Ozempic (Semaglutide) Dosing
For type 2 diabetes, start Ozempic at 0.25 mg subcutaneously once weekly for 4 weeks, then increase to 0.5 mg weekly (standard maintenance dose), with optional escalation to 1 mg weekly after at least 4 weeks if additional glycemic control is needed, and a maximum dose of 2 mg weekly for diabetes management. 1, 2, 3
Standard Dosing Protocol for Type 2 Diabetes
Initiation Phase:
- Week 1-4: 0.25 mg subcutaneously once weekly 1, 2, 3
- This low starting dose minimizes gastrointestinal side effects 1, 2
Maintenance Dosing:
- Week 5 onward: Increase to 0.5 mg once weekly 1, 2, 3
- This is the standard maintenance dose for most patients 2
Dose Escalation (if needed for glycemic control):
- After ≥4 weeks at 0.5 mg: May increase to 1.0 mg weekly 1, 2, 3
- After ≥4 weeks at 1.0 mg: May increase to 2.0 mg weekly (maximum approved dose for diabetes) 2, 3
Administration Details
- Inject subcutaneously in the abdomen, thigh, or upper arm 1, 2
- Administer once weekly at any time of day, with or without meals 1, 2
- Inject on the same day each week 1
- Rotate injection sites systematically within one anatomical area to minimize absorption variability 2
Higher Dose for Weight Management
For obesity or overweight with weight-related complications (not the standard Ozempic indication):
- Continue titration beyond 2 mg to reach 2.4 mg weekly over 16-20 weeks 1, 4, 5
- Week 1-4: 0.25 mg weekly 1, 4
- Week 5-8: 0.5 mg weekly 1, 4
- Week 9-12: 1.0 mg weekly 1, 4
- Week 13-16: 1.7 mg weekly 1, 4
- Week 17+: 2.4 mg weekly (maintenance for weight management) 1, 4, 5
Note: The 2.4 mg dose is marketed as Wegovy for weight management, not Ozempic 4, 5
Special Populations
Renal Impairment:
- No dose adjustment required for any degree of renal impairment, including end-stage renal disease 1, 2
Hepatic Impairment:
Elderly Patients:
- No dose adjustment based on age alone 3
Missed Dose Management
- If 1 dose missed: Resume next scheduled dose 4
- If 2 consecutive doses missed: Resume at current dose if previously tolerated well; otherwise consider stepping back to lower dose 4
- If 3+ consecutive doses missed: Restart the titration schedule from 0.25 mg 4
Concomitant Medication Adjustments
When initiating semaglutide:
- Reduce insulin dose by 20% to prevent hypoglycemia 6
- Consider discontinuing or reducing sulfonylurea doses due to hypoglycemia risk 4, 2
- Do NOT combine with other GLP-1 receptor agonists or DPP-4 inhibitors 4, 6
Critical Contraindications
Absolute contraindications:
- Personal or family history of medullary thyroid cancer 1, 4, 2
- Multiple endocrine neoplasia syndrome type 2 (MEN2) 1, 4, 2
- Pregnancy or lactation 2
- History of severe hypersensitivity reaction to semaglutide 2
Expected Clinical Outcomes
Glycemic Control:
Weight Loss:
- Mean weight loss of 3.8-5.5 kg at 56 weeks with 0.5-1.0 mg doses for diabetes 3
- Mean weight loss of 9.6% with 2.4 mg dose for weight management 5, 7
Common Adverse Effects and Mitigation
Gastrointestinal effects (most common):
- Nausea occurs in 18-40% of patients 4, 2
- Diarrhea in 12-13% 4
- Vomiting in 8-16% 4
- These are typically mild-to-moderate and transient 4, 5
Mitigation strategies:
- Gradual dose titration (as outlined above) minimizes GI effects 1, 4, 2
- Reduce meal size and limit alcohol/carbonated beverages 6
- If GI symptoms are severe, maintain current dose for additional 4 weeks before continuing escalation 4
Monitoring Requirements
During titration (first 16-20 weeks):
- Assess every 4 weeks for GI tolerance, weight, blood pressure, and signs of pancreatitis/gallbladder disease 6
After reaching maintenance dose:
- Monitor every 3 months for weight, blood pressure, cardiovascular risk factors, and medication adherence 4, 6
- Check for signs of pancreatitis (persistent severe abdominal pain) and gallbladder disease 4, 2