Does ALBIGLUTIDE Cause Device leakage? 1,195 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,195 reports of Device leakage have been filed in association with ALBIGLUTIDE. This represents 13.8% of all adverse event reports for ALBIGLUTIDE.
1,195
Reports of Device leakage with ALBIGLUTIDE
13.8%
of all ALBIGLUTIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device leakage From ALBIGLUTIDE?
Of the 1,195 reports, 3 (0.3%) required hospitalization.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBIGLUTIDE. However, 1,195 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)
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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
ABATACEPT (671)
Which ALBIGLUTIDE Alternatives Have Lower Device leakage Risk?
ALBIGLUTIDE vs ALBUMIN
ALBIGLUTIDE vs ALBUMIN HUMAN
ALBIGLUTIDE vs ALBUTEROL
ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE
ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM