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Method of treating chronic recurrent vulvovaginitis |
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IPC classes for russian patent Method of treating chronic recurrent vulvovaginitis (RU 2423978):
Method of treating nonspecific aerobic vaginitis / 2422147
Claimed is method of treating nonspecific aerobic vaginitis by vagina sanitation with medication "Bioprost" in dose 1 suppository per night for 10 days. Method ensures complex therapeutic effect due to anti-inflammatory action of pumpkin seed oil, improving vigaina microecology, and thymol, which suppresses development of Gram-positive, Gram-negative bacteria, fungi, and possesses activity with respect to protozoa and herpes virus.
Suppositories for treating proctologic and gynecologic diseases / 2421210
Invention refers to suppositories for treating proctologic and gynaecologic diseases. Said suppositories contain a drug in the form of the dehydrated preparation 'Baliz' or a power-predried form of the preparation 'Baliz', or an active substance pre-recovered from the preparation 'Baliz' in the form of comenic acid or its salts, and also a base representing fatty substances, and a food or medicinal emulsifier.
Method of treating urogenital infection of lower parts of genital tracts in women / 2420274
Invention relates to medicine, namely to gynecology, and can be used in treatment of urogenital infection of lower parts of genital tracts in women. For this purpose carried out are per oral antibiotic therapy and additional irrigation with oxygenated solution of antimicrobial preparations for 1-3 min in volume 50-100 ml. Course constitutes 1-2 procedures per day for 3-7 days.
Method of preventing endometritis after cesarean section / 2412729
Invention relates to medicine, namely to operational obstetrics, and can be used for prevention of endometritis after Cesarean section. For this purpose irrigation of vagina with 0.25% water solution of chlorhexidine bigluconate in amount 150-200 ml is carried out 1-1.5 h before operation of planned Cesarean section and during 3-5 days after operation 2 times per day in the morning and in the afternoon.
Composition and method to control and maintain bacterial microflora and acidity of vagina / 2409368
Invention relates to medicinal agents and to application of benzoic acid and/or its sodium salt in combination with saccharide (saccharides) as active components to make vaginal composition, to stimulate growing number of gram-positive bacilli and production of acids in vagina, in case gram-positive bacilli in vagina are scarce, and vagina acidity is far too weak, and to inhibit production of acids into vagina, in case of high number of gram-positive bacilli in vagina and excessive acidity of vagina, by maintenance of vaginal secretion pH value in the range from 3.5 to 4.5. Also vaginal composition is described, as well as method to control microflora and acidity of vagina.
Method for treatment of anogenital warts / 2404743
Invention relates to medicine, in particular to dermatovenerology and gynaecology and to treatment of anogenital warts. For this purpose 30% glicifon ointment is applied onto lesion foci. Ointment is applied daisy in a thin layer for 6-8 hours. Course of treatment is 5-14 days.
Pharmaceutical composition for treating urogenital infections / 2401102
Offered pharmaceutical composition for treating urogenital infections in a unit dosage form contains antiseptics, a biologically active additive, an ingredient for natural vaginal acidity, an antifungal agent, an anesthetic and a base. Even in minimum dosage, the pharmaceutical composition exhibits an effective action for treating urogenital infections since it has a wide spectrum of antimicrobial action, such as antiseptic and antifungal, removes painful symptoms of urogenital infections, normalises a disturbed microflora and ensures a regenerative effect.
Method of treating bacterial vaginosis / 2393870
Invention refers to medicine, particularly to gynecology, and concerns treating bacterial vaginosis. That is ensured by administration of a herbal tincture containing camomile flowers, pine buds, birch buds, celandine herb, bird cherry, oak bark and alder collective fruits at the equal ratio, dosed 250.0 ml once a day. Additionally, sterile tissues wetted in said tincture are introduced intravaginally. The therapeutic course is 20 days.
Method of acute bacterial vaginitis treatment / 2391977
Invention belongs to medicine, notably to gynaecology and dermatovenerology, and concerns treating of acute bacterial vaginitis. Before suppository insertion vagina must be treated with cotton or gauze pad soaked with 30-50 ml of Tantum Rosa solution. Vaginal suppository Bifilis must be inserted in the morning and midday, and suppository Syntomycin must be inserted in the evening. Course of treatment lasts 5-7 days.
Method of treating chronic recurrent urogenital bacterial and viral diseases / 2390339
Invention refers to medicine, particularly to gynaecology and urology, and concerns treating chronic recurrent urogenital bacterial and viral infections. That is ensured by producing lymphocyte self-cells of the patient's blood. Then said lymphocytes are cultivated with an immunomodulator. It is followed with intrauterine introduction of 0.5-2.0 ml of a lymphocyte suspension in an acceptable medium at their concentration 106-107 cel/ml.
New benzothiazolone derivatives / 2415136
Compounds of the invention exhibit properties of β2- adrenoreceptor agonists. In formula (I) , R1 represents hydrogen; each R2, R3, R4, R5, R4' and R5' independently represents hydrogen or C1-C6alkyd; e is equal to 0 or 1; A represents C(O); D represents oxygen or sulphur; m is equal to an integer 0 to 3; n is equal to an integer 0 to 3; R6 represents the group -(X)p-Y-(Z)q-R10; each X and Z independently represents C1-C6akylene group; each p and q is independently equal to 0 or 1; Y represents a bond, oxygen, CH2 or NR9; R7a and R7b independently represent hydrogen or C1-C6alkyl; R9 represents C1-C6alkyl; R10 represents hydrogen or saturated or unsaturated 6-members ring system optionally containing at least one ring heteroatom, chosen of nitrogen. And this ring system is optionally substituted by C1-C6alkoxycarbonyl; R7 represents 6-12-members aromatic ring system which is optionally substituted by halogen, trifluoromethyl, hydroxyl, C1-C6alkyl, C1-C6alkoxy or NH2; provided R6 does not represent hydrogen or unsubsituted C1-C6alkyl group. Also, the invention refers to methods for producing compounds of formula (I), to a pharmaceutical composition exhibiting properties of β2- adrenoreceptor agonists containing the compound of formula (I) as an active ingredient, to application of the compound of formula (I) in preparing a drug, to a combination containing the compound of formula (I) and one or more agents.
New cis-imidazolines / 2408593
Invention relates to compounds of formula I and its pharmaceutically acceptable salts. In formula (I) , R stands for 6-unit ring, containing one ore two heteroatoms of nitrogen, and substituted with group selected from the following groups: (lower)alkyl, -C(O)-R1, (lower)alkyl, substituted with group -SO2-(lower)alkyl, (lower)alkyl, substituted with group -C(O)-R1, -SO2-(lower)alkyl, or 5-unit saturated ring, containing one heteroatom of nitrogen, R1 is selected from group, including (lower)alkyl, -N((lower)alkyl)2, or R1 stands for 6-unit saturated ring, containing two heteroatoms, selected from N and O, X1 and X2 are independently selected from group, including hydrogen, (lower)alkoxy, each Y1 and Y2 are independently selected from group, including -Cl and -Br, and absolute stoichiometric configuration in position 4 and 5 imidazoline ring includes S and R configuration, accordingly. Invention also relates to pharmaceutical composition, having inhibiting activity regarding interaction of MDM2 - p-53, containing efficient amount of invention compound.
Modulators of alpha 7 nicotinic acetylcholine receptors alpha 7 and their therapeutic applications / 2403247
Claimed invention relates to compound of general formula (I) and its pharmaceutically acceptable salts. In general formula (I) , Y represents group -CONH(Q)- or -NHCONH(Q)-; Q represents 6-member aromatic ring or 5-10-member heteroaromatic ring, containing one or two N heteroatoms or two O heteroatoms; R represents hydrogen, halogen, linear or branched (C1-C6)alkyl; (C1-C6)alkoxy; di-(C1-C6)alkylamino, 5-member heteroaromatic ring, containing one O or S heteroatom; 6- or 9-member heteroaromatic ring, containing one or two N heteroatoms; phenyl, mono- or disubstituted with halogen, (C1-C6)alkyl, halogeno(C1-C6)alkyl, (C1-C6)alkoxy, acyl; hydroxy; piano; di-(C1-C6)alkylamino, acylamino' carbamoyl; X represents group : where Z represents CH2, N or O; m represents integer number from 1 to 3; p is equal 0, 1; R" is selected from group, consisting of di-( C1-C6)alkylaminocarbonyl, (C1-C6)alkyl, acyl. Invention also relates to pharmaceutical composition, containing as active ingredient, invention compound, to application of invention compound for manufacturing pharmaceutical composition, to method of inhibition of nicotinic acetylcholine receptor α7.
Anetholdithiolthiones and other dithiolthiones for treating conditions associated with monoamine neurotransmission dysfunction / 2402543
In embodiments of the invention, specific compounds are used to prepare a medicinal agent for treating, relieving and preventing conditions associated with dysfunction of monoamine transmission. The compounds have general formula (1) , where: R1 and R2 are identical or different and denote hydrogen, alkyl, alkenyl, alkynyl, aryl, thio or alkylthio, or R1 and R2 may have extra substitutes which are selected from hydrogen, alkyl, alkenyl, alkynyl, aryl, alkyloxy, morpholin-4-ylalkoxy, piperidin-1-ylalkyloxy, alkylamino, dialkylamino, arylamino.
3-ethylidenehydrazine-substituted heterocyclic compounds as thrombopoietin receptor activators / 2395505
Invention relates to compounds of formula (1), their tautomers and pharmaceutically acceptable salts. The disclosed compounds have thromobopoietin receptor agonist properties. In formula (1) , A is a nitrogen atom or CH, when A is a nitrogen atom, B is NR9 (where R9 is a C1-10 alkyl group), and when A is CH, B is a sulphur atom, R1 is a phenyl group (the phenyl group is substituted with one or more substitutes selected from a group consisting of halogen atoms, C1-10 alkyl groups and C1-10 alkoxy groups (C1-10 alkyl groups and C1-10 alkoxy groups are unsubstituted or substituted with one or more halogen atoms)), L1 is bond, X is OH, R2 is a C1-10 alkyl group, L2 is a bond, L3 is NH, L4 is a bond or NH, Y is a sulphur atom, and when L4 is a bond, R3 is a piperidinyl group, a piperazinyl group (the piperidinyl group and the piperazinyl group are substituted with substitutes selected from a group containing C1-10 alkoxycarbonyl groups, carboxyl group, hydroxyl groups, di-C1-10 alkylaminocarbonyl groups, C1-10 alkylaminocarbonyl groups and C1-10 alkyl groups (C1-10 alkylaminocarbonyl groups and C1-10 alkyl groups are substituted with a substitute selected from a group containing pyridyl groups, hydroxyl groups and carboxyl groups)), or when L4 is NH, R3 is a C1-10 alkyl group (C1-10 alkyl group is substituted with a substitute selected from a group containing C1-10 alkoxy groups, C1-10 alkoxycarbonyl groups or carboxyl groups).
3-carbamoyl-2-pyridone derivatives / 2392271
Invention refers to compounds of the formula (I): , where R1 is C1-C8alkyl optionally substituted with one to three substitutes selected out of substitute group A; R2 is C1-C6alkyl or C1-C6alkoxyC1-C6alkyl; R3 is C1-C6alkyl or C1-C6alkoxy; or R2 and R3 together with adjoining carbon atoms form optionally substituted non-aromatic 5-10-member carbon ring; R4 is hydrogen; G is group represented by the formula: or the rest as provided in the invention claim; and to pharmaceutical composition, application of claimed compounds, and method of atopic dermatitis prevention or treatment.
Novel cyclic derivative of aminobenzoic acid / 2391340
Present invention relates to cyclic derivatives of aminobenzoic acid and to their pharmaceutically acceptable salts of general formula , in which ring Ar is a phenyl group, a 5-member aromatic heterocyclic group containing 1-2 heteroatoms selected from nitrogen, sulphur and oxygen, or a benzothiazolyl group; where the said groups can have 1-2 substitutes selected from a group comprising lower alkyl; a phenyl group; a phenyl group substituted with 1-2 halogens; a phenyl group substituted with a lower alkoxy group; a phenyl group substituted with a halogen-substituted lower alkyl group; a phenoxy group substituted with a halogen; a halogen; Z is an oxygen atom or -(CH2)-n (where n equals 0, 1 or 2); Y is C1-C4 alkylene, C2-C4 alkenylene or general formula (2) -T-A-U- (2) in which T is a single bond, C1-C4 alkylene or C2-C4 alkenylene; U is single bond, C1-C4 alkylene; values of the rest of radicals are given in the formula of invention.
Novel piperidine-substituted diaminothiazoles / 2382784
Invention relates to compounds of formula and their pharmaceutically acceptable salts and esters. The disclosed compounds have cdk4 inhibition properties. In formula (I) n equals 0 or 1; R1 and R2 are each independently selected from a group consisting of H, lower alkyl, CO2R5, SO2R6 and COR6; or alternatively, R1 and R2 can form a ring containing 5-6 atoms in the ring, where the said ring contains carbon atoms, where the said carbon atoms are optionally substituted with oxygen, and the said atoms in the ring are optionally substituted with OR6; R3 is selected from a group consisting of H, lower alkyl, O-lower alkyl, halogen, OH, CN, NO2 and COOH; R4 is selected from a group consisting of H, lower alkyl, C3-C6-cycloalkyl, O-lower alkyl, halogen, NO2, S-lower alkyl, NR5R6, CONR7R8, OH and CN; or alternatively R3 and R4, together with two carbon atoms and the bond between them from the benzene ring, to which R3 and R4 are bonded, can form a ring containing 5-7 atoms, where the said 5-7-member ring contains carbon atoms, where the said carbon atoms are optionally substituted with one or two heteroatoms selected from O and N, and the said atoms in the ring are optionally substituted with CO2R6; R4 represents H or halogen; R5 and R6 are each independently selected from a group consisting of H and lower alkyl; R7 and R8 each represents H. The invention also relates to a pharmaceutical composition for treating or controlling diseases progression of which can be enhanced by inhibiting cdk4, containing an effective amount of the disclosed compound as an active ingredient, to use of disclosed compounds for preparing medicinal agents and method of producing said compounds.
Polyheterocyclic compounds and use thereof as metabotropic glutamate receptor antagonists / 2381226
Present invention relates to compounds of formula I and their pharmaceutically acceptable salts which have inhibitory properties towards mGluR5. In formula I , P represents phenyl; R1 is bonded to P through a carbon atom on ring P and is selected from a group consisting of halogen, C1-6alkylhalogen, OC1-6alkylhalogen, C1-6alkyl, OC1-6alkyl and C0-6alkylcyano; X1 is selected from a group consisting of N, NR4 and CR4; X2 is selected from a group consisting of C and N; X3 is selected from a group consisting of N and O; X4 is selected from a group consisting of N and O; X5 is selected from a group consisting of a bond, CR4R4', NR4, O, S, SO, SO2; X6 represents N; X7 is selected from a group consisting of C and N; Q represents triazolyl.
Chemical compounds i / 2381216
Invention relates to a novel compound N-(1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl) piperidin-4-yl]propyl}piperidin-4-yl)-N-ethyl-2-[4- (methylsufonyl)phenyl]acetamide or its pharmaceutically acceptable salts. The invention also relates to a method for synthesis of the compound in paragraph 1, as well as to a pharmaceutical composition.
Method for treatment of allergy by using substituted pyrazoles / 2259202
Invention relates to a method for treatment of patient suffering with allergic disease. Method involves administration to patient the therapeutically effective dose of pharmaceutical composition comprising compound of the formula (I)
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FIELD: medicine. SUBSTANCE: invention relates to medicine, namely to dermato-venerology and gynecology, and can be applied for treatment of chronic recurrent candidal vulvovaginitis. For this purpose together with antifungal medications inside prescribed is antihistaminic medication erius in day dose 5 mg for 10 days. Then, monthly 5 days before menstruation and during 5 days after it. After that, in pills in day dose 5 mg inside for 6 months. EFFECT: method insures adequacy and safety of therapy and makes it possible to reduce dosage of antifungal medications, quickly reduce disease symptoms and reduce of relapse frequency of recurrences. 3 ex
The invention relates to medicine, in particular to the gynecologist, and for the treatment of chronic recurrent chronic Candida vulvovaginitis. There is a method of treatment of vulvovaginal candidiasis in pregnant women by adjuvant therapy, including basic combo antimycotic drug and intravaginal introduction proteoliticeski immobilized enzyme - kasimasi at a dose of 5 ml (300 PE) in the 1st, 5th and 10th days of treatment [RF patent № 2262948 from 12.04.2004, IPC7AC 38/43, OR 43/00, publ. 27.10.2005 St]. As a result, through the full rehabilitation of the vagina decreases the number of complications during pregnancy, childbirth, postpartum and early neonatal periods. The disadvantage of this method is that it is recommended only for pregnant women. In addition, this method does not completely eliminate the fungal infection from the body and its application to chronic forms of the disease is not possible to achieve full cure and does not reduce the recurrence rate. There is a method of treatment of vulvovaginal candidiasis, including medication antifungal therapy, electrophoresis, zinc, prodigiozana, ultraviolet irradiation region of the perineum, in the beginning spend bipolar electrophoresis solutions of sulphate of zinc and prodigiozana for 15-20 min, after which the wasp is estlat ultraviolet irradiation of the perineum, and with 5-6 days before the procedure of electrophoresis carried out deep laser therapy by introducing the light of the nozzle into the vagina until it stops in the cervix, the course of treatment consists of 10 treatments carried out daily [description of the invention to the patent of Russian Federation № 2155613 from 08.07.1997, IPC7A61N 1/30, A61N 5/067, AK 33/30, AK 35/74, publ. 10.09.2000]. As a result, increases antimycotic effect of the treatment, reducing the rate antifungal therapy, increases the immunological reactivity of the organism and achieved long-term remission. The disadvantage of this method is the need for regular visits to health facilities and use of physiotherapy equipment. In addition, its disadvantage is its limited indications, because the success of it can be applied only for sexually active women. In the most General sense is a method of treatment of chronic vulvovaginal candidiasis includes vaginal douching solutions of antifungal substances in 3-5 days morning produce irrigation with 3%solution of protargol followed by the introduction of crushed tablets nystatin sprayed onto the wall of the vagina and its arches, and in the evening irrigation with 5%sodium bicarbonate, followed by the introduction of sodium tetraborate in glycerol [RF patent № 2113852 from 01.09.1994, IPC 6AC 33/38, AK 33/00, AK 35/70, A61N 5/06, AV 17/42, publ. 27.06.1998]. As a result, the background stimulation of nonspecific resistance of the organism is provided as a local treatment of vulvovaginal candidiasis. The disadvantage of this method is that in chronic forms of the disease local treatment is not always effective. In addition, this method allows to effectively treat acute exacerbation of chronic recurrent vulvovaginal candidiasis, but does not prevent the emergence of new relapses. The task of the invention is the efficiency of the treatment method, ensure the adequacy and safety of therapy at lower dosages of antifungal drugs, the rapid reduction of symptoms and reduce the frequency of relapses. To solve the problem and achieve the claimed technical effect in the treatment of chronic recurrent vulvovaginal candidiasis, including the oral use of antifungal drugs, together with anti-fungal prescribed drugs inside antihistamine drug Arius in a daily dose of 5 mg for 10 days, and then monthly for 5 days before menstruation and during 5 days after it, and then tablets in a daily dose of 5 mg orally for 6 months. Thus, the claimed ability is b the treatment of chronic recurrent vulvovaginal candidiasis involves the use of antifungal drugs type Fluconazol and/or Itraconazole, assigned based on the severity of the disease (relapse and their frequency, persistent option currents and other), the anatomical localization of infection (vagina, vulva, skin, etc. and in accordance with the sensitivity of isolates of Candida, in addition prescribe antihistamines drug Arius mainly third generation, in a daily dose of 5 mg, orally, for 10 days, and then monthly for 5 days before menstruation and for 5 days thereafter, in tablets, in a daily dose of 5 mg orally for 6 months. As anihistamines drug use desloratadin (Arius) (registration number P # 014704/02 07.09.2004) in the course dose of 350 mg Analyze the materiality of the features of the invention. Candida albicans is a powerful allergen (Moraes PS, de Lima Goiaba S, Taketomi EA. Candida albicans allergen immunotherapy in recurrent vaginal candidiasis // J Investig Aliegol Clin Lmmunol. - 2000/ - Vol.5, No. 10. - P.305-309), and suggested that local hypersensitivity to these yeast may be a factor in the prolongation and the recurrence of the disease. Colonization of Candida albicans in the vagina and the vulva supports mycotic sensitization of the body, helps hyperproductive Ig E and increases the willingness to giperergicakie reactions to damaging antigen. Elevated levels of total Ig E in blood and the presence of foci of fungal infection supports persistent, chronic Kida the dose candidiasis. For this reason, in addition to the recommended antifungal drugs type Fluconazol and/or Itraconazole recommended to administer antihistamines. Antihistamines new generation are divided into inactive metabolites (prodrugs) and pharmacologically active metabolites. Representatives of inactive metabolites - Bastin (kestin), acrivastine (semprex), loratadine (claritin, lomilan) are prodrugs, as the ingestion they become not only a pharmacologically active metabolites, but in the other metabolites, competing in the binding of H1-receptors. Therefore, they are non-competitive contact with H1receptors and in violation of the metabolism of these tools, especially when used concomitantly with other drugs, such as macrolides and antifungal agents, can accumulate and have undesirable side effects, in particular, to be present. Of particular importance are pharmacologically active metabolites cetirizine, Fexofenadine, desloratadine and levocetirizine. These drugs selectively associated with H1-receptors do not have competition for places on these receptors, their action does not depend on food intake or drugs, and therefore they are more effective, safe, predpochtitel the s. Among the products of a new generation of the most potent and selective antagonist of the N1receptor is desloratadin, as it has the greatest affinity for H1-rapeporn and longest half-life (27 hours). In controlled studies proved that the effect of the first dose of desloratadine in the morning lasts until the next morning. It acts quickly and extended, its effect does not depend on food intake or drugs, the absorbance decreases with the consumption of fatty food, taking antacids, the high content of salt in the diet. In addition to antihistaminic actions desloratadin also has anti-allergic and anti-inflammatory effects. Desloratadine inhibits the effects of many mediators involved in the development of allergic inflammation, including cytokines (TNFand, IL-3, IL-4, IL-8), chemokines, and intercellular adhesion molecules, including P-selectin and ICAM-1. Thus, the essence of the proposed invention is that to the basic therapy of chronic recurrent vulvovaginal candidiasis, including antimycotic drugs, joins an antihistamine, desloratadine (Arius) (registration number P # 014704/02 07.09.2004). Reception of desloratadine promotes rapid relief the main symptom is the disease: itching, burning sensation, swelling of the external genitalia. All patients with the use of desloratadine led to considerable improvement and to reduce the frequency of relapses during the year of follow up. In the first days of use of desloratadine in comparison with the control group received the recommended antimycotic therapy (40 observed patients received traditional treatment)were found to reduce itching, burning, swelling of the vulva, improve quality of life. The efficiency of this method was confirmed in 43 volunteers (women of reproductive age) in the age groups from 18 to 45 years, suffering from chronic recurrent vulvovaginal candidiasis from 1 year to 7 years. Example 1. Patient L., 32 years old, married, profession credit inspector came for a consultation with complaints cheesy discharge from the genital organs, expressed itching, burning, swelling of the vulva, frequent painful urination, irritability, poor sleep, decreased attention. Ill Candida vulvovaginitis about seven years. Onset links with the operational delivery by caesarean section. Exacerbation of the disease 10-11 times a year, often treated with oral antimycotics and local action. Index questionnaire William G. Crook [see adaskevich VP diagnostic industries, the ski indices in dermatology. - Moscow: a Medical book. - 2004, 165 S.] for patients with candidiasis 16 points. The General condition is satisfactory. Systolic blood pressure of 110 mm Hg, diastolic 60 mm Hg, heart rate of 78 beats per minute, satisfactory filling and tension. Objective examination: redness, swelling, white bloom and maceration of the labia, the vaginal mucosa, phenomena cervicitis, rich cheesy discharge. Microscopic examination of smears detected yeast. Microbiological study was identified Candida albicans at a concentration of 109COE/ml Diagnosis: Chronic recurrent vulvovaginal candidiasis in the acute stage. In General, the analysis of blood: b 128 g/l, er. of 4.2×1012/l; L 8,2-109/l 1%, P.60%, A%, limp. 30%, mon. 8%; ESR 10 mm/h in Serum IgE 110 (ke/l). Patients received comprehensive treatment of the proposed method with the purpose of desloratadine (Arius) in a daily dose of 5 mg, orally, for 10 days. At the end of treatment achieved clinical and microbiological cure. Over the next 6 months follow up, the patient courses were conducted preventive anti-relapse therapy Ericom tablets, orally, in a daily dose of 5 mg, on a monthly basis for 5 days before menstruation and for 5 days thereafter. Recurrence within 12 months was not observed. <> Example 2. Sick So 40 years old, married, by profession a teacher in the school. He complained of frequent painful urination, itching and burning in the genital area, dragging pain in the perineum, the impossibility of intimate relationships. Ill vulvovaginal candidiasis more than 5 years. Onset connects with antibiotics. Exacerbation of the disease last year, almost every month, mainly before or after menstruation. Repeatedly treated with oral antimycotics and local action. Index questionnaire William G. Crook for patients with candidiasis 18 points.The General condition is satisfactory. Systolic blood pressure 120 mm Hg, diastolic 70 mm Hg heart rate of 74 beats per minute, satisfactory filling and tension. Objective examination: redness and swelling of the openings of the urethra, labia minora, vulva and the vaginal mucosa, rich cheesy discharge. Microscopic examination of smears detected yeast. Microbiological study was identified Candida albicans at a concentration of 1010COE/ml Diagnosis: Chronic recurrent vulvovaginal candidiasis in the acute stage. Complete blood count: b 130 g/l, er. 4,0-1012/l; L 7,1 109/l, 4%, P.65%, A%, limp. 22%, mon. 8%, erythrocyte sedimentation rate of 12 mm/h in Serum IgE 80 (ke/l). Patients received a comprehensive treatment of marinatin techniques with simultaneous prescription of desloratadine (Arius) in a daily dose of 5 mg, inside, within 10 days. At the end of treatment achieved clinical and microbiological cure. Over the next six months follow up, the patient courses were conducted preventive anti-relapse therapy Ericom tablets, orally, in a daily dose of 5 mg, on a monthly basis for 5 days before menstruation and for 5 days thereafter. Clinical observation of the patient over 1 year acknowledged the absence of acute vulvovaginal candidiasis. Example 3. Patient W., 22 years old, single, student. He complained of cheesy discharge, itching and burning in the genital area, dragging pain in the abdomen, depressed, anxious mood because of illness, the impossibility of sexual life and sports. Ill Candida vulvovaginitis about 2 years. Disease associates with the beginning of sexual life. Exacerbation of the disease notes 6-7 times a year. Repeatedly treated with oral antimycotics and local action. Index questionnaire William G. Crook for patients with candidiasis 15 points. The General condition is satisfactory. Systolic blood pressure 120 mm Hg, diastolic 60 mm Hg heart rate of 70 beats per minute, satisfactory filling. Objective examination: redness and swelling of the mucous membrane of the vagina, cervix, labia, whitish plaque and the matzah is the situation of the vaginal mucosa, cervical, cheesy discharge. Microscopic examination of smears detected yeast. Microbiological study was identified Candida albicans at a concentration of 1010COE/ml Diagnosis: Chronic recurrent vulvovaginal candidiasis in the acute stage. Complete blood count: b 142 g/l, er. 4,4-1012/l; L 6,0-109/l, 2%, P.66%, A%, limp. 24%, mon. - 6%, erythrocyte sedimentation rate of 4 mm/h in Serum IgE 60 (ke/l). Patients received comprehensive treatment according to standard techniques with simultaneous appointment of ERISA in a daily dose of 5 mg, orally, for 10 days. At the end of treatment achieved clinical and microbiological cure. Over the next 6 months follow up, the patient courses were conducted preventive counter-recurrent therapy Ericom tablets, orally, in a daily dose of 5 mg, on a monthly basis for 5 days before menstruation and for 5 days thereafter. Recurrence was not observed for 1 year. Thus, the use of the proposed method has been able to reduce the dosage of antifungal drugs has improved the treatment efficiency rapidly decreased symptoms, a positive effect on psycho-emotional status of patients with chronic recurrent vulvovaginal candidiasis. Conducted preventive against the recurrent therapy Ericom extended periods of remission, improved the quality of life for this group of patients. A method for the treatment of chronic recurrent vulvovaginal candidiasis, including the oral use of antifungal agents, characterized in that together with anti-fungal prescribed drugs inside antihistamine drug Arius in a daily dose of 5 mg for 10 days, and then monthly for 5 days before menstruation and during 5 days after it, and then tablets in a daily dose of 5 mg orally for 6 months.
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