Product image of Myrelez (Lanreotide Acetate) supplied by GNH India

Myrelez

Active Ingredient:
Lanreotide Acetate
Origin:
EU

Myrelez (Lanreotide Acetate)

Lanreotide acetate, the active ingredient in Myrelez, is a somatostatin analog presented as an injectable solution for subcutaneous use. It is used to control hormone excess in conditions such as acromegaly and certain neuroendocrine tumors.
GNH India supplies Myrelez as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Amdipharm Limited

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Indications & Clinical Uses

Myrelez is a somatostatin analog indicated for endocrine disorders where excess hormone secretion is a problem.

  • Acromegaly: reduces growth hormone levels and helps control disease activity.
  • Neuroendocrine tumors: inhibits secretion of vasoactive peptides and can stabilize tumor‑related symptoms.

How It Works

  • Lanreotide acetate is a synthetic analogue of somatostatin that binds with high affinity to somatostatin receptor subtypes (especially sst2 and sst5). Receptor activation inhibits adenylate cyclase activity, reduces calcium influx, and suppresses the release of growth hormone, insulin‑like growth factor‑1, and various peptide hormones, thereby controlling hormone‑driven disease processes.

Side Effects

Myrelez may cause a range of adverse reactions, most of which are mild to moderate in severity.

Common Side Effects

  • Injection site pain: mild discomfort at the injection site.
  • Diarrhea: loose stools occurring shortly after dosing.
  • Nausea: transient feeling of queasiness.
  • Abdominal pain: cramping or discomfort in the abdomen.
  • Headache: mild to moderate headache episodes.
  • Fatigue: general tiredness or lack of energy.

Serious or Rare Side Effects

  • Gallbladder disease: formation of gallstones or cholecystitis.
  • Hyperglycemia: elevated blood glucose levels, especially in diabetic patients.
  • Pancreatitis: inflammation of the pancreas, presenting with severe abdominal pain.
  • Allergic reactions: rash, itching, or anaphylaxis in rare cases.

Precautions & Warnings

Before initiating Myrelez, consider the following safety measures.

  • Monitor glucose: check blood sugar regularly in patients with diabetes or risk factors.
  • Gallbladder assessment: evaluate for gallstones or biliary disease prior to treatment.
  • Cardiac evaluation: assess heart rhythm in patients with known arrhythmias.
  • Pregnancy and lactation: discuss potential risks with a healthcare professional before use.
  • Storage: Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Myrelez can interact with other medicines; awareness of the interaction level helps manage risk.

Major Interactions (Avoid)

  • Cytochrome P450 inducers: may reduce lanreotide exposure.
  • Somatostatin analogs combination: can increase risk of gallbladder complications.

Moderate Interactions (Monitor Closely)

  • Antidiabetic agents: may require dose adjustment due to altered glucose control.
  • Antiplatelet or anticoagulant drugs: monitor for increased bleeding risk if gallbladder disease develops.

Frequently Asked Questions

Myrelez is prescribed for patients with acromegaly to lower excess growth hormone and for certain neuroendocrine tumors to reduce hormone‑related symptoms and tumor activity.

Lanreotide acetate mimics natural somatostatin, binding to somatostatin receptors on endocrine cells. This binding blocks hormone release pathways, decreasing growth hormone and other peptide hormones that drive disease processes.

The dosage of Myrelez is individualized by the prescribing clinician based on the patient’s condition, disease severity, and response to therapy. Only a qualified healthcare professional should determine the appropriate regimen.

Safety data for Myrelez in pregnancy and lactation are limited. Women who are pregnant, planning pregnancy, or breastfeeding should discuss potential risks and benefits with their healthcare provider before starting treatment.

To request Myrelez, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and import documentation.

Myrelez (lanreotide acetate) and other analogs such as octreotide share a similar mechanism of receptor binding but differ in dosing frequency, formulation, and specific receptor affinity. Clinicians may choose based on patient convenience, tolerability, and individual therapeutic response.

Myrelez should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until ready for use.

Myrelez is given as a subcutaneous injection, typically by a healthcare professional. The injection site is rotated to minimize local irritation, and the device is prepared according to the manufacturer’s instructions.

Serious risks include gallbladder disease such as gallstones or cholecystitis, hyperglycemia that may worsen diabetes, and rare cases of pancreatitis or severe allergic reactions. Patients should be monitored for these events throughout therapy.

Myrelez is contraindicated in patients with known hypersensitivity to lanreotide acetate or any excipients in the formulation. Caution is also advised for individuals with severe uncontrolled diabetes, active gallbladder disease, or significant cardiac arrhythmias.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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