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CABERGOLINE (DOSTINEX) (25 MG/TAB. – 10 TAB)
(0)33,83 £SHORT DESCRIPTION
Cabergoline works by preventing the production of prolactin. Prolactin is key to a number of processes in the body, especially the female body. Generally, reducing its production can have several benefits.
Because it minimizes the production of prolactin, it helps to suppress the worst side effects of testosterone spiking substances like SARMs, making it a good PCT supplement, like Nolvadex or Clomid (both Selective Estrogen Receptor Modulators).
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ESSENTIALE FORTE (LIVER PROTECTION) (300 MG/CAPS – 30 CAPS)
(0)20,82 £Essentiale Forte (polyenylphosphatidylcholine or PPC, with or without synergistic vitamins) is a preparation of essential phospholipids. Essentiale normalizes the metabolism of lipids and proteins, improves the detoxification function of the liver, restores the cellular structure of the liver and retards the producing of conjunctive tissue. Essentiale medications are indicated for the treatment of fatty degeneration of the liver, hepatitis (including toxic hepatitis, liver damage caused by medicines or alcohol abuse), cirrhosis of the liver, and disturbances in liver function associated with different illnesses.
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ESSENTIALE FORTE (LIVER PROTECTION) (600 MG/CAPS – 30 CAPS)
(0)25,15 £Essentiale Forte (polyenylphosphatidylcholine or PPC, with or without synergistic vitamins) is a preparation of essential phospholipids. Essentiale normalizes the metabolism of lipids and proteins, improves the detoxification function of the liver, restores the cellular structure of the liver and retards the producing of conjunctive tissue. Essentiale medications are indicated for the treatment of fatty degeneration of the liver, hepatitis (including toxic hepatitis, liver damage caused by medicines or alcohol abuse), cirrhosis of the liver, and disturbances in liver function associated with different illnesses.
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HCG 1000 IU (1000IU/VIAL – 1 VIAL)
(0)17,34 £HCG 1000IU is a synthetic analogue of the naturally occurring human chorionic gonadotropin (hCG), which plays a key role by mimicking the hCG hormone found in the placenta during pregnancy.
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HCG 2000 IU (2000IU/VIAL – 1 VIAL)
(0)21,68 £HCG 2000IU represents a synthetic analogue of the naturally occurring Chorionic Gonadotropin Human peptide, pivotal in mimicking the hCG hormone found in the placenta during pregnancy.
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MESTEROLONE (PROVIRON) (25 MG/TAB. – 50 TABS)
(0)25,15 £Mesterolone 25 is used to treat potency disturbances, infertility, and declining physical and
mental M alertness in the aging male due to reduced androgen formation. It is an oral
androgen which does not aromatize estrogen. It does not stimulate the body to produce
testosterone but may act as an oral androgen substitute to compensate for a lack of the
natural male androgen. It is suitable för treatment of all conditions caused by deficient
endogenous androgen formation without impairment of spermato- genesis. It is effective as
an anti-aromatase in the body, preventing or slowing the conversion of androgens into
estrogens. Mesterolone 25 is well tolerated by the liver. -
PREGNYL (HUMAN CHORIONIC GONADOTROPIN) (5000 IU/VIAL – 1 VIAL)
(0)20,82 £Human chorionic gonadotropin (HCG), a polypeptide hormone produced by the human placenta, is composed of an alpha and a beta subunit. The alpha sub-unit is essentially identical to the alpha subunits of the human pituitary gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), as well as to the alpha subunit of human thyroid-stimulating hormone (TSH). The beta subunits of these hormones differ in amino acid sequence.
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TAMOXIFEN CITRATE (NOLVADEX) (20 MG/TAB. – 50 TABS)
(0)20,82 £Tamoxifen citrate 20 is a nonsteroidal agent that has demonstrated potent antiestrogenic
effects related to its ability to compete with estrogen for binding sites in target tissues.
Tamoxifen citrate is an oral anti- estrogen and estrogen antagonist which competes with
estrogen at the receptor sites reducing estrogenic expression. Tamoxifen citrate is a
Selective Estrogen Receptor Modular (SERM) acting via estrogen site competition as
opposed to Aromatase Inhibitor (Al) drugs which prevent aromatase derived estrogens from
being created.