Adex 1mg – Nakon Medical Int

$31.00

Availability: Out of Stock

ACTIVE HALF-LIFE: 2 days
CLASSIFICATION: Non-steroidal aromatase inhibitor
DOSAGE: 0.5-1 mg/day
ACNE: No
WATER RETENTION: No
HBR: No
HEPATOTOXICITY: No
AROMATIZATION: No
MANUFACTURER: Nakon Medical
WAREHOUSE: International Warehouse 12
SUBSTANCE: Anastrozole

Out of stock

Description

Oxy 50, the active ingredient is Oxymetholone.

The effects of the drug:

Awesome set of muscle mass.
Increased hemoglobin synthesis.
Growth of the power indicators.
Acceleration of protein synthesis.
Eliminating pain in the joints.

Possible side effects:

Hepatotoxicity (negative effect on the liver at moderate doses can be reduced).
High blood pressure (due to heavy water retention).
Diarrhea.
Headaches, nausea, vomiting, stomach pain, apathy, lethargy, lack of appetite.
Progestin activity.
Acne.

Side effects can be avoided in advance by making analyzes and carrying out post-cycle therapy.

Oxy 50 Cycles

Oxy 50 cycle for beginners – 6 weeks of cycle, the first week of receiving Oxy 50 at 50 mg per day, the second week, 100 mg per day until the end of the cycle, but you should know one truth: you will lose 70% of gained weight, but there is a plus, it depends on your body’s response to the drug.

Oxy 50 cycle for experienced users – 10 weeks of taking, the first seven weeks Sustanon 350 at 750 mg per week + Oxy 50 at 150 mg per day, the last three weeks, Dianabol at 30-50 mg per day + Propionat 100 at 400 mg per week, to maintain the obtained results.

Warnings: Keep out of reach of children. For adults only.

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DescriptionACTIVE HALF-LIFE: 2 days CLASSIFICATION: Non-steroidal aromatase inhibitor DOSAGE: 0.5-1 mg/day ACNE: No WATER RETENTION: No HBR: No HEPATOTOXICITY: No AROMATIZATION: No MANUFACTURER: Nakon Medical WAREHOUSE: International Warehouse 12 SUBSTANCE: AnastrozoleActive Ingredient: Sibutramine hydrochloride monohydrate 20mg Tablet Count: 100 Tabs Concentration: 20 mg/Tab Presentation: 100 Tablet (Total box 2000 mg) Trade name: Sibutramine Ship From: USAActive Ingredient: T3 25mcg Tablet Count: 50 Counts Active Half-life: 9 Hours Classification: Peptides Dosage Men: 50-100 Mcg/day Dosage Women: 50-100 Mcg/day Acne: Rarely Water Retention: No Hbr: No Hepatology: Low Aromatization: NoACTIVE INGREDIENT: Exemestane 25 mg TABLET COUNT: 30 COUNTS ACTIVE HALF-LIFE: 9 HOURS CLASSIFICATION: ANABOLIC STEROID DOSAGE MEN: 25-50 MG/DAY DOSAGE WOMEN: 5-30 MG/DAY ACNE: RARELY WATER RETENTION: NO HBR: NO HEPATOXITY: LOW Ship From: EuropeActive Ingredient: Exemestane 25 Mg Tablet Count: 25 Counts Active Half-life: 9 Hours Classification: Anabolic Steroid Dosage Men: 25-50 Mg/day Dosage Women: 5-30 Mg/day Acne: Rarely Water Retention: No Hbr: No Hepatoxity: LowActive Ingredient: Oxandrolone 10mg Active Half-life: 9 Hours Classification: Anabolic Steroid Dosage Men: 50-100 Mg/day Dosage Women: 5-30 Mg/day Acne: Rarely Water Retention: No Hbr: No Hepatoxity: Low Aromatization: No
ContentOxy 50, the active ingredient is Oxymetholone. The effects of the drug: Awesome set of muscle mass. Increased hemoglobin synthesis. Growth of the power indicators. Acceleration of protein synthesis. Eliminating pain in the joints. Possible side effects: Hepatotoxicity (negative effect on the liver at moderate doses can be reduced). High blood pressure (due to heavy water retention). Diarrhea. Headaches, nausea, vomiting, stomach pain, apathy, lethargy, lack of appetite. Progestin activity. Acne. Side effects can be avoided in advance by making analyzes and carrying out post-cycle therapy. Oxy 50 Cycles Oxy 50 cycle for beginners - 6 weeks of cycle, the first week of receiving Oxy 50 at 50 mg per day, the second week, 100 mg per day until the end of the cycle, but you should know one truth: you will lose 70% of gained weight, but there is a plus, it depends on your body’s response to the drug. Oxy 50 cycle for experienced users - 10 weeks of taking, the first seven weeks Sustanon 350 at 750 mg per week + Oxy 50 at 150 mg per day, the last three weeks, Dianabol at 30-50 mg per day + Propionat 100 at 400 mg per week, to maintain the obtained results. Warnings: Keep out of reach of children. For adults only.Sibutramine hydrochloride monohydrate 20mg x 100 tab Sibutramine affects chemicals in the brain that affect weight maintenance. Sibutramine is used together with diet and exercise to treat obesity that may be related to diabetes, high cholesterol, or high blood pressure. Sibutramine may also be used for other purposes not listed in this medication guide. Exemestane is a synthetic androgen analogue. It’s is a steroidal inhibitor of aromatase which  binds irreversibly to and inhibits the enzyme aromatase, thereby blocking the conversion of cholesterol to pregnenolone and the peripheral aromatization of androgenic precursors into estrogens. Exemestane has been associated with a low rate of serum enzyme elevations during therapy and rare instances of clinically apparent liver injury. This medication is used to treat certain types of breast cancer (such as hormone-receptor-positive breast cancer) in women after menopause. Exemestane is also used to help prevent the cancer from returning. Some breast cancers are made to grow faster by a natural hormone called estrogen. Exemestane decreases the amount of estrogen the body makes and helps to slow or reverse the growth of these breast cancers. Exemestane is usually not used in women of childbearing age. Exemestane is usually taken once a day after a meal. Take Exemestane at around the same time every day. You may need to take Exemestane for several years or longer. Continue to take Exemestane even if you feel well. Do not stop taking Exemestane without talking to your doctor. Effect On Estrogens Plasma estrogen (estradiol, estrone, and estrone sulfate) suppression is seen starting at a 5-mg daily dose of Exemestane, with a maximum suppression of at least 85% to 95% achieved at a 25-mg dose. Exemestane 25 mg daily reduces whole body aromatization (as measured by injecting radiolabeled androstenedione) by 98% in postmenopausal women with breast cancer. After a single dose of Exemestane 25 mg, the maximal suppression of circulating estrogens occurres 2 to 3 days after dosing and persisted for 4 to 5 days. Effect On Corticosteroids In multiple-dose trials of doses up to 200 mg daily, Exemestane selectivity was assessed by examining its effect on adrenal steroids. Exemestane did not affect cortisol or aldosterone secretion at baseline or in response to ACTH at any dose. Thus, no glucocorticoid or mineralocorticoid replacement therapy is necessary with Exemestane treatment. Other Endocrine Effects Exemestane does not bind significantly to steroidal receptors, except for a slight affinity for the androgen receptor (0.28% relative to dihydrotestosterone). The binding affinity of its 17dihydrometabolite for the androgen receptor, however, is 100 times that of the parent compound. Daily doses of Exemestane up to 25 mg had no significant effect on circulating levels of androstenedione, dehydroepiandrosterone sulfate, or 17-hydroxyprogesterone, and were associated with small decreases in circulating levels of testosterone. Increases in testosterone and androstenedione levels have been observed at daily doses of 200 mg or more. A dose-dependent decrease in sex hormone binding globulin (SHBG) has been observed with daily Exemestane doses of 2.5 mg or higher. Slight, nondose-dependent increases in serum luteinizing hormone (LH) and follicle-stimulating hormone (FSH) levels have been observed even at low doses as a consequence of feedback at the pituitary level. Exemestane 25 mg daily had no significant effect on thyroid function [free triiodothyronine (FT3), free thyroxine (FT4), and thyroid stimulating hormone (TSH). Absorption Exemestane is distributed extensively into tissues. Exemestane is 90% bound to plasma proteins and the fraction bound is independent of the total concentration. Albumin and α11-acid glycoprotein both contribute to the binding. The distribution of Exemestane and its metabolites into blood cells is negligible. Metabolism Exemestane is extensively metabolized. The initial steps in the metabolism of Exemestane are oxidation of the methylene group in position 6 and reduction of the 17-keto group with subsequent formation of many secondary metabolites. Each metabolite accounts only for a limited amount of drug-related material. The metabolites are inactive or inhibit aromatase with decreased potency compared with the parent drug. One metabolite may have androgenic activity [see Pharmacodynamics]. Studies using human liver preparations indicate that cytochrome P 450 3A4 (CYP 3A4) is the principal isoenzyme involved in the oxidation of Exemestane. Exemestane is metabolized also by aldoketoreductases.
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