Does INSULIN GLARGINE Cause Device use issue? 469 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 469 reports of Device use issue have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 0.5% of all adverse event reports for INSULIN GLARGINE.
469
Reports of Device use issue with INSULIN GLARGINE
0.5%
of all INSULIN GLARGINE reports
1
Deaths
33
Hospitalizations
How Dangerous Is Device use issue From INSULIN GLARGINE?
Of the 469 reports, 1 (0.2%) resulted in death, 33 (7.0%) required hospitalization.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 469 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)
Device issue (3,175)
What Other Drugs Cause Device use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
LEVODOPA (443)
Which INSULIN GLARGINE Alternatives Have Lower Device use 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