UPA

UPA=SARMS TESTOLONE(RAD-140) 10MG/TABLET=50 TABLETS. Testolone (RAD-140) Testosterone Replacement Testolone (RAD-140) is designed to make hormonal receptors in the tissues act as though they are getting a strong dose of testosterone. This gives the same effect as if running a cycle of anabolics and/or prohormones without the negative side effects that correlate with use.

UPA TB500(5MG=1 POWDER+WATER) Thymosin Beta 4, or TB-500, is a synthetic version of a naturally occurring 43-amino acid peptide present in nearly all human and animal cells studied.

Decreases HPTA function: Yes, dose and administration period dependent Oral Dianabol was reported to be a highly effective mass AAS which provided impressive weight and strength gains. Most users experienced a 2-4 LB bodyweight increase per week with heavy water retention.

UPA BPC 157(PENTADECAPEPTIDE 5MG=1 POWDER+WATER))

Nandrolone Decanoate is a very anabolic, moderate androgenic form of nortestosterone that was the most commonly used drug to create a rapid build-up of lean muscle mass or as a diet “protein- sparing” drug by athletes of all kinds. This is a longer lasting nandrolone than Durabolin so some water retention resulted with long term administration (especially in higher dosages). A prominent positive nitrogen balance occurs with the use of nandrolones and therefore a high protein intake was a must for all reported users.

Oral Dianabol was reported to be a highly effective mass AAS which provided impressive weight and strength gains. Most users experienced a 2-4 LB bodyweight increase per week with heavy water retention. With higher dosages gynecomastia (bitch tits) was a common negative side effect. Obviously much of this was avoided by those who reported co-addministration of Proviron and/or Novladex. When stacked with a nandrolone, some gyno problems seemed to lessen. This was probably due to Nandrolones aromatization to a weaker estrogen called Norestrogen and the resulting mild anti-estrogenic effect that results in moderate dosage administration. Methandrostenlone becomes active in 1-3 hours with a half-life of about 3.5-4.5 hours. For this reason, dosages were spread through out the day to maintain blood serum concentrations at an elevated state. Massive dosages just were not necessary since a single 10-mg dose has increase androgen anabolic activity 5 times over normal with a correlating reduction in natural cortisol activity of 50-70%. Males using 5mg per 25-LBS of body weight broken into 3-5 equal dosages throughout the day have experienced impressive results. At dosages above 50 mg per day, results were not progressively quantitative. Most first time AAS users who used a daily dosage of 20-30mg daily experience significant results over a 4-6 week period. Women should not utilize Methandrostenolone but a surprising number did report the inclusion of the drug in AAS protocols. For those who insisted, no more than 10-mg daily for 3-4 weeks stacked with a very low androgenic product minimized masculization type negative side effects.