Effects of Primobolan
This steroid has the chemical name of 17ß-hydroxy-1-methyl-5a-androst-1-en-3-one acetate and its anabolic/androgenic ratio is 88:44-57. The molecular weight of Primobolan is 344.488 g/mol at the base and this anabolic compound has the molecular formula is C 22 H 32 O 3 . Primobolan can be detected over a period of 4-5 weeks and its anabolic/androgenic ratio is 88:44-57. This anabolic androgenic steroid is available both as an injectable (enanthate) and oral (acetate). The active life of oral Methenolone is 4-6 hours and active life of liquid (injectable) Methenolone is 10-14 days.
I am just saying we are two different individuals both hell bent on our opinions on this matter, we don’t see eye to eye. but we don’t have to. I have read through a lot of your posts and you are DEFINITELY a Knowledgeable bro for sure. but. can I ask– what is YOUR Goal. Are You a competitive bodybuilder/strongman/powerlifter. do you lift for the sake of being a large scale male (big-o-rexia). do you know your stuff from years of trial and error or from reading the science of this stuff on websites dedicated to this.
The most popular brand names of Methenolone Acetate tablets (generic Primobolan) in 2015 are:
– A minimum rollback phenomenon after the end of the course
All patients received prophylactic induction therapy consisting of an antilymphocyte antibody preparation, corticosteroids and azathioprine. Where bodybuilding, athletics, and performance enhancement is concerned, beginner Primobolan dosages for the injectable format normally start at about 400mg per week. Intermediate Primobolan dosages are usually in the range of 400 пїЅ 700mg per week, which should be adequate enough, and advanced users may venture as high as 800 пїЅ 1,000mg per week. Female Primobolan dosages in terms of safety and minimal virilization are usually in the range of 50 пїЅ 100mg per week. Injectable Primo tends to be used far less frequently by females than the oral variant, which is the preferred form. Potent inhibition of CYP Primobolan and both hepatic and intestinal CYP 3A45 activities were observed after first dose and steady state. Thus, it is difficult to predict the net effect of Primobolan administered with ritonavir on oral bioavailability and plasma concentrations of drugs that are dual substrates of Primobolan 3A Primobolan P-gp. Follow-up studies indicated that impaired fertility was due to an effect on the female.