Active substanceDesogestrel + EthinylestradiolDesogestrel + Ethinylestradiol
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  • Dosage form: & nbspfilm-coated tablets
    Composition:

    Active substances: Ethinylestradiol 0.020 mg, desogestrel 0.150 mg;

    Excipients: dye quinoline yellow E 104, α-tocopherol, magnesium stearate, silicon colloidal dioxide, stearic acid, povidone, potato starch, lactose monohydrate;

    film sheath: propylene glycol, macrogol 6000, hypromellose.

    Description:

    Round, biconvex tablets of light yellow color with marking "P9" on one side and "RG" another.

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

    G.03.A.A   Progestogens and estrogens (fixed combinations)

    G.03.A.A.09   Desogestrel and ethinyl estradiol

    Pharmacodynamics:

    Novinet® is a combined oral contraceptive whose main contraceptive effect is inhibition of gonadotropin synthesis and suppression of ovulation. In addition, by increasing the viscosity of cervical mucus, the movement of spermatozoa through the cervical canal slows down, and a change in the state of the endometrium prevents the implantation of a fertilized egg. Ethinylestradiol is a synthetic analogue of endogenous estradiol, desogestrel has a pronounced gestagenic and antiestrogenic action, similar to endogenous progesterone, weak androgenic and anabolic activity. Novinet® has a beneficial effect on lipid metabolism: it increases the concentration of high-density lipoprotein (HDL) in the blood plasma, without affecting the content of low-density lipoprotein (LDL). Against the background of the use of the drug, there is a significant decrease in the amount of monthly lost blood (with the initial menorrhagia), the menstrual cycle is normalized, and a favorable effect on the skin is noted (especially with acne vulgaris).

    Pharmacokinetics:

    Desogestrel

    Suction

    When taken orally desogestrel is absorbed from the gastrointestinal tract (GIT) quickly and almost completely. Metabolised in 3-keto-desogestrel, which is a biologically active metabolite of desogestrel. Mean maximum serum concentration (FROMmax) 2 ng / ml, is achieved after 1.5 hours (TmOh) after taking the pill. Bioavailability of the drug is 62-81%.

    Distribution in the body

    3-keto-desogestrel binds to blood plasma proteins, mainly with albumins and with globulin binding sex hormones (SHBG). The volume of distribution is 1.5 l / kg.

    Metabolism

    In addition to 3-keto-desogestrel, which is formed in the liver and in the intestinal wall, other metabolites are formed: 3α-OH-desogestrel, 3β-OH-desogestrel, 3α-OH-5α-H-desogestrel (metabolites of the first phase). They do not have pharmacological activity and in part, by conjugation (the second phase of metabolism), they turn into polar metabolites (sulfates and glucuronates). Clearance from the blood plasma - about 2 ml / min per 1 kg of body weight.

    Excretion from the body

    The average half-life of 3-keto-desogestrel is 30 hours.Metabolites are excreted by the kidneys and through the intestine (in a ratio of 4: 6).

    Stable concentration is established by the second half of the cycle. At this time, the level of ketogestrel is increased by 2-3 times.

    Ethinylestradiol

    Suction

    Ethinyl estradiol is absorbed from the gastrointestinal tract quickly and completely. Mean maximum serum concentration (FROMmax) is 80 pg / ml - after 1-2 hours (Tmax) after taking the pill. Bioavailability due to presystemic conjugation and first-pass effect - about 60%.

    Distribution in the body

    Ethinyl estradiol completely binds to blood plasma proteins, mainly with albumins. The volume of distribution is 5 l / kg.

    Metabolism

    Pre-systemic conjugation of ethinyl estradiol is significant. Passing the intestinal wall (the first phase of metabolism), it undergoes conjugation in the liver (the second phase of metabolism). Ethinylestradiol and its conjugates of the first phase of metabolism (sulfates and glucuronides) are isolated in bile and enter enterohepatic circulation. Clearance from the blood plasma - about 5 ml / min per 1 kg of body weight.

    Isolation from the body

    The average half-life of ethinylestradiol is about 24 hours.About 40% is excreted by the kidneys and about 60% by the intestine.

    Stable concentration is established by 3-4 days, while the level of ethinyl estradiol in the serum is 30-40% higher than after a single dose

    Indications:

    Contraception.

    Contraindications:

    - Pregnancy or suspicion of it;

    - lactation;

    - presence of severe and / or multiple risk factors for venous or arterial thrombosis (including moderate or severe arterial hypertension with blood pressure of 160/100 mm Hg or more);

    - harbingers of thrombosis (including transient ischemic attack, angina pectoris), including in the anamnesis;

    - Migraine with focal neurologic symptoms, including in history;

    - venous or arterial thrombosis / embolism (including deep vein thrombosis tibia, pulmonary embolism, myocardial infarction, stroke) and currently anamnesis,

    - presence of venous thromboembolism in relatives;

    - diabetes mellitus (with the presence of angiopathy);

    - pancreatitis (including in the anamnesis), accompanied by severe hypertriglyceridemia;

    - dyslipidemia;

    - severe liver disease, cholestatic jaundice (including during pregnancy), hepatitis, incl. in the history (before normalization of functional and laboratory parameters and within three months after returning of these indicators in norm);

    - jaundice due to taking drugs containing steroids;

    - cholelithiasis at present or anamnesis;

    - Gilbert syndrome, Dubin-Johnson syndrome, Rotor syndrome;

    - liver tumors (including in the anamnesis);

    - severe itching, otosclerosis or progression of otosclerosis during a previous pregnancy or when taking glucocorticosteroids;

    - hormone-dependent malignant neoplasms of genital organs and mammary glands (including suspicion of them);

    - vaginal bleeding of unclear etiology;

    - Smoking over the age of 35 (more than 15 cigarettes a day);

    - individual hypersensitivity to the drug or its components.

    Carefully:

    Conditions that increase the risk of venous or arterial thrombosis / thromboembolism: age over 35 years, smoking, family history, obesity (body mass index more than 30 kg / m 2), dyslipoproteinemia, arterial hypertension, migraine, epilepsy, valvular heart disease, fibrillation atria, prolonged immobilization, extensive surgical intervention, surgical intervention on the lower extremities, severe trauma, varicose veins and superficial thrombophlebitis, postpartum period, presence of severe depression, incl.in the history, changes in biochemical parameters (resistance of activated protein C, hyperhomocysteinemia, deficiency of antithrombin III, deficiency of protein C or S, antiphospholipid antibodies, incl. antibodies to cardiolipin, lupus anticoagulant).

    Diabetes mellitus not complicated by vascular disorders, systemic lupus erythematosus (SLE), Crohn's disease, ulcerative colitis, sickle-cell anemia; hypertriglyceridemia (including in family history), acute and chronic liver disease.

    Pregnancy and lactation:

    The use of the drug during pregnancy and during breastfeeding is contraindicated.

    Dosing and Administration:

    Inside. Tablets are taken from the first day of the menstrual cycle and take 1 tablet a day for 21 days, if possible at the same time of day.

    After taking the last pill from the package, a 7-day break occurs, during which menstrual bleeding occurs due to withdrawal of the drug. The next day after a 7-day break (four weeks after taking the first tablet, on the same day of the week), the drug is resumed from the next package, also containing 21 tablets, even if the bleeding did not stop.Such a regimen of taking tablets is adhered to as long as there is a need for contraception. If the rules of admission are observed, the contraceptive effect is maintained even for a 7-day break.

    The first drug intake

    The first pill should be taken from the first day of the menstrual cycle. In this case, no additional methods of contraception are needed.

    You can start taking pills from the 2nd-5th day of menstruation, but in this case, in the first cycle of using the drug, you need to apply additional methods of contraception in the first 7 days of taking the tablets.

    If more than 5 days have passed since the onset of menstruation, it should be postponed the start of the drug until the next menstruation.

    Taking the drug after giving birth

    Non-breastfeeding women can start taking pills no earlier than 21 days after giving birth, after consulting with a doctor. In this case, there is no need to use other methods of contraception.

    If after the birth had already had sexual contact, then with taking the pills you need to wait until the first menstruation.

    If a decision is made to take the drug later than 21 days after the birth, then in the first 7 days it is necessary to use additional methods of contraception.

    Admission after abortion

    After abortion, in the absence of contraindications, the taking of tablets should begin from the first day, and in this case there is no need for additional methods of contraception.

    Transition from another oral contraceptive

    Taking Novinet® after using another hormonal oral contraceptive containing 30 μg of ethinylestradiol, according to the 21 day schedule: nThe first Novinet® tablet should be taken the day after the completion of the previous drug. It is not necessary to withstand a 7-day break or wait for the onset of menstruation. There is no need for additional methods of contraception.

    When switching to Novinet® from a drug containing 28 tablets, the next day after the tablets in the package have run out, start a new Novinet® package.

    Go to Novinet® after the use of oral hormone preparations containing only progestogen (the so-called "mini-pili"):

    The first tablet of Novinet® should be taken on the first day of the cycle. There is no need for additional methods of contraception.

    If there is no menstruation when taking a mini-drink,then after the exclusion of pregnancy, you can start taking Novinet® any day of the cycle, but in this case, additional methods of contraception must be used in the first 7 days.

    In the above cases, the following nonhormonal methods are recommended as additional methods of contraception: use cervical cap with spermicidal gel, condom, or abstinence from sexual intercourse. The use of the calendar method in these cases is not recommended.

    Delayed menstrual cycle

    If there is a need to delay menstruation, you should continue taking the pills from the new package, without a 7-day break, according to the usual scheme. When delaying menstruation, breakthrough or spotting bleeding may occur, but this does not reduce the contraceptive effect of the drug. Regular intake of Novinet® can be restored after an ordinary 7-day break.

    Missed tablets

    If the woman forgot to take the pill on time, and after the pass was passed no more than 12 hours, you just need to take a forgotten pill, and then continue the reception at the usual time.

    If between the reception of tablets passed more than 12 hours, this is considered a missing tablet, the reliability of contraception in this cycle is not guaranteed and the use of additional methods of contraception is recommended.

    If you miss one tablet on the first or second week of the cycle, you need to take 2 tablets the next day and then continue with regular reception, using additional contraceptive methods until the end of the cycle.

    If you miss a pill on the third week of the cycle, you must take a forgotten pill, continue with regular intake and do not take a 7-day break. It is important to remember that in connection with the minimal dose of estrogen, the risk of ovulation and / or bleeding is increased when a pill is missed and therefore additional methods of contraception are recommended.

    What should I do if I vomit or have diarrhea?

    If vomiting or diarrhea occurs after taking the drug, then the absorption of the drug may be inadequate. If the symptoms have stopped within 12 hours, then you need to take another pill in addition. After this, you should continue taking the tablets in the usual way. If symptoms continue for more than 12 hours, then additional methods of contraception should be used during vomiting or diarrhea and for the next 7 days.

    Side effects:

    Side effects, when the appearance of which requires immediate discontinuation of the drug:

    - arterial hypertension;

    - hemolytic-uremic syndrome;

    - porphyria;

    - loss of hearing due to otosclerosis.

    Rarely encountered: arterial and venous thromboembolism (including myocardial infarction, stroke, deep vein thrombosis of the lower extremities, thromboembolism of the pulmonary artery); exacerbation of reactive systemic lupus erythematosus.

    Very rare: arterial or venous thromboembolism of the hepatic, mesenteric, renal, retinal arteries and veins; Sydenham's chorea (passing after withdrawal of the drug).

    Other side effects, less severe, but more common. The expediency of continuing the use of the drug is decided individually after consultation with the doctor, based on the benefit / risk ratio.

    - Reproductive system: Acyclic bleeding / spotting from the vagina, amenorrhea after drug withdrawal, change in the state of vaginal mucus, the development of inflammatory processes of the vagina (eg: candidiasis).

    - Mammary gland: tension, pain, enlargement of the mammary glands, galactorrhea.

    - Gastrointestinal tract and hepatobiliary system: nausea, vomiting, Crohn's disease, ulcerative colitis, the appearance or exacerbation of jaundice and / or itching associated with cholestasis, cholelithiasis.

    - Leather: nodal / exudative erythema, rash, chloasma.

    - central nervous system: headache, migraine, mood changes, depressive states.

    - Metabolic disorders: fluid retention in the body, change (increase) in body weight, reduced tolerance to carbohydrates.

    - Eyes: increased sensitivity of the cornea when wearing contact lenses.

    - Other: allergic reactions

    Overdose:

    Possible nausea, vomiting, girls - spotting from the vagina.

    The drug does not have a specific antidote, the treatment is symptomatic.

    If overdose symptoms occur within the first 2-3 hours after taking the drug, gastric lavage is possible.

    Interaction:

    Drugs that induce hepatic enzymes, such as hydantoin, barbiturates, primidon, carbamazepine, rifampicin, oxcarbazepine, topiramate, felbamate, griseofulvin, Drugs containing St. John's wort reduce the effectiveness of oral contraceptives and increase the risk of bleeding "breakthrough".The maximum level of induction is usually achieved no earlier than 2-3 weeks, but can last up to 4 weeks after drug withdrawal.

    Ampicillin, tetracycline - reduce efficiency (the mechanism of interaction is not established).

    If it is necessary to share, it is recommended to use an additional barrier method of contraception throughout the course of treatment and for 7 days (for rifampicin - for 28 days) after drug withdrawal.

    Oral contraceptives can reduce tolerance to carbohydrates, increase the need for insulin or oral antidiabetics.

    Special instructions:

    Before starting the use of the drug and every 6 months thereafter, it is recommended to collect a detailed family and personal history and undergo a general medical and gynecological examination (gynecologist examination, cytological smear, breast examination and liver function, blood pressure control, blood cholesterol concentration, Analysis of urine). These studies need to be repeated periodically, due to the need for timely detection of risk factors or contraindications.

    The drug is a reliable contraceptive drug: the Perl index (the indicator of the number of pregnancies that occurred during the application of the method of contraception in 100 women for 1 year), when properly applied, is about 0.05.

    In each case, before the appointment of hormonal contraceptives individually evaluated the benefits or possible negative effects of their reception. This issue should be discussed with the patient, who after receiving the necessary information will make a final decision on the preferences of hormonal or some other method of contraception. The state of women's health must be carefully monitored.

    If during the reception of the drug appears or worsens any of the below listed conditions / diseases, you must stop taking the drug and go to another, non-hormonal method of contraception:

    - diseases of the hemostasis system;

    - conditions / diseases, predisposing to the development of cardiovascular, renal failure;

    - epilepsy;

    - migraine;

    - risk of developing an estrogen-dependent tumor or estrogen-dependent gynecological diseases;

    - diabetes mellitus not complicated by vascular disorders;

    - severe depression (if depression is associated with a violation of tryptophan metabolism, then for the purpose of correction, you can use vitamin B6);

    - sickle cell anemia, because in some cases (for example, infections, hypoxia), estrogen-containing drugs in this pathology can provoke thromboembolic events;

    - the appearance of abnormalities in laboratory tests assessing liver function.

    Thromboembolic diseases

    Epidemiological studies have shown that there is a link between the intake of oral hormonal contraceptives and an increased risk of arterial and venous thromboembolic diseases (including myocardial infarction, stroke, deep vein thrombosis of the lower limbs, pulmonary embolism). The increased risk of venous thromboembolic diseases has been proven, but it is significantly less than in pregnancy (60 cases per 100,000 pregnancies).

    When using oral contraceptives, arterial or venous thromboembolism of hepatic, mesenteric, renal vessels or retinal vessels is very rare.

    The risk of arterial or venous thromboembolic disease increases:

    - with age;

    - when smoking (intensive smoking and age over 35 are among the risk factors);

    - if there is a family history of thromboembolic diseases (for example, in parents, a brother or a sister). If you suspect a genetic predisposition, you must consult a specialist before using the drug.

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

    - with dyslipoproteinemia;

    - with arterial hypertension;

    - with diseases of the heart valves complicated by hemodynamic disorders;

    - with atrial fibrillation;

    - with diabetes mellitus, complicated by vascular lesions;

    - with prolonged immobilization, after a large surgical intervention, after surgery on the lower limbs, after severe trauma.

    In these cases, a temporary discontinuation of the drug is expected: it is advisable to discontinue no later than 4 weeks before the surgery, and resume not earlier than 2 weeks after remobilization.

    Increased risk of venous thromboembolic disease in women after childbirth.

    Diseases such as diabetes mellitus, systemic lupus erythematosis, hemolytic uremic syndrome, Crohn's disease, ulcerative colitis, sickle cell anemia, increase the risk of venous thromboembolic disease.

    Such biochemical abnormalities as resistance to activated protein C, giperhromotsisteinemiya, protein deficiency FROM, S, deficiency of antithrombin III, the presence of antiphospholipid antibodies, increase the risk of arterial or venous thromboembolic disease.

    When assessing the benefit / risk ratio of taking the drug, one should keep in mind that targeted treatment of this condition reduces the risk of thromboembolism.

    The signs of thromboembolism are:

    - sudden pain in the chest, which radiates into the left arm;

    - sudden shortness of breath;

    - Any unusually severe headache, which lasts a long time or appearing for the first time, especially when combined with a sudden complete or partial loss of vision, or diplopia, aphasia, dizziness, collapse, focal epilepsy), weakness or severe numbness in half of the body, movement disorders, severe unilateral pain gastrocnemius muscle, sharp abdomen).

    Tumor diseases

    Some studies have reported an increase in the incidence of cervical cancer in women who have been taking hormonal contraceptives for a long time, but the results of research are contradictory. In the development of cervical cancer, sexual behavior, infection with human papillomavirus and other factors play a significant role.

    A meta-analysis of 54 epidemiological studies showed that there is a relative increase in the risk of breast cancer among women taking oral hormonal contraceptives, but a higher detection of breast cancer could be associated with a more regular medical examination. Breast cancer is rare among women younger than 40, regardless of whether they take hormonal contraceptives or not, and increases with age. The intake of tablets can be regarded as one of many risk factors. Nevertheless, a woman should be informed about the possibility of a risk of developing breast cancer, based on an assessment of the relationship between benefit and risk (protection against ovarian cancer and endometrium).

    There are few reports of the development of a benign or malignant liver tumor in women who take long-term hormonal contraceptives. This should be borne in mind in the differential diagnosis of abdominal pain, which may be associated with an increase in liver size or intra-abdominal hemorrhage.

    A woman should be warned that the drug does not protect against HIV infection (AIDS) and other sexually transmitted diseases.

    The effectiveness of the drug may decrease in the following cases: missed tablets, vomiting and diarrhea, simultaneous use of other drugs that reduce the effectiveness of birth control pills.

    If the patient simultaneously takes another drug that may decrease the effectiveness of birth control pills, additional contraceptive methods should be used.

    The effectiveness of the drug may decrease if after several months of their application irregular, spotting or breakthrough bleeding occurs, in such cases it is advisable to continue taking the tablets before their end in the next package.If at the end of the second cycle menstrual bleeding does not begin or acyclic spotting does not stop, stop taking the pills and resume it only after the pregnancy is excluded.

    Chlazmy

    Chloasma can occasionally occur in women who have had a history in pregnancy. For women who are at risk of developing chloasma, avoid contact with sunlight or ultraviolet light while taking the tablets.

    Changes in laboratory indicators

    Under the influence of oral contraceptive pills, in connection with the estrogen component, the level of certain laboratory parameters (functional parameters of the liver, kidneys, adrenal glands, thyroid gland, hemostatic parameters, levels of lipoproteins and transport proteins) can vary.

    After acute viral hepatitis should be taken after the normalization of liver function (not earlier than 6 months).

    With diarrhea or intestinal disorders, vomiting contraceptive effect may decrease (without stopping the drug, it is necessary to use additional non-hormonal methods of contraception).

    Smoking women have an increased risk of developing vascular diseases with serious consequences (myocardial infarction, stroke).

    The risk depends on the age (especially in women older than 35 years) and on the number of cigarettes smoked.

    During lactation, milk production may decrease, in small amounts, the drug is excreted in breast milk.

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

    Studies to study the possible effects of the drug on the ability to drive a car or other mechanisms were not conducted.

    Form release / dosage:Tablets, film-coated, 150 μg + 20 μg.
    Packaging:

    21 tablet in a blister (Al / PVC / PVDC).

    1 or 3 blisters in a cardboard box with instructions for use.

    Storage conditions:

    At a temperature of 15-30 ° C.

    Keep out of the reach of children.

    Shelf life:

    3 years.

    Do not use after expiry date.

    Terms of leave from pharmacies:On prescription
    Registration number:П N014994 / 01
    Date of registration:10.10.2008
    Expiration Date:Unlimited
    The owner of the registration certificate:GEDEON RICHTER, OJSC GEDEON RICHTER, OJSC Hungary
    Manufacturer: & nbsp
    Representation: & nbspGEDEON RICHTER OJSC GEDEON RICHTER OJSC Hungary
    Information update date: & nbsp23.06.2018
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