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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 ETRUMADENANT Cause Dyspnoea? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Dyspnoea have been filed in association with ETRUMADENANT. This represents 8.6% of all adverse event reports for ETRUMADENANT.

6
Reports of Dyspnoea with ETRUMADENANT
8.6%
of all ETRUMADENANT reports
6
Deaths
6
Hospitalizations

How Dangerous Is Dyspnoea From ETRUMADENANT?

Of the 6 reports, 6 (100.0%) resulted in death, 6 (100.0%) required hospitalization.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETRUMADENANT. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does ETRUMADENANT Cause?

Disease progression (19) Febrile neutropenia (16) Platelet count decreased (15) Pyrexia (14) Hyponatraemia (12) Drug hypersensitivity (11) Vomiting (11) Diarrhoea (10) Nausea (10) Acute kidney injury (7)

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)

Related Pages

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