Product image of Medi-Exametazim (Exametazime) supplied by GNH India

Medi-Exametazim

Active Ingredient:
Exametazime
Origin:
EU

Medi-Exametazim (Exametazime)

Exametazime, the active ingredient in Medi-Exametazim, is a radiopharmaceutical presented as a sterile injectable solution for intravenous use. It is employed to label white blood cells for imaging infection and inflammation in patients undergoing diagnostic evaluation.
GNH India supplies Medi-Exametazim as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Radiopharmacy Laboratórium Kft.

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Indications & Clinical Uses

Medi-Exametazim is used in nuclear medicine to visualize sites of infection and inflammation through leukocyte labeling.

  • Infection detection: enables visualization of bacterial infection sites using radiolabeled white blood cells.
  • Osteomyelitis imaging: assists in locating bone infection and assessing treatment response.
  • Fever of unknown origin: helps identify occult infectious foci when conventional tests are inconclusive.
  • Inflammatory disease imaging: highlights active inflammatory lesions in conditions such as vasculitis or sarcoidosis.

How It Works

  • Exametazime penetrates leukocyte membranes and binds intracellular components, allowing the cells to be labeled with a technetium‑99m radionuclide. After intravenous administration, the labeled leukocytes migrate to areas of active infection or inflammation, where they emit gamma radiation detectable by SPECT imaging, thereby localizing pathological sites.

Side Effects

Adverse reactions may occur following intravenous administration of Exametazime‑labeled leukocytes.

Common Side Effects

  • Nausea: mild, transient feeling of stomach upset.
  • Headache: occasional mild to moderate intensity.
  • Injection site pain: brief discomfort at the infusion site.
  • Flushing: transient warmth or redness of the skin.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure that may cause dizziness or fainting.
  • Pulmonary embolism: rare clot formation in the lungs associated with radiolabeled cell aggregates.

Precautions & Warnings

Use of Medi-Exametazim requires careful assessment of patient-specific factors and handling requirements.

  • Pregnancy: safety not established; avoid unless benefits outweigh potential risks.
  • Breastfeeding: unknown excretion in milk; consider discontinuation of nursing.
  • Renal impairment: monitor as altered clearance may affect image quality.
  • Concurrent immunosuppressive therapy: may reduce leukocyte labeling efficiency.
  • Known hypersensitivity to radiopharmaceutical components: assess risk before administration.

Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Exametazime may interact with other agents that affect leukocyte function or radiation exposure.

Major Interactions (Avoid)

  • Concurrent radiolabeled leukocyte agents: may cause overlapping radiation dose.
  • High‑dose corticosteroids: can suppress leukocyte labeling and reduce imaging sensitivity.
  • Chemotherapeutic drugs causing leukopenia: diminish available leukocytes for labeling.

Moderate Interactions (Monitor Closely)

  • Anticoagulants: may alter vascular imaging interpretation.
  • Beta‑blockers: could mask cardiovascular side effects of the radiotracer.

Frequently Asked Questions

Medi-Exametazim is a radiopharmaceutical used to label white blood cells for SPECT imaging, helping clinicians locate sites of infection, osteomyelitis, fever of unknown origin, and other inflammatory conditions.

Exametazime penetrates leukocyte membranes and binds intracellular components, allowing the cells to be tagged with technetium‑99m. The labeled cells travel to infection or inflammation sites, where their gamma emissions are captured by imaging equipment.

The dose of Medi-Exametazim is determined by the prescribing physician based on the specific imaging protocol, patient weight, and clinical indication. No fixed regimen is provided here.

Safety data for Exametazime in pregnancy and lactation are limited. It should only be used if the potential diagnostic benefit justifies any possible risk to the fetus or infant, and under close medical supervision.

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 and required import documentation.

Compared with non‑radiolabeled alternatives, Exametazime‑labeled leukocytes provide high specificity for active infection and inflammation, offering superior lesion localization in complex cases such as osteomyelitis, though they require specialized handling and imaging facilities.

The product must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. Use aseptic technique during preparation and administer promptly after reconstitution.

Medi-Exametazim is administered intravenously by a qualified healthcare professional. The radiolabeled leukocyte preparation is injected into a peripheral vein, followed by a waiting period before imaging to allow cell migration.

Serious risks include severe allergic reactions such as anaphylaxis, marked hypotension, and rare events like pulmonary embolism. Immediate medical attention is required if any of these symptoms occur.

Patients with known hypersensitivity to Exametazime or any component of the radiopharmaceutical, those with severe uncontrolled hypertension, or individuals who cannot safely undergo nuclear imaging should avoid this product.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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