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Testosterone propionate is, therefore, comparatively much faster-acting than other testosterone esters such ascypionate or enanthate, and requires a much more frequent dosing schedule. By most accounts testosterone propionate is an older and cruder form of injectable testosterone, made obsolete by the slower-acting and more comfortable esters that were developed subsequent to it. Still, those who are not bothered by the frequent injection schedule find testosterone propionate every bit as acceptable. How it is suppliedNandrolone decanoate is widely available in human and veterinary drug markets.

  • Therapeutic useModern (approved) medical applications for the drug are even more refined than they were in the mid-1970’s.
  • The subcutaneous administration of somatropin may cause redness, itching, or lumps at the site of injection.
  • The usual dosage for physique-or performance-enhancing purposes is between 15 mg and 25 mg per day, or three five 5 mg tablets, taken for no longer than 6-8 weeks.
  • Intramuscular injection will cause the drug to be released too rapidly, potentially resulting in hypoglycaemia.
  • Testosterone cypionate is not recommended for women for physique-or performance-enhancing purposes due to its strong androgenic nature, tendency to produce virilising side effects, and slow-acting characteristics (making blood levels difficult to control).

Drug descriptionClomiphene citrate is an anti-oestrogenic drug that is prescribed to women to treat anovulatory infertility (inability to ovulate). In clinical medicine it is specifically referred to as a nonsteroidal ovulatory stimulant. The drug works by interacting with oestrogen receptors, often in an antagonistic manner, in various tissues of the body including the hypothalamus, pituitary, ovary, endometrium, vagina, and cervix. One main focus is that the drug will oppose the negative feedback of oestrogens on the hypothalamic-pituitary-ovarian axis, enhancing the release of gonadotropins (LH and FSH).

Clomiphene Citrate (Clomid)

The drug is typically taken in cycles of 6-12 weeks in length, which is usually a sufficient period of time to notice the benefits of drug therapy. For womenThe original prescribing guidelines for Anavar did not offer separate dosing recommendations for women, although it was indicated that women who were pregnant, or may become pregnant, should not use the drug. The current guidelines for Oxandrin also do not make special dosing recommendations for women. Women who fear the masculinizing effects of many steroids would be quite comfortable using this drug, as these properties are very rarely seen with low doses. For physique-or performance-enhancing purposes, a daily dosage of 5-10 mg should illicit considerable growth without the noticeable androgenic side effects of otherdrugs. Side effectsMethandrostenolone is aromatised by the body, and is a moderately oestrogenic steroid.

  • Drug descriptionOxymetholone is a potent oral anabolic steroid derived from dihydrotestosterone.
  • As such, it may act as an oestrogen in some tissues while blocking the action of oestrogen in others.
  • This is an early symptom of hypoglycemia, and a clear sign the user should be consuming more carbohydrates.
  • Therapy is initiated 2-3 years after tamoxifen has failed to elicit a desirable response, at which point tamoxifen is discontinued.

How it is usedWhen used to mitigate the oestrogenic side effects of anabolic/androgenic steroid use or increase muscle definition, male athletes and bodybuilders will commonly take 12.5 mg to 25 mg of exemestane per day. In some instances a half of a tablet (12.5 mg) taken every other day is sufficient to prevent the onset of oestrogenic side effects. Drug descriptionTrenbolone acetate is an injectable (generally) anabolic steroid derived from nandrolone.

Clomifene Citrate (Clomid)

It was mainly applied to cases of maleandrogen insufficiency, and those issues normally surrounding low testosterone levels such as reduced sex drive and impotence in adults, and cryptorchidism (undescended testicles) in teenagers and young adults. Food & Drug Administration, however, and by the 1980’s, testosterone propionate was being largely applied only to male patients. The injectable is usually not advised with women for physique-or performance-enhancing purposes, as it allows for less control over blood hormone levels.

  • Among bodybuilders, dosages of regular insulin (Humulin-R) used are usually in the range of 11U per pounds of lean bodyweight; 10IU is perhaps the most common dosage.
  • It is synthesized in … the placenta, and is responsible for increasing the production of progesterone, a pregnancy-sustaining hormone.
  • (©William Llewellyn, Taken from “Anabolics 2009”)Ephedrine is often found in over the counter “fat burners”.
  • Nandrolone is not c-17 alpha alkylated, and not known to have hepatotoxic effects in healthy subjects.
  • Female athletes occasionally use clomiphene citrate for the reduction of estrogenicity near the time of a bodybuilding contest.

It is also advised to rotate subcutaneous injection sites regularly to avoid the localized buildup of subcutaneous fat due to the lipogenic properties of this hormone. Among athletes, mesterolone is primarily used to increase androgen levels when dieting or preparing for a contest, and as an anti-oestrogen due to its intrinsic ability to antagonize the aromatase enzyme. Due to the ability of LH to stimulate the Leydig’s cells in the testes to manufacture testosterone, hCG is also used with men to treat hypogonadotropic hypogonadism, a disorder characterized by low testosterone levels and insufficient LH output. The drug is also used in the treatment of prepubertal cryptochidism, a condition in which one or both of the testicles have failed to descend into the scrotum. The medical dosage will vary depending on the individual requirements of the patient. Furthermore, changes in such things as diet, activity level, or work/sleep schedule may affect the required insulin dose.

Oxandrolone is noted for being quite mild as far as oral steroids are concerned, well-tailored for the promotion of strength and quality muscle tissue gains without significant side effects. However, it is also an expensive drug by comparison to other similar anabolic agents. The original prescribing guidelines for Winstrol called for a daily dosage of 4mg (one 2mg tablet twice daily) with young women particularly susceptible to the androgenic effects of anabolic steroids. This dosage was increased to 6mg (the same as the recommended dose for males) when necessary.

How it is suppliedTamoxifen citrate is most commonly supplied in tablets of 10 mg or20 mg. For womenWhen used to induce ovulation and pregnancy in anovulatory infertile woman, a dose of 5,000 to 10,000 units is administered one day following the last dose of menotropins. The timing is specific so that the hormone is given precisely at the right moment in the ovulation cycle. It is also important to make sure others are aware of your use of the drug so that they may inform emergency medical technicians should you lose consciousness or the ability to inform others of your condition due to hypoglycemia. This information can spare valuable (perhaps life saving) time in helping medical professionals establish a diagnosis and provide supportive treatment.


Side effectsAlthough classified as an anabolic steroid, androgenic side effects are still possible with this substance, especially with higher doses. Women are warned of the potential virilising effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Lt is also important to point out that due to its mild androgenic nature and ability to suppress endogenous testosterone, nandrolone is prone to interfering with libido in males when used without another androgen. Side effectsOxandrolone is not aromatised by the body, and is not measurably oestrogenic.

CLENBUTEROL SOPHARMA 0,02 mg * 50 tablets

However, there is some limited evidence to show long term use can lead to weight gain and sexual dysfunction. Many athletes believe that its short window of effect makes it an ideal insulin medication for physique-or performance-enhancing purposes, as most of its action can be concentrated in the post-training enhanced-nutrient uptake window. Therapeutic useIn the veterinary market, boldenone undecylenate is most commonly applied to horses, although in many regions it is indicated for use in other animals as well. Additionally, the 5-alpha reductase enzyme does not metabolize mesterolone, so its relative androgenicity is not affected by finasteride or dutasteride. Injecting carries several risks, both from the process and from the drugs themselves. It is important to be aware of these risks before attempting to inject any substance.

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