GNH USA

Europe — EMA

Lanreotid Zentiva

GNH USA supplies Lanreotid Zentiva (Lanreotide), a somatostatin analog for acromegaly and neuroendocrine tumors. Request a quote for global supply today.

Lanreotide

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What is Lanreotide?

Lanreotide, the active ingredient in Lanreotid Zentiva, is a somatostatin analog presented as a sterile solution for subcutaneous injection. It is used to control excess growth hormone secretion in acromegaly and to inhibit hormone‑producing neuroendocrine tumors in adult patients.

GNH USA supplies Lanreotid Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, ensuring quality‑assured product availability across regulated markets. The product complies with European Union marketing authorisation standards and is distributed under strict cold‑chain conditions.

What is Lanreotide used for?

Lanreotid Zentiva (lanreotide) is employed in the management of disorders driven by excess growth hormone or peptide hormone secretion.

Acromegaly: reduces serum IGF‑1 levels and controls disease activity. Neuroendocrine tumors (e.g., carcinoid): alleviates hormone‑related symptoms and may slow tumor progression. VIPoma: suppresses vasoactive intestinal peptide secretion, improving diarrhoea and electrolyte balance.

What are the side effects of Lanreotide?

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

Common Side Effects: - Injection site pain or erythema - Nausea or vomiting - Diarrhoea or abdominal cramps - Headache - Hyperglycaemia or altered glucose tolerance - Fatigue

Serious or Rare Side Effects: - Gallstone formation or biliary colic - Acute pancreatitis - Severe allergic reactions (anaphylaxis, angio‑edema) - Cardiac arrhythmias - Pituitary apoplexy in patients with pre‑existing adenomas - Severe hepatic dysfunction

What precautions apply to Lanreotide?

Before initiating therapy, clinicians should consider several safety aspects.

Monitor glucose levels: assess for hyperglycaemia, especially in diabetic patients. Assess gallbladder status: evaluate for gallstones or biliary disease prior to treatment. Evaluate pituitary tumor size: watch for signs of apoplexy in acromegaly patients. Adjust dose in hepatic or renal impairment: use caution and consider dose modification. Avoid in known hypersensitivity: discontinue if allergic reaction occurs. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Lanreotide interact with?

Lanreotide can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid): - Octreotide: additive suppression of hormone secretion may lead to excessive hormonal inhibition. - Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase lanreotide plasma concentrations. - Cyclosporine: elevated lanreotide levels can enhance adverse effects.

Moderate Interactions (Monitor Closely): - Antidiabetic agents: monitor blood glucose as lanreotide may affect glycaemic control. - Anticoagulants: observe for altered bleeding risk. - Diuretics: watch electrolyte balance, especially potassium. - Other peptide hormone therapies: assess for overlapping pharmacodynamic effects.

Frequently asked questions

What conditions is Lanreotid Zentiva used to treat?+
Lanreotid Zentiva, containing lanreotide, is indicated for the treatment of acromegaly and for symptom control in neuroendocrine tumors such as carcinoid tumors and VIPoma. It helps reduce excess hormone secretion that drives disease activity in these conditions.
How does lanreotide work in the body?+
Lanreotide mimics the natural hormone somatostatin and binds to somatostatin receptors (mainly SSTR2 and SSTR5) on target cells. This binding inhibits adenylate cyclase, lowers cyclic AMP levels, and suppresses the release of growth hormone, insulin‑like growth factor‑1, and other peptide hormones involved in tumor growth and symptom generation.
What is the usual dose of Lanreotid Zentiva?+
The dosage of Lanreotid Zentiva is individualized by the prescribing clinician based on the patient’s condition, disease severity, and response to therapy. Only a qualified healthcare professional can determine the appropriate dosing schedule and amount.
Is Lanreotid Zentiva safe to use during pregnancy or breastfeeding?+
The safety of lanreotide in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.
How do I order Lanreotid Zentiva from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain logistics if needed), and necessary import documentation.
How does Lanreotid Zentiva compare with other somatostatin analogues?+
Lanreotid Zentiva is comparable to other long‑acting somatostatin analogues such as octreotide LAR. Both provide sustained receptor activation, but lanreotide is formulated for subcutaneous administration and may have a different dosing interval, which can influence convenience and patient preference.
What are the storage and handling requirements for Lanreotid Zentiva?+
Lanreotid Zentiva should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. The product should be kept in its original packaging until use to maintain stability.
How is Lanreotid Zentiva administered?+
The medication is supplied as a sterile solution for subcutaneous injection. A healthcare professional administers the injection, typically into the abdomen or thigh, following aseptic technique and the dosing schedule prescribed by the clinician.
What are the most serious risks associated with Lanreotid Zentiva?+
Serious risks include gallstone formation, acute pancreatitis, severe allergic reactions such as anaphylaxis, cardiac arrhythmias, and pituitary apoplexy in patients with pre‑existing adenomas. Patients should be monitored for these events and advised to seek immediate medical attention if symptoms arise.
Who should not use Lanreotid Zentiva?+
Lanreotid Zentiva is contraindicated in individuals with known hypersensitivity to lanreotide or any of the formulation excipients. Caution is also advised for patients with severe hepatic impairment, uncontrolled diabetes, or active gallbladder disease.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Lanreotide
Route
Subcutaneous Use
Manufacturer
Zentiva Pharma Gmbh
Origin
EU

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