Does INSULIN GLARGINE Cause Incorrect product administration duration? 215 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 215 reports of Incorrect product administration duration have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 0.2% of all adverse event reports for INSULIN GLARGINE.
215
Reports of Incorrect product administration duration with INSULIN GLARGINE
0.2%
of all INSULIN GLARGINE reports
1
Deaths
23
Hospitalizations
How Dangerous Is Incorrect product administration duration From INSULIN GLARGINE?
Of the 215 reports, 1 (0.5%) resulted in death, 23 (10.7%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 215 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 administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which INSULIN GLARGINE Alternatives Have Lower Incorrect product administration duration 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