Active substancePalm Creeping Fruit ExtractPalm Creeping Fruit Extract
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  • Dosage form: & nbspcapsules
    Composition:

    Contents of the capsule:

    Active substance:

    Serenoa creeping fruits extract lipidosterol - Serenoa repens - (LSESR) 160 mg.

    Excipients:

    Macrogol 10 000 - 290 mg

    Capsule (base and lid):

    Yellow iron oxide E172 - 0.38 mg indigo carmine E132 (Indigo) - 0.02 mg titanium dioxide E171 - 3.08 mg, gelatine - 77 mg (100%)

    Description:

    Capsules of light green color. The contents of the capsule are greenish pasty substance with a characteristic odor. The size of capsule number 1.

    Pharmacotherapeutic group:treatment of benign prostatic hyperplasia of plant origin
    ATX: & nbsp

    G.04.C.X   Other drugs for the treatment of benign prostatic hyperplasia

    G.04.C.X.02   Palm Creeping Fruit

    Pharmacodynamics:

    Permikson has complex effects on the pathogenesis and symptoms of benign prostatic hyperplasia, effects due to complementary constituent ingredients of the plant extract.Permixon has antiandrogenic, anti-inflammatory, anti-edematous and antiproliferative effects, selectively manifested at the level of the prostate gland. In this case, the drug does not affect the level of sex hormones in the blood, does not cause impairment of sexual functions, libido, potency and does not change the serum PSA (prostate-specific antigen) level. The local anti-androgenic effect of Permixon is associated with inhibition of the enzyme 5-alpha-reductase 1 and 11 types, which is responsible for the conversion of testosterone in the prostate into its active form, dihydrotestosterone, and a decrease in binding of the latter to specific receptors. Reducing the formation of dihydrotestosterone results in a decrease in further growth in prostate volume.

    Local anti-inflammatory effect is caused by the effect of lipidosterol extract of serenoid creeping on the main mediators of cellular inflammation - inhibits the activity of phospholipase A2, cyclooxygenase and lipoxygenase. Permixon during the first weeks of treatment reduces capillary permeability and vascular stasis, relieves edema and inflammation of the prostate, eliminates the compression of the neck of the bladder and urinary canal, like alpha blockers improves urodynamics.The local antiproliferative effect of the drug is manifested by a decrease in the activity of growth factors (primarily epidermal and fibroblastic) and the acceleration of apoptosis of prostate cells, which is reflected in inhibition of growth and a subsequent decrease in the volume of the prostate gland. These properties of the drug contribute, on the one hand, to a reduction in the pathological symptoms of benign prostatic hyperplasia (dysuria, pollakiuria, nocturia, painful sensations and a feeling of tension during urination, incomplete emptying of the bladder), an increase in the volume and strength of urination. On the other hand, Permixon contributes to inhibition of further growth and volume of the prostate gland.

    Indications:

    Benign hyperplasia (adenoma) of the prostate of the I and II stages.

    Contraindications:

    Hypersensitivity to the components of the drug.

    Dosing and Administration:

    Inside for 160 mg (1 capsule) 2 times a day or once in the morning, without chewing, while eating. The duration of treatment should be at least 3 months.

    The optimal scheme and repeated courses of treatment is established and appointed by the doctor individually in each specific case on the basis of a diagnostic examination.

    Side effects:Adverse reactions are classified according to the medical vocabulary for regulatory legal activity MedDRA and systematized according to the frequency of development in accordance with the WHO Classification:
    very frequent - 1/10 appointments (≥ 10%);
    frequent - 1/100 appointments (≥ 1%, but <10%);
    infrequent - 1/1000 appointments (≥ 0.1%, but <1%);
    rare - 1/10000 prescriptions (≥ 0.01%, but <0.1%);
    very rare - less than 1 / 10,000 appointments (<0.01%).
    Disturbances from the nervous system: often - headache.
    Violations with hand gastro-intestinal tract: often - abdominal pain; infrequently - nausea.
    Violations with hand liver and bile ducts: infrequently - an increase in the activity of gamma-glutamyl transferase, an increase activity of transaminases.
    Disturbances from the skin and subcutaneous tissues: infrequently - rash.
    Violations of the genitals and breast: infrequently - gynecomastia (reversible after discontinuation of treatment).
    Allergic Reagents: frequency is unknown (can not be estimated from available data) - edema.
    If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, inform the doctor about it.

    Overdose:

    Cases of overdose are not described. If you accidentally take a large amount of the drug, you need to do a gastric lavage.

    Interaction:

    Not found.

    Form release / dosage:

    Capsules 160 mg.

    Packaging:For 15 capsules in a blister of PVC / aluminum foil, 2 blisters per pack of cardboard along with instructions for use.
    Storage conditions:

    At a temperature of no higher than 25 ° C. Keep in a place inaccessible to children.

    Shelf life:

    3 years.

    Do not use after the expiry date printed on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:П N012687 / 02
    Date of registration:30.07.2007
    The owner of the registration certificate:Pierre Fabre Medication ProductionPierre Fabre Medication Production France
    Manufacturer: & nbsp
    Representation: & nbspPIER FABR PIER FABR France
    Information update date: & nbsp14.08.2015
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