HD

Pretty much everything written thus far about Stanozolol injectable (*See “Winstrol Depot” under “Injectable Anabolic Androgenic Steroids” for more info) was also attributed also to the oral form. It was often said that the oral form is less effective than the injectable. In truth, it was usually due to dosages, and this in turn was due to price. Athletes usually administered a lower dosage orally because it seemed like 25 pills daily was mega dosing. In my personal opinion this was true to a point. Oral use of any 17-alfa-alkylated steroid is hard on the liver.

Nandrolone Phenylpropionate is an anabolic steroid that is very similar to the popular Nandrolone Decanoate compound. However, Nandrolone Phenylpropionate was the first Nandrolone compound ever commercially sold. Nandrolone Phenylpropionate hit the shelves in the 1950’s and was brought to the market by Organon under the name Durabolin. Soon after Organon would release its Decanoate cousin under the name Deca Durabolin.

Testosterone was generally toted as the big daddy of injectable steroids. No other steroid was consistently reported to bring such high returns as quickly in weight gain and strength increases. Due to its high anabolic/high androgenic effects, many athletes used this drug in an off-season mass cycle. Water retention during administration of ENANTHATE was not reportedly as high as that realized during the use of OMNADREN. but darn close. Like all testosterone esters, Enanthate aromatized easily and has a high conversion rate to DHT. Those with prostate problems or who were sensitive to gyno and female pattern fat deposits, readily agreed that they should have either left it alone or taken steps to suppress estrogenic activity due to aromatization. Drugs such as PROVIRON and NOVLADEX were often utilized for this reason. DHT conversion enzyme blockers such as Proscar were commonly co-administered with testosterones for the former reason. Testosterone enanthate notably suppressed HPTA function severely. HCG/Clomid were considered almost a must to stimulate normal endogenous (natural) testosterone production within a positive period of time at post use. My personal experience has been that if a cycle containing testosterone enanthate lasted longer than 6 weeks, HCG and usually Clomid were introduced for 10 days beginning at the end of week #4. (5000 i.u. of HCG 3 times in 10 days usually normalized sperm and endogenous testosterone production to a respectable extent) Without the use of HPTA stimulating compounds normalization did occur, only at a much slower rate. For this reason, gains made during “enanthate only” administrations were not well maintained after use was discontinued, and much was lost needlessly by most regardless. Perhaps this was why so many uninformed individuals stayed on the stuff almost year round.

200MG/ML NANDROLONE DECANOATE 100MG/ML TESTOSTERONE ENANTHATE 100MG/ML TESTOSTERONE CYPIONATE 100MG/ML TRENBOLONE ENANTHATE

Primobolan tablets are a moderately anabolic and low androgenic oral steroid that was reported as limited in use by most bodybuilders. This was likely simply because alone and when it was administered in listed dosages the drug was not very effective. However, gains were made in muscle mass and strength were consistently reported to be of a very high quality and were mostly retained post-cycle. Acetates are “said” to aid in fat burning, so this drug was mostly used in a stack pre-contest. The problem in effectiveness lies in the fact that PRIMOBOLAN ACETATE is not a c17-ALFA-ALKYLATED steroid and is therefore mostly deactivated during the first pass through the liver. As the reader is aware, oral AAS are commonly altered to decrease liver deactivation. The most common alteration is called a c-17 alfa-alkylated drug. This alteration makes the liver work over-time to deactivate it and is therefore said to be highly liver toxic. (But so are most oral birth control drugs) But another alteration in structure allows Primobolan orals to be somewhat resistant to liver deactivation. It is referred to as unsaturation in the 1-position.This alteration allows the compound to resist metabolic deactivation by significantly shifting the 17-Keto redox potential toward creation of active 17-beta hydroxyl AAS. The result is an active oral AAS that is not liver toxic except in very high dosages. Some have recalled the injectable form of Primobolan acetate with great fondness for its supposed fat burning/lean mass building qualities. The vials contained only 20-mg of METHENOLONE ACETATE (MA) yet it was reported far more effective than 150- mg of the oral. A commonly reported method to obtain greater blood circulatory levels of the oral form was to mix 20-25-mg of the ground tables with either DMSO gel or a 50/50 solution of DMSO and water. Users then simply applied the mixture to their skin (especially in areas of stubborn fat deposits). 10-20% absorbed and passed directly into the blood stream thus avoiding first pass liver deactivation. This was done 1-5 times daily. DMSO is a solvent that carries smaller molecule structures mixed with it directly through the skin. It is said to be found at some health food stores and chemical supply warehouses. Another reported method was mixing ground Primobolan tabs with Vitamin-E oil. The users then ingested it orally. This caused a great deal of the active steroid to be absorbed through the lymph system like Andriol and therefore avoid first pass deactivation. *There is a great deal of research under way in the OTC supplement industry that employs a similar pharmacological solution to liver destruction of micronutrients. Back to reported tablet use… Primobolan tabs were reportedly used most by women and steroid novices because they do not aromatize or cause water retention. Women who utilized 50-100mg daily of this drug seldom noted virilizing side effects. Most report a distinct harder look and a 3-4 LB muscle mass gain in 6-8 weeks. Obviously many females also stacked Primobolan tabs with other drugs to heighten results. Males normally ingested 100-200 mg daily in 2-4 divided doses (due to short half-life 4-6 daily divided dosages were more effective at maintaining plasma concentrations of the active drug) and report fair gains. Stacked with more androgenic steroids such as testosterone, Parabolan, or even moderate androgenics such as Deca Durabolin or Equipoise, males made high quality muscle mass and strength gains with safer low side effect results.