Does DEVICE\POLYURETHANE Cause Device dislocation? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device dislocation have been filed in association with DEVICE\POLYURETHANE. This represents 9.6% of all adverse event reports for DEVICE\POLYURETHANE.
5
Reports of Device dislocation with DEVICE\POLYURETHANE
9.6%
of all DEVICE\POLYURETHANE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device dislocation From DEVICE\POLYURETHANE?
Of the 5 reports, 3 (60.0%) required hospitalization.
Is Device dislocation 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 Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)