Allergen from pollen dandelion medicinal for diagnosis and treatment (Allergena ex pollene toraxaci, platensium and cultorum oramimem pro diagnostica et curatione (Taraxacum officinale))

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Dosage form: & nbspsolution for cutaneous scarification, intradermal and subcutaneous administration
Composition:

Allergen is a water-salt extract of protein-polysaccharide complexes - 10000 PNU/ ml *, isolated from pollen of dandelion by drug extraction in a neutral phosphate-buffered saline solution.

Phosphate-buffered saline contains (in 1 ml): sodium chloride - 5.0 mg, sodium hydrogen phosphate dodecahydrate (equivalent to 0.56 mg sodium hydrophosphate) - 1.4 mg, potassium dihydrogen phosphate - 0.36 mg, phenol (preservative) 2.0-4.0 mg, water for injections - up to 1 ml. The concentration of these salts is calculated, in the finished product is not determined.

Note:

* PNU (protein N unit) - an international unit adopted to express the concentration of protein nitrogen in allergens, equal to the content of 1x10-5 mg of protein nitrogen.

In a set with an allergen, test-control and dilution fluids are produced.

Test-control liquid - phosphate buffered saline contains (in 1 ml): sodium chloride - 5.0 mg, sodium hydrophosphate dodecahydrate (equivalent to 0.56 mg sodium hydrophosphate) - 1.4 mg, potassium dihydrogen phosphate - 0.36 mg, phenol (preservative ) - 2,0-4,0 mg, water for injections - up to 1 ml.

Dilution liquid - phosphate buffered saline, in which polysorbate-80 is added, contains (in 1 ml): sodium chloride - 5.0 mg, sodium hydrophosphate dodecahydrate (equivalent to 0.56 mg sodium hydrophosphate) - 1.4 mg, potassium dihydrogen phosphate - 0,36 mg, phenol (preservative) - 2,0-4,0 mg, polysorbate-80 - 0,005 μl, water for injections - up to 1 ml.

Description:Allergen is a clear liquid from yellow to brown.
Test-control liquid and diluent fluid are colorless, clear liquids.
Pharmacotherapeutic group:MIBP is an allergen
ATX: & nbsp
  • Allergens of grass pollen
  • Pharmacodynamics:

    The main active principle of the allergen is the protein-polysaccharide complex, which makes it possible to diagnose a hypersensitivity to the dandelion of the medicinal pollen in the patient, and apply it to immunotherapy for pollinosis and atopic bronchial asthma.

    Indications:

    Specific diagnosis and specific immunotherapy of pollinosis and atopic bronchial asthma, caused by hypersensitivity to dandelion medicinal pollen.

    Indications for diagnosis are clinical manifestations of the disease and history data.

    Indications for specific immunotherapy are determined by the allergist doctor on the basis of the history, clinical manifestations of the disease, the results of skin testing, taking into account contraindications.

    Contraindications:

    In order to identify contraindications, the doctor on the day of setting allergic tests and on the day of specific immunotherapy conducts an examination of the patient.

    1. An aggravation of an allergic disease.

    2. Acute infection.

    3. Chronic diseases in the stage of exacerbation and / or decompensation.

    4. Immunodeficiency conditions.

    5. Autoimmune diseases.

    6. Tuberculosis of any localization in the period of exacerbation.

    7. Severe bronchial asthma, poorly controlled by pharmacological drugs (volume of forced expiration in 1 s less than 70% after adequate pharmacotherapy).

    8. Malignant neoplasms and blood diseases.

    9. Mental illness in the period of exacerbation.

    10. Systemic diseases of connective tissue.

    11. Children under 5 years of age (for specific immunotherapy); up to 6 months (for specific diagnostics).

    12. Pregnancy and lactation.

    13. Cardiovascular diseases, in which complications are possible when using adrenaline (epinephrine) (for specific immunotherapy).

    14. Severe form of atopic eczema (for specific immunotherapy).

    15. Therapy with β-adrenoblockers (for specific immunotherapy).

    16. Systemic glucocorticosteroid therapy, β-adrenomimetic therapy and antihistamines (for specific diagnostics).

    Pregnancy and lactation:

    Contraindicated.

    Dosing and Administration:

    I. Specific diagnostics

    The preparation is used for setting up skin tests (scarification, prik-test and intradermally). Specific diagnostics, as a rule, are carried out simultaneously with other pollen allergens. During one procedure, up to 15 samples with pollen allergens of various denominations are allowed to be carried out. For 2-3 days before the setting of skin tests, antihistamines should be canceled. With doubtful results of skin tests, they can be repeated two days after the local reaction to the previous samples subsided. In case of a positive result, skin tests with pollen allergens can be repeated no more than once a month.

    Setting scarification skin tests, prik-tests

    Scarification skin tests, prik-tests put on the inner surface of the forearm or, if necessary, on the skin of the back.

    Simultaneously with the allergen, dermal samples were made with a test-control fluid and with a 0.01% histamine solution, which was prepared by dilution 0.1% histamine dihydrochloride solution (1 part) of sodium chloride solution of 0.9% (9 parts), a positive reaction to which no less than "+" indicates the presence of sufficient skin reactivity. The diluted solution of histamine is suitable for 6 hours from the moment of preparation.

    The metal cap of the vials (with the allergen, test-control liquid) is rubbed with alcohol. Remove the central cap of the cap using a sterile forceps, and pierce the rubber stopper, pretreated with 70% ethyl alcohol, with a sterile needle.

    The skin of the inner surface of the forearm is wiped with 70% ethyl alcohol and allowed to dry. A drop of the tested allergen is applied to the disinfected skin using a sterile syringe, a drop of test-control fluid and a drop of 0.01% histamine solution at a distance (30 ± 10) mm from each other. Allergen, typed in a syringe, can not be poured back into the vial.

    When setting skarifikatsionnyh skin tests through drops of applied solutions with sterile scarifiers or injection needles, two parallel scratches with a length of 5 mm are applied.

    When prik-tests are applied through droplets of applied solutions with sterile injecting needles, shortened or with the depth stop of the prick or needles for prik-test (lancets), the skin is injected to a depth of 1.0-1.5 mm. When using injection needles, the skin is pierced at an angle of 45 ° so that blood does not protrude; then the needle is removed, slightly lifting the skin.

    After 15-20 minutes, sterile cotton swabs "drip" the drops of applied solutions at the site of scratches or puncture of the skin (a cotton swab should be separate for each drop of applied solutions) and take into account the skin reaction.

    Injection of intradermal samples

    Intradermal tests are set in cases where the scarification skin test gives a negative reaction, and the anamnesis is suspected of increased sensitivity to the dandelion drug, and / or if allergometric titration is necessary before the initiation of specific immunotherapy.

    Intradermal tests are performed on the inner surface of the forearm.The skin is pulled downward by moving the finger downwards, the needle is inserted at an angle of 15 ° to the surface of the skin, and it must be ensured that the needle hole is completely hidden in the epidermis, the needle must be thin with a short point.

    Sterile, individual for the allergen and test control fluid, marked syringes with a scale of 0.02 ml, strictly intracutaneously injected 0.02 ml of the allergen and test-control fluid, a sample with 0.01% histamine solution is put by the method of scarification. Allergen, typed in a syringe, can not be poured back into the vial.

    Evaluation of diagnostic skin tests

    The local skin reaction during the formulation of scarifying skin tests, prik-tests are taken into account after 15-20 minutes, intradermal tests - after 20 minutes in the absence of reaction to the test control fluid and in the presence of a positive sample for histamine (not less than "+") (Table. 1).

    Table 1. Scheme of accounting for scarification skin tests, prik-tests

    Evaluation of reaction

    Power manifestations reactions *

    The size and nature of the reaction

    Negative

    -

    Absence of blister (papules), hyperemia with dimensions both in control with test-control fluid

    Doubtful

    ±

    Absence of blister (papules), hyperemia with sizes exceeding those in control with test-control fluid

    Positive

    +

    Blister (papule) 2-3 mm, visible only when stretching the skin, hyperemia (for scarification tests);

    Blister (papule) 3-5 mm, visible only when stretching the skin, hyperemia (for prik-tests)

    Positive

    ++

    Blister (papule) 4-5 mm, hyperemia (for scarification tests);

    Blister (papule) 5-10 mm, hyperemia (for prik-tests)

    Positive

    +++

    Blister (papule) 6-10 mm, hyperemia or blister (papule) 6-10 mm with pseudopodia, hyperemia (for scarification tests); Blister (papule) 10-15 mm, hyperemia (for prik-tests)

    Positive

    ++++

    Blister (papule) more than 10 mm, hyperemia or blister (papule) more than 10 mm with pseudopodia, hyperemia (for scarification tests); Blister (papule) more than 15 mm with pseudopodia, hyperemia (for prik-tests)

    Scheme of recording intradermal samples

    Evaluation of reaction

    Power manifestations reactions *

    The size and nature of the reaction

    Negative

    -

    Absence of blister (papules), hyperemia with dimensions both in control with test-control fluid

    Doubtful

    ±

    Absence of blister (papules), hyperemia with sizes exceeding those in control with test-control fluid

    Positive

    +

    Blister (papule) 2-3 mm, visible only when stretching the skin, hyperemia (for scarification tests);

    Blister (papule) 3-5 mm, visible only when stretching the skin, hyperemia (for prik-tests)

    Positive

    ++

    Blister (papule) 4-5 mm, hyperemia (for scarification tests);

    Blister (papule) 5-10 mm, hyperemia (for prik-tests)

    Positive

    +++

    Blister (papule) 6-10 mm, hyperemia or blister (papule) 6-10 mm with pseudopodia, hyperemia (for scarification tests);

    Blister (papule) 10-15 mm, hyperemia (for prik-tests)

    Positive

    ++++

    Blister (papule) more than 10 mm, hyperemia or blister (papule) more than 10 mm with pseudopodia, hyperemia (for scarification tests);

    Blister (papule) more than 15 mm with pseudopodia, hyperemia (for prik-tests)

    Note:

    * Degree of severity of reaction:

    - Negative;

    ± Doubtful;

    + Weakly positive;

    ++ Positive;

    +++ Sharply positive;

    ++++ Very sharply positive.

    II. Specific immunotherapy

    Specific immunotherapy is carried out in those cases when it is impossible to exclude the contact of a sensitized patient with an allergen.

    Immunotherapy starts with a dose 10 times lower than the one that caused a minimal positive reaction with intradermal administration.

    Allergen for specific immunotherapy is administered subcutaneously.

    For the correct preparation and use of dilutions of the allergen with compliance with asepsis, the responsibility is borne by the allergist doctor.

    The dilutions of the drug, the volume administered (dose) and the recommended scheme of application are given in Table. 2.

    Table 2. An example scheme of specific immunotherapy in pollinosis

    Breeding allergen

    Dose (ml)

    Notes

    1

    2

    3

    10-5

    1:100000 0,1 PNU/ ml

    0,1

    0,2

    0,4

    0,8

    Specific immunotherapy begins after diagnosis of atopic disease no later than 3-4 months. before flowering and complete no later than 1,5 months. before the flowering of plants.

    Injections are made strictly subcutaneously in the region of the lower third of the shoulder. The first injection (when diluting the allergen 10-5, 10-4, 10-3) are doing daily or every other day, subsequent injections (dilutions of 10-2, 10-1) - with an interval of 7-10 days. The dose of the allergen is 0.9-1.0 ml in dilution 10-1 repeat with an interval of 5-7 days before the beginning of flowering of plants. The period of use of the allergen after its dilution is 1 month.

    After each injection of the patient's allergen, the patient is observed in the office for at least 60 minutes. The doctor notes the skin reaction at the site of the allergen injection and the general condition of the patient.

    Contraindication to increase the dose is a local reaction in the form of an infiltrate larger than 25 mm, arising during the day at the injection site, the general reaction of the body, exacerbation of the underlying disease. In these cases, the dose is reduced, the intervals between injections are extended until good tolerability is established.

    10-4

    1:10000 1,0 PNU/ ml

    0,1

    0,2

    0,4

    0,8

    10-3

    1:1000

    10 PNU/ ml

    odes

    0,2

    0,4

    0,8

    10-2

    1:100

    100 PNU/ ml

    0,1

    0,2

    0,3

    0,4

    0,5

    0,6

    0,7

    0,8

    0,9

    1,0

    10-1

    1:10

    1000 PNU/ ml

    0,1

    0,2

    0,3

    0,4

    0,5

    0,6

    0,7

    0,8

    0,9

    1,0

    Side effects:

    When introducing an allergen, local and general reactions are possible.

    In some cases, in highly sensitive patients with specific immunotherapy, an allergen may appear general reactions, which are manifested by symptoms of varying severity: from moderately expressed - coughing, sneezing, headache, urticaria, facial edema, conjunctivitis, rhinitis, bronchospasm, exacerbation of the underlying disease to anaphylactic shock in rare cases.

    Local Reactions expressed by education at the site of administration of edema, hyperemia.

    After each injection of the allergen, the patient should be observed by an allergist for at least 60 minutes. During this time the doctor should note the reaction of the skin to the administration of the drug and the general condition of the patient. On remote reactions the patient should inform the doctor.

    In the room where specific immunotherapy of patients is carried out, pharmacological preparations and tools for emergency care should be located.

    Overdose:

    If the prescribed dose is exceeded, the risk of side effects increases, which requires symptomatic treatment.

    Interaction:

    Skin tests and treatment with an allergen should be carried out not earlier than through:

    - 1 week after tuberculin test;

    - 1 month after vaccination with inactivated vaccines;

    - 3 months after vaccination with live vaccines (both viral and bacterial, including BCG vaccine).

    Do not use simultaneously with the use of β-blockers. Simultaneous reception of symptomatic drugs for the treatment of allergies is possible for better tolerability of ASIT (β2-adrenomimetikov, corticosteroids, inhibitors of degranulation of mast cells, if necessary later in the course of immunotherapy, it is possible to use H1antigistamines).

    It is possible to use other names simultaneously with pollen allergens.

    Special instructions:

    Precautions for use

    In particularly sensitive patients, a systemic allergic reaction and anaphylactic shock can occur. In this regard, in the office, where specific diagnostics and specific immunotherapy of patients are carried out, there should be pharmacological preparations and tools for emergency care.

    Assisting with general reactions and anaphylactic shock

    After the introduction of the allergen, symptoms of clinical manifestations of hypersensitivity to the allergen may develop. With parenteral administration of an allergen, it is possible to develop an immediate-type reaction, incl. anaphylaxis, which manifests itself in the form of urticaria and vascular edema, laryngeal edema, shortness of breath and suffocation. These symptoms often occur after feeling generalized itching, burning sensation, skin flushing, and a sense of fear of death.

    As a result of anaphylactic shock, non-occuring bronchospasm, asphyxia due to edema of the upper respiratory tract, and collapse can develop.

    In this case, urgent medical measures are required.

    Prehospital care for anaphylactic shock

    1. Immediately stop the introduction of the allergen that caused the reaction, put the patient on the couch (head below the legs), turn the head to the side, push the lower jaw, remove the existing dentures.

    2. Apply the tourniquet in place above the injection of the allergen, if possible.

    3. In finiteness, free from the tourniquet, add 0.3-0.5 ml of 0.1% adrenaline solution intramuscularly (IM) or intravenously (IV) (children 0.01 mg / kg, maximum to 0.3 mg ).If necessary, the administration of these doses is repeated at intervals of 10-20 minutes. The total dose of epinephrine should not exceed 1 ml of 0.1% solution. The multiplicity and dose of adrenaline administered depends on the severity of the shock and blood pressure. Repeated administration of small doses of epinephrine is more effective than single administration of a large dose.

    4. Finish the injection site with 0.3-0.5 ml of adrenaline solution (1 ml of 0.1% solution of epinephrine diluted in 3-5 ml of sodium chloride solution 0.9%).

    5. Apply an ice pack to the injection site.

    6. Provide access to fresh air or give oxygen. If the rhythm of breathing is disturbed or if it is difficult, perform artificial ventilation (IVL).

    7. Urgent call the doctor, simultaneously called the resuscitation team.

    Before the arrival of the resuscitation team, it is necessary to provide medical care and carry out constant monitoring of hemodynamic parameters and the state of the function of external respiration (FVD).

    Hospital care for anaphylactic shock

    1. In extremely serious condition of the patient and with severe hemodynamic disorders, 5 ml of 0.01% solution of epinephrine are injected slowly into IV, when the effect is achieved, the administration is stopped. Children 0,1 ml / kg 0,01% solution is injected slowly for several minutes.

    2. If blood pressure (BP) does not stabilize, urgently begin intravenous drip injection of norepinephrine (phenylephrine, dopamine) 0.2% 1.0-2.0 ml per 500 ml of 5% glucose solution for infusion or sodium chloride solution of 0.9%.

    3. Intravenously injected glucocorticosteroids: prednisolone - 60-180 mg (children 5 mg / kg) or dexamethasone - 8-20 mg (children 0,3-0,6 mg / kg), or hydrocortisone - 200-400 mg (children 4-8 mg / kg). As of the introduction of hormones, repeat and continue at least 4-6 days to prevent allergic reactions by immunocomplex or delayed type.

    4. Only with the stabilization of blood pressure intramuscularly enter 2.0 ml of a 2% solution of chloropyramine (children 6-12 months - 0.25 ml, 1-6 years - 0.5 ml, 7-18 years - 0.5-1.0 ml) or 0.1% clemastine (children 0,025 mg / kg / day for two injections).

    5. Symptomatic therapy according to indications. At bronhospazme 10.0 ml of a 2.4% solution of aminophylline on sodium chloride solution 0.9% (2-3 mg / kg for children) is injected intravenously. If necessary, enter cardiac glycosides, respiratory analeptics.

    6. If necessary, suck from the respiratory tract accumulated secret and vomit, begin oxygen therapy.

    7. In acute edema of the larynx, intubation or tracheotomy is indicated.

    All patients with anaphylactic shock are subject to compulsory admission for a period of at least 10 days in order to continue monitoring and treatment, In 2-5% of patients who have had anaphylactic shock, late allergic reactions are observed.

    Doses of drugs administered and the tactics of the doctor are determined by the clinical picture, but in all cases it is necessary, first of all, the introduction of adrenaline, glucocorticosteroid preparations. The administration of preparations of phenothiazine series and calcium preparations is contraindicated.

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

    Not studied.

    Form release / dosage:

    Solution for cutaneous scarification, intradermal and subcutaneous administration, 10000 PNU/ ml.

    Packaging:

    A solution for cutaneous scarification, intradermal and subcutaneous administration - 5.0 ml in the vial; test-control liquid - 4.5 ml in the vial; diluting liquid of 4.5 ml in a vial.

    Issued in the kit: 1 bottle of allergen, 7 bottles of dilution fluid, 1 bottle of test-control fluid, 1 empty sterile bottle in a pack of cardboard along with instructions for use.

    Storage conditions:

    AT According to JV 3.3.2.1248-03 in a place protected from light and inaccessible to children, at a temperature from 2 before 8 ° C.

    Freezing is not allowed.

    Shelf life:

    Allergen - 2 years, test-control and dilution of fluids - 5 years.

    The drug with expired shelf life is not subject to application.

    Terms of leave from pharmacies:On prescription
    Registration number:LS-000876
    Date of registration:11.09.2012 / 19.07.2013
    The owner of the registration certificate:MICROGEN FGUP Scientific and Production Association MICROGEN FGUP Scientific and Production Association Russia
    Manufacturer: & nbsp
    Representation: & nbspMICROGEN FGUP Scientific and Production Association MICROGEN FGUP Scientific and Production Association Russia
    Information update date: & nbsp10.03.2016
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