRA vs AROMASIN ARIXTRA vs ARSENIC TRIOXIDE ARIXTRA vs ARTEMETHER\LUMEFANTRINE ARIXTRA vs ARTESUNATE

ARIXTRA Full Profile All Investigation Reports All Drugs Causing Investigation ARIXTRA Demographics