Does APIDRA SOLOSTAR Cause Incorrect product storage? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Incorrect product storage have been filed in association with APIDRA SOLOSTAR. This represents 6.8% of all adverse event reports for APIDRA SOLOSTAR.
9
Reports of Incorrect product storage with APIDRA SOLOSTAR
6.8%
of all APIDRA SOLOSTAR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From APIDRA SOLOSTAR?
Of the 9 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APIDRA SOLOSTAR. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does APIDRA SOLOSTAR Cause?
Blood glucose increased (33)
Visual impairment (11)
Malaise (9)
Blood glucose decreased (8)
Feeling abnormal (8)
Wrong drug administered (8)
Dyspnoea (7)
Drug dose omission (6)
Drug administration error (5)
Drug ineffective (5)
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 APIDRA SOLOSTAR Alternatives Have Lower Incorrect product storage Risk?
APIDRA SOLOSTAR vs APIXABAN
APIDRA SOLOSTAR vs APOMORPHINE
APIDRA SOLOSTAR vs APRACLONIDINE
APIDRA SOLOSTAR vs APREMILAST
APIDRA SOLOSTAR vs APREPITANT