UPA

This product becomes active after one day, but through the series of the other 3 testosterones, remains active for 3 weeks. This mixture had a reported better over all effect milligram for milligram than any other testosterone alone. Users experienced a rapid increase in strength and an even increase in solid mass during administration. SUSTANON aromatized less and caused less water retention when compared to other single testosterones and much less than OMNADREN. Liver toxicity was low (Except in ridiculous dosages) as the liver metabolizes testosterone very efficiently. Like all testosterones, SUSTANON provided improved muscle pumps, better post-training recuperation, and an elevation in aggressiveness toward training.

This is probably the strongest oral compound ever made. Taking one tab a day (10mg) should be sufficient for a maximum of 5 to 6 weeks. These doses might sound low but considering its potency athletes are warned to not compare it to doses being taken of other products they are familiar with. Some users reported a dose of around 20mg but this was found to be very high and the side effects of high blood pressure and toxicity at those doses became rapidly evident. Some describe M1T’s characteristics as a mix between Primabolan, Stanazol and Trenbolone. I personally like comparing it to Oxymethelone (Anapolon) by comparing its anabolic rating. Anapolon is seen as one of the strongest orals in the world and has an anabolic rating of 320. M1T has an anabolic rating of 900-1600. This is between four and five times the anabolic rating of Anapolon (Oxymethelone)

Oral Turinabol is an anabolic steroid developed and made famous by scientists in East Germany years ago. Actually, this is more a steroid of infamy actually, as it was one of the closely held secrets inside the “East German Doping Machine” I am referring to a state sponsored doping program, called “State Plan 14.25” that operated in East Germany for a period of time between the 1960’s and 80’s. It was an aggressive anabolic steroid administration program, designed with one goal in mind: cheating the Olympic drug test. In many cases, the Olympic athletes, both male and female, were unwitting participants, simply told by their trainers and coaches that they were being given “vitamins” Many of these blue vitamins turned out to be Oral Turinabol, a potent and undetectable (at the time) anabolic steroid. As many as 10,000 unsuspecting athletes were given anabolic steroids during the time the program was active. For a more in-depth look at this dramatic historic event, including the trials of several former East German officials for their participation, I recommend you look at the book “Faust’s Gold: Inside the East German Doping Machine”by Steven Ungerleider. OT, as it is called, is a potent derivative of Dianabol. It is structurally a cross between methandrostenolone and clostebol (4-chlorotestosterone), having the same base structure as Dianabol with the added 4-chloro alteration of clostebol. This makes OT a “kinder, gentler Dianabol” the new steroid displaying a much lower level of androgenic activity in comparison to its more famous counterpart. Its anabolic activity of chlorodehydromethyltestosterone is somewhat lower than that of Dianabol as well, but it does maintain a much more favorable balance of anabolic to androgenic effect overall. This means that at any given level of muscle-building activity, OT will be much less likely to produce the classic androgenic side effects such as oily skin, acne, aggression, and male-pattern hair loss (if genetically prone) than would Dianabol. The 4-chloro attachment used with this steroid also inhibits its ability to be aromatized. Therefore, OT is not going to present its user with unwanted estrogenic side effects like water retention, increased fat deposition, or gynecomastia. While Dianabol tends to produce puffiness and a little fat retention in its users, which hides muscle definition, the exact opposite effect usually happens with OT. OT tends to promote gain in lean tissue mass, accompanied by an increased look of density, hardness, and definition due to the intensified androgen to estrogen ratio. For bodybuilding purposes, this makes OT a great pre-contest or cutting steroid, not really a bulking agent of choice. Athletes in sports where speed tends to be a primary focus would also find favor in OT, obtaining a strong anabolic benefit without having to carry around any extra water or fat weight

Decreases HPTA function: No, the drug has been accredited with HPTA up-regulating effects. Arimidex is an anti-estrogen type drug. It is usually provided in 0.5 MG tabs. The drug works in a non-steroid form by inhibiting the aromatase enzyme which converts testosterone and other androgens into estrogen. This means that there is less estrogen to cause female pattern fat deposits, gyno, and water retention.

Haltestin is an oral c17-alfa-alkylated AAS that provided good strength gains and low-moderate anabolic qualities. This means that the drug alone failed to provide significant muscle mass gains. Obviously power lifters seeking improved strength while maintaining a certain body weight liked this drug. Bodybuilders used Haltestin to improve muscle hardness during the last 4-6 weeks of dieting before competition.

This was/is a very nasty but effective steroid that was removed from the market about 1987 or so. Not all that long ago it began showing up on the black market from Australia. Upon testing the 50-ml vials, it was discovered that it actually contained 31-mg/ml of Trenbolone acetate. Most Fina Jet now found is bogus. It contains either a testosterone ester, ground Finaplix pellets, or just oil. But the original has been discontinued.