Does DEVICE Cause Complication of device removal? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Complication of device removal have been filed in association with DEVICE. This represents 0.1% of all adverse event reports for DEVICE.
11
Reports of Complication of device removal with DEVICE
0.1%
of all DEVICE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Complication of device removal From DEVICE?
Of the 11 reports, 3 (27.3%) required hospitalization.
Is Complication of device removal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
Product use issue (1,076)
Intercepted product preparation error (1,033)
Wrong technique in product usage process (935)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
What Other Drugs Cause Complication of device removal?
COPPER (7,895)
ETONOGESTREL (3,578)
LEVONORGESTREL (2,039)
MIRENA (44)
INTERFERON BETA-1A (37)
TREPROSTINIL (24)
IMPLANON (21)
ETHINYL ESTRADIOL\ETONOGESTREL (15)
UNSPECIFIED INGREDIENT (14)
BUPRENORPHINE (11)
Which DEVICE Alternatives Have Lower Complication of device removal Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN