Drug Safety

, Volume 32, Issue 5, pp 409–418 | Cite as

Hypoglycaemia with Oral Antidiabetic Drugs

Results from Prescription-Event Monitoring Cohorts of Rosiglitazone, Pioglitazone, Nateglinide and Repaglinide
  • Veronika Vlckova
  • Victoria Cornelius
  • Rachna Kasliwal
  • Lynda Wilton
  • Saad A. W. Shakir
Original Research Article


Background: Hypoglycaemia is an acute complication associated with intensive treatment of patients with diabetes mellitus. This complication poses a major challenge in diabetes management. Furthermore, severe hypoglycaemia may be life threatening. Although hypoglycaemia is more often associated with insulin treatment, oral hypoglycaemic agents have the potential to trigger hypoglycaemia.

Aim: The aim of this study was to quantify the incidence of hypoglycaemic events and to describe the pattern of these incident events during the first 9 months of treatment with four oral antidiabetic drugs, rosiglitazone, pioglitazone, nateglinide and repaglinide, prescribed in general practice in England.

Methods: We used data collected for prescription-event monitoring (PEM) studies of rosiglitazone, pioglitazone, nateglinide and repaglinide. PEM is an observational, non-interventional, incept cohort study. Observation time for each patient and incidence rate (IR) per 1000 patient-years of treatment for hypoglycaemia was calculated for each drug cohort. Smoothed hazard estimates were plotted over time. Case/non-case analysis was performed to describe and compare patients who had at least one hypoglycaemic event in the first 9 months of treatment with those who did not.

Results: The total number of patients included in the analysis was 14373, 12768, 4549 and 5727 in rosiglitazone, pioglitazone, nateglinide and repaglinide cohorts, respectively. From these, 276 patients experienced at least one episode of hypoglycaemia. The IR was between 50% and 100% higher in patients receiving treatment with meglitinides compared with those treated with the thiazolidinediones (TZDs) [IR = 9.94, 9.64, 15.71 and 20.32 per 1000 patient-years for rosiglitazone, pioglitazone, nateglinide and repaglinide, respectively]. The plot of the hazard function and the estimated shape parameter from the Weibull regression model showed that pioglitazone, nateglinide and repaglinide had non-constant (decreasing) hazards over time, whereas the hazard for rosiglitazone-treated patients was approximately constant over time. Nateglinide and repaglinide had similar shape hazard function, indicating a significantly higher number of hypoglycaemic episodes shortly after starting treatment. For women treated with TZDs, hypoglycaemia was reported more frequently than for men.

Conclusion: This analysis shows that the frequency of reported hypoglycaemia within the study cohorts was relatively low. The rates of hypoglycaemia were not equal between drug classes. Treatment with nateglinide or repaglinide was characterized by a higher incidence of hypoglycaemia at the beginning of treatment. Further investigation is necessary to assess whether women treated with TZDs are more prone to hypoglycaemia than men. Findings from this study should be taken into account with other clinical and pharmacoepidemiological studies.


Rosiglitazone Pioglitazone Repaglinide Nateglinide Hypoglycaemic Event 
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We are grateful to all the staff at the DSRU who contributed to this study, particularly Mr Shayne Freemantle, Mrs Neera Soor for data management and information technology support and Mrs Lesley Flowers for her assistance in the preparation of this study. The DSRU is an independent, registered medical charity (No. 327206) associated with the University of Portsmouth, Portsmouth, UK.

The DSRU receives unconditional donations from pharmaceutical companies for the conduct of studies. The companies have no control on the conduct or the publication of such studies. No external funding was received for this study but the manufacturers of the products included have made previous donations.

Veronika Vlckova, Victoria Cornelius, Rachna Kasliwal and Lynda Wilton have no conflicts of interest to declare that are directly relevant to the content of this study. Saad Shakir was an employee of Glaxo Wellcome more than 10 years previously and has received remuneration for consultancy work and lecturing from Takeda Pharmaceutical Company Ltd.


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Copyright information

© Adis Data Information BV 2009

Authors and Affiliations

  • Veronika Vlckova
    • 1
    • 3
  • Victoria Cornelius
    • 1
    • 2
  • Rachna Kasliwal
    • 1
    • 2
  • Lynda Wilton
    • 1
    • 2
  • Saad A. W. Shakir
    • 1
    • 2
  1. 1.Drug Safety Research UnitSouthamptonUK
  2. 2.University of PortsmouthPortsmouthUK
  3. 3.Department of Social and Clinical PharmacyCharles University in Prague, Faculty of PharmacyHradec KraloveCzech Republic

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