Finished product reference
Rhenium (188re) Sulfide Colloid
Injection, Suspension · Parenteral · 10 mCi
- List code
- 52642
- Pharmacologic class
- Therapeutic radiopharmaceutical (rhenium-188 colloid)
What it is and how it works
Rhenium-188 sulfide colloid consists of particles labelled with rhenium-188, a beta and gamma emitter with a half-life of about 17 hours. After intra-articular injection the particles are phagocytosed by synovial cells, and the beta radiation ablates inflamed synovium (radiosynoviorthesis).
Indications
Radiosynovectomy of joints with chronic synovitis (e.g. rheumatoid arthritis, haemophilic arthropathy) unresponsive to conventional therapy; investigational and local uses include other locoregional therapies.
Dosage and administration (summary)
Dosing is individualised by the nuclear medicine specialist according to protocol and joint size; given by intra-articular injection under aseptic conditions, often with imaging guidance.
Contraindications
Pregnancy and breast-feeding, local infection or skin lesion at the injection site, ruptured Baker’s cyst and extensive joint destruction with bone loss.
Warnings and precautions
Extra-articular leakage may cause radiation necrosis of tissue; the joint should be immobilised for about 48 hours after injection to reduce leakage. Radiation-protection measures are required.
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.
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