Oxandrolone Oral Anabolic Steroids Avanar 20mg Raw Powder For Cutting Phases

Anavar (oxandrolone), unlike most oral compounds is categorized as a Class I anabolic steroid, most efficiently stacked with Class II compounds such as Dianabol or Anadrol

Product name: Oxandrolone

Other name: anavar; lonavar; oxandrin

CAS register number: 53-39-4

EINECS: 200-172-9

Molecular formula: C19H30O3

Molecular weight: 306.4

Assay: 97-100.5%

Appearance: White or almost white crystalline powder

Usage: Oxandrolone is widely used due to its exceptionally small level of androgenicity[citation needed] accompanied by moderate anabolic effect. Although oxandrolone is a 17-alpha alkyloid, its liver toxicity is very small as well.

It adds little if anything to high-dose use of Anabolic Steroids such as Trenbolone , or to high-dose testosterone, which is classified as having mixed activity. It can be an aid, albeit an expensive one, to moderate dose testosterone usage.

Anavar has often been called a weak steroid. Part of the reason for this is that use of a Class I steroid alone never is maximally effective. The other cause is that bodybuilders and authors in the field sometimes make unfortunate and unreasonable comparisons when judging anabolic steroids. If say 8 tablets per day does little, then a drug is pronounced useless or weak. And traditionally, oxandrolone was available in 2.5 mg Anavar tablets, proving only 20 mg daily with such usage, which totals to only 140 mg/week. For comparison, testosterone at that dose also gives little results. Indeed, few anabolic steroids give dramatic results at that dose, but they are not called weak on that account. The proper conclusion is that such Anavar tablets were individually weak, but not that the drug lacks potency.

As higher-dose Anavar tablets have become available, the oxandrolone’s reputation has improved. However, it still is not a particularly cost-effective Class I steroid, and if used alone cannot match the performance of a good stack.

Anavar does not aromatize or convert to DHT, and has an 8 hour half-life. Thus, a moderate dose taken in the morning is largely out of the system by night, yet supplies reasonable levels of androgen during the day and early evening.

Oxandrolone to be superior to testosterone and to Deca (nandrolone) for reducing abdominal fat in men, or at least in obese older men at the specific low doses studied, which were not necessarily equipotent. From this, some have made broad generalizations to bodybuilding. However, this does not necessarily carry over to anabolic steroid cycles at doses commonly used in bodybuilding. In the case of the study in question, I expect the difference in outcomes was dose-related.

In practice, at total androgen doses typically used, one can cut just as effectively without oxandrolone as with, given any of various possible substitutions for the oxandrolone. This is not to say this drug is ineffective, but rather that other androgens including testosterone are also effective at high dose for abdominal fat loss.

Among bodybuilders it is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 20-50mg per day, a level that should produce noticeable results.

It can be further combined with anabolics like Primobolan and Winstrol to elicit a harder, more defined look without added water retention. Such combinations are very popular and can dramatically enhance the show physique. One can also add strong non-aromatizing androgens like Halotestin, Proviron or trenbolone.

However, in the case of low-dose use, I think it is a correct conclusion that for most, low-dose Anavar use is more effective for most other synthetic metabolic steroids. This may be partially or completely derived from the addition of natural testosterone: the use of octreotide may not inhibit its production, the user can enjoy the full effect of his natural testosterone and the effect of oxazolone. In contrast, the use of low-dose testosterone or norbornone can lead to a large number of natural testosterone inhibition, so the overall effect is poor.

As with other 17-alkylated steroids, oxazolones are hepatotoxic. Once again, this is not, but Oxandrin's clinical and practical experience shows that hepatotoxicity is indeed a long-term use. I think that when oxethazone is used, it should be used at the same time to limit the use of 17-alkylation to a six-week general principle, just like any alkylated oral administration.

Terence or Primobolan is an appropriate alternative to Anavar, no liver toxicity problems. As a substitute, Primobolan has low inhibitory properties while talbolone does not have.

An interesting application of the drug for its oral administration is as soon as the morning bridging agent between circulation and I should be done - only after the complete recovery of normal testosterone production from the previous cycle can be used. At least 20 mg of the present application is generally acceptable. Ideally, testosterone levels will be measured to monitor this bridge. One factor limiting this bridging is hepatotoxicity.

With regard to the use of women, although it is widely believed that Anavar has the least toxic side effects on women, in fact, at 20 mg / day, deterioration is not common and may occur at a fairly low dose. Even 5 mg / day for everyone is not without side effects.

In a cycle, odrolone is not particularly recommended because there are more cost-effective options that will fully achieve the same goal without increasing liver toxicity .

50ml @ 50mg/ml
2.5 grams Anavar
2.5ml BA
2.5ml BB
5ml guaiacol
37.5ml Oil

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