SMALL DESCRIPTION
Initially Anastrozole was G created in an effort to combat breast cancer in post- menopausal
women. The drug is also used by bodybuilders / powerlifters. Anastrozole is a powerful
anti-estrogen medication, which belongs to the aromatase inhibitor (Al) family. Anastrozole is
not an anabolic steroid, but isole commonly used in conjunction with anabolic steroids to
combat related side-effects.
SHORT DESCRIPTION
Bacteriostatic Water for Injection, USP, is sterile, nonpyrogenic, distilled water for
intravenous administration after addition of a suitable solute. It may also be used as a
dispensing container for diluent use. No antimicrobial or other substance has been added.
The pH is 5.5 (5.0 to 7.0). The osmolarity is 0.
Boldenone Undecylenate 250 is an oily solution of boldenone undecylenate for IM injection.
Boldenone Undecylenate 250 is designed to release boldenone slowly from the injection
site. Boldenone serum levels will remain elevated for 5 to 8 days after administration.
Boldenone is an anabolic steroid possessing anabolic properties with moderate androgenic
activity. Anabolic and androgenic agents are widely used in the treatment of catabolic
processes where accelerated strength and muscular development are indicated.
SHORT DESCRIPTION
The drug is extensively distributed throughout the body. Cabergoline is moderately bound (40% to 42%) to human plasma proteins in a concentration-independent manner. Concomitant dosing of highly protein
bound drugs is unlikely to affect itsdisposition.
SHORT DESCRIPTION
CJC-1295 DAC, also known as growth hormone releasing factor (GRF MOD (1-29) or GRF),
is an analogue of GHRH (growth hormone releasing hormone). CJC-1295 is a GHRH (the
44- amino acid long version) with 15 aminos removed, thus a total of 29 amino acids, and
bound to DAC it is also called Drug Affinity Complex, and CJC-1295 is often referred to as
GHRH with Drug Affinity Complex, this essentially lengthens its life span. CJC-1295 DAC
stimulates HGH and its interaction with GHRH in the body produces a family of growth
hormones. No other peptides will not produce such a wide spectrum of growth hormones
such as CJC-1295. Unique characteristics of CJC- 1295 is a fact that can influence an
increase in the amount of secretory cells and pituitary growth hormone, which can produce.
SHORT DESCRIPTION
Clenbuterol is a therapeutic drug for asthma and Chronic obstructive pulmonary disease.
Also used as weight-loss drug. This drug has an active life of approximately 68 hours and
has a half life of about 36-39 hours. The chemical name of Clenbuterol (Clenbuterol
Hydrochloride) is 4-Amino- alpha-[(tert-butylamino) R methyl]-3, 5-dichlorobenzyl alcohol
Monohydrochloride and it has the molecular weight of 277.193 g/mol at the base.
Clenbuterol is featured by an oral bioavailability of 89 to 98 percent and can be detected in
semen or urine.
SHORT DESCRIPTION
Clomiphene citrate 50 is a non-steroidal fertility medicine. It causes the pituitary gland to
release hormones needed to stimulate ovulation (the release of an egg from the ovary).
Clomiphene citrate 50 is used to cause ovulation in women with certain medical conditions
(such as polycystic ovary syndrome) that prevent naturally occurring ovulation. Clomiphene
citrate 50 may also be used for purposes not listed in this medication guide.
Cut Stack is an injectable steroid that contains ob is testosterone propionate, trenbolone
acetate and drostanolone propionate. Testosterone propionate is designed to reach peak
testosterone serum levels within 24 hours of IM administration and remain elevated for 2 to 3
days. Testosterone propionate is suitable for the treatment of hypogonadism and other
disorders related to androgen deficiency. Testosterone Propionate has both anabolic and
androgenic effects. Testosterone supplementation has been demonstrated to increase
strength and growth of new muscle tissue, frequently with increases in libido. Trenbolone
Acetate is an anabolic steroid with significant anabolic and androgenic effects.
Drostanolone Enanthate 200 is a synthetic derivative of dihydrotestosterone, producing an
anabolic effect and promoting protein synthesis as well as creating positive nitrogen balance
in humans. Since it is a derivative of dihydrotestosterone, drostanolone does not aromatize
to estrogens. Drostanolone Enanthate 200 has significant anabolic and androgenic
properties promoting an increase in Te strength and growth of muscle tissue while acting as
an estrogen antagonist. The combination of a short-acting propionate ester with a longacting enanthate ester pro- duces rapid increases in serum drostanolone levels with a
Sustained duration of 5-8 days.
Drostanolone Propionate 100 is a synthetic derivative of dihydrotestosterone, producing an
anabolic effect and promoting protein synthesis as well as creating positive nitrogen balance
in humans. Since it is a derivative of dihydrotestosterone, drostanolone does not aromatize
to estrogens. Drostanolone Propionate 100 has significant anabolic and androgenic
properties promoting an increase in 2 strength and growth of muscle tissue while acting as
an estrogen antagonist. The combination of a short-acting propionate ester with a longacting enanthate ester pro- duces rapid increases in serum drostanolone levels with a
sustained duration of 5-8 days.
SHORT DESCRIPTION
Exemestane is a synthetic androgen analogue. It is a steroidal inhibitor of aromatase which
binds irreversibly to and inhibits the enzyme aromatase, thereby blocking the conversion of
cholesterol to pregnenolone and the peripheral aromatization of androgen precursors into
estrogens. Exemestane has been associated with a low rate of serum enzyme elevations
during therapy and rare instances of clinically apparent liver injury.
SHORT DESCRIPTION
Growth hormone releasing peptide-2 (GHRP-2) is a synthetic ghrelin analogue. Like ghrelin,
it stimulates release of endogenous growth hormone from somatotrophs in the anterior
pituitary; also like ghrelin, it is synergistic with endogenous growth hormone releasinghormone (GHRH) as well as with synthetic GHRH analogues such as Sermorelin or
GRF(1-29). Whereas GHRP-2 and other ghrelin analogues increase the number of
somatotrophs involved in the GH pulse by inhibiting somatostatin, GHRH increases the
pulse amplitude per pituitary cell or somatotroph by other means.