What is the use of Ozempic (semaglutide)?

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Last updated: May 6, 2025View editorial policy

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From the Guidelines

Ozempic (semaglutide) should be initiated at a dose of 0.25 mg subcutaneously once weekly and titrated as needed to achieve glycemic control, with consideration of its benefits in reducing major adverse cardiovascular events and its potential for weight loss, as supported by recent guidelines and studies 1.

Key Considerations for Ozempic Use

  • The medication is primarily used for the treatment of type 2 diabetes but has also been recognized for its potential in weight management.
  • Common side effects include nausea, vomiting, diarrhea, abdominal pain, and constipation, which often improve over time.
  • Patients should inject Ozempic subcutaneously in the abdomen, thigh, or upper arm, rotating injection sites, and it's crucial to take it on the same day each week.
  • Ozempic requires refrigeration before first use but can be stored at room temperature for up to 56 days after opening.

Clinical Guidelines and Evidence

  • Recent studies and guidelines, such as those from 2024, emphasize the importance of considering the use of GLP-1 receptor agonists like semaglutide for their glycemic efficacy and cardiovascular benefits 1.
  • The American Gastroenterological Association suggests using semaglutide 2.4 mg with lifestyle modifications for the long-term treatment of obesity, highlighting its potential beyond diabetes management 1.
  • The choice of medication should be guided by efficacy, side effects, cost, access, and individual preferences, with a focus on minimizing hypoglycemia risk, particularly in individuals with established cardiovascular disease or indicators of high cardiovascular risk.

Important Safety Information

  • Ozempic has been associated with an increased risk of pancreatitis and gallbladder disease, and patients should be monitored for these potential adverse effects.
  • It may delay gastric emptying, leading to nausea and vomiting, which can be mitigated by gradual dose titration.
  • The medication is contraindicated in patients with a history of serious hypersensitivity reaction to the drug, pregnancy, breastfeeding, severe renal impairment, or end-stage renal failure, among other conditions, as outlined in detailed guidelines and studies 1.

From the FDA Drug Label

The FDA drug label does not answer the question.

From the Research

Ozempic (Semaglutide) Overview

  • Ozempic, also known as semaglutide, is a glucagon-like peptide-1 (GLP-1) analogue used for the treatment of type 2 diabetes and obesity.
  • It is administered via subcutaneous injection once a week.

Efficacy in Weight Loss

  • Studies have shown that semaglutide 2.4 mg is associated with significant weight loss in individuals with overweight or obesity, with or without type 2 diabetes 2, 3.
  • In the STEP trials, semaglutide 2.4 mg resulted in mean weight losses of 14.9%-17.4% in individuals with overweight or obesity without type 2 diabetes, and -9.6% in individuals with type 2 diabetes 2, 3.
  • A higher dose of semaglutide (up to 16 mg) has also been shown to provide additional weight loss, although with more adverse events 4.

Efficacy in Glycemic Control

  • Semaglutide has been shown to improve glycemic control in individuals with type 2 diabetes, with significant reductions in HbA1c levels 5, 4, 6.
  • The combination of semaglutide with metformin has been shown to be effective in improving glycemic control and weight loss in individuals with type 2 diabetes and overweight or obesity 6.

Safety Profile

  • The safety profile of semaglutide is generally consistent across trials, with gastrointestinal adverse events being the most commonly reported 2, 5, 3, 4.
  • Higher doses of semaglutide have been associated with more adverse events and treatment discontinuations 4.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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