Does INSULIN GLARGINE Cause Product administration error? 136 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 136 reports of Product administration error have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 0.1% of all adverse event reports for INSULIN GLARGINE.
136
Reports of Product administration error with INSULIN GLARGINE
0.1%
of all INSULIN GLARGINE reports
4
Deaths
77
Hospitalizations
How Dangerous Is Product administration error From INSULIN GLARGINE?
Of the 136 reports, 4 (2.9%) resulted in death, 77 (56.6%) required hospitalization, and 18 (13.2%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 136 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which INSULIN GLARGINE Alternatives Have Lower Product administration error 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