Primobolan Depot by
Bayer Schering Turkey is a steroid injection which contains 100 mg/ml of the
hormone Methenolone Enanthate , and it is available in a 1ml ampoule.
The Enanthate ester of this steroid makes this compound slow acting, that's why a 2 times a week schedule is enough.
Usually known as Primo , Primobolan is one of the oldest steroids, and it is still one of the most popular between bodybuilders and athletes which are in their cutting phase of the cycle, but wouldn't want to gain any fat. Due to it's mild nature, Primobolan works really great with diets with restricted calories.
Primobolan Depot does not produce aromatization, so there is no need in an estrogen blocker. This steroid will give a pronounced quantity of muscles definition and hardness, especially to Bodybuilders and athletes with a low body fat.
Primobolan was the favourite anabolic steroid of well known Arnold Schwarzenegger. This was the steroid that helped Arnold to maintain his really small waist.
Promobolan is very well known as a binding steroid, which means that athletes use a stable dose of this steroid between the regular cycle. This type of use of Primobolan will give to bodybuilders an anabolic state more than it is natural, but it is not shutting down the natural process of producing testosterone as other steroids would do.
Bodybuilders who want to include Primobolan Depot in their cycle, can stack it with Testosterone and an oral compound like Winstrol tabs or Anavar.
Due to it's mild nature and a low rate of androgenic effects, Primobolan is a very good choise for female bodybuilders.
Average dose men: 300-800 mg/week
Average dose women: 50-100 mg/week
Primobolan Depot is very mild on the system, probably the reason why both are strongly favored as base compounds in stacks. Methenolone has no estrogenic side-effects whatsoever, on account of its structure. Its effects on the cholesterol levels are barely noticeable. In doses of 200 mg or less (injectable) blood pressure is rarely, if at all, altered. As for hepatoxicity, long-term use will of course increase liver values but gradually and only slightly. The injections of course, since they only pass the liver once, have roughly half the liver-toxic effects of the tabs. The low liver-toxicity is accounted for that the bio-availability of Methenolone is carried by a 1-methyl-group, which lessens the need for a carrier attachment such as a 17-alpha-akylated group, the main culprit in steroid-related liver afflictions.