Active substanceDrospirenone + EthinylestradiolDrospirenone + Ethinylestradiol
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  • Dosage form: & nbspfilm-coated tablets
    Composition:

    1 tablet contains: active substances: drospirenone 3.00 mg, ethinyl estradiol 0.03 mg;

    auxiliary substances (core): lactose monohydrate 43.370 * mg, corn starch 12.80 mg, pregelatinized starch 15.40 mg, povidone-K25 3.40 mg, croscarmellose sodium 1.60 mg, magnesium stearate 0.40 mg;

    auxiliary substances (shell): Fade yellow 03B38204 2.00 mg (hypromellose-6cR 62.50%, titanium dioxide 29.50%, macrogol-400 6.25%, iron-oxide dye yellow 1.75%).

    * - the amount of lactose monohydrate may vary depending on the purity of the substance of the active substances.

    Description:

    Round biconvex tablets covered with a film coating of light yellow color, marked "D3" on one side of an embossed tablet. On the cross section, the core of the tablet is from white to almost white.

    Pharmacotherapeutic group:Contraceptive agent combined (estrogen + progestogen)
    ATX: & nbsp

    G.03.A.A.12   Drospirenone and ethinylestradiol

    Pharmacodynamics:

    MODEL PRO is a low-dose combined monophasic oral hormonal contraceptive containing ethinyl estradiol and drospirenone. The contraceptive effect of MODEL PRO is mainly carried out by suppressing ovulation, increasing the viscosity of the secretion of the cervix and changing the endometrium. In women taking combined oral contraceptives (COCs), the menstrual cycle becomes more regular, less painful menstruation is observed, menstrual bleeding is less frequent, and the risk of iron deficiency anemia is reduced.Besides, there is evidence of a reduced risk of developing endometrial cancer and ovarian cancer.

    Drospirenone contained in the MODEL PRO preparation has an antimineralocorticoid action and is able to prevent weight gain and other symptoms (for example, peripheral edema) associated with hormone-dependent fluid retention. Drospirenone also has anti-androgenic activity and helps reduce acne (acne), oiliness of the skin and hair. This action of drospirenone is similar to the action of natural progesterone, produced in the female body. This should be considered when choosing a contraceptive, especially for women with hormone-dependent fluid retention, as well as women with acne and seborrhea.

    When used correctly, Perl's index (the indicator reflecting the number of pregnancies in 100 women who use the contraceptive during the year) is less than 1. When missing tablets or improperly used, the Pearl index may increase.

    Pharmacokinetics:

    Drospirenone

    Suction. After ingestion drospirenone quickly and almost completely absorbed from the gastrointestinal tract.After a single dose, the maximum concentration (CmOh) drospirenone in the blood plasma is achieved after 1-2 hours and is 37 ng / ml. The bioavailability of drospirenone is 76-85%. Eating does not affect its bioavailability.

    Distribution. After oral administration, there is a two-phase decrease in the concentration of drospirenone in the blood plasma.

    Drospirenone binds to serum albumin and is not bound by globulin binding to sex steroids (SHBG) or corticosteroid-binding globulin (CSG). Estradiol-induced increase in SHBG does not affect the binding of drospirenone to plasma proteins.

    During the cycle of taking the drug, the equilibrium concentration of drospirenone is reached in the second half of the cycle.

    A further increase in the concentration is observed after approximately 1-6 cycles of the drug intake, subsequent increase in the concentration is not observed.

    Metabolism. After ingestion, drospirenone is completely metabolized. Most metabolites in the plasma are represented by acid forms of drospirenone, which are formed without the participation of cytochrome P450 isoenzymes.

    Excretion. It is excreted as metabolites through the intestine and kidneys in a ratio of approximately 1.2: 1.4. The half-life (T1/2) metabolites is approximately 40 h.

    Renal failure. The equilibrium concentration of drospirenone in blood plasma in women with mild renal insufficiency (creatinine clearance 50-80 ml / min) is comparable to that of women with a normal function of the nights. In women with renal insufficiency of moderate severity (creatinine clearance 30-50 ml / min), the concentration of drospirenone in the blood plasma is on average 37% higher than in women with normal renal function.

    Violation of the function of the liver. In women with moderate impaired liver function (class B on the Child-Pugh scale), the area under the concentration-time curve (AUC) is comparable with the corresponding index in healthy women with close values ​​of CmOh in the phases of absorption and distribution. T1 / 2 drospirenone in patients with moderate impairment of liver function is 1.8 times higher than in healthy volunteers with preserved liver function.

    In patients with moderate impairment of liver function, a decrease in clearance of drospirenone by approximately 50% compared with women with preserved liver function was noted, and there was no difference in the potassium concentration in the blood plasma in the study groups.There was no change in potassium concentration even in the case of a combination of factors predisposing to its increase (concomitant diabetes mellitus or spironolactone treatment).

    Ethinylestradiol

    Suction. After taking the drug inside ethinyl estradiol quickly and completely absorbed from the gastrointestinal tract.

    FROMmOh in blood plasma is achieved after 1-2 hours and is 54-100 pg / ml. Ethinylestradiol is subjected to the effect of "first passage" through the liver, resulting in its bioavailability when ingested at an average of 60%.

    Distribution. The connection with blood plasma proteins (with albumin) is about 08%. Ethinylestradiol induces synthesis of SHBG.

    Reduction in concentration ethinyl estradiol and in blood plasma is biphasic in nature. The equilibrium concentration is established during the second half of the first cycle of drug administration.

    Metabolism. Ethinyl estradiol undergoes presystemic conjugation in the mucosa by race of the intestine and in the liver. The main pathway of metabolism is aromatic hydroxylation.

    Excretion. Ethinyl estradiol is excreted as metabolites by the kidneys and through the intestine in a ratio of approximately 4: 6.T1 / 2 metabolites about 24 h.

    Indications:

    - Contraception.

    Contraindications:

    - Thrombosis (venous and arterial) at present or in the anamnesis (including deep vein thrombosis, pulmonary embolism, myocardial infarction, cerebrovascular disorders);

    - conditions preceding thrombosis (including transient ischemic attacks, atrial fibrillation, angina) now or in the anamnesis;

    - identified acquired or hereditary predisposition to venous or arterial thrombosis, including resistance to activated protein C, deficiency of antithrombin III, deficiency of protein C, protein deficiency S, hyperhomocysteinemia, antibodies to phospholipids (antibodies to cardiolipin, lupus anticoagulant);

    - Migraine with focal neurologic symptoms at present or in the anamnesis;

    - diabetes mellitus with diabetic angiopathy;

    - Multiple or expressed risk factors for venous or arterial thrombosis (including complicated heart valve disease, atrial fibrillation, cerebrovascular or coronary artery disease, uncontrolled arterial hypertension, long immobilization, volumetric surgical intervention, operative interference on the lower extremities, extensive injuries, smoking over the age of 35, obesity and body mass index more than 30 kg / m2);

    - Pancreatitis with severe hypertriglyceridemia at present or in the anamnesis;

    - hepatic failure and severe liver disease (before the normalization of liver function);

    - liver tumors (benign or malignant) at present or in the anamnesis;

    - severe and / or acute renal failure;

    - identified hormone-dependent malignant diseases (including genitals or mammary glands) or suspected of them;

    - bleeding from the vagina of unknown origin;

    - pregnancy or suspected of it;

    - the period of breastfeeding;

    - hypersensitivity to the components of the drug;

    - hereditary lactose intolerance, lactase deficiency or glucose-galactose malabsorption.

    If any of the above diseases or conditions develop for the first time against the background of taking the drug, then it should be immediately canceled.

    Carefully:

    The ratio of potential risk to expected benefits should be assesseduse of MODEL PRO in each individual case in the presence of the following diseases / conditions and risk factors:

    - Risk factors for thrombosis and thromboembolism: smoking, obesity <30 kg / m2, dyslipoproteinemia, controlled arterial hypertension, migraine without focal neurological symptoms, uncomplicated heart valve defects, hereditary predisposition to thrombosis (thrombosis, myocardial infarction, or impaired cerebral circulation at a young age in any of the next of kin);

    - other diseases in which peripheral circulation disorders may occur: diabetes mellitus without diabetic angiopathy, systemic lupus erythematosus (SLE), hemolytic-uremic syndrome, Crohn's disease and ulcerative colitis, sickle cell anemia, phlebitis of superficial veins;

    - hereditary angioedema;

    - hypertriglyceridemia;

    - liver disease, not related to contraindications (see "Contraindications");

    - diseases that first appeared or worsened during pregnancy or against the background of previous reception of sex hormones (eg, jaundice and / or itching associated with cholestasis,cholelithiasis, otosclerosis with deterioration of hearing, porphyria. Herpes during the previous pregnancy, Sydenham's chorea);

    - the postpartum period.

    Pregnancy and lactation:

    Pregnancy. If the pregnancy is detected during the MODEL PRO treatment, the drug should be immediately discontinued. Extensive epidemiological studies did not reveal an increased risk of developmental defects in children born to women who received sex hormones before pregnancy, or teratogenicity in cases where sexual hormones were mistaken for early pregnancy.

    In animal studies, the effects of drospirenone and ethinylestradiol were related to their pharmacological action. In particular, in studies of reproductive toxicity, embryotoxic and fetotoxic effects were detected in animals, but these effects were considered to be related to the specificity of a particular animal species. At exposure levels in animals exceeding the corresponding levels in women taking drospirenone and ethinyl estradiol, there was an effect on sex differentiation of rat embryos, which was absent in small monkeys.According to the data obtained in animal studies, it is impossible to exclude the possibility of developing undesirable effects caused by the hormonal activity of the active substances in humans. However, the combined experience of the use of COC in pregnancy did not provide evidence of the development of unwanted effects in humans.

    Data on the results of the MODEL PRO treatment during pregnancy are limited, which does not allow us to draw any conclusions about the negative effect of the drug on pregnancy, fetal and newborn health. Currently, there are no significant epidemiological data.

    Breastfeeding period. The drug is contraindicated in the period of breastfeeding. It can reduce the amount of breast milk and change its composition, so its use is not recommended until the end of breastfeeding. A small amount of sex hormones and / or their metabolites can be excreted in milk, but there is no evidence of their negative impact on the health of the child.

    Dosing and Administration:

    Tablets should be taken orally in the order given on the package, every day at about the same time, with a small amount of water. Take 1 tablet continuously for 21 days.The taking of tablets from the next package begins after a 7-day break, during which menstrual-like bleeding (bleeding "cancellation") is usually observed. As a rule, it begins on the 2-3 day after the last pill and may not end before taking the tablets from the new package.

    The beginning of the drug MODELL PRO. If there is no reception of any hormonal contraceptives in the previous month, the MODEL PRO treatment begins on the 1st day of the menstrual cycle (ie, on the 1st day of menstrual bleeding). It is allowed to start taking the menstrual cycle on the 2nd-5th day, but in this case it is recommended to use the barrier method of contraception during the first 7 days of taking the tablets from the first package.

    The transition from other combined hormonal contraceptive drugs (COC, vaginal ring or contraceptive patch). It is preferable to start taking MODEL PRO on the next day after taking the last tablet from the previous package, but in any case not later than the next day after an ordinary 7-day break. Receiving MODEL PRO should begin on the day of removal of the vaginal ring or patch, but not later than the day when a new ring is to be inserted or a new patch is stuck.

    Transition from contraceptives containing only gestagens ("mini-pili", injectable forms, implant or intrauterine devices (IUDs) with controlled release of progestogen). You can go from "mini-drills" to taking MODEL PRO on any day (without a break), from the implant or the IUD - on the day they are removed, from the injection contraceptive - the day the next injection is to be taken. In all cases, it is necessary to use an additional barrier method of contraception during the first 7 days of taking the tablets.

    After abortion in the first trimester of pregnancy. You can start taking the drug immediately - on the day of abortion. If this condition is met, the woman does not need additional methods of contraception.

    After childbirth or abortion in II trimester of pregnancy. It is recommended to start taking the drug on days 21-28 after giving birth (if there is no breastfeeding) or abortion in the second trimester of pregnancy. If the reception is started later, it is necessary to use an additional barrier method of contraception during the first 7 days of taking the tablets. If sexual contact took place, before pregnancy MODEL PRO should be excluded pregnancy or it is necessary to wait for the first menstruation.

    Acceptance of missed tablets. If the delay in taking the drug was less than 12 hours, contraceptive protection does not decrease. A woman should take the pill as soon as possible, the next pill is taken at the usual time.

    If the delay in taking the drug is more than 12 hours, contraceptive protection can be reduced. The more pills are missed and the closer the pass to the 7-day break in taking pills, the more likely it is to become pregnant.

    In this case, you can follow the following two basic rules:

    - drug intake should never be interrupted for more than 7 days;

    - to achieve adequate suppression of the hypothalamic-pituitary-ovarian system, 7 days of continuous intake of tablets are required.

    Accordingly, if the delay in taking the tablets was more than 12 hours (the interval from the time of taking the last tablet is more than 36 hours), the woman should observe the following recommendations:

    The first week of taking the drug. It is necessary to take the last missed pill as soon as possible, as soon as a woman remembers it (even if you need to take two tablets at the same time). The next tablet is taken at the usual time.In addition, a barrier method of contraception (for example, a condom) should be used for the next 7 days. If sexual intercourse took place within a week before passing the pill, it is necessary to consider the likelihood of pregnancy.

    The second week of taking the drug. It is necessary to take the last missed pill as soon as possible, as soon as a woman remembers it (even if you need to take two tablets at the same time). The next tablet is taken at the usual time. Provided that the woman took the tablets correctly within 7 days preceding the first missed pill, there is no need for additional contraceptive measures. Otherwise, as well as when two or more tablets are missed, barrier methods of contraception (for example, a condom) should be used additionally within 7 days.

    The third week of taking the drug. The risk of pregnancy is increased because of the upcoming pause in taking pills. A woman should strictly adhere to one of the following two options. In this case, if within 7 days preceding the first missed tablet, the weight of the pill was taken correctly, there is no need to use additional contraceptive methods.Otherwise it is necessary to use the first of the following schemes and additionally use the barrier method of contraception (for example, a condom) for 7 days.

    - It is necessary to take the last missed pill as soon as possible, as soon as a woman remembers it (even if you need to take two tablets at the same time). The following tablets are taken at the usual time, until the tablets in the current packaging run out. The next package should be started immediately without interruption. Bleeding "cancellation" is unlikely until the second package ends, but there may be "spotting" spotting and "breakthrough" bleeding during taking the tablets.

    - You can also interrupt the taking of tablets from the current package, thus starting a 7-day break (including the day of skipping the tablets), and then start taking the tablets from the new package.

    If a woman misses taking pills, and then during a break in admission she does not have a bleeding "withdrawal", it is necessary to exclude pregnancy.

    Recommendations in case of occurrence of disorders from the gastrointestinal tract (GIT). In the case of severe gastrointestinal disorders (vomiting, diarrhea), absorption may be incomplete, therefore additional methods of contraception should be used.If vomiting occurs within 4 hours after taking the pill, recommendations should be followed when skipping tablets.

    Changing the day of the beginning of the menstrual cycle. In order to delay the onset of menstruation, it is necessary to continue taking the tablets from the new MODEL PRO package without a 7-day break. Tablets from a new package can be taken for as long as necessary, including until the packaging is finished. Against the background of taking the drug from the second package, it is possible "smearing" spotting from the vagina or "breakthrough" uterine bleeding. Resume regular reception MODEL PRO from the next package follows the usual 7-day break. In order to transfer the onset of menstruation on the next day of the week, the woman should shorten the nearest break in taking the tablets for the desired number of days. The shorter the interval, the higher the risk that it will not have the bleeding of "cancellation", and thereafter there will be "smears" and "breakthrough" bleeding during the second package (as well as in the case when it would like to delay the onset menses).

    Additional information for specific patient categories

    Use in children. The efficacy and safety of the drug as a contraceptive is studied in women of reproductive age. It is assumed that the efficacy and safety of the drug in post-pubertal age under 18 years are similar to those in women after 18 years of age. The use of the drug before menarche is not indicated.

    Application in the elderly. After the onset of menopause, the drug MODELL PPO not shown.

    Application for violations of the liver. Contraindicated the use of the drug in the presence at present or in history of severe liver disease (before the normalization of indicators of "liver" samples), the present or in the history of benign or malignant liver tumors.

    Use in cases of impaired renal function. Contraindicated use of the drug in acute renal failure and severe renal failure.

    Side effects:

    The following undesirable reactions were identified when the drug was used.

    System

    organ class

    Frequency of adverse reactions


    Often

    Infrequently

    Rarely


    1/100 - < 1/10

    ≥ 1/1000 -< 1/100

    ≥ 1/10000 -< 1/1000

    Immune system disorders



    Bronchial asthma
    Hypersensitivity reactions

    Disturbances from the nervous system

    Headache



    Disorders from the psyche

    Depressive mood

    Changing libido


    Hearing disorders



    Hearing loss

    Disorders from the vascular system

    Migraine

    Increased blood pressure
    Lowering blood pressure

    Thromboembolism

    Disorders from the gastrointestinal tract

    Nausea

    Vomiting

    Diarrhea


    Disturbances from the skin and subcutaneous tissue


    Acne

    Eczema

    Itching

    Nodular erythema Erythema multiforme

    Disorders from the reproductive system and breast

    Menstrual irregularities
    Acyclic bleeding
    Pain in the mammary glands
    Hypersensitivity of the breast
    Beli
    Candidiasis vulvovaginitis

    Breast Enlargement
    Vaginitis

    Discharge from the mammary glands

    Common violations


    Fluid retention Change in body weight


    The following serious adverse events were reported in women using COCs:

    - venous thromboembolism;

    - arterial thromboembolism;

    - Increase in blood pressure:

    - Liver tumors;

    - the appearance or deterioration of conditions, the relationship of which with the administration of COC has not been fully established: Crohn's disease, ulcerative colitis, epilepsy, migraine, uterine myoma, porphyria, systemic lupus erythematosus, herpes during previous pregnancy, Sydenham's chorea, haemolytic uremic syndrome, cholestatic jaundice ;

    - Chloasma.

    In women with hereditary angioedema, estrogen use may cause or aggravate its symptoms.

    Overdose:

    No serious violations were reported in case of an overdose. Based on experience with the use of COCs symptoms, which can be noted during an overdose: nausea, vomiting, "smearing" spotting from the vagina or metrorrhagia.

    Treatment: conduct symptomatic therapy. There is no specific antidote.
    Interaction:

    The interaction of oral contraceptives with other drugs can lead to "breakthrough" bleeding and / or a decrease in contraceptive reliability. Women taking these drugs should temporarily use barrier methods of contraception in addition to the MODEL PRO product or choose another method of contraception.

    Interactions that lead to a decrease in the effectiveness of MODEL PRO

    Influence on hepatic metabolism. The use of drugs that induce microsomal enzymes of the liver can lead to an increase in the clearance of sex hormones, which, in turn, can lead to "breakthrough" bleeding or a decrease in the reliability of contraception. Such medicines include phenytoin, barbiturates, primidon, carbamazepine, rifampicin, rifabutin, it is also possible oxcarbazepine, topiramate, felbamate, griseofulvin and preparations containing St. John's wort.

    During the administration of drugs that affect microsomal enzymes of the liver, and within 28 days after their withdrawal, the barrier method of contraception should be used additionally.

    HIV protease inhibitors (eg, ritonavir) and non-nucleoside reverse transcriptase inhibitors (eg, nevirapine) and their combinations also have the potential to affect hepatic metabolism.

    Effect on intestinal hepatic recirculation. Some antibiotics (for example, penicillins and tetracycline) can reduce the intestinal hepatic circulation of estrogens, thereby lowering the concentration of ethinylestradiol.

    During the reception of antibiotics (such as penicillins and tetracyclines) and within 7 days after their withdrawal, the barrier method of contraception should be used additionally. If the period of use of the barrier method of protection ends later than the tablets in the package, you need to go to the next MODEL PRO package without the usual break in taking the tablets.

    Other interactions

    The major metabolites of drospirenone are formed in the plasma without the involvement of the cytochrome P450 system. Therefore, the effect of inhibitors of the cytochrome P450 system on the metabolism of drospirenone is unlikely.

    COCs can affect the metabolism of other drugs, leading to an increase (for example, ciclosporin) or decrease (for example, lamotrigine) of their concentration in plasma and tissues.

    Based on interaction studies in vitro, as well as research on women volunteers taking omeprazole, simvastatin and midazolam. it was found that the effect of drospirenone at a dose of 3 mg on the metabolism of other drugs is unlikely.

    There is a theoretical possibility of increasing serum potassium concentration in women receiving MODEL PRO along with other drugs that can increase the serum potassium concentration.These drugs include angiotensin-converting enzyme inhibitors, angiotensin II receptor antagonists, some anti-inflammatory drugs, potassium-sparing diuretics, and aldosterone antagonists. However, in studies evaluating the interaction of drospirenone with angiotensin-converting enzyme inhibitors or indomethacin, there was no significant difference between serum potassium concentration in comparison with placebo.

    Special instructions:

    Before starting or resuming the use of MODEL PRO, it is necessary to familiarize yourself with the history of life, the family history of a woman, to conduct a thorough medical examination (including measurement of blood pressure, heart rate, body mass index) and gynecological examination, including breast examination and cytological examination of scrapings from the neck (test for Pap test), to exclude pregnancy. The volume of additional studies and the frequency of follow-up examinations are determined individually. Usually, follow-up examinations should be conducted at least once every 6 months.

    A woman should be informed that MODEL PRO does not protect against HIV infection (acquired immunodeficiency syndrome - AIDS) and other sexually transmitted diseases.

    If any of the conditions, diseases and risk factors identified below are present, careful consideration should be given to the potential risk and expected benefit of using COCs in each individual case and to discuss it with the woman before she decides to start taking the drug. With weighting, strengthening, or with the first manifestation of risk factors, it may be necessary to cancel the drug.

    Diseases of the cardiovascular system. The results of epidemiological studies indicate the existence of a relationship between the use of COCs and an increase in the incidence of venous and arterial thrombosis and thromboembolism, such as deep vein thrombosis, pulmonary embolism, myocardial infarction, cerebrovascular disease. These diseases are rare.

    The risk of developing venous thromboembolism (VTE) is maximal in the first year of taking such drugs. The increased risk is present after the initial use of COC or the resumption of the use of the same or different COCs (after a break between doses of 4 weeks or more).Data from a large prospective study with 3 groups of patients show that this increased risk is present mainly during the first 3 months.

    The overall risk of VTE in patients taking low-dose COCs (containing <50 μg ethinylestradiol) is 2-3 times higher than in non-pregnant patients who do not take COC, however this risk remains lower compared to the risk of VTE during pregnancy and childbirth. VTE can lead to death (in 1-2% of cases).

    VTE, manifested as deep vein thrombosis or pulmonary embolism, can develop with any COCs.

    Very rarely, when using COC, thrombosis occurs in other blood vessels, for example, liver, mesenteric, renal, cerebral veins and arteries or retinal vessels. A common opinion regarding the relationship between the occurrence of these events and the use of COC is absent. Symptoms of deep vein thrombosis (DVT) include: unilateral swelling of the lower limb or along the vein on the lower limb, pain or discomfort in the lower extremity only in the upright position or walking, local fever in the affected lower limb, redness or change the color of the skin on the lower limb.

    Symptoms of thromboembolism of the pulmonary artery (PE) are as follows: shortness of breath or rapid breathing; sudden cough, incl. with hemopoiesis; acute pain in the chest, which can increase with a deep breath; sense of anxiety; severe dizziness; rapid or irregular heartbeat. Some of these symptoms (eg, dyspnea, cough) are nonspecific and may be misinterpreted as symptoms of other more or less severe events (eg, respiratory tract infection).

    Arterial thromboembolism can lead to stroke, vascular occlusion or myocardial infarction. Symptoms of a stroke: sudden weakness or loss sensitivity of the face, limbs, especially on one side of the body, sudden confusion, problems with speech and understanding; sudden one- or two-sided loss of vision; sudden gait disturbance, dizziness, loss of balance or coordination of movements; sudden, severe or prolonged headache for no apparent reason; loss of consciousness or fainting with or without an epileptic seizure. Other signs of vascular occlusion: sudden pain, puffiness and weak blueing of the extremities, "sharp" abdomen.

    Symptoms of myocardial infarction include: pain; discomfort; feeling of pressure, gravity, a feeling of contraction or bursting in the chest, in the hand or behind the breastbone; discomfort in the left half of the chest with irradiation in the back, cheekbone, larynx, arm, epigastric region; cold sweats, nausea, vomiting or dizziness, severe weakness, anxiety, or shortness of breath; rapid or irregular heartbeat.

    Arterial thromboembolism can be fatal.

    The risk of developing thrombosis (venous and / or arterial) and thromboembolism increases:

    - with age;

    - for smokers (with an increase in the number of cigarettes or an increase in the age, the risk increases, especially in women over 35);

    - with obesity (body mass index more than 30 kg / m2);

    - in the presence of a family history (for example, venous or arterial thromboembolism ever at close relatives or parents at a relatively young age). In the case of a hereditary or acquired predisposition, a woman should be examined by an appropriate specialist to decide on the possibility of taking COC;

    - with prolonged immobilization, serious surgical intervention, any operation on the lower limbs or extensive trauma.In these situations, it is desirable to stop using COCs (in the case of a planned operation, at least four weeks before) and not to resume admission within two weeks after the end of immobilization;

    - with dyslipoproteinemia;

    - with arterial hypertension;

    - with migraine;

    - with diseases of the valvular heart;

    - with atrial fibrillation.

    The question of the possible role of varicose veins and superficial thrombophlebitis in the development of venous thromboembolism remains controversial. An increased risk of thromboembolism in the postpartum period should be considered.

    Violations of peripheral circulation can also occur in diabetes mellitus, SLE, hemolytic uremic syndrome, chronic inflammatory bowel disease (Crohn's disease or ulcerative colitis) and sickle cell anemia.

    An increase in the frequency and severity of migraine attacks during the use of COCs (which may precede cerebrovascular disorders) should be grounds for the immediate discontinuation of these medications.

    To biochemical indicators indicating a hereditary or acquired predisposition to venous or arterial thrombosis,include: resistance to activated protein C, hyperhomocysteinemia, insufficiency of antithrombin III, deficiency of protein C, protein deficiency S, presence of antibodies to phospholipids (antibodies to cardiolipin, lupus anticoagulant).

    When assessing the relationship between risk and benefit, it should be borne in mind that adequate treatment of the relevant condition can reduce the risk of thrombosis associated with it. It should also be taken into account that the risk of thrombosis and thromboembolism in pregnancy is higher than when taking low-dose COCs (containing less than 50 μg ethinyl estradiol). Drugs containing levonorgestrel, norgestimate or norethindrone. have a low risk of venous thromboembolism. In drugs that contain drospirenone, the risk of developing thromboembolic complications is 2 times higher, therefore, before the woman is recommended the drug MODEL PRO, she should be warned about this increased risk.

    Tumors. The most significant risk factor for developing cervical cancer is persistent papillomavirus infection. There are reports of a slight increase in the risk of developing cervical cancer with prolonged use of COCs.However, the connection with the reception of the COC has not been proven. Controversial data remain regarding the extent to which these data are associated with screening for the diagnosis of cervical pathology or with features of sexual behavior (the more rare use of barrier methods of contraception).

    A meta-analysis of 54 epidemiological studies has shown that there is a slightly increased relative risk of developing breast cancer diagnosed in women taking COCs at the present time (relative risk 1.24). The increased risk gradually disappears within 10 years after discontinuation of these medications. Due to the fact that breast cancer is rarely seen in women under 40 years of age, an increase in the number of diagnoses of breast cancer in women who are currently taking COCs or who have recently taken COC is insignificant in relation to the overall risk of this disease. The relationship between the development of breast cancer and the use of COC has not been proven. The observed increase in risk may also be due to careful follow-up and earlier diagnosis of breast cancer in women using COCs.Women who have ever used COC have earlier stages of breast cancer than women who have never used them.

    In rare cases, the development of benign, and extremely rare, malignant liver tumors, which in some cases led to life-threatening intraabdominal hemorrhage, was observed with the use of COCs. In the case of severe pain in the abdominal region, enlarged liver, or signs of intra-abdominal bleeding, this should be taken into account when making a differential diagnosis.

    Other condition. Clinical studies showed no effect of drospirenone on serum potassium concentration in patients with mild to moderate renal failure. Theoretically, there is a risk of developing hyperkalemia in patients with impaired renal function and the initial content of potassium at the upper limit of the norm or against the background of taking medications leading to a delay in potassium in the body.

    In women with hypertriglyceridemia (or in the presence of this condition in a family history), an increased risk of developing pancreatitis during COC administration is possible.Despite the fact that a small increase in blood pressure was described in many women taking COC, clinically significant hypertension was rare. Nevertheless, if a persistent, clinically significant increase in blood pressure develops during the administration of COC, these drugs should be discontinued and the treatment of hypertension should begin. The administration of COCs can be continued if normal values ​​are achieved with the help of antihypertensive therapy blood pressure.

    The following conditions have been reported to develop or worsen, both during pregnancy and when taking COC, but their relationship with COC use has not been proven: jaundice and / or pruritus associated with cholestasis; formation of stones in the gallbladder; porphyria; SLE; hemolytic-uremic syndrome; chorea; herpes pregnant; hearing loss associated with otosclerosis. Cases of Crohn's disease or ulcerative colitis are also described against the background of COC use.

    In women with hereditary forms of angioedema, exogenous estrogens can cause or worsen symptoms of angioedema.

    In acute or chronic violations of the liver, it may be necessary to cancel the drug until the liver function indicators return to normal.Recurrent cholestatic jaundice, which develops for the first time during pregnancy or previous admission of sex hormones, requires discontinuation of COCs.

    Although COCs may affect insulin resistance and glucose tolerance, there is no need to change the therapeutic regimen in diabetics using low-dose COCs (containing less than 50 μg ethinyl estradiol). Nevertheless, women with diabetes mellitus need careful monitoring of blood glucose concentrations during the application of the drug.

    When using the drug, it is possible to develop chloasma. especially in women with a history of pregnant chloasma. Women with a tendency to chloasma while taking COC should avoid prolonged exposure to the sun and exposure to ultraviolet radiation.

    The effectiveness of COCs can be reduced by missing tablets, vomiting and diarrhea, or as a result of drug interactions.

    Influence on the menstrual cycle. Against the background of the use of COC, irregular (acyclic) bleeding ("spotting" bleeding or "breakthrough" bleeding) can occur, especially during the first months of use.Therefore, any irregular bleeding should be assessed only after an adaptation period of approximately 3 cycles.

    If irregular bleeding recurs or develops after previous regular cycles, a thorough examination should be conducted to exclude malignant neoplasms or pregnancy.

    Some women during the break in taking pills may not develop a bleeding "cancellation". If the COC was administered in accordance with the directions, pregnancy is unlikely. Nevertheless, if before the reception of COC was carried out irregularly or if there are no consecutive two bleeding "cancellations", then the continuation of the drug should be excluded from pregnancy.

    Influence neither of the indicators of laboratory tests. Acceptance of COC can affect the results of some laboratory tests, including liver, kidney, thyroid, adrenal, transport protein in plasma, carbohydrate metabolism, coagulation and fibrinolysis parameters. Changes usually do not go beyond the limits of normal values. Drospirenone increases the activity of plasma renin and aldosterone, which is associated with its antimineralocorticoid effect.

    Effect on the ability to drive transp. cf. and fur:Studies to study the effect of the drug on the ability to drive vehicles and mechanisms were not conducted. There was no influence of the COC on the ability to drive vehicles and mechanisms.

    Form release / dosage:Tablets, film-coated 3 mg + 0.03 mg.

    Packaging:

    For 21 tablets in a blister of PVC / Aluminum foil. 1, 3 or 6 blisters together with instructions for use in a cardboard box.

    Storage conditions:

    Store at a temperature not exceeding 25 ° C.

    Keep out of the reach of children.

    Special precautions for the destruction of unused medications

    Special precautions for the destruction of unused drug ns required.

    Shelf life:

    3 years. Do not use after the expiration date.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-002882
    Date of registration:27.02.2015
    Expiration Date:27.02.2020
    The owner of the registration certificate:Teva Pharmaceutical Enterprises Co., Ltd.Teva Pharmaceutical Enterprises Co., Ltd. Israel
    Manufacturer: & nbsp
    Representation: & nbspTeva Teva Israel
    Information update date: & nbsp16.11.2017
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