Those who have more patience or are afraid of potential side effects will usually be very satisfied with Primobolan Depot.
It is is the “Cleanest and Gentles” anabolic steroid, will not aromatize, non-toxic, low in androgens. Primobolan depot may be taken by both Men and Women. Dosages for men are 100-300 mg/week, Women 1/2 dosage.
Primobolan depot is the only steroid that works well on a low calorie diet. Effective for bulking, but tends to harden and add muscle tone more that build big muscles. Primobolan depot works great when added to a cycle (stacked) with other steroids, it tends to lessen water retention and harshness when stacked with more heavy duty testosterone injectables, like Omnadren / Sustanon, Cypoinate / Propionate, ect. It is an analog immune-stimulating steroid used by people with Aids and others with depressed immune systems to build up the immune system and add lean muscle mass. Primobolan is one of the finest steroids in the world today.
Primobolan is a well-known and popular steroid as well. Like nandrolone it’s most often used as a base compound for stacking with other steroids. Methenolone however, is a DHT-based steroid (actually, DHB or dihydroboldenone, the 5-alpha reduced of the milder boldenon). Meaning when it interacts with the aromatase enzyme it does not form estrogens at all. That makes it ideal for use when cutting when excess estrogen is best avoided because of its retentive effects on water and fat. Methenolone is mostly only used in such instances, or by people who are very succeptible to estrogenic side-effects, because the anabolic activity of methenolone is slightly lower than that of nandrolone, quite likely BECAUSE it is non-estrogenic.
Like nandrolone, methenolone 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.
For athletes who wish to maintain a “natural” status in competition, the tablets are quite well-suited as detection chances for the acetate-form are quite slim. However tests have improved and quite a number of metabolites of methenolone can be detected with a simple urine sample. But an English study documented that there is a liability in eating methenolone contaminated meats, which could provide a possible defense if found out. One could always claim they ate the meat of a chicken or cow injected with methenolone since the test concluded eating such meat does not improve performance, but can deliver positive tests for several methenolone metabolites almost 24 hours after ingestion. That’s for those of you seeking a viable defense against a possible methenolone-positive.
There is no use for alternate drugs since it does not aromatize, is quite mild and the gains are fairly easy to maintain, so post-cycle use of clomid or Nolvadex is not warranted.