Finished product reference · In the Hanpars portfolio
Meglumine Compound
Injection · Parenteral · 66 %/10 % · 100 mL
- List code
- 798
- Pharmacologic class
- Ionic iodinated radiographic contrast medium (meglumine and sodium amidotrizoate/diatrizoate)
What it is and how it works
A mixture of the meglumine and sodium salts of amidotrizoic (diatrizoic) acid, a tri-iodinated benzoic acid derivative. The iodine atoms absorb X-rays, opacifying the vessels, body cavities or gastrointestinal tract into which the solution is introduced; it is excreted unchanged, mainly by the kidneys.
Indications
Injection: radiographic procedures such as urography, angiography and other contrast examinations. Oral/rectal solution: radiographic examination of the gastrointestinal tract, particularly when barium sulfate is contraindicated (e.g. suspected perforation).
Dosage and administration (summary)
Dose, concentration and route are individualised by the radiologist according to the examination and the patient’s age, weight and renal function.
Contraindications
Hypersensitivity to iodinated contrast media; manifest hyperthyroidism. The injection must not be given intrathecally.
Warnings and precautions
Hypersensitivity and anaphylactoid reactions may occur, so resuscitation facilities should be available; risk is higher with a history of asthma or previous contrast reaction. Contrast-induced nephropathy may occur, particularly in renal impairment, diabetes and dehydration; ensure adequate hydration. Oral use of the hyperosmolar solution can cause fluid shift and dehydration and, if aspirated, pulmonary oedema.
Pregnancy
Use only if essential; iodinated contrast may affect fetal thyroid function, so neonatal thyroid function should be checked after exposure.
Storage and supply
Store below 25 °C, protected from light and X-rays.
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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