Ultima-Gonadorelin 2mg-int

$14.97

Availability: In Stock

ACTIVE HALF-LIFE
?CLASSIFICATION
?DOSAGE
?ACNE
?WATER RETENTION
?HBR
?HEPATOTOXICITY
?AROMATIZATION

SKU: ULTIMA-AAS-5596 Categories: , , ,

Description

Products are shipping without brand label for security reasons.

Gonadorelin – is one of the hormones produced by the body. It increases the secretion of gonadotropins, which provokes an increase in testosterone levels. Today there are a lot syntactic gonadorelin analogues. They are actively used in sports and bodybuilding.

Gonadorelin peptide can surely be called an activator of the pituitary gland works. The production of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) is activated under the influence of this substance. These hormones affect the reproductive power of the human body. The luteinizing hormone is especially important for the athletes since it affects the testosterone level in the blood. Therefore Gonadorelin administration helps to increase the level of this component.

The effects of Gonadorelin use:

muscle growth;
increase of the testosterone level in blood;
improving the sexual life;
increase of endurance and strength.
great for PCT

Gonadorelin reviews show that during the course of the preparation the decrease of the body fluid is noticed. This is especially important during the cutting cycle and preparation for a competition for bodybuilders. Immediately after intake it reaches its maximal concentration within 30-40 minutes. Then it excreted through the kidneys and bladder.

Application and dosage of Gonadorelin

In order to prevent complications the peptide is administered in courses. The following scheme is acceptable: 100-200 mcg every four hours. Gonadorelin course lasts for four weeks and consists of 4 injection per day. Then the pause must be made in order to recover normal operation of organism?s own endocrine organs.

Side effects and contraindications

The course of the Gonadorelin may cause several side effects such as strong headache, alteration in bowel habits, allergic reactions, as well as local reactions in the form of congestion. In case of intake process violation there is a possibility of thrombosis.

Gonadorelin 2mg is hardly absorbed into the digestive tract that is why it is recommended to use the injectable form of the peptide. A linear intake of the preparation will cause the decrease of the pituitary gland function, which leads to the testosterone production stopping. That is why the experts recommend to buy Gonadorelin 2mg for the pulse administration, i.e. high dosage for 3-4 months followed by a break. During the break the work of the internal body organs is normalized and the organism starts to produce its own hormone again. It is also important to note that prolonged use of the peptide lowers organism?s sensibility to a preparation, significantly reducing its effectiveness.

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DescriptionACTIVE HALF-LIFE ?CLASSIFICATION ?DOSAGE ?ACNE ?WATER RETENTION ?HBR ?HEPATOTOXICITY ?AROMATIZATIONACTIVE HALF-LIFE 12-36 hours  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION No
ContentProducts are shipping without brand label for security reasons. Gonadorelin - is one of the hormones produced by the body. It increases the secretion of gonadotropins, which provokes an increase in testosterone levels. Today there are a lot syntactic gonadorelin analogues. They are actively used in sports and bodybuilding. Gonadorelin peptide can surely be called an activator of the pituitary gland works. The production of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) is activated under the influence of this substance. These hormones affect the reproductive power of the human body. The luteinizing hormone is especially important for the athletes since it affects the testosterone level in the blood. Therefore Gonadorelin administration helps to increase the level of this component. The effects of Gonadorelin use: muscle growth; increase of the testosterone level in blood; improving the sexual life; increase of endurance and strength. great for PCT Gonadorelin reviews show that during the course of the preparation the decrease of the body fluid is noticed. This is especially important during the cutting cycle and preparation for a competition for bodybuilders. Immediately after intake it reaches its maximal concentration within 30-40 minutes. Then it excreted through the kidneys and bladder. Application and dosage of Gonadorelin In order to prevent complications the peptide is administered in courses. The following scheme is acceptable: 100-200 mcg every four hours. Gonadorelin course lasts for four weeks and consists of 4 injection per day. Then the pause must be made in order to recover normal operation of organism?s own endocrine organs. Side effects and contraindications The course of the Gonadorelin may cause several side effects such as strong headache, alteration in bowel habits, allergic reactions, as well as local reactions in the form of congestion. In case of intake process violation there is a possibility of thrombosis. Gonadorelin 2mg is hardly absorbed into the digestive tract that is why it is recommended to use the injectable form of the peptide. A linear intake of the preparation will cause the decrease of the pituitary gland function, which leads to the testosterone production stopping. That is why the experts recommend to buy Gonadorelin 2mg for the pulse administration, i.e. high dosage for 3-4 months followed by a break. During the break the work of the internal body organs is normalized and the organism starts to produce its own hormone again. It is also important to note that prolonged use of the peptide lowers organism?s sensibility to a preparation, significantly reducing its effectiveness.Euro-HMG 75IU Injection or hMG for short is used to treat infertility in women. It is also known by the name of Menotropin. It is a hormonally active drug that stimulates the production of eggs in the ovaries in cases of women who suffer from ovarian failure. Euro-HMG 75IU Injection is extricated from the urine of postmenopausal females. The urine of a postmenopausal woman contains high levels of follicle stimulating hormone (FSH), lutropin hormone (LH) and also gonadotropins. Euro-HMG 75IU Injection is injected into the body through the muscle. Using Euro-HMG 75IU Injection may show these side effects; headaches, mood swings, weakness, weight gain, swelling in the area where the injection has been given, enlargement of the breasts and also breast tenderness. The other most common effect of using Euro-HMG 75IU Injection is pain in the abdominal area caused by ovarian hyperstimulation (OHSS). This happens when too many eggs are produced and the ovaries subsequently swell up. The other risk that may arise from taking these shots is that of conceiving twins in case you were not planning for it. Before taking this medication it is advised that you consult and inform your doctor if you have any of the conditions mentioned below: If your are allergic to menotropins or gonadotropins. If you suffer from vaginal bleeding. If you have a ovarian cyst. Dosage differs from person to person. It is generally fixed according to the individual requirement of each patient. Ideally, if you time your conception and try to have intercourse within 12 to 36 hours after Euro-HMG 75IU Injection has been given, chances of you becoming pregnant are higher. In case the first cycle therapy does not work then re-evaluate it. You should have second thoughts about taking Euro-HMG 75IU Injection and consult your doctor if ovulation does not occur even after three cycles of treatment.Insulin-like growth factor-1 (IGF-1) helps encourage normal bone and tissue growth and development and also has the ability to decrease blood glucose levels. IGF-1 advances to fat cells and therefore burns fat. Subsequently, it increases lean body mass and decreases fat. These effects are desired mostly by athletes and bodybuilders. Increased IGF-1 levels are also comparable to weight gain. This weight gain is a result of lean body mass growth, not fat production. IGF-1 is favored in the bodybuilding industry and for people who workout regularly. It helps enhance recovery time after workout and improves energy during the workout. IGF-1 injections are common for adults and children if they have a growth hormone deficiency. IGF-1 contains many necessary amino acids that can help children who are not developing at a standard rate and supplement adults that are deficient. Research has also shown that the anabolic effects of IGF-1 may reflect inhibited protein breakdown and stimulated protein synthesis in skeletal muscle and that this response may be caused by a direct effect of IGF-1 on muscle tissue, therefore assisting burns on the skin and other tissue abnormalities. Mechanism of Action IGF-1 is a hormone found naturally in human blood. Its primary function is to manage the effects of growth hormone in the body. Normal IGF-1 and growth hormone functions include tissue and bone growth. IGF-1 is formed in different tissues as a result of growth hormone in the blood. IGF-1 promotes systemic body growth, and has growth-stimulating effects on mostly every cell in the body, mainly bone, cartilage, skeletal muscle, liver, kidney, nerve, skin and lung cells. As well as the insulin-like effects, IGF-1 can also manage cellular DNA synthesis. Administration Mode of Administration: Subcutaneous injection to a fleshy part of the body, typically to the stomach or abdominal area. IGF-1 can also be administered intramuscularly. Before administering IGF-1, always be sure to use a clean and sterile syringe. Hold the IGF-1 vial upright and insert the syringe in the center of the cap. Draw the plunger until you have the correct amount (see ‘Dosage’ below) in the syringe and carefully remove it. Before administering the syringe, use alcohol to cleanse the area of skin. Pinch the skin around the area to be injected, leave about 2 cm on each side. Hold the syringe at a 90 degree angle to your skin and swiftly insert the syringe. Depress the plunger fully, until the syringe is empty, and carefully draw out. Dosage Dosage Amount: For lean muscle growth and fat loss 40 mcg - 50 mcg daily (men) 10 mcg - 20 mcg daily (women) IGF-1 should not be injected more than twice daily A typical dosage cycle of IGF-1 will continue for 2 to 12 weeks Children and adults who are prescribed IGF-1 for development deficiency should consult with a care provider about correct dosing. Side Effects The side effects of IGF-1 can be similar to those of other growth hormones. These include growth of excess body tissue, also known as acromegaly, and damage to the joints, liver, and heart. IGF-1 could possibly cause joint pain, muscle pain, headaches and nausea. IGF-1 can also decrease levels of blood glucose, resulting in hypoglycemia. Researchers also associate IGF-1 with an increased risk of developing some cancers, such as lung, breast, colorectal and prostate. Benefits Facilitation of protein synthesis in the body Regulation of stored fat and channeling it to be used for energy production, resulting in fat loss Promotion of positive effects on metabolism and increasing lean body mass and muscle growth Protection against autoimmune disease, heart disease and plaque buildup Aid development in young children and adults deficient in essential amino acids Improvement in blood sugar regulation Promotion of optimal health, wellness and fitness in usersIpamorelin is a pentapeptide and a ghrelin mimetic with growth hormone releasing activity. Ipamorelin imitates ghrelin and ties to the ghrelin receptor in the brain, thus selectively stimulating the release of growth hormone from the pituitary gland. Usage Growth hormones are frequently released and more abundant in children. When humans begin to age, the production of growth hormones decelerates and lessens gradually over time. The use of Ipamorelin can encourage these growth hormones to be created and released regularly. Ipamorelin is used to help increase growth hormone production, which can assist in the reduction of body fat, enhancement of lean muscle mass, improvement of sleep, and increase of energy and over all wellness. Ipamorelin is mostly used for collagen production, wrinkle reduction, acceleration of healing and recovery, and enhancement of mood and sleep; therefore being a peptide that is sought after for it’s anti-aging benefits. Mechanism of Action The function of Ipamorelin is to mimic ghrelin. The hormone ghrelin, discovered in 1999, has extreme effects on metabolism, restraining stored fat breakdown, and most importantly gherlin performs to regulate growth hormone release from the pituitary gland. Ipamorelin fastens to ghrelin receptors on the pituitary gland, activating them identically to the way ghrelin naturally would. The activation of these receptors work collectively with no effect on the rest of the body’s hormones. Administration Mode of Administration: Subcutaneous injection to a fleshy part of the body, typically to the stomach or abdominal area. Before administering Ipamorelin, always be sure to use a clean and sterile syringe. Hold the Ipamorelin vial upright and insert the syringe in the center of the cap. Draw the plunger until you have the correct amount (see ‘Dosage’ below) in the syringe and carefully remove it. Before administering the syringe, use alcohol to cleanse the area of skin. Pinch the skin around the area to be injected, leave about 2 cm on each side. Hold the syringe at a 90 degree angle to your skin and swiftly insert the syringe. Depress the plunger fully, until the syringe is empty, and carefully draw out. Dosage Dosage Amount: 100mcg - 500mcg (0.1mg to 0.5mg) Dosage Frequency: 1-3 times daily Recommended dose of 300mcg, 3 times daily (injection under the skin) for strength gain and performance enhancement Recommended dose of 200mcg, 1 time daily (injection under the skin) for anti-aging purposes For best results, it is recommended to administer Ipamorelin at the same time daily. Avoid consumption of food and liquids at least one hour before and after administering Ipamorelin. Expectations Ipamorelin typically takes time to show results. While some patients will notice significant changes in the body after the first month, the full-benefits are usually noticed after three to six months of administering the peptide daily. Ipamorelin is most successful with diet, exercise, consistency and time. Side Effects The most common reaction to Ipamorelin is redness and irritation around the injection site. This reaction is typically short term and normally goes away on its own. Ipamorelin is can also increase hunger and cause dry mouth in some patients. In less than 1% of patients that use Ipamorelin, other side effects have occurred, including: severe drowsiness, hives, vomiting, headache, nausea, difficulty swallowing, hyperactivity, chest tightness and pallor, distortion in perception of taste, and flushing of the skin. Benefits Anti-aging: collagen production and wrinkle reduction Increase of lean muscle mass and muscle growth Accelerated recovery time from exercising, weight lifting and physical activity Improvement in cellular repair and regeneration Increase of energy, the immune system and overall wellness Improvement in bone strength and bone mineral density composite Higher metabolic rate and improved circulation resulting in body fat reduction Improvement in sleep cycle, resulting in heightened mood and energyTesamorelin (Tesamorelin) is made with growth hormone-releasing factor (GRF). Tesamorelin is used to reduce excess fat around the stomach that is caused by taking certain HIV medications. This condition is also called lipodystrophy (LYE-poe-DIS-troe-fee). Tesamorelin is not a weight-loss medication and should not be used to treat obesity. Tesamorelin (Tesamorelin for injection) is indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy. Limitations of Use: Since the long-term cardiovascular safety and potential long-term cardiovascular benefit of Tesamorelin treatment have not been studied and are not known, careful consideration should be given whether to continue Tesamorelin treatment in patients who do not show a clear efficacy response as judged by the degree of reduction in visceral adipose tissue measured by waist circumference or CT scan. Tesamorelin is not indicated for weight loss management (weight neutral effect). There are no data to support improved compliance with anti-retroviral therapies in HIV-positive patients taking Tesamorelin. General Dosing Information The recommended dose of Tesamorelin is 2 mg injected subcutaneously once a day. The recommended injection site is the abdomen. Injection sites should be rotated to different areas of the abdomen. Do not inject into scar tissue, bruises or the navel. Reconstitution Procedure Tesamorelin must be reconstituted with the diluent provided with the product. Reconstitute the 2 mg vial of Tesamorelin with 2.1 mL of diluent. Mix by rolling the vial gently in your hands for 30 seconds. Do not shake. Detailed instructions for reconstituting Tesamorelin are provided in the INSTRUCTIONS FOR USE leaflet enclosed in the boxes containing Tesamorelin and diluent. Administer Tesamorelin immediately following reconstitution and throw away any unused Tesamorelin solution. If not used immediately, the reconstituted Tesamorelin solution should be discarded. Do not freeze or refrigerate the reconstituted Tesamorelin solution. Administration Reconstituted Tesamorelin solution should always be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Tesamorelin must be injected only if the solution is clear, colorless and without particulate matter. Tesamorelin should be injected subcutaneously into the skin on the abdomen. Injection sites should be rotated to different areas of the abdomen. Do not inject into scar tissue, bruises or the navel.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. The difference between CJC-1295 and CJC-1295 DAC is that CJC-1295 DAC version CJC-1295 with the addition of so-called. Drug Affinity Complex (DAC), which significantly prolong their effects and action. This means that the product will act in the body much longer than is usual in CJC-1295 (without DAC), namely up to 14 days. The main effects of CJC-1295 DAC enhances secretion of growth hormone in the blood; helps achieve significant muscle hardness; promotes muscle growth and strength; helps burn fat effectively; visibly improves skin quality, has a rejuvenating effect and smooths wrinkles; increases bone density; effectively strengthens ligaments and joints; has a significant positive effect on sleep, regeneration and vitality. CJC 1295 DAC Stack/Cycle In order to regenerate the various systems of the body, take CJC-1295 just before going to bed, once per day. In bodybuilding, for muscle building, a CJC-1295 injection is produced three times a day. The optimum dose is considered to be 300 mcg per day and it should be divided into three equal parts, to perform injections in the morning, afternoon and evening. In order to achieve a synergistic effect, in which substantially increases the release of growth hormone, it is practiced co-administration of CJC-1295 and GHRP-2 or GHRP-6. Duration of CJC-1295 cycle does not have any limitations. The drug is injected into the body via intramuscular or subcutaneous injection.
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