anastrozole bodybuilding

Tien for the anastrozole bodybuilding is used to treat infections of moderate to severe currents, caused by susceptible to aerobic and anaerobic microorganisms. And also for the empirical treatment of infectious process before defining its bacterial pathogens Tien is indicated for the treatment of:

  • Lower respiratory infections, including pneumonia, bronchitis, as well as exacerbation of chronic obstructive pulmonary disease caused by Streptococcus pneumoniae and of Haemophilus influenzae ;
  • Intra-abdominal infections, including acute gangrenous and perforated appendix, including complicated by peritonitis caused by Streptococcus Group D, including of Enterococcus faecalis , a group of Streptococcus viridans ; of Escherichia coli, of Klebsiella pneumoniae, of Pseudomonas aeruginosa, of Bacteroides spp. , Including V.fragilis, B.distasonis , B.intermedius, B.thetaiotaomicron; andFusobacterium spp. , and Peptostreptococcus spp.
  • Infections of the skin and soft tissues, including abscess, phlegmon, infected ulcers and wound infections caused by of Staphylococcus aureus , including penicillinase-producing strains; of Streptococcus pyogenes; Streptococcus Group D, including Enterococcus faecalis; Spp Acinetobacter. , Including A.calcoaceticus; Citrobacter spp .; Escherichia coli, Enterobacter cloacae, Klebsiella pneumoniae , Pseudomonas aeruginosa, and Bacteroides spp., Including B.fragilis .
  • Gynecologic infections, including postpartum endomyometritis caused by Streptococcus group , including Enterococcus faecalis; Escherichia coli; Klebsiella pneumoniae; Bacteroides intermedius andPeptostreptococcus spp .


  • Hypersensitivity to any component of the drug, other beta-lactam antibiotics, penicillins and cephalosporins.
  • When using lidocaine hydrochloride as a solvent administration of the drug is contraindicated in patients with known hypersensitivity to amide anesthetics local action and in patients with severe shock and intracardiac conduction blockade.
  • Patients with creatinine clearance less than 20 mL / min / 1.73 m 2 .
  • Children up to 12 years.Carefully:
  • pseudomembranous colitis anastrozole bodybuilding
  • Patients with a history of gastrointestinal disease.
  • Patients with creatinine clearance of 20 to 70 ml / min / 1.73 m 2 .
  • Patients with central nervous system diseases.Use of the drug during pregnancy and lactation: Studies using tienama for i / m administration in pregnant women has been conducted,stanabol 50 the drug should therefore be used during pregnancy only if the benefit of treatment justifies the potential risk to the fetus. Imipenem is found in breast human milk. If the application tienama deemed necessary, breast-feeding should be discontinued in breast milk.

    Use in pediatric patients: In children older than 12 years, the drug is used for the same indications as in adults. Data on the efficacy and safety of tienama for i / m administration in children under 12 years are not enough.

    Use in elderly patients: In clinical studies the efficacy and safety tienama with the / m introduction of the elderly over 65 years old are not different from those of a younger age in people. However, considering the characteristic of this age group is reduced function of the cardiovascular system, liver, kidneys, and the presence of comorbidities and concomitant drug therapy, care should be taken in dose selection, adhering to the lower limits of the recommended doses. It is advisable to monitor renal excretory function.

    Dosage and administration:

    The dosing recommendations given tienama mipenema amount to be administered. Tienama dosage for adults and children 12 years of age is determined depending on the location and severity of infection, as well as the sensitivity of the pathogen anastrozole bodybuilding renal function and body weight of the patient. In patients with lower respiratory tract infections, skin and appendages, and gynecological infections recommended introduction tienama (500 mg imipenem) every 12 hours, and patients with intra-abdominal infections -. 750 mg imipenem every 12 hours for a total daily dose by intramuscular administration should not exceed 1.5 g of imipenem. If there is a need for higher doses of the drug, it should be used intravenous route of administration. The duration of treatment depends on the type of pathogen and severity of the disease caused by it, the treatment is usually continued for at least two days after disappearance of all symptoms of an infectious disease. Safety and efficacy of treatment over 14 days has not been established. Thienyl be administered deep into large muscles (such as the gluteal muscles or lateral thigh muscles), with obligatory test aspiration to avoid contact with the drug in the lumen of the vessel. In patients with a creatinine clearance ≥ 20 ml / min / 1,73m 2 thien for intramuscular injections may be administered, without reducing the dosage.

    Preparation of solution: The solution tienama for intramuscular injection is prepared by dissolving a sterile powder in a vial 1% lidocaine hydrochloride (without epinephrine), or water for injection or saline, as indicated in the Table.The prepared solution is white or slightly yellow color.

    Stability tienama dosage form for intramuscular injection: The preparation in the form of a dry powder must be stored at a temperature not higher than 25 ° C. The prepared solution should be used within an hour. Thienyl intramuscular injection can not be mixed or added to other antibiotics.

    Adverse Reactions: Tien is generally well tolerated. In clinical studies showed thienyl same tolerability as cefazolin, cefotaxime and cephalothin. Side effects as a rule, do not require discontinuation of therapy and are usually transient and Just noticeable; serious anastrozole side effects are rare. The most common side effects are tienama: Local reactions The most frequent of the reported local reactions were pain at the site of administration. Allergic reactions Rash, pruritus, urticaria, erythema multiforme, Stevens-Johnson syndrome, angioedema, toxic epidermal necrolysis (rare), exfoliative dermatitis (rarely), candidiasis, fever, including dosage, anaphylactic reactions. The reactions of the gastro-intestinal tract Nausea, vomiting, diarrhea, staining of the teeth and / or tongue. As in the case of treatment by almost all broad-spectrum antibiotics, there were reports of pseudomembranous colitis.

  • The reactions of the central nervous system as well as in the treatment of other antibiotics of the beta-lactams, with the / m introduction tienama described cases of side effects from the central nervous system in the form of myoclonus, and seizures. Normally, such phenomena are observed in patients with CNS (brain injuries, or a history of seizures) and / or in patients with impaired renal function, although isolated cases were reported in patients without CNS disease. To avoid complications it is necessary to strictly adhere to the recommended dosage and treatment regimen (see section “Dosage and method of application.”), And in patients with established convulsive disorder should continue taking anticonvulsants.
  • Changes in laboratory parameters blood – decrease in the number of red blood cells, hemoglobin level, and hematocrit, eosinophilia , leukocytosis and leukopenia, thrombocytosis anastrozole bodybuilding and thrombocytopenia, prolonged prothrombin time.
  • liver enzymes – an increase in serum transaminases, bilirubin and / or serum alkaline phosphatase.
  • The excretory system – increase in serum levels of urea and creatinine. Possible eritrotsit-, leykotsit-, cylinder- and bacteriuria.

anastrozole 1mg

Levodopa absorbed by active transport from the gastrointestinal tract, its passage through the blood-brain barrier is also carried out by active mechanisms. Barriers to absorption of levodopa is the presence of dopa decarboxylase in the intestinal wall. Levodopa anastrozole 1mg is absorbed from the stomach in a limited amount. The rate of gastric emptying plays a key role in the absorption of the drug. Factors that slow gastric emptying (food, m-anticholinergic agents), delaying the passage of the drug into the duodenum, and slow its absorption. The maximum concentration of the drug in the blood observed after 1-2 hours after administration. Distribution: The volume of distribution of levodopa is 0.9-1.6 l / kg. While maintaining the total clearance dopa decarboxylase activity in plasma levodopa is 0.5 l / kg / hr.

Levodopa penetrates through the blood-brain barrier by facilitated diffusion. The endothelium of the brain capillaries also contains a dopa decarboxylase as a second potential barrier to receipt of levodopa to the brain, however, in these capillaries is decarboxylated a small portion of the administered dose of levodopa. Metabolism: Approximately 70-75% of input into the levodopa is metabolized in the gut wall (the effect of “first pass “). Liver first-pass metabolism does not substantially participate. With increasing doses of levodopa, the amount of drug in the intestine undergoes  decreases.Levodopa is not bound to plasma proteins. The  of levodopa-dopa decarboxylase is the main way of the formation of dopamine levodopa. A large anastrozole 1mg number of this enzyme in the intestine, liver and kidneys.

Methoxylation levodopa influenced by catechol-O-methyltransferase to form a 3-O-is the second metildofy by metabolism of levodopa. With long-term treatment of this metabolite may accumulate. Transamination is an additional route of metabolism of levodopa. The end product of this pathway is vanilpiruvat, vanilatsetat and 2,4,5-trigidroksifeniluksusnaya acid. All pathways except transamination are irreversible. Selection: In combination with carbidopa, levodopa half-life is increased to 3 hours. Up to 69% of levodopa can be detected in the urine of a human dopamine and its metabolites – vinilinmindalnoy acid, norepinephrine, homovanillic acid digidrofeniluksusnoy acid.

b. Carbidopa
At recommended doses, carbidopa does not penetrate the blood-brain barrier. The maximum plasma concentration is reached after 4.2 hours. Approximately 50% of carbidopa is excreted in the urine and feces. 35% of carbidopa are excreted renally, it appears unchanged.



Hypersensitivity to the drug, a form-closure glaucoma, severe psychosis or neurosis, pregnancy and lactation, melanoma or suspected it, skin disease of unknown etiology, Huntington’s disease, essential tremor. It should not be used for the treatment of secondary parkinsonism caused by the use of antipsychotic drugs (neuroleptics). Do not assign patients up to 18 years.


The drug is taken with caution in patients with erosive and ulcerative lesions of gastric and / or duodenal ulcer, epileptic seizures in history of myocardial infarction with cardiac arrhythmias in the history of, heart failure, diabetes, asthma, diseases of the endocrine system, mental disorders, as well as heavy violations of liver and kidney function.

Dosing and Administration

With a small amount of food or after a meal, with water and without chewing. Since there is competition between the aromatic amino acids and levodopa by sucking, while anastrozole 1mg use of the drug should avoid consuming large amounts of protein. The average daily dose of carbidopa needed to inhibit peripheral conversion of levodopa, is 70-100 mg. Exceeding 200 mg carbidopa does not entail further enhance the therapeutic effect. The daily dose of levodopa should not exceed 2000 mg.
The starting dose – 1/2 tablets 2 times a day, can be increased by half pill daily as needed. Typically, at the beginning of substitution therapy, the daily dose should not exceed 3 tablets per day (1st tablet 3 times a day). The use of this dosage is recommended in the early treatment of severe cases of Parkinson’s disease. The daily dose of the drug as an exception may be raised during monotherapy, but should not exceed 8 tablets (1 tablet minutes 8 times a day). The use in an amount of more than 6 tablets per day should be carried out with great care.
Tidomet Forte when replacing levodopa
levodopa discontinued 12 hours prior to start of treatment Tidometom Forte, and in the case of receiving prolonged forms levokarbidopy – 24 hours. Dosage Tidometa Forte in this case should be no more than 20% of the previous dose of levodopa. The maintenance dose is 3-6 tablets per day for most patients.

Side effect

Nervous system: Dyskinesia, including choreoathetosis, focal dystonia, with prolonged use – “on-off” syndrome, dizziness, ataxia, seizures, anorexia, sedation, drowsiness, nightmares, nervousness, irritability, anxiety, insomnia, psychotic reactions, hallucinations, depression, paranoid state, hypomania, increased libido, euphoria, dementia. Gastrointestinal tract: loss of appetite, nausea, vomiting, constipation, epigastric pain, dysphagia, ulcerogenic action in predisposed patients. Cardiovascular system: orthostatic hypotension, collapse, heart arrhythmia, tachycardia. hemopoiesis system: moderate leukopenia, thrombocytopenia, hemolytic anemia. The change in laboratory parameters: changes in the level glutumatoksalattransaminazy, glutamatpiruvatoksalazy, alkaline phosphatase, lactate dehydrogenase, urea nitrogen, bilirubin, iodine-related protein, positive direct Coombs’ test . Others: blepharospasm, mydriasis, diplopia, a slight increase in body weight during long-term use. Side effects are usually dependent on the dose received and the individual patient’s sensitivity. Side effects can be eliminated temporary dose reduction without interruption in treatment. If side effects do not regress, the treatment should be stopped gradually.


Symptoms: The first increase and then decrease in blood pressure, sinus tachycardia, confusion, agitation, insomnia, anxiety. It may also develop orthostatic hypotension. Symptoms of anorexia and insomnia may persist for several days. Treatment: gastric lavage, activated charcoal. If necessary, carrying out symptomatic treatment in a hospital. There is no specific antidote.

Drug interactions


  • Simultaneous with the appointment of antihypertensive drugs requires special attention due to the risk of postural hypotension.
  • when combined with tricyclic antidepressants may cause hypertension and dyskinesia, and reduced bioavailability of levodopa.
  • the combined use of phenothiazines, and butirofenonov Tidometa Forte reduces the effect of the latter.
  • Tidomet Forte should not be administered in conjunction with non-selective monoamine oxidase inhibitors, as can develop hypertensive crisis. monoamine oxidase inhibitors, treatment should be discontinued for at least 14 days prior to drug administration. The exception is selegiline (a selective inhibitor of monoamine oxidase – B) that can be used as an adjuvant in the treatment of levodopa.
  • may increase the effects of sympathomimetics, and therefore it is recommended to reduce the dose. With simultaneous use of levodopa with β-adrenostimulyatorov, means for inhalation anesthesia may increase the risk of cardiac arrhythmias.
  • when used with levodopa amantadine marked potentiating effect.
  • methyldopa and levodopa may potentiate the side effects of each other.
  • pyridoxine is a cofactor dopa decarboxylase – an enzyme responsible for peripheral decarboxylation of levodopa and dopamine education. When his appointment in patients receiving levodopa (without dopa decarboxylase inhibitors), there is a growing peripheral metabolism of levodopa and a smaller amount of it penetrates through the blood-brain barrier. Thus, pyridoxine reduces the therapeutic effect of levodopa, dopa decarboxylase peripheral inhibitors if not assigned additionally.
  • when supplemental dopa decarboxylase inhibitors, the daily dose of levodopa can be reduced by 70-80% while maintaining the same clinical outcome.
  • when combined with diazepam, phenytoin, clonidine, thioxanthene derivatives, papaverine, reserpine, may decrease the antiparkinsonian action.
  • while the use of drugs anastrozole 1mg increases the risk of dyskinesias and hallucinations.

special instructions

Should not be used in cases of secondary parkinsonism, caused by the use of antipsychotic drugs (neuroleptics).
Discontinuation of therapy should be gradual, since the sudden discontinuation of the drug may develop symptom complex resembling neuroleptic malignant syndrome (muscular rigidity, increased body temperature, increased content serum ). Requires monitoring of patients who took a sudden reduce the dose or interrupt reception. The absorption of levodopa in elderly patients is higher than in the young. These data confirm the information on the reduction of the activity of dopa decarboxylase in tissues with age, as well as long-term administration of levodopa.
When erosive and ulcerative lesions of gastric and / or duodenal ulcer, epileptic seizures in history of myocardial infarction, rhythm disturbances in the history of, heart disease, diabetes , bronchial asthma, diseases of the endocrine system, mental disorders, as well as severe liver or kidney function should take the drug with caution. In such cases, patients should be under close medical supervision.
In long-term treatment is necessary to carry out periodic monitoring of liver function, kidney, hematopoietic system and the cardiovascular system are also necessary to monitor the patient’s mental status.
In general anesthesia during surgical operations Tidomet Forte administered without reducing the dose if the patient is able to take drugs and fluids inside. When using halothane and cyclopropane use of the drug is stopped for at least 8 hours before surgery. Treatment continued after the operation at the same dose.
Patients with glaucoma in patients receiving the drug should regularly monitor the intraocular pressure.
The impact on driving: anastrozole 1mg you must refrain from transport management, as well as activities requiring psychomotor speed reactions.


After oral administration of ornidazole is rapidly absorbed. The average absorption is 90%. Maximum plasma concentrations are reached within 3 hours.


The binding of ornidazole with anastrozole the proteins is approximately 13%. Active substance tiberal very well into the cerebrospinal fluid, and other body fluids and tissues.

Ornidazole plasma concentrations are in the optimal range for the various indications. Cumulation factor after receiving multiple doses of 500 mg or 1000 mg in healthy volunteers after every 12 hours is equal to 1.5-2.5.


Ornidazole is metabolized in the liver to form mainly hydroxymethyl-2 and a -gidroksimetilmetabolitov. Both metabolites are less active against Trichomonas vaginalis and anaerobic bacteria than the unmodified ornidazole.


The half-life is about 13 hours. After a single oral dose is excreted 85% in the first 5 days, mainly as metabolites. About 4% of the dose is eliminated via the kidneys in unchanged form.


Trichomoniasis (urinary infections in women and men caused by Trichomonas vaginalis); amebiasis (all of intestinal infections caused by Entamoeba histolytica, including amoebic dysentery, and all forms of extra-intestinal amebiasis, especially amebic liver abscess); giardiasis.

Mode of application

Tiberal always taken after meals.


2 1 tablet twice a day (morning and evening) for 5 days.

To eliminate the possibility of re-infection, the sexual partner, in all cases, should receive the same treatment.

The daily dose anastrozole for children is 25 mg / kg body weight and is administered once.

Hypersensitivity to the drug or other nitroimidazole derivative.

Side effects

Weakly expressed drowsiness, headaches and gastrointestinal disorders (nausea). In some cases side effects, such as dizziness, tremor, rigidity, loss of coordination, convulsions, fatigue, temporary loss of consciousness, signs of sensory or mixed peripheral neuropathy. There have been cases of perversion of taste sensations, changes in liver function tests, skin reactions and hypersensitivity reactions.

Precautionary measures

Care should be taken in patients with anastrozole diseases such as epilepsy, brain lesions, multiple sclerosis. If you exceed the recommended doses there is a risk in patients with liver disease, alcohol abuse, pregnant and lactating mothers and children.

Pregnancy and lactation

Extensive research on the different kinds of animals did not reveal any teratogenic or toxic effect of the drug on the fetus. Controlled studies in pregnant women have been conducted. However, for general health reasons appoint Tiberal early in pregnancy or nursing mothers only if absolutely indicated.

Drug interactions

Unlike other nitroimidazole derivative, ornidazole did not inhibit aldehyde dehydrogenase and is therefore incompatible with alcohol. However, ornidazole potentiates the anastrozole action of oral anticoagulants coumarin, which requires their respective dose adjustment. Ornidazole lengthens muscle relaxant action of vecuronium bromide.

anastrozole for men

Anastrozole for men administration of 200 mg tiapride maximum drug concentration in plasma – 1.3 ug / ml – achieved 1 hour. After intramuscular injection of 200 mg tiapride maximum drug concentration in plasma – 2.5 mcg / ml – 30 minutes is achieved. The bioavailability of the tablets is 75%. When receiving them directly before ingestion bioavailability is increased by 20% and the maximum plasma concentration – 40%.

Absorption is slowed in the elderly. The distribution in the body is rapid (less than 1 h). Penetrates through the blood-brain barrier and the placenta, accumulation does not occur. Animals in drug penetration mentioned milk with a ratio of concentrations in milk and blood of 1.2. Contact with plasma proteins and erythrocytes weak. Metabolism tiapride is very low: 70% of the dose found in the urine in unchanged form. Women and in men 3.6 hours. Selection takes place mainly in the urine, and renal clearance of up to 330 ml / min. In patients with renal function impaired excretion correlates with creatinine clearance. If creatinine clearance below 20 ml / min, the daily dose should be installed depending on the severity of renal failure: use half the dose when creatinine clearance 11-20 ml / min, and a quarter of the dose when creatinine clearance 10 mL / min.

Indications Tablets Adults:

  • Relief of psychomotor agitation and aggressive states, especially in chronic alcoholism or in old age.
  • Intense chronic pain syndrome.

In adults and children older than 6 years:

  • Different types of chorea, Gilles de la Tourette syndrome

In children older than 6 years:

  • Conduct disorder with agitation and aggressiveness.


  • Relief of psychomotor agitation and aggressive states, especially in chronic alcoholism or in old age. Intense chronic pain syndrome.


: Hypersensitivity to tiaprid or to other components of the preparation.

  • Diagnosed or suspected prolactin-dependent tumors, such as pituitary gland prolactinoma and breast cancer.
  • Confirmed or suspected pheochromocytoma.
  • In combination with sultopride;
  • Pregnancy (I term)
  • lactation
  • Children’s age (up to 6 years)
  • Hypertensive crisis anastrozole for men
  • Severe renal and / or hepatic impairment
  • In combination with dopaminergic agonists (amantadine, apomorphine, bromocriptine, cabergoline, entacapone, lisuride, pergolide, piribedil, pramipexole, quinagolide, ropinirole), except in patients suffering from Parkinson’s disease.

In combination with medicines that can cause heart rhythm disturbance: antiarrhythmics Ia class (quinidine, gidrohinidin, disopyramide) and class III (amiodarone, sotalol, dofetilide, Ibutilide), some antipsychotics (thioridazine, chlorpromazine, Levomepromazine, trifluoperazine, tsiamemazin, amisulpride, sulpiride, pimozide, haloperidol, droperidol), and with the following medications: levodopa, bepridil, cisapride, difemanil, erythromycin, mizolastine, intravenous vincamine, sparfloxacin, moxifloxacin. (see. section “Interaction with other medicinal products” ).



  • Epilepsy, in connection with the possibility of lowering the seizure threshold;
  • Cardiovascular diseases in the stage of decompensation;
  • Parkinson’s disease;
  • Combined use of drugs containing alcohol;
  • In old age, bradycardia , hypokalaemia, congenital  prolongation, and in the combined use of drugs that can cause severe bradycardia, hypokalaemia, decreased cardiac conduction, or prolongation of the interval QT.


Pregnancy and lactation The drug is contraindicated in the I trimester of pregnancy and lactation. Regarding the effect of neuroleptics used during pregnancy, fetal brain, the data are not available (preferably not be used during pregnancy tiaprid). However, if the drug is still applied during pregnancy, it is recommended whenever possible to limit the dose and duration of treatment. Prolonged treatment and / or use of high doses and / or late pregnancy justified control neurological neonate functions.

Breastfeeding known whether tiapride penetrates breast milk, so breast-feeding is forbidden.


Dosing and Administration The tablets only for adults and children over 6 years. It is always necessary to select the minimum effective dose. If the patient’s condition allows, treatment should be started at a low dose and then gradually increasing it.

  • Relief of psychomotor anastrozole for men agitation and aggressive states, especially in chronic alcoholism or in old age:
    • In adults: 200 – 300 mg / day course of treatment 1 – 2 months.
    • In old age: 50 mg twice a day. The dose can be gradually increased to 50 to 100 mg every 2-3 days to a maximum daily dose of 300 mg.
  • Chorea, Gilles de la Tourette syndrome
    • In adults: 300 – 800 mg / day
    • Treatment should start with a dose – 25 mg a day, and then slowly raise it until the minimum effective dose.
    • In children older than 6 years: 3-6 mg / kg / day
    • Intense chronic pain syndrome.
    • The usual dose for adults is 200 – 400 mg / day.
  • Conduct disorder with agitation and aggression in children older than 6 years -Dose is 100 – 150 mg / day.

Solution for injection Intramuscular or intravenous

only adults
should always choose the minimum effective dose. If the patient’s condition allows, treatment should be started at a low dose and then gradually increasing it.
Relief of psychomotor agitation and aggressive states, especially in chronic alcoholism or in old age:

  • In adults:
    The usual dose is 200 – 300 mg / day.
    When delirious predelirioznom syndrome or condition. 400 – 1200 mg / day (up to 1800 mg / day)
    Injection be administered every 4-6 hours.
  • In old age:
    200 – 300 mg / day, 2-3 injections i.e. to 6-hour intervals.
    Not more than a single dose of 100 mg.


  • Intense chronic pain syndrome.

The usual dose is 200 – 400 mg / day, ie, 2-4 capsules a day.



Side effect

  • Asthenia, fatigue (9.4%)
  • Drowsiness (6.6%)
  • Insomnia (4.4%)
  • Agitation, agitation (3.7%)
  • Apathetic state (2.8%)
  • Dizziness (2.6%)
  • Headache (2%)
  • Parkinson’s syndrome: tremor (2.3%), increased blood pressure, bradykinesia (1.2%), hypersalivation (1.2%).
  • Much less:
    • Early dyskinesia and dystonia (spasmodic torticollis, oculogyric crises, lockjaw), akathisia (0.9%).
    • These symptoms are usually reversible upon discontinuation of the drug or destination protivoparkinsonnyh anticholinergic agents.
    • Tardive dyskinesia (involuntary stereotypic movements of the tongue, face and limbs) occurring with prolonged use (anticholinergic antiparkinsonian agents appointed as correctors may worsen the patient’s condition).
    • Hyperprolactinemia and mating with her disorder (<0.2%): amenorrhea, galactorrhea, breast swelling, chest pain, impotence and ejaculation disorders,
    • Weight gain
    • QT prolongation
    • atrial fibrillation
    • postural hypotension
    • Neuroleptic malignant syndrome.


Overdose Symptoms: excessive sedation, drowsiness, depression of consciousness up to coma, hypotension, extrapyramidal symptoms. Treatment: removal of the drug, gastric lavage (in case of poisoning pills), symptomatic and detoxification therapy, monitoring of vital functions of the body (especially of cardiac function up to the complete disappearance of symptoms of intoxication In case of severe extrapyramidal symptoms -.. anticholinergic treatment As tiaprid weakly dialyzed to remove the substance is not recommended dialysis Antidote tiapride unknown..


Interaction with other drugs not recommended combinations

  • When used in conjunction with anti-arrhythmic drugs 1a class (quinidine, gidrohinidin, disopyramide) and III-class (amiodarone, sotalol, dofetilide, Ibutilide), antiarrhythmic drugs, some antipsychotics (thioridazine, chlorpromazine, levomepromazine, trifluoperazine, tsiamemazin, sulpiride, amisulpride, pimozide, haloperidol, droperidol), and other drugs such as bepridil, cisapride, difemanil, erythromycin, mizolastine, vincamine, an increased risk of ventricular arrhythmias, and atrial fibrillation.
  • Alcohol
    Alcohol increases the sedative effect of neuroleptics.
  • Levodopa
    There is a joint action antagonism of levodopa and neuroleptics. In patients with Parkinson’s disease, it is recommended to use the minimum effective dose of levodopa and tiapride.
  • Dopaminergic agonists may cause or exacerbate psychotic disorders. If you need neuroleptic treatment to a patient suffering from Parkinson’s disease receiving dopaminergic drug, the dose should be gradually reduce the latter to cancel (abrupt withdrawal may lead to the development of neuroleptic malignant syndrome).
  • Sparfloxacin, moxifloxacin:
    There is a growing risk of ventricular arrhythmias, and atrial fibrillation. If the combination can not be avoided, you should first check the QT interval and provide ECG monitoring.

Combinations requiring caution

  • Drugs associated with bradycardia (blockers “slow” calcium channel blockers: diltiazem, verapamil, beta-blockers, clonidine, guanfacine; digitalis drugs that are inhibitors of cholinesterase: donezepil, rivastigmine, galantamine, pyridostigmine, neostigmine).
  • Drugs that can cause hypokalaemia: potassium carve diuretics, laxatives, amphotericin B, glucocorticoids, tetrakozaktid. There is a growing risk of ventricular arrhythmias, and atrial fibrillation.

Combinations to be taken into account

  • Antihypertensive drugs (all):
    An additive effect, increasing the risk of postural hypotension.
  • Preparations depressing central nervous system function:
    Morphine derivatives (analgesics, cold preparations and means of substitutional therapy); barbiturates; benzodiazepines and other anxiolytics; sleeping pills; antidepressants with sedative effect; HI antihistamines with sedative effect; antihypertensive medications central action; baclofen; Thalidomide contributed to increasing oppression of the central nervous system.


Cautions Neuroleptic malignant syndrome: Neuroleptic malignant syndrome, characterized by paleness, hyperthermia, muscle rigidity, dysfunction of the peripheral nervous system, impaired consciousness.Signs of peripheral nervous system dysfunction, such as increased perspiration, and blood pressure lability may precede onset of hyperthermia, and thus, be an early warning signals. Some risk factors, such as dehydration or organic brain damage, despite the fact that such action can be attributed to antipsychotics idiosyncrasy probably are predisposing. Lengthening the  interval: tiaprid causes dose-dependent lengthening of the  interval. It is known that this effect increases the risk of serious ventricular arrhythmia, it is enhanced by bradycardia, with hypokalemia as well as in the case of congenital or acquired long interval QT (combination with drugs that prolong the anastrozole for men interval). Hypokalemia should be adjusted prior to use of the drug, except it should ensure that control of clinical, and electrolyte balance. When extrapyramidal syndrome induced by neuroleptics, instead of using dopamine agonists should be prescribed anticholinergic drugs. In the period of treatment should refrain from activities potentially hazardous activities that require high concentration and psychomotor speed reactions.

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