Does INSULIN GLARGINE Cause Incorrect product storage? 341 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 341 reports of Incorrect product storage have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 0.3% of all adverse event reports for INSULIN GLARGINE.
341
Reports of Incorrect product storage with INSULIN GLARGINE
0.3%
of all INSULIN GLARGINE reports
1
Deaths
69
Hospitalizations
How Dangerous Is Incorrect product storage From INSULIN GLARGINE?
Of the 341 reports, 1 (0.3%) resulted in death, 69 (20.2%) required hospitalization, and 7 (2.1%) were considered life-threatening.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 341 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
CYCLOSPORINE (203)
Which INSULIN GLARGINE Alternatives Have Lower Incorrect product storage 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