What are the doses of Ozempic (semaglutide)?

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Last updated: October 9, 2025View editorial policy

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Ozempic (Semaglutide) Dosing Guidelines

Ozempic (semaglutide) subcutaneous injection is administered once weekly with a standard dosing schedule of 0.25 mg initially for 4 weeks, then increased to 0.5 mg, with further titration to 1 mg or 2 mg as needed for glycemic control. 1

Standard Dosing Schedule

  • Initial dose: 0.25 mg subcutaneously once weekly for 4 weeks (this is a titration dose, not intended for glycemic control) 2
  • Maintenance dose: 0.5 mg subcutaneously once weekly after the initial 4 weeks 1
  • Dose escalation: If additional glycemic control is required after at least 4 weeks on the 0.5 mg dose, the dose can be increased to 1 mg once weekly 1
  • Higher dose option: For patients requiring additional glycemic control, a 2 mg once weekly dose is available (after at least 4 weeks on the 1 mg dose) 3

Administration Guidelines

  • Ozempic can be administered at any time of day, with or without meals 1, 2
  • The injection should be given on the same day each week 2
  • If a dose is missed, it should be administered as soon as possible within 5 days after the missed dose. If more than 5 days have passed, skip the missed dose and administer the next dose on the regularly scheduled day 2
  • Ozempic is administered subcutaneously in the abdomen, thigh, or upper arm 2

Special Populations

  • Renal Impairment: No dosage adjustment is required for patients with renal impairment, including those with end-stage renal disease 1
  • Hepatic Impairment: Limited experience in patients with severe hepatic impairment; use with caution 1
  • Elderly: No specific dose adjustment is required based on age 1

Weight Management Dosing

  • For weight management in patients with obesity (BMI ≥30 kg/m²) or overweight (BMI ≥27 kg/m²) with at least one weight-related comorbidity, the target dose is 2.4 mg once weekly 1
  • In clinical trials, higher doses of semaglutide (7.2 mg) have shown greater weight reduction in patients with obesity and type 2 diabetes, but this dose is not yet FDA-approved 4

Practical Considerations

  • Gradual dose titration is essential to minimize gastrointestinal adverse effects 5
  • Each pen delivers multiple doses: the 0.25 mg or 0.5 mg pen contains 2 mg of semaglutide total, while the 1 mg pen contains 4 mg of semaglutide total 2
  • Store unused pens in the refrigerator between 36°F to 46°F (2°C to 8°C) 2
  • After first use, the pen can be stored at room temperature between 59°F to 86°F (15°C to 30°C) or in a refrigerator for up to 56 days 2

Common Side Effects and Management

  • Gastrointestinal effects are the most common adverse events, including nausea (20-24%), diarrhea (11-13%), and vomiting 6
  • These side effects are typically transient and can be minimized with gradual dose titration 7
  • The risk of hypoglycemia is low when used as monotherapy but increases when combined with insulin secretagogues (e.g., sulfonylureas) 7, 3

Clinical Efficacy

  • In clinical trials, semaglutide 0.5 mg and 1.0 mg reduced HbA1c by 1.2% and 1.6%, respectively, compared to 0.8% with insulin glargine 7
  • Weight reduction of 3.5 kg with 0.5 mg and 5.2 kg with 1.0 mg semaglutide has been observed, compared to weight gain with insulin glargine 7
  • Semaglutide 2.0 mg provides additional HbA1c reduction (-0.2%) compared to the 1.0 mg dose in patients with inadequate glycemic control 3

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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