Millions shed pounds on Ozempic and Mounjaro, only to watch them return faster than ever after stopping—exposing a harsh truth about these blockbuster drugs.

Story Snapshot

  • BMJ review of 37 studies shows GLP-1 drugs like semaglutide cause rapid weight regain at 0.4 kg per month post-discontinuation, four times faster than diet alone.
  • Cardiometabolic benefits reverse in 1.4-1.7 years, risking diabetes and heart disease rebound.
  • Average treatment lasts 39 weeks; follow-up reveals real-world limitations beyond clinical trials.
  • Researchers urge combining drugs with lifestyle changes for sustainable obesity control.

BMJ Review Reveals Post-Discontinuation Realities

A systematic review by BMJ Group examined 37 studies with 9,341 participants using GLP-1 receptor agonists such as semaglutide in Ozempic and Wegovy, and tirzepatide in Mounjaro and Zepbound. These drugs delivered initial weight loss of 10-17%. Discontinuation triggered regain at 0.4 kg per month. This rate exceeded lifestyle interventions by nearly four times. Researchers applied three analytical methods to project outcomes despite data limits.

GLP-1 Drugs Evolve from Diabetes to Weight Loss Mainstay

Semaglutide started as a type 2 diabetes treatment, suppressing appetite and slowing gastric emptying to control blood sugar. Post-2021 STEP trials showed 17.3% average weight loss after one year, sparking off-label use. Tirzepatide gained approvals from 2023-2025 with dual GLP-1/GIP action for enhanced results. Real-world persistence dropped to 33% at 12 months for Ozempic and 70% at 24 months overall, driven by plateaus, side effects, and costs. Metabolic adaptations reduced energy expenditure, fueling regain.

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Stakeholders Navigate High Stakes and Power Shifts

Novo Nordisk dominates with Ozempic and Wegovy, generating over $20 billion annually while expanding indications. Eli Lilly competes via tirzepatide’s superior profile amid patent disputes and supply battles. BMJ researchers provide evidence-based caution, influencing guidelines. Patients in studies and online reviews prioritized efficacy despite 62% gastrointestinal side effects. FDA regulators weigh approvals against long-term data gaps. Pharma funds R&D, but academics and patients shape narratives through real-world insights.

Recent Developments Underscore Sustainability Challenges

The BMJ review released January 29, 2026, after compiling studies through February 2025. Average treatment ran 39 weeks with 32 weeks post-stop follow-up, maxing at 12 months. Only eight GLP-1 studies exceeded one year. Researchers stated drugs alone fail long-term; prevention and combinations work better. Infoveillance from 60 reviews confirmed plateaus after one year. Ongoing trials like NCT06751589 test tirzepatide and semaglutide feasibility.

Impacts Reshape Patient Outcomes and Policy

Short-term, patients achieved satisfaction ratings of 7.5-8.5 with rapid 10-17% loss, tolerating common GI issues. Long-term, full regain hits in 1.7 years; health markers revert in 1.4 years. Obese individuals risk yo-yo cycling; low-income groups face cost barriers. Pharma gains revenue from continuous use, but savings from initial loss fade with regain treatments. Narrative shifts from miracle cures to adjunct tools, spurring prevention policies and combo trials grounded in common-sense lifestyle integration.

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Sources:

JMIR infoveillance on Ozempic perceptions
BMJ systematic review on GLP-1 agonists
PubMed abstract on related GLP-1 study
Ozempic and weight loss in 2026 real people insights
MSU expert on Ozempic craze
NAM on understanding GLP-1 drugs
ClinicalTrials.gov NCT06751589

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