Hormone Therapy – Arenis Medico https://arenismedico.eu Wed, 28 Sep 2022 11:25:05 +0000 es hourly 1 https://wordpress.org/?v=5.6.13 https://arenismedico.eu/wp-content/uploads/2021/02/favicons.png Hormone Therapy – Arenis Medico https://arenismedico.eu 32 32 Prognyl — 5.000IU HCG https://arenismedico.eu/product/prognyl-5-000iu-hcg/ Sun, 07 Feb 2021 12:26:54 +0000 https://arenismedico.eu/?post_type=product&p=75974 Prognyl (Human Chorionic Gonadotropin) is a prescription medication containing chorionic gonadotropin obtained from a natural origin. Chorionic gonadotropin is a polypeptide hormone normally found in the female body during the early months of pregnancy. It is synthesized in syncytiotrophoblast cells of the placenta, and is responsible for increasing the production of progesterone, a pregnancy-sustaining hormone. Prognyl (Human Chorionic Gonadotropin) is used by male athletes for its ability to increase endogenous testosterone production, generally during, or at the conclusion of, a steroid cycle, when natural hormone production has been interrupted.

Side effects

Common side effects associated with the administration of Prognyl (Human Chorionic Gonadotropin) include headache, irritability, restlessness, fatigue, depression, swelling, appareance of female breasts in men, pain in the area where you received the injection. Less common side effects include abdominal or stomach pain, bloating, decreased amount of urine, indigestions, nausea, vomiting, diarrhea, pelvic pain, shortness of breath, weight gain.

General Administration

Prognyl (Human Chorionic Gonadotropin) is generally given by intramuscular injection. Peak concentrations of chorionic gonadotropin occur approximately 6 hours after intramuscular injection, and 16 to 20 hours after subcutaneous injection.

Administration for men

Bodybuilders and athletes use Prognyl (Human Chorionic Gonadotropin) either on cycle, in an effort to maintain testicular integrity during steroid administration, or after a cycle, to help restore hormonal homeostasis more quickly. Both types of use are deemed effective when properly applied.

Post-Cycle

Prognyl (Human Chorionic Gonadotropin) is often used with other medications as part of an in- depth Post Cycle Therapy (PCT) program focused on restoring endogenous testosterone production more rapidly at the end of a steroid cycle. Protocols for the post-cycle use of Prognyl (Human Chorionic Gonadotropin) generally call for the administration of 2000-3000 Units every 2nd or 3rd day, taken for no longer than 2 or 3 weeks.

On-Cycle

Bodybuilders and athletes may also administer Prognyl (Human Chorionic Gonadotropin) throughout a steroid cycle, in an effort to avoid testicular atrophy and the resulting reduced ability to respond to LH stimulus. It is important to remember that the dosage needs to be carefully monitored with this type of use, as high levels of Prognyl (Human Chorionic Gonadotropin) may cause increased testicular aromatase expression (raising estrogen levels), and also desensitize the testes to LH. Current protocols for the use of Prognyl (Human Chorionic Gonadotropin) in this manner involve administering 250 IU subcutaneously every 3rd or 4th day throughout the length of the steroid cycle. Higher doses may be necessary for some individuals, but still no point should exceed 500 IU per injection.

Administration for women

Prognyl (Human Chorionic Gonadotropin) is not used by women for physique- or performance- enhancing purposes.]]> Prognyl (Human Chorionic Gonadotropin) is a prescription medication containing chorionic gonadotropin obtained from a natural origin. Chorionic gonadotropin is a polypeptide hormone normally found in the female body during the early months of pregnancy. It is synthesized in syncytiotrophoblast cells of the placenta, and is responsible for increasing the production of progesterone, a pregnancy-sustaining hormone. Prognyl (Human Chorionic Gonadotropin) is used by male athletes for its ability to increase endogenous testosterone production, generally during, or at the conclusion of, a steroid cycle, when natural hormone production has been interrupted.

Side effects

Common side effects associated with the administration of Prognyl (Human Chorionic Gonadotropin) include headache, irritability, restlessness, fatigue, depression, swelling, appareance of female breasts in men, pain in the area where you received the injection. Less common side effects include abdominal or stomach pain, bloating, decreased amount of urine, indigestions, nausea, vomiting, diarrhea, pelvic pain, shortness of breath, weight gain.

General Administration

Prognyl (Human Chorionic Gonadotropin) is generally given by intramuscular injection. Peak concentrations of chorionic gonadotropin occur approximately 6 hours after intramuscular injection, and 16 to 20 hours after subcutaneous injection.

Administration for men

Bodybuilders and athletes use Prognyl (Human Chorionic Gonadotropin) either on cycle, in an effort to maintain testicular integrity during steroid administration, or after a cycle, to help restore hormonal homeostasis more quickly. Both types of use are deemed effective when properly applied.

Post-Cycle

Prognyl (Human Chorionic Gonadotropin) is often used with other medications as part of an in- depth Post Cycle Therapy (PCT) program focused on restoring endogenous testosterone production more rapidly at the end of a steroid cycle. Protocols for the post-cycle use of Prognyl (Human Chorionic Gonadotropin) generally call for the administration of 2000-3000 Units every 2nd or 3rd day, taken for no longer than 2 or 3 weeks.

On-Cycle

Bodybuilders and athletes may also administer Prognyl (Human Chorionic Gonadotropin) throughout a steroid cycle, in an effort to avoid testicular atrophy and the resulting reduced ability to respond to LH stimulus. It is important to remember that the dosage needs to be carefully monitored with this type of use, as high levels of Prognyl (Human Chorionic Gonadotropin) may cause increased testicular aromatase expression (raising estrogen levels), and also desensitize the testes to LH. Current protocols for the use of Prognyl (Human Chorionic Gonadotropin) in this manner involve administering 250 IU subcutaneously every 3rd or 4th day throughout the length of the steroid cycle. Higher doses may be necessary for some individuals, but still no point should exceed 500 IU per injection.

Administration for women

Prognyl (Human Chorionic Gonadotropin) is not used by women for physique- or performance- enhancing purposes.]]> Primoten — 100mg Methenolone Enanthate https://arenismedico.eu/product/primoten-100mg-methenolone-enanthate/ Sun, 07 Feb 2021 12:24:05 +0000 https://arenismedico.eu/?post_type=product&p=75972 Primoten (Methenolone Enanthate) is an injectable steroid that exhibits moderately strong anabolic properties with very low androgenic properties.

Estrogenic Side Effects

Primoten (Methenolone Enanthate) is not aromatized by the body, and is not measurably estrogenic. Estrogen linked side effects should not be seen when administering this steroid. Primoten (Methenolone Enanthate) can cause side effects like development of gynecomastia, water retention and strong elevations in blood pressure but these are very rare.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still possible with this substance. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Primoten (Methenolone Enanthate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Primoten (Methenolone Enanthate) is likely to have a stronger negative effect on the hepatic management of cholesterol than testosterone or nandrolone due to its non-aromatizable nature, but a much weaker impact than c-17 alpha alkylated steroids. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 200 – 400 mg per week. The dosage schedule can be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. Primoten (Methenolone Enanthate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

When used for physique- or performance-enhancing purposes, women take much lower doses of Primoten (Methenolone Enanthate) than men, typically 50 – 100 mg per week.]]> Primoten (Methenolone Enanthate) is an injectable steroid that exhibits moderately strong anabolic properties with very low androgenic properties.

Estrogenic Side Effects

Primoten (Methenolone Enanthate) is not aromatized by the body, and is not measurably estrogenic. Estrogen linked side effects should not be seen when administering this steroid. Primoten (Methenolone Enanthate) can cause side effects like development of gynecomastia, water retention and strong elevations in blood pressure but these are very rare.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still possible with this substance. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Primoten (Methenolone Enanthate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Primoten (Methenolone Enanthate) is likely to have a stronger negative effect on the hepatic management of cholesterol than testosterone or nandrolone due to its non-aromatizable nature, but a much weaker impact than c-17 alpha alkylated steroids. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 200 – 400 mg per week. The dosage schedule can be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. Primoten (Methenolone Enanthate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

When used for physique- or performance-enhancing purposes, women take much lower doses of Primoten (Methenolone Enanthate) than men, typically 50 – 100 mg per week.]]> Provibolic — 25mg Mesterolone https://arenismedico.eu/product/provibolic-25mg-mesterolone/ Sun, 07 Feb 2021 12:17:58 +0000 https://arenismedico.eu/?post_type=product&p=75970 Provibolic (Mesterolone) is an oral anabolic steroid derived from dihydrotestosterone. Provibolic (Mesterolone) is highly favored by athletes for its ability to increase androgen levels when dieting or preparing for a contest, and as an anti-estrogen due to its intrinsic ability to antagonize the aromatase enzyme.

Estrogenic Side Effects

Provibolic (Mesterolone) is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as the drug is unlikely to induce gynecomastia, water retention, or other estrogen-related side effects.

Androgenic Side Effects

Provibolic (Mesterolone) is classified as an androgenic steroid. Androgenic side effects are common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Provibolic (Mesterolone) is not c17-alpha alkylated, and not known to produce hepatotoxic effects; liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Provibolic (Mesterolone) should not be used when cardiovascular risk factors preclude the use of other oral steroids. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Provibolic (Mesterolone) has a very weak suppressive effect on gonadotropins and serum testosterone. Studies show that when given in moderate doses (150 mg per day or less), significant suppression of testosterone levels does not occur. In studies with higher doses (300 mg per day and above), the agent strongly suppressed serum testosterone. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 50-150mg per day. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-12 weeks. Provibolic (Mesterolone) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

Provibolic (Mesterolone) is rarely used with women in clinical medicine. Provibolic (Mesterolone) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.  ]]> Provibolic (Mesterolone) is an oral anabolic steroid derived from dihydrotestosterone. Provibolic (Mesterolone) is highly favored by athletes for its ability to increase androgen levels when dieting or preparing for a contest, and as an anti-estrogen due to its intrinsic ability to antagonize the aromatase enzyme.

Estrogenic Side Effects

Provibolic (Mesterolone) is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as the drug is unlikely to induce gynecomastia, water retention, or other estrogen-related side effects.

Androgenic Side Effects

Provibolic (Mesterolone) is classified as an androgenic steroid. Androgenic side effects are common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Provibolic (Mesterolone) is not c17-alpha alkylated, and not known to produce hepatotoxic effects; liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Provibolic (Mesterolone) should not be used when cardiovascular risk factors preclude the use of other oral steroids. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Provibolic (Mesterolone) has a very weak suppressive effect on gonadotropins and serum testosterone. Studies show that when given in moderate doses (150 mg per day or less), significant suppression of testosterone levels does not occur. In studies with higher doses (300 mg per day and above), the agent strongly suppressed serum testosterone. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 50-150mg per day. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-12 weeks. Provibolic (Mesterolone) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

Provibolic (Mesterolone) is rarely used with women in clinical medicine. Provibolic (Mesterolone) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.  ]]> Winnybol — 50mg Stanozolol https://arenismedico.eu/product/winnybol-50mg-stanozolol/ Tue, 12 Jan 2021 21:06:17 +0000 https://arenismedico.eu/?post_type=product&p=535 Winnybol (Stanozol) is an injectable anabolic steroid derived from dihydrotestosterone. Winnybol (Stanozol) is highly favored by dieting bodybuilders and competitive athletes for its ability to promote muscle growth without water-retention.

Estrogenic Side Effects

Winnybol (Stanozolol) is not aromatized by the body, and is not measurably estrogenic. An anti- estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Winnybol (Stanozolol) is a c17-alpha alkylated compound. C17-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life-threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain. The use of a liver detoxification supplement is advised while taking any hepatotoxic anabolic/androgenic steroids. Relative hepatotoxicity increases as the dosage escalates, so hepatic dysfunction should still be a concern.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 100 – 150mg per week. The dosage schedule should be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. Winnybol (Stanozolol) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

It is most commonly used at a dosage of 35-50mg per week. The dosage schedule should be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 4-6 weeks. Although this compound is weakly androgenic, the risk of virilization symptoms cannot be completely excluded.
]]> Winnybol (Stanozol) is an injectable anabolic steroid derived from dihydrotestosterone. Winnybol (Stanozol) is highly favored by dieting bodybuilders and competitive athletes for its ability to promote muscle growth without water-retention.

Estrogenic Side Effects

Winnybol (Stanozolol) is not aromatized by the body, and is not measurably estrogenic. An anti- estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Winnybol (Stanozolol) is a c17-alpha alkylated compound. C17-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life-threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain. The use of a liver detoxification supplement is advised while taking any hepatotoxic anabolic/androgenic steroids. Relative hepatotoxicity increases as the dosage escalates, so hepatic dysfunction should still be a concern.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 100 – 150mg per week. The dosage schedule should be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. Winnybol (Stanozolol) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

It is most commonly used at a dosage of 35-50mg per week. The dosage schedule should be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 4-6 weeks. Although this compound is weakly androgenic, the risk of virilization symptoms cannot be completely excluded.
]]> Undebolic — 250mg Testosterone Undecanoate https://arenismedico.eu/product/undebolic-250mg-testosterone-undecanoate/ Tue, 12 Jan 2021 21:04:38 +0000 https://arenismedico.eu/?post_type=product&p=533 Undebolic (Testosterone Undecanoate) is an injectable steroid that exhibits strong anabolic and moderately androgenic properties.

Estrogenic Side Effects

Undebolic (Testosterone Undecanoate) is aromatized in the body to estradiol (estrogen). Elevated estrogen levels can cause side effects such as increased water retention, body fat gain, and gynecomastia. An anti-estrogen may be necessary to prevent estrogenic side effects. One may alternately use an aromatase inhibitor which more efficiently controls estrogen by preventing its synthesis.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Undebolic (Testosterone Undecanoate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession.

Administration for Men

For the treatment of low androgen levels, it is most commonly used at an initial dosage of 120 – 160 mg daily for 2-3 weeks. Based on the level of effect, a daily maintenance dosage of 40-120 mg is usually continued at this point. For bodybuilding purposes, it is most commonly used at a dosage of 240 – 480 mg per day. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-8 weeks or more in duration. Undebolic (Testosterone Undecanoate) should always be taken with meals, preferably containing a moderate fat content (20 grams) to maximize lymphatic absorption. The total daily dosage should be divided into a minimum of two applications, taken in the morning and evening. Undebolic (Testosterone Undecanoate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

Undebolic (Testosterone Undecanoate) is rarely used with women in clinical medicine. Undebolic (Testosterone Undecanoate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> Undebolic (Testosterone Undecanoate) is an injectable steroid that exhibits strong anabolic and moderately androgenic properties.

Estrogenic Side Effects

Undebolic (Testosterone Undecanoate) is aromatized in the body to estradiol (estrogen). Elevated estrogen levels can cause side effects such as increased water retention, body fat gain, and gynecomastia. An anti-estrogen may be necessary to prevent estrogenic side effects. One may alternately use an aromatase inhibitor which more efficiently controls estrogen by preventing its synthesis.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Undebolic (Testosterone Undecanoate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession.

Administration for Men

For the treatment of low androgen levels, it is most commonly used at an initial dosage of 120 – 160 mg daily for 2-3 weeks. Based on the level of effect, a daily maintenance dosage of 40-120 mg is usually continued at this point. For bodybuilding purposes, it is most commonly used at a dosage of 240 – 480 mg per day. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-8 weeks or more in duration. Undebolic (Testosterone Undecanoate) should always be taken with meals, preferably containing a moderate fat content (20 grams) to maximize lymphatic absorption. The total daily dosage should be divided into a minimum of two applications, taken in the morning and evening. Undebolic (Testosterone Undecanoate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

Undebolic (Testosterone Undecanoate) is rarely used with women in clinical medicine. Undebolic (Testosterone Undecanoate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> Turabolic — 10mg Turinabol https://arenismedico.eu/product/turabolic-10mg-turinabol/ Tue, 12 Jan 2021 21:03:05 +0000 https://arenismedico.eu/?post_type=product&p=531 Turabolic (Turinabol) is an anabolic steroid that is derived from testosterone.

Estrogenic Side Effects

Turabolic (Turinabol) is not aromatized by the body, and is not measurably estrogenic. An anti- estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Turabolic (Turinabol) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 15-40mg per day. The drug is administered for 3 consecutive weeks, followed by a break for 3 weeks. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-8weeks. For maximum utilization Turabolic (Turinabol) should be taken on an empty stomach. Turabolic (Turinabol) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

It is most commonly used at a dosage of 2.5-5mg per day. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-8weeks. For maximum utilization Turabolic (Turinabol) should be taken on an empty stomach.
]]> Turabolic (Turinabol) is an anabolic steroid that is derived from testosterone.

Estrogenic Side Effects

Turabolic (Turinabol) is not aromatized by the body, and is not measurably estrogenic. An anti- estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

Turabolic (Turinabol) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 15-40mg per day. The drug is administered for 3 consecutive weeks, followed by a break for 3 weeks. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-8weeks. For maximum utilization Turabolic (Turinabol) should be taken on an empty stomach. Turabolic (Turinabol) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

It is most commonly used at a dosage of 2.5-5mg per day. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 6-8weeks. For maximum utilization Turabolic (Turinabol) should be taken on an empty stomach.
]]> TrenE — 200mg Trenbolone Enanthate https://arenismedico.eu/product/trene-200mg-trenbolone-enanthate/ Tue, 12 Jan 2021 21:01:12 +0000 https://arenismedico.eu/?post_type=product&p=529 TrenE (Trenbolone Enanthate) is an injectable steroid that exhibits strong anabolic and androgenic properties TrenE (Trenbolone Enanthate) is highly favored by athlete for its capability of promoting strong gains in lean muscle mass, often with an accompanying increase in relative hardness and definition.

Estrogenic Side Effects

TrenE (Trenbolone Enanthate) is not aromatized by the body, and is not measurably estrogenic. This steroid displays significant binding affinity for the progesterone receptor.The side effects associated with progesterone including negative feedback inhibition of testosterone production, body fat gain and gynecomastia can occur. The use of an anti-estrogen is often sufficient to mitigate gynecomastia caused by progestational anabolic/androgenic steroids.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

TrenE (Trenbolone Enanthate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely. Although unlikely, hepatotoxicity cannot be completely excluded, especially with high doses.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession.

Administration for Men

It is most commonly used at a dosage of 150 – 300 mg per week. The dosage schedule can be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. TrenE (Trenbolone Enanthate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

TrenE (Trenbolone Enanthate) is rarely used with women in clinical medicine. TrenE (Trenbolone Enanthate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> TrenE (Trenbolone Enanthate) is an injectable steroid that exhibits strong anabolic and androgenic properties TrenE (Trenbolone Enanthate) is highly favored by athlete for its capability of promoting strong gains in lean muscle mass, often with an accompanying increase in relative hardness and definition.

Estrogenic Side Effects

TrenE (Trenbolone Enanthate) is not aromatized by the body, and is not measurably estrogenic. This steroid displays significant binding affinity for the progesterone receptor.The side effects associated with progesterone including negative feedback inhibition of testosterone production, body fat gain and gynecomastia can occur. The use of an anti-estrogen is often sufficient to mitigate gynecomastia caused by progestational anabolic/androgenic steroids.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

TrenE (Trenbolone Enanthate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely. Although unlikely, hepatotoxicity cannot be completely excluded, especially with high doses.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession.

Administration for Men

It is most commonly used at a dosage of 150 – 300 mg per week. The dosage schedule can be further divided to reduce the volume of each injection if necessary, perhaps administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. TrenE (Trenbolone Enanthate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

TrenE (Trenbolone Enanthate) is rarely used with women in clinical medicine. TrenE (Trenbolone Enanthate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> TrenA — 100mg Trenbolone Acetate https://arenismedico.eu/product/trena-100mg-trenbolone-acetate/ Tue, 12 Jan 2021 20:59:06 +0000 https://arenismedico.eu/?post_type=product&p=527 TrenA (Trenbolone Acetate) is an injectable non-estrogenic steroid derived from nandrolone. Trenbolone is highly favored by athlete for its ability to increase muscle hardness, definition, and raw strength, without unwanted water retention and fat mass gains.

Estrogenic Side Effects

TrenA (Trenbolone Acetate) is not aromatized by the body, and is not measurably estrogenic. This steroid displays significant binding affinity for the progesterone receptor. The side effects associated with progesterone including negative feedback inhibition of testosterone production, body fat gain and gynecomastia can occur. The use of an anti-estrogen is often sufficient to mitigate gynecomastia caused by progestational anabolic/androgenic steroids.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

TrenA (Trenbolone Acetate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely. Although unlikely, hepatotoxicity cannot be completely excluded, especially with high doses.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 100 – 300 mg per week. Due to the short-acting nature of acetate esters the total week’s dosage is to be be further divided to reduce the volume of each injection administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. TrenA (Trenbolone Acetate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

TrenA (Trenbolone Acetate) is rarely used with women in clinical medicine. TrenA (Trenbolone Acetate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> TrenA (Trenbolone Acetate) is an injectable non-estrogenic steroid derived from nandrolone. Trenbolone is highly favored by athlete for its ability to increase muscle hardness, definition, and raw strength, without unwanted water retention and fat mass gains.

Estrogenic Side Effects

TrenA (Trenbolone Acetate) is not aromatized by the body, and is not measurably estrogenic. This steroid displays significant binding affinity for the progesterone receptor. The side effects associated with progesterone including negative feedback inhibition of testosterone production, body fat gain and gynecomastia can occur. The use of an anti-estrogen is often sufficient to mitigate gynecomastia caused by progestational anabolic/androgenic steroids.

Androgenic Side Effects

Although classified as an anabolic steroid, androgenic side effects are still common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxicity Side Effects

TrenA (Trenbolone Acetate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely. Although unlikely, hepatotoxicity cannot be completely excluded, especially with high doses.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

It is most commonly used at a dosage of 100 – 300 mg per week. Due to the short-acting nature of acetate esters the total week’s dosage is to be be further divided to reduce the volume of each injection administering the drug two to three times per week. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. The positive effects of this drug become most apparent when it is used for longer cycles, usually lasting 8 weeks or more in duration. TrenA (Trenbolone Acetate) is a very versatile drug, and can be combined with a number of other agents depending on the desired result.

Administration for Women

TrenA (Trenbolone Acetate) is rarely used with women in clinical medicine. TrenA (Trenbolone Acetate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> Testop — 100mg Testosterone Propionate https://arenismedico.eu/product/testop-100mg-testosterone-propionate/ Tue, 12 Jan 2021 20:57:14 +0000 https://arenismedico.eu/?post_type=product&p=525 Testop (Testosterone Propionate) is an injectable form of the primary male androgen testosterone. The added propionate ester slows the rate in which testosterone is released from the injection site. Still, Testosterone Propionate is much faster-acting than other testosterone esters and therefore requires a much frequent dosing schedule.

Estrogenic Side Effects

Testop (Testosterone Propionate) is readily aromatized in the body to estradiol (estrogen). The aromatase (estrogen synthetase) enzyme is responsible for this metabolism of testosterone. Elevated estrogen levels can cause side effects such as increased water retention, body fat gain, and gynecomastia. Testop (Testosterone Propionate) is considered a moderately estrogenic steroid. An anti-estrogen may be necessary to prevent estrogenic side effects. One may alternately use an aromatase inhibitor which more efficiently controls estrogen by preventing its synthesis. Estrogenic side effects will occur in a dose-dependant manner, with higher doses (above normal therapeutic levels) more likely to require the concurrent use of an anti-estrogen or aromatase inhibitor.

Androgenic Side Effects

Testosterone is the primary male androgen, responsible for maintaining secondary male sexual characteristics. Elevated levels of testosterone are likely to produce androgenic side effects including oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids, especially with a strong androgen such as testosterone. These may include deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxic Side Effects

Testop (Testosterone Propionate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Testop (Testosterone Propionate) tends to have a much less dramatic impact on cardiovascular risk factors than synthetic steroids. This is due in part to its openness to metabolism by the liver, which allows it to have less effect on the hepatic management of cholesterol. The aromatization of testosterone to estradiol also helps to mitigate the negative effects of androgens on serum lipids. Due to the positive influence of estrogen on serum lipids, aromatase inhibitors are preferred for those concerned with cardiovascular health, as they offer a partial estrogenic effect in the liver. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

To treat androgen insufficiency, the recommended dosage is 25 – 50 mg two to three times per week. The usual dosage among male athletes is in the range of 50 – 100 mg per injection, given every second or third day. Testop (Testosterone propionate) is commonly used at a weekly cumulative dosage between 200 – 400 mg. This level is sufficient for most users to notice exceptional gains in muscle size and strength. Testop (Testosterone propionate) is usually incorporated into bulking phases of training, when added water retention will be of little consequence, the user more concerned with raw mass than definition. Testop (Testosterone propionate) is a very effective anabolic drug, and is often used alone with great benefit. However, it is ultimately very versatile, and can be combined with many other anabolic/androgenic steroids to tailor the desired effect.

Administration for Women

Testop (Testosterone propionate) is rarely used with women in clinical medicine. Testop (Testosterone propionate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> Testop (Testosterone Propionate) is an injectable form of the primary male androgen testosterone. The added propionate ester slows the rate in which testosterone is released from the injection site. Still, Testosterone Propionate is much faster-acting than other testosterone esters and therefore requires a much frequent dosing schedule.

Estrogenic Side Effects

Testop (Testosterone Propionate) is readily aromatized in the body to estradiol (estrogen). The aromatase (estrogen synthetase) enzyme is responsible for this metabolism of testosterone. Elevated estrogen levels can cause side effects such as increased water retention, body fat gain, and gynecomastia. Testop (Testosterone Propionate) is considered a moderately estrogenic steroid. An anti-estrogen may be necessary to prevent estrogenic side effects. One may alternately use an aromatase inhibitor which more efficiently controls estrogen by preventing its synthesis. Estrogenic side effects will occur in a dose-dependant manner, with higher doses (above normal therapeutic levels) more likely to require the concurrent use of an anti-estrogen or aromatase inhibitor.

Androgenic Side Effects

Testosterone is the primary male androgen, responsible for maintaining secondary male sexual characteristics. Elevated levels of testosterone are likely to produce androgenic side effects including oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids, especially with a strong androgen such as testosterone. These may include deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxic Side Effects

Testop (Testosterone Propionate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Testop (Testosterone Propionate) tends to have a much less dramatic impact on cardiovascular risk factors than synthetic steroids. This is due in part to its openness to metabolism by the liver, which allows it to have less effect on the hepatic management of cholesterol. The aromatization of testosterone to estradiol also helps to mitigate the negative effects of androgens on serum lipids. Due to the positive influence of estrogen on serum lipids, aromatase inhibitors are preferred for those concerned with cardiovascular health, as they offer a partial estrogenic effect in the liver. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

To treat androgen insufficiency, the recommended dosage is 25 – 50 mg two to three times per week. The usual dosage among male athletes is in the range of 50 – 100 mg per injection, given every second or third day. Testop (Testosterone propionate) is commonly used at a weekly cumulative dosage between 200 – 400 mg. This level is sufficient for most users to notice exceptional gains in muscle size and strength. Testop (Testosterone propionate) is usually incorporated into bulking phases of training, when added water retention will be of little consequence, the user more concerned with raw mass than definition. Testop (Testosterone propionate) is a very effective anabolic drug, and is often used alone with great benefit. However, it is ultimately very versatile, and can be combined with many other anabolic/androgenic steroids to tailor the desired effect.

Administration for Women

Testop (Testosterone propionate) is rarely used with women in clinical medicine. Testop (Testosterone propionate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> Testem — 250mg Testosterone Enanthate https://arenismedico.eu/product/testem-250mg-testosterone-enanthate/ Tue, 12 Jan 2021 20:55:40 +0000 https://arenismedico.eu/?post_type=product&p=523 Testem (Testosterone Enanthate) is a slow-acting injectable form of the androgen testosterone. Testosterone is the principle anabolic hormone in men, highly favored by athletes for its ability to promote strong increases in muscle mass and strength.

Estrogenic Side Effects

Testem (Testosterone Enanthate) is readily aromatized in the body to estradiol (estrogen). The aromatase (estrogen synthetase) enzyme is responsible for this metabolism of testosterone. Elevated estrogen levels can cause side effects such as increased water retention, body fat gain, and gynecomastia. Testem (Testosterone Enanthate) is considered a moderately estrogenic steroid. An anti-estrogen may be necessary to prevent estrogenic side effects. One may alternately use an aromatase inhibitor which more efficiently controls estrogen by preventing its synthesis. Estrogenic side effects will occur in a dose-dependant manner, with higher doses (above normal therapeutic levels) more likely to require the concurrent use of an anti-estrogen or aromatase inhibitor.

Androgenic Side Effects

Testosterone is the primary male androgen, responsible for maintaining secondary male sexual characteristics. Elevated levels of testosterone are likely to produce androgenic side effects including oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids, especially with a strong androgen such as testosterone. These may include deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxic Side Effects

Testem (Testosterone Enanthate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Testen (Testosterone Enanthate) tends to have a much less dramatic impact on cardiovascular risk factors than synthetic steroids. This is due in part to its openness to metabolism by the liver, which allows it to have less effect on the hepatic management of cholesterol. The aromatization of testosterone to estradiol also helps to mitigate the negative effects of androgens on serum lipids. Due to the positive influence of estrogen on serum lipids, aromatase inhibitors are preferred for those concerned with cardiovascular health, as they offer a partial estrogenic effect in the liver. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

To treat androgen insufficiency, the recommended dosage is 50 – 400 mg of Testen (Testosterone enanthate) every 2 to 4 weeks. Although active in the body for a longer time, Testen (testosterone enanthate) is usually injected on a weekly basis for muscle-building purposes. The usual dosage for physique- or performance- enhancing purposes is in the range of 200 – 600 mg per week, taken in cycles 6 to 12 weeks in length. This level is sufficient for most users to notice exceptional gains in muscle size and strength. Testem (testosterone enanthate) is usually incorporated into bulking phases of training, when added water retention will be of little consequence, the user more concerned with raw mass than definition. Testem (testosterone enanthate) is a very effective anabolic drug, and is often used alone with great benefit. However, it is ultimately very versatile, and can be combined with many other anabolic/androgenic steroids to tailor the desired effect.

Administration for Women

Testem (Testosterone Enanthate) is rarely used with women in clinical medicine. Testem (Testosterone Enanthate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
]]> Testem (Testosterone Enanthate) is a slow-acting injectable form of the androgen testosterone. Testosterone is the principle anabolic hormone in men, highly favored by athletes for its ability to promote strong increases in muscle mass and strength.

Estrogenic Side Effects

Testem (Testosterone Enanthate) is readily aromatized in the body to estradiol (estrogen). The aromatase (estrogen synthetase) enzyme is responsible for this metabolism of testosterone. Elevated estrogen levels can cause side effects such as increased water retention, body fat gain, and gynecomastia. Testem (Testosterone Enanthate) is considered a moderately estrogenic steroid. An anti-estrogen may be necessary to prevent estrogenic side effects. One may alternately use an aromatase inhibitor which more efficiently controls estrogen by preventing its synthesis. Estrogenic side effects will occur in a dose-dependant manner, with higher doses (above normal therapeutic levels) more likely to require the concurrent use of an anti-estrogen or aromatase inhibitor.

Androgenic Side Effects

Testosterone is the primary male androgen, responsible for maintaining secondary male sexual characteristics. Elevated levels of testosterone are likely to produce androgenic side effects including oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids, especially with a strong androgen such as testosterone. These may include deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Hepatotoxic Side Effects

Testem (Testosterone Enanthate) does not have hepatotoxic effects and therefore, liver toxicity is unlikely.

Cardiovascular Side Effects

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Testen (Testosterone Enanthate) tends to have a much less dramatic impact on cardiovascular risk factors than synthetic steroids. This is due in part to its openness to metabolism by the liver, which allows it to have less effect on the hepatic management of cholesterol. The aromatization of testosterone to estradiol also helps to mitigate the negative effects of androgens on serum lipids. Due to the positive influence of estrogen on serum lipids, aromatase inhibitors are preferred for those concerned with cardiovascular health, as they offer a partial estrogenic effect in the liver. To help reduce cardiovascular strain, it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active steroid administration. Supplementing with fish oils and a natural cholesterol/antioxidant formula is also recommended.

Testosterone Suppression

All anabolic/androgenic steroids are expected to suppress endogenous testosterone production. Testosterone is the primary male androgen, and offers strong negative feedback on endogenous testosterone production. Testosterone-based drugs will, likewise, have a strong effect on the hypothalamic regulation of natural steroid hormones. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration for Men

To treat androgen insufficiency, the recommended dosage is 50 – 400 mg of Testen (Testosterone enanthate) every 2 to 4 weeks. Although active in the body for a longer time, Testen (testosterone enanthate) is usually injected on a weekly basis for muscle-building purposes. The usual dosage for physique- or performance- enhancing purposes is in the range of 200 – 600 mg per week, taken in cycles 6 to 12 weeks in length. This level is sufficient for most users to notice exceptional gains in muscle size and strength. Testem (testosterone enanthate) is usually incorporated into bulking phases of training, when added water retention will be of little consequence, the user more concerned with raw mass than definition. Testem (testosterone enanthate) is a very effective anabolic drug, and is often used alone with great benefit. However, it is ultimately very versatile, and can be combined with many other anabolic/androgenic steroids to tailor the desired effect.

Administration for Women

Testem (Testosterone Enanthate) is rarely used with women in clinical medicine. Testem (Testosterone Enanthate) is not recommended for women for performance enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects.
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