Does INSULIN GLARGINE Cause Product use complaint? 119 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Product use complaint have been filed in association with INSULIN GLARGINE (Lantus Solostar). This represents 0.1% of all adverse event reports for INSULIN GLARGINE.
119
Reports of Product use complaint with INSULIN GLARGINE
0.1%
of all INSULIN GLARGINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product use complaint From INSULIN GLARGINE?
Of the 119 reports, 3 (2.5%) required hospitalization, and 1 (0.8%) were considered life-threatening.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE. However, 119 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 use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which INSULIN GLARGINE Alternatives Have Lower Product use complaint 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