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what is testosterone propionate

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what is testosterone propionate

Testosterone propionate is one of the most popular steroids in bodybuilding. Testosterone propionate is for the development of muscle mass and strength, but due to the nature of the action, it is more often used during the drying period. Is one of the testosterone esters. Rosuvastatin is effective in adults with hypercholesterolaemia, with and without hypertriglyceridaemia, regardless of race, gender or age, including patients with diabetes mellitus and familial hypercholesterolemia. 80% of patients with hypercholesterolemia IIa and what is testosterone propionate classification Fredrickson at application rosuvastatin concentration reaches the values in patients with heterozygous familial hypercholesterolemia treated with rosuvastatin in dosages from 20 to 80 mg scheme for accelerated titration dose, there was a positive dynamics of the lipid profile. After titration to a daily dose of 40 mg per day (12 weeks) concentration decreased by 53%. In 33% of patients had achieved a reduction in the concentration . In patients with homozygous familial hypercholesterolemia treated with rosuvastatin at doses of 20 and 40 mg, the mean reduction. The additive effect was observed in combination with fenofibrate against the concentration of TG and nicotinic acid (more than 1 g per day) in relation to the concentration . in patients with lower risk for coronary heart disease and subclinical atherosclerosis, which is estimated by the thickness of the complex “intima-media” carotid artery, rosuvastatin 40 mg / day significantly slowed the rate of progression IMT for maximum of 12 segments of the carotid artery compared to placebo at a rate – 0.0145 mm / year . The dose of 40 mg should be used only in patients with severe hypercholesterolaemia and high risk for cardiovascular disease. The maximum concentration of rosuvastatin plasma levels achieved approximately 5 hours after oral administration. The absolute bioavailability of ≈ 20%. The distribution of Rosuvastatin is metabolized mainly by the liver, which is the main site of cholesterol synthesis . The volume of distribution of rosuvastatin is approximately 134 liters french press exercise. Approximately 90% of rosuvastatin is bound to plasma proteins, mainly to albumin. Metabolism Biotransformation exposed to a limited number of what is testosterone propionate (approximately 10%). The metabolism of rosuvastatin marginally associated with cytochrome isozymes system. The main identified metabolites of rosuvastatin are what is testosterone propionate and lactone metabolites. N-desmetilrozuvastatin approximately 50% less active than rosuvastatin lactone metabolites are pharmacologically inactive. Over 90% of the pharmacological activity for the inhibition of the circulating HMG-CoA reductase inhibitor rosuvastatin is provided, and the rest – its metabolites. Excretion Approximately 90% of the accepted dose of rosuvastatin is excreted unchanged through the intestines (including unabsorbed and absorbed rosuvastatin), and the rest excreted by the kidneys. In unaltered by the kidneys is displayed for about 5% of the administered dose. The of 19 hours, does not change with increasing dose. The geometric mean plasma clearance of approximately 50 l / h (coefficient of variation 21.7%). As in the case , a process of “hepatic” capture involved rosuvastatin membrane transporter of cholesterol through the membrane. This vector plays an important role in the removal of rosuvastatin is the liver. The linearity Systemic exposure of rosuvastatin increases in proportion to dose. superdrol for sale preparation h bodybuilding melatonin 10 mg bestellen bodybuilding and stretch marks Related Posts testosterone cypionate vs propionate testosterone propionate cycle testosterone propionate vs enanthate...

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Buy testosterone propionate may cause drowsiness, especially at the beginning of treatment, so you should refrain from drinking alcohol and use caution when co-administered with drugs depressing the central nervous system. In connection with the presence of anti-histamine effect, cinnarizine may affect the result of doping control athletes (false positive result), and can also neutralize the positive reaction during skin diagnostic samples (4 days prior to study treatment should be discontinued). with long-term use of the drug is recommended to perform the control of liver function examination, renal, clinical analysis of peripheral blood. Patients suffering from Parkinson’s disease, cinnarizine should be used only in cases where the benefits from its destination exceeds the possible risk of deterioration. Patients with these rare genetic disorders like galactose intolerance, lactase deficiency or malabsorption syndrome glucose / galactose should not take cinnarizine as the preparation contains 175 mg of lactose monohydrate, exercise climber. Overdose The maximum recommended dose buy testosterone propionate should not exceed 225 mg (9 tablets) per day. In case of overdose There is no specific antidote, you need to take a gastric lavage and activated charcoal. Treatment – symptomatic. The action of the drug on the ability to drive vehicles and to operate machinery with an increased risk of injury Because the drug can cause drowsiness, especially at the beginning of treatment should refrain from driving and potentially hazardous activities that require high buy testosterone propionate concentration and psychomotor reactions. steroids anabolic for sale hgh uk buy steroid online Related Posts testosterone propionate vs enanthate testosterone propionate cycle testosterone cypionate vs propionate testosterone propionate dosage what is testosterone propionate testosterone propionate...

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testosterone propionate cycle

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testosterone propionate cycle

The drug testosterone propionate is resorbed in the stomach testosterone propionate cycle and intestines. Maximum plasma concentration of the drug after oral administration is 1-3 hours. Contact cinnarizine plasma protein is 91%. Completely metabolized in the liver (by glyukuronirovaniya). Displays in the form of metabolites: 1/3 – 2/3 and kidneys – intestines. Therapeutic indications Adults Treatment of cerebrovascular origin symptoms (dizziness, tinnitus, headache vascular genesis, irritability, impaired memory and concentration), vestibular disorders (including Meniere’s disease, vertigo, tinnitus, nystagmus, nausea and vomiting labyrinthine origin), prevention kinetoses ( “road of disease” – sea and air sickness), migraine (prevention of attacks); peripheral circulatory disorders ( “intermittent” claudication, Raynaud’s disease, diabetic angiopathy, thrombophlebitis, trophic disorders (including trophic and varicose ulcers), akrotsianoz, paresthesia, nocturnal cramps and cooling in the limbs). Children older than 5 years Prevention kinetoses ( “traffic’s disease” – sea and air sickness) Contraindications: Hypersensitivity, pregnancy, lactation. Age 5 years (effectiveness and safety have been established). Precautions In Parkinson’s disease. Pregnancy and lactation Although pre-clinical studies testosterone propionate cycle have not revealed teratogenic effects of cinnarizine, the drug can be assigned during pregnancy only if the expected benefit to the mother outweighs the potential risk to the fetus. There are no data on the penetration of cinnarizine in mother’s milk, so in while receiving breastfeeding drug should be discontinued. Dosing and Administration Inside, after a meal. If you violate the circulation of the brain – 25-50 mg (1-2 tablets) three times a day; in violation of the peripheral circulation – at 50-75 mg (2-3 tablets) three times a day; during vestibular disorders – 25 mg three times a day; when kinetoses ( “Road” disease): adults – 25 mg half an hour before the trip (if necessary repeated reception of 25 mg every 6 hours). The maximum dose should not exceed 225 mg (9 tablets) per day. The dose for children aged 5 to 12 years – 14 doses, the recommended adult dose for children over 12 years corresponds to the dose recommended for adult patients. With a high sensitivity to the drug treatment is initiated with half the dose, increasing it gradually. The course of treatment from a few weeks to several months. Interaction with other drugs increases the effects of alcohol and sedatives, tricyclic antidepressants. In an application with nootropic, antihypertensive and vasodilator enhances their effect, while the use of drugs prescribed for hypotension – reduces their effect. Side effect On the part of the nervous testosterone propionate cycle system: drowsiness, fatigue, headache, extrapyramidal disorders (tremor of the limbs and increased muscle tone, hypokinesia elderly patients in long-term treatment, in such cases, treatment should be discontinued), romanian deadlift, depression. From the digestive system: dry mouth, epigastric pain, dyspepsia, cholestatic jaundice (extremely rare). For the skin: sweating, development volchanochnopodobnogo syndrome, lichen planus (extremely rare), skin rash. Other: Allergic reactions, increased body mass index. men’s health metandienone for sale anastrozole bodybuilding dosage bodybuilding grocery list bodybuilding workouts for men over 40 buy ghrp6 bodybuilding gyms Related Posts buy testosterone propionate testosterone propionate vs enanthate what is testosterone propionate testosterone cypionate vs propionate testosterone propionate buy testosterone propionate half...

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testosterone cypionate vs propionate

in the complex therapy of chronic heart failure II (in the presence of clinical manifestations) testosterone cypionate, III and IV functional class; tachysystolic form of flicker and flutter and paroxysmal chronic course (especially when combined with chronic heart failure). Contraindications: Hypersensitivity to the drug, glycoside intoxication, testosterone cypionate vs buy testosterone propionate online, atrioventricular block II degree, intermittent complete blockade. Precautions (comparing the benefit / risk): atrioventricular block I degree, sick sinus syndrome without pacemaker, the probability of unstable conduct on the atrioventricular node, specifying a history of attacks of Morgagni-Adams-Stokes, hypertrophic subaortic stenosis, isolated mitral stenosis with a rare frequency heart rate, cardiac asthma in patients testosterone propionate vs cypionate with mitral stenosis (in the absence of the one-hisistolicheskoy atrial fibrillation), acute myocardial infarction, unstable angina, arteriovenous shunt, hypoxia, heart failure with diastolic dysfunction (restrictive cardiomyopathy, amyloidosis heart, constrictive pericarditis, tamponade heart), arrythmia, marked dilatation of the heart cavities, “pulmonary” heart. Electrolyte disorders: hypokalemia, hypomagnesemia, hypercalcemia, hypernatremia. Hypothyroidism, alkalosis, myocarditis, advanced age, renal hepatic insufficiency, obesity. Dosage and administration by slow intravenous injection. Dose selected testosterone cypionate vs propionate individually depending on the nosology and patient response to therapy. The maximum single dose – 0.25 mg daily mg -1. The drug is administered in low doses of 0.1-015 mg at intervals of from 30 minutes to 2 hours. At an average rate digitaliza-tion yk11 side effects in the saturation period is usually 0.25 mg administered two times a day at intervals of 12 hours. The period saturation averages 2 days. Maintenance dose strofantinom-G does not exceed 0.25 mg / day. Side effects: Occasionally allergic reactions. Other side effects are mainly due to drug overdose or increased sensitivity to the patient’s cardiac glycosides. Overdose Symptoms of overdose strofantinom-T varied. Cardio-vascular system: arrhythmia, including bradycardia, AV-block, ventricular tachycardia or extrasystole, ventricular fibrillation. On the part of the digestive tract: anorexia, nausea, vomiting, diarrhea. On the part of the central nervous system and sensory organs: headache , fatigue. dizziness, rarely – staining the surrounding objects in green and yellow colors, a sense of flicker flies before his eyes, blurred vision, scotoma, macro- and micropsia: very rarely confusion, sinkoialnye state. With the development of glycoside intoxication drug buy testosterone propionate should be discontinued; assign the patient potassium supplements, parenteral administration unitiola, symptomatic therapy. Interaction with other drugs agonists, methylxanthines, reserpine, tricyclic antidepressants increases the risk of heart rhythm disorders. Beta-blockers, and antiarrhythmics class, verapamil and magnesium sulfate increase the severity of reducing the conductivity . Quinidine, methyldopa, clonidine, spironolactone, amiodarone, verapamil , captopril, erythromycin and tetracycline increase the concentration in the blood, female bodybuilding (competitive decreased secretion of the proximal renal tubules). Corticosteroids and diuretics increase the risk of hypokalemia and hypomagnesemia, angiotensin-converting enzyme inhibitors and angiotensin receptor – reduce. calcium salts, catecholamines, diuretics ( more kartoangidrazy thiazide and inhibitors), glucocorticosteroids, insulin, increase the risk of glycoside intoxication. Cautions With extreme caution in patients with hyperthyroidism and atrial premature beats. In view of the low therapeutic range during treatment requires testosterone cypionate vs enanthate careful medical monitoring and individual dose selection. In case of violation of renal excretory function should be reduced dose (prevention glycoside intoxication). Overdose probability increases with hypokalemia , hypomagnesemia, hypercalcemia, hypernatremia, marked dilatation of the heart cavities, “pulmonary” heart, alkalosis, in elderly patients. Particular caution and testosterone cypionate...

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testosterone propionate vs enanthate

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Testosterone propionate. Paracetamol blocks cyclooxygenase I and II only in the central nervous system, affecting the pain and thermoregulatory centers (in inflamed tissues cellular peroxidase neutralize the effect of paracetamol on cyclooxygenase), which explains the almost complete absence of anti-inflammatory effect. No effect on prostaglandin synthesis in peripheral tissues causes lack of a testosterone propionate vs enanthate negative effect on water-salt exchange (sodium and water retention), and gastrointestinal mucosa.The possibility of formation metgemoglobina- unlikely. Indications . Moderately or weakly expressed pain (headache, toothache, migraine pain, neuralgia, myalgia) Increased body temperature in cold and other infectious and inflammatory diseases. Contraindications: Hypersensitivity to paracetamol. Children under 15 years old. Be wary – kidney and liver failure, benign hyperbilirubinemia (including Gilbert’s syndrome, viral hepatitis, alcoholic liver disease), alcoholism, pregnancy, lactation, old age, lack of glucose-6-phosphate dehydrogenase. Dosage and administration: Administered orally with plenty of fluids 1-2 tablets 2-3 times a day at intervals of at least 4 hours. The maximum single dose for adults and children over 15 years is 2 tablets (1000 mg) daily – 8 tablets (4000 mg). In patients with impaired liver testosterone propionate vs enanthate and kidney function, with Gilbert’s syndrome and in elderly patients with an interval between doses of the drug should be at least 8 hours and the daily dose should be reduced. The duration of the maximum of 5 days when administered as an analgesic and 3 days as an antipyretic. Side effects: Nausea, vomiting, epigastric pain, allergic reactions (skin rash, pruritus, urticaria, angioedema). Rarely – anemia, leukopenia, grombotsitopeniya, agranulocytosis. With prolonged use at high doses – gepatotoksicheekoe effects, hemolytic anemia, aplastic anemia, methemoglobinemia, pancytopenia. Renal toxicity (renal colic, Piura, interstitial nephritis, papillary necrosis). Overdose: Symptoms: pale skin, anorexia, nausea, vomiting; gepatonekroz (necrosis severity is directly dependent on the degree of overdose). The toxic effect of the drug in adults is possible after receiving more than 10-15 g of paracetamol: increased activity of “liver” transaminases, increased prothrombin time, detailed clinical picture of liver damage manifests itself in 1-6 days. Rarely hepatic dysfunction develops lightning speed and can be complicated by renal insufficiency (tubular necrosis). Treatment: stop taking the drug, gastric lavage, activated charcoal to take. Further therapeutic measures should be undertaken in a hospital: the introduction of donators of and precursors of glutathione synthesis – through methionine 8-9 h after the overdose . The need for additional therapeutic measures is determined depending on the concentration of paracetamol in the blood, and the time elapsed after administration. Interaction: Stimulants microsomal oxidation in the liver (phenytoin, ethanol, barbiturates, rifampicin, phenylbutazone, tricyclic antidepressants) increase the production of hydroxylated active metabolites, which makes the possibility of severe intoxication with small overdoses. Ethanol contributes to the development of acute pancreatitis. Inhibitors of microsomal oxidation (including cimetidine) reduce the risk of hepatotoxicity. Reduces the effectiveness of uricosuric drugs. Special instructions: With caution and under medical supervision should testosterone propionate vs enanthate use the drug to patients with impaired hepatic or renal function, in conjunction with other anti-inflammatory and analgesic agents, as well as with anticoagulants and drugs that affect the central nervous system. When receiving metoclopramide, domperidone or cholestyramine also need to consult with your doctor. Distorts the performance of laboratory tests cypionate vs enanthate for the quantitative determination of uric acid in the plasma. In order to prevent liver...

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Testosterone propionate stimulates the synthesis and regeneration of the visual pigment rhodopsin, helping to improve visual acuity, improve adaptation to darkness and low light conditions. It has angioproteguoe effect and improves blood flow to the retina eyes. The product testosterone propionate results has an antioxidant effect. Indications for use: – Manifestations of the syndrome eye fatigue during prolonged work with a computer and reading; – myopia varying degrees; – violation of the mechanisms of adaptation of a dark (day-blindness); – diabetic retinopathy; – central and peripheral retinal dystrophy; – in the complex of primary glaucoma therapy – in the period recovery after surgery on the eyes. Contraindications Individual hypersensitivity to the drug, children under 7 years (due to the lack of clinical data). Use during pregnancy and breast-feeding During pregnancy and lactation are used testosterone propionate results only if the expected benefit to the mother outweighs risk to the fetus and infant. Dosing and Administration Children from 7 years of age: 1 tablet a day. Adults: 2 tablets per day. The tablet drink the required amount of water. The course of treatment – 1 month. Repeated courses on doctor’s advice. Side effect. If you are hypersensitive to the drug, possible allergic reactions. special instructions Do not exceed the stated daily dose. Product form. Tablets, film-coated. 30 tablets in blister testosterone propionate results film and aluminum foil. 1 blister with instruction on use is placed in a cardboard box. steroiden kaufen anabolika steroide kaufen Related Posts testosterone propionate half life testosterone propionate buy testosterone propionate cream testosterone propionate vs enanthate testosterone cypionate vs propionate propionate...

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The half-life after propionate testosterone intravenous injection of 1500000 IU streptokinase – 1 hour, streptokinase-plasminogen complex – about 23 minutes. Biotransformed in the liver by hydrolysis. It is displayed in a small amount of the kidneys. In diseases of the liver is slowed down clearance, renal insufficiency does not affect clearance. Indications Indications for use of streptokinase are: propionate testosterone pulmonary embolism and its branches, thrombosis and embolism, peripheral arterial thrombosis of superficial and deep veins (legs, pelvis), acute myocardial infarction (during the first 12 hours), thrombosis, vascular retinal and other conditions, proceeding with acute thrombosis or embolism, and the threat of blood clots. Dosing and dosing regimen Enter streptokinase intravenously, and in necessary cases – intra. Usually administered intravenously in an initial dose of 250,000 IU in 50 ml isotonic sodium chloride solution for 30 min (30 drops per minute). The dose is usually the beginning of a blood clot lysis. Streptokinase administration was then continued per hour. The total duration of administration is usually 16-18 hours. The subsequent treatment is carried out with heparin and indirect anticoagulants. With extensive arterial and venous thrombosis sometimes need long-term administration of the drug. Intra-arterial administration of streptokinase is used in acute myocardial infarction (initial dose of 20,000 IU; maintenance – 2000-4000 IU per minute for 30-90 minutes). In all cases, the introduction of streptokinase propionate testosterone should be initiated as early as possible, as the best effect is observed in fresh thrombi. streptokinase treatment is carried out under the control of the thrombin time and fibrinogen content of the blood. Side effect When using streptokinase can develop non-specific reactions to the protein: headache, nausea, vomiting, allergic reactions (use of corticosteroids is recommended when expressed allergic reactions). With rapid intravenous possible development of hypotension, heart rhythm disturbances. Keep in mind the possibility of emboli (due to the mobilization of the elements of the thrombus). Contraindications The drug is contraindicated in acute bleeding, hemorrhagic diathesis, fresh ulcers of the gastrointestinal tract, after recent surgery, and severe hypertension, bacterial endocarditis, cerebral circulatory disorders, pulmonary tuberculosis (cavernous forms), in the first trimester of pregnancy. Overdose Symptoms: increased side effects (most often – hemorrhage) Treatment: haemorrhage (if available), purpose of antifibrinolytic agents (tranexamic acid paraaminometilbenzoynaya acid, or kallikrein protease inhibitors, including aprotinin, aminocaproic acid – 5 g / h, followed by 1 g / hr for 4-8 hours to achieve the effect), replacement of blood loss (except dextran and hydroxyethyl starch), symptomatic treatment. Precautionary measures Treatment is carried out under the supervision of indicators thrombin or partial thromboplastin time. With extreme caution is used when expressed violations of liver and kidney function, diabetes, asthma, streptococcal infections, including rheumatism, bronchiectasis with hemoptysis, varicose veins of the esophagus, the recent appointment of anticoagulants, states after cardiopulmonary resuscitation, mechanical ventilation, bleeding accompanying urological diseases, including urolithiasis, as well as chronic diseases of the gastrointestinal tract, menorrhagia, menstrual bleeding, earlier (from 5 days to 1 year) conducted a course of treatment with streptokinase in old age (over 75 years). The drug is used in a hospital environment. special instructions Do not use the system in myocardial propionate testosterone infarction after 24 hours or more, deep vein thrombosis – 14 days or more, thrombosis of retinal vessels: arterial occlusions – 6-8 hours or more, venous – 10 days or more,...

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