Does INSULIN GLARGINE Cause Device mechanical issue? 725 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 725 reports of Device mechanical issue have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 0.7% of all adverse event reports for INSULIN GLARGINE.
725
Reports of Device mechanical issue with INSULIN GLARGINE
0.7%
of all INSULIN GLARGINE reports
3
Deaths
22
Hospitalizations
How Dangerous Is Device mechanical issue From INSULIN GLARGINE?
Of the 725 reports, 3 (0.4%) resulted in death, 22 (3.0%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device mechanical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 725 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 mechanical issue?
SOMATROPIN (6,411)
INSULIN GLARGINE-YFGN (853)
ALBUTEROL (455)
DEVICE (226)
ETANERCEPT (145)
FLUTICASONE\SALMETEROL (127)
GLATIRAMER (124)
EXENATIDE (108)
MEDROXYPROGESTERONE (99)
ADALIMUMAB-AFZB (76)
Which INSULIN GLARGINE Alternatives Have Lower Device mechanical 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