Anavar Dosage and Stack

Unlike most of the oral compounds, anavar (oxandrolone) is classified as class 1 of anabolic steroids, which most effectively accumulates with two kinds of compounds, such as dianabol or anadrol.
It has little effect on the high-dose use of class I anabolic steroids such as trenbolone or high-dose testosterone (classified as having mixed activity). It may be a help, though an expensive one, to moderate the dose of testosterone used.
Anavar is often referred to as a weak steroid. Part of the reason is that class I steroids alone will never be the most effective. Another reason is that bodybuilders and authors in the field sometimes make unfortunate and unreasonable comparisons when judging anabolic steroids. If eight tablets a day have little effect, a drug is declared useless or weak. Traditionally, oxandrone has been used in 2.5 mg of anavar, proving to be only 20 mg per day, for a total of 140 mg / week. In contrast, this dose of testosterone has no effect. In fact, few anabolic steroids can produce significant effects at this dose, but they are not so called weak. The correct conclusion is that this anavar tablet is individually weak, but not that the drug lacks efficacy.
With the available of higher doses of Anavar,anavar's reputation has improved. However, it is still not a particularly cost-effective class I steroid, and if used alone, it cannot achieve a good stack performance.
In pharmacology, it has been found that oxandrolone has weak binding with androgen receptor. This seems to be inconsistent with they system, but it has been found. Maybe it's because what happens in vivo is different from what happens in vitro, or maybe another interesting phenomenon has happened.
However, from a practical point of view, the stacking behavior of oxandrolone requires that it be classified as one kind of steroids: it combines with steroids classified as two kinds, but only with one kind of compounds. From a practical point of view, it is a quite effective drug, that is to say, it has a good curative effect per milligram. Combined with class II steroids, anavar is quite effective at 75 mg / day or even 50.
Anavar does not aromatize or convert to DHT, with a half-life of 8 hours. Therefore, the medium dose taken in the morning is not in the system at night, but provides a reasonable level of androgen in the daytime and evening.
One study found that oxandrolone was superior to testosterone and deca (nandrolone) in reducing abdominal fat in men, or at least at a specific low dose in the study, and was not necessarily equivalent in obese older men. Therefore, some people have made a broad summary of bodybuilding. However, this does not necessarily extend to anabolic steroid cycles in doses commonly used for bodybuilding. In this study, I think the difference in results is related to dose.
In fact, under the total androgen dosage usually used, if oxandrolone is not used, as long as various possible substitutes of oxandrolone are used, it can be cut equally effectively. This is not to say that the drug is ineffective, but other androgens, including testosterone, are also effective in reducing abdominal fat at high doses.
However, in the case of low-dose use, I think this is a correct conclusion. For most people, low-dose use of anavar is more effective than most other steroids of the same dose. This may be partly or completely due to the additive effect of natural testosterone: the use of this kind of oxandrone can not inhibit its production, and users can enjoy the full effect of natural testosterone and the effect of oxandrone at the same time. In contrast, the use of low-dose testosterone or nandolone can lead to a large amount of inhibition of natural testosterone, so the overall effect is small.
Oxandrolone, like 17 other alkylated steroids, is hepatotoxic. It has been thought that it is not, but clinical and practical experience have shown that long-term use of oxandrin does cause liver toxicity. I think the general principle of limiting the use of 17 alkylation to 6 weeks should be applied when aucxion is used, just like any alkylation taken orally.
Trenbolone or Primobolan are suitable substitutes for anavar, and there is no hepatotoxicity problem. As a substitute, resveratrol has low inhibition, while chuanbolong has no low inhibition.
An interesting use of oral administration of the drug is to use it as the only linker in the morning between cycles, which, in my opinion, should be done - if done - only in the complete return to normal testosterone production from the last cycle. In this application, at least 20 mg is generally acceptable. Ideally, testosterone levels would be measured to monitor this bridging. One factor limiting this bridging is the problem of liver toxicity.
With regard to use by women, while there is a common belief that Anavar is minimally virilizing to female, in fact virilization is not unusual at 20 mg/day and can occur at considerably lower doses than that. Even 5 mg/day is not side-effect-free for all.

During a cycle, oxandrolone is not particularly recommended because there are more cost-efficient choices that will fully accomplish the same goals and do not add to liver toxicity.

The two best uses for Anavar are in optional bridging periods between cycles, if such are employed, while keeping care to avoid excessive duration of continuous 17-alkylated use; and, if short-acting injectables are not available, to supplement cycles as levels fall between the time of last injection and the start of post-cycle therapy so that that time period can remain effective for gains.