| Description | ACTIVE HALF-LIFE?9 Hours
?CLASSIFICATION?Anabolic Steroid
?DOSAGE?Men 30-50 mg/day
?ACNE?Rarely
?WATER RETENTION?No
?HBR?No
?HEPATOTOXICITY?Low
?AROMATIZATION?No | Active Ingredient: Clomiphene Citrate (Clomid)
Tablet Count: 50 Tab
Molar Mass: 405.966 G/mol
Formula: C26h28clno
Trade Name: Clomid
Concentration: 50 mg/cap
Presentation: 50 Tablets (Total box 2500mg)
Ship From: Europe | Product 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: None | Active 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: USA | ACTIVE INGREDIENT: LETROZOLE 5mg
TABLET COUNT: 100 COUNTS
ACTIVE HALF-LIFE: 9 HOURS
CLASSIFICATION: ANTI ESTROGEN
DOSAGE: 5mg
ACNE: NONE
WATER RETENTION: NO
HBR: NO
HEPATOXITY: LOW
AROMATIZATION: NO | ACTIVE 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]Ultima-Oxa is an anabolic steroid that is created in a synthetic way and is used by beginners and experienced athletes to form a qualitative, relief structure of muscles.
The active substance of the drug is a synthetic steroid Oxandrolone, created in the 60?s for medical purposes (as an immunostimulator for HIV patients, anemia). Initially, this anabolic was produced under the trade name Anavar, but since the 80s of the last century, many analogues have been produced in the market of sports pharmacology.
Ultima-Oxa Effects:
- Increased protein synthesis in muscle fibers;
- Formation of well-delineated, relief musculature;
- A significant increase in strength, endurance;
- Marked burning of subcutaneous fat;
- Anti-catabolic effect.
How to Use Ultima-Oxa: Dosage, Cycle, PCT
Making a solo course with Ultima-Oxa, it is easy to avoid possible side effects (decreased libido, lack of appetite, increased pressure, sluggish erections, etc.), if you adhere to several general recommendations:
- The steroid should be started with a minimum dosage (10-20 mg/day), gradually increasing it.
- The maximum dose for an adult male is 80-100 mg/day.
- At the end of the course, during the last two weeks, the dosage should be gradually reduced to the minimum value.
- The course duration of Ultima-Oxa solo averages from 6 to 8 weeks.
Ultima-Oxa, according to reviews, is often used to increase the strength or the formation of muscles? relief, also women can use it, observing a maximum dosage of 40 mg.
Ultima-Oxa Combination Cycles
Since the last week of the course, it is recommended to buy Tamoxifen (or buy Nolvadex), use it at the rate of 10 mg per day, to resume Testosterone production, within 2-3 weeks.
You can take the drug with other steroids (for example, you can buy Sustanon or buy Testosterone or buy Primobolan) to increase the effectiveness of weight gain courses. Do not avoid consulting a doctor to check beforehand your body?s predisposition to such stresses on the liver.
Ultima-Oxa Reviews
Leaving Ultima-Oxa reviews, most athletes on the forums warn of the low effectiveness of the drug in the period of weight gain. The steroid is used primarily before the competition, as it provides a fat burning effect and forms a quality, well-defined musculature. Ultima-Oxa, according to reviews, has a low toxicity on the liver, while there is no effect of aromatization.
Warnings: Keep out of reach of children. For adults only.[/vc_column_text][/vc_column][/vc_row] | [vc_row][vc_column][vc_column_text]
Clomiphene – Post Cycle Therapy
The basic need in bodybuilding is the right amount of testosterone secretion of an athlete. It enables them to perform and also gaining the ripped structure. Preference for the testosterone is on top. The testosterone level can be maintained by a right regimen and also with the help of some steroids. One of them is Clomiphene, which can also be quoted as recoveree for testosterone. If the level of testosterone is not up to the mark or the bodybuilder need more push, then it should be used.
What is Clomiphene?
Clomid is extensively used for the enhancement of testosterone production. It takes a vital place after anabolic steroid cycles. It is the next step after taking anabolic steroids.
It works by taking the space of binding sites of estrogen receptors without activating. If the estrogen levels will be low then there is a supposition for hypothalamus. Hypothalamus is gland beneath the brain which secretes hormones.
Generally, Clomiphene dosage is at 50mg/day. It has a long life. The body contains the Clomipheneof past dosage, simultaneously keeping the present dose of any bodybuilder. It takes time to get going. For example, if you are taking Clomiphene from last week, and today you have taken the dose, your body also has that amount of past Clomiphenein the system. It’s fine if the blood level is right.
Benefits
- In bodybuilding, it enables those athletes who are already on anabolic steroids but want to reduce their side effects especially that of steroids action changing to increase female sex hormone. One of the examples of this is the excessive size of chest or man boobs (gyno).
- It also stimulates the testosterone level after completing the course of anabolic steroids.
- The popularity of clomiphene is due to the resisting factor which enables the bodybuilder to avoid loss of strength and muscle mass. It also improves the appearance of bodybuilders. This is done, due to its binding nature of brain receptors which are solely taken care of male hormonal level. If the male hormones are timely kept in check and the need is fulfilled timely.
Excessive dosage after the first day, if taken more than 50 mg is not recommended. It may cause serious side effects, rather than giving much advantage.
Clomiphene is popularly known as Clomid, as it is the brand name. Clomid is generally available in almost all pharmaceuticals. Moreover, it is also available for research purposes mostly in liquid form. The dosage of Clomid is not preferable with any other drug. But, combining with Nolvadex can give maximum results and half of the dose can perform the work of full dosage. As using excessive or full dosage increase the risk of side effects rather than enhancing much.
The usage for bodybuilding is quite extensive, as any of the legitimate trainers will give preference to testosterone level. Testosterone level plays a very important role in bodybuilding.
[/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. | 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.
| Letrozole 5mg x 100 tablets
Letrozole is a third generation Aromatase Inhibitor (AI) that works by attaching to -and eliminating the aromatase enzyme resposible for producing estrogen. This makes it a perfect choice to combat gynocomastia which it will completely prevent. Letrozole also quite raises LH levels which deems it suitable for post-cycle use. The human body does need estrogen to maintain proper immune function and balance cholesterol ratios in the blood. Since letrozole is so strong at eliminating estrogen, it is not suited for long term use. | 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. |
Create a password
Select how much to transfer and select the correct country/currency
Choose personal transfer
Choose local bank account and fill information
For recipient choose “Someone Else”
You can skip entering the email and fill in the information here
Review Detail of your transfer and confirm
You can choose either debit or credit card or bank ACH
Pay with your card
Afterwards go to all activity and click on detail to check transfer progress
[/vc_column_text][/vc_column][/vc_row]
[/vc_column_text][/vc_column][/vc_row]
Reviews
There are no reviews yet.