Active substancePyracetamPyracetam
Similar drugsTo uncover
  • Lucetam®
    solution w / m in / in 
  • Lucetam®
    pills inwards 
  • Memotropil®
    pills inwards 
  • Nootropil®
    capsules inwards 
    YUSB Farma S.A.     Belgium
  • Nootropil®
    solution w / m in / in d / infusion 
    YUSB Farma S.A.     Belgium
  • Nootropil®
    solution inwards 
    YUSB Farma S.A.     Belgium
  • Nootropil®
    pills inwards 
    YUSB Farma S.A.     Belgium
  • Pyracetam
    solution w / m in / in 
    ORGANICS, JSC     Russia
  • Pyracetam
    pills inwards 
    ORGANICS, JSC     Russia
  • Pyracetam
    pills inwards 
    MARBIOFARM, OJSC     Russia
  • Pyracetam
    pills inwards 
    DALHIMFARM, OJSC     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
    DALHIMFARM, OJSC     Russia
  • Pyracetam
    solution w / m in / in 
    VEROPHARM SA     Russia
  • Pyracetam
    solution w / m in / in 
    Mapichem AG     Switzerland
  • Pyracetam
    solution w / m in / in d / infusion 
  • Pyracetam
    solution w / m in / in d / infusion 
  • Pyracetam
    solution in / in d / infusion 
    Company DEKO, LLC     Russia
  • Pyracetam
    pills inwards 
    BIOSINTEZ, PAO     Russia
  • Pyracetam
    capsules inwards 
  • Pyracetam
    solution w / m in / in d / infusion 
  • Pyracetam
    solution w / m in / in d / infusion 
  • Pyracetam
    capsules inwards 
    FARMPROJECT, CJSC     Russia
  • Pyracetam
    capsules inwards 
    ATOLL, LLC     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
    BIOCHEMIST, OJSC     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
    ELLARA, LTD.     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
    SYNTHESIS, OJSC     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
  • Pyracetam
    capsules inwards 
    SYNTHESIS, OJSC     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
    ATOLL, LLC     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
    BIOSINTEZ, PAO     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
  • Pyracetam
    capsules inwards 
    AVVA RUS, OJSC     Russia
  • Pyracetam
    capsules inwards 
    VERTEKS, AO     Russia
  • Pyracetam
    capsules inwards 
    AKRIKHIN HFK, JSC     Russia
  • Pyracetam
    solution w / m in / in d / infusion 
    GROTEKS, LLC     Russia
  • Pyracetam
    solution in / in d / infusion 
  • Pyracetam
    pills inwards 
    IRBITSK HFZ, OJSC     Russia
  • Pyracetam
    capsules inwards 
  • Pyracetam
    pills inwards 
  • Pyracetam
    capsules inwards 
    URALBIOFARM, OJSC     Russia
  • Pyracetam
    capsules inwards 
    MINSKINTERKAPS, UP     Republic of Belarus
  • Pyracetam
    capsules inwards 
    BELMEDPREPARATY, RUP     Republic of Belarus
  • Pyracetam
    solution w / m in / in d / infusion 
    BELMEDPREPARATY, RUP     Republic of Belarus
  • Pyracetam
    solution in / in d / infusion 
  • Pyracetam
    pills inwards 
    OZONE, LLC     Russia
  • Pyracetam
    capsules inwards 
  • Pyracetam
    capsules inwards 
    NGO Farmvilar, OOO     Russia
  • Pyracetam of Avexime
    pills inwards 
  • Pyracetam Beefus
    solution w / m in / in d / infusion 
    UPDATE OF PFC, CJSC     Russia
  • Pyracetam Welfarm
    solution w / m in / in 
    VELFARM, LLC     Republic of San Marino
  • Piracetam MS
    pills inwards 
    MEDISORB, CJSC     Russia
  • Pyracetam Obolenskoe
    pills inwards 
  • Piracetam-Vial
    solution w / m in / in d / infusion 
    VIAL, LLC     Russia
  • Piracetam-Richter
    pills inwards 
  • Piracetam-SZ
    capsules inwards 
    NORTH STAR, CJSC     Russia
  • Piracetam-Ferein®
    solution w / m in / in d / infusion 
    BRYNTSALOV-A, CJSC     Russia
  • Piracetam-Ferein®
    capsules inwards 
    BRYNTSALOV-A, CJSC     Russia
  • Piracetam-Eskom
    solution w / m in / in d / infusion 
    ESKOM NPK, OAO     Russia
  • The escotropel
    solution in / in d / infusion 
    ESKOM NPK, OAO     Russia
  • The escotropel
    solution in / in d / infusion 
    ESKOM NPK, OAO     Russia
  • Dosage form: & nbspfilm-coated tablets
    Composition:

    1 tablet contains:

    Active substance: piracetam 800 mg or 1200 mg.

    Excipients:

    Tablets 800 mg: microcrystalline cellulose - 28.34 mg; carboxymethyl starch sodium - 25,33 mg; potato starch - 7.38 mg; silicon dioxide colloidal - 4.33 mg; magnesium stearate - 0.62 mg.

    Tablets 1200 mg: microcrystalline cellulose - 42,50 mg; sodium carboxymethyl starch - 38.00 mg; potato starch - 11.07 mg; silicon dioxide colloid - 6.50 mg; magnesium stearate - 0.93 mg.

    Sheath:

    Tablets 800 mg: hypromellose - 14.54 mg; macrogol 6000 - 7.47 mg; talc - 4.72 mg; titanium dioxide - 4.43 mg; propylene glycol - 4.43 mg; dye quinoline yellow (E 104) 41 mg.

    Tablets 1200 mg: hypromellose - 22,00 mg; macrogol 6000 - 30 mg; talc - 8.50 mg; titanium dioxide - 6.70 mg; propylene glycol 6.70 mg; dye sunset sunset yellow (E 110) - 0.80 mg.

    Description:

    Tablets 800 mg - oblong with rounded ends, biconvex, with a risk, covered with a filmy coating of yellow, on a broken white with a yellow edge.

    Tablets 1200 mg - oblong with rounded ends, biconvex, with a risk, covered with a film shell of orange color, on a broken white with an orange edge.

    Pharmacotherapeutic group:Nootropic remedy
    ATX: & nbsp

    N.06.B.X.03   Pyracetam

    Pharmacodynamics:

    Nootropic agent, has an effect on the nervous system in various ways: it modifies neurotransmission in the brain; improves the conditions conducive to neuronal plasticity; improves microcirculation, affecting the rheological characteristics of the blood and not causing vasodilation. The use of pyracetam in patients with cerebral dysfunction increases concentration and improves cognitive function, which is accompanied by changes in the electroencephalogram (increase in α and β activity, decrease in δ-activity).

    Promotes restoration of cognitive functions due to various disorders, such as hypoxia, intoxication or electroconvulsive therapy.Reduces the duration of induced vestibular neuronitis. Pyracetam inhibits increased aggregation of activated platelets and, in the case of pathological rigidity of red blood cells, improves their deformity and ability to filter.

    Pharmacokinetics:

    After oral administration piracetam quickly and almost completely absorbed from the gastrointestinal tract. Well penetrates into various organs and tissues. Bioavailability is about 95 %. After a single dose in a dose of 2 g, the maximum concentration in the blood plasma (Cmax), 40-60 μg / l, is achieved within 0.5 h and in the cerebrospinal fluid after about 5 hours. The volume of distribution is 0.7 l / kg. It penetrates through the blood-brain and placental barriers, as well as through membranes used in hemodialysis. When tested on animals piracetam selectively accumulates in the tissues of the cerebral cortex, mainly in the frontal, parietal and occipital lobes, in the cerebellum and basal ganglia. It does not bind to blood plasma proteins, is not metabolized in the body and is excreted by the kidneys in an unchanged form by renal filtration.

    The half-life of the drug (T1/2) from the blood plasma is 4-5 hours and 8.5 hours from the cerebrospinal fluid, prolonged with renal failure. The renal clearance of piracetam in healthy volunteers is 86 ml / min. The pharmacokinetics of pyracetam do not change in patients with hepatic insufficiency.

    Indications:

    Symptomatic treatment of intellectual-mnestic disorders in the absence of an established diagnosis of dementia. Reduction of the manifestations of cortical myoclonia in piracetam sensitive patients both as monotherapy and as part of complex therapy. (In order to determine sensitivity to pyracetam in a particular case, a trial treatment course can be performed).

    Contraindications:
    • Hypersensitivity to pyracetam or pyrrolidone derivatives, as well as other components of the drug;
    • Hemorrhagic stroke;
    • Terminal stage of chronic renal failure;
    • Huntington's disease.
    Carefully:

    - Violation of hemostasis;

    - Extensive surgical interventions;

    - After dental interventions;

    - Simultaneous reception of anticoagulants and antiplatelet agents,including acetylsalicylic acid (in antiplatelet doses);

    - heavy bleeding;

    - patients with risk of bleeding (with gastric ulcer);

    - chronic renal failure (creatinine clearance 20-80 ml / min).

    Pregnancy and lactation:

    Preclinical studies did not show a direct or indirect effect on pregnancy, embryo / fetal development, childbirth or postnatal development. There were no controlled studies of the drug during pregnancy. The concentration of the drug in newborns reaches 70-90% of its concentration in the blood of the mother. The appointment in pregnancy is possible if the potential benefit to the mother exceeds the potential risk to the fetus. It should be refrained from breastfeeding with the appointment of a woman piracetam.

    Dosing and Administration:

    Inside, during meals or on an empty stomach, squeezed with liquid.

    Attention! The last single dose should be taken no later than 17 hours.

    In memory disorders, intellectual disorders:

    On 2,4-4,8 g / day in several receptions during the first several weeks, then pass to supporting therapy of 2,4 g / day in 2-3 receptions, reception of 1,2 g / day is possible.

    Treatment of cortical myoclonia: Treatment begins with a dose of 7.2 g / day, increasing it by 4.8 g / day every 3-4 days to a maximum dose of 24 g / day. The daily dose of piracetam should be divided into 2-4 admission. The dose of other drugs for the treatment of myoclonus does not change. Then, in the future, according to the results of treatment, it is allowed to review the dose of other drugs for the treatment of myoclonus.

    After initiation of piracetam treatment, treatment is continued as long as the symptoms of the disease persist. In patients with acute course of the disease, spontaneous improvement can occur over time, therefore every 6 months, attempts should be made to reduce the dose or to abolish the drug.

    For this, the dose of piracetam is reduced by 1.2 g every 2 days (every 3-4 days in the case of Lance and Adams syndromes, in order to avoid a sudden relapse of myoclonus). This allows you to know the average effective dose.

    Elderly patients with renal insufficiency a dose adjustment should be performed (see "Renal failure" below). With long-term treatment to assess the need for dose adjustment, creatinine clearance should be assessed regularly.

    Renal insufficiency

    Piracetam is excreted almost exclusively by the kidneys, care should be taken when treating patients with renal insufficiency or requiring renal function control.

    The elimination half-life increases in direct proportion to the impairment of kidney function and creatinine clearance; this is also true for the elderly, in whom the excretion of creatinine depends on age.

    In this regard, the dose is adjusted in accordance with the table below:

    Kidney function

    CK (ml / min)

    Dosing regimen

    Norm

    >80

    The standard dose of 2-4 admission

    Mild renal insufficiency

    50-79

    2/3 of the standard dose in 2-3 doses

    Mean renal insufficiency

    30-49

    1/3 of the standard dose in 2 divided doses

    Severe renal insufficiency

    <30

    1/6 of the standard dose once

    Terminal Renal Failure

    -

    Contraindicated


    Liver failure

    Patients with isolated dysfunction of the liver do not need correction of the dose. Patients with dysfunction of the liver and kidneys are dosed according to the scheme above (see "Renal failure").

    Side effects:

    Depending on the frequency of occurrence, the following groups of side effects are distinguished: very often: ≥1 / 10; often: ≥1 / 100, <1/10; infrequently: ≥1 / 1000, <1/100; rarely: ≥1 / 10000, <1/1000; very rarely: <1/10000, including individual cases; the frequency is unknown: the frequency of development can not be estimated from the available data.

    On the part of the organs of hematopoiesis and lymphatic system: frequency unknown - hemorrhagic disorders.

    From the nervous system: often - hyperkinesia; frequency unknown irritability, drowsiness, asthenia, headache, insomnia, imbalance, ataxia, exacerbation of epilepsy, tremor.

    From the side of the psyche: often - mental excitement, nervousness; infrequently - depression frequency unknown agitation, anxiety, confusion, hallucinations.

    From the digestive system: frequency unknown - nausea, vomiting, diarrhea, abdominal pain (including in the upper parts).

    From the side of metabolism: often - weight gain.

    From the side of the organ of hearing and labyrinth: frequency unknown - vertigo.

    From the skin and subcutaneous tissues: frequency unknown - Quincke's edema, dermatitis, itching, urticaria.

    From the immune system: frequency is unknown - hypersensitivity, anaphylactoid reactions.

    On the part of the reproductive system: frequency unknown - increased sexual desire.
    Overdose:

    Symptoms: a single case of development of dyspeptic phenomena in the form of diarrhea with blood and pain in the abdomen when taking the drug inside a daily dose of 75 g,which was most likely due to the presence of a high concentration of sorbitol in the preparation.

    Treatment: In case of an overdose, symptomatic therapy is recommended, which may include hemodialysis. There is no specific antidote. The efficacy of hemodialysis for piracetam is 50-60%.

    Interaction:

    Piracetam improves the effectiveness of thyroid hormones and antipsychotics (neuroleptics). With simultaneous appointment with neuroleptics piracetam reduces the risk of extrapyramidal disorders.

    With simultaneous use with drugs that exert a stimulating effect on the central nervous system, it is possible to enhance the stimulating effect on the central nervous system.

    No interaction with clonazepam, phenytoin, phenobarbital, valproic acid was observed.

    High doses (9.6 g / day) of pyracetam increase the effectiveness of indirect anticoagulants in patients with venous thrombosis (there was a greater decrease in platelet aggregation, fibrinogen level, vWF, blood and plasma viscosity compared with the use of only indirect anticoagulants).

    The possibility of changing the pharmacodynamics of piracetam under the influence of other drugs is low, since 90% of the drug is excreted unchanged in urine.

    Pyracetam does not inhibit cytochrome P450 isoenzymes. Metabolic interaction with other drugs is unlikely.

    Receiving piracetam at a dose of 20 mg / day did not change the maximum concentration and area under the concentration-time curve of antiepileptic drugs (carbamazepine, phenytoin, phenobarbital, valproic acid) in the serum of the patient with epilepsy, receiving a constant dosage.

    Joint reception with alcohol did not affect the level of serum piracetam concentration, and the serum concentration of alcohol did not change with the intake of 1.6 g of piracetam.

    Special instructions:

    Be wary appoint patients with hemostasis, before the forthcoming extensive surgical interventions or in patients with symptoms of severe bleeding.

    When treating patients with cortical myoclonia, sudden interruption in treatment should be avoided, as this may cause a resumption of seizures.

    With prolonged treatment of elderly patients, regular monitoring of renal function,if necessary, dose adjustment is performed depending on the creatinine clearance.

    It penetrates the hemodialysis apparatus through the filter membranes. Effect on platelet aggregation: due to antiplatelet effect (see section "Pharmacodynamics"), piracetam should be administered with caution to patients with severe hemorrhagic disorders, risk of bleeding (eg, gastric ulcer), homeostatic disorders, patients with a history of hemorrhagic stroke, patients with surgical interventions, including dental interventions, in patients taking anticoagulants and antiplatelet agents, including low doses of acetylsalicylic acid.

    Dye sunset yellow sunset (E 110) in tablets of 1200 mg can cause allergic reactions.

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

    During the treatment period, care must be taken when driving vehicles and engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.

    Form release / dosage:

    Tablets, film-coated 800 mg, 1200 mg.

    Packaging:

    For 5 or 10 tablets in a foil blister Al / PVC.

    2 or 6 blisters for 10 tablets or, 4 or 12 blisters for 5 tablets (20 or 60 tablets, respectively), along with instructions for use are placed in a cardboard box.

    Storage conditions:

    At a temperature of no higher than 25 ° C. Keep out of the reach of children.

    Shelf life:

    3 years.

    Do not use the drug after the expiration date.

    Terms of leave from pharmacies:On prescription
    Registration number:П N011764 / 02
    Date of registration:01.06.2011
    Expiration Date:Unlimited
    The owner of the registration certificate:Pharmaceutical factory "POLFARMA" JSCPharmaceutical factory "POLFARMA" JSC Poland
    Manufacturer: & nbsp
    Representation: & nbspAKRIKHIN OJSC AKRIKHIN OJSC Russia
    Information update date: & nbsp28.04.2018
    Illustrated instructions
      Instructions
      Up