Effectiveness, persistence of use, and safety of orlistat and liraglutide in a group of patients with obesity

Expert Opin Pharmacother. 2023 Mar;24(4):535-543. doi: 10.1080/14656566.2023.2178900. Epub 2023 Feb 15.

Abstract

Background: To determine the effectiveness, persistence of use, adverse reactions, interactions of orlistat and liraglutide taken for weight loss by a group of obese patients in Colombia.

Research design and methods: A retrospective follow-up study of a cohort of patients with obesity treated with orlistat or liraglutide. Sociodemographic, clinical, and pharmacological variables were identified. The effectiveness for weight loss at 12-16 and 52 weeks, persistence of use, and safety were determined.

Results: A total of 294 patients were followed up. At 12-16 weeks after starting orlistat and liraglutide, weight losses of -1.2kg (p=0.002) and -4.1kg (p<0.001) were observed, respectively, and at 52 weeks, reductions of -1.6kg (p=0.208) and -7.8kg (p<0.001) were observed. A total of 8.8% and 31.3% of patients treated with orlistat and liraglutide, respectively, persisted with treatment 1 year after initiation. A total of 17.3% had adverse drug reactions. Older adults with grade II or III obesity who performed physical activity and those treated with liraglutide were more likely to have lost at least 5% of their body weight at 12-16 weeks.

Conclusion: Orlistat and liraglutide users presented weight loss at 12-16 weeks. However, this effect was greater and sustained with liraglutide, especially when combined with physical activity.

Keywords: (MeSH): liraglutide; obesity; orlistat; pharmacoepidemiology; pharmacovigilance; weight loss.

MeSH terms

  • Aged
  • Anti-Obesity Agents* / adverse effects
  • Follow-Up Studies
  • Humans
  • Lactones / adverse effects
  • Liraglutide* / adverse effects
  • Obesity / drug therapy
  • Orlistat / adverse effects
  • Retrospective Studies
  • Weight Loss

Substances

  • Orlistat
  • Liraglutide
  • Anti-Obesity Agents
  • Lactones