Does INSULIN GLARGINE\LIXISENATIDE Cause Device defective? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device defective have been filed in association with INSULIN GLARGINE\LIXISENATIDE. This represents 0.3% of all adverse event reports for INSULIN GLARGINE\LIXISENATIDE.
9
Reports of Device defective with INSULIN GLARGINE\LIXISENATIDE
0.3%
of all INSULIN GLARGINE\LIXISENATIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From INSULIN GLARGINE\LIXISENATIDE?
Of the 9 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE\LIXISENATIDE. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does INSULIN GLARGINE\LIXISENATIDE Cause?
Blood glucose increased (419)
Product storage error (379)
Accidental exposure to product (258)
Off label use (205)
Visual impairment (136)
Inappropriate schedule of product administration (132)
Nausea (132)
Exposure via skin contact (125)
Drug ineffective (98)
Blood glucose decreased (94)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which INSULIN GLARGINE\LIXISENATIDE Alternatives Have Lower Device defective Risk?
INSULIN GLARGINE\LIXISENATIDE vs INSULIN GLULISINE
INSULIN GLARGINE\LIXISENATIDE vs INSULIN HUMAN
INSULIN GLARGINE\LIXISENATIDE vs INSULIN LISPRO
INSULIN GLARGINE\LIXISENATIDE vs INSULIN LISPRO-AABC
INSULIN GLARGINE\LIXISENATIDE vs INSULIN NOS