Does LANTUS SOLOSTAR Cause Incorrect product storage? 167 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 167 reports of Incorrect product storage have been filed in association with LANTUS SOLOSTAR. This represents 6.9% of all adverse event reports for LANTUS SOLOSTAR.
167
Reports of Incorrect product storage with LANTUS SOLOSTAR
6.9%
of all LANTUS SOLOSTAR reports
0
Deaths
10
Hospitalizations
How Dangerous Is Incorrect product storage From LANTUS SOLOSTAR?
Of the 167 reports, 10 (6.0%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LANTUS SOLOSTAR. However, 167 reports have been filed with the FAERS database.
What Other Side Effects Does LANTUS SOLOSTAR Cause?
Blood glucose increased (555)
Visual impairment (229)
Injection site pain (177)
Drug dose omission (169)
Malaise (129)
Blood glucose decreased (124)
Visual acuity reduced (107)
Injection site haemorrhage (106)
Injury associated with device (99)
Feeling abnormal (79)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which LANTUS SOLOSTAR Alternatives Have Lower Incorrect product storage Risk?
LANTUS SOLOSTAR vs LAPATINIB
LANTUS SOLOSTAR vs LAPATINIB DITOSYLATE
LANTUS SOLOSTAR vs LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN
LANTUS SOLOSTAR vs LARONIDASE
LANTUS SOLOSTAR vs LAROTRECTINIB