Does ALBIGLUTIDE Cause Product preparation error? 691 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 691 reports of Product preparation error have been filed in association with ALBIGLUTIDE. This represents 8.0% of all adverse event reports for ALBIGLUTIDE.
691
Reports of Product preparation error with ALBIGLUTIDE
8.0%
of all ALBIGLUTIDE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product preparation error From ALBIGLUTIDE?
Of the 691 reports, 4 (0.6%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBIGLUTIDE. However, 691 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)
Underdose (663)
Wrong technique in product usage process (527)
Nausea (441)
Blood glucose increased (333)
What Other Drugs Cause Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
SODIUM OXYBATE (222)
Which ALBIGLUTIDE Alternatives Have Lower Product preparation error Risk?
ALBIGLUTIDE vs ALBUMIN
ALBIGLUTIDE vs ALBUMIN HUMAN
ALBIGLUTIDE vs ALBUTEROL
ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE
ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM