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The preservative benzyl alcohol has been associated with serious adverse events, including the "gasping syndrome", and death in pediatric patients. Although normal therapeutic doses of this product ordinarily deliver amounts of benzyl alcohol that are substantially lower than those reported in association with the "gasping syndrome", the minimum amount of benzyl alcohol at which toxicity may occur is not known. The risk of benzyl alcohol toxicity depends on the quantity administered and the liver and kidneys' capacity to detoxify the chemical. Premature and low-birth weight infants may be more likely to develop toxicity.

Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds). However it seems likely that much of its suppressive nature still stems from its powerful androgen action. With the strong impact trenbolone has on endogenous testosterone, of course the use of a stimulating drug such as HCG and/or Clomid®/Nolvadex® is recommended when concluding steroid therapy (a combination is preferred). Without their use it may take a prolonged period of time for the hormonal balance to resume, as the testes may at first not be able to normally respond to the resumed output of endogenous gonadotropins due to an atrophied state. Those who have used Parabolan regularly would often claim it to be indispensable. A weekly dosage of 3 ampules (228mg) was the most popular range when running a cycle, however many did find it highly effective in lesser amounts. Although a weekly administration schedule would prove sufficient, athletes usually injected a single ampule per application, the total amount spread evenly throughout the week. While Parabolan is quite potent when used alone, it was generally combined with other steroids for an even greater effect. Leading up to a show one could successfully add a non-aromatizing anabolic such as Winstrol® or Primobolan®. Such combinations will elicit a greater level density and hardness to the build, often proving dramatic to a stage appearance. We could also look for bulk with this drug, and addition stronger compounds like Dianabol or Testosterone. While the mass gain would be quite formidable with such a stack, some level of water retention would probably also accompany it. Moderately effective anabolics such Deca-Durabolin® or Equipoise® would be somewhat of a halfway point, providing extra strength and mass but without the same level of water bloat we see with more readily aromatized steroids.


The mixture of testosterone is subject to the effects of the enzyme aromatase in the body, among the side effects of T-400 are side effects of estrogen. The rate of aromatization is directly related to the amount of used substance, and together with increasing doses aromatization is higher. Estrogenic side effects include: excessive water retention and bloating, elevated blood pressure (. due to water retention in the body), accelerated fat deposition and gynecomastia. The side effects of estrogen can be reduced or completely avoided by using aromatase inhibitors or SERMs (selective estrogen receptor modulators. Among androgenic side effects are: increased secretion of sebum (oily skin), acne (in terms of increased secretion of sebum), body hair growth, and increased risk of inducing male pattern baldness (MPB) in persons with a genetic predisposition. Anabolic / androgenic steroids can have deleterious effects on blood cholesterol levels. This includes a tendency to reduce HDL (good) cholesterol and increase LDL (bad) cholesterol. All anabolic steroids have the ability to suppress or shut down the natural endogenous production of testosterone in the body, and T-400 is no exception. After the end of the cycle, it is highly recommended to use a suitable PCT (Post Cycle Therapy).  

Teratogenicity studies in mice using the subcutaneous route resulted in fetotoxicity at the highest dose tested (1 mg/kg) and teratogenicity at all dose levels tested down to mg/kg. These doses are approximately and times, respectively, the human topical dose of clobetasol propionate ointment. Abnormalities seen included cleft palate and skeletal abnormalities. In rabbits, clobetasol propionate was teratogenic at doses of 3 and 10 mcg/kg. These doses are approximately and times, respectively, the human topical dose of clobetasol propionate ointment. Abnormalities seen included cleft palate, cranioschisis, and other skeletal abnormalities.

Test propionate opis

test propionate opis

Teratogenicity studies in mice using the subcutaneous route resulted in fetotoxicity at the highest dose tested (1 mg/kg) and teratogenicity at all dose levels tested down to mg/kg. These doses are approximately and times, respectively, the human topical dose of clobetasol propionate ointment. Abnormalities seen included cleft palate and skeletal abnormalities. In rabbits, clobetasol propionate was teratogenic at doses of 3 and 10 mcg/kg. These doses are approximately and times, respectively, the human topical dose of clobetasol propionate ointment. Abnormalities seen included cleft palate, cranioschisis, and other skeletal abnormalities.

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