As with nearly all sympathomimetic stimulant based fat loss compounds (and most fat loss compounds in general), the Albuterol doses for the purpose of performance and physique enhancement are generally inflexible. Albuterol is utilized in much the same manner that Clenbuterol or Ephedrine is utilized. Albuterol doses and the protocols in which it is used is actually more similar to Ephedrine than it is to Clenbuterol, although Albuterol’s effects at the cellular level are identical as a beta-2 receptor adrenergic agonist. The manner in which Albuterol doses are administered is closer to Ephedrine in that the half-lives of both compounds are very similar (3 – 6 hours). However, the general manner of use of all stimulants for the purpose of fat loss is normally uniform in the following fashion: a peak dose is selected, which is the maximal daily dose that will be used during the cycle for fat loss. The first several days (normally spanning the first week or two) of use, the dose will be slowly ramped upwards until the final peak dose is achieved, after which the user will remain at the peak dose for the duration of use.
Finnea Albuterol
AUD90.00
Albuterol – 5mg/tab 50 tabs.
Related products
Finnea Anavar
50 Tabs of 25mg Oxandrolone
Anavar or Oxandrolone was first developed in 1964 by Searle Laboratories to combat and treat conditions like rapid weight loss and muscle wasting like many other anabolic steroids. Compared to other anabolic steroids, Anavar is considered to be the safest for use for both males and females and its used quite extensively by athletes.
Suggested Dosage: (men) 50-80mg a day, (women) 10-20mg per day
Finnea Proviron
50 tabs each tab 25mg Mesterolone
Proviron is also known as Provironum
Mesterolone is an orally active, 1-methylated DHT. Like Masteron, but then actually delivered in an oral fashion. DHT is the conversion product of testosterone at the 5-alpha-reductase enzyme, the result being a hormone that is 3 to 4 times as androgenic and is structurally incapable of forming estrogen. One would imagine then that mesterolone would be a perfect drug to enhance strength and add small but completely lean gains to the frame. Unfortunately there is a control mechanism for DHT in the human body. When levels get too high, the 3alpha hydroxysteroid dehydrogenase enzyme converts it to a mostly inactive compound known as 3-alpha (5-alpha-androstan-3alpha,17beta-diol), a prohormone if you will. It can equally convert back to DHT by way of the same enzyme when low levels of DHT are detected. But it means that unless one uses ridiculously high amounts, most of what is administered is quite useless at the height of the androgen receptor in muscle tissue and thus mesterolone is not particularly suited, if at all, to promote muscle hypertrophy.
Proviron has four distinct uses in the world of bodybuilding. The first being the result of its structure. It is 5-alpha reduced and not capable of forming estrogen, yet it nonetheless has a much higher affinity for the aromatase enzyme (which converts testosterone to estrogen) than testosterone does. That means in administering it with testosterone or another aromatizable compound, it prevents estrogen build-up because it binds to the aromatase enzyme very strongly, thereby preventing these steroids from interacting with it and forming estrogen. So Mesterolone use has the extreme benefit of reducing estrogenic side-effects and water retention noted with other steroids, and as such still help to provide mostly lean gains. Its also been suggested that it may actually downgrade the actual estrogen receptor making it doubly effective at reducing circulating estrogen levels.
