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Teslac
Teslac-
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Profiles >>
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Teslac belongs to
the group of sex hormones and from a biochemical
perspective, is a relative of the testosterones.
Although this catego-rizes it as an androgenic
steroid, from a technical point of view it is
neither an androgenic nor an anabolic steroid.
Teslac is very similar to the structure of
androgenic steroids but it has only a very low
androgenic and no anabolic effect. In school
medicine this compound is used in the treatment
of advanced mammary carcinomas in women. Before
you discard Teslac as a completely useless drug
and stop reading we want to tell you that Teslac
does have his justified application in
bodybuilding. Two reasons speak for an intake of
Teslac: First, it is the most effective
antiestrogen and second, it causes a distinct
increase of the endogenic (body's own)
testosterone produc-tion. Teslac is unique in
its effectiveness as an antiestrogen. Like
Proviron, it prevents the aromatizing process of
the steroids from the basis. Thus, Teslac
prevents almost completely the introduction of
more estrogens into the blood and subsequent
bonding with the estrogen receptors. Athletes
who want to be absolutely certain com-bine
Teslac with Proviron 50 mg/day and obtain a
complete sup-pression of the estrogens. What
makes Teslac different from Proviron, however,
and so desirable is the characteristic that it
can lead to an irreversible and permanent
suppression of the estrogens in male ath-letes.
Studies, in the meantime, have proven that
Teslac makes male athletes resistant to an
aromatization of steroids over a prolonged
period. A water retention caused by the
estrogens and gynecomastia is thus avoided in
the long term. Another advantage of Teslac is
that it directly influences the hypothalamus and
upon its "signal" the hypophysis
releases more gonadotropine, leading to a
significant increase of the endogenic
testosterone level. The strength of the
tes-tosterone-stimulating effect of Teslac can
be compared with the one of HCG (see also HCG).
Unlike HCG which after only a few-hours results
in an elevated plasmatestosterone level, Teslac
does require a longer initial period. Thus a
regular intake over several days is a
preliminary. Although we have initially
mentioned that Teslac does not have an anabolic
effect, based on the increased testosterone
level, a gain in muscles and strength can occur.
This could lead to androgenically-linked side
effects but they are very unlikely.
Side effects from Teslac are very rare. Since
this compound, above all, was developed for
women, it was extremely important to ex-clude
the androgenic effect component as much as
possible. This was successfully accomplished so
that females very rarely experi-ence
masculinizing symptoms such as, for example,
increased growth of body hair or deep voice.
Possible side effects from Teslac are given on
the package insert by the German manufacturer,
Bristol Arzneimittel GmbH, for the remedy
Fludestrin: "cutaneous erup-tions (maculopapular
erythema), high blood pressure, sensations such
as itching and pricking (paresthesia), pain in
the arms and legs and swelling, tongue
infection, loss of appetite, nausea and vomit-ing."
These side effects, as already mentioned, are
extremely rare. The plasma calcium level of
athletes should, however, be checked since
Teslac could lead to hypercalcemia (increased
calcium level).
Perhaps the greatest negative side effect of
Teslac is its high price. A package of fifty 50
mg tablets costs about $200 on the black mar-ket.
Every single tablet thus costs $4. The
recommended daily dose of 10-20 tablets - that
is 500-1000 mg/day! Usually 4-5 tablets daily
(200-250 mg/day) are sufficient. However even
such a dosage will discourage most athletes
because of the high cost. An alterna-tive would
be to limit the intake of Teslac to two tablets
per day and to supplement them with the
similarly effective Proviron (50 mg/ day).
| Substance:
Testolactone |
| Trade
Names: |
| Fludestrin |
100
mg/ml; |
Bristol
G |
| Fludestrin |
50
mg/ml; |
Bristol
G |
| Teslac |
50
mg tab.; |
Squibb
B, NL; Squibb Mark U.S.; Mead Johnson
U.S. |
|
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