Does ALBIGLUTIDE Cause Wrong technique in device usage process? 929 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 929 reports of Wrong technique in device usage process have been filed in association with ALBIGLUTIDE. This represents 10.8% of all adverse event reports for ALBIGLUTIDE.
929
Reports of Wrong technique in device usage process with ALBIGLUTIDE
10.8%
of all ALBIGLUTIDE reports
0
Deaths
7
Hospitalizations
How Dangerous Is Wrong technique in device usage process From ALBIGLUTIDE?
Of the 929 reports, 7 (0.8%) required hospitalization.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBIGLUTIDE. However, 929 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)
Product preparation error (691)
Underdose (663)
Wrong technique in product usage process (527)
Nausea (441)
Blood glucose increased (333)
What Other Drugs Cause Wrong technique in device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which ALBIGLUTIDE Alternatives Have Lower Wrong technique in device usage process Risk?
ALBIGLUTIDE vs ALBUMIN
ALBIGLUTIDE vs ALBUMIN HUMAN
ALBIGLUTIDE vs ALBUTEROL
ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE
ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM