Active substanceProcainProcain
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  • Dosage form: & nbspinjection
    Composition:

    1 ml of the preparation contains:

    active substance: Novocaine (procaine hydrochloride) 5.0 mg;

    Excipients: 0.1 M hydrochloric acid solution to pH from 3.8 to 4.5, water for injection to 1 ml.

    Description:

    A clear, colorless solution.

    Pharmacotherapeutic group:local anesthetic
    ATX: & nbsp

    N.01.B.A   Ethers of aminobenzoic acid

    N.01.B.A.02   Procain

    Pharmacodynamics:

    A local anesthetic with moderate anesthetic activity and a large breadth of therapeutic effect.Being a weak base, it blocks sodium channels, prevents the generation of pulses in the endings of the sensory nerves and impulses along nerve fibers. Changes the action potential in the membranes of nerve cells without a pronounced effect on the resting potential. Suppresses carrying out not only pain, but also impulses of another modality.

    With absorption and direct vascular injection into the blood flow reduces the excitability of peripheral cholinergic systems, reduces the formation and release of acetylcholine from preganglionic endings (possesses some ganglion-blocking action), eliminates spasm of smooth muscles, reduces the excitability of the myocardium and motor cortex areas of the brain.

    Eliminates the descending inhibitory effects of the reticular formation of the brain stem. Oppresses polysynaptic reflexes. In large doses can cause seizures. Has a short anesthetic activity (the duration of infiltration anesthesia is 0.5-1 h).

    Pharmacokinetics:

    It is subject to complete systemic absorption. The degree of absorption depends on the site and route of administration (especially on vascularization and blood flow velocity in the area of ​​administration) and the final dose (amount and concentration).It is rapidly hydrolyzed by plasma and liver esterases with the formation of two basic pharmacologically active metabolites: diethylaminoethanol (has a moderate vasodilating effect) and para-aminobenzoic acid (a competitive antagonist of sulfanilamide chemotherapeutic drugs and can weaken their antimicrobial effect). Half-life 30-50 s, in the neonatal period - 54-114 s. It is excreted mainly by kidneys in the form of metabolites, in unchanged form it is deduced no more than 2%.

    Indications:

    - Infiltration anesthesia;

    - vagosympathetic cervical, paranephalic, circular and paravertebral blockades.

    Contraindications:

    - Hypersensitivity (including para-aminobenzoic acid and other local anesthetic esters);

    - children's age till 12 years;

    - pronounced fibrotic changes in the tissues (for anesthesia using the creeping infiltrate method).

    Carefully:

    - Emergency operations, accompanied by acute blood loss;

    - conditions accompanied by a decrease in hepatic blood flow (eg, in chronic heart failure, liver disease);

    - progression of cardiovascular insufficiency (usually due to the development of heart block and shock);

    - inflammatory diseases or infection of the injection site;

    - Pseudocholinesterase deficiency;

    - kidney failure;

    - Children's age (from 12 to 18 years);

    - in elderly patients (over 65 years);

    - Weakened patients;

    - Pregnancy and the period of childbirth, lactation period.

    Pregnancy and lactation:

    Application in pregnancy and during lactation is possible in cases where the expected benefit to the mother exceeds the potential risk to the fetus or child.

    Dosing and Administration:

    For infiltration anesthesia, solutions of 2.5 mg / ml, 5 mg / ml; for anesthesia by the method of Vishnevsky (tight creeping infiltration) - solutions of 1.25 mg / ml, 2.5 mg / ml. To reduce the absorption and lengthening of the action with local anesthesia, an additional 0.1% solution of epinephrine is added, 1 drop per 2-5-10 ml of procaine solution.

    With paranephric blockade (according to AV Vishnevsky) 50-80 ml of a solution of 5 mg / ml or 100-150 ml of a solution of 2.5 mg / ml are injected into the peritoneal cellulose.

    With vagosympathetic blockade injected 30-100 ml of a solution of 2.5 mg / ml.

    For a circular or paravertebral block intradermally injected solution of 2.5 mg / ml or 5 mg / ml.

    Higher doses for infiltration anesthesia for adults: the first single dose at the beginning of the operation is not more than 500 ml of a solution of 2.5 mg / ml or 150 ml of a solution of 5 mg / ml. The maximum dose for use in children older than 12 years is 15 mg / kg.

    The procedure for working with a polymer ampoule:

    1. Take an ampoule and shake it, holding it by the neck.

    2. Press the ampoule with your hand, while the drug should not be isolated, and rotate and separate the valve with rotating movements.

    3. Through the formed hole, immediately connect the syringe with the ampoule.

    4. Turn the ampoule over and slowly put the contents into the syringe.

    5. Put the needle on the syringe.

    Side effects:

    Headache, dizziness, drowsiness, weakness, increase or decrease in blood pressure, collapse, peripheral vasodilation, bradycardia, arrhythmia, chest pain, trismus, tremor, visual and hearing impairment, nystagmus, persistent anesthesia, hypothermia, methemoglobinemia, allergic reactions up to anaphylactic shock).

    Overdose:

    Symptoms: pallor of the skin and mucous membranes, dizziness, nausea, vomiting, "cold" sweat, quickening of the breath, tachycardia, lowering of blood pressure, including collapse, apnea, methemoglobinemia.Action on the central nervous system is manifested by a feeling of fear, hallucinations, convulsions, motor excitement.

    Treatment: maintenance of adequate pulmonary ventilation, detoxification and symptomatic therapy.

    Interaction:

    Strengthens the depressing effect on the central nervous system of funds for general anesthesia, hypnotics and sedatives, narcotic analgesics and tranquilizers.

    Anticoagulants (ardeparin sodium, dalteparin sodium, sodium danaparoid, sodium enoxaparin, heparin sodium, warfarin) increase the risk of bleeding.

    When treating the site of injection of a local anesthetic with disinfectant solutions containing heavy metals, the risk of developing a local reaction in the form of tenderness and swelling increases.

    When used simultaneously with local anesthetic drugs for epidural anesthesia with guanadrel, guanethidine, mecamylamine, trimetaphan camsylate, the risk of a sharp decrease in blood pressure and bradycardia increases.

    Simultaneous use with monoamine oxidase inhibitors (furazolidone, procarbazine, selegiline) increases the risk of a pronounced decrease in blood pressure.

    Strengthens and prolongs the action of muscle relaxants.

    With the simultaneous use of procaine in conjunction with narcotic analgesics, an additive effect is noted, while respiratory depression is increased. Vasoconstrictors (epinephrine, methoxamine, phenylephrine) extend the local anesthetic effect.

    Procaine reduces the effect of antimiasthenic drugs, especially when used in high doses, which requires an additional correction of the treatment of myasthenia gravis.

    Cholinesterase inhibitors (antimiasthenic drugs, cyclophosphamide, democaria bromide, eco-iodide iodide, thiotepa) reduce the metabolism of procaine.

    Metabolite procaine (paraaminobenzoic acid) is a sulfonamide antagonist.

    Special instructions:

    During the treatment period it is necessary to monitor the functions of the cardiovascular, respiratory and central nervous systems.

    It is necessary to abolish monoamine oxidase inhibitors 10 days before the administration of procaine. Before use, it is recommended that samples be taken for individual sensitivity to the drug. It should be borne in mind that when conducting a local anesthesia with the same total dose, the toxicity of procaine is higher the more concentrated solution is used.

    Effect on the ability to drive transp. cf. and fur:

    During the period of treatment it is necessary to refrain from driving motor vehicles and practicing potentially dangerous activities that require an increased concentration of attention and speed of psychomotor reactions.

    Form release / dosage:

    Solution for injection, 5 mg / ml.

    Packaging:

    By 5 or 10 ml in polymer ampoules, manufactured by the technology "blow-fill-seal"" blow-fill-seal ".

    For 5 or 10 polymer ampoules, along with the instructions for medical use, put in a pack of cardboard.

    Storage conditions:

    In the dark place at a temperature of no higher than 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.

    Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-002112
    Date of registration:25.06.2013
    The owner of the registration certificate:SLAVYANSKAYA APTEKA, LLC SLAVYANSKAYA APTEKA, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp02.09.2015
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