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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ALBIGLUTIDE Cause Product quality issue? 1,004 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,004 reports of Product quality issue have been filed in association with ALBIGLUTIDE. This represents 11.6% of all adverse event reports for ALBIGLUTIDE.

1,004
Reports of Product quality issue with ALBIGLUTIDE
11.6%
of all ALBIGLUTIDE reports
0
Deaths
6
Hospitalizations

How Dangerous Is Product quality issue From ALBIGLUTIDE?

Of the 1,004 reports, 6 (0.6%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALBIGLUTIDE. However, 1,004 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) 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 Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which ALBIGLUTIDE Alternatives Have Lower Product quality issue Risk?

ALBIGLUTIDE vs ALBUMIN ALBIGLUTIDE vs ALBUMIN HUMAN ALBIGLUTIDE vs ALBUTEROL ALBIGLUTIDE vs ALBUTEROL\BUDESONIDE ALBIGLUTIDE vs ALBUTEROL\IPRATROPIUM

Related Pages

ALBIGLUTIDE Full Profile All Product quality issue Reports All Drugs Causing Product quality issue ALBIGLUTIDE Demographics