Does LANTUS SOLOSTAR Cause Product quality issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product quality issue have been filed in association with LANTUS SOLOSTAR. This represents 0.4% of all adverse event reports for LANTUS SOLOSTAR.
9
Reports of Product quality issue with LANTUS SOLOSTAR
0.4%
of all LANTUS SOLOSTAR reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From LANTUS SOLOSTAR?
Of the 9 reports, 3 (33.3%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LANTUS SOLOSTAR. However, 9 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)
Incorrect product storage (167)
Malaise (129)
Blood glucose decreased (124)
Visual acuity reduced (107)
Injection site haemorrhage (106)
Injury associated with device (99)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which LANTUS SOLOSTAR Alternatives Have Lower Product quality issue 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