There is limited information available on the pharmacokinetics of oxymetholone.  It appears to be well-absorbed with oral administration .  Oxymetholone has very low affinity for human serum sex hormone-binding globulin (SHBG), less than 5% of that of testosterone and less than 1% of that of DHT.  The drug is metabolized in the liver by oxidation at the C2 position, reduction at the C3 position, hydroxylation at the C17 position, and conjugation .   The C2 hydroxymethylene group of oxymetholone can be cleaved to form mestanolone (17α-methyl-DHT), which may contribute to the effects of oxymetholone.  The elimination half-life of oxymetholone is unknown.  Oxymetholone and its metabolites are eliminated in the urine .  
Intermediate Primobolan dosages are usually in the range of — mg per week, which should be adequate enough, and advanced users may venture as high as — 1,mg per week. Primobolan, as other synthetic anabolic androgenic steroids , produce a number of benefits as far as athletes are concerned. Therefore, since only the enanthate version is available for injections. The recommended dosage for women is milligrams mgs per day for oral primobolan, and mgs per week for the depot. Hence, it is a very good cutting steroid that can be used alone, or cycled with other AAS. None of their products are condoned nor recommended for non-medical use such as athletics or bodybuilding. One can easily see where the allure of this anabolic steroid comes from within the athletic and bodybuilding community, as it is a compound that exhibits weak androgenic effects with very little to no side effects.
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