GP Methan 10
GP Methan 10
Manufacturer: Geneza Pharmaceuticals
Active substance: Methandienone
Pack: 100 tabs (10 mg/tab)
Administration Route: Oral
Active Life: 6-8 hours
Drug Class: Anabolic/Androgenic Steroid (Oral)
Average Dose: Men 15-50 mg/day......Women 5-10 mg/day
Acne: Yes, especially in higher dosages
Water Retention: Yes, similar to testosterone
High Blood Pressure: Yes
Liver Toxic: Yes
Aromatization: Yes
DHT Conversion: No
Decrease HPTA function: Yes, dose and cycle length dependant
Methandrostenolone
is a derivative of testosterone, exhibiting strong anabolic and
moderate androgenic properties. This compound was first made available
in 1960, and it quickly became the most favored and widely used
anabolic steroid in all forms of athletics. This is likely due to the
fact that it is both easy to use and extremely effective. In the U.S.
Dianabol production had meteoric history, exploding for quite some
time, then quickly dropping out of sight. Many were nervous in the late
80's when the last of the U.S. generics were removed from pharmacy
shelves, the medical community finding no legitimate use for the drug
anymore. But the fact that Dianabol has been off the U.S. market for
over 10 years now has not cut its popularity. It remains the most
commonly used black market oral steroid in the U.S. As long as there
are countries manufacturing this steroid, it will probably remain so.
Similar to testosterone and Anadrol 50, Dianabol is a potent steroid,
but also one which brings about noticeable side effects. For starters
methandrostenolone is quite estrogenic. Gynecomastia is often a concern
during treatment, and may present itself quite early into a cycle
(particularly when higher doses are used). At the same time water
retention can become a pronounced problem, causing a notable loss of
muscle definition as both subcutaneous water and fat build. Sensitive
individuals may therefore want to keep the estrogen under control with
the addition of an anti-estrogen such as Nolvadex and/or Proviron. The
stronger drugs Arimidex, Femara, or Aromasin (antiaromatase) would be a
better choice if available.
In addition, androgenic side effects are common with this substance,
and may include bouts of oily skin, acne and body/facial hair growth.
Aggression may also be increased with a potent steroid such as this, so
it would be wise not to let your disposition change for the worse
during a cycle. With Dianabol there is also the possibility of
aggravating a male pattern baldness condition. Sensitive individuals
may therefore wish to avoid this drug and opt for a milder anabolic
such as Deca-Durabolin. While Dianabol does convert to a more potent
steroid via interaction with the 5-alpha reductase anzyme (the same
enzyme responsible for converting testosterone to dihydrotestosterone),
it has extremely little affinity to do so in the human body's. The
androgenic metabolite 5alpha dihydromethandrostenolone is therefore
produced only in trace amounts at best. Therefore the use of
Proscar/Propecia would serve no real purpose.
Being moderately androgenic, Dianabol is really only a popular steroid
with men. When used by women, strong virilization symptoms are of
course a possible result. Some do however experiment with it, and find
low doses (5mg) of this steroid extremely powerful for new muscle
growth. Whenever taken, Dianabol will produce exceptional mass and
strength gains. It's effectiveness is often compared to other strong
steroids like testosterone and Anadrol 50, and it is likewise a popular
choice for bulking purposes. A daily dosage of 20-40mg is enough to
give almost anybody dramatic results. Some do venture much higher in
dosage, but this practice usually leads to a more profound incidence of
side effects. It additionally combines well with a number of other
steroids. It is noted to mix particularly well with the mild anabolic
Deca-Durabolin. Together one can expect an exceptional muscle and
strength gains, with side effects not much worse than one would expect
from Dianabol alone. For all out mass, a long acting testosterone ester
like enanthate can be used. With the similarly high
estrogenic/androgenic properties of this androgen, side effects may be
extreme with such a combination however. Gains would be great as well,
which usually makes such an endeavor worthwhile to the user. As
discussed earlier, ancillary drugs can be added to reduce the side
effects associated with this kind of cycle.
In order to withstand oral administration, this compound is c17 alpha
alkylated. We know that this alteration protects the drug from being
deactivation by the liver (allowing nearly all of the drug entry into
the bloodstream), however it can also be toxic to this organ. Prolonged
exposure to c17 alpha alkylated substances can result in actual damage,
possibly even the development of certain kinds of cancer. To be safe
one might want to visit the doctor a couple of times during each cycle
to keep an eye on their liver enzyme values. Cycles should also be kept
short, usually less than 8 weeks long to avoid doing any noticeable
damage. Jaundice (bile duct obstruction) is usually the first visible
sign of liver trouble, and should be looked out for. This condition
produces an unusual yellowing of the skin, as the body has trouble
processing bilirubin. In addition to the skin, the whites of the eyes
may also yellow, a clear indicator of trouble. Should this occur the
drug should be discontinued immediately and a doctor visited. This is
usually a point where further, permanent damage can be avoided.
It is also interesting to note that methandrostenolone is structurally
identical to boldenone (EQ), except that it contains the added c17
alpha alkyl group discussed above. This fact makes clear the impact of
altering a steroid in such a way, as these two compounds appear to act
very differently in the body. The main dissimilarity seems to lie in
the tendency for estrogenic side effects, which seems to be much more
pronounced with Dianabol. Equipoise is known to be quite mild in this
way, and users therefore commonly take this drug without any need of an
anti-estrogen. Dianabol is much more estrogenic not because it is more
easily aromatized, as in fact the 17 alpha methyl group and c1-2 double
bond both slow the process of aromatization. The problem is that
methandrostenolone converts to l7alpha methylestradiol, a more
biologically active form of estrogen than regular estradiol. But
Dianabol also appears to be much more potent in terms of muscle mass
compared to boldenone, supporting the notion that estrogen does play an
important role in anabolism. In fact boldenone and methandrostenolone
differ so much in their potencies as anabolics that the two are rarely
though of as related. As a result, the use of Dianabol is typically
restricted to bulking phases of training while Equipoise is considered
an excellent cutting or lean-mass building steroid.
The half-life of Dianabol is only about 3 to 4 hours, a relatively
short time. This means that a single daily dosage schedule will produce
a varying blood level, with ups and downs throughout the day. The user
likewise has a choice, to either split up the tablets during the day or
to take them all at one time. The usual recommendation has been to
divide them and try to regulate the concentration in your blood. This
however, will produce a lower peak blood level than if the tablets were
taken all at once, so there may be a trade off with this option. The
steroid researcher Bill Roberts also points out that a single-episode
dosing schedule should have a less dramatic impact on the
hypothalamic-pituitary-testicular axis, as there is a sufficient period
each day where steroid hormone levels are not extremely exaggerated. I
tend to doubt hormonal stability can be maintained during such a cycle
however, but do notice that anecdotal evidence often still supports
single daily doses to be better for overall results. Perhaps this is
the better option. Since we know the blood concentration will peak
about 1.5 to 3 hours after administration, we may further wonder the
best time to take our tablets. It seems logical that taking the pills
earlier in the day, preferably some time before training, would be
optimal. This would allow a considerable number of daytime hours for an
androgen rich metabolism to heighten the uptake of nutrients,
especially the critical hours following training.
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