Does ALBIGLUTIDE Cause Device breakage? 56 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 56 reports of Device breakage have been filed in association with ALBIGLUTIDE. This represents 0.7% of all adverse event reports for ALBIGLUTIDE.
56
Reports of Device breakage with ALBIGLUTIDE
0.7%
of all ALBIGLUTIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device breakage From ALBIGLUTIDE?
Of the 56 reports, 1 (1.8%) required hospitalization.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBIGLUTIDE. However, 56 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 Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which ALBIGLUTIDE Alternatives Have Lower Device breakage Risk?
ALBIGLUTIDE vs ALBUMIN
ALBIGLUTIDE vs ALBUMIN HUMAN
ALBIGLUTIDE vs ALBUTEROL
ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE
ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM