Milife tablets 500 mg 30 pcs.

• chronic fatigue syndrome and immune dysfunction;
• complex therapy for the treatment of viral and toxic liver injury (including.
• complex therapy for the treatment of viral and toxic liver injury (including alcoholic genesis)
• complex therapy in the treatment of autoimmune diseases (autoimmune thyroiditis, diabetes);
• as a therapeutic and prophylactic agent for influenza, latent forms of herpes (6 types of herpes), chlamydial, ureaplasma infections;
• HIV and hepatitis C infections, as well as infections caused by yellow fever and malaria;
• Radiation and chemotherapy in cancer patients;
• Period of pre- and postoperative rehabilitation;
• neuroendocrine disorders (mastitis, ovarian dysfunction and cystic changes, uterine myoma, endometriosis, infertility);
• different manifestations of climacteric syndrome
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• to people engaged in physical education and sport (all ages – from junior to veteran) in training and competition cycles, as a means of increasing efficiency and increasing the fatigue threshold;
• rehabilitation of athletes after trauma and when leaving the “big” sport.

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Composition

One tablet contains: lactose monohydrate, 164.2 mg; strawberry leaf, 40 mg; grape leaf, 40mg; wheat starch 3.3 mg.

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How to take, the dosage

Tablets: sublingually (sucked up), after meals.

Capsules: orally, after meals.

Two dosages were developed during the study of the drug’s effect on the body systems and the body as a whole:

1 capsule is equal to 5 tablets.

The use of different dosages and their alternation is determined by the specific preventive and therapeutic objectives. When the dose of 1 tablet 3 times a day disrupted connections in the body at the molecular and submolecular level are detected and restored; subjectively this is manifested by various clinical symptoms of chronic pathology present in the person. At a dose of 1 capsule from 6 to 12 times a day directly a positive effect on the pathological focus and replacement of defective cells occurs, subjectively – relief of clinical manifestations. Selection of the scheme of taking Milife® is individual and depends on the initial status (immunological, neurohumoral, etc.).

The initial regimen of Milife®:

After taking the starting scheme, the doctor decides the need for further administration of Milife® on an individual scheme. For athletes and persons intensively engaged in physical training, the starting scheme is the same, but in the pre-start and starting periods, the dose increases to 12 capsules This scheme is approved by the Laboratory of Clinical Pharmacology and Anti-Doping Control of the Moscow Research Center for Sports Medicine.

Interaction

Special Instructions

Based on 15 years of observation of people of different sex and age taking Milife®, the following results were obtained.

There was normalization of all blood parameters (clinical and biochemical).

There was normalization of T- and B-cell immune system parameters.

The study of the hormone profile showed correlation influence of the drug Milife® on the level of pituitary and ovarian hormones in the I and II phases of the menstrual cycle, the reliable increase of progesterone in the ovulatory phase of the menstrual cycle. The anovulatory cycle was not observed in any woman of childbearing age.

The data obtained point to the reliable stabilization and normalization of the neurohormonal profile in the reproductive ring of the hypothalamus-pituitary-adrenal-ovarian system, which allows us to recommend the drug Milife® to girls of pre-puberty period to relieve the syndrome of psycho-emotional lability, to establish and normalize the menstrual cycle.

In ultrasound examination we found a reduction in the size of subserosal interstitial fibromatous nodules up to their complete lysis, while a small percentage of women experienced a “birth” of submucosal fibromatous nodules and disappeared cellularity of the myometrium and cystic ovarian degeneration.

After taking the drug, positive EEG dynamics in the form of normalization of the alpha rhythm, appearance of zonal differences, disappearance of paroxysmal changes at functional loads were revealed. The revealed positive EEG dynamics indicates the normalization of the functional state of mesodiencephalic brain structures against the background of taking Milife® in more than 90% of those who took the drug.

The functional studies of the cerebral vessels showed no signs of venous stasis, improved blood filling of the carotid arteries, normalized the tone of vessels in the vertebrobasilar basin. Milife® improves microcirculation not only due to restoration of rheological properties of blood, but also due to improvement of blood supply of the vessel wall itself (in particular epithelium).

Milife® restores earlier disturbed processes of neurohumoral regulation and myocardial energy resources, which is reflected in improvement of contractility, relaxation function and positive inotropic stimulation of the heart.

Restoration of bioenergetic processes improves compensatory abilities of the body, contributing to the work of the heart in a more economical mode.

In chronic latent forms of genital herpes and chlamydia, a massive exit of infectious agents from cells and their subsequent elimination was found, which is associated with the development of the body’s “short” immunity. This contributed to the restoration of the microscopic structure of mucosal and muscle fibers of smooth muscles.

Milife® , when administered for 21 days with a course of treatment, improves the overall athletic performance by at least 30%, as shown by the increase of time to failure on the treadmill with a stepped-up physical load.

A powerful antioxidant effect of the drug in the same period was found. Morphologically, this effect was expressed in the stabilization of muscle mass against the background of fat mobilization, whereas in the control group there were signs of maladaptation to similar loads in the form of a total decrease of three morphological indices (body weight, muscle mass, fat mass).

Milife® with a course of use prevents an increase in urea concentration in the blood of athletes (statistically significant by 17.8%), as well as a decrease in hematocrit and lactate. There was an increase of myocardial contractility and improvement of cardiac propulsive work.

An economization of circulatory system function was achieved by increasing the ability of muscles to use oxygen and improving the ability to isotonic contraction of the heart muscle.

Positive dynamics was noted in the contractility of the myocardium and the phase structure of systole. The lengthening of the pre-systole period indicated an improvement in myocardial ability to create the necessary tension for powerful contraction. The decreased value of intraventricular pressure created conditions for decreased tension in the left ventricular wall, which together with decreased systolic indices of left ventricular posterior wall thickness and size contributed to some reduction of systolic meridional and circulatory stress and increased values of structural functioning index. Assessment of diastolic function showed improvement of myocardiocyte ability to accumulate the necessary energy reserve.

Restoring immunological reactivity in high-class athletes, as manifested by normalization of reduced concentration of immunoglobulins A, M and G; normalization of complement components CK and C4 levels, reduced due to debilitating physical activity in endurance athletes.

Favors cellular immunity (phagocytic activity, the intensity of phagocytosis, lysosomal activity, monocyte activity, increases the number of T- and B-lymphocytes). It normalizes the factors of non-specific defense, such as level of alpha-1-glycoprotein and alpha-2-glycoprotein, while the concentration of seromucoid and haptoglobin remains practically unchanged.

Pregnancy use