Does DEVICE Cause Blood glucose abnormal? 269 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 269 reports of Blood glucose abnormal have been filed in association with DEVICE. This represents 2.1% of all adverse event reports for DEVICE.
269
Reports of Blood glucose abnormal with DEVICE
2.1%
of all DEVICE reports
3
Deaths
30
Hospitalizations
How Dangerous Is Blood glucose abnormal From DEVICE?
Of the 269 reports, 3 (1.1%) resulted in death, 30 (11.2%) required hospitalization, and 3 (1.1%) were considered life-threatening.
Is Blood glucose abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 269 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 Blood glucose abnormal?
INSULIN GLARGINE (2,463)
INSULIN LISPRO (2,460)
DULAGLUTIDE (912)
INSULIN HUMAN (900)
METFORMIN (563)
EXENATIDE (556)
EMPAGLIFLOZIN (445)
SITAGLIPTIN (334)
ADALIMUMAB (285)
TIRZEPATIDE (267)
Which DEVICE Alternatives Have Lower Blood glucose abnormal Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN