Oxydrol steroids side effects

What are you talking about??? The OP was asking if his product was legit and was trying to assure him that it probably was. I mean that was what the whole thread was about or did you not know that.. As far as oxys are concerned, I know what the fuk Im doing, I was born at night but not last night... Im a competitive powerlifter, the best thing for me to take for immediate streghth gains far out from competition is oxys... I only take em for 3 or 4 weeks at the start of a heavy androgenic frontload with a limited dosage, so its like once a year... And btw everyone responds different to anabolics. My blood levels where better after a cycle where i included oxys than they were when I did a simple test and var run... I contribute that mostly to a better diet at the time.... Dont think everybody doesnt know what they are doing, b/c I do. Maybe you should preach to some of the Olympic Bodybuilders and try to get them to lower the dose or quit using what they are.

A lot of bodybuilders consider Oxymetholone to be the strongest oral that there is for sheer mass gain. It is important to note that some of this mass will be from water bloat caused by the steroid. While Oxydrol is a DHT derived compound and therefore can’t convert directly to estrogen, it still is known for many estrogenic related side effects. Some have speculated that Oxydrol 50 somehow triggers the body’s natural estrogen receptors into overdrive. Stronger anti-estrogens such as Letrozole and Exemestane have been shown to greatly suppress the body’s estrogen levels and can both be very effective in keeping these types of side effects to a minimum while using Oxymetholone.

Oxydrol is an oral drug with a dosage of 50mg per tablet. It is the strongest oral on the market. It has both high androgenic and anabolic effects. Strength and weight gains are very significant. It is highly toxic to the liver. Oxydrol also aromatizes fairly easily. Oxymetholone has been reported to produce gynecomastia in users (not all probably around 50%). An anti-estrogen should be used to counteract the aromatization. Nolvadex is an suggested anti-estrogen. Many side effects are associated including acne, hair loss, abdominal pains, headaches, gynecomastia, hypertension, and heavy water retention. Loss of weight and strength usually occurs after the cycle. Oxydrol also shuts down natural testosterone production. It is regarded by the bodybuilding community as the most effective oral steroid in building strength and size. Oxydrol has many side effects however, which make it relatively dangerous to use when compared to other steroids. Average dose is from 50-100 mg a day to 200 mg a day. Oxydrol is used on bulking cycle with sustanon and deca-durabolin.

There is limited information available on the pharmacokinetics of oxymetholone. [4] It appears to be well-absorbed with oral administration . [4] 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. [1] 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 . [4] [2] The C2 hydroxymethylene group of oxymetholone can be cleaved to form mestanolone (17α-methyl-DHT), which may contribute to the effects of oxymetholone. [3] The elimination half-life of oxymetholone is unknown. [2] Oxymetholone and its metabolites are eliminated in the urine . [1] [2]

Oxydrol steroids side effects

oxydrol steroids side effects

There is limited information available on the pharmacokinetics of oxymetholone. [4] It appears to be well-absorbed with oral administration . [4] 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. [1] 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 . [4] [2] The C2 hydroxymethylene group of oxymetholone can be cleaved to form mestanolone (17α-methyl-DHT), which may contribute to the effects of oxymetholone. [3] The elimination half-life of oxymetholone is unknown. [2] Oxymetholone and its metabolites are eliminated in the urine . [1] [2]

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