Product image of Octreoscan (Indium In-111 Pentetreotide) supplied by GNH India

Octreoscan

Active Ingredient:
Indium In-111 Pentetreotide
Origin:
EU

Octreoscan (Indium In-111 Pentetreotide)

Indium In-111 pentacarbamoyl‑methyl‑DTPA‑octreotide (Indium In-111 pentetreotide), the active ingredient in Octreoscan, is a somatostatin analog presented as a diagnostic radiopharmaceutical for intravenous use. It binds to somatostatin receptors to help visualize neuroendocrine tumors and related lesions in patients undergoing evaluation.

GNH India supplies Octreoscan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Curium Netherlands B.V.

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Indications & Clinical Uses

Octreoscan is a radiolabeled somatostatin analog used in diagnostic imaging of neuroendocrine tumor pathways. It assists clinicians in locating and staging disease.

  • Gastroenteropancreatic neuroendocrine tumors: enables whole‑body scintigraphic detection of somatostatin‑receptor positive lesions.
  • Bronchial and thymic carcinoids: highlights receptor‑rich tumors for surgical planning.
  • Metastatic disease assessment: determines extent of spread to guide therapeutic decisions.

How It Works

  • Indium In-111 pentetreotide binds with high affinity to somatostatin receptor subtypes 2 and 5 on the surface of neuroendocrine cells. After intravenous administration, the radiolabelled complex is internalized, and the emitted gamma photons are captured by a gamma camera, producing images that reflect receptor density and tumor location.

Side Effects

Adverse reactions are generally mild and related to the radiopharmaceutical or injection process.

Common Side Effects

  • Nausea: transient feeling of queasiness after injection.
  • Flushing: brief warmth or redness of the face and neck.
  • Mild headache: short‑lasting discomfort.
  • Injection site pain: soreness at the venipuncture site.
  • Transient hypotension: temporary drop in blood pressure.

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis): difficulty breathing, hives, or swelling.
  • Significant hypotension: prolonged low blood pressure requiring intervention.
  • Radiation‑induced marrow suppression: decreased blood counts.
  • Renal toxicity: impaired kidney function in susceptible patients.

Precautions & Warnings

Octreoscan should be administered by qualified personnel in a setting equipped for nuclear medicine procedures.

  • Pregnancy: avoid use unless clearly needed, as radiation may affect fetal development.
  • Breastfeeding: discontinue breastfeeding for an appropriate period after administration.
  • Renal function: assess kidney function before use; adjust protocol if impairment is present.
  • Allergy history: verify no prior hypersensitivity to somatostatin analogs or indium‑111 compounds.
  • Storage: Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Octreoscan may interact with agents that affect somatostatin receptors or alter radiation distribution.

Major Interactions (Avoid)

  • Long‑acting somatostatin analog therapy (e.g., octreotide LAR): may compete for receptor binding and reduce imaging sensitivity.

Moderate Interactions (Monitor Closely)

  • Diuretics: can modify renal clearance of the radiotracer.
  • ACE inhibitors: may influence blood pressure response during injection.
  • Antihistamines: may mask early signs of an allergic reaction.
  • Radioprotective agents: could alter image quality if administered concurrently.

Frequently Asked Questions

Octreoscan is a radiolabeled somatostatin analog used in nuclear medicine to image somatostatin‑receptor positive neuroendocrine tumors. It helps clinicians locate primary lesions, assess metastatic spread, and plan appropriate therapeutic strategies.

Indium In-111 pentetreotide binds selectively to somatostatin receptor subtypes 2 and 5 on neuroendocrine cells. After intravenous injection, the complex is internalized and emits gamma photons that are captured by a gamma camera, producing detailed images of receptor‑rich tissues.

The administered activity of Octreoscan is determined by the prescribing physician based on patient weight, age, and the imaging protocol. Dosage is individualized and should follow local regulatory and institutional guidelines.

Octreoscan involves a radioactive tracer, so it is generally avoided in pregnancy unless the diagnostic benefit outweighs the risk. Breastfeeding mothers should discontinue nursing for a period advised by the treating physician to prevent infant exposure.

To request Octreoscan, 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.

Octreoscan (Indium‑111) is a well‑established agent for somatostatin‑receptor imaging, offering whole‑body scintigraphy. Newer PET agents such as Ga‑68 DOTATATE provide higher resolution and faster imaging, but Octreoscan remains useful where PET facilities are unavailable or for specific regulatory approvals.

Octreoscan must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. The product should be kept in its original container until ready for preparation and administration by qualified nuclear medicine staff.

Octreoscan is administered intravenously by a trained nuclear medicine professional. After injection, patients typically wait a few hours before imaging to allow optimal tumor uptake and clearance of background activity.

Serious risks include severe allergic reactions (anaphylaxis), significant hypotension, radiation‑induced bone‑marrow suppression, and potential renal toxicity. Patients are monitored during and after injection to promptly identify and manage any adverse events.

Octreoscan is contraindicated in patients with known hypersensitivity to indium‑111 compounds or somatostatin analogs, and it should be avoided in pregnant women unless absolutely necessary. Caution is also advised for individuals with severe renal impairment or uncontrolled cardiovascular conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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