Does INSULIN GLARGINE Cause Device breakage? 237 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 237 reports of Device breakage have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 0.2% of all adverse event reports for INSULIN GLARGINE.
237
Reports of Device breakage with INSULIN GLARGINE
0.2%
of all INSULIN GLARGINE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Device breakage From INSULIN GLARGINE?
Of the 237 reports, 11 (4.6%) required hospitalization.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 237 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 breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which INSULIN GLARGINE Alternatives Have Lower Device breakage 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