Deca is a good basic steroid which, for muscle buildup, can be combined with many other steroids. Although Deca is not an optimal steroid when preparing for a competition, many athletes also achieve good results during this phase. Since Deca is a long-term anabolic, there is risk that with a higher dosage, the competing athlete will retain too much water. A conversion into estrogen, that means an aromatizing process, is possible with deca but usually occurs only at a dose of 400 mg/week. During competitions with doping tests Deca must not be taken since the metabolites in the body can be proven in a urine analysis up to 18 months later. Those who do not fear testing can use Deca as a high-anabolic basic compound in a dosage of 400 mg/week. The androgens contained in 400 mg/week also help to accelerate the body's regeneration.Many athletes who use Clenbuterol claim that it promotes dramatic strength increases and a very noticeable reduction in body fat and weight loss. Keep Clomid in a tightly closed container and out of reach of children. Store Clomid at room temperature and away from excess heat and moisture (not in the bathroom). by Bill Roberts - Nolvadex is very comparable to Clomid, behaves in the same manner in all tissues, and is a mixed estrogen agonist/antagonist of the same type as Clomid. The two molecules are also very similar in structure.Cypionate = C8 H4 O = 124.2mg = 69.90mg Testosterone enanthate is an oil based injectable steroid, designed to release testosterone slowly from the injection site. Once Testosterone Enanthate is administered, serum concentrations of this hormone will rise for several days, and remain markedly elevated for approximately two weeks. It may actually take three weeks for the action of Testosterone Enanthate to fully diminish. For medical purposes Testosterone Enanthate is the most widely prescribed testosterone, used regularly to treat cases of hypogonadism and other disorders related to androgen deficiency. Since patients generally do not self-administer such injections, a long acting steroid like this is a very welcome item. Therapy is clearly more comfortable in comparison to an ester like propionate, which requires a much more frequent dosage schedule. Testosterone Enanthate product has also been researched as a possible male birth control option. Regular injections will efficiently lower sperm production, a state that will be reversible when the drug is removed.Clenbuterol is a prescribed asthma medication which is catabolic to fat and anabolic to muscle. Clenbuterol is not a steroid hormone but a beta-2-symphatomimetic. There have been an increasing number of American bodybuilders that are experimenting with this drug. The question of the right dosage, as well as the type and duration of application, is very difficult to answer. Since there is no scientificresearch showing how STH should be taken for performance improvement, we can only rely on empirical data, that is experimental values. The respective manufacturers indicate that in cases of hypophysially stunted growth due to lacking or insuffieient release of growt hormones by the hypophysis, a weekly average dose of 0.3 I.U/ week per pound of body weight should be taken. An athlete weighting 200 pounds, therefore, would have to inject 60 I.U. weekly. The dosage would be divided into three intramuscular injections of 20 I.U. each. Subcutaneous injections (under the skin) are another form of intake which, however would have to be injected daily, usually 8 I.U. per day. Top athletes usually inject 8-20 I.U./day. Ordinarily, daily subcutaneous injections are preferred. Since STH has a half life time of less than one hour, it is not surprising that some athletes divide their dail dose into three or four subcutaneous injections of 2-4 I.U. each. Application of regular small dosages seems to bring the most effective results. This also has its reasons: When STH is injected, serum concentration in the blood rises quickly, meaning that the effect is almost immediate. As we know, STH stimulates the liver to produce and release somatomedins and insulin like growth factors which in turn effect the desired results in the body. Since the liver can only produce a limited amount of these substances, we doubt that larger STH injections will induce the liver to produce instantaneously a larger quantity of somatomedins and insulin-like growth factors. It seems more likely that the liver will react more favorably to smaller dosages. If the STH solution is injected subcutaneously several consecutive times at the same point of injection, a loss of fat tissue is possible. Therefore, the point of injection, or even better, the entire sisde of the body should be continuously, changed in order to avoid a loss of local fat tissue (lipoathrophy) in the injection cell. One thing has manifested itself over the years: The effect of STH is dosage-dependent. This means either invest a lot of money and do it right or do not even begin. Half-hearted attempts are condemned to failure Minimum effective dosages seem to start at 4 I.U. per day. For comparison: the hypophysis of a healthy; adult, releases 0.5-1.5 I.U. growth hormones daily. The duration of intake usually depends on the athlete's financial resources. Our experience is that STH is taken over a prolonged period, from at least six weeks to several (3-4)months. It is interesting to note that the effect of STH does not stop after a few weeks; this usually allows for continued improvements at a steady dosage. Bodybuilders who have had positive results with STH have reported that the build-up strength and, in particular, the newly-gained muscle system were essentially maintained after discontinuance of the product. It remains to be clarified what happens with the insulin and LT-3 thyroid hormone. Athletes who take STH in their build-up phase usually do not need exogenous insulin. It is recommended, in this case, that the athlete eats a complete meal every three hours, resulting in 6-7 meals day. This causes the body to continuously release insulin so that the blood sugar level does not fall too low. The use of LT-3 thyroid hormones, in this phase, is carried out reluctantly by athletes. In any case, you must have a physician check the thyroid hormone level during the intake of STH. Simultaneous use of anabolic /androgenic steroids and/or Clenbuterol is usually appropriate. During the preparation for a competition the use of thyroid hormones steadily inereases. Sometimes insulin is taken together with STH, as well as with steroids and Clenbuterol. Apart from the high damage potential that exogenous insulin can have in non-diabetics, incorrect use will simply and plainly make you "FAT! Too much insulin activates certain enzymes which convert glucose into glycerol and finally into triglyceride. Too little insulin, especially during a diet, reduces the anabolic effect of STH. The solution to this dilemma? Visiting a qualified physician who advises the athlete during this undertaking and who, in the event of exogenous insulin supply, checks the blood sugar level and urine periodically. According to what we have heard so far, athletes usually inject intermediately-effective insulin having a maximum duration of effect of 24 hours once a day. Human insulin such as Depot-H-Insulin Hoechst is generally used. Briefly-effective insulin with a maximum duration of effect of eight hours is rarely used by athletes. Again a human insulin such as H-Insulin Hoechst is preferred.Drug Class: High androgenic/anabolic steroid (Oral) Please discuss the treatment with your doctor again if any of the conditions above apply to you. Aromatization: Low, converts to less active norestrogens Releaser HGH products are essentially amino acid "multi- vitamins". They typically contain L- group amino acids such as valine and glutamine that are the building blocks for human growth hormone. While these ingredients are essential components of actual human growth hormone, they still need to undergo a chemical change to produce true HGH. Many of the less- expensive pill supplements touted as "HGH" today are simple amino acid releaser products.Androfort-Richt. 10, 25 mg/ml; Gedeon Richter HU If the person loses consciousness, you should place them in either a "lateral" or "coma" position, tilting the head fully back and jaw forward, in order to ensure an open airway and protect them from possible aspiration. Keep them in this position while medical assistance is being sought.Bonalone,brand name for supstance oxymetholone,produced by Body research,Thailand is a very potent oral steroid.Some studies says that is a strongest oral steroid. The first made was available in 1960, by firm Syntex. Oxymetholone have ability to increase red blood cell production which leads to medical indication to heal a few kinds of anemia. Erythropoietin change it in a medical sphere because of side effects typical for a oral androgen. Tablets are light orange pentagon shaped tablets, with a score on one side, sealed in bags of 500 tablets. A number of athletes claim that GH is not that effective on its own, but in a stack with steroids it can do remarkable things. Perhaps there is some type of actual synergism created by the concomitant use of these two agents. Empirical data suggests that the efficacy of GH is dose related and that the majority of users may not have been taking enough of it to get positive results. Despite speculation concerning its efficacy, synthetic GH is being used by thousands of elite athletes. These include men and women bodybuilders, strength athletes, as well as a multitude of Olympic competitors. Although Growth Hormone is banned by athletic committees, there is no method for the detection of it which allows drug tested competitors to use this product freely without any ramifications. Adverse reactions to GH use are rare but technically could involve acromegaly (elongation of the feet, forehead and hands). Other possible side effects involve overgrowth of the elbows or jaw, thickening of the skin and a type of diabetes. There are numerous counterfeit versions of this product which are merely cashing in on the drug's mystique and high price tag. The legitimate versions must be refrigerated at all times, before and after they are reconstituted. Effective dosages seem to be in the area of 2 I.U., 2-4 times a week. Cycle length is usually determined by how long the athlete can afford it. Some take the product for 6 week cycles, others use it year round. It's of course used in other stacks with products such as methandrostenolone, boldenone and nandrolone to reduce estrogenic activity and increase muscle hardness. The addition of proviron makes boldenone a dead lock for a cutting stack and for some may even make it possible to use nandrolone while cutting, although the use of Winstrol or a receptor antagonist in conjunction is wishful as well. The benefit of adding it to a nandrolone stack is that it may also help you reduce the decrease in libido suffered from nandrolone, since the latter is mostly deactivated by 5-alpha reductase, an enzyme that makes other hormones more androgenic.Testosteron 10 mg/ml; Sopharma BG Xenical, additional information Tell your doctor or pharmacist: about all other medicines you are taking, including non-prescription medicines; if you are a frequent user of drinks with caffeine or alcohol; if you smoke; or if you use illegal drugs. These may affect the way your medicine works. Check before stopping or starting any of your medicines. Viagra is used to treat impotence in men. Viagra increases the body's ability to achieve and maintain an erection during sexual stimulation. Viagra does not protect you from getting sexually transmitted diseases, including HIV.The second option is to take propionate during the entire period of intake. This, however, requires a periodic injection every second day. Best results can be obtained with 50-100 mg per day or every second day. The bodybuilder as already mentioned, will experience visibly lower water retention than with the depot testosterones so that propionate is well liked by body builders who easily draw water with enanthate. A good stack for gaining muscle mass would be, for example, 100 mg Testosterone propionate every 2 days, 50 mg Winstrol Depot every 2 days, and 30 mg Dianabol/day. Propionate is mainly used in the preparation for a competition and used by female athletes. And in this phase, dieting is often combined with, testosterone to maintain muscle mass and muscle density at their maximum. Propionate has always proven effective in this regard since it fulfills these requirements while lowering possible water retention. This water retention can be tempered by using Nolvadex and Proviron. A combination of 100 mg Testosterone propionate every 2 days, either 50 mg Winstrol Depot/day or 76 mg Parabolan every 2 days, and 25 mg Oxandrolone/day help achieve this goal and are suitable for building up "quality muscles."The trick of using Clenbuterol successfully seems to be avoiding receptor downgrade which occurs rapidly with the use of this beta agonist. In fact, one clinical study showed downgrade at receptor as much as 50% experienced after using Clenbuterol for as little as 18 days consecutively. The same study showed that attenuation can be avoided if Clenbuterol is taken in a '2 day on' then '2 day off' pattern. Athletes using Clenbuterol in this manner have reported much greater results than those who use the product continualy which seems to support the theory that attenuation can be at least partially avoided by staggering the dosage. Athletes have also made a habit of cycling Clenbuterol in an effort to minimize side effects as well as prevent receptor downgrade. Average cycle length on Clenbuterol is 8-10 weeks with a 4-6 week off period.HCG is a glycoprotein that is secreted in the urine by pregnant women. It is legally used as a fertility drug for women to help induce ovulation. This drug is used by male athletes to elevate natural levels of testosterone production, mostly after a steroid cycle. This drug is used to kick start your testosterone after a cycle. While on steroids for long periods of time (more than 3 - 4 weeks) your natural testosterone shuts down. A shot of this each week for 2 weeks straight will get things going again. It should be used for no more than 2 weeks at a time because it also raises a male's natural production of estrogen. For that reason take some Nolvadex with it also. HCG is always packaged in 2 different vials, one with a powder and the other with a sterile solvent. These vials need to be mixed before injecting.Withdrawal of treatment leads to gradual reversal of effect within 12 months. It is also important to remember that endogenous Testosterone production is likely to be suppressed after a cycle of Testosterone enanthate. When this occurs, one runs the risk of losing muscle mass once the steroid is discontinued. HCG and/or Clomid are in most cases considered to be a necessity, used effectively to restore natural Testosterone production and avoid a post-cycle "crash".Uses: The third reason which speaks well for an intake of Oxandrolone is that even in a very high dosage this compound does not influence the body's own testosterone production. To make this clear: Oxandrolone does not suppress the body's own hormone production. The reason is that it does not have a negative feedback mechanism on the hypothalamohypophysial testicular axis, meaning that during the intake of Oxandrolone, unlike during the intake of most anabolic steroids, the testes signal the hypothalamus not to reduce or to stop the release of GnRH (gonadotropin releasing hormone) and LHRH (luteinizing hormon releasing hormone). This special feature of Oxandrolone can be explained by the fact that the substance is not converted into.Primobolan Depot, although with a weaker effect than Deca Durabolin, is a good basic steroid with a predominantly anabolic effect and, depending on the goal, can be effectively combined with almost any steroids. Serious side effects with diazepam include: Just read an article in my local Sacramento CA Newspaper Titled "Study:Tamoxifen's Effectiveness Fades".
Rifampin is a potent hepatic enzyme inducer and can accelerate the hepatic metabolism of diazepam. Patients should be monitored closely for signs of reduced diazepam effects if given rifampin concomitantly. Most athletes, however, use HCG at the end of a treatment in order to avoid a crash, to achieve the best possible transition into natural training. A precondition is that the steroid intake or dosage be reduced slowly and evenly before taking HCG. Although HCG causes a quick and significant increase of the endogenic plasma- testosterone level, unfortunately it is not a perfect remedy to prevent the loss of strength and mass at the end of a steroid treatment. Although HCG does stimulate endogenous testosterone production, it does not help in reestablishing the normal hypothalamic/pituitary testicular axis. The hypothalamus and pituitary are still in a refractory state after prolonged steroid usage, and remain this way while HCG is being used, because the endogenous testosterone produced as a-result of the exogenous HCG represses the endogenous LH production. Once the HCG is discontinued, the athlete must still go through a readjustment period. This is merely delayed by the HCG use. For this reason experienced athletes often take Clomid and Clenbuterol following HCG intake or they immediately begin another steroid treatment. Some take HCG merely to get off the steroids for at least two to three weeks.- If you have hypervitaminosis A ( having high levels of vitamin A in your body). How does it work? Alprostadil is the same as a naturally occurring chemical called prostaglandin E1. This prostaglandin is thought to cause some types of blood vessels to widen by relaxing the thin layer of muscle found in the vessel wall. An erection is produced via a complex chain of events, involving signals from the nervous system and the release of active chemicals, including prostaglandin E1 within the tissues of the penis. These chemicals cause blood vessels entering the penis to widen, allowing more blood to enter. They also cause less blood to leave the penis. Prostaglandin E1 plays an important role in this process and alprostadil, when administered directly into the penis, will ultimately cause the penis to become rigid and erect by increasing the blood flow into its tissues. This preparation is administered by injection directly into the penis. What is it used for? Aid to diagnosis of erectile dysfunction Impotence (erectile dysfunction).Omeprazole can increase the plasma concentrations and the elimination half-life of diazepam, presumably due to inhibition of the hepatic metabolism of diazepam. Although the pharmacodynamics of this interaction are not clear, it is recommended that patients receiving omeprazole and diazepam concomitantly should be monitored for enhanced diazepam response.Type of insulin: short acting insulin preparations are considerably safer than long acting preparations because with short acting types, it is much easier to avoid hypoglycemia with adequate food intake. With the non-medical use of longer acting insulin preparations, a person is at real risk of experiencing hypoglycemia late in the day, particularly in between meals, during or after exercise and when asleep. Regardless of this advice, some people are in reality using a mixture of short and long acting insulin preparations and exposing themselves to unnecessary increased risk.Testosterone enanthate is currently the most popular ester of testosterone available to athletes. Unlike cypionate, enanthate is manufactured by various companies all over the world. Ampules of Testoviron from Schering are probably the most popular although many others exist. Enanthate is a long acting testosterone similar to cypionate. Injections are taken once weekly. It remains the number one product for serious growth, every serious bodybuilder took it at least once usualy it is stacked with deca durabolin and dianabol.Testosterone Enanthate has very strong anabolic effects as well as strong androgenic side effects. Being an injectable testosterone, liver values are generally not elevated much by this product.During a typical Testosterone Propionate cycle one will see action that is consistent with a testosterone. Users sensitive to gynecomastia may therefore need to addition an antiestrogen. Those particularly troubled may find that a combination of Nolvadex and Proviron works especially well at preventing/halting this occurrence. Also unavoidable with a testosterone are androgenic side effects like oily skin, acne, increased aggression and body/facial hair growth. Those who may have a predisposition for male pattern baldness may also find that propionate will aggravate this condition. To help combat this we also have the option of adding Proscar, which will reduce the buildup of DHT in many androgen target tissues. This will help minimize related side effects (particularly hair loss) although it offers us no guarantees. And as with all testosterone products, propionate will also suppress endogenous testosterone production. The use of a testosterone stimulating drug like HCG and/or Clomid is therefore almost a requirement in order to avoid enduring a post-cycle crash.Use: The administration of valproic acid to patients receiving diazepam can cause an increase in diazepam serum concentrations and a concurrent increase in absence seizures. This interaction appears to be the result of inhibited metabolism of diazepam during concurrent use. If absence seizures increase in patients receiving these medications, an alternative anticonvulsant should be instituted. Phentermine Drug Interactions If you want to use IGF for localization growth get some rhIGF-1. It binds to the wound only and does not go into the bloodstream. This helps repair the injection wound and makes new cells in that area only. While Long R3 IGF binds somewhat to the would then makes its way to the blood stream causing growth throughout the body..All versions of Upjohn and Steris in multi-dose vials should be looked at with extreme caution as they are very difficult to get on the black market. Counterfeits are quite easy to obtain. T Jenapharm (o.c.) 25 mg/ml; Jenapharm G Do not take this medicine if you have had an allergic reaction to it in the past or to any other ingredient that is found in it. Testosterone cypionate is a long acting ester of testosterone which is increasingly difficult to find. Before the scheduling of anabolics in the U.S., this was the most common form of testosterone available to athletes. Cyp had gained a reputation as being slightly stronger than Enanthate and became the testosterone of choice for many.Virormone 25, 50 mg/ml; Paines & Byrne GB Nandrolone is chemically related to the male hormone testosterone. Compared to testosterone, it has an enhanced anabolic and a reduced androgenic activity. This has been demonstrated in animal bioassays and explained by receptor binding studies. The low androgenicity of nandrolone is confirmed in clinical use. In the human, nandrolone has been shown to positively influence calcium metabolism and to increase bone mass in osteoporosis. In women with disseminated mammary carcinoma, nandrolone has been reported to produce objective regressions for many months. Furthermore, nandrolone has a nitrogen-saving action. This effect on protein metabolism has been established by metabolic studies and is utilised therapeutically in conditions where a protein deficiency exists such as during chronic debilitating diseases and after major surgery and severe trauma. In these conditions, nandrolone phenylpropionate serves as a supportive adjunct to specific therapies and dietary measures as well as parenteral nutrition, due to it's faster acting nature nandrolone phenylpropionate is preffered in situations where a faster clinical response is required over it's chemical variant nandrolone decaonate.KAMAGRA is not for newborns, children, or women. Do not let anyone else take your KAMAGRA. KAMAGRA must be used only under a healthcare provider's supervision. Prolonged use of Clomid may increase the risk of a borderline or invasive ovarian tumor. Description 4: Stanabol 50 (Winstrol Depot) (stanozolol) Since, when taking Testosterone Heptylate Termex, a certain percentage of the substance converts into estrogens in the body, athletes will also have to take antiestrogens. The administration of testosteronestimulating sub-stances such as HCG, Clornifen citrate or Cyclofenil could be indicated since the endogenous testosterone production is considerably reduced by Testosterone heptylate.Be aware that 1.0 ml of insulin contains one hundred International Units (100 IU), 0.1 ml of insulin contains ten (10) IU and 0.01 ml contains one (1.0) IU. So take care in measuring out your insulin ….it is very concentrated! Post Cycle Therapy: Danabol / Dianabol / Methandrostenolone Serious side effects with diazepam include:Xenical is indicated for obesity management including weight loss and weight maintenance when used in conjunction with a reduced-calorie diet. Xenical is also indicated to reduce the risk for weight regain after prior weight loss. If the person loses consciousness, you should place them in either a "lateral" or "coma" position, tilting the head fully back and jaw forward, in order to ensure an open airway and protect them from possible aspiration. Keep them in this position while medical assistance is being sought. If you have low blood pressure or uncontrolled high blood pressure. Day 15: offSince Trenbolone binds so tightly to androgen receptors, and those receptors are found in lipid cells as well as muscle cells (10), Trenbolone seems to have a profound effect on the AR in both of these types of cells to catalyze anabolism as well as lipolysis (fat-burning) (11). Finally, Trenbolone significantly promotes red blood cell production and also increases the rate of glycogen replenishment, both of which serve to profoundly improve recovery. (12) by Bill Roberts - Topically (on the scalp itself) it is of some effect in minimizing further loss. In combination with Nizoral and spironolactone (which smells awful, by the way) it can actually reverse loss moderately.Day 15: off Androgenic: Anabolic Ratio:N/A Water Retention: Yes, but less than testosterone Clomid at recommended dosages, is generally well tolerated. Adverse reactions usually have been mild and transient and most have disappeared promptly after treatment has been discontinued. Like all medicines, VIAGRA can cause some side effects. These effects are usually mild and do not last long. Some of these side effects are more likely to occur with higher doses. VIAGRA is generally well tolerated. Side effects are rare, but if experienced they are usually mild and temporary.Alternate your injection sites in order to minimize tissue damage ("lipoatrophy" or "lipohypertrophy"; Yes technically it has a longer half-life. Why? Because it either gets rapidly taken up by a cell receptor or... Just floats around. Until it can find a receptor or is destroyed by the immune system or some other metabolizing mechanism. BUT THIS MEANS ***NOTHING***!!! Why does it mean nothing? BECAUSE once it attaches to a cell receptor, it initiates a cellular response that will take about 72 hours to be complete. THIS CELLULAR RESPONSE IS ALL THAT INTERESTS US. Not "blood levels", that's utter bullshit. As a matter of fact, the one thing YOU DO NOT WANT IS FOR BLOOD LEVELS OF IGF-1 TO BE ELEVATED. Because that means you are growing everywhere and this means first and foremost your guts. Sure it feels like it's working while you're on. Just you wait 9 months and see that you look like Craig Kovacs. Bravo, you now have the biggest intestines in the world.Additional comments: Water Retention: No Trenbolones chemical structure makes it resistant to the aromatize enzyme (conversion to estrogen) thus absolutely no percentage of trenbolone will convert to estrogen. Trenbolone administration would not promote estrogenic side effects such as breast tissue growth in men (gynecomastia, bitch tits) accelerated fat gain, decline in fat break down and water retention trenbolone. Trenbolone is also resistant to the 5- alpha-reductase enzyme, this enzyme reduces some steroid hormones into a more androgenic form, in trenbolones case however this does not matter, trenbolone boasts an androgenic ratio of 500, it can easily cause adverse androgenic side effects in any steroid.com members who are prone cases of hair loss, prostate enlargement, oily skin and acne have been reported. Unfortunately trenbolones potential negative side effects do not end there. Trenbolone is also a noted progestin: it binds to the receptor of the female sex hormone progesterone (with about 60% of the actual strength progesterone). In sensitive steroid.com members this can lead to bloat and breast growth worse still, trenbolones active metabolite17beta-trenbolone has a binding affinity to the progesterone receptor (PgR) that is actually greater than progesterone itself. No need to panic though, the anti-estrogens letrzole or fulvestrant can lower progesterone levels, and combat any progestenic sides. The use of a 19-nor compound like trenbolone also increases prolactin&. bromocriptine or cabergoline are often recommended to lower prolatin levels. Testicular atrophy (shrunken balls) may also occur; HCG used intermittently throughout a cycle can prevent this. It is also wise for Tren users to closely monitor their cholesterol levels, as well as kidney function and liver enzymes, as Tren has the potential to negatively affect all of those functions. Trenbolone, being a powerful progestin, will also shut down natural testosterone production which even a relatively small dose and keep the testosterone level suppressed for an extended period of time, this can lower libido and cause erectile dysfunction (fina dick). It is essential that you always stack trenbolone with testosterone. |
According to many an opinion this drug delivers the best gains, qualitatively speaking, for money. You notice two names on top of this profile, but unfortunately finaject hasn't been made in quite a while now. Since 1987. This is quite a shame. Both Finaplix and finaject are veterinary steroids and were readily and easily available for democratic prices. Finaject was an injectable and provided you could find a sterile source it was quite convenient. Now only finaplix remains as the original source of trenbolone acetate. The Ttokkyo brand trenbol75 surfaces from time to time as well, but its derived from the same material, though qualitatively not as pure. The problem with finaplix as opposed to finaject is that it comes in veterinary implant pellets, and trust me, you don't want to get one of these babies shot in your butt. So it needs to be converted to either a transdermal (often using DMSO) or an injectable. There are kits to achieve both. Trenbolone nasal sprays are gaining popularity as well.
Trenbolone acetate is rather short-acting but well liked because of its great availability and price. The alternative is the limited availability of Parabolan, a longer-acting trenbolone ester made for human use. Unfortunately certain lots only surface from time to time and they never sell cheap. They do act quite a bit longer. Parabolan (trenbolone as hexahydrobencylcarbonate) has the half-life of an enanthate meaning it requires less frequent injections. One of the major problems with finaplix however is that beginners making sterile injectable compounds isn't a wishful thing, and often leads to abscesses and infections.
The fun with Fina is that it causes small, well-maintainable and quality gains. Naturally it won't give you the sort of mass that testosterone or methandrostenolone would give, but it makes up for it by adding only quality mass (no estrogen formation, so no fat and water retention) which is quite easy to keep on your frame. In contradiction to many aromatizing steroids such as testosterone where a large portion of the gained mass is quickly lost again after discontinuation of the product.
It's also a very versatile product that can be used in a lot of different ways. One could easily stack it with testosterone, anadrol or dianabol for mass gains where the actions of trenbolone cause severe strength gains and add some quality to the mass. Since trenbolone was found to be roughly 3 to 4 times as anabolic as most testosterone esters it quite easily boosts strength over short periods of time. It acts well on the androgen receptor with as a result that it can have certain side-effects. Most notably the normal androgenic side-effects such as increased acne and a risk for prostate hypertrophy, definitely increased aggression leading to roid rage in prolonged use of high doses and in some cases an aggravation of an existing hair loss problem.
On the other hand trenbolone just as easily combines with stanozolol or methenolone for purposes of reducing body-fat. Bill Roberts recently claimed that trenbolone doesn't reduce body-fat and that nothing in the literature proves it does. But I beg to differ. Either Mr.Roberts isn't too bright or he doesn't know how to perform a medline search, since after a mere minute of searching I found a study1 that clearly documented the fat-loss aspects of trenbolone acetate. It clearly concluded (even said so in the abstract) that trenbolone does indeed reduce body-fat (as androgens do, we discuss this in our profile of Masteron), but only when not competing with circulating estrogen. This means as a fat-loss agonist, trenbolone is best used late in a cycle and only combined with non-aromatizing steroids since it competes with circulating estradiol. Body-fat percentage when cutting would drop regardless, simply because of the qualitative lean mass gain made while no extra body-fat is deposited.
And finally in doses of 50-100 mg daily, trenbolone acetate can be used just fine by itself and quite favorably. In fact for people starting out, not too concerned with the side-effects and looking solely for a quality increase in lean muscle, small doses of fina (50mg/day injectable) would be very suitable.
The mechanism by which trenbolone mediates skeletal muscle hypertrophy is diversified and not very well understood. On the one hand trenbolone is a very active agonist of the androgen receptor, as illustrated by its increasing strength and aggression at the level it does. While this is a large contributor there is evidence that it mediates muscle growth by another pathway entirely2,3, namely the increasing of satellite cell sensitivity to an increase in IGF-1 (Insulin-Like growth factor 1) and FGF (Fibroblast growth factor). This would result in a much, much greater nutrient uptake and protein synthesis and explain why trenbolone is so much more potent in building lean muscle than other non-aromatizing, AR-mediated steroids like drostanolone and mesterolone.
In fact, in veterinary cycles the androgenic hypertrophy is regarded as the strongest of any steroid, which is why instead of using aromatizing compounds to enhance mass in cattle, they now inject them with products like Revalor-S, which contains trenbolone and estradiol, to make up for the lack of estrogenic mass accrual.
The points one may wish to consider during use of Fina is the low sterility of some home-brewed concoctions along with the already relatively painful injections (high alcohol content). This can lead to multiple problems when it is injected daily. Lumps due to plentiful same-site injections, abscesses and infections caused by faulty filtering and so on. Trenbolone is not particularly toxic though. Liver values are barely elevated while using it. Though there is no evidence or explanation to support this, some users reported a certain kidney-toxicity. Blood in urine and all that. While this was no doubt the result of a fake (Finaject used to be an often faked steroid shortly after its discontinuation) but I figured I'd mention it. Other than that mild androgenic effects such as acne and an increase in hair loss are noted as well.
For those seeking to use trenbolone there are many online sources on how to make injectable, transdermal and intranasal forms if you can get your hands on fina. Some sites even sell conversion kits that make the whole even easier.
Use:
Trenbolone is relatively safe steroid all in all. There is some concern about kidney toxicity, but usually exaggerated. The beauty of trenbolone is that its one steroid that has it all : Its highly effective in its own, provides all lean gains which are fairly easy to maintain and isn't very prone to cause side-effects. Finaplix particularly provides you with a cheap source of trenbolone as well. The problem is making the cartridges into a sterile injectable or transdermal.
A transdermal is made quite easily. Option number one is simply to get your hands on some DMSO, mix up a 50/50 mix of DMSO and water, add in the crushed up fina pellets and apply to the skin. The second is to make an alcohol carrier. You can find the necessary products at any local pharmacy and the more you buy, the cheaper it gets. All of it perfectly legal, easy to obtain since pharmacies are supplied 5 times a day and not too expensive. You need ethanol (as pure as it gets, I use SD40) and Isopropyl Myristate (IPM), a mix of isopropyl alcohol and myristic acid. Mix up 70% ethanol and 30% IPM and dissolve 50 mg per ml trenbolone in your solution. Meaning if you had a solution of half a liter (500 ml) you could add in 25 grams of trenbolone. Again, simply apply and let it dry. These methods will give you roughly 25% absorption of trenbolone.
To get the maximum it is recommended that you inject the stuff of course, but that's slightly more complex as you need to get rid of a lot of the crap they put in these cartridges. You will need sterile oil, solvent (lipophillic), 1 empty sterile container, A syringe filter, two syringes and 2 18gauge needles. Start by putting your pellets in your solvent, and let it sit. You want the pellets to become completely undone and dissolved in your fluid. This is imperative. Shake it up real good and then let it sit for 12-48 hours to let all the crap sink to the bottom. Now take one of your syringes and start transferring the fluid into the sterile oil. You can decant as well, but you really don't want any of the crud on the bottom to make it into this solution, so using the syringe and doing it slowly is the best way. Now take your empty sterile container and use a new syringe to transfer the oil. Attach a syringe filter between syringe and needle and slowly put the oil into your container, slowly filtering it. For everytime you repeat this step you need uncouple the filter/needle from the syringe, or else dirt will gather at the wrong side of the filter and get into your solution. In fact, if your container is a vial its advised that you leave the needle in the vial with the filter on it and you just use the syringe to refill and filter. This solution is now fit to be injected. Its still advised to hold the syringe with the trenbolone under some hot streaming water before injecting first though.
One may also want to note that finaplix has decent oral availability as well. In fact, because of the acetate ester its transdermal availability is less than it would be for a pure steroid, so actually its oral potential is greater than its transdermal potential. When taking oral fina, to account for the difference in availability between this and injectable, one would have to consume 240 mg ( 3 times 4 pellets) every day for 6-8 weeks. But it does work and it saves you the time and cost of making a transdermal.
Nasal sprays and sublingual forms are also popular, and while they too have some minor success, they are the worst way to go. It's a steroid, and with the added ester its even more lipophillic. Since the mucous membranes in the mouth and nose only let hydrophilic substances through, the rate of absorption is extremely limited. Usually to achieve this cyclodextrins are used, sugars that are lipophillic on the inside and can hold a steroid inside, but are hydrophilic on the outside, making the whole absorbable through these channels. But since fina does not have this and most of us do not possess the skills to make cyclodextrin complexes in our own kitchens, this is not a path one should consider.
There is little or no need to stack secondary drugs with fina. It does not aromatize. There is some concern as to fina being progestagenic, so you should you opt to stack it with an aromatizable compound it may worsen potential gynocomastia so adding winstrol or Nolvadex, or even both to such a stack may be wise. But in itself or in a non-aromatizing stack this is not necessary. The use for post-cycle estrogen antagonists is limited as well, so Nolva or clomid to boost natural test will have little use. It is a very strong androgen receptor agonist however, so perhaps using some HCG after a cycle may help you retain more gains and prevent testicular shrinkage, but since HCG does increase estrogen that does reinstate the use of Nolvadex or clomid as well.