Clinical and pharmacological group: & nbsp

Insulins

Included in the formulation
  • Humalog® Mix 25
    suspension PC 
    Eli Lilly East SA     Switzerland
  • Humalog® Mix 50
    suspension PC 
    Eli Lilly East SA     Switzerland
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    VED

    ONLS

    АТХ:

    A.10.A.B.04   Insulin LizPro

    Pharmacodynamics:

    The two-phase suspension consists of short-acting insulin analogues (lyspro 25%) and an average duration of action (lyspro protamine 75%), in molecules of which the reverse sequence of lysine and proline amino acid residues is observed at positions 29 and 28 of the B chain of insulin.

    Insulin lyspro soluble (25%) provides action for 15 minutes after administration.

    The protamine suspension of insulin lispro (75%) creates a depot under the skin with a slow release of insulin, which begins to act after 30 minutes and lasts for 15 hours.

    It interacts with insulin receptors of fat and muscle tissues, increasing intracellular transport of glucose, simultaneously inhibits the formation of glucose in the liver. Due to the assimilation of glucose by cells, a reduction in its level in the blood plasma is achieved.

    Pharmacokinetics:

    After subcutaneous administration 25% soluble insulin lyspro quickly absorbed from the subcutaneous tissue. The maximum concentration in the blood plasma is achieved after 0.5-2.5 hours.It is distributed unevenly in the tissues. It does not penetrate the placental barrier and into breast milk.

    The elimination half-life is 3-4 hours. The level of insulin in the blood plasma returns to the original in 8-9 hours. The duration of the action is about 15 hours.

    Indications:

    It is used for the treatment of diabetes mellitus I type, as well as II insulin-dependent type, in combination with oral hypoglycemic agents.

    IV.E10-E14.E11   Non-insulin-dependent diabetes mellitus

    IV.E10-E14.E10   Insulin-dependent diabetes mellitus

    Contraindications:

    Hypoglycemia, individual intolerance. The safety and effectiveness of the drug in patients under 18 years of age has not been studied.

    Carefully:

    Hypersensitivity.

    Pregnancy and lactation:

    Recommendations for FDA - Category B. It is used during pregnancy and lactation.

    Dosing and Administration:

    Subcutaneously, immediately before meals, or immediately after meals.

    The dose is calculated individually and depends on the concentration of glucose in the blood plasma. With diabetes mellitus II type recommended initial dose is 6 units before breakfast and 6 units before dinner in conjunction with metformin.Depending on the level of glucose in the blood plasma, the dose can be increased to 30 units per day for 2 or 3 injections.

    Side effects:

    Central and peripheral nervous system: rapid stabilization of blood glucose levels at the beginning of therapy can lead to acute pain neuropathy, which is transient.

    Dermatological reactions: lipodystrophy at the injection site.

    Sense organs: refractive disorders, decreased visual acuity - is also associated with the rapid stabilization of blood glucose at the beginning of therapy, is transient.

    Allergic reactions.

    Overdose:

    Very rarely - hypoglycemia. It develops in those cases when the administered dose of the drug exceeds its need.

    Treatment in mild form - ingestion of glucose (sugar, candy, sweet fruit juice).

    In severe hypoglycemia - intramuscular injection of glucagon in an amount of 0.5-1 mg. Intravenous - a solution of dextrose 40% in an amount corresponding to the injected insulin preparation.

    Interaction:

    Hypoglycemic action increases α- and β-adrenoblockers, salicylates, disopyramide, tetracyclines, monoamine oxidase inhibitors, ACE inhibitors, alcohol, sulfonamides, anabolic steroids.

    Weaken the action of insulin β-adrenomimetics, glucocorticoids, sympathomimetics, thiazide diuretics.

    Special instructions:

    The drug is not intended for intravenous administration. Insulin suspensions are not used in insulin pumps (pumps) for subcutaneous administration.

    Store the used syringe pen at room temperature. Unused syringe pen - in the refrigerator. The drug should be administered only after thoroughly mixing the contents of the syringe to a uniform whitish color.

    Intensive physical activity, as well as concomitant infectious and inflammatory processes require an additional amount of insulin.

    At the beginning It is not recommended to drive vehicles and work with moving mechanisms due to visual impairment. With constant intake of the drug should be careful in connection with the possible development of hypoglycemia.

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