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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 DEVICE\POLYURETHANE Cause Dyspnoea exertional? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Dyspnoea exertional have been filed in association with DEVICE\POLYURETHANE. This represents 9.6% of all adverse event reports for DEVICE\POLYURETHANE.

5
Reports of Dyspnoea exertional with DEVICE\POLYURETHANE
9.6%
of all DEVICE\POLYURETHANE reports
0
Deaths
3
Hospitalizations

How Dangerous Is Dyspnoea exertional From DEVICE\POLYURETHANE?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Dyspnoea exertional Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE\POLYURETHANE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does DEVICE\POLYURETHANE Cause?

Dermatitis contact (29) Infusion site pain (17) Infusion site erythema (14) Nausea (12) Diarrhoea (10) Dyspnoea (10) Infusion site swelling (9) Dizziness (7) Headache (7) Infusion site infection (7)

What Other Drugs Cause Dyspnoea exertional?

TREPROSTINIL (3,378) ALBUTEROL (2,190) MACITENTAN (1,660) AMBRISENTAN (1,655) PREDNISONE (1,319) TIOTROPIUM (1,137) MEPOLIZUMAB (1,109) BUDESONIDE\FORMOTEROL (1,038) OMALIZUMAB (995) EPOPROSTENOL (938)

Related Pages

DEVICE\POLYURETHANE Full Profile All Dyspnoea exertional Reports All Drugs Causing Dyspnoea exertional DEVICE\POLYURETHANE Demographics