Clomid 50

$43.00

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ACTIVE HALF-LIFE 5-7 Days
CLASSIFICATION SERM
DOSAGE 50-100 mg/day
ACNE No
WATER RETENTION No
HBR Rare
HEPATOTOXICITY Low
AROMATIZATION No
MANUFACTURER Pharmaqo
SUBSTANCE Clomiphene Citrate

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Description

[vc_row][vc_column][vc_column_text]Clomid (commercially known as Clomiphene Citrate) – a synthetic estrogen, which is usually assigned to women that have difficulty conceiving a child. As for men, the application of Clomid increases the level of hormones that stimulate the testicles. That is Clomid acts directly on the pituitary gland. This increases the natural production of testosterone by the body.

Chemically for athletes this is highly a favorable effect, since at the end of cycle Testosterone levels are higher than normal. Once the athlete stops taking medication, testosterone levels significantly decreased and its natural level must be returned. Because of this, there are considerable loss of muscle mass and volume. Studies show that when taking Clomid in the amount of 50-100 mg per day, in the evening or in the morning, after meals, in the two-week period or more natural testosterone production is back to normal.

Clomid Effects

During the period of Clomid use, it raises testosterone levels. As effective is Clomid as an anti-estrogen. Many athletes experience a surplus in it after completing the cycle. A high level of the hormone in combination with low testosterone may lead to the development of gynecomastia. Clomid – solves two problems: blocks unwanted effect of estrogen; rising natural level of testosterone in the body.

In this regard as of side effects, it is considered a fairly safe drug. Clomid is both women and men, in that there are no contraindications. Women who use this drug helps to achieve tighter appearance before the competition. There may be temporary visual disturbances.

How to Use Clomid: Dosage, Cycle, Reviews

In the early cycle apply two tablets a day (it is 100 mg). Then, the dosage can go to one tablet per day.

Warnings: Keep out of reach of children. For adults only.[/vc_column_text][/vc_column][/vc_row]

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SettingsClomid 50 removeClomimed 50mg – Clomiphene Citrate – Deus Medical removeCytomed 25mcg – Liothyronine Sodium – Deus Medical removeProvimed 25mg – Mesterolone – Deus Medical removeHalozone - Halotestin 10mg. removeExemestane 25mg - Hilma Biocare remove
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SKUpharmaqo-008101AAS-DM-0-119101AAS-DM-0-118101AAS-DM-0-104RF-AlphaZone-upline2674101AAS-HB-0-138
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DescriptionACTIVE HALF-LIFE 5-7 Days CLASSIFICATION SERM DOSAGE 50-100 mg/day ACNE No WATER RETENTION No HBR Rare HEPATOTOXICITY Low AROMATIZATION No MANUFACTURER Pharmaqo SUBSTANCE Clomiphene CitrateActive Ingredient: Clomiphene Citrate (Clomid) Teblets Count: 50 Tab Molar Mass: 405.966 G/mol Formula: C26h28clno Trade Name: Clomidothers Concentration: 50 mg/cap Presentation: 50 Teblets (Total box 2500mg)Active 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: Mesterolone 10mg Bottle Count: 50 Tablets Active Half-life: 12 Hours Classification: Anabolic Steroid Dosage Men: 30-100 mg/day Acne: Yes Water Retention: No Concentration: 10 mg/Pill Presentation: 50 Tablets (Total box 500 mg) Dosage: 30-100mg per day over the course of 8-12 weeksProduct Name: Halotestin 10mg Active Ingredient: Fluoxymesterone 10mg Active Life: 9 Hours Drug Class: Androgen; Anabolic Steroid Detection Time: 11 Months Common Doses: 10-20 mg/day Blood pressure: Perhaps Acne: Yes Water retention: No Aromatisation: No Liver toxicity: High Decrease HPTA function: NoneACTIVE 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: Europe
Content[vc_row][vc_column][vc_column_text]Clomid (commercially known as Clomiphene Citrate) – a synthetic estrogen, which is usually assigned to women that have difficulty conceiving a child. As for men, the application of Clomid increases the level of hormones that stimulate the testicles. That is Clomid acts directly on the pituitary gland. This increases the natural production of testosterone by the body. Chemically for athletes this is highly a favorable effect, since at the end of cycle Testosterone levels are higher than normal. Once the athlete stops taking medication, testosterone levels significantly decreased and its natural level must be returned. Because of this, there are considerable loss of muscle mass and volume. Studies show that when taking Clomid in the amount of 50-100 mg per day, in the evening or in the morning, after meals, in the two-week period or more natural testosterone production is back to normal. Clomid Effects During the period of Clomid use, it raises testosterone levels. As effective is Clomid as an anti-estrogen. Many athletes experience a surplus in it after completing the cycle. A high level of the hormone in combination with low testosterone may lead to the development of gynecomastia. Clomid – solves two problems: blocks unwanted effect of estrogen; rising natural level of testosterone in the body. In this regard as of side effects, it is considered a fairly safe drug. Clomid is both women and men, in that there are no contraindications. Women who use this drug helps to achieve tighter appearance before the competition. There may be temporary visual disturbances. How to Use Clomid: Dosage, Cycle, Reviews In the early cycle apply two tablets a day (it is 100 mg). Then, the dosage can go to one tablet per day. Warnings: Keep out of reach of children. For adults only.[/vc_column_text][/vc_column][/vc_row]Fluoxymesterone 10mg x 100 tablets Fluoxymesterone has established itself as a high-quality drug with a high androgenic index. Fluoxy mesteronegives a great increase in strength. Suitable for preparation for competitions, when an athlete needs strength without a large set of muscle mass. In this case, the musculature gets the necessary hardness.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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