GLP-1 Receptor Agonist
Semaglutide is the compound that went mainstream. Sold as Ozempic (for type 2 diabetes), Wegovy (for obesity), and Rybelsus (oral tablet). Compounded semaglutide is the same molecule sourced from compounding pharmacies, typically as a lyophilized powder you reconstitute with bacteriostatic water. It mimics GLP-1, a gut hormone that tells your brain you're full and slows your stomach down. The result is dramatically reduced appetite without the white-knuckle willpower of traditional dieting. People describe it as food noise just stopping. The trade-off is real GI side effects, especially when you increase the dose too fast. Slow and steady wins here. Rushing the titration is the number one mistake people make.
Dose: 0.25mg-2.4mg per week (titrated up) | Frequency: Once weekly | Cycle: Ongoing (not cycled) | Route: SubQ
Reconstitution: 2mL bacteriostatic water per 5mg vial for compounded versions. Free reconstitution calculator.
Start at 0.25mg for 4 weeks, then 0.5mg for 4 weeks, and keep titrating up. Do not rush this. Your GI system needs time to adjust. Same day each week, any time of day.
| Condition | Dose | Duration | Notes |
|---|---|---|---|
| Weight loss (primary indication) | 0.25mg to 2.4mg weekly, titrated | Ongoing, minimum 16 weeks for meaningful results | Start at 0.25mg. Hold 4 weeks. Increase to 0.5mg, hold 4 weeks. Continue: 1mg, 1.7mg, 2.4mg. Most people find their effective dose between 1-1.7mg. The 2.4mg dose showed 15% average weight loss in STEP trials. Don't skip the low doses even if you feel nothing. Your gut needs the ramp. |
| Type 2 diabetes management | 0.25mg to 1mg weekly (Ozempic dosing) | Ongoing | FDA-approved as Ozempic for this indication. A1C reductions of 1.5-1.8% in SUSTAIN trials. If you're on insulin or sulfonylureas, your prescriber needs to adjust those down. Low blood sugar risk is real when combining diabetes meds. |
| Cardiovascular risk reduction | 2.4mg weekly | Ongoing | The SELECT trial (2023) showed a 20% reduction in major cardiovascular events in obese non-diabetics. This is the first GLP-1 with proven heart benefit independent of diabetes. The cardiovascular data is what moved semaglutide from a weight loss drug to a metabolic medicine. |
| Metabolic syndrome and insulin resistance | 0.5mg to 1mg weekly | Ongoing | Lower doses work for metabolic improvement without aggressive weight loss. Fasting glucose, triglycerides, blood pressure all improve. Some people stay at 0.5-1mg long-term for metabolic benefits without needing the higher obesity doses. |
Compounded semaglutide is the same active molecule as Ozempic and Wegovy, prepared by compounding pharmacies instead of Novo Nordisk. It typically comes as a lyophilized powder (you reconstitute with bacteriostatic water) or a pre-mixed liquid vial. The molecular structure is identical. The difference is manufacturing oversight: branded versions are FDA-inspected, compounded versions are regulated by state pharmacy boards. Compounded semaglutide became widely available during the FDA-declared shortage of Ozempic/Wegovy and is significantly cheaper.
Start at 0.25mg once weekly for 4 weeks. Increase to 0.5mg for 4 weeks. Then 1mg for 4 weeks. Then 1.7mg for 4 weeks. Maximum maintenance dose is 2.4mg weekly. This is the Wegovy titration schedule. The entire ramp takes 16-20 weeks. For compounded semaglutide from a vial, you need to convert mg to syringe units based on your vial concentration. A 5mg vial reconstituted with 2mL gives 2.5mg/mL. For a 0.25mg dose, draw 10 units on a U-100 insulin syringe.
Nausea (44%), diarrhea (30%), constipation (24%), vomiting (24%), and fatigue (11%). GI side effects are worst during dose increases and usually settle within 1-2 weeks at each level. Smaller, slower meals help. Serious but rare risks include pancreatitis, gallbladder disease, and a boxed warning for a rare thyroid cancer (showed up in rats, hasn't been confirmed in humans, but it's serious enough to earn a boxed warning). The compounded-specific risk is dosing error. Pen users have fixed doses. Vial users calculate their own. Getting the unit conversion wrong is the most common compounded-specific issue.
Semaglutide mimics GLP-1, a hormone your gut releases after eating. GLP-1 tells your brain you're full, slows down how fast your stomach empties (food sits in there longer, so you feel full longer), and increases insulin secretion. The synthetic version has a much longer half-life (about 7 days vs minutes for natural GLP-1), which is why you only inject once a week. The appetite suppression is the primary driver of weight loss. You eat less because your brain genuinely isn't hungry, not because you're white-knuckling it.
For a 5mg lyophilized vial: add 2mL of bacteriostatic water. That gives you 2.5mg per mL. For a 0.25mg dose, draw 10 units on a U-100 insulin syringe. For 0.5mg, draw 20 units. For 1mg, draw 40 units. Aim the water at the glass wall, not directly onto the powder. Swirl gently. Never shake. If your compounded semaglutide comes pre-mixed, check the concentration on the label and use our calculator to determine the correct units.
In the STEP 1 trial, participants lost an average of 14.9% of body weight at the 2.4mg dose over 68 weeks. That's roughly 33 pounds for someone starting at 220 lbs. About a third of participants lost 20% or more. Real-world results vary with diet, exercise, starting weight, and dose reached. Weight regain after stopping is common. The STEP 1 extension showed participants regained about two-thirds of their lost weight within a year of stopping.
Same molecule, three products. Ozempic is semaglutide injection approved for type 2 diabetes (max 2mg/week). Wegovy is semaglutide injection approved for obesity (max 2.4mg/week). Rybelsus is oral semaglutide for diabetes (daily pill, 14mg max). Ozempic is widely prescribed off-label for weight loss. Compounded semaglutide is the same molecule from a compounding pharmacy, usually at a fraction of the branded price.
The longest published trial data is 2 years (STEP 5). The SELECT cardiovascular trial ran 3+ years. No new safety signals emerged with longer use. The cardiovascular data is actually positive. 20% reduction in major cardiac events in obese non-diabetics. The main long-term concerns are muscle loss (eat enough protein), gallbladder issues (risk increases with rapid weight loss), and the theoretical thyroid risk from the rodent data. For compounded versions, the molecular safety is the same. The variable is manufacturing quality. Verify your compounding pharmacy is accredited.
Often run with: Tirzepatide, Tesamorelin.
Strong evidence. The most studied weight-loss compound on the planet. Multiple Phase 3 trials, FDA-approved as both Ozempic (diabetes) and Wegovy (obesity). Average weight loss of ~15% body weight in the STEP trials. The SELECT trial showed cardiovascular benefit in non-diabetics. The science is settled. This works.
Approval status: FDA-approved (branded)
These statements have not been evaluated by the FDA. This content is for educational purposes only. Consult a healthcare professional before starting any protocol. vialprep sells injection supplies, not compounds.