Finished product reference
Rhenium (Sup186/Supre) Etidronic Acid
Injection, Solution · Parenteral · 80 mCi
- List code
- 51099
- Pharmacologic class
- Therapeutic radiopharmaceutical (bone-seeking; rhenium-186 etidronate)
What it is and how it works
Rhenium-186 etidronate (186Re-HEDP) is a phosphonate complex that localises in bone at sites of increased osteoblastic activity, such as skeletal metastases. Rhenium-186 emits beta particles that irradiate the metastatic sites and gamma photons that allow imaging; its half-life is about 3.7 days.
Indications
Palliation of pain from osteoblastic bone metastases (e.g. prostate and breast cancer) confirmed by bone scintigraphy.
Dosage and administration (summary)
Dosing is individualised by the nuclear medicine specialist according to protocol; given as a single slow intravenous injection, which may be repeated after haematological recovery.
Contraindications
Pregnancy and breast-feeding, severe bone marrow suppression, severe renal impairment and spinal cord compression or pathological fractures requiring other treatment.
Warnings and precautions
Causes transient myelosuppression (mainly thrombocytopenia), so monitor blood counts for several weeks; a transient flare of bone pain may occur. Patients should be well hydrated and empty the bladder frequently to reduce radiation dose; radiation-protection measures apply.
Pregnancy
Therapeutic radiopharmaceuticals are contraindicated in pregnancy; pregnancy must be excluded before administration.
Storage and supply
Store in appropriate lead shielding in accordance with national regulations for radioactive materials and the manufacturer’s instructions; use within the stated shelf-life after calibration.
Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.
Other presentations of the same active ingredient
Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.
Tell us the quantity, the market and the timing.
Send the molecule or ingredient, the specification and the destination. We reply from Tehran with the questions, the documents and the next step.