Does DEVICE\POLYURETHANE Cause Therapy non-responder? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Therapy non-responder have been filed in association with DEVICE\POLYURETHANE. This represents 9.6% of all adverse event reports for DEVICE\POLYURETHANE.
5
Reports of Therapy non-responder with DEVICE\POLYURETHANE
9.6%
of all DEVICE\POLYURETHANE reports
1
Deaths
4
Hospitalizations
How Dangerous Is Therapy non-responder From DEVICE\POLYURETHANE?
Of the 5 reports, 1 (20.0%) resulted in death, 4 (80.0%) required hospitalization.
Is Therapy non-responder 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 Therapy non-responder?
ETANERCEPT (3,472)
APREMILAST (3,360)
METHOTREXATE (2,965)
RITUXIMAB (2,731)
ADALIMUMAB (2,595)
PREDNISONE (2,563)
TREPROSTINIL (2,289)
INFLIXIMAB (2,122)
TOCILIZUMAB (1,775)
HYDROXYCHLOROQUINE (1,699)