Finished product reference

Phosphorous [32p] Chromic Phosphate Colloid

Injection, Solution · Parenteral · 5 mCi

List code
50196
Pharmacologic class
Therapeutic radiopharmaceutical (beta-emitting colloid)

What it is and how it works

Chromic phosphate P 32 is an insoluble colloidal suspension that, when instilled into a body cavity or joint, is phagocytosed and distributed over serosal or synovial surfaces. Phosphorus-32 emits pure beta radiation (mean tissue range a few millimetres, half-life about 14.3 days), delivering local radiation that causes fibrosis and destruction of superficial tumour cells or inflamed synovium.

Indications

Intracavitary (intraperitoneal or intrapleural) treatment of malignant effusions and as adjuvant therapy in selected ovarian cancers; radiosynovectomy in some chronic synovitis and haemophilic arthropathy settings.

Dosage and administration (summary)

Dosing is individualised: activity is determined by the nuclear medicine specialist according to the cavity or joint and protocol. For intracavitary or intra-articular use only; never given intravenously.

Contraindications

Intravenous administration, loculated cavities or evidence of poor distribution, large open wounds or communication with other cavities, and pregnancy.

Warnings and precautions

Correct intracavitary placement must be confirmed before administration, as leakage into the bowel wall or subcutaneous tissue may cause radiation necrosis and fibrosis. Bone marrow suppression may occur. Handle only by trained personnel under radiation protection regulations.

Pregnancy

Contraindicated.

Storage and supply

Store at room temperature in lead shielding in accordance with radiation protection regulations; use within the expiry period stated by the manufacturer.

Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.

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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