Does ALBIGLUTIDE Cause Device use error? 4,056 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,056 reports of Device use error have been filed in association with ALBIGLUTIDE. This represents 46.9% of all adverse event reports for ALBIGLUTIDE.
4,056
Reports of Device use error with ALBIGLUTIDE
46.9%
of all ALBIGLUTIDE reports
0
Deaths
18
Hospitalizations
How Dangerous Is Device use error From ALBIGLUTIDE?
Of the 4,056 reports, 18 (0.4%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBIGLUTIDE. However, 4,056 reports have been filed with the FAERS database.
What Other Side Effects Does ALBIGLUTIDE Cause?
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)
Blood glucose increased (333)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
TREPROSTINIL (563)
Which ALBIGLUTIDE Alternatives Have Lower Device use error Risk?
ALBIGLUTIDE vs ALBUMIN
ALBIGLUTIDE vs ALBUMIN HUMAN
ALBIGLUTIDE vs ALBUTEROL
ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE
ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM