Profile of Commonly Used IPEDs Image and Performance Enhancing Drugs IPEDs

It is also important to stress that before one considers using insulin they should also become familiar with using a glucometer. This is a medical device that can give you a quick and accurate reading of your blood glucose levels. How is it suppliedThe most common way for Melanotan to be supplied as a white lyophilised powder, in multi dose vials, which require dilution at home.

• 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.
• This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favours greater risk of arteriosclerosis.
• Lt is also estimated to display about three times more androgenic potency than testosterone, making it one of the strongest injectable anabolic steroids ever commercially manufactured.
• How it is suppliedClomiphene citrate is most commonly supplied in tablets of 50 mg.

How it is suppliedStanozolol is widely available in both human and veterinary drug markets. Stanozolol was originally designed as an oral anabolic steroid, containing’i 2mg of drug per tablet (Winstrol). Oestrogenic side effects will occur in a dose-dependent manner, with higher doses (above normal therapeutic levels) of testosterone cypionate more likely to require concurrent use of ananti-oestrogen or aromatase inhibitor. Since water retention and loss of muscle definition common with higher doses of testosterone cypionate, this drug is usually considered a poor choice for dieting cutting phases of training. 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. When used for physique-or performance-enhancing purposes, a dosage of 5 mg to 10 \g daily is most common, taken for no longer than 4-6 weeks.

Clomiphene Citrate (Clomid)

Its activity is quite removed from its structural parent, however, such that direct comparisons between the two are difficult. Trenbolone is a non-oestrogenic steroid, and is considerably more anabolic and androgenic than nandrolone on a milligram for milligram basis. In appearance, it is much more commonly compared to a stronger androgen such as drostanolone, than it is to nandrolone. Lt is also estimated to display about three times more androgenic potency than testosterone, making it one of the strongest injectable anabolic steroids ever commercially manufactured.

• This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favours greater risk of arteriosclerosis.
• It was designed to have a very strong separation of anabolic and androgenic effect, and no significant estrogenic or progestational activity.
• Mesterolone should not be used when cardiovascular risk factors preclude the use of other oral steroids.
• Drug descriptionDNP is one of the most controversial drugs in use by bodybuilders.
• 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.

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).

OTHER IPEDS: ANTI-OESTROGENIC

The administration schedule is often more conservative as well, with a small injection (25 mg at most) given every 5 to 7 days, and cycle duration limited to 6-8 weeks or less. Allanabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Stanozolol is no exception, and is noted for its strong influence on the hypothalamic-pituitary-testicular axis Clinical studies giving 10 mg per day to healthy male subjects for 14 days caused the mean plasma testosterone level to fall by 55%. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production.

• Men with a genetic predisposition for hair loss (androgenetic alopecia) may, notice accelerated male pattern balding.
• How it is suppliedTestosterone propionate is widely available in human and veterinary drug markets.
• This surge in gonadotropins may cause egg release (follicular rupture), ideally leading to conception.
• Nandrolone is very similar to testosterone in structure, although it lacks a carbon atom at the 19th position (hence its other name, 19-nortestosterone).
• Studies have demonstrated that a majority of women will notice acne, which is indicative of androgenicity, at a dosage of only 10 mg per day.

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.

Human Growth Hormone (Somatropin)

The undecylenate ester extends the activity of the drug greatly (the undecylenate ester is only one carbon atom longer than decanoate), so that injections need to be repeated only once every 3 or 4 weeks. Trenbolone is not c-17 alpha alkylated, and is generally not considered a hepatotoxic steroid; liver toxicity is unlikely. This steroid does have a strong level of resistance to hepatic breakdown, however, and severe liver toxicity has been noted in bodybuilders abusing trenbolone.

When administered, ephedrine will notably increase the activity of the central nervous system, as well as have a stimulatory effect on other target cells. (©William Llewellyn, Taken from “Anabolics 2009”)Ephedrine is often found in over the counter “fat burners”. Administration (Intermediate-acting, Long-acting, and Biphasic insulins)Intermediate-acting, CJC 1295 DAC 2 mg long-acting, and biphasic insulins are designed for subcutaneous injection. Intramuscular injection will cause the drug to be released too rapidly, potentially resulting in hypoglycaemia. Following subcutaneous injection, the injection site should be left alone and not rubbed, to prevent the drug from releasing into circulation too quickly.

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.

Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. The use of oxymetholone should be undertaken only after careful consideration in people with high cholesterol or a familial history of heart disease. Women are warned of the potential virilising effects of anabolic/androgenic steroids, especially with a strong androgen such as testosterone. These may include deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.