Mounjaro KwikPen 15 — Tirzepatide 15 mg, 1 pcs, Eli Lilly
100% original product

Mounjaro KwikPen 15 (Tirzepatide) 15 mg Cold chain · Storage +2…+8 °C

21769 23557 -8%
Cold chain Storage +2…+8 °C

This medicine requires temperature control. We pack it in a thermal box with cold packs for safe delivery.

Please return the thermal box with cold packs after delivery. An additional charge applies only if you wish to keep the box.

Mounjaro 15 mg KwikPen is a first-in-class, novel pharmaceutical preparation containing Tirzepatide. It represents the first dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist. Mounjaro is indicated for the treatment of type 2 diabetes mellitus and for chronic weight management in adults with obesity or overweight. By simultaneously targeting both GIP and GLP-1 receptors, Tirzepatide enhances glucose-dependent insulin secretion, improves insulin sensitivity, delays gastric emptying, and acts on central brain pathways to significantly reduce appetite and body weight.

Manufacturer: Eli Lilly and Company (USA). A global leader in biopharmaceuticals and metabolic healthcare, renowned for strict manufacturing standards, extensive clinical trial programs, and pioneering innovations in diabetes and endocrinology care.

⚠️ Important Commercial & Packaging Notice: Mounjaro is supplied in a pre-filled, multi-dose Mounjaro KwikPen 15 mg/0.6 ml device containing a total volume of 2.4 ml. Each KwikPen device delivers exactly 4 doses of 15 mg (one weekly subcutaneous injection for a 4-week treatment course). The 15 mg strength represents the maximum maintenance dosage of Tirzepatide available in the Mounjaro line.

Key Clinical Advantages and Features of Mounjaro 15 mg KwikPen:

  • Dual Receptor Agonism (GIP/GLP-1): Delivers synergistic metabolic benefits, achieving superior glycemic control and weight reduction compared to selective GLP-1 receptor mono-agonists.
  • Maximum Clinical Potency: The 15 mg dose demonstrated the highest efficacy in the SURPASS and SURMOUNT clinical trials, achieving up to 20–22.5% body weight reduction in adults with obesity and profound HbA1c lowering.
  • User-Friendly KwikPen System: Multi-dose pen designed for convenient, once-weekly subcutaneous administration, providing a complete 4-week treatment regimen per pen.
  • Cardiometabolic Optimization: Positively impacts cardiometabolic risk factors, including blood pressure, lipid profiles, and intrahepatic fat accumulation.

Mounjaro 15 mg KwikPen is supplied as a clear, colorless to slightly yellow solution for subcutaneous injection in a pre-filled multi-dose KwikPen injector:

  • Packaging Configuration: 1 pre-filled multi-dose KwikPen containing 2.4 ml of solution (delivering 4 doses of 0.6 ml).
  • Active Ingredient: Tirzepatide — 15 mg per single dose (0.6 ml). Total active drug content per pen is 60 mg.
  • Inactive Excipients: Sodium phosphate dibasic heptahydrate, sodium chloride, benzyl alcohol (preservative), water for injections, sodium hydroxide and/or hydrochloric acid (for pH adjustment).

Pharmacodynamics: Tirzepatide is a 39-amino-acid synthetic peptide engineered with a C20 fatty diacid moiety that enables non-covalent binding to human albumin, extending its half-life to approximately 5 days. Tirzepatide binds to and activates both GIP and GLP-1 receptors. Simultaneous activation stimulates glucose-dependent insulin secretion, suppresses glucagon release, lowers fasting and postprandial glucose levels, slows gastric emptying, and acts on hypothalamic feeding centers to increase satiety and reduce caloric intake.

Pharmacokinetics: Following subcutaneous administration, maximum plasma concentration (Cmax) is attained within 8 to 72 hours. Absolute bioavailability is approximately 80%. Steady-state plasma concentrations are achieved following 4 weeks of once-weekly administration. Tirzepatide is metabolized via proteolytic cleavage of the peptide backbone and beta-oxidation of the fatty acid side chain. The terminal elimination half-life (T1/2) is approximately 5 days (120 hours), supporting once-weekly dosing. Elimination occurs via urine and feces as metabolic fragments.

Mounjaro 15 mg KwikPen is indicated for adult patients in the following therapeutic areas:

  • 🔹 Type 2 Diabetes Mellitus: As an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus, either as monotherapy (when metformin is inappropriate) or in combination with other antihyperglycemic agents (metformin, sulfonylureas, SGLT-2 inhibitors, insulin).
  • 🔹 Chronic Weight Management: As an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial Body Mass Index (BMI) of ≥ 30 kg/m² (obesity) or ≥ 27 kg/m² to < 30 kg/m² (overweight) in the presence of at least one weight-related comorbid condition (e.g., hypertension, dyslipidemia, obstructive sleep apnea, cardiovascular disease).

Mounjaro 15 mg KwikPen is formulated strictly for subcutaneous injection:

  • 💊 Dose Escalation Schedule: Therapy must be initiated at 2.5 mg once weekly for 4 weeks. After 4 weeks, increase the dose in 2.5 mg increments every 4 weeks (2.5 mg ➔ 5 mg ➔ 7.5 mg ➔ 10 mg ➔ 12.5 mg ➔ 15 mg). The 15 mg dose is the maximum maintenance dose and should only be administered after completing all lower dose steps.
  • ⏱️ Administration Schedule: Administer once weekly, on the same day each week, at any time of day, with or without food. Inject subcutaneously into the abdomen, thigh, or upper arm. Rotate injection sites with each weekly dose.
  • 💉 KwikPen Operation: The multi-dose KwikPen is pre-configured to deliver a fixed 0.6 ml dose (15 mg Tirzepatide) per injection. Attach a new sterile pen needle before each administration.
  • 🚫 Missed Dose Management: If a dose is missed, administer it as soon as possible within 4 days (96 hours) after the missed dose. If more than 4 days have elapsed, skip the missed dose and resume the regular weekly schedule on the next planned day.

Mounjaro 15 mg KwikPen is strictly contraindicated in patients presenting with:

  • ❌ Hypersensitivity to Tirzepatide or to any of the inactive excipients in the formulation.
  • ❌ Personal or family history of Medullary Thyroid Carcinoma (MTC).
  • ❌ Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
  • ❌ Type 1 diabetes mellitus or treatment of diabetic ketoacidosis.
  • ❌ Severe gastrointestinal disease, including severe gastroparesis.
  • ❌ Pregnancy and breastfeeding.
  • ❌ Pediatric patients under 18 years of age (safety and efficacy not established).

Consider the following interactions when administering Mounjaro 15 mg KwikPen:

  • ⚠️ Insulin and Insulin Secretagogues (Sulfonylureas): Co-administration increases the risk of hypoglycemia. A dose reduction of insulin or sulfonylurea may be required.
  • ⚠️ Oral Medications: Mounjaro causes a delay in gastric emptying, which may impact the rate and extent of absorption of concomitantly administered oral medications (e.g., oral contraceptives, antibiotics, narrow therapeutic index drugs). Patients taking oral contraceptives should switch to a non-oral method or add a barrier method for 4 weeks after initiation and for 4 weeks after each dose escalation.

Mounjaro 15 mg KwikPen is **contraindicated during pregnancy**. Animal reproduction studies have shown potential embryofetal toxicity. Women of childbearing potential should use effective contraception during treatment. Discontinue Mounjaro at least 2 months prior to a planned pregnancy. It is unknown whether Tirzepatide is excreted in human milk; breastfeeding should be discontinued during treatment.

Mounjaro 15 mg KwikPen at the 15 mg dose may cause adverse reactions, most commonly involving the gastrointestinal tract, which typically subside over time:

  • 🤢 Gastrointestinal (Very Common): Nausea, diarrhea, vomiting, constipation, abdominal pain, dyspepsia, eructation, flatulence, gastroesophageal reflux disease.
  • 💆 General Disorders: Fatigue, asthenia, dizziness, injection site reactions (erythema, pruritus, hematoma).
  • 📉 Metabolic & Laboratory: Hypoglycemia (when used with insulin or sulfonylureas), decreased appetite, elevated serum lipase/amylase.
  • ⚠️ Rare but Serious Events: Acute pancreatitis, gallbladder disease (cholelithiasis, cholecystitis), acute kidney injury (secondary to dehydration from GI adverse reactions), severe hypersensitivity reactions (anaphylaxis, angioedema).

Overdose Symptoms: Massive overdosage of Tirzepatide may lead to severe gastrointestinal distress (severe nausea, persistent vomiting, diarrhea) and significant hypoglycemia, particularly if co-administered with other antidiabetic agents.

Overdose Management: Provide supportive medical treatment according to clinical symptoms. Monitor blood glucose levels closely and maintain adequate fluid and electrolyte balance. No specific antidote exists.

Storage instructions for Mounjaro 15 mg KwikPen:

  • ❄️ Unopened Pens: Store refrigerated between 2 °C to 8 °C. Do not freeze! Discard if the device has been frozen.
  • 🌡️ In-Use / Room Temperature Storage: An in-use or unopened pen may be stored at room temperature up to 30 °C for a maximum period of 30 days. Discard the pen after 30 days, even if medication remains inside.
  • 💧 Light Protection: Store in the original outer carton to protect from direct light. Keep the cap on the pen when not in use.
  • 👶 Safety Precautions: Keep out of reach and sight of children. Store the pen without a needle attached.

To ensure the authenticity of your Mounjaro 15 mg KwikPen device, check for the following anti-counterfeiting security features:

  • 🛡️ Packaging Design: The original carton features crisp graphics with a distinct red corner accent block, prominent Mounjaro® and KwikPen® trademarks, and official Lilly branding. The front panel explicitly indicates "15 mg" and "15mg/0.6 ml".
  • 🔍 Batch and Expiry Markings: The side panel of the carton and the pen label display deeply stamped or thermal-printed Lot Number (LOT) and Expiration Date (EXP), which must be identical.
  • 📦 KwikPen Build Quality: The authentic device consists of a sturdy grey body with a purple cap and dose knob matching the official 15 mg color code. The dose window clearly displays fixed unit indicators. The liquid solution inside the glass cartridge must be completely clear, colorless to light yellow, and free of visible particles.

Notice. The information on this page is for reference only and does not replace medical consultation. Always consult a healthcare professional and read the manufacturer's instructions before using any medicine. Self-medication may be dangerous. Information updated: 20.08.2026

Active ingredient
Storage temperature
Cold chain · Storage +2…+8 °C

Shipped in a thermal box with cold packs

Dosage form Solution for subcutaneous injection in a pen injector
Volume 0.6 ml
Units per pack 1
Packaging Pen injector in a carton box
100% original product
Delivery across Ukraine
1
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