Clinical and pharmacological group: & nbsp

Alpha-blockers

Means that affect the metabolism of the prostate gland, and correctors urodynamics

Included in the formulation
  • Hyperprost
    capsules inwards 
  • Glansin
    capsules inwards 
  • Mikotisin
    capsules inwards 
    Sandoz d.     Slovenia
  • Omnik®
    capsules inwards 
    Astellas Farma Europe BV     Netherlands
  • Omnik Okas
    pills inwards 
    Astellas Farma Europe BV     Netherlands
  • Omsulosin
    capsules inwards 
  • Proflosin®
    capsules inwards 
       
  • Sonizin®
    capsules inwards 
    GEDEON RICHTER, OJSC     Hungary
  • Tamzelin®
    capsules inwards 
    VELFARM, LLC     Republic of San Marino
  • Tamsulosin
    capsules inwards 
  • Tamsulosin
    capsules
    VERTEKS, AO     Russia
  • Tamsulosin Bacher
    pills inwards 
    Bakter, OOO     Russia
  • Tamsulosin Canon
    capsules inwards 
  • Tamsulosin retard
    pills inwards 
  • Tamsulosin-OBL
    capsules inwards 
  • Tamsulosin-Teva
    pills inwards 
  • Tamsulon®
    capsules inwards 
  • Tanise® ERAS
    pills inwards 
    KRKA-RUS, LLC     Russia
  • Tulosin®
    capsules inwards 
  • Focussin®
    capsules inwards 
    Zentiva c.s.     Czech Republic
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    VED

    ONLS

    АТХ:

    G.04.C.A.02   Tamsulosin

    Pharmacodynamics:

    Selectively blocks postsynaptic α1A-adrenoceptors located on the neck of the bladder and smooth muscle cells of the prostate gland, as well as the prostatic urethra.

    It improves the outflow of urine, reduces irritation and eliminates the manifestations of obstruction of the urinary tract due to benign prostatic hyperplasia.

    Pharmacokinetics:

    After oral administration, it is completely absorbed in the gastrointestinal tract. The maximum concentration in the blood plasma is reached after 4-5 hours. The connection with plasma proteins is up to 99%.

    Therapeutic effect develops 2 weeks after the beginning of the admission. Metabolism in the liver to metabolites that retain pharmacological activity.

    The half-life is 9-13 hours. Elimination of the kidneys in the form of metabolites, about 9% unchanged.

    Indications:

    It is used to treat dysuric disorders in benign prostatic hyperplasia.

    XIV.N40-N51.N40   Hyperplasia of the prostate

    Contraindications:

    Renal and hepatic insufficiency, individual intolerance, children under 18 years of age.

    Carefully:

    Orthostatic hypotension, including in history, hypersensitivity.

    Pregnancy and lactation:

    Not applicable.

    Dosing and Administration:

    Inside, 400 mg once a day after breakfast.

    The highest daily dose: 400 mg.

    The highest single dose: 400 mg.

    Side effects:

    Central and peripheral nervous system: asthenia, headache, dizziness, syncope, sleep disorders.

    The cardiovascular system: orthostatic hypotension, tachycardia, cardialgia.

    Digestive system: nausea, vomiting, diarrhea, or constipation.

    Musculoskeletal system: backache.

    Sense organs: rhinitis, visual impairment.

    Dermatological reactions: a rash.

    Reproductive system: priapism, violation of libido, retrograde ejaculation.

    Allergic reactions.

    Overdose:

    Increased side effects.

    Treatment is symptomatic.

    Interaction:

    Cimetidine increases the concentration of tamsulosin in the blood plasma.

    Furosemide lowers the concentration of tamsulosin in the blood plasma.

    Warfarin and diclofenac increase the rate of excretion of tamsulosin.

    When used simultaneously with other α1-adrenoceptor increases the risk of developing arterial hypotension.

    Special instructions:

    Before using tamsulosin, a full examination of patients is recommended to exclude malignant neoplasm of the prostate.

    In the treatment it is not recommended to drive vehicles and work with moving mechanisms.

    Instructions
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