Product image of Octreoteva Long Acting (Octreotide Acetate) supplied by GNH India

Octreoteva Long Acting

Active Ingredient:
Octreotide Acetate
Origin:
EU

Octreoteva Long Acting (Octreotide Acetate)

Octreotide acetate, the active ingredient in Octreoteva Long Acting, is a somatostatin analog presented as a long‑acting formulation for intramuscular, intravenous use. It is employed in the management of hormone‑secreting tumors and related endocrine disorders in adults.

GNH India supplies Octreoteva Long Acting as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Octreotide acetate is used in several endocrine‑related conditions where inhibition of hormone secretion is required.

  • Acromegaly: reduces excessive growth hormone production and helps control disease activity.
  • Neuroendocrine tumors: controls hormone‑related flushing and diarrhea associated with carcinoid syndrome.
  • VIPoma and other functional pancreatic tumors: decreases vasoactive intestinal peptide secretion and mitigates severe watery diarrhea.

How It Works

  • Octreotide acetate mimics natural somatostatin, binding with high affinity to somatostatin receptor subtypes (particularly sst2 and sst5). This interaction inhibits adenylate cyclase activity, reduces cyclic AMP formation, and suppresses the release of various hormones and peptides, leading to decreased secretion of growth hormone, insulin, glucagon, and gastrointestinal peptides.

Side Effects

Adverse reactions to Octreotide acetate may vary in frequency and severity.

Common Side Effects

  • Gastrointestinal discomfort: nausea, abdominal cramping, or pain.
  • Injection site reactions: erythema, swelling, or induration.
  • Gallbladder abnormalities: biliary sludge or gallstones.
  • Hyperglycaemia or hypoglycaemia: altered blood glucose levels.
  • Headache or dizziness.

Serious or Rare Side Effects

  • Pancreatitis: inflammation of the pancreas.
  • Severe hypersensitivity: anaphylaxis or severe skin reactions.
  • Cardiac arrhythmias: irregular heart rhythms.
  • Acute cholecystitis: inflammation of the gallbladder.
  • Severe hyperglycaemia requiring medical intervention.

Precautions & Warnings

Before initiating therapy with Octreotide acetate, clinicians should assess patient‑specific factors and monitor for potential complications.

  • Cardiovascular assessment: evaluate for pre‑existing arrhythmias or heart disease.
  • Glycaemic monitoring: check blood glucose regularly, especially in diabetic patients.
  • Gallbladder surveillance: perform periodic imaging to detect sludge or stones.
  • Drug interactions: review concomitant medications that affect glucose or cardiac function.
  • Pregnancy and lactation: weigh potential benefits against risks; use only if clearly needed.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Octreotide acetate can influence the pharmacokinetics of several co‑administered medicines.

Major Interactions (Avoid)

  • Insulin or oral hypoglycaics: may require dose adjustment due to altered glucose control.
  • Cytochrome P450 substrates metabolised by CYP3A4: risk of increased exposure.

Moderate Interactions (Monitor Closely)

  • Somatostatin analog‑containing regimens: additive hormonal suppression.
  • QT‑prolonging agents: potential for enhanced cardiac repolarisation effects.
  • Anticoagulants: monitor clotting parameters as gastrointestinal effects may alter absorption.

Frequently Asked Questions

Octreoteva Long Acting is indicated for the control of hormone‑related symptoms in acromegaly, neuroendocrine (carcinoid) tumors and functional pancreatic tumors such as VIPoma. It helps reduce excess growth hormone, flushing, diarrhea and other peptide‑mediated effects in these endocrine disorders.

Octreotide acetate is a synthetic analogue of somatostatin. It binds to somatostatin receptors (mainly sst2 and sst5) on endocrine cells, inhibiting adenylate cyclase and lowering cyclic AMP levels. This suppresses the release of several hormones and peptides, including growth hormone, insulin, glucagon and gastrointestinal secretions.

The dosage of Octreoteva Long Acting is individualized. A qualified prescriber determines the amount, frequency and route of administration based on the patient’s specific condition, response to therapy and clinical guidelines.

Octreoteva Long Acting should be used in pregnancy or while breastfeeding only if the potential benefit justifies the potential risk to the fetus or infant. Clinicians must evaluate each case carefully and discuss possible effects with the patient.

To place an order, 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.

Octreoteva Long Acting offers a prolonged dosing interval compared with short‑acting formulations like octreotide immediate‑release, reducing injection frequency. Its efficacy in controlling hormone secretion is comparable to other long‑acting analogues such as lanreotide, while the choice often depends on clinician preference, patient tolerance and specific regulatory approvals.

Octreoteva Long Acting should be stored at 2‑8 °C (refrigerated), protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.

The product is supplied for intramuscular or intravenous injection by a healthcare professional. It is typically given as a deep intramuscular depot injection, allowing slow release of the drug over several weeks.

Serious risks include pancreatitis, severe hypersensitivity reactions (including anaphylaxis), gallbladder complications such as acute cholecystitis, and significant disturbances in blood glucose that may require medical intervention.

Patients with known hypersensitivity to octreotide or any excipients, those with uncontrolled severe cardiac arrhythmias, and individuals with active gallbladder disease should avoid using Octreoteva Long Acting unless a clinician determines that benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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