Does ALBIGLUTIDE Cause Wrong technique in product usage process? 527 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 527 reports of Wrong technique in product usage process have been filed in association with ALBIGLUTIDE. This represents 6.1% of all adverse event reports for ALBIGLUTIDE.
527
Reports of Wrong technique in product usage process with ALBIGLUTIDE
6.1%
of all ALBIGLUTIDE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ALBIGLUTIDE?
Of the 527 reports, 5 (0.9%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBIGLUTIDE. However, 527 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)
Nausea (441)
Blood glucose increased (333)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ALBIGLUTIDE Alternatives Have Lower Wrong technique in product usage process Risk?
ALBIGLUTIDE vs ALBUMIN
ALBIGLUTIDE vs ALBUMIN HUMAN
ALBIGLUTIDE vs ALBUTEROL
ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE
ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM