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Study · Observational study · 2014

2 results

A prospective, claims-based assessment of the risk of pancreatitis and pancreatic cancer with liraglutide compared to other antidiabetic drugs.

Funch D, Gydesen H, Tornøe K, Major-Pedersen A, Chan KA

Diabetes, obesity & metabolism26 Nov 2013Cited by 64 (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-ND. 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 US adults with diabetes in a claims database, acute pancreatitis incidence with liraglutide (187.5 per 100,000 person-years) did not differ significantly from non-GLP-1-based therapies (154.4; adjusted RR 1.10).

    In plain wordsIn US insurance data, people using liraglutide did not have a clearly higher rate of acute pancreatitis than people using other non-GLP-1 diabetes drugs.

    Outcome
    No significant changeAcute pancreatitis
    Study

    n: not reported in source

    Comparator
    All non-GLP-1-based therapies
    Outcome group
    Adverse events · Gastrointestinal
    Studied dose
    Dose not stated

    Measurements

    Incidence rate
    187.5 per 100 000 person-years
    liraglutide
    Incidence rate
    154.4 per 100 000 person-years
    non-GLP-1-based therapies
    Adjusted rate ratio
    1.1
    95% CI 0.81-1.49

    Source sentences

    Summary
    The IR for acute pancreatitis for liraglutide was 187.5 compared with 154.4 for all non-glucagon-like peptide-1 (GLP-1)-based therapies (adjusted RR 1.10; CI 0.81-1.49).
    1 context sentence
    Summary · context
    Initiators of liraglutide, exenatide, metformin, pioglitazone or groups containing initiators of dipeptidyl peptidase-4 inhibitors or sulfonylureas were identified in a US commercial health insurance claims database (1 February 2010 to 31 March 2013) and followed for a median of 15 months.
  2. 02HumanObservational studySafety outcome

    In US adults with diabetes in a claims database, pancreatic cancer incidence with liraglutide (19.9 per 100,000 person-years) did not differ significantly from non-GLP-1-based therapies (33.0; adjusted RR 0.65).

    In plain wordsIn US insurance data, people using liraglutide did not have a clearly different rate of pancreatic cancer than people using other non-GLP-1 diabetes drugs.

    Outcome
    No significant changePancreatic cancer
    Study

    n: not reported in source

    Comparator
    All non-GLP-1-based therapies
    Outcome group
    Adverse events · Cancer
    Studied dose
    Dose not stated

    Measurements

    Incidence rate
    19.9 per 100 000 person-years
    liraglutide
    Incidence rate
    33 per 100 000 person-years
    non-GLP-1-based therapies
    Adjusted rate ratio
    0.65
    95% CI 0.26-1.60

    Source sentences

    Summary
    The IR for pancreatic cancer was 19.9 for liraglutide compared with 33.0 for all non-GLP-1-based therapies (adjusted RR 0.65; 95% CI 0.26-1.60).
    1 context sentence
    Summary · context
    Initiators of liraglutide, exenatide, metformin, pioglitazone or groups containing initiators of dipeptidyl peptidase-4 inhibitors or sulfonylureas were identified in a US commercial health insurance claims database (1 February 2010 to 31 March 2013) and followed for a median of 15 months.

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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 2Current

    12 Oct 2026, 12:10 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:05 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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