Does DEVICE Cause Device mechanical issue? 226 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 226 reports of Device mechanical issue have been filed in association with DEVICE. This represents 1.8% of all adverse event reports for DEVICE.
226
Reports of Device mechanical issue with DEVICE
1.8%
of all DEVICE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device mechanical issue From DEVICE?
Of the 226 reports.
Is Device mechanical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 226 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 mechanical issue?
SOMATROPIN (6,411)
INSULIN GLARGINE-YFGN (853)
INSULIN GLARGINE (725)
ALBUTEROL (455)
ETANERCEPT (145)
FLUTICASONE\SALMETEROL (127)
GLATIRAMER (124)
EXENATIDE (108)
MEDROXYPROGESTERONE (99)
ADALIMUMAB-AFZB (76)
Which DEVICE Alternatives Have Lower Device mechanical issue Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN