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primobolan cycle

Symptoms: dizziness, nausea, and vomiting. With intravenous administration of ranolazine following symptoms were further noted: diplopia, confusion, fainting. Severity of symptoms can be enhanced by increasing the dose. Treatment: . Symptomatic primobolan cycle under careful medical supervision for 30 minutes after taking the drug can take measures to prevent its absorption from the gastrointestinal tract (gastric lavage, administration of activated charcoal). Hemodialysis is ineffective.

Interaction with other drugs

Ranolazine is a substrate of cytochrome. The simultaneous use of ranolazine  isoenzyme inhibitors increases the concentration in plasma ranolazine. Probability of development of dose-related side effects (eg, nausea, dizziness) may also increase with an increase in ranolazine plasma concentrations.

Concomitant use contraindicated: Strong inhibitors Concomitant use of ranolazine and strong inhibitors  (eg, itraconazole, ketoconazole, voriconazole, posaconazole, HIV protease inhibitors, clarithromycin, telithromycin, nefazodone) is contraindicated (see section. “Contraindications” ). Simultaneous treatment with ketoconazole 200 mg 2 times a day increases the of ranolazine by 3.0 – 3.9 times. Grapefruit juice is also a potent inhibitor isoenzyme.

Concomitant use with caution: Moderate inhibitors Inducers of CYP3A4 should not start taking ranolazine to patients receiving treatment with inducers of  (rifampicin, phenytoin, phenobarbital, carbamazepine, St. John’s wort (Hypericum perforatum)). Since, for example, rifampicin (600 mg once daily) reduces the equilibrium concentration in the blood plasma ranolazine of about 95%. Inhibitors isozyme Ranolazine partially metabolized isoenzyme. The simultaneous use of ranolazine isozyme  inhibitors may increase the ranolazine plasma concentrations. The simultaneous use of ranolazine 1000 mg 2 times a day with a potent inhibitorisozyme paroxetine 20 mg 1 time per day increases the average concentration of ranolazine plasma at steady state is about 1.2 times. No dose adjustment is required. The simultaneous use of ranolazine 500 mg 2 times a day, a potent inhibitor of CYP2D6 isozyme may lead to an increase in AUC of ranolazine of about 62%.The inhibitors / substrates of P-gp (P-glycoprotein) Ranolazine is a substrate of P-gp. Inhibitors of P-gp (such as cyclosporine, verapamil) increase the concentration of ranolazine plasma. Verapamil (120 mg tid) increases the equilibrium concentration of ranolazine 2.2 times. For patients treated with inhibitors of P-gp, ranolazine recommended dose titration. You may need to decrease the dose of ranolazine. On the other hand, ranolazine is a moderate inhibitor of P-gp and may increase the concentration of P-gp substrates in plasma. Tissue distribution of drugs which are transported by P-gp, may be increased.Substrates isozyme There is evidence that ranolazine is a weak inhibitor isozyme. Receiving ranolazine 750 mg 2 times a day increases in the plasma concentration of metoprolol in 1.8 times. Therefore, while the use of ranolazine, may potentiate metoprolol or other substrates isoenzyme primobolan cycle (e.g., propafenone and flecainide, to a lesser extent, tricyclic antidepressants and neuroleptics) thereby may require dose reduction of these drugs. Substrates isoenzyme  potential to inhibit isoenzyme  is not installed. During the appointment, together with the isoenzyme substrates (eg bupropion, efavirenz, cyclophosphamide) recommend caution. Digoxin There is evidence of increasing the concentration of digoxin in the blood plasma of on average 1.5 times, while the use of digoxin and ranolazine. Therefore, a control digoxin concentrations at the beginning and after the end of therapy with ranolazine. Substrates isoenzyme  is a weak inhibitor of isozyme  which may lead to increased concentrations isoenzyme  substrates in plasma and require dose correction sensitive substrates isoenzyme for example, simvastatin, lovastatin) and substrates  with narrow therapeutic range (eg, cyclosporine, tacrolimus, sirolimus, everolimus). simvastatin metabolism and clearance of simvastatin are highly dependent on  isoenzyme. Receiving ranolazine 1000 mg two times a day increases the concentration of the simvastatin lactone and simvastatinovoy acid in blood plasma at about 2 times. Simvastatin in high doses associated with the development of rhabdomyolysis, also cases of rhabdomyolysis while the use of ranolazine and simvastatin have been described. The maximum dose of simvastatin for patients receiving simultaneously primobolan cycleranolazine, should not exceed 20 mg / day. buy anabolic steroids online bruce lee’s workout anabolic steroids online uk

primobolan dosage

primobolan for saleData on the use of ranolazine in pregnant women are not available. Penetration of ranolazine in breast milk has not been studied. In the absence of data to use the drug primobolan dosage during pregnancy and lactation is contraindicated.

The tablets should be swallowed whole, drinking plenty of fluids, do not pulverize, without breaking or chewing. Food does not affect the bioavailability of the drug, so it can be taken without regard to meals. The recommended initial dose primobolan depot of the for adults is 500 mg two times a day. After 2-4 weeks the dose, if necessary, can be increased to 1000 mg two times a day. The maximum daily dose is 2,000 mg. When side effects caused by drug intake for example, dizziness, nausea, or vomiting), it is necessary to reduce the dose to 500 mg. If after that the symptoms do not disappear, use of the drug should be discontinued. For patients with chronic heart failure (III-IV functional class classification), with renal insufficiency mild to moderate (creatinine clearance 30-80 ml / min), hepatic insufficiency mild (5-6 points on a scale Child-Pugh) with patients weighing less than 60 kg, and patients over 65 years and for patients taking isoenzyme inhibitors and P-gp (P-glycoprotein), dose titration is recommended.

Side effect

Side effects seen in patients taking in most cases characterized by mild or moderate severity and usually develop within the first 2 weeks of application. The following are the side effects, which has been recognized as a possible link with .

On the part of metabolism and nutrition: Uncommon: decreased appetite, anorexia, dehydration. On the part of the psyche:Uncommon: anxiety, insomnia, dizziness, hallucinations. rare: disorientation . From the nervous system: Common: dizziness, headache. Uncommon: lethargy, syncope, hypoesthesia, somnolence, tremor, postural dizziness, paresthesia. rare: amnesia, confusion, loss of consciousness, gait ataxia, gait disturbance, parosmiya. With the organ of vision: Uncommon: blurred vision, visual disturbances, diplopia.On the part of the organ of hearing and labyrinth disorders: Uncommon: vertigo, tinnitus. rare: hearing loss. On the part of the cardiovascular system: Infrequent: “tides” of blood to the face primobolan side effects, marked reduction in blood pressure. rare: cold extremities, postural hypotension. The respiratory system, organs, thoracic and mediastinal disorders: Uncommon: dyspnoea, cough, epistaxis. rare: feeling of constriction in the throat. On the part primobolan dosage of the digestive tract: Common: constipation, nausea , vomiting. Uncommon: abdominal pain, dryness of the oral mucosa, dyspepsia, flatulence, stomach discomfort.rare: pancreatitis, erosive duodenitis, hypoesthesia oral cavity. For the skin and subcutaneous tissue disorders: Uncommon: pruritus, rash. rare: allergic dermatitis, urticaria, cold sweat, skin rash, angioedema. From the musculoskeletal system: Uncommon: pain in the extremities, muscle cramps, swelling of the joints. rare: muscle weakness. On the part of the kidney and urinary tract:Uncommon: dysuria , hematuria, chromaturia. rare: acute renal failure, urinary retention. With the genitourinary system: rare: erectile dysfunction. General disorders: Common: asthenia. Uncommon:fatigue, peripheral edema. Other disorders: Uncommon: increased creatinine concentration in blood plasma , increasing concentrations of urea in blood plasma, lengthening the QTc interval primobolan dosage corrected, thrombocytosis and leukocytosis, weight loss. rare: increased activity of “liver” enzymes.

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oral primobolan

After receiving the highest concentration of ranolazine inside ranolazine plasma , usually reached in 2 – 6 hours When receiving ranolazine 2 times a day equilibrium concentration is usually achieved within 3 days.. The mean absolute bioavailability of ranolazine after oral administration is 35-50%, with a high degree of individual variability. At higher oral primobolan doses of 500 to 1000 mg per day, 2 times a 2.5-3 fold increase observed AUC (area under the curve “concentration-time”) in an equilibrium state. In healthy volunteers, C max at steady state is about 1770 ng / ml at steady state AUC 0-12 on average equal to 13700 hr x ng / mL after administration of 500 mg two times a day. Food does not affect the speed and completeness of absorption of ranolazine. Distribution: Approximately 62% of ranolazine binds to plasma proteins, mainly alpha-1 acid glycoprotein and albumin slightly. The mean volume of distribution at steady state  is about 180 l. Metabolism: Ranolazine undergoes rapid and almost complete metabolism predominantly in the liver. The most important metabolic pathways are ranolazine O-demethylation and N-dealkylation. Ranolazine is metabolized mainly isoenzyme CYP3A4, and isoenzyme CYP2D6. Upon receiving 500 mg 2 times a day for people with insufficient activity of the isoenzyme CYP2D6, AUC indicator exceeds the same amount for people with a normal metabolic rate by 62%. A similar difference for a dose of 1000 mg 2 times per day was 25%.

Excretion: unchanged to the kidneys and the bowel is allocated less than 5% of the dose of ranolazine. Clearance of ranolazine is dose-dependent, decreasing with the increase it. The half-life of ranolazine in an equilibrium state after oral administration is about 7 hours.

Oral primobolanactive metabolites increased 5 times in patients with severe renal failure severity. Duration finding ranolazine plasma increases 1.2 times in patients with moderate renal impairment (creatinine clearance of 30-60 ml / min). In patients with severe renal failure severity (creatinine clearance <30 mL / min) increasing the length of stay in the blood plasma ranolazine was found to 1.3-1.8 times. Effect of dialysis on the pharmacokinetics of ranolazine has not been evaluated. Hepatic impairment the AUC of ranolazine is not changed in patients with hepatic insufficiency mild, but increased by 1.8 times in the case of hepatic failure, moderate (7-9 points on a scale Child-Pugh); in these patients was more pronounced elongation of the QTc interval. Experience in the use of ranolazine in patients with hepatic insufficiency, severe gravity (more than 9 points on a scale Child-Pugh) is absent. Advanced age is clinically significant changes in pharmacokinetic parameters of ranolazine as a function of age was observed. Older patients due to age-related decrease in renal function may increase ranolazine actions. Body weight The patients weighing 40 kg, it was noted that the effect of ranolazine 1.4 times greater than its effect in patients with a body weight of 70 kg.




  • Hypersensitivity to the active substance or to any of the excipients (see section. Composition );
  • lactase deficiency, hereditary lactose intolerance, glucose-galactose malabsorption (for 1000 mg);
  • severe renal insufficiency (creatinine clearance <30 mL / min);
  • liver failure secondary (7-9 points on a scale Child-Pugh) or severe (more than 9 points on a scale Child-Pugh) severity;
  • simultaneous application of potent inhibitors isoenzyme CYP3A4 (itraconazole, ketoconazole, voriconazole, posaconazole, HIV protease inhibitors, clarithromycin, telithromycin, nefazodone);
  • simultaneous application of antiarrhythmics of class IA (e.g., quinidine) or a class III (e.g., dofetilide) except amiodarone; with sotalol.
  • children under 18 years of age (efficacy and safety have not been established);
  • pregnancy;
  • during breastfeeding.Carefully
  • liver failure, mild ;
  • renal failure mild or moderate (creatinine clearance 30-80 ml / min);
  • age over 65 years;
  • patient body weight less than 60 kg;
  • Chronic heart failure (III-IV functional class NYHA classification);
  • syndrome of congenital long  history, family history; diagnosed acquired prolongation of the interval ;
  • failure isozyme;
  • simultaneous use with moderate inhibitors of isoenzyme (diltiazem, fluconazole, erythromycin);
  • simultaneous use with inducers isoenzyme (rifampicin, phenytoin, phenobarbital, carbamazepine, St. John’s wort (Hypericum perforatum));
  • simultaneous oral primobolan application of inhibitors of P-gp (P-glycoprotein) (verapamil, cyclosporin).
    In patients with a combination of several of the above conditions may increase the action of ranolazine, includingIt increases the risk of side effects.In this case, requires regular monitoring of the state for the purpose of early detection of adverse effects, if necessary, may require dose reduction or withdrawal of the drug.

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primobolan only cycle

Treatment and prevention of erectile dysfunction. To restore and enhance sexual function, stimulation of sexual desire, as well as prevention of their primobolan only cycle violations. Physical and emotional stress, convalescence after somatic and infectious diseases, to increase the efficiency of the organism.

Contraindications: Hypersensitivity to the drug, anatomical deformation of the penis (including angulation, cavernous fibrosis or Peyronie’s disease), hypertension, convulsive conditions (including epilepsy), bleeding tendency, chronic heart failure decompensation, unstable angina, transferred in the last 6 months: myocardial infarction, stroke, or life-threatening arrhythmia; liver dysfunction, age 18 years. Precautions: chronic heart failure, older age.

Dosing and Administration In order to avoid complications of the drug should be used primobolan cycle by a physician! The drug is administered orally. For the treatment and prevention of erectile dysfunction, restore and enhance sexual function, stimulation of sexual desire, as well as prevention of their violations, drug use 1-2 capsules per day morning. The duration of the 2-3 months. Recommended repeated 2-3 month course of the drug 2 times a year at intervals between courses of 3-4 weeks. When physical or emotional primobolan only cycle strain, to improve the efficiency of the organism – 1 capsule per day (in the morning ) within one month.

Side effects Possible allergic reactions, increased blood pressure, tachycardia, headache, hypoglycemia, insomnia, nasal bleeding.

Overdose In applying the drug in doses exceeding recommended, may increase side effects.

Interaction with other drugs increases the effects of psychostimulants and analeptikov (including caffeine, camphor and others.) Antagonize the interaction with drugs that depress the central nervous system (antiepileptic drugs, antipsychotics, tranquilizers, sedatives). It enhances the effect of hypoglycemic drugs, warfarin. It increases the risk of developing resistance primobolan to loop diuretics. Perhaps strengthening the action of antianginal drugs.

Cautions Raylis promotes erection offensive only in the presence of sexual arousal. Spontaneous erection without erotic stimulation medication is not causing. For the diagnosis of erectile dysfunction, identify possible reasons for their choice and adequate treatment is necessary to collect a complete medical history and conduct a thorough examination. Due to lack of data for the study reprotoksicheskih properties of the drug, when used should provide for methods of effective contraception to patients of both sexes. Preparations for the treatment of erectile primobolan only cycle dysfunction, should not be given to men for whom sexual activity is undesirable. No negative interactions with alcohol is not revealed.


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