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Adipotide
Weight Management
AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
DSIP
Sleep & Recovery
Epithalon
Anti-Aging
GHK-Cu
Anti-Aging
GHRP-2
Growth Hormone
HCG
Hormone Support
Hexarelin
Growth Hormone
HGH
Growth Hormone
IGF-1 LR3
Growth Hormone
Kisspeptin
Hormone Support
Melanotan-2
Cosmetic
MOTS-C
Metabolic
NAD+
Anti-Aging
Oxytocin Acetate
Hormone Support
PEG-MGF
Recovery
PNC-27
Cancer Research
PT-141
Sexual Health
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Snap-8
Cosmetic
SS-31
Mitochondrial
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
Weight Management
Total Peptides: 32
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Weight Management Protocol

LiraglutideComplete Dosing & Administration Guide

FDA-approved once-daily GLP-1 receptor agonist (Victoza/Saxenda) that reduces HbA1c by 0.9–1.6%, promotes 5–10% body weight loss, and demonstrated a 13% reduction in major adverse cardiovascular events in the landmark LEADER trial of 9,340 patients

Dose Range

0.6-3.0mg

Frequency

Once daily

Route

Subcutaneous injection

Cycle Length

Ongoing/indefinite

Dosing

How much
do I take?

Starting Dose

0.6 mg subcutaneous once daily

Frequency

Once daily

Duration

1 week (tolerability assessment)

Begin at 0.6 mg daily for the first week to assess gastrointestinal tolerability before dose escalation. This starting dose is sub-therapeutic for both diabetes and obesity indications. Inject in abdomen, thigh, or upper arm at any time of day regardless of meals. Rotate injection sites. GI side effects (nausea) are most common during the initial titration period.

Standard Dose

1.2–1.8 mg subcutaneous once daily

Frequency

Once daily

Duration

Ongoing chronic therapy

Standard therapeutic dose range for type 2 diabetes (Victoza). Escalate from 0.6 mg to 1.2 mg at week 2 and optionally to 1.8 mg at week 3 for additional glycemic benefit. Maximum diabetes dose is 1.8 mg/day. No dose adjustment needed for renal or hepatic impairment. If combining with sulfonylureas, reduce sulfonylurea dose by 50% to minimize hypoglycemia. Store in-use pen at room temperature or refrigerated for up to 30 days.

Advanced Dose

3.0 mg subcutaneous once daily

Frequency

Once daily

Duration

Ongoing chronic therapy with 16-week efficacy assessment

Obesity dose (Saxenda) reached through weekly 0.6 mg increments: 0.6→1.2→1.8→2.4→3.0 mg over 5 weeks. Evaluate response at 16 weeks — if <4% body weight loss, consider discontinuation as unlikely to achieve meaningful benefit. Must be combined with reduced-calorie diet and increased physical activity. Approved for BMI ≥30 or BMI ≥27 with weight-related comorbidities. Do not use simultaneously with Victoza or any other GLP-1 RA.

Timing

Best time to take

Administer Liraglutide at the same time each day (or on the same day each week for weekly injections). Many users prefer morning or evening administration. Pick a time you'll remember consistently.

With food?

Liraglutide injections can be given regardless of meal timing. However, if GI effects occur, administering on an empty stomach or with a light meal may help reduce discomfort.

If stacking

Liraglutide should be used as directed by your healthcare provider. If combining with other medications or supplements, discuss potential interactions with your provider. Avoid combining with compounds that have overlapping mechanisms unless specifically guided by a medical professional.

Adjusting Your Dose

Increase if

  • +You've tolerated the current dose for the recommended period without significant side effects
  • +Therapeutic goals haven't been met at the current dose level
  • +Your healthcare provider recommends dose escalation based on your response
  • +Lab work or clinical assessments support a higher dose

Decrease if

  • -Side effects are bothersome or impacting daily life despite management strategies
  • -You experience any signs of an adverse reaction
  • -Lab results indicate the need for dose reduction
  • -Your healthcare provider recommends a lower dose based on your response

Signs of right dose

  • Therapeutic goals being met with minimal side effects
  • Stable and consistent response to treatment
  • Lab values or clinical markers trending in the right direction
  • Good tolerance with manageable or absent side effects

Dosing Calculator

Calculate Your Exact Dose

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Administration

How do I
use it?

Reconstitution

What you need

  • Liraglutide vial (lyophilized powder or solution)
  • Bacteriostatic water or sterile sodium chloride for reconstitution
  • Alcohol swabs for cleaning vial tops and injection sites
  • Appropriately sized syringes with fine-gauge needles (27-30 gauge)
  • Sharps disposal container

Example

Add the recommended volume of bacteriostatic water to the Liraglutide vial. Gently swirl (do not shake) until the powder is fully dissolved. The resulting solution should be clear. Calculate your individual dose based on the concentration and your prescribed amount.

Your dose of Liraglutide is determined by your healthcare provider. Using an insulin syringe marked in units, draw up the exact amount prescribed. For example, if the reconstituted concentration is 1mg/mL and your dose is 0.5mg, draw up 0.5mL (50 units on an insulin syringe). Always double-check calculations before injection.

Injection

Route

Subcutaneous injection (into the fatty tissue just under the skin)—allows for consistent absorption and can be self-administered at home after proper training

Best sites

  • Abdomen (stomach area)—at least 2 inches from the belly button, most popular choice for self-injection
  • Front of thighs—middle to upper portion of the outer leg
  • Back of upper arm—outer area (may need assistance from another person)

Technique

  • 1.Wash your hands thoroughly with soap and water before handling supplies
  • 2.Clean the injection site with an alcohol swab and let it air dry completely
  • 3.Pinch a fold of skin at the chosen injection site
  • 4.Insert the needle at a 45-90 degree angle (depending on needle length and body composition)
  • 5.Inject the medication slowly and steadily over 5-10 seconds
  • 6.Release the skin fold and remove the needle, applying gentle pressure with a clean swab
  • 7.Rotate injection sites to prevent tissue irritation or lipodystrophy
  • 8.Dispose of the needle safely in a sharps container—never recap or reuse needles
Full Injection Guide

Storage

Before reconstitution

Store Liraglutide in the refrigerator at 36-46°F (2-8°C) in its original packaging. Protect from light and moisture. Do not freeze. Check the expiration date before use. Some formulations may be stored at room temperature for limited periods—check your specific product labeling.

After reconstitution

Once reconstituted, Liraglutide should be kept refrigerated at 36-46°F (2-8°C) and used within the timeframe specified on your product labeling (typically 14-28 days). Label the vial with the reconstitution date. Do not use if the solution appears cloudy, discolored, or contains particles.

Signs of degradation

  • Solution appears cloudy, discolored, or contains visible particles (should be clear)
  • Product has been exposed to temperatures outside the recommended storage range
  • Product has been frozen (unless specifically designed for freeze-thaw stability)
  • Expiration date has passed or reconstituted solution has exceeded its use-by date
  • Unusual odor, color change, or visible contamination

Sample Daily Schedule

As prescribed (once daily)

As prescribed by your healthcare provider injection

Site: Subcutaneous injection—rotate sites if applicable

Maintain a consistent schedule for optimal results with Liraglutide. Set reminders if needed. If you miss a dose, follow your healthcare provider's instructions—do not double up on doses to compensate.

Safety

Is it
safe?

Safety Profile

Liraglutide (Victoza, Saxenda) is FDA-approved with extensive safety data from 15+ years of clinical use in diabetes (GLP-1 agonist) and obesity indications. Gastrointestinal side effects (nausea, vomiting, diarrhea) occur in 30-40% of patients during dose escalation but diminish significantly after 2-3 weeks of stable dosing. Black box warnings include risk of medullary thyroid carcinoma and pancreatitis, though absolute incidence remains rare. Injection site reactions are minimal. The compound shows no hepatotoxicity, nephrotoxicity, or major drug interactions at approved doses.

Liraglutide safety derives from LEAD Phase 3 diabetes trials (2008-2009) enrolling thousands of patients, SCALE obesity trials (2013-2014), and decades of post-marketing surveillance. Published in New England Journal of Medicine and Diabetes Care, these studies establish favorable cardiovascular outcomes and weight reduction with well-characterized adverse event profiles. Regulatory oversight by FDA and EMA continues monitoring thyroid-related safety signals.

Common Side Effects

Experienced by some users

Nausea

Most frequent adverse effect (20–40% incidence), typically dose-dependent and most pronounced during the first weeks of therapy and dose escalation. Generally mild to moderate and transient.

Management: Gradual dose titration per prescribing schedule. Eat smaller, more frequent meals. Avoid high-fat or very large meals. Most patients develop tolerance within 4–8 weeks.

Diarrhea

Occurs in 15–20% of patients, usually mild to moderate in severity. Related to GLP-1 receptor-mediated effects on gastrointestinal motility.

Management: Stay well hydrated. Dietary adjustments (BRAT diet if needed). Usually self-limiting within the first few weeks of therapy.

Vomiting

Reported in 9–15% of patients, typically during dose escalation. Dose-dependent and generally decreases with continued therapy.

Management: Slow dose titration. Temporarily hold at current dose if vomiting is persistent. Anti-emetics may be used short-term if needed.

Decreased appetite and headache

Reduced appetite (therapeutic effect for weight management) and headache (5–10%) are common during initiation. Constipation (10–15%) may also occur.

Management: Appetite reduction is expected and therapeutic. Headache typically resolves with hydration and time. Constipation managed with adequate fiber and fluid intake.

Less Common

  • Injection site reactions

These typically resolve with continued use or dose adjustment.

Stop and Seek Help If

  • ×Severe or worsening side effects that don't improve with dose adjustment or supportive care
  • ×Signs of an allergic reaction—rash, hives, swelling, or difficulty breathing
  • ×Your healthcare provider recommends discontinuation based on your clinical response
  • ×Development of any new medical condition that may be contraindicated with Liraglutide
  • ×Pregnancy or planning to become pregnant (unless specifically approved for use during pregnancy)
  • ×Abnormal lab results or clinical markers that suggest adverse effects

Liraglutide should only be started, adjusted, or discontinued under medical supervision. This information is for educational purposes only and does not replace professional medical advice. Never stop a prescribed treatment without consulting your healthcare provider first, as abrupt discontinuation may have consequences.

Interactions

With other peptides

  • May be used together under medical guidance.
  • May be used together under medical guidance.
  • May be used together under medical guidance.

With medications

  • !Other GLP-1 receptor agonists (semaglutide, exenatide, dulaglutide) — redundant mechanism with increased adverse effects and no additional benefit - Use with caution—discuss with your healthcare provider.
  • !DPP-4 inhibitors (sitagliptin, saxagliptin) — overlapping incretin pathway mechanism; inferior to liraglutide monotherapy in head-to-head trials - Use with caution—discuss with your healthcare provider.
  • !Sulfonylureas at full dose — increased hypoglycemia risk requires 50% sulfonylurea dose reduction when adding liraglutide - Use with caution—discuss with your healthcare provider.

With supplements

  • Multivitamins - Generally safe to take alongside Liraglutide. Space doses apart if taking oral formulations to ensure optimal absorption.
  • Electrolyte supplements - Helpful if experiencing any GI side effects that could lead to dehydration. Safe to combine.

Want the Full Picture?

View the complete Liraglutide research profile including mechanism of action, clinical studies, effectiveness timeline, and FAQ.

View Full Liraglutide Profile

Medical Disclaimer

Liraglutide is an investigational research compound not approved by the FDA for human therapeutic use. This information is for educational purposes only and should not be construed as medical advice. Always consult with a qualified healthcare provider before starting any new supplement or treatment protocol.

Last updated: 2/8/2026