Does ALBIGLUTIDE Cause Incorrect product storage? 100 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Incorrect product storage have been filed in association with ALBIGLUTIDE. This represents 1.2% of all adverse event reports for ALBIGLUTIDE.
100
Reports of Incorrect product storage with ALBIGLUTIDE
1.2%
of all ALBIGLUTIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product storage From ALBIGLUTIDE?
Of the 100 reports, 2 (2.0%) 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 ALBIGLUTIDE. However, 100 reports have been filed with the FAERS database.
What Other Side Effects Does ALBIGLUTIDE Cause?
Device use error (4,056)
Drug dose omission (1,270)
Device leakage (1,195)
Accidental exposure to product (1,182)
Product quality issue (1,004)
Wrong technique in device usage process (929)
Product preparation error (691)
Underdose (663)
Wrong technique in product usage process (527)
Nausea (441)
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 ALBIGLUTIDE Alternatives Have Lower Incorrect product storage Risk?
ALBIGLUTIDE vs ALBUMIN
ALBIGLUTIDE vs ALBUMIN HUMAN
ALBIGLUTIDE vs ALBUTEROL
ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE
ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM