22 Sep

chlorodehydromethyltestosterone pcti

Effective bactericidal and fungicidal. Inhibits the synthesis of ergosterol membranes fungal cells, causing his death, blocks the synthesis of bacterial proteins. It is active against dermatophytes (. Trichophyton spp, Microsporum spp, Epidermophyton spp, etc….); molds, yeasts and yeast-like fungi Candida spp, Pityrosporum orbiculare / ovale (chlorodehydromethyltestosterone pcti), Corynebacterium minutissimum -. erythrasma pathogen, trichomonas and Gram-positive bacteria Staphylococcus spp, Streptococcus spp..

Diflukortolon – glucocorticosteroid topical. It has anti-inflammatory, antiekssudativnoe, antiallergic and antipruritic effect.

Studies on the pharmacokinetics have not been conducted. Oral testosterone steroids


Dermatoses combined etiology, sensitive to therapy with glucocorticosteroids infected fungal / bacterial flora. Fungal skin lesions, including secondarily infected boldenone acetate, accompanied by severe inflammatory or ekzemopodobnye symptoms:

– Tinea pedis and chlorodehydromethyltestosterone pcti smooth the skin, including the localization of the folds, interdigital spaces, the external genitalia (including balanoposthitis): mikrosporiya, trihofitia, rubrofitii, athlete; – candidiasis; – erythrasma.


Hypersensitivity to the drug. TB, syphilis, viral (varicella, herpes zoster), skin lesions, skin reactions after vaccination, pregnancy – I trimester, children up to 2 years.

Precautions – Pregnancy II and III trimester, lactation.

Dosing and Administration

Outwardly. Travokort applied thinly to the affected skin and gently rubbed 2 times a day (morning and night). The maximum treatment duration is 2 weeks.

Side effect

Travokort usually well tolerated, even when applied chlorodehydromethyltestosterone pcti to sensitive skin. In rare cases, may develop skin irritation and allergic reactions. Given that the product contains a glucocorticosteroid for external use in applying cream boldenone to the large surface (greater than 10% of the skin surface) for a long time (over 4 weeks) and / or by using occlusive dressings may cause side effects characteristic of glucocorticosteroids : skin atrophy, telangiectasia, striae, aknepodobny dermatitis, perioral dermatitis, hypertrichosis, as well as systemic side effects (suppression of the hypothalamic-pituitary-adrenal axis).


The phenomena of acute overdose have not been described, however, the excessive or prolonged use of the drug can be a chronic overdose accompanied described under “Side effects” symptoms. Treatment: symptomatic.


22 Sep

chlorodehydromethyltestosterone wikipedia deutsch

The maximum concentration travoprost free acid plasma levels achieved within 10-30 minutes of topical application . travoprost free acid is rapidly cleared from the plasma concentration over hours drops below the threshold of detection (less than 10 pg / ml). Free acid travoprost in humans has not been established because of its low concentration in plasma and the rapid clearance of the organism after topical drug application. The metabolism is the main route of elimination of travoprost free acid and travoprost. Systemic pathway parallel pathways of metabolism of endogenous prostaglandin chlorodehydromethyltestosterone wikipedia deutsch, are characterized by reduction of 13-14 double bond, oxidation of 15-hydroxyl group and a β-link upper oxidative cleavage of the side chain. The free acid travoprost and its metabolites are primarily excreted by the kidneys. No dose adjustment in patients with impaired hepatic function, drostanolone enanthate from weakly expressed to severe, and in patients with impaired renal function, from weakly expressed to severe (with creatinine clearance below 14 ml / min) not required.


Reduction of elevated intraocular pressure in: – open-angle glaucoma; – increased intraocular pressure.


Individual hypersensitivity to the drug chlorodehydromethyltestosterone wikipedia deutsch, children under 18 years, pregnancy and lactation.


In patients with aphakia; patients at break psevdofakiey posterior lens capsule, or in patients with anterior chamber IOL patients; in patients at risk of cystoid macular edema in patients at risk of developing iritis, uveitis.


Locally. 1 drop into the conjunctival sac eye (eye) 1 time per day in the evening. To reduce the risk of systemic side effects is recommended after instillation of the drug pinch nasolacrimal duct by pushing in its projection at the inner corner of the eye. If the dose was missed, the treatment should be continued with the next dose. The daily dose should not exceed 1 drop in the conjunctival sac 1 eye once a day. If the drug chlorodehydromethyltestosterone wikipedia deutsch is appointed as a substitute for another ophthalmic preparation turinabol for the treatment of glaucoma, the latter should be repealed, and the following day to start .

Side effect

Local. In 10% of cases observed bloodshot eyes. In 1-10% of cases – punctate keratitis, eye pain, photophobia, eye irritation, foreign body sensation, dry eye, eye pruritus, conjunctival hyperemia. In 0.1-1% of cases – blurred vision, increased lacrimation, itching and erythema of eyelid, crusting on the edges of the eyelids. Systemic side effects. In 1-10% of cases – skin hyperpigmentation, discoloration of the skin. In 0.1-1% of cases -. Dry mouth, headache Side effects that do not have the frequency (post-marketing experience). Local. Macular edema, eye iris color change, darkening, thickening and lengthening eyelashes / or an increase in their number, eyelid skin darkening. Systemic side effects. Bradycardia, tachycardia, exacerbation of asthma, dizziness, ringing in the ears, increased prostate specific antigen side effects of famara, a violation of the hair growth.


There is currently no reported cases of overdoses. Symptoms: mucous membrane irritation of the eyes, conjunctival hyperemia or episclera. In the case of a local drug should wash your eyes with warm water overdose. In case of suspicion of the use of oral treatment of symptomatic medication.

Interaction with other drugs

Be used in combination with other topical ophthalmic preparations for reducing intraocular pressure. In this case, the interval between their use should be at least 5 minutes.

special instructions

The may cause a gradual change in eye color by increasing the amount of brown pigment in the iris. This effect is detected predominantly in patients with mixed colored irises, eg, blue-brown, gray-brown, green-brown or yellowish-brown, which is explained by an increase in melanin content in the stromal melanocytes of the iris. This effect was also observed in patients with brown eye color. Usually brown pigmentation spreads concentrically around the pupil to the periphery of the iris, and the entire iris or parts of it may acquire a more intense brown color. The long-term effects on the melanocytes and the consequences of this effect are currently unknown . Changing the iris color occurs slowly and may go unnoticed for a number of months or years. After discontinuation of the drug was observed to further increase the amount of brown pigment, but has evolved color change may be irreversible. In the presence of nevus or lentigo on the iris were observed their changes under the influence therapy with chlorodehydromethyltestosterone wikipedia deutsch . The drug can cause darkening, thickening and lengthening eyelashes / or increase their number; rarely darkening of the eyelid skin. The mechanism of these changes is not currently installed. Prior to treatment, patients t3 dosage should be informed about the possibility of changing eye color. Treatment of only one eye can lead to permanent heterochromia. Necessary to avoid contact with skin, since in experiments on rabbits demonstrated, percutaneous absorption travoprost. Prostaglandins and prostaglandin analogs – biologically active substances that can be absorbed through the skin. Women during pregnancy, and women who plan to become pregnant, should avoid direct contact with substances containing prostaglandins. In case of contact with a large amount of the drug on the skin should immediately rinse the water area of the skin. Before using the product, contact lenses must be removed and set back no earlier than 15 minutes after application of the preparation. The product contains propylene glycol, which can cause irritation to the skin! The product contains macrogol glitserilgidroksistearat that can cause reactions on the part of the skin! Do not touch the tip of the dropper bottle to any surface to avoid contamination of the vial-dropper and its contents. The vial must be closed after each use.

Effects on ability to drive vehicles and management mechanisms

If the patient after treatment temporarily chlorodehydromethyltestosterone wikipedia deutsch reduced sharpness of vision, to its recovery is not recommended to drive and engage in activities that require attention.


22 Sep

chlorodehydromethyltestosterone pct trail

Paracetamol is rapidly and completely absorbed after oral administration. The absolute bioavailability after oral administration is about 80% and is dose-dependent within the dose range of turinabol chlorodehydromethyltestosterone pct trail. It practically does not bind to plasma proteins, and its volume distribution of about 0.91 kg.

After of paracetamol plasma in healthy adults is about 2.3 hours, varying from 1.5 to 3.0 h. Paracetamol biotrasformatsii undergoes intense in the liver and its major metabolites are inactive and fenolsulfatnye glucuronide conjugates. The intermediate product of the metabolism of paracetamol are usually excreted by the kidneys in the form mercapturic acid and cysteine conjugates. Glutathione conjugate can be excreted in the bile, but in this case it is cleaved by intestinal peptidases and cleavage products are reabsorbed.

Chlorpheniramine maleate : After oral administration, it is almost completely absorbed and distributed in the tissues. Maximum plasma concentrations were reached in 2-3 hours after a single dose fasted 12 mg. In human urine chlorpheniramine found unchanged (35%) and monodemetilirovannye (20%) and didemetilirovannye (10%) metabolites. Chlorpheniramine and its demethylated metabolites are slowly excreted over time.

Dextromethorphan hydrobromide : Following oral administration of dextromethorphan is well absorbed but undergoes extensive first-pass metabolism in the liver, resulting in its plasma chlorodehydromethyltestosterone pct trail concentration is only 0.1 g / l after 0.5 h and the average maximum concentration of 2.5 hours after a single dose is 20 mg 1.8 mg / l. Dextromethorphan is extensively metabolized in the liver and about 50% of the dose is excreted by the kidneys within 24 hours. Excreted bowel less than 1% of the dose. About 8% of the dose is excreted unchanged by the kidneys for 6 hours. Phenylephrine hydrochloride : The absorption of phenylephrine after oral administration varies considerably, it is subjected to intensive first-pass metabolism. As a result, its systemic bioavailability is only 40% and the maximum plasma concentration is achieved 1-2 hours after ingestion. The volume of distribution of 200-500 L and the median T ½ of the plasma is about 2-3 hours. After intensive absorption Phenylephrine undergoes biotransformation in the gut wall. Following oral administration deaminiruetsya 24% phenylephrine, since most of the ingested drug is metabolized by sulfation even before reaching the liver.



Symptomatic treatment of colds, flu, SARS, infectious and allergic rhinitis (a feverish syndrome, pain, rhinorrhea).

: Hypersensitivity to the drug; concomitant use of tricyclic antidepressants, monoamine oxidase inhibitors (MAOIs), beta-blockers; deficiency of chlorodehydromethyltestosterone pct trail dehydrogenase; blood diseases; liver and / or kidney failure; angle-closure glaucoma; prostatic hyperplasia; Gilbert’s syndrome; arterial hypertension; hyperthyroidism; pheochromocytoma; diabetes; bronchial asthma; bronchitis; pregnancy; lactation;children, age (under 14 years).

angina pectoris, hypertrophic obstructive cardiomyopathy (GOKMP), advanced age.

Dosing and Administration
Inside, adults – one capsule every 4-6 hours, but not more than 4 capsules per day.
Admission as an antipyretic means no more than 3 days without consulting a doctor.

Side effect On the part of the cardiovascular system : hypertension. From the nervous system and sensory organs : dizziness, drowsiness, irritability, mydriasis, paresis of accommodation, increased intraocular pressure. Digestive system: dry mouth, epigastric pain, nausea, vomiting, hepatotoxic effect. On the part of hematopoiesis : anemia, thrombocytopenia, hemolytic anemia, aplastic anemia. From the urinary system : urinary retention, renal toxicity (papillary necrosis). Allergic reactions (including skin rash, pruritus, angioedema), bronchial obstruction.


symptoms (due to paracetamol, appears after taking more than 10-15 grams): pale skin, anorexia, nausea, vomiting, gepatonekroz, increased activity of “liver” transaminases, increased prothrombin time.
Treatment: gastric lavage, followed by the appointment of activated charcoal, symptomatic therapy.

Interaction with other drugs
Enhances effects of MAO inhibitors, sedatives, ethanol.
Antidepressants, antiparkinsonian agents, antipsychotics, phenothiazine derivatives increase the risk of urinary retention, dry mouth, constipation. Glucocorticosteroids  increase the risk of developing glaucoma. Paracetamol reduces the effectiveness of uricosuric drugs.
Chlorpheniramine appointed simultaneously  inhibitors and furazolidone, can lead to a hypertensive crisis, agitation, increase in temperature.
Tricyclic antidepressants increase the sympathomimetic effects,chlorodehydromethyltestosterone pct trail of halothane increases the risk of ventricular arrhythmias.
Decreases hypotensive effect of guanethidine, which in turn, increases the activity of alpha-adrenostmuliruyuschuyu phenylephrine.

During treatment should not take other medicines that contain substances that are part of the drug.
In persons suffering from chronic alcoholism, receiving therapeutic doses of the drug can cause severe hepatic insufficiency.
The period of treatment should refrain from the use of ethanol (development of hepatotoxicity ), car driving and other activities potentially hazardous activities that require high concentration and psychomotor speed reactions.


22 Sep

chlorodehydromethyltestosterone 10mg ritalin

There have been severe complications, while the use of sertraline  (including selective effect (selegiline) and reversible type of action (moclobemide). Perhaps the development of serotonin syndrome. Similar complications, sometimes fatal, occur in the appointment chlorodehydromethyltestosterone 10mg ritalin during treatment with antidepressants, depressing neuronal uptake of monoamines or immediately after their withdrawal. with simultaneous use of selective inhibitors of reverse neyronalnogo serotonin  arise: hyperthermia, rigidity, myoclonus, lability of the autonomic nervous system (rapid fluctuations in the parameters of the respiratory and cardiovascular systems ), mental status changes, including increased irritability, marked agitation, confusion, which in some cases can go into delirious state or coma. Medications that suppress the central nervous system, and ethanol.

The combined use of sertraline and substances which depress the central nervous system requires attention, and also prohibited the use of alcoholic beverages during treatment with sertraline. The derivatives of coumarin – when coadministered with sertraline showed a significant increase in prothrombin time – in these cases it is recommended to monitor the prothrombin time at the beginning of treatment with sertraline and after its cancellation.  Sertraline is associated with plasma proteins. It is therefore necessary to consider the possibility of interaction with other drugs that bind to the protein (eg, diazepam, tolbutamide and warfarin).Cimetidine: simultaneous use significantly reduces the clearance of sertraline. Drugs metabolized isoenzyme : long-term treatment with sertraline 50 mg per day accompanied by increased concentrations of de zipramina.

Drugs metabolized other enzyme cytochrome  systems. Experimental chlorodehydromethyltestosterone 10mg ritalin studies in vitro interaction showed that carried isozymes  betagidroksilirovanie endogenous cortisol, as well as the metabolism of carbamazepine and terfenadine prolonged appointment sertraline prolonged assignment of sertraline in the same dose also varies. Thus, we can conclude that sertraline does not inhibit  isoenzyme. Sertraline has no effect on the concentration of diazepam in blood serum, which indicates the absence of inhibition of isoenzyme . According to in vitro studies, sertraline has virtually no effect or minimally inhibits  isoenzyme. Lithium. The pharmacokinetics of lithium is not changed by concomitant administration of sertraline. However, the tremor occurs more often when they are used together.

As well as the appointment of other selective inhibitors of reverse neuronal uptake of serotonin, the combined use of sertraline with drugs that affect the serotonergic transmission (eg, lithium), requires increased caution.Agents acting on serotonergic transmission. When you replace one inhibitor of neuronal serotonin reuptake another there is no need to “washout period”. However, you want to be careful with changes in the course of treatment. Avoid concomitant administration of tryptophan or fenfluramine with sertraline. The induction of microsomal liver enzymes. Sertraline causes minimal induction of liver enzymes. Co-administration of sertraline and antipyrine at a dose of 200 mg leads to a significant reduction in the half-life of antipyrine, although there is only 5% of cases. Atenolol: when co-administered sertraline does not change its p-adrenoceptor blocking action. Glibenclamide and digoxin: the introduction of sertraline in a daily dose 200 mg of drug interactions with these drugs have been identified.


Sertraline should not be used in conjunction with MAOIs, and within 14 days after discontinuation of treatment . Similarly, after the abolition of sertraline for 14 days did not prescribe chlorodehydromethyltestosterone 10mg ritalin.
It should be noted that in patients undergoing electroconvulsive therapy, sufficient experience with sertraline is not. The possible success or the risk of such combined treatment has not been studied.
Patients with depression are at risk for suicide attempts. This risk persists until the development of remission. Therefore, from the beginning of the treatment and to achieve optimal clinical response for patients should establish a permanent medical supervision.

Pregnancy and breast-feeding: Controlled results of the application of sertraline in no pregnant women, so assign them the drug is only if the expected benefit to the mother outweighs the potential risk to the fetus. Women of reproductive age, which is supposed to appoint sertraline should be advised to use effective contraception. Sertraline is found in breast milk, therefore the treatment with this drug is not recommended during breast-feeding chlorodehydromethyltestosterone 10mg ritalin. No reliable data on safety of its use in this case. If treatment is necessary, it is better to stop breast-feeding. Effects on ability to drive vehicles and management mechanisms: Purpose, sertraline, are generally not accompanied by a breach of psychomotor functions. However, its use in conjunction with other drugs may impair attention and motor coordination. Therefore, during treatment with sertraline drive vehicles, special equipment or practice associated with an increased risk of the activity is not recommended.


22 Sep

chlorodehydromethyltestosterone reviews for horrible bosses

Absorption of sertraline from the gastrointestinal tract significantly, but is slow. Maximum plasma concentration is achieved through 4,5-8,4 hours after ingestion of the drug.The equilibrium concentration of sertraline in blood plasma is achieved within a week for a single daily reception. Bioavailability food during reception increases by 25%, while the time to reach maximum concentration is shortened.

Distribution. Total binding sertraline plasma chlorodehydromethyltestosterone reviews for horrible bosses protein is 98%. The volume of distribution> 20L / kg. Metabolism and excretion. Sertraline is extensively metabolized during the first passage through the liver, subjected to N-demethylation. Its main metabolite  active as compared to the parent compound. The metabolites are excreted with urine and faeces in equal amounts. About 0.2% of sertraline excreted by the kidneys unchanged. Half-life time is 22-36 hours, regardless of age or sex. For this figure is 62-104 hours. The half-life of sertraline time and area under the plasma concentration curve ( increase with abnormal liver function. Regardless of the severity of renal failure the pharmacokinetics of sertraline in his constant use is not changed. Sertraline passes into breast milk. Data about its ability to pass through the blood-placental barrier there. Sertraline is not dialyzed.


Indications for use:


  • Depression different etiology (treatment and prevention)
  • Obsessive-Compulsive Disorder
  • Panic disorder (With or without agoraphobia).
  • Post-traumatic stress disorder chlorodehydromethyltestosterone reviews for horrible bosses.Contraindications
  • Hypersensitivity to the active substance or any other ingredients in the drug,
  • concomitant use of sertraline inhibitors. When replacing one drug to another should avoid antidepressants within 14 days,
  • concomitant use of sertraline with tryptophan or fenfluramine
  • unstable epilepsy,
  • Children under 6 years of age;
  • pregnancy and lactation (see “Osobyeukazaniya.”).
  • Precautions: organic brain disease (including mental retardation), manic state, epilepsy, liver and / or kidney failure, weight loss, in children older than 6 years.Dosing and Administration Depression  Adults The initial dose is 50 mg Thorin once a day, morning or evening. The daily dose can be gradually, not earlier than one week increased to 50 mg, to a maximum daily dose of 200 mg.
  • Panic disorders  initial dose is 25 mg Thorin once a day, in the morning or evening. A week later, the doctor can increase the dose to 50 mg of sertraline once a day, and then gradually, not earlier than one week, the daily dose can be gradually increased from 50 mg up to a maximum daily dose of 200 mg. A satisfactory therapeutic results achieved typically after 7 days from the start of treatment. However, to achieve full therapeutic effect requires regular intake of the drug for 2-4 weeks.
  • Patients chlorodehydromethyltestosterone reviews for horrible bosses with obsessive-compulsive disorder to achieve a good result may require 8-12 weeks. The minimum dose that provides the therapeutic effect is retained in the future as a support. Children for children from 6 to 12 years, the starting dose is 25 mg sertraline once a day, morning or evening. After one week, the dose can be increased to 50 mg once a day. For children aged 12 to 17 years of the initial dose is 50 mg once a day, in the morning or evening. The daily dose can be gradually, not earlier than one week increased to 50 mg, to a maximum daily dose of 200 mg. To avoid overdose, consideration should be given less weight in children than adults, and by increasing the dose of 50 mg / day should be carefully monitored for this category of patients, and at the first sign of overdose repeal the drug. In elderly patients there is no need for a special dose selection.
  • Patients with liver function disorders require special attention in the treatment of Mr. sertrali. In severe liver function disorder the dose should be reduced dose or increase the interval between receptions. In patients with impaired renal function specially select a dose is not required 

    Side effects:
    dry mouth, increased sweating, drowsiness, headache, dizziness, tremors, insomnia, anxiety, agitation, hypomania, mania, decreased appetite (rarely – increased) up to anorexia, dyspepsia (bloating, nausea, vomiting, diarrhea ), abdominal pain, weight loss, gait disturbance.
    It is also possible weakness, redness, blurred vision, ejaculation disorder, decreased libido.
    During sertraline treatment were marked extrapyramidal disorder, dyskinesia, tremor, cramps, menstrual disorders, hyperprolactinemia, galactorrhea, skin rash, occasionally erythema multiforme. Movement disorders were more common in patients with indications of their presence in the history or concomitant use of antipsychotics.
    When stopping treatment with sertraline described rare cases of withdrawal. May appear paresthesia, gipostezii, depressive symptoms, hallucinations, aggressive reaction, agitation, anxiety or psychotic symptoms that are indistinguishable from symptoms of the underlying disease. Laboratory tests Data: rarely – in 0.8% of cases, with prolonged use – there is asymptomatic increase transaminase activity in serum. Cancel the drug in this case leads to the normalization of the activity of enzymes. During treatment with sertraline may occur transient hyponatremia. It occurs more frequently in elderly patients, as well as when taking diuretics or several other drugs. This side effect associated with the syndrome of inappropriate secretion of antidiuretic hormone.

    Serious symptoms of an overdose chlorodehydromethyltestosterone reviews for horrible bosses of sertraline is not revealed even in the appointment of the drug in high doses. However, simultaneous administration with other drugs or ethanol may occur severe poisoning.
    Overdose can cause serotonin syndrome with nausea, vomiting, somnolence, tachycardia, agitation, dizziness, agitation, diarrhea, sweating, myoclonus and hyperreflexia. Treatment: No specific antidote. It requires intensive supportive care and constant monitoring of vital body functions. Induce vomiting is not recommended. Introduction of the activated carbon can be more effective than gastric lavage. It is necessary to maintain airway patency. At the large volume of distribution of sertraline, in this regard, increased diuresis, dialysis, hemoperfusion or blood transfusion may be inconclusive.