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GLP-1 dose escalation schedules, four labels side by side

Every one of these labels starts a patient below the dose that does the work, and every one gives a different ladder to climb. The four schedules below are printed as four separate tables, each read from its own label’s dosage section, because they are not variants of one schedule and merging them would be the fastest way to attach a real number to the wrong drug.

Reviewed by Ellis Brandt. Sources checked September 2026.

This guide draws on the cited FDA-approved prescribing information and other FDA sources. It is not medical advice; discuss treatment with your clinician. See the medical disclaimer.

Ozempic (semaglutide) injection

The Ozempic label sets an initiation dosage and then two optional increases, each gated on glycemic control rather than on the calendar alone: “If additional glycemic control is needed after at least 4 weeks” on the current dose.

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Ozempic dosage escalation — label version 20, effective 2026-06-01
StepDosageWhat the label says about moving on
Initiation0.25 mg once weeklyFor 4 weeks. The label calls this an initiation dosage.
After 4 weeks0.5 mg once weeklyA maintenance dosage.
Optional increase1 mg once weeklyAfter at least 4 weeks on 0.5 mg, if additional glycemic control is needed.
Optional increase2 mg once weeklyAfter at least 4 weeks on 1 mg. The maximum recommended dosage is 2 mg once weekly.

The same label sets a separate rule for one population: in patients with type 2 diabetes and chronic kidney disease, increase to the 1 mg maintenance dosage after at least 4 weeks on 0.5 mg.

Wegovy (semaglutide)

Wegovy’s ladder is on the clock rather than on a response, and the label prints it as a table of week ranges. It is also the only one of the four whose label covers two dosage forms, so there are two schedules here and they are not related to each other.

Wegovy injection dosage escalation, 5 steps — label version 19, effective 2026-06-18
  1. Weeks 1 through 4

    0.25 mg once weekly

    Starting dosage

  2. Weeks 5 through 8

    0.5 mg once weekly

    Dosage escalation

  3. Weeks 9 through 12

    1 mg once weekly

    Dosage escalation

  4. Weeks 13 through 16

    1.7 mg once weekly

    Dosage escalation

  5. Week 17 and onward

    1.7 mg or 2.4 mg once weekly, by indication

    Maintenance dosage. The label states “See the indication below for the recommended maintenance dosage(s)” rather than a single figure.

Every step above is from the Wegovy prescribing information, section 2.2, Table 1 — one document. No step is carried across from another label, and no interval is inferred.

Wegovy prescribing information, label version 19, effective 2026-06-18, read September 2026. This is the injection schedule only; the tablet schedule in the same label is below and the two are not related.

For weight reduction in adults the recommended maintenance dosage is 2.4 mg once weekly, with 1.7 mg as the alternative. The label then adds a step above it: for patients who tolerate 2.4 mg for at least 4 weeks and for whom additional weight reduction is clinically indicated, “the dosage may be increased to a maximum dosage of 7.2 mg subcutaneously once weekly.” For cardiovascular risk reduction the maintenance dosage is 2.4 mg or 1.7 mg, and for noncirrhotic MASH with moderate to advanced fibrosis it is 2.4 mg, reducible to 1.7 mg if 2.4 mg is not tolerated.

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Wegovy tablet dosage escalation — label version 19, effective 2026-06-18
DaysOnce-daily tablet dosageStage
1 through 301.5 mgStarting dosage
31 through 604 mgDosage escalation
61 through 909 mgDosage escalation
91 and onward25 mgMaintenance dosage

Mounjaro and Zepbound (tirzepatide)

Both tirzepatide labels start at 2.5 mg once weekly and both move in 2.5 mg increments after at least 4 weeks on the current dose. They differ in where they stop and in what they say about the starting dose.

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Tirzepatide dosage escalation, 2 labels — Mounjaro version 40 effective 2026-08-27, Zepbound version 40 effective 2026-08-28
LabelStarting dosageEscalationMaintenance dosages the label namesMaximum
Mounjaro2.5 mg once weeklyIncrease in 2.5 mg increments after at least 4 weeks on the current dose, if additional glycemic control is neededThe label does not enumerate maintenance dosages separately15 mg once weekly in adults; 10 mg once weekly in patients aged 10 and older
Zepbound2.5 mg once weekly for 4 weeks. The label states that this dosage “is for treatment initiation and is not approved as a maintenance dosage”After 4 weeks increase to 5 mg, then in 2.5 mg increments after at least 4 weeks on the current doseWeight reduction and long-term maintenance: 5 mg, 10 mg or 15 mg. Obstructive sleep apnea: 10 mg or 15 mg15 mg once weekly, for all indications

What the schedules do not cover

The four ladders above describe four FDA-approved products. Some telehealth providers supply compounded semaglutide or compounded tirzepatide instead, and a compounded preparation has no FDA-approved label — so there is no approved escalation schedule to read, no approved strength list, and nothing on this page that describes one. The FDA states plainly that “compounded drugs are not FDA approved” and that “the agency does not review compounded drugs for safety, effectiveness or quality before they are marketed.”

The same FDA page records what has gone wrong when a dose schedule is written outside an approved label: reports of adverse events, “some requiring hospitalization, that may be related to dosing errors associated with compounded injectable semaglutide products”, and further reports involving patients “prescribed compounded semaglutide or tirzepatide products in doses beyond what is in the FDA-approved drug label” — including “increasing the amount more quickly (titration schedule).”

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1 question this page cannot answer from an approved label
QuestionWhy the labels do not answer itStatus here
The escalation schedule for a compounded semaglutide or tirzepatide preparationA compounded drug is not FDA-approved and is not reviewed by the FDA for safety, effectiveness or quality before it is sold, so it has no prescribing information to read.No approved label to read, so nothing to print here.

A reader on a compounded product has the schedule their own prescriber wrote, and it is worth asking that prescriber which approved schedule, if any, it follows. Related: what each label says about a missed dose, and what Zepbound’s own trials reported at each of its three maintenance doses.

Sources

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Sources: 4 FDA-approved labels, read September 2026
LabelApplicant on the labelSPL versionLabel effective dateWhere it was read
Ozempic (semaglutide)Novo Nordisk Pharmaceutical Industries, LP202026-06-01DailyMed, set id adec4fd2-6858-4c99-91d4-531f5f2a2d79
Wegovy (semaglutide)Novo Nordisk Pharmaceutical Industries, LP192026-06-18DailyMed, set id ee06186f-2aa3-4990-a760-757579d8f77b
Mounjaro (tirzepatide)Eli Lilly and Company402026-08-27DailyMed, set id d2d7da5d-ad07-4228-955f-cf7e355c8cc0
Zepbound (tirzepatide)Eli Lilly and Company402026-08-28DailyMed, set id 487cd7e7-434c-4925-99fa-aa80b1cc776b

Every figure and quotation comes from the label’s own tables and text. Each label is the FDA-approved version that was current when it was read in September 2026, identified in the table by its version number and effective date.

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1 FDA page, read September 2026
PagePublisherContent current as ofAddress
FDA’s Concerns with Unapproved GLP-1 Drugs Used for Weight LossU.S. Food and Drug Administration2026-09-01fda.gov

Each page is quoted as the FDA publishes it. The date beside it is the “content current as of” date the agency prints on the page itself.

See the providers

Once you know the schedule, the boards list the providers who sell each drug on it and what each one publishes.

More, read from the same labels

  • First-year GLP-1 costsresearch guide

    A low monthly headline does not tell you what a year of treatment will cost. Compare the same medication and service package, then separate the total you expect to spend from the amount you must pay before treatment begins.

  • Cancellation and refundsresearch guide

    Canceling future membership charges, stopping an upcoming medication order and requesting a refund are three different requests. Get a written answer for each one that applies to you.

  • Insurance denial documentsresearch guide

    The next step depends on why coverage was denied. A missing document, a formulary restriction and an excluded benefit are different problems. Start with the written decision before paying someone to submit another request.

  • Savings and cash-pay eligibilityresearch guide

    A manufacturer savings card and a self-pay offer can have different eligibility rules, even for the same medicine. Match the offer to your coverage and exact product before using its advertised price in your budget.

  • Verify your GLP-1 pharmacyresearch guide

    The website taking your payment, the clinician prescribing and the pharmacy dispensing may be different businesses. Identify each one. A recognizable brand or a reassuring badge does not tell you who will fill the prescription.

  • Changing GLP-1 providersresearch guide

    Before ending your current service, establish what the new practice needs, what it will charge and when it can evaluate you. Transferring your records does not guarantee that another clinician will continue the same prescription.

  • Weight regain after stoppingresearch guide

    Weight regain occurred after treatment withdrawal in studies of semaglutide and tirzepatide. The findings support planning follow-up and affordability before an interruption, but they do not predict exactly what will happen to one person.

  • Semaglutide vs tirzepatideresearch guide

    What the four FDA-approved labels say each molecule is, what each is approved to treat, and where the two differ.

  • How they workresearch guide

    The receptor each molecule switches on, what the labels say that does to appetite, blood sugar and the stomach, and why one dose lasts a week.

  • Is Ozempic insulin?research guide

    What the Ozempic label calls semaglutide, how that differs from insulin, and where insulin appears on these labels as a separate medicine.

  • Zepbound vs Ozempicresearch guide

    Four brand names, two molecules and two kinds of approval: which of these products are the same drug, and what each one is actually approved to do.

  • Side effect ratesresearch guide

    What each label reports for nausea, vomiting, diarrhea and constipation — and the sentence every label prints above those numbers.

  • Hair lossresearch guide

    Which labels report hair loss, the rate against placebo where a trial measured it, and why two of them put no number on it.

  • Fatigue and tirednessresearch guide

    Which labels list fatigue, the rate against placebo where a trial measured it, and what each label counts as fatigue.

  • Missed dose rulesresearch guide

    The window each label gives for a late dose, and the minimum gap it requires when the injection day changes.

  • Drug interactionsresearch guide

    Insulin and sulfonylureas, oral medications, and the oral-contraceptive precaution that appears on two of these four labels and not the other two.

  • Buying one onlineresearch guide

    The agency's own warning signs for a telehealth GLP-1 seller, its 28-day vial rule, and what it says about drugs that arrive warm.

  • Zepbound by doseresearch guide

    What each Zepbound dose achieved in the trials printed in its label, what the label says about choosing a maintenance dose, and what the higher doses cost in side effects.

  • Zepbound at 3 monthsresearch guide

    What does the Zepbound label report about three-month weight loss and maintenance dosing?

  • Injecting tirzepatideresearch guide

    The injection sites, the rotation rule and the steps for the single-dose pen, the KwikPen and the vial and syringe, exactly as the FDA-approved Instructions for Use give them.

  • Refrigeration and storageresearch guide

    How cold each pen is kept, how many days it can spend at room temperature, and what the labels say about heat and freezing.

  • Who should not take oneresearch guide

    The boxed warning every one of these labels carries, the two contraindications, and which warnings appear on which product.

The one thing all four agree on

Each label ties escalation to gastrointestinal tolerance, in almost identical words: follow the escalation “to reduce the risk of gastrointestinal adverse reactions”. The ladder is not a formality; it is the label’s stated mitigation.

Four labels, read September 2026. Versions and effective dates at the foot of this page.

About our comparisons. Our scores measure published information, not medical quality. We do not assign an overall provider rating or rank providers by treatment outcomes.