Finished product reference

Insulin Biphasic Lispro 50/50

Injection, Suspension · Parenteral · 100 IU/1mL · 3 mL

List code
52207
Pharmacologic class
Biphasic rapid-acting insulin analogue (insulin lispro 25% / insulin lispro protamine 75%)

What it is and how it works

A premixed suspension containing 25% soluble insulin lispro for rapid prandial action and 75% insulin lispro protamine for intermediate-acting basal cover. Insulin lowers blood glucose by stimulating peripheral glucose uptake in muscle and fat and inhibiting hepatic glucose output.

Indications

Diabetes mellitus requiring insulin treatment.

Dosage and administration (summary)

Subcutaneous injection, usually twice daily immediately before (within 15 minutes of) meals; dose individualised according to blood glucose monitoring. Must not be given intravenously.

Contraindications

Hypoglycaemia; hypersensitivity to insulin lispro or excipients.

Warnings and precautions

Hypoglycaemia is the main risk, especially with missed meals, exercise or dose errors. Resuspend by gentle rolling before use; rotate injection sites to avoid lipodystrophy. Hypokalaemia and fluid retention (with pioglitazone) may occur.

Pregnancy

May be used in pregnancy with close glucose monitoring; insulin requirements change across trimesters.

Storage and supply

Unopened: 2–8 °C refrigerated, do not freeze, protect from light; in-use pen may be kept below 30 °C for up to 28 days.

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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