Does DEVICE Cause Device breakage? 108 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 108 reports of Device breakage have been filed in association with DEVICE. This represents 0.9% of all adverse event reports for DEVICE.
108
Reports of Device breakage with DEVICE
0.9%
of all DEVICE reports
1
Deaths
11
Hospitalizations
How Dangerous Is Device breakage From DEVICE?
Of the 108 reports, 1 (0.9%) resulted in death, 11 (10.2%) required hospitalization, and 2 (1.9%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 108 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 Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which DEVICE Alternatives Have Lower Device breakage Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN