anti estrogen pills

Topiramate is absorbed quickly and efficiently. Its bioavailability is 81%. Food intake has no clinically significant effect on the bioavailability of topiramate. Since plasma protein binds to 13-17% of topiramate.After receiving a single dose of 1200 mg the average volume of distribution is 0,55-0,8 l / kg. The anti estrogen pills value of volume of distribution depends on sex: for women it is about 50% of the values observed in men, which is associated with higher levels of body fat women.

After oral administration, it is metabolized about 20% of the dose. However, in patients receiving concomitant therapy with antiepileptic drugs that induce the enzymes responsible for drug metabolism, the metabolism of topiramate is increased to 50%. Six virtually inactive metabolites have been isolated and identified from the plasma, urine and human faeces. The main route of excretion of unchanged topiramate (70%) and its metabolites are the kidneys. Following oral administration of topiramate plasma clearance is 20-30 ml / min. The pharmacokinetics of topiramate is linear, plasma clearance remains constant anadrol, and the area under the curve “concentration-time» anti estrogen pills in the dose range from 100 to 400 mg increases proportionally with dose. In patients with normal renal function in order to achieve stable plasma concentrations may need 4 to 8 days. The value of maximum concentration after repeated oral administration of 100 mg twice a day averaged 6.76 ug / ml. After receiving multiple doses of 50 and 100 mg twice a day half-life of plasma topiramate averaged 21 hour.

In patients with impaired renal function, moderate and severe plasma and renal clearance of topiramate is reduced as a consequence may increase the equilibrium concentration of topiramate in plasma when compared with patients having normal renal function. In addition, in patients with impaired renal function, it takes longer to reach equilibrium concentration of topiramate in the blood. Patients with moderate or severe renal insufficiency is recommended to use half the recommended initial and maintenance dose.

Topiramate effectively derived from the plasma by hemodialysis. Long term hemodialysis may reduce the concentration of topiramate in the blood below the quantity required anastrozole bodybuilding to maintain the anticonvulsant activity. To avoid rapid fall topiramate plasma concentration during hemodialysis, may require the appointment of an additional dose of the drug Topamax ®. When dose adjustment should be taken into account:

  1. dialysis duration,
  2. the value of clearance anti estrogen pills used hemodialysis systems,
  3. effective renal clearance of topiramate in patients on dialysis.

Plasma clearance of topiramate is reduced by an average of 26% in patients with hepatic insufficiency, moderate or severe. Therefore, patients with hepatic impairment topiramate should be used with caution.

In elderly patients without renal disease, the plasma clearance of topiramate is unchanged.

The pharmacokinetics of topiramate in children up to 12 years

The pharmacokinetic parameters of topiramate in children as well as adults receiving this drug as an adjunct therapy, are linear, while its ground clearance is independent of dose, and the equilibrium concentration in the plasma increases proportionally to increasing doses. It should be noted, however, that the clearance of topiramate in children increased, and the period of its half-life is shorter.Consequently, anti estrogen pills for the same dose per 1 kg of body weight anavar only cycle, the plasma concentrations of topiramate in children may be lower than in adults. In children as in adults, antiepileptic drugs that induce liver enzymes cause a reduction in the plasma concentrations of topiramate. bodybuilding coupon code 10

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nolvadex side effects

Absorption – high, bioavailability – 80%. Food intake has no clinically significant effect on bioavailability.The time to reach maximum concentration in plasma -2 hours after ingestion of 400 mg. The nolvadex side effects maximum blood concentration after repeated oral administration of 100 mg 2 times a day – 6.76 pg / ml. Relationship to plasma proteins – 13-17%.

The volume of distribution (1.2 g after administration) – 0,55-0,8 l / kg, depends on sex (female – 50% of the values observed in men). The equilibrium concentration is reached after 4-8 days, with renal failure – 10-15 days. It penetrates into breast milk. It is metabolized in the liver by hydroxylation, hydrolysis and glyukuronirovaniya 6 to form a pharmacologically inactive metabolites. Pharmacokinetics after single oral buy testosterone cypionate uk administration is linear, plasma clearance remains constant – 20-30 ml / min; value of the area under the curve “concentration – time» in the dose range of 100-400 mg increases proportionally with dose. The e after multiple-dose 100 and 50 mg 2 times a day -21 hours. In severe hepatic and renal (creatinine clearance less than 60 mL / min) and the plasma deficiency reduces renal clearance. Excreted by the kidneys in unchanged form (70%) and in the form of metabolites. Removed from the plasma by dialysis.

Indications for use as monotherapy – newly diagnosed epilepsy. As a subsidiary of the drug in adults and children older than 3 years – partial or generalized tonic-clonic seizures; seizures on the background of Lennox-Gastaut syndrome.

Contraindications: Hypersensitivity, pregnancy, lactation, children’s age (up to 3 years).

Precautions Renal or hepatic impairment, nolvadex side effects nefrourolitiaz (in history, including a family), hypercalciuria.

Dosing and Administration Inside, regardless of meals. Tablets should not be divided. When used as monotherapy, it is necessary to take into account the possible impact of the abolition of concomitant anticonvulsant therapy on seizure frequency. In cases where sharp cancel undesirable concomitant anticonvulsant therapy, reduce the dose of drug gradually reducing the dose to 1/3 every 2 weeks. If you cancel the drugs that are inducers of microsomal “liver” enzymes, topiramate plasma concentrations are increased. In such situations, if clinically indicated dose can be reduced. Adults masteron in the early monotherapy – 25 mg 1 time a day at bedtime for 1 week. Then increase the dose at intervals of 1 – 2 weeks at 25-50 mg / day (daily dose divided into 2 admission). At intolerance of such regimen, the dose is increased by a smaller amount, or over large intervals. The dose is adjusted depending on the effect. The recommended dose – 100 mg / day, maximum daily dose – 500 mg. In nolvadex side effects some cases, monotherapy for refractory epilepsy treatment topiramate dose of 1 g / day. Children over 3 years as monotherapy in the first week of treatment – 0.5-1 mg / kg / day (daily dose divided into 2 admission). The size of the dose and its rate of increase determined by the clinical efficacy and tolerability of therapy. The recommended dose range of topiramate monotherapy in children over 3 years – 3-6 mg / kg / day. When newly diagnosed partial seizures – up to 500 mg / day. When administered in combination with other antiepileptic drugs in adults the initial dose – 50 mg 1 time a day at night for 1 week. Further dose increase of 25-50 mg weekly until the effective dose. The average daily dose -200-400 mg, the multiplicity of reception – 2 times a day. If necessary, can be increased to a maximum daily dose – 1600 mg. The criterion for selection of the dose is the clinical effect, in some patients it may be achieved by taking the drug one time per day.

In carrying out the combination anticonvulsant therapy in children older than 3 years, the recommended total daily dose – 5-9 mg / kg in 2 divided doses. Selection of doses begin with 25 mg / day at night for 1 week. Further the dose can be increased to 1.3 mg / kg per 1-2 weeks and to take 2 doses. The daily dose of 30 mg / kg is generally well tolerated. In the days of hemodialysis, topiramate should be administered in addition to a dose equal to half the daily dose in 2 divided doses (before and after the procedure). Cancel the drug should be gradual to minimize the possibility of increasing the frequency seizures (100 mg / week).

Side effects of ataxia, decreased ability to concentrate, confusion, dizziness, fatigue, paresthesia, drowsiness, abnormal thinking; seldom – agitation, amnesia, decreased appetite, aphasia, depression, emotional lability, impaired speech, nystagmus, visual disturbances (including diplopia), perversion of taste sensations, nausea, nefrourolitiaz, weight loss. occurrence of the syndrome is possible nolvadex side effects (usually through 1 month after initiation of therapy), characterized by myopia accompanied by increased ocular hypertension. It also noted a sharp decrease in visual acuity and / or pain in the eye. Ophthalmic manifestations include: myopia, reducing the depth of the anterior chamber of the eye, bloodshot eyes and mucosa increased intraocular pressure. In some cases – mydriasis. A possible mechanism methenolone of this syndrome is the increase supratsiliarnogo effusion, leading to forward displacement of the lens and the iris, and as a result the development of secondary angle-closure glaucoma. Treatment includes discontinuation and measures aimed at reducing the intraocular pressure. Perhaps the development of allergic reactions.

Overdosing Symptoms: increased side effects. Treatment: gastric lavage, symptomatic therapy. The use of activated charcoal is ineffective because in in vitro experiments have shown that it does not adsorb topiramate. An effective way to removing topiramate from the body – hemodialysis.

Interaction with other drugs reduces the effectiveness of oral estrogensoderjath contraceptives. Reduces the AUC of digoxin by 12%. It is not recommended concomitant use of ethanol and other drugs which depress the central nervous system. When concomitantly with carbamazepine nolvadex side effects of carbamazepine remains constant or varies slightly (by less than 10 .%), whileof topiramate reduced by 40% When coadministered phenytoin remains unchanged or is increased by 25%, whereas the primobolan enanthate of topiramate reduced by 48%; may require correction dosing regime of the latter. While the use of valproic acid valproic acid is reduced by 11%, topiramate – nA 14%. Carbonic anhydrase inhibitors (acetazolamide) increase the risk of kidney stones.

Cautions In patients with a predisposition to nefrourolitiaz increases the risk of kidney stones, to prevent which to adequately increase the volume of fluid intake. Effects on ability to drive and use other mechanisms.In the period of treatment must be careful when driving and occupation of other potentially hazardous activities that require high concentration and speed of psychomotor reactions.

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tamoxifen weight gain

Symptoms: marked reduction of tamoxifen weight gain blood pressure, sometimes accompanied by fainting. Treatment: the patient immediately to be placed in a horizontal position, lift the leg. Symptomatic therapy. Hemodialysis is ineffective.

Interaction with Drug

Doxazosin increases the hypotensive effect of antihypertensive drugs. There were no adverse interaction with the simultaneous use of doxazosin and thiazide diuretics, furosemide, beta-blockers, blockers “slow” calcium channel blockers,inhibitors, antibiotics, oral hypoglycaemic agents, uricosuric agents, and anticoagulants. The drug has no effect on the degree of binding to plasma proteins blood digoxin, phenytoin. in an application with inducers of microsomal oxidation methandienone 10mg in the liver may increase the effectiveness of doxazosin with inhibitors – lowering. Nonsteroidal anti-inflammatory drugs (especially indomethacin), estrogen and sympathomimetic agents may reduce the antihypertensive effect of doxazosin. Eliminating alpha adrenostimuliruyuschee effects of epinephrine, doxazosin may lead to tachycardia and hypotension. Cimetidine increases tamoxifen weight gain of doxazosin. Inhibitors of phosphodiesterase-5 may enhance the hypotensive effect of doxazosin (be careful)

special instructions

Doxazosin should be used with caution in patients with:

  • impaired liver function, especially in cases of appointment of drugs that can affect liver function. In case of deterioration of the functional state of the liver drug overturned immediately.
  • to prevent orthostatic reactions, patients should avoid unexpected and sudden shifts in body position (transition from a lying position to a standing position)
  • Caution should be exercised when used together with phosphodiesterase inhibitors (for the treatment of erectile dysfunction), as in some patients it can lead to symptomatic hypotension
  • Due to the fact that doxazosin can cause orthostatic reaction initially or during the treatment of increasing dosage, it is advisable to refrain from all potentially dangerous activities, in tamoxifen weight gain particular from car driving, in other vehicles and mechanisms
  • Drinking alcohol can increase adverse reactions.
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side effects of tamoxifen

After oral administration of therapeutic doses, doxazosin is well absorbed, absorption  (simultaneous reception of food slows the absorption of 1 hour). The maximum concentration in plasma is created in 3 hours. When evening reception time to maximum concentration is prolonged to 5 hours.
Bioavailability – 60-70% (first pass metabolism). Contact with blood proteins – about 98%. Excretion of plasma takes place in two phases, with a finite half-life 19-22 hours, allowing to take the drug once daily.
Doxazosin is side effects of tamoxifen extensively metabolized in the liver by demethylation of hydroxylation and,
in patients with impaired liver function, as well as the reception drugs that can alter hepatic metabolism, the process can break down the drug biotransformation. Main excretion through the intestine (65% as metabolites and about 5% of intact). The kidneys remove 10%  studies with doxazosin in the elderly and in patients with kidney disease showed no significant pharmacokinetic differences.


Benign prostatic hyperplasia: for the treatment of difficulty or delay the outflow of urine associated with benign prostatic hyperplasia (BPH). The drug can be used in the presence of hypertension and with normal blood pressure. Hypertension is used in combination with other antihypertensive agents such as thiazide diuretics, beta-blockers, blockers “slow” calcium channel blockers or angiotensin-converting enzyme  inhibitors.



  • Increased sensitivity to doxazosin, other quinazoline derivatives or any of the components of the drug support.
  • age of 18 years (effectiveness and safety have been established).
  • lactation

Precautions: in patients with side effects of tamoxifen hepatic impairment, aortic and mitral stenosis, orthostatic hypotension.


In the absence of adequate and well-controlled studies in pregnant Tonokardina safe use during pregnancy has not been established. Tonokardin should be used in these groups of patients only where, in the opinion of the physician, the potential benefits outweigh the potential risk to the fetus and / or child


Dosing and Administration

Doxazosin should be 1 time per day (morning or evening), regardless of the meal, not chewing and drinking plenty of water. Benign prostatic hyperplasia initial dose is 1 mg per day, in order to minimize the possibility of orthostatic hypotension / or fainting. If necessary, depending on the performance and availability of urodynamicssymptoms increase the dose (1-2 week intervals) to 4.2 mg / day. The maximum permissible dose is 8 mg per day. The recommended maintenance dose – 2-4 mg / day.

Hypertension The initial dose is 1 mg per day at bedtime. After the first dose the patient should remain in bed for 6 – 8 hours. This is required in connection with the side effects of tamoxifen opportunity, “first dose phenomenon”, especially pronounced on the background of the previous diuretics. In case of insufficient therapeutic effect, the daily dose can be increased to 2 mg every 1-2 weeks. Subsequently, every 1-2 weeks the dose can be increased to 2 mg. The vast majority of patients, the optimal therapeutic effect is achieved at a dose of 8 mg per day. The maximum daily dose of 16 mg per day should not be exceeded. After reaching a stable dose of a therapeutic effect is usually reduced (average therapeutic dose for maintenance therapy is typically 2 – 4 mg daily). The drug Tonokardin take long. Duration of treatment is determined by the physician.


Side effect

Hypertension is
the most frequently observed in clinical trials, especially in the early treatment of orthostatic hypotension, which in rare cases may cause fainting. Common reactions: asthenia, fatigue, malaise: the part of the central nervous system and the peripheral system: headache, dizziness, drowsiness. Allergic reactions: skin rash, urticaria. from the digestive system: nausea. On the part of the cardiovascular system:peripheral edema, fainting. The respiratory system: . rhinitis and notes the following adverse reactions in patients with arterial hypertension (cause-and-effect relationship has not been established .): bradycardia, tachycardia, palpitations, chest pain, angina pectoris, myocardial infarction, cerebrovascular accident, arrhythmias.

Benign prostatic hyperplasia (BPH) in patients with side effects of tamoxifen found the same side effects as the patients with arterial hypertension, as well as: Common reactions: allergic reactions, skin rash, pruritus, urticaria, back pain, joint pain, muscle aches, muscle weakness, muscle cramps, feeling of heat ( “hot flushes”), an increase in body weight. On the part of the central nervous and peripheral system: hypoesthesia , priapism, paraesthesia, tremor, impotence, insomnia, irritability, anxiety, nervousness, depression, sleep disorders. Since the cardiovascular system: decrease in blood pressure, orthostatic hypotension. respiratory system: bronchospasm, cough, shortness of breath, nasal bleeding. from the endocrine: gynecomastia. from the digestive system: nausea, dry mouth, abdominal pain, constipation, diarrhea, dyspepsia, flatulence, loss of appetite, nausea, anorexia, cholestasis, jaundice, hepatitis, abnormal laboratory values of liver function . From the urogenital system: dysuria, hematuria, violation of urination, nocturia, polyuria, urinary incontinence On the part of hematopoiesis and hemostasis system: thrombocytopenia, thrombocytopenic purpura, leukopenia. With the skin: alopecia, purpura. From the senses: blurred vision , noise in ears.


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tamoxifen citrate

Tomudex diluted with water for injection to a concentration of 0.5 mg / ml and further diluted in 50-250 ml of 0.9% sodium chloride or 5% dextrose (glucose) immediately prior to intravenous infusion.
Other drugs should not be mixed with Tomudex in one package.
The dissolved drug should be stored at 2- 8 o C for up to 24 hours.
Infusion tomudeksa recommended to begin tamoxifen citrate immediately after the dilution of the drug.
Divorced tomudeksa solution must be completely used within 24 hours or destroyed.
There is no need to protect from light and diluted dilute the drug.
Do not store partially used vials or dissolved preparation for later use.

Side effect On the part of the digestive system: nausea, vomiting, diarrhea, anorexia, mucositis, stomatitis, ulceration of the mucous membrane of the mouth, dyspepsia, constipation, gastrointestinal bleeding (in the background of inflammation of the mucous membranes of the gastrointestinal tract thrombocytopenia), increased activity of “liver” transaminases , hyperbilirubinemia, and increased alkaline phosphatase. The most commonly nausea ). Typically, these events are mild to moderate harkter (1-2 degrees according to thetamoxifen citrate scale). Diarrhea, which can occur at any time tomudeksa therapy, observed in 36% of cases and is also usually wears a light or moderate (grade 1-2 on the scale). However, it may develop severe diarrhea, especially pronounced when combined with gematotoksichnosti (in particular with leukopenia).

Hematopoietic system: leukopenia, neutropenia, anemia, thrombocytopenia. Inhibition of bone marrow blood is usually seen in the first 2 weeks after administration of Tomudex. Perhaps the development of neutropenia and thrombocytopenia 4 severity on a scale of WHO, which may be severe and life-threatening, especially in combination with toxic effects on the gastrointestinal tract. Metabolic and Nutritional Disorders: weight loss, dehydration, peripheral edema. On the part of the musculoskeletal system : arthralgia. From the nervous system: increased muscle tone (usually in the form of spasms), headache. skin and skin appendages: rash, sometimes accompanied by itching, desquamation of the epidermis, alopecia, increased sweating. From the senses: taste change, conjunctivitis. other: asthenia, fever, flu-like symptoms, less often – abdominal pain, pain at other sites, accession secondary infections, superficial abscess and sepsis.


Expected symptoms: increased suppression of bone marrow hematopoiesis and severity of dyspeptic disorders.
Treatment. Antidote to raltitrexed with proven clinical efficacy is unknown. Given the preclinical data that indicate a decrease in the toxic effect tomudeksa when using leucovorin, as well as clinical experience with other antifolates, an overdose as soon as possible is recommended to start the administration of folinic acid 25 mg / m 2 intravenously every 6 hours until the symptoms permit.
In the case of occurrence of toxicity tamoxifen citrate should be applied and supportive symptomatic treatment.

Interaction with other drugs and other forms of interaction.
Leucovorin (folinic acid), folic acid and vitamin preparations containing them, reduce the effectiveness of Tomudex, and therefore, these drugs should not be used right before or during administration of Tomudex.
Safety Study application raltitreksida in patients receiving  or warfarin did not reveal clinically significant interactions.

Specific guidance
Treatment Tomudex should be conducted only under the supervision of a physician who is experienced in the use of anticancer drugs.
Patients receiving therapy Tomudex should be carefully monitored for early signs of possible toxic and unwanted effects.
When using Tomudex should pay special attention to the condition of patients with suppressed function bone marrow, poor general condition, or after radiation therapy.
Patients with tumor progression after prior treatment of advanced chemotherapy disease with inclusion of 5-FU may also be insensitive to the action of Tomudex.
Before each administration of the drug required to monitor patterns of peripheral blood (including blood count and platelets) , the activity of “liver” transaminases, bilirubin and creatinine in serum.
The drug can be administered only under the following parameters of blood: white blood cell count ≥ 4000/mkl, neutrophil count ≥ 2000/mkl, platelet count ≥ 100000/mkl.
Repeated administration of the drug can only be with the disappearance of all signs of toxicity (particularly gastrointestinal and hematologic).
if signs of gastrointestinal toxicity, it is necessary to control the picture of peripheral blood (including blood count and platelets), at least 1 time per week to detect hematologic toxicity.
in the case of 4 degree of gastrointestinal toxicity (diarrhea or mucositis) or in the case of a combination of grade 3 gastrointestinal toxicity with grade 4 hematologic toxicity treatment Tomudex should stop and immediately begin to standard supportive care, which includes intravenous fluids and therapeutic measures to support bone marrow hematopoiesis . Perhaps intravenous leucovorin (folinic acid) at a dose of 25 mg / m 2 every 6 hours until symptoms disappear.
Further use of Tomudex in such patients is not recommended.
Men and women of childbearing age during treatment with Tomudex and for at least 6 months after cessation of therapy should use reliable methods of contraception.
Tomudex belongs to the class of cytotoxic drugs and must be handled according to accepted rules for such substances.
in case of contact of the drug with its skin should be rinsed thoroughly with water immediately. In case of eye medication, they should be rinsed with clean water by opening the eyelids, for at least 10 minutes. Necessary tamoxifen citrate medical follow up.
Some side effects of Tomudex, such as malaise and fatigue, may adversely affect driving ability and the performance of potentially hazardous activities that require high concentration and speed of psychomotor reactions.


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