PHARMACOM BOLD 500
PHARMACOM BOLD 500(500MG/ML BOLDENONE UNDECYLENATE=10ML)
Active-Life: 7-9 days
Drug Class: Anabolic /Androgenic steroid (for injection)
Average Reported Dosage: Men 150-500mg weekly Women 50-150mg weekly
Water Retention: Low
High Blood Pressure: Rare
Aromatization: About 50% less than testosterone
Liver Toxic: None
Noted comments: High anabolic/moderate androgenic
DHT Conversion: Low
Decreases HPTA function: Moderately (Dose dependent)
Boldenone is available as a veterinary steroid under various trade names and was commonly refereed to as EQ by athletes polled. However, the quality is normally quite high due to its use in million dollar race horses. Boldenone was reported as one of the safest and most effective anabolic / androgenic injectable steroids used by both power lifters and bodybuilders. This drug brought slow but continuous muscle mass and strength gains over a prolonged period. Gains were mostly of a high quality lean mass nature and were maintained for several weeks after use was discontinued. Improved pumps and vascularity were normal are common attributes while low aromatization brought an improved hardness to users musculature.
Males normally reported a dosage range of 150-500mg weekly total, usually utilizing an every other day (EOD) injection schedule. Women made excellent progress with dosages of 50-150mg total weekly with a 1-2 injections weekly schedule. In this dose range, women seldom reported virilizing side effects. Most experienced an elevate libido (cool) with few other negative side effects reported. But in some cases, increased hair growth on face and legs were noted. This was usually due to higher dosages however and predominantly limited to existing hair (not new hair growth).
Due to Boldenone's reported "non-toxic to the liver" structure, most users experienced great gains with none or few negative side effects. The appetite and red blood cell production stimulating effects of Equipoise marked this drug as a standard for those who sought few negative side effects with quality muscle mass gains. Obviously with increased red blood cell count an increase in oxygen transport was also realized, as was improved nutrient transport.
Due to a double carbon bond between carbons one and two, boldenone experiences only slight DHT conversion by the 5-alfa-reductase enzyme and is fairly resistant to aromatization to estrogens.
Male athletes commonly stacked Boldenone with testosterone and/or Anadrol-50 for mass and strength cycles. Pre-contest cycles utilizing this drug often included Trenbolones, Winstrol, and anti-estrogens to create the ultra hard and vascular look.
*Personal experiences with Boldenone have resulted in very high quality lean tissue and freaky vascularity. This quite beneficial from a competitive appearance stand-point but long term use resulted in an unfavorable CBC result. I believe my error was in protocol length.
Boldenone (1,4-androstadiene-3-one-17β-ol, available as the undecylenate ester)is an anabolic steroid developed for veterinary use, mostly for treatment of horses. It is not indicated for use in humans in the US and is only available through veterinary clinics.
The activity of boldenone is mainly anabolic, with a low androgenic potency. It has a very long half-life, with minimal blood levels present up to 8 weeks after discontinued use.
Boldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys. The drug is commonly used in doping within bodybuilding. If intended to assist in bodybuilding, the drug is taken as part of a steroid stack of other anabolic steroids, usually with a potent androgen like testosterone as the 'base' of the stack.
Boldenone has a low rate of aromatization (about 50% of Testosterone), which means it does not convert to estrogen easily and does not cause very much water retention. Many Bodybuilders will find that it is a good replacement drug for Nandrolone.
It is a poor drug of choice for any athlete who will be subject to a blood test due to its long metabolic half-life. Trace amounts of the drug can easily be detected for months after discontinued use.