Short answer: Per the FDA label (2.1, 2.2), Zepbound starts at 2.5 mg once weekly for 4 weeks, then 5 mg. The dose may rise in 2.5 mg steps after at least 4 weeks on the current dose. Weight-management maintenance is 5, 10 or 15 mg weekly; OSA maintenance is 10 or 15 mg; the maximum is 15 mg.
Per label section 1, Zepbound is a GIP and GLP-1 receptor agonist indicated, with a reduced-calorie diet and increased physical activity, to reduce excess body weight and maintain weight reduction long term in adults with obesity, or with overweight plus at least one weight-related condition, and to treat moderate to severe obstructive sleep apnea (OSA) in adults with obesity. This page summarizes the current FDA prescribing information (revised 8/2026). It is not personalized medical advice; your prescriber sets your dose.
The label's dosing schedule (label section 2.1; 2.2):
| Period | Dose | Label note |
|---|---|---|
| Weeks 1–4 | 2.5 mg once weekly | Initiation dose; the label says 2.5 mg is not approved as a maintenance dosage |
| Weeks 5–8 | 5 mg once weekly | Lowest weight-management maintenance dose |
| Weeks 9–12 | 7.5 mg once weekly | Escalation step (+2.5 mg after at least 4 weeks); not listed as a maintenance dose |
| Weeks 13–16 | 10 mg once weekly | Maintenance dose option |
| Weeks 17–20 | 12.5 mg once weekly | Escalation step; not listed as a maintenance dose |
| Week 21 onward | 15 mg once weekly | Maximum dosage for all indications |
Maintenance: For weight reduction and long-term maintenance, the label lists 5 mg, 10 mg or 15 mg once weekly as maintenance dosages, chosen with treatment response and tolerability in mind. The maximum dosage for all indications is 15 mg once weekly (2.2).
Below is the label schedule laid out week by week, using the earliest timing the label allows. The label lets prescribers stay at a step longer, so a real calendar is often slower. The blank columns are for your own record.
| Week | Label dose | Date | Site / time | Weight | Notes |
|---|---|---|---|---|---|
| Week 1 | 2.5 mg once weekly | ||||
| Week 2 | 2.5 mg once weekly | ||||
| Week 3 | 2.5 mg once weekly | ||||
| Week 4 | 2.5 mg once weekly | ||||
| Week 5 | 5 mg once weekly | ||||
| Week 6 | 5 mg once weekly | ||||
| Week 7 | 5 mg once weekly | ||||
| Week 8 | 5 mg once weekly | ||||
| Week 9 | 7.5 mg once weekly | ||||
| Week 10 | 7.5 mg once weekly | ||||
| Week 11 | 7.5 mg once weekly | ||||
| Week 12 | 7.5 mg once weekly | ||||
| Week 13 | 10 mg once weekly | ||||
| Week 14 | 10 mg once weekly | ||||
| Week 15 | 10 mg once weekly | ||||
| Week 16 | 10 mg once weekly | ||||
| Week 17 | 12.5 mg once weekly | ||||
| Week 18 | 12.5 mg once weekly | ||||
| Week 19 | 12.5 mg once weekly | ||||
| Week 20 | 12.5 mg once weekly | ||||
| Week 21 | 15 mg once weekly | ||||
| Week 22 | 15 mg once weekly | ||||
| Week 23 | 15 mg once weekly | ||||
| Week 24 | 15 mg once weekly | ||||
| Week 25 | 15 mg once weekly |
Printing this page prints the schedule and calendar without the site navigation.
| Product | What it delivers | Doses per pen / vial | Contents |
|---|---|---|---|
| Single-dose pen (carton of 4 pens) | 2.5, 5, 7.5, 10, 12.5 or 15 mg per injection | 1 dose per pen (4 pens = 4 weekly doses) | 2.5 mg/0.5 mL, 5 mg/0.5 mL, 7.5 mg/0.5 mL, 10 mg/0.5 mL, 12.5 mg/0.5 mL or 15 mg/0.5 mL |
| Single-dose vial (carton of 1 or 4 vials) | 2.5, 5, 7.5, 10, 12.5 or 15 mg per injection | 1 dose per vial | 2.5 mg/0.5 mL, 5 mg/0.5 mL, 7.5 mg/0.5 mL, 10 mg/0.5 mL, 12.5 mg/0.5 mL or 15 mg/0.5 mL |
| Single-patient-use KwikPen 2.5 mg | 2.5 mg per dose | 4 doses | 10 mg/2.4 mL (4.17 mg/mL) |
| Single-patient-use KwikPen 5 mg | 5 mg per dose | 4 doses | 20 mg/2.4 mL (8.33 mg/mL) |
| Single-patient-use KwikPen 7.5 mg | 7.5 mg per dose | 4 doses | 30 mg/2.4 mL (12.5 mg/mL) |
| Single-patient-use KwikPen 10 mg | 10 mg per dose | 4 doses | 40 mg/2.4 mL (16.7 mg/mL) |
| Single-patient-use KwikPen 12.5 mg | 12.5 mg per dose | 4 doses | 50 mg/2.4 mL (20.8 mg/mL) |
| Single-patient-use KwikPen 15 mg | 15 mg per dose | 4 doses | 60 mg/2.4 mL (25 mg/mL) |
| Multi-dose vial 2.5 mg | 2.5 mg/0.6 mL per dose | 4 doses | 10 mg/2.4 mL (4.17 mg/mL) |
| Multi-dose vial 5 mg | 5 mg/0.6 mL per dose | 4 doses | 20 mg/2.4 mL (8.33 mg/mL) |
| Multi-dose vial 7.5 mg | 7.5 mg/0.6 mL per dose | 4 doses | 30 mg/2.4 mL (12.5 mg/mL) |
| Multi-dose vial 10 mg | 10 mg/0.6 mL per dose | 4 doses | 40 mg/2.4 mL (16.7 mg/mL) |
| Multi-dose vial 12.5 mg | 12.5 mg/0.6 mL per dose | 4 doses | 50 mg/2.4 mL (20.8 mg/mL) |
| Multi-dose vial 15 mg | 15 mg/0.6 mL per dose | 4 doses | 60 mg/2.4 mL (25 mg/mL) |
The label reports these rates from placebo-controlled trials (label section 6.1, Table 1). Percentages are the share of trial participants who reported each reaction.
| Adverse reaction | Placebo (N=958) | Zepbound 5 mg (N=630) | Zepbound 10 mg (N=948) | Zepbound 15 mg (N=941) |
|---|---|---|---|---|
| Nausea | 8% | 25% | 29% | 28% |
| Diarrhea (incl. frequent bowel movements) | 8% | 19% | 21% | 23% |
| Vomiting | 2% | 8% | 11% | 13% |
| Constipation (incl. feces hard) | 5% | 17% | 14% | 11% |
| Abdominal pain (grouped terms) | 5% | 9% | 9% | 10% |
| Dyspepsia | 4% | 9% | 9% | 10% |
| Injection site reactions (grouped terms) | 2% | 6% | 8% | 8% |
| Fatigue (incl. asthenia, lethargy, malaise) | 3% | 5% | 6% | 7% |
| Hypersensitivity reactions | 3% | 5% | 5% | 5% |
| Eructation | 1% | 4% | 5% | 5% |
| Hair loss | 1% | 5% | 4% | 5% |
| Gastroesophageal reflux disease | 2% | 4% | 4% | 5% |
| Flatulence | 2% | 3% | 3% | 4% |
| Abdominal distension | 2% | 3% | 3% | 4% |
| Dizziness | 2% | 4% | 5% | 4% |
| Hypotension (incl. blood pressure decreased, orthostatic hypotension) | 0% | 1% | 1% | 2% |
When do they happen? Per the label, the majority of nausea, vomiting and/or diarrhea events occurred during dose escalation and decreased over time; gastrointestinal adverse reactions overall occurred in 56% at each Zepbound dose versus 30% on placebo. Most patients who stopped Zepbound for adverse reactions did so during the first few months, due to gastrointestinal reactions (6.1).
The label also carries warnings that are not in this table (for example, a boxed warning or pancreatitis and gallbladder warnings where applicable). Read the full label linked under Sources, and report side effects to your prescriber.
Per the label, a missed dose is given as soon as possible within 4 days (96 hours); if more than 4 days have passed, the missed dose is skipped and the next dose is given on the regular day. The weekly day can be changed if the two doses are at least 3 days (72 hours) apart. (label section 2.3) The full walk-through is on the Zepbound missed-dose page.
The label describes once-weekly subcutaneous injection at any time of day, with or without meals, together with a reduced-calorie diet and increased physical activity. Sites are the abdomen or thigh, or the back of the upper arm when another person injects, rotated with each dose. (label section 2.4)
A simple log makes each titration step easier to talk through with your prescriber. These are the things worth writing down, and how Dose Track handles them:
Your log stays on your phone. See GLP-1 tracking in Dose Track for the full feature list.
Reviewed as of . Section numbers above refer to the FDA prescribing information.
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