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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ARIXTRA Cause Dyspnoea? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Dyspnoea have been filed in association with ARIXTRA. This represents 3.0% of all adverse event reports for ARIXTRA.

9
Reports of Dyspnoea with ARIXTRA
3.0%
of all ARIXTRA reports
0
Deaths
7
Hospitalizations

How Dangerous Is Dyspnoea From ARIXTRA?

Of the 9 reports, 7 (77.8%) required hospitalization, and 1 (11.1%) were considered life-threatening.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ARIXTRA. However, 9 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 Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

Which ARIXTRA Alternatives Have Lower Dyspnoea Risk?

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

Related Pages

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