Does INSULIN GLARGINE Cause Device issue? 3,175 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,175 reports of Device issue have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 3.2% of all adverse event reports for INSULIN GLARGINE.
3,175
Reports of Device issue with INSULIN GLARGINE
3.2%
of all INSULIN GLARGINE reports
3
Deaths
144
Hospitalizations
How Dangerous Is Device issue From INSULIN GLARGINE?
Of the 3,175 reports, 3 (0.1%) resulted in death, 144 (4.5%) required hospitalization, and 5 (0.2%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 3,175 reports have been filed with the FAERS database.
What Other Side Effects Does INSULIN GLARGINE Cause?
Blood glucose increased (19,234)
Inappropriate schedule of product administration (8,982)
Product storage error (7,743)
Off label use (6,842)
Visual impairment (5,793)
Blood glucose decreased (4,552)
Drug ineffective (4,351)
Hypoglycaemia (4,212)
Injection site pain (3,574)
Incorrect dose administered (3,070)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
EVOLOCUMAB (1,659)
Which INSULIN GLARGINE Alternatives Have Lower Device issue Risk?
INSULIN GLARGINE vs INSULIN GLARGINE-YFGN
INSULIN GLARGINE vs INSULIN GLARGINE\LIXISENATIDE
INSULIN GLARGINE vs INSULIN GLULISINE
INSULIN GLARGINE vs INSULIN HUMAN
INSULIN GLARGINE vs INSULIN LISPRO