Product image of Octreotide Arrow (Octreotide Acetate) supplied by GNH India

Octreotide Arrow

Active Ingredient:
Octreotide Acetate
Origin:
EU

Octreotide Arrow (Octreotide Acetate)

Octreotide acetate, the active ingredient in Octreotide Arrow, is a peptide presented as a formulation for injectable use. It modulates hormone secretion and is employed in the management of certain endocrine‑related disorders in adults.

GNH India supplies Octreotide Arrow as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and specialty pharmacies worldwide.

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

Octreotide Arrow is a synthetic analogue of somatostatin that acts on neuroendocrine pathways. It is indicated for:

  • Acromegaly: reduces growth hormone and IGF‑1 levels, helping control disease activity.
  • Carcinoid syndrome: lessens flushing and diarrhoea by inhibiting serotonin release.
  • VIPoma/Medullary thyroid carcinoma associated diarrhea: controls severe secretory diarrhoea.
  • Preventive control of postoperative pancreatic fistula after major pancreatic surgery, where evidence supports its use.
  • Management of hypoglycaemia related to insulinoma or nesidioblastosis by suppress of insulin secretion.
  • Control of bleeding from varice various gastro‑intestinal bleeds where som­ som pathways are involved.

How It Works

  • Octreotide acetate is a synthetic somatostatin analogue that binds with high affinity to somatostatin receptor subtypes 2 and 5. Activation of these G‑protein‑coupled receptors inhibits adenylate cyclase, reduces cyclic AMP levels and suppresses the release of several hormones and peptides, including growth hormone, insulin, glucagon, gastrin and serotonin. This broad inhibition underlies its therapeutic effects in hormone‑driven disorders.

Side Effects

Octreotide Arrow may cause a range of adverse reactions.

Common Side Effects

  • Gastrointestinal discomfort: nausea, abdominal cramping or diarrhoea.
  • Injection‑site reactions: erythema, pain or induration.
  • Gallbladder changes: biliary sludge or gallstones.
  • Metabolic alterations: hyperglycaemia or hypoglycaemia.
  • Headache or fatigue.

Serious or Rare Side Effects

  • Pancreatitis.
  • Severe hypersensitivity reactions, including anaphylaxis.
  • Cardiac arrhythmias.
  • Acute cholecystitis.
  • Significant electrolyte disturbances.

Precautions & Warnings

Octreotide Arrow should be used with clinical oversight and consideration of patient‑specific factors.

  • Renal impairment: dose adjustment may be required.
  • Hepatic dysfunction: monitor liver enzymes and gallbladder status.
  • Diabetes mellitus: monitor blood glucose closely, as the drug can affect glycaemic control.
  • Cardiovascular disease: observe for brady‑cardia or arrhythmias.
  • Pregnancy and lactation: only use if the potential benefit outweighs risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • Cytochrome P450 substrates metabolised by CYP3A4 (e.g., midazolam) – may have reduced exposure.
  • Long‑acting octreotide formulations – risk of additive hormonal suppression.

Moderate Interactions (Monitor Closely)

  • Insulin or oral hypoglycaemic agents – risk of hypoglycaemia or hyperglycaemia.
  • Antiplatelet or anticoagulant drugs – potential for altered bleeding risk.
  • Thyroid hormone replacement – may require dose adjustment.

Frequently Asked Questions

Octreotide Arrow is a synthetic somatostatin analogue indicated for conditions such as acromegaly, carcinoid syndrome, VIP‑oma related diarrhoea, and for preventing postoperative pancreatic fistula. It works by inhibiting excess hormone secretion that drives these disorders.

Octreotide acetate binds to somatostatin receptors 2 and 5 on target cells, triggering a cascade that lowers cyclic AMP and suppresses the release of several hormones—including growth hormone, insulin and serotonin—thereby reducing the clinical manifestations of hormone‑driven diseases.

The dosing regimen for Octreotide Arrow is individualized by the prescribing clinician based on the specific indication, patient characteristics and response to therapy. Healthcare professionals determine the appropriate dose and administration schedule.

Octreotide Arrow should only be used during pregnancy or lactation when the potential therapeutic benefit justifies any potential risk to the fetus or infant. Clinicians must evaluate the risk‑benefit profile for each 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 where required) and import documentation.

Octreotide Arrow is comparable to other long‑acting somatostatin analogues such as lanreotide, offering similar receptor affinity and clinical efficacy. Differences may lie in formulation, dosing frequency and specific regulatory approvals, which clinicians consider when selecting therapy.

Octreotide Arrow must be stored at 2‑8 °C, protected from light, and should not be frozen or shaken. It should be kept in its original packaging until use to maintain stability.

Octreotide Arrow is supplied as an injectable solution that is administered subcutaneously or intravenously by a qualified healthcare professional, following the dosing schedule prescribed for the specific indication.

Serious risks include pancreatitis, severe hypersensitivity reactions such as anaphylaxis, cardiac arrhythmias, acute cholecystitis and significant electrolyte disturbances. Patients should be monitored closely for these events.

Octreotide Arrow is contraindicated in patients with known hypersensitivity to octreotide or any excipients in the formulation, and should be used with caution in individuals with severe hepatic impairment, uncontrolled diabetes, or active gallbladder disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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