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    Liraglutide (6mg)

    SubcutaneouslyOnce daily6mg

    Reviewed by the AllPeptides.eu Editorial Team·Last reviewed: 2026-06-16

    🇺🇸 FDA (Victoza®)
    🇪🇺 EMA (Victoza®)
    🇯🇵 PMDA (Victoza®)
    🇨🇦 Health Canada (Victoza®)

    Educational information. Not medical advice, and no efficacy claim is implied. Regulatory approval is not a use recommendation by AllPeptides.eu.

    FDA & EMA approved — for specific indications
    Educational information. Not medical advice or a recommendation for use.

    ⚠️ For informational/educational purposes only. Not medical advice. We do not sell any products. Self-treatment carries serious risks — consult a healthcare professional. Disclaimer

    Available sizes:
    6mg
    3mg

    Research monograph

    See the full Liraglutide encyclopedia page with mechanism, evidence tier, related variants and research context.

    Open monograph
    Free Access

    How It Works

    Liraglutide mimics GLP-1, enhancing glucose-dependent insulin, reducing glucagon, slowing gastric emptying, and reducing appetite.

    Quick Start

    • Reconstitution: Add 2.0 mL bacteriostatic water → 3.0 mg/mL concentration.
    • Daily range: 0.6–3.0 mg once daily.
    • Storage: 2–8 °C.
    Detailed Protocol Data

    Gradual Titration (2 mL = 3.0 mg/mL)

    Educational only
    Vial Size— affects syringe units
    BAC Water2 mL
    Concentration3.00 mg/mL

    Route: Subcutaneously | Frequency: Once daily

    WeekDoseUnits (per injection)
    Week 1
    0.6 mg
    20 Units (0.20 mL)
    Week 2
    1.2 mg
    40 Units (0.40 mL)
    Week 3
    1.8 mg
    60 Units (0.60 mL)
    Week 4
    2.4 mg
    80 Units (0.80 mL)
    Week 5+
    3.0 mg
    100 Units (1.00 mL)

    Studies report administration once daily. Increase +0.6 mg/wk. A 6 mg vial = ~2 days at the maximum dose.

    Related compounds

    Reconstitution Steps

    1. Withdraw 2.0 mL of bacteriostatic water.
    2. Inject slowly.
    3. Swirl gently.
    4. Refrigerate at 2–8 °C.

    Protocol Overview

    • Goal: Weight loss / glycemic control.
    • Schedule: Daily, long-term.
    • Half-life: ~13 hours.

    Dosing Protocol

    • Start: 0.6 mg/day.
    • Max: 3.0 mg/day.
    • Titration: +0.6 mg/wk.
    • Break between cycles: Gradual reduction before discontinuation.

    Washout & Cycle Restart

    When can I restart?

    Gradual reduction before discontinuation.

    Minimum wait period: 2 weeks

    Storage Instructions

    • Powder: 2–8 °C.
    • Solution: 2–8 °C, use within 30 days.

    Important Notes

    • FDA-approved.
    • Larger vial = fewer changes.
    • Gradual titration is essential.
    Clinical Analysis & Safety

    Potential Benefits & Side Effects

    Potential Benefits:

    • Proven weight loss.
    • Glycemic control.
    • Cardiovascular benefits.

    Potential Side Effects:

    • Nausea, diarrhea.
    • Headache.
    • Rare: pancreatitis.

    ⚠️ Serious Warnings & Long-Term Risks

    The following warnings are based on published literature, FDA labels, and post-marketing surveillance. They do not constitute medical advice. Consult a healthcare professional.

    🎗️ Cancer Markers
    ⬛ FDA Black Box Warning

    Thyroid C-cell tumors (medullary thyroid carcinoma)

    In rodents, liraglutide caused dose-dependent thyroid C-cell tumors. Contraindicated in patients with personal/family history of MTC or MEN 2.

    📄 FDA Boxed Warning — Saxenda® Label
    ⚠️ Other
    🔴 High Risk

    Acute pancreatitis

    Reports of acute pancreatitis in post-marketing surveillance. Discontinue if suspected.

    📄 FDA Label — Victoza®
    ❤️ Cardiovascular
    🟡 Moderate / Theoretical

    Increased heart rate

    Small increase in heart rate (2-3 bpm) observed in clinical trials. Monitor in patients with cardiac conditions.

    📄 LEADER Trial — NEJM 2016

    References

    1. NEJM — SCALE — Liraglutide 3.0 mg for obesity
      View Source
    2. NEJM — LEADER — Liraglutide cardiovascular outcomes
      View Source

    Recommended Supplements

    Research Sources & Verified Data
    …
    Clinical Trials
    …
    PubMed Studies
    Approved
    FDA Status
    4
    Regulatory Approvals
    Verified across ClinicalTrials.gov, PubMed & FDA

    External Sources & Regulatory Status

    Regulatory Approvals

    🇺🇸
    FDA
    Approved

    Victoza® / Saxenda® · Type 2 diabetes / Obesity (2010)

    🇪🇺
    EMA
    Approved

    Victoza® / Saxenda® · Type 2 diabetes / Obesity (2009)

    🇯🇵
    PMDA
    Approved

    Victoza® · Type 2 diabetes (2010)

    🇨🇦
    Health Canada
    Approved

    Victoza® / Saxenda® · Type 2 diabetes / Obesity (2010)

    FDA/EMA approved (Victoza®/Saxenda®)

    No official regulatory source available yet — research peptide.

    Educational information. Not medical advice, and no efficacy claim is implied. Regulatory approval is not a use recommendation by AllPeptides.eu.

    Summary:
    4 Approvals
    0 PubMed
    0 Clinical Studies

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