Rx Anabolics
120 itemsBELIGAS Pharmaceuticals
113 itemsLIVEWELL Pharmaceuticals
102 itemsUltima Pharmaceuticals
56 itemsBuy anabolics online - Best Steroids for sale
An extensive selection of anabolic steroids are available for purchase on the reliable website Rx Pharmaceutical Juice. They serve the demands of both fitness enthusiasts and professional athletes with their wide assortment of high-quality items. Rx Pharmaceutical Juice provides everything you need to improve your overall appearance, increase muscle mass, or improve performance.
The dedication of Rx Pharmaceutical Juice to provide genuine and safe products is what makes them unique. They get their steroids from reputable producers, so you know you're getting real, pharmaceutical-quality ingredients. Their discrete packaging and safe delivery techniques, which guarantee that your item reaches securely and without any problems, further demonstrate their commitment to quality. For those wishing to purchase anabolics online and safely and successfully reach their fitness objectives, Rx Pharmaceutical Juice is the go-to choice thanks to its user-friendly website, competitive pricing, and top-notch customer service.
Primo E 100mg
- Promotes nitrogen retention Enhances immune system Gain a lead and hard physique For bulking and mass gains Strength
Anavar
- Muscle gain Fat loss Strength-building Mild side effects Female-friendly Enhanced athletic performance Big pumps
Turinabol
- Increased muscularity Enhanced strength Fat loss No Estrogenic effects Weak Androgen
Deca Durabolin
- Muscular Size and Strength Well Tolerated Joint Anti-Inflammatory No Hepatotoxic Effects Long Esters
Anadrol
- Rapid weight gain Muscle-building Enhances strength Oral form Joint support Fat loss
Human Chorionic Gonadotropin (HCG)
- Burning of adipose tissue (fat) for energy Improved metabolic function Energy boost Confidence boost Hormone regulation Less hunger Preserve muscle integrity Whole-body weight loss Lower cholesterol
S4 (ANDARINE)�
- Andarine provides benefits in strengthening bones by improving bone density which is an advantage for weight lifting athletes where the musculoskeletal system needs to be of sufficient strength to support the growth in muscle mass you’re trying to ach
S4 (ANDARINE)�
- Andarine provides benefits in strengthening bones by improving bone density which is an advantage for weight lifting athletes where the musculoskeletal system needs to be of sufficient strength to support the growth in muscle mass you’re trying to ach
Human Chorionic Gonadotropin (HCG)
- Burning of adipose tissue (fat) for energy Improved metabolic function Energy boost Confidence boost Hormone regulation Less hunger Preserve muscle integrity Whole-body weight loss Lower cholesterol
Human Growth Hormone (HGH)
- Overall Health Brain Function Muscle Growth, Recovery Strength Control Stamina Fat Loss Joint Protection
Human Growth Hormone (HGH)
- Overall Health Brain Function Muscle Growth Recovery
SR9009 10 (Stenabolic)�
- Endurance and stamina Fat Loss Increase Lean Muscle Mass Inflammation Cholesterol
SR9009 10 (Stenabolic)�
- Endurance and stamina Fat Loss Increase Lean Muscle Mass Inflammation Cholesterol
MK677 10 (Ibutamoren)
- Muscle Mass Gains Bone Density Strength Recovery and Sleep Muscle Retention Skin and Nails
MK677 10 (Ibutamoren)
- Muscle Mass Gains Bone Density Strength Recovery and Sleep Muscle Retention Skin and Nails
LGD4033 10 (Ligandrol)�
- Muscle Building Muscle Repair Fat Loss Stamina, Endurance, Strength
LGD4033 10 (Ligandrol)�
- Muscle Building Muscle Repair Fat Loss Stamina, Endurance, Strength
MK2866 10 (Ostarine)
- Lean Muscle Gains Muscle Recovery Bones Joints Resolves Heart Issues
MK2866 10 (Ostarine)
- Lean Muscle Gains Muscle Recovery Bones Joints Resolves Heart Issues
GW501516 10 (Cardarine)�
- Exceptionally improved physical performance is where Cardarine shines. Without the anabolic activity of true SARMs and steroids, Cardarine is not a muscle growth compound. Instead it has found popularity with athletes wanting incredible improvements in perf
GW501516 10 (Cardarine)�
- Exceptionally improved physical performance is where Cardarine shines. Without the anabolic activity of true SARMs and steroids, Cardarine is not a muscle growth compound. Instead it has found popularity with athletes wanting incredible improvements in perf
Ultima-Accutane is a potent and widely used steroid medication that is primarily prescribed for the treatment of severe acne. It belongs to a class of drugs called retinoids, specifically isotretinoin. Ultima-Accutane is known for its effectiveness in reducing the production of sebum, an oily substance that can clog pores and lead to the formation of acne.
Here are some key characteristics and features of Ultima-Accutane steroids:
1. Mechanism of Action: Ultima-Accutane works by targeting and regulating the activity of sebaceous glands, which are responsible for producing sebum. It reduces the size of these glands and inhibits the production of sebum, ultimately leading to a significant reduction in acne breakouts.
2. Acne Treatment: Ultima-Accutane is typically prescribed for severe cases of acne, particularly when other treatments have failed. It is highly effective in treating nodular acne, cystic acne, and acne that is resistant to other medications. This steroid helps to clear existing acne lesions and prevents the formation of new ones.
3. Duration of Treatment: The duration of Ultima-Accutane treatment can vary depending on the severity of acne and individual response. Typically, a treatment course lasts for a period of 4 to 6 months. However, some individuals may require longer treatment durations to achieve optimal results.
4. Side Effects: While Ultima-Accutane can be highly effective, it is important to note that it may also have potential side effects. The most common side effects include dry skin, dry eyes, chapped lips, and joint/muscle pain. Additionally, Ultima-Accutane has been associated with more serious side effects such as psychiatric disorders, liver damage, and birth defects if taken during pregnancy. Therefore, it is crucial to use this medication under the guidance of a healthcare professional and follow all safety precautions.
5. Monitoring and Safety Measures: Due to its potential side effects, patients prescribed Ultima-Accutane are closely monitored throughout the treatment period. Regular visits to the healthcare provider are required to assess the patient's response, monitor any side effects, and ensure overall safety.
6. Contraindications: Ultima-Accutane is contraindicated in pregnant women or women planning to become pregnant, as it can cause severe birth defects. It is also not recommended for individuals with a history of liver disease, high blood lipid levels, depression, or hypersensitivity to retinoids.
7. Precautions: Patients taking Ultima-Accutane should avoid excessive sun exposure and use appropriate sun protection, as the medication can make the skin more sensitive to sunlight. Additionally, it is important to avoid the use of other medications that may interact with Ultima-Accutane, especially those containing vitamin A or retinoids.
In summary, Ultima-Accutane is a powerful steroid medication used for the treatment of severe acne. It effectively reduces sebum production, clears existing acne lesions, and prevents new breakouts. However, it should only be used under the guidance of a healthcare professional, as it can have potential side effects and requires careful monitoring throughout the treatment period.
ACTIVE HALF-LIFE
CLASSIFICATION Glycoprotein hormones, alpha polypeptide
DOSAGE 500-3000IU 1-3 times/week
ACNE Possible
WATER RETENTION No
HBR No
HEPATOTOXICITY No
AROMATIZATION No
MANUFACTURER RX Pharmaceuticals
SUBSTANCE Human Chorionic Gonadotropin
HCG 5000iu is an injectable drug that contains as active substance Human Chorionic Gonadotropin (hCG). This is a hormone produced during pregnancy that is made by the developing placenta after conception, and later by the placental component syncytiotrophoblast. One of the uses of hCG is to suppress hunger and trigger the human body’s use of fat for fuel. hCG is used also to cause ovulation and treat infertility in women and increase sperm count in men. bodybuilders use it in steroids cycles and in post-cycle therapy to lose gain and increase testosterone production.
HCG is utilized among bodybuilders and athletes at the end of an anabolic-androgenic steroid cycle to prevent the breakdown of muscle tissue. It is also important in restoring the testes to their normal abilities. Many times after a period of anabolic steroids usage the testes of an athlete may shrink. HCG is effective in returning them to normal size. When used along with a very low-calorie diet, athletes burn off that extra fat over their muscle mass. Females may also use HCG with a very low-calorie diet to burn off unnecessary fat.
The average dosage of HCG during a cycle is between 500iu to 3000iu every week (1-3 times per week). If the injection is taken more frequently the blood level of the athlete is more stable while taking it in one shot may increase the estrogen levels caused by the aromatization of normal Testosterone and result in gynecomastia. There are sources showing that some bodybuilders used 6000iu for 6 days, but this is a risky affair and depends on the individual features of men. As post cycle therapy HCG should be used in smaller doses, about 250 – 500iu every day for 2 or 3 weeks. Smaller doses are enough to begin the reversal process of testicular atrophy. When starting a cycle of hCG, bodybuilders must follow it for a 2 to 3-week range with a least one month off in between and follow this course with no concern. HCG can be used with Clomid or Nolvadex in the PCT and continue using them after HCG is no longer part of the cycle. It is also recommended to start an hCG cycle near the end of a normal steroids cycle, most effective in the last week.
The most serious side effects that may occur while using HCG are severe pelvic pain, swelling of the hands or legs, stomach pain and swelling, shortness of breath, weight gain, diarrhea, nausea, or vomiting. Other common side effects of HCG are headache, feeling restless or irritable, mild swelling or water weight gain, depression, breast tenderness or swelling; or pain, swelling, or irritation where the injection is given. The medicine can cause early signs of puberty among boys, such as a deepened voice, pubic hair growth, and increased acne or sweating.
Hexarelin is a synthetic growth hormone-releasing peptide (GHRP) that belongs to the class of peptides known as growth hormone secretagogues. It is a hexapeptide consisting of six amino acids and is primarily used in research and medical settings.
Hexarelin works by stimulating the release of growth hormone (GH) from the pituitary gland in the brain. It does this by binding to the ghrelin receptor, which is present in various tissues throughout the body. Activation of this receptor triggers a cascade of signaling pathways that ultimately leads to the release of growth hormone.
One of the main advantages of hexarelin is its ability to selectively stimulate the release of GH without affecting other hormones. This specificity makes it a valuable tool in scientific research and clinical studies aiming to understand the role of growth hormone in various physiological processes.
Hexarelin has shown potential therapeutic applications in the areas of growth disorders, muscle wasting conditions, and age-related decline in growth hormone levels. It has been studied for its ability to promote muscle growth, enhance strength and endurance, and improve overall body composition.
Furthermore, hexarelin has been investigated for its potential neuroprotective effects. Studies suggest that it may have a positive impact on brain health and cognitive function. It has also been explored for its potential role in wound healing and tissue repair.
In terms of administration, hexarelin is typically given via subcutaneous or intravenous injection. The dosage and frequency of administration may vary depending on the specific research or clinical application.
It is important to note that hexarelin is still in the experimental stage and is not approved for use in humans. Its use is primarily limited to scientific research, and any potential therapeutic applications should be further validated through rigorous clinical trials.
As with any peptide or medication, hexarelin may have side effects, including but not limited to increased appetite, water retention, and potential effects on cortisol and prolactin levels. It is crucial to consult with a qualified healthcare professional or researcher before using hexarelin or any other peptide for experimental or therapeutic purposes.
Boldenone Undecylenate, also known by its trade name Equipoise, is a synthetic anabolic androgenic steroid (AAS) that has gained popularity among athletes and bodybuilders for its various benefits. It was originally developed for veterinary use, specifically for the treatment of horses, but it has since found its way into the world of human performance enhancement.
Boldenone Undecylenate belongs to the family of testosterone-derived AAS, and its chemical structure is derived from testosterone by adding a double bond between carbon atoms 1 and 2 of the steroid backbone. This modification enhances its anabolic properties while reducing its androgenic effects, making it a favorable choice for many users.
One of the primary reasons why Boldenone Undecylenate is highly regarded is its ability to promote lean muscle mass growth. It stimulates protein synthesis within the muscle cells, leading to an increase in muscle size and strength. This effect is accompanied by a significant improvement in nitrogen retention, which further aids in muscle growth. Users often report experiencing lean muscle gains that are more sustainable compared to other steroids.
Another noteworthy characteristic of Boldenone Undecylenate is its relatively slow but steady release into the bloodstream. This is due to the undecylenate ester attached to the parent compound, which allows for a prolonged action. As a result, users typically require fewer injections, making it a convenient choice for those who prefer less frequent dosing.
One of the unique qualities of Boldenone Undecylenate is its ability to increase red blood cell production, a process known as erythropoiesis. This results in improved oxygen-carrying capacity and enhanced endurance. Athletes who engage in endurance-based sports often appreciate this effect as it allows for longer and more intense training sessions without experiencing fatigue.
In addition to its anabolic and erythropoietic properties, Boldenone Undecylenate also exhibits a mild androgenic activity. This means that it can promote masculine characteristics such as increased facial and body hair growth, deepening of the voice, and improved libido. However, the androgenic effects are generally milder compared to other AAS, making it a popular choice for female athletes and bodybuilders.
When it comes to dosing, the recommended range for Boldenone Undecylenate is typically between 200 to 600 mg per week. However, some experienced users may opt for higher doses, although this increases the risk of potential side effects. The compound has a long half-life, estimated to be around 14 days, which contributes to its sustained action in the body.
As with any AAS, the use of Boldenone Undecylenate carries the risk of side effects. These can include acne, oily skin, increased aggression, mood swings, and potential suppression of natural testosterone production. It is important to note that individual response to the compound may vary, and some users may be more susceptible to certain side effects than others.
To mitigate the potential side effects and optimize the benefits of Boldenone Undecylenate, it is crucial to follow appropriate cycling protocols and engage in post-cycle therapy (PCT). This involves the use of medications and strategies to restore natural testosterone production and minimize the risk of hormonal imbalances.
In conclusion, Boldenone Undecylenate is a versatile and popular synthetic AAS that offers numerous benefits to athletes and bodybuilders. Its ability to promote lean muscle mass growth, enhance endurance, and exhibit mild androgenic properties make it an attractive choice for many users. However, it is important to approach its use with caution, adhere to recommended dosing guidelines, and prioritize post-cycle therapy to ensure optimal results and minimize potential side effects.
The recent boom in biotechnology has opened the door for studying new biologically-active compounds, including “cognitive enhancers” or “nootropics.”
One such compound is Selank — previously known as “TP-7” — which belongs to a class of molecules called synthetic peptides, or small artificially-designed proteins.
Selank has been touted as an “anti-anxiety” compound, and has also been claimed to improve learning and increase energy — supposedly without side-effects or the risk of addiction.
Selank is small and only a fraction of the size of most naturally-occurring proteins. It was developed at the Institute of Molecular Genetics (Russian Academy of Sciences) in cooperation with the V.V. Zakusov Research Institute of Pharmacology (Russian Academy of Medical Sciences), along with its “cousin” drug, Semax.
Selank was derived by combining the sequence of a peptide called tuftsin with another sequence that improves its molecular stability. Tuftsin is naturally-occurring, and makes up one part of the natural antibody IgG.
Both tuftsin and Selank have been reported to reduce anxiety and increased serotonin levels in rats, with Selank being slightly more effective.
Selank has been approved in Russia for the treatment of generalized anxiety disorder (GAD) and for its use as a nootropic. However, the FDA has not approved its use for any conditions. Nonetheless, Selank continues to be available in several countries, where it is often sold as a “nutritional supplement.”
Selank Mechanism of Action
Although the mechanisms behind Selank are not yet fully known for certain, Selank is believed to act in part by stabilizing enkephalins in the blood. Enkephalins are natural peptides in the body that are believed to counteract the stress response.
However, one animal study in mice did not demonstrate the stabilization of enkephalins following dosing with Selank, and the treated mice also did not appear to benefit from any significant “anti-anxiety” effects.
According to some cell studies, Selank may bind to GABA receptors. By extensions, most compounds that bind to GABA receptors generally cause “sedative” effects. In one study of mice treated with Selank, researchers reported increased activity in inhibitory neurons, which rely on GABA. This resulted in less overall brain activity, which is generally consistent with a sedative effect.
In addition, some researchers have reported an increase in BDNF, an important brain-growth compound (neurotropic factor) which has been implicated in learning and memory. Some researchers have suggested that this mechanism may be responsible for some of Selank’s claimed cognitive effects.
Selank has also been reported to influence the levels of the neurotransmitters norepinephrine, dopamine, and serotonin in mice. These neurotransmitters are widely believed to be involved in motivation, focus, and pleasure.
However, according to one animal study in mice, Selank was reported to increase norepinephrine, but reportedly decreased dopamine and serotonin levels. In contrast, in some other treated mice, Selank was reported to increase norepinephrine and dopamine levels, and did not change serotonin. Therefore, its exact effects and mechanisms remain unclear.
Possibly Effective for:
Anxiety
According to one preliminary clinical trial on 62 people, those given Selank reported fewer anxiety symptoms, with a greater decrease being observed in those suffering from pre-existing anxiety disorders.
In another trial, similar benefits were reported in 60 patients suffering from anxiety and phobias, with these effects lasting up to a week after the final dose.
Additionally, in one study of 70 anxiety patients, Selank was reported to increase the effects of phenazepam (an anti-anxiety drug banned in some U.S. states for its recreational use), while also reportedly reducing its rates of negative side-effects (such as drowsiness and memory loss).
In one animal study, Selank was reported to reduce anxiety in mice. The more anxious the mice were to begin with, the more significant the observed changes in their behavior after treatment.
Additionally, Selank was reported to show “anti-anxiety” effects in one study of rats who received 4 weeks of daily treatment.
Although limited, some of the above evidence suggests that Selank may potentially help curb anxiety, although much more research will still be needed to confirm its effectiveness and safety in human users. If you suffer from anxiety, you could have a discussion with your doctor about whether taking Selank might help you — however, always remember that you should never take this supplement in place of what your doctor recommends or prescribes.
Memory
Selank was reported to stabilize memory traces (i.e. potentially improve memory storage) in rats during one 30-day trial. However, it is unclear how these measurements were performed, as memory traces are not detectable as discrete locations in the brain.
One other animal study has reported that Selank may also preserve memory in monkeys.
However, appropriate human studies are lacking, and remains unknown what effects — if any — Selank might have in healthy human users. It is also unclear whether or not this compound would be safe for such users to take (either in the short- or long-term), and so caution would be advised until much more additional research is performed.
Brain Damage Recovery
In one study, researchers gave Selank supplements to rats with toxin-induced brain damage. This drug reportedly restored their brain activity to normal levels.
Depression
Selank has been reported to decrease depression symptoms (immobility during a forced swimming test) in mice. Curiously, it was reported to be more effective at relatively lower rather than higher doses.
Antioxidant Activity in the Liver
In one preliminary animal study, injection of Selank was reported to increase the levels of antioxidants in the livers of stressed mice.
Blood Flow
In one animal study of sedated cats, Selank was reported to decrease blood pressure by about 30% for up to 3 minutes.
It also increased blood flow to the cats’ brain by about 24% for up to 10 minutes [30].
While these preliminary findings are interesting in that they suggest that Selank may have some short-term cardiovascular effects on blood flow, the relatively short durations of these effects is hard to interpret, and may suggest that these effects are not strong or medically significant.
Additionally, these were only observed in animals, and so whether these effects would be similar in healthy human users remains unclear.
Alcohol Withdrawal
Anxiety is one of the more common symptoms involved in alcohol withdrawal. To mimic high alcohol intake, rats were given a 10% solution of ethanol (alcohol) as their sole drinking source for 24 weeks. Selank reportedly decreased the anxiety of these rats after a 48-hour alcohol withdrawal period.
Preventing Weight Gain and Reducing Cholesterol
According to one animal study, rats who were fed a high-fat diet reportedly showed 35% less weight gain when treated with Selank. Additionally, total cholesterol levels for these rats were reportedly reduced by over 58%, and blood glucose levels were reduced by 23.5%.
Cancer
In one animal study, mice with breast cancer were treated with daily doses of Selank and had slower tumor growth. Also, these mice reportedly lived longer than their untreated counterparts.
However, this preliminary finding doesn’t mean that Selank has any value in anticancer therapy. Much more research would be needed to verify and extend these early findings into legitimate medical treatments for cancer. Do not under any circumstances attempt to replace conventional cancer therapies with Selank (or any other supplements)!
Inflammation in the Spleen
After treatment with Selank, the spleens of mice were reported to show increased levels of several inflammatory response genes, which may suggest some degree of protection against the harmful effects of inflammation.
Ulcers
Selank has been reported to reduce the size (area) of stomach ulcers in animal models.
Some researchers have speculated that this may be because this drug increases the flow of lymph — an important component of the immune system — to the stomach.
Nonetheless, much more research in humans would be needed to confirm this effect, as well as its potential mechanisms.
Immune Function
Selank reportedly increased IL-6 in blood cells collected from patients suffering from depression. IL-6 is an inflammatory protein that is believed to help fight off infections.
Additionally, according to one cell-based study, Selank was reported to stimulate the release of interferons, which are anti-viral molecules.
Selank has also been proposed to potentially protect cells against some viral infections. However, one animal study in mice infected with a virus did not report any anti-viral benefits from Selank treatment, which casts doubt on this potential use.
Title: Tamoxifen: A Comprehensive Guide to Usage, Mechanism, and Side Effects
Introduction:
Tamoxifen is a medication that has been widely used for the treatment of breast cancer for several decades. It is an important drug in the field of oncology and has played a crucial role in improving the survival rates and quality of life for many patients. This article aims to provide a detailed description of Tamoxifen, including its usage, mechanism of action, and potential side effects.
Usage:
Tamoxifen is primarily used for the treatment of hormone receptor-positive breast cancer, both in pre-menopausal and post-menopausal women. It can be administered as an adjuvant therapy after surgery, radiation, or chemotherapy, or as a first-line treatment for advanced or metastatic breast cancer. Furthermore, Tamoxifen has proven effective in reducing the risk of breast cancer in high-risk individuals, such as those with a family history of the disease or certain genetic mutations.
Mechanism of Action:
Tamoxifen exerts its effects by acting as a selective estrogen receptor modulator (SERM). It competes with estrogen for binding to estrogen receptors in breast tissue, effectively blocking the estrogen signaling pathway. This inhibitory action prevents the growth and proliferation of hormone receptor-positive breast cancer cells, ultimately leading to tumor regression. Additionally, Tamoxifen has been shown to enhance the production of certain proteins that inhibit cell growth and promote cell death, further contributing to its anti-cancer effects.
Side Effects:
While Tamoxifen is generally well-tolerated, it is important to be aware of its potential side effects. The most common side effects include hot flashes, vaginal dryness, and irregular menstrual periods in pre-menopausal women. Post-menopausal women may experience menopausal symptoms such as night sweats and mood swings. These side effects are usually mild and can be managed with symptomatic treatment or hormone replacement therapy if necessary.
Tamoxifen may also have an impact on bone health, as it can reduce bone mineral density and increase the risk of osteoporosis. Regular bone density assessments and appropriate interventions, such as calcium and vitamin D supplementation, are important for minimizing this risk. Additionally, Tamoxifen has been associated with a slightly increased risk of blood clots, which can manifest as deep vein thrombosis or pulmonary embolism. Patients on Tamoxifen should be educated about the signs and symptoms of blood clots and seek immediate medical attention if they occur.
Another important consideration is Tamoxifen's potential effect on the endometrium. It has been associated with a slightly increased risk of endometrial cancer, although this risk is outweighed by the drug's benefits in treating breast cancer. Regular gynecological examinations and monitoring for any signs of abnormal vaginal bleeding are crucial for early detection and management of endometrial changes.
It is worth noting that Tamoxifen may interact with certain medications, including selective serotonin reuptake inhibitors (SSRIs) and aromatase inhibitors. Therefore, it is important for patients to inform their healthcare providers about any other medications they are taking to avoid potential drug interactions.
Conclusion:
Tamoxifen is a vital medication in the treatment of hormone receptor-positive breast cancer. Its ability to modulate estrogen receptor signaling has been instrumental in improving outcomes for patients. While Tamoxifen is generally well-tolerated, it is essential for patients and healthcare providers to be aware of its potential side effects and take appropriate measures to minimize risks. Overall, Tamoxifen's benefits in treating breast cancer far outweigh its potential risks, making it an indispensable tool in the fight against this disease.
ACTIVE HALF-LIFE 16 hours
CLASSIFICATION Anabolic Steroid
DOSAGE 20-40 mg/day
ACNE Yes
WATER RETENTION Low
HBR Perhaps
HEPATOTOXICITY Yes
AROMATIZATION No
MANUFACTURER RX Pharmaceuticals
SUBSTANCE Chlorodehydro Methyltest
Oral Turinabol is somewhat of a unique anabolic steroid. Specifically, Oral Turinabol is a cross between Methandrostenolone and Clostebol. This provides a steroid with powerful anabolic action while at the same time minimizing androgenic characteristics. Oral Turinabol also carries somewhat of an interesting history behind it. Oral Turinabol was first released by Jenapharm out of East Germany in 1962. The steroid would enjoy a very high safety rating for decades not only among men but in women and even children in a therapeutic setting. This steroid was proven to be very effective in the effort to build or protect lean mass and bone mass without severe complications. However, Oral Turinabol would gain worldwide attention in the 1990’s when the East German steroid scandal became public knowledge. From 1974 to 1989 what would be known as the East German Doping Machine had been successful in administering anabolic steroids to its Olympic athletes. Not only were they cheating but they were getting away with it as steroids like Oral Turinabol were, at the time, undetectable. State Plan Research Theme 14.25 as it was officially known would also make use of epitestosterone during this period in order to skew testosterone readings in drug testing. When Oral Turinabol was discovered as being an integral part of the East German scandal Jenapharm would discontinue the product in 1994. Two years later the pharmaceutical powerhouse out of Germany Schering, makers of such steroids as Primobolan, Testoviron and Proviron would acquire Jenapharm but chose not to bring Oral Turinabol back to the market. Since that time this anabolic steroid has never been manufactured by a true pharmaceutical compounding entity and has become a strictly black market underground anabolic steroid.
Oral Turinabol Functions & Traits: Oral Turinabol, officially known as 4-chlorodehydromethyltestosterone is basically a structurally altered form of Dianabol (Methandrostenolone), which itself is a derivative of testosterone. The structural makeup of Oral Turinabol is very simple. The compound is simply the testosterone hormone with an added double bond at carbon 1 and 2, which alters the anabolic to androgenic ratio in favor of anabolic. It also carries an added Chloro group at carbon 4, which inhibits the hormone from aromatizing and further reduces its androgenic nature. The final change is an added methyl group at the 17th carbon position, which protects the hormone through oral administration. This final change officially classifies Oral Turinabol as a C17-alpha alkylated (C17-aa) anabolic androgenic steroid. On a functional basis the traits of Oral Turinabol are very simple. Like most anabolic steroids it should have a positive impact on protein synthesis and nitrogen retention, as well as in increasing red blood cell count. These traits are all important as they enhance the anabolic atmosphere of the individual. Protein synthesis in that protein is the primary building block of muscle and synthesis representing the rate by which cells build proteins, and nitrogen retention in that it represents an important part of lean tissue composition. A deficiency in nitrogen will lead to a catabolic state, where as a higher amount retained will promote a more favorable anabolic atmosphere. Then we have red blood cells, which are responsible for carrying oxygen to and through the blood. More red blood cells will equate to greater blood oxygenation, which in turn will equate to greater muscular endurance. All of these traits will also be tremendously beneficial in terms of the body’s ability to recover. While the protein, nitrogen and red blood cells traits are present, they are not as pronounced in Oral Turinabol as they might be with many other steroids. But they are still notable and quite beneficial. However, the steroid will promote such traits with a milder nature in that it lacks the ability to aromatize and carries such mild androgenic activity. This can be very beneficial to the individual who while he needs to make progress he needs to keep it as clean as possible. The mild nature of Oral Turinabol makes it very appealing but there is another trait that greatly enhances its worthwhile. This steroid has the ability to significantly reduce Sex Hormone Binding Globulin (SHBG). It doesn’t carry this ability as strongly as a few other steroids but it is still more than notable. This reduction in SHBG allows for more active and available free testosterone. Perhaps more importantly, it keeps the other steroids you may be using from falling into a bound state. Basically the individual should be able to get more out of the other steroids being used without a need for increasing the dose simply due to the synergy created by Oral Turinabol.
Effects of Oral Turinabol:
Without question the effects of Oral Turinabol will be most valuable to the athlete and by athlete we actually mean athlete. We’re not talking about the bodybuilder or gym rat that lives like one but rather someone who competes in a competitive sport of physical skill. The use of Oral Turinabol will significantly promote muscular endurance, they won’t tire out as fast and their overall rate of recovery should be greatly improved. As the season wanes on, they should also find they have taken less of a beating and are closer to the physical peak they enjoyed at the beginning of the season. This would not occur without the anabolic protectant nature. The athlete should also find his strength is noticeably improved upon. Yes, he should be stronger, which can directly translate into physical power and speed. No, it will not create the athlete, it will not create athletic ability, affect coordination or turn a sloth into a star, but it will enhance the existing athlete within. If it wasn’t phenomenal for this purpose you can bet the East Germans wouldn’t have been using it and successfully so for nearly two decades. In a direct physical sense, as an off-season bulking steroid Oral Turinabol is not what we’d label phenomenal. It’s not going to pack a ton of mass on anyone’s frame but it can provide some decent growth. You will definitely grow more when using Dianabol or Anadrol, and it’s not going to build mass like Deca Durabolin, but it should still be notable and clean. Remember, as it doesn’t aromatize all weight gained due to use will be lean mass. Due to its ability to reduce SHBG, this could also make the other steroids you’re taking, such as Deca Durabolin far more valuable during your off-season use. As a cutting agent, Oral Turinabol can be a decent steroid. It’s probably a little more valuable in the cutting phase than in a true off-season cycle. The steroid will provide solid protection against lean tissue loss and a lot of users often report an increase in hardness. How much hardness will it provide? This is a tough question to answer but it’s not going to be near the level of Winstrol or Masteron and most certainly not near the level provided by Trenbolone. However, the lean tissue protection and increases in endurance and recovery can prove invaluable during this phase of training. Many find this is a great steroid to use at the frontend of a long cutting cycle and then once a little leaner to switch over to more powerful hardening agents.
Side Effects of Oral Turinabol:
We can say with confidence that the side effects of Oral Turinabol are some of the mildest of any anabolic steroid on earth. However, we will also find that it can have a strong, negative impact on cardiovascular health. This should be controllable for the healthy adult but it will be something you need to keep an eye on. Both men and women will be able to use this steroid. This is not our first choice in female use, but it is a viable option. In order to help you understand the possible side effects of Oral Turinabol we have broken them down into their separate categories along with all the information you’ll need.
Estrogenic:
The side effects of Oral Turinabol do not include any of an estrogenic nature. This steroid does not aromatize and carries no progestin related traits making side effects like gynecomastia and excess water retention impossible. This should also greatly reduce the risk of high blood pressure as high blood pressure due to steroid use is most commonly linked to severe water retention.
Androgenic:
On a structural basis Oral Turinabol appears to carry no androgenic activity but the total information we have at our disposal is inconclusive. As the steroid is no longer manufactured legitimately and probably never will be again, more than likely its androgenic nature may always remain a slight mystery. However, we do know that it displays very little androgenic activity but we cannot say as some have attempted to say that it doesn’t posses any. Androgenic side effects of Oral Turinabol are possible, although unlikely. Such side effects may include acne, accelerated hair loss in those predisposed to male pattern baldness and body hair growth. Such effects will be highly dependent on genetics but the androgenic effects will not be affected by inhibitors. 5-alpha reductase inhibitors will have little effect on this steroid’s androgenicity as it is not significantly metabolized by the 5-alpha reductase enzyme.
When looking at the androgenic side effects of Oral Turinabol, the most concerning will be female virilization symptoms. Women can use this steroid without virilization, but the dose must be kept low or virilization will absolutely occur. Virilization symptoms include a deepening of the vocal chords, body hair growth and clitoral enlargement. If such symptoms begin to show, discontinue use immediately and they will fade away. If such symptoms are ignored it is possible that they may become irreversible.
Cardiovascular:
Oral Turinabol can have a significant impact on cholesterol in increasing LDL levels (bad cholesterol) and suppressing/reducing HDL levels (good cholesterol). This negative effect on cholesterol will carry a stronger probability than with just about any injectable steroid you could use. Further, while we wouldn’t necessarily call it the unfriendliest oral steroid in this category it is far from the friendliest.
If you suffer from high cholesterol you should not use this steroid. If you cannot live a cholesterol friendly lifestyle and actually give it some attention you should not use this steroid. For those who are disciplined enough for use, ensure your diet is low in saturated fats and simple sugars. Also ensure your diet is rich in omega fatty acids. A large amount of fish oils daily is advised. It’s also a good idea to consider a cholesterol antioxidant and always include plenty of cardiovascular training into your routine. If you’re a healthy adult and you do these things, unless there is an underlying issue you shouldn’t run into any problems.
Testosterone:
Oral Turinabol is suppressive to natural testosterone and should be used in conjunction with exogenous testosterone. Men who use Oral Turinabol without exogenous testosterone will risk a low testosterone condition. Such a condition can come with a host of possible symptoms ranging from physical, mental and sexually related. However, while physical related symptoms are unlikely when steroids are being used the others are a very real possibility.
Once the use of Oral Turinabol comes to an end natural testosterone production will begin again on its own. However, natural levels will still be very low and it will take a large amount of time to recover proper or healthy levels. For this reason most men are encouraged to implement a Post Cycle Therapy (PCT) plan once the use of anabolic steroids is discontinued. This will greatly speed up the recovery process and protect your lean tissue. Without a PCT plan it is possible for cortisol to become dominant for a period of time, destroy muscle tissue and promote fat gain. While a PCT plan will promote recovery, it will not return you to normal on its own. There is no PCT plan on earth that has this ability. However, a well planned PCT will speed up the process and ensure you have enough testosterone for proper bodily function while your levels continue to naturally rise.
There are a few important notes on natural recovery, the primary being that no low testosterone condition existed prior to anabolic steroid use. Further, natural recovery assumes no severe damage was done to the Hypothalamic-Pituitary-Testicular-Axis (HPTA) through improper anabolic steroid use. As a final note, women have no need to supplement with exogenous testosterone when using Oral Turinabol.
Hepatotoxic:
As a C17-aa anabolic steroid, Oral Turinabol is hepatotoxic. Liver enzyme values will increase with use due to the stress it will place on the liver. However, it’s important to remember an increase in enzyme values does not automatically equate to damage, but it is an indicator of stress. This is not the most hepatotoxic C17-aa steroid at our disposal but it is far from the mildest. With proper use it is more than possible to avoid any liver damage, but this will require responsible use.
If you already suffer from any liver related issues, you should not supplement with Oral Turinabol. If you are healthy enough for use, you should ensure you do all you can to promote a healthy liver. First and foremost, avoid all excess alcohol consumption when using this steroid. Heavy consumption will present even more stress to the liver and greatly increase the potential for damage. In fact, avoiding all alcohol during use isn’t the worst idea. Always keep in mind alcohol is perhaps the most anti-performance substance on earth and your very reason for supplementing with Oral Turinabol is to promote performance.
Beyond alcohol regulation, avoiding all over the counter medications when possible is highly advised. Many over the counter medications are quite hepatotoxic and should be limited to when only absolutely necessary. The use of a liver detoxification supplement is also advised when using Oral Turinabol.
If the individual does these things and had a healthy liver to begin with, although enzyme values will rise during use they should return to normal shortly after use is discontinued. The liver carries some of the most remarkable rejuvenation characteristics of any organ in the body and if proper steps are followed and no underlying issues exist no damage should be done.
ACTIVE HALF-LIFE 8-12 hours
CLASSIFICATION Anabolic Steroid
DOSAGE 10-20 mg/day
ACNE Rarely
WATER RETENTION No
HBR Yes
HEPATOTOXICITY High
AROMATIZATION No
MANUFACTURER Rx Pharmaceuticals
SUBSTANCE Methyldrostanolone,
Superdrol – trademark of anabolic steroid Methyldrostanolone.
Also called Metasteron, this steroid is a powerful oral anabolic agent, which was never produced as a commercial medical product.
Its chemical structure is very similar to Masteron (Drostanolone).
The only difference – the addition being 17 alpha-methyl group, a modification that gives this steroid a highly availability by oral administration.
In many cases, with 17 alpha-alkylation, it changes the nature of the steroid, in this case this does not happen.
Like its parent Drostanolone – aromatizing, so there is no estrogenic difference in these two steroids. Neither should not produce the side effects of estrogen. In addition, both steroids remain with very favorable ratio of anabolic effect of androgen.
Laboratory tests have shown that its anabolic activity is 4 times higher than that of oral Methyltestosterone and its relationship to androgenic anabolic effect of 20:1.
Masteron tests, as shown, that it is as powerful as an anabolic agent as Testosterone, but only 25-40% of androgens. It is – still a very good anabolic steroid, but by all accounts its rate is 3:1 instead of 20:1.
The effective Ultima-Superdrol dosage seems to start in the range of 10-20 mg per day for men. At this dosage level, it provides good anabolic effect which is usually accompanied by loss of fat and muscle expression appearance. But do not expect to obtain 10-15 kg with this steroid, growth is mostly 5-7 kg of quality weight if used solo.
In determining the optimum daily dosage, some do find that the drug is more effective in the range of up to 30mg. At higher dosage begins to develop the potential hepatotoxicity of the drug. In many cases, the best choice would be to use Ultima-Superdrol at 20 mg per day + any non-toxic injectable steroid (Nandrolone or Boldenone).
You can consider the possibility of using injectable Primobolan or Trenbolone for such cycles, instead of adding 17-alpha alkylated anabolic steroids.
Since this steroid has a very high ratio of the anabolic effect of androgen, it may be interesting for representatives of women’s bodybuilders. Ultima-Superdrol is less androgenic than the majority of popular Winstrol and Primobolan. The closest to it is Anavar (Oxandrolone), which according to some ratio of anabolic and androgenic effect is 30:1.
However, this steroid deserves interest. The main point of the problems with the use of women may be the dosage that is too high (10mg per tablet) Women are better to experiment with 1-2mg per day.
Admittedly not a comfortable experience, but nevertheless it will be effective. As with all steroids, there is a danger of virilization.
When using 17 alpha alkylation oral steroids is necessary to bear in mind the possibility of liver damage. For the most, Ultima-Superdrol best cycle is 4-6 weeks in length, that does not prevent some bodybuilders to use it for 8 consecutive weeks. This is due to the fact that among bodybuilders is widely believed that Ultima-Superdrol is less toxic to the liver than Oxymetholone, Dianabol and Winstrol.
We can tell you with little confidence that this is – a lie!
Ultima-Superdrol – really powerful oral anabolic steroid, it is an effective drug with a very favorable ratio of anabolic to androgenic effect, but also there is a significant possibility of liver damage in the event of misuse.
Warnings: Keep out of reach of children. For adults only.
Product Categories
Product Tags
- Steroids For Sale Online UK
- Buy Legal HGH Injections Online
- Human Growth Hormone HGH For Sale Online
- Buy High-Quality Anabolic Steroids Online
- Legal Anabolic Steroids For Sale Online
- Injectable Human Growth Hormone For Sale UK
- Buy Legal Anabolics Steroids Online UK
- Testosterone Enanthate For Sale Online
- Testosterone Cypionate For Sale Online
- Buy Cheap Anabolic Steroids Online
Fast Delivery
Across USA, CANADA & EUROPE
safe payment
100% Secure Payment
Online Discount
Add Multi-buy Discount
Help Center
Dedicated 24/7 Support
Curated items
From Handpicked Producers