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Study · Observational study · 2023

2 results

Assessing adverse drug reaction reports for antidiabetic medications approved by the food and drug administration between 2012 and 2017: a pharmacovigilance study.

Stottlemyer BA, McDermott MC, Minogue MR, Gray MP, Boyce RD, Kane-Gill SL

Therapeutic advances in drug safety12 Jun 2023Cited by 22 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: CC BY-NC. Results still quote short attributed sentences.

Results from this study2

2 results from studies that gave the peptide. 2 results from people.

  1. 01HumanObservational studySafety outcome

    In FAERS reports, dulaglutide was associated with greater reporting of gastrointestinal adverse reactions than other approved drugs in its class.

    In plain wordsIn safety reports, dulaglutide was linked to more gastrointestinal reaction reports than other drugs in its class.

    Outcome
    IncreaseGastrointestinal adverse reaction reporting
    Study

    n: not reported in source

    Comparator
    Other approved drugs in the therapeutic class
    Outcome group
    Gastrointestinal adverse events · Gastrointestinal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Assessing glucagon-like peptide-1 (GLP-1) receptor agonists, dulaglutide and semaglutide were associated with greater reports of gastrointestinal adverse drug reactions.
    2 context sentences
    Summary · context
    A disproportionality analysis of spontaneously reported ADRs was conducted.
    Summary · context
    Reporting odds ratios were calculated for the top 10 ADRs, comparing new diabetic agents to the other approved drugs in their therapeutic class.
  2. 02HumanObservational studySafety outcome

    In FAERS reports, semaglutide was associated with greater reporting of gastrointestinal adverse reactions than other approved drugs in its class.

    In plain wordsIn safety reports, semaglutide was linked to more gastrointestinal reaction reports than other drugs in its class.

    Outcome
    IncreaseGastrointestinal adverse reaction reporting
    Study

    n: not reported in source

    Comparator
    Other approved drugs in the therapeutic class
    Outcome group
    Gastrointestinal adverse events · Gastrointestinal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Assessing glucagon-like peptide-1 (GLP-1) receptor agonists, dulaglutide and semaglutide were associated with greater reports of gastrointestinal adverse drug reactions.
    2 context sentences
    Summary · context
    A disproportionality analysis of spontaneously reported ADRs was conducted.
    Summary · context
    Reporting odds ratios were calculated for the top 10 ADRs, comparing new diabetic agents to the other approved drugs in their therapeutic class.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 3Current

    22 Oct 2026, 02:25 UTC

    Study results updated

  2. Version 2

    21 Oct 2026, 18:59 UTC

    Study data updated · source update from Europe PMC

  3. Version 1

    9 Oct 2026, 03:06 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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