The National Institute of Clinical Excellence (NICE) has recommended that Xenical is used under the following conditions:Many athletes will get sleepy after injecting insulin. This may be a symptom of hypoglycemia, and an athlete should probably consume more carbohydrates. Avoid the temptation to go to bed since the insulin may take its peak effect during sleep and significantly drop glucose levels. Being unaware of the warning signs during his slumber, the athlete is at a high risk of going into a state of severe hypoglycemia without anyone realizing it. Humulin R usually remains active for only 4 hours with a peak at about two hours after injecting. An athlete would be wise to stay up for the 4 hours after injecting.Its effectiveness at the androgen receptor of muscle tissue is superior to that of testosterone: it binds better. Yet, it gives only about half the muscle-building results per milligram. This I think is a result of its being less effective or entirely ineffective in non-AR-mediated mechanisms for muscle growth. PATIENT INFORMATION: Many have speculated as to what makes Anapolon so troublesome in terms of estrogenic side effects. Some have suggested that it has progestational activity, similar to nandrolone, and Anapolon is not actually estrogenic at all. Since the obvious Anapolon side effects of both estrogens and progestins are very similar, this explanation might be a plausible one. However we do find medical studies looking at this possibility. Anapolon (Oxymetholone) is also a very potent androgen. This trait tends of Anapolon to produce many pronounced, unwanted androgenic side effects.If overdose of anadrol is suspected, contact your local poison control center or emergency room immediately. Being a testosterone product, all the standard androgenic side effects are also to be expected. Oily skin, acne, aggressiveness, facial/body hair growth and male pattern baldness are all possible. Older or more sensitive individuals might therefore choose to avoid testosterone products, and look toward milder anabolics like Deca-Durabolin or Equipoise which produce fewer side effects. Others may opt to add the drug Proscar/Propecia which will minimize the conversion of testosterone into DHT (dihydrotestosterone). With blood levels of this metabolite notably reduced, the impact of related side effects should also be reduced. With strong bulking drugs however, the user will generally expect to incur strong side effects and will often just tolerate them. Most athletes really do not find the testosterones all that uncomfortable (especially in the face of the end result), as can be seen with the great popularity of such compounds.Being a strong androgen, we can expect the typical side effects. This includes oily skin, acne body/facial hair growth and premature balding. The addition of Proscar/Propecia should be able to minimize such side effects, as it will limit the testosterone to DHT (dihydrotestosterone) conversion process. Sustanon will also suppress natural testosterone production rather quickly. The use of HCG (human chorionic gonadotropin) and/or Clomid (clomiphene citrate)/Nolvadex (tamoxifen citrate) may be necessary at the conclusion of a cycle in order to avoid a hormonal crash. Remember though, Sustanon will remain active in the body for up to a month after your last injection was given. Beginning you ancillary drug therapy immediately after the steroid has been discontinued will not be very effective. Instead, HCG or Clomid/Nolvadex should be delayed two or three weeks, until you are near the point where blood androgen levels are dropping significantly.Pharmacokinetics of 194mg Testosterone enanthate injection. Source: Comparison of Testosterone, dihydrotestosterone, luteinizing hormone, and follicle- stimulating hormone in serum after injection of Testosterone enanthate or Testosterone cypionate. Schulte-Beerbuhl M, Nieschlag E. Fertility and Sterility 33(1980)201-3.Each 10ml multidose vial contains 150mg per ml of dromastolone enanthate and 50mg of dromastolone propionate. Flip-off tops are gray-coloured and have Mastabol Depot stamped on them. These include: Winstrol (stanozolol) is a relatively low androgenic steroid which does not seem to aromatize. Winstrol can be toxic to the liver in excessive dosages. Winstrol is a popular all purpose steroid; many stack with Primobolan or Parabolan for cutting, others stack it with testosterone for size and strength gains. Women often use winstrol but occasionally it can cause virilization, even at low dosages. Winstrol gives a solid muscle gain and an overproportionally strong strength, which usually remains after use of Winstrol is discontinued.Consider giving this paper to the person who is going to be with you when you use insulin, so they are aware of the things to look out for and what to do if you should experience a hypoglycemic reaction. The following instructions are for a peer observer or other person who may find you experiencing difficulty as a result of overdosing on insulin or any other drug or combination of drugs.How to Buy Bonavar Oxanabol is mild low androgenic 17-alphalkylated anabolic steroid with very low toxicity. Possible side effects • It improves skin texture (71%) and skin elasticity ( 71%) Anabolic Rating: 1900 (!) Testosterone is a powerful hormone with notably prominent side effects. Much of which stem from the fact that Testosterone exhibits a high tendency to convert into estrogen. Related side effects of Testosterone enanthate may therefore become a problem during a cycle. For starters, water retention can become quite noticeable side effect of Testosterone enanthate. This can produce a clear loss of muscle definition, as subcutaneous fluids begin to build. Being a Testosterone product, all the standard androgenic side effects are also to be expected. Side effects of Testosterone enanthate are oily skin, acne, aggressiveness, facial/body hair growth and male pattern baldness are all possible. Older or more sensitive individuals might therefore choose to avoid Testosterone products, and look toward milder anabolics like Deca Durabolin® or Equipoise® which produce fewer side effects. Others may opt to add to Testosterone enanthate the drug Proscar®/Propecia®, which will minimize the conversion of Testosterone into DHT (dihydrotestosterone). With blood levels of this metabolite notably reduced, the impact of related side effects of Testosterone enanthate should also be reduced. With strong bulking drugs however, the user will generally expect to incur strong side effects and will often just tolerate them. Most athletes really do not find the Testosterones all that uncomfortable (especially in the face of the end result), as can be seen with the great popularity of such compounds.
Testosterone + 5 esters
Formula of Acetate ester: C2 H4 O2 Formula of Propionate ester: C3H6O2 Formula of Phenylpropionate ester:C9 H10 O2 Formula of Cypionate ester: C8 H14 O2 Formula of Decanoate ester: C10 H20 O2 Manufacturer: British Dragon Effective dose (injectable): (Men) 550mgs-1,100mgs+/week Active Life: 14 days Detection Time: 3 months (projected) Anabolic/Androgenic Ratio (Range):100:100 Averbol is an injectable form of methandienone. Methandienone is a derivative of testosterone and has a very strong anabolic and androgenic effect. It has a great effect on protein metabolism and promotes protein synthesis. This effect manifests itself in by creating a positive nitrogen balance, supporting the builidup of protein and, thus, skeletal muscle mass. Methandienone also induces an improved sense of well-being. Norditropin ® is the Novo Nordisk A/S registered trademark for somatropin, a polypeptide hormone of recombinant DNA origin.After a cycle, mainly due to the high aromatization and increased levels of estradiol in the blood after discontinuing, natural testosterone levels will be severely suppressed. This means steps need to be taken to assure the quick return of natural testosterone, or we stand to lose a lot of the gains we made while using testosterone. Since it's a non-toxic, potent mass-builder its mostly used in long 10-12 week cycles. So some testicular shrinkage will have occurred too. Its very important that people see that HCG and Nolvadex/clomid are essential as a post-cycle therapy, and that both are equally important in achieving our goal. HCG injections should be started the last week of the cycle and continued for 3-4 weeks, using 1500-3000 IU every 5-6 days. HCG will act as an alternative to LH and start the endogenous testosterone cycle, thereby increasing testicle size once again. Then about 2 weeks after the last shot of testosterone is given, Nolvadex/Clomid cycle should be started. 40 mg of Nolva or 150 mg of Clomid per day for two weeks, followed by two more weeks with either 20 mg of Nolva or 100 mg of Clomid per day should be adequate. Always remember that HCG is suppressive of natural testosterone itself and should be discontinued at least 2 weeks prior to finishing Nolvadex/Clomid.VIAGRA Is Not for Everyone: Alcohol abuse (or history of) or Patients receiving levodopa for Parkinson's disease experienced an exacerbation of parkinsonian symptoms when benzodiazepines were added to their regimen. Benzodiazepines should be administered cautiously to such patients. This product is also not picked up on steroid tests, so some athletes use it to keep androgen levels high before a contest that has drug testing. HCG must be refergerated after it is mixed together, and it then has a life of about 10 weeks. It is taken intramuscularly only; this drug is often available by order of a physician if you show symptoms of hypogonadism. It is hard to find on the black market.Keep anadrol in a tightly closed container and out of reach of children. Store anadrol at room temperature and away from excess heat and moisture (not in the bathroom). Testosterone is usually attached to an ester (i.e. when you buy testosterone propionate, the subject of this profile, you are buying testosterone with a propionate ester attached). The ester determines how long it takes your body to dispose of the steroid in question, and propionate is the shortest ester available with a testosterone base (of course, testosterone suspension has no ester). There are enzymes, called esterases, in your body which have the function of removing the ester from steroids, and leaving you with just the steroid molecule with the ester cleaved off. Depending on how heavy the ester chain is, that determines how long it takes the esterase to remove it. And that amount of time determines how long the drug stays active in your body. Great, right? Not really...see, the ester takes up "room" in the injection. Check out this chart:The drug seems to have estrogenic effects on mood, which can be beneficial (improving relationships with women by improving empathy) or can yield depression or PMS-like symptoms, but for most users there is no significant effect either way.If you are interested in taking clenbuterol for anything other than fat loss then you might as well stay away from this compound. There is a lot of talk as to how clenbuterol compares to ephedrine as well. Most "experts" feel that clen gives a better bang for the buck than the ECA stack. It should be noted that clenbuterol’s results and effects are much shorter lived. They work through very similar mechanisms. Both products stimulate the beta-receptors but clenbuterol seems to be a more refined version, called a second generation beta-agonist drug, than ephedrine. Clenbuterol targets the proper receptors, being the beta-2 and 3 receptors than ephedrine more specifically which should in theory make clenbuterol more effective of a fat burner. Again, most of the so called "experts" say that clenbuterol is more effective than ephedrine. I, personally, get worse results with clen vs. the good old ECA stack. Clenbuterol also didn't blunt my hunger either and I ate more while taking it as well. I also seem to get much better effects out of cytomel as a fat burner as well. Even better than the ECA stack or clenbuterol. But, again, that is my personal opinion.IGF also mimic's insulin in the human body. It makes muscles more sensitive to insulin's effects, so if you are a person that currently uses insulin you can lower your dosage by a decent margin to achieve the same effects, and as mentioned IGF will keep the insulin from making you fat. - You must not take Roaccutane if you are pregnant. By minimizing the production of DHT, we should greatly reduce many of these harsh side effects and make our testosterone cycles more comfortable. In many instances, Proscar/Propecia can allow the athlete the use of steroid compounds (testosterone esters such as cypionate, enanthate, Sustanon etc.), Halotestin and methyltestosterone with much less androgenic side activity.Viagra tablets. Each Viagra tablet contains 100 mg. sildenafil citrate. Viagra comes in packs of 4 tablets and is manufactured by Pfizer. - If you are breastfeeding. Precautions Rohypnol has never been approved for medical use in the United States, therefore, doctors cannot prescribe it and pharmacists cannot sell it. However, it is legally prescribed in over 50 other countries and is widely available in Mexico, Colombia, and Europe where it is used for the treatment of insomnia and as a pre-anesthetic. Therefore, it was placed into Schedule IV of the Controlled Substances Act in 1984 due to international treaty obligations and remains under that classification.Pharmacokinetics of 194mg Testosterone enanthate injection. Source: Comparison of Testosterone, dihydrotestosterone, luteinizing hormone, and follicle- stimulating hormone in serum after injection of Testosterone enanthate or Testosterone cypionate. Schulte-Beerbuhl M, Nieschlag E. Fertility and Sterility 33(1980)201-3.Description 3:
(17beta-Hydroxyestra-4,9,11-trien-3-one) Phentermine Storage By minimizing the production of DHT, we should greatly reduce many of these harsh side effects and make our testosterone cycles more comfortable. In many instances, Proscar/Propecia can allow the athlete the use of steroid compounds (testosterone esters such as cypionate, enanthate, Sustanon etc.), Halotestin and methyltestosterone with much less androgenic side activity. Testosterone Prop. 100 mg/ml; Steris U.S.Yellow bodily fluids - Some don't notice this, but others find that all of their bodily fluids take on a yellowish appearance. Urine is a darker yellow, and even semen and vaginal secretions may be affected. According to current knowledge, this is not known to be harmful in and of itself. Formula (base): C19 H28 O2 CLONAZEPAM is also known as RIVOTRIL. VIAGRA Is Not for Everyone: Novaquimaca: Deposteron (Brazil) - 100 mg/ml The anti-estrogenic properties of Provironum© are not unique to this compound. A number of steroids have in fact demonstrated similar activity. Dihydrotestosterone and Masteron (2methyl-dihydrotestosterone) for example have been successfully used as therapies for gynecomastia and breast cancer due to their strong anti-estrogenic effect. It has been suggested that nandrolone may even lower aromatase activity in peripheral tissues where it is more resistant to estrogen conversion (the most active site of nandrolone aromatization seems to be the liver). The antiestrogenic effect of all of these compounds is presumably caused by their ability to compete with other substrates for binding to the aromatase enzyme. With the aromatase enzyme bound to the steroid, yet being unable to alter it, and inhibiting effect is achieved as it is temporarily blocked from interacting with other hormones.It is not known whether anabolic steroids can cause problems in nursing babies. There is very little experience with their use in mothers who are breast-feeding. The most common side effects with CIALIS were headache and upset stomach. Backache and muscle ache were also reported, sometimes with delayed onset. Most men weren't bothered by the side effects enough to stop taking CIALIS. Although a rare occurrence, men who experience an erection for more than 4 hours (priapism) should seek immediate medical attention. Discuss your medical conditions and medications with your doctor to ensure CIALIS is right for you and that you are healthy enough for sexual activity.Boldenone is very common in the precontest arena for two main reasons. First off, there is a low amount of aromitization and secondly there is very little water retention while taking equipoise. This makes equipoise a good precontest steroid. Boldenone is well known to give a good increase in the pumps you get while working out. This is caused from the increase in red blood cells that you will experience while taking this steroid. It is also well known to help cause a dramatic increase in appetite. When taken with a good mass building steroid like dianabol, this is a sure formula for successful gains in muscle mass.Clomid is also effective as an anti-estrogen. Most athletes will suffer from an elevated estrogen level at the conclusion of a cycle. A high estrogen level combined with a low testosterone level puts an athlete in serious risk of developing gynocomastia. With the intake of Clomid, the athlete gets the dual effect of blocking out some of the effects of estrogen, while also increasing endogenous testosterone production.Deca durabolin (Organon): Generic Name - Nandrolone Decanoate The blend of testosterones allows it to be recognized by the receptors for longer periods of time than other testosterones. As with all testosterone products it has a strong anabolic activity, with a pronounced androgenic component. Thus it can provide significant gains in strength and muscle mass, as well a noticeable increase in libido. An added benefit of testosterone is relief from joint and tendon pain also athletes are able to maintain physical out put much longer due to the oxygen rich blood along wih the increase in red blood cells. Although when taken at low at dosages this product will not aromatize excessively some patient may wish to use an anti-estrogen as insurance. In this case a low dosage of Tamoxifen Citrate or Mesterolone would be appropriate.
For this reason Oxandrolone combines very well with Andriol, since Andriol does not
aromatize in a dosage of up to 240 mg daily and has only slight influence on the hormone
production. The daily intake of Bonavar (Oxandrolone) Side EffectsTestosterone enanthate is an oil based injectable steroid, designed to release testosterone slowly from the injection site (depot). Once 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 this drug to fully diminish. For medical purposes this 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 selfadminister 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.For females only: Gastrointestinal events may increase when Xenical is taken with a diet high in fat (>30% total daily calories from fat). Xenical (Orlistat) additional information: This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.The authors of this research commented that "theoretically, this could provide a biochemical environment conducive to accelerating the rate of muscle hypertrophy and inhibiting protein degradation". However, the writer knows of no scientific studies which support this theory.50mg tablets are pink hexagon shaped tablets, with "50" imprinted on one side and a score on the reverse, sealed in bags of 100 tabs. As with no other doping drug, growth hormones are still surrounded by an aura of mystery. Some call it a wonder drug which causes gigantic strength and muscle gains in the shortest time. Others consider it completely useless in improving sports performance and argue that it only promotes the growth process in children with an early stunting of growth. Some are of the opinion that growth hormones in adults cause severe bone deformities in the form of overgrowth of the lowerjaw and extremities. And, generally speaking, which growth hormones should one take the human form, the synthetically manufactured version, recombined or genetically produced form and in which dosage? All this controversy about growth hormones is so complex that the reader must have some basic information in order to understand them. The growth hormones is a polypeptide hormone consisting of 191 amino acids. In humans it is produced in the hypophysis and released if there are the right stimuli (e.g. training, sleep, stress, low blood sugar level). It is now important to understand that the freed HGH (human growth hormones) itself has no direct effect but only stimulates the liver to produce and release insulin-like growth factors and somatomedins. These growth factors are then the ones that cause various effects on the body. The problem, however, is that the liver is only capable of producing a limited amount of these substances so that the effect is limited. If growth hormones are injected they only stimulate the liver to produce and release these substances and thus, as already mentioned, have no direct effect. The use of these STH somatotropic hormone compounds offers the athlete three performance-enhancing effects. STH (somatotropic hormone) has a strong anabolic effect and causes an increased protein synthesis which manifests itself in a muscular hypertrophy (enlargement of muscle cells) and in a muscular hyperplasia (increase of muscle cells.) The latter is very interesting since this increase cannot be obtained by the intake of steroids. This is probably also the reason why STH is called the strongest anabolic hormone. The second effect of STH is its pronounced influence on the burning of fat. It turns more body fat into energy leading to a drastic reduction in fat or allowing the athlete to increase his caloric intake. Third, and often overlooked, is the fact that STH strengthens the connective tissue, tendons, and cartilages which could be one of the main reasons for the significant increase in strength experienced by many athletes. Several bodybuilders and powerlifters report that through the simultaneous intake with steroids STH protects the athlete from injuries while inereasing his strength.Xenical can also help to improve risk factors. such as high blood pressure. high cholesterol and high blood sugar which, if not treated, could lead to other diseases such as hypertension and diabetes. Each Xenical capsule contains 120 mg of the active substance orlistat, which acts as a lipase inhibitor.Third, and often overlooked, is the fact that STH strengthens the connective tissue, tendons, and cartilages which could be one of the main reasons for the significant increase in strength experienced by many athletes. Several bodybuilders and powerlifters report that through the simultaneous intake with steroids STH protects the athlete from injuries while inereasing his strength. 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.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.Strong gains are never really made while using stanozolol (it's a weak androgen since it has no 3-keto group needed for androgen binding), but decent and fairly easy to maintain gains are possible. Its limited time of use however makes most experienced users opt for other steroids in that regard. Winny, in bodybuilding circles at least, is used mostly during cutting cycles to maintain mass. Winstrol, like a DHT compound also gives a distinct increase in muscle hardness and striations in people with a low body-fat percentage. This lends further credence that it too may be a an anti-estrogen. But most likely it has more to do with the overall lower levels of circulating estrogen. Winny is also quite effective at promoting strength because it binds very well at the androgen receptor. Short term stanozolol use can promote drastic strength, a feat often employed early in a bulking cycle (although d-bol would be more suited in that case) or late in a cutting cycle to prevent a decrease in performance. This combined with the red blood cell count-stimulating properties of its androgen affinity make it popular among track athletes as well in order to beget better results. As many, including Ben Johnson, did not take into account it can be detected for quite some time after last use so its not advisable for drug tested athletes. Many have assumed otherwise due to the short half-life, but apparently some inactive metabolites are easily esterified, so they can be found up to 5 months after the last injection. |
PRODUCT NAME: Oxydrol
SUBSTANCE: Oxymetholone
CONTENT: 100 Tabs/50mg
MANUFACTURER: British Dragon / Thailand
Oxydrol is the only oral anabolic-androgenic steroid indicated in the treatment of anemias caused by deficient red cell production. Oxymetholone is contraindicated in: male patients with carcinoma of the prostate or breast; females with hypercalcemia with carcinoma of the breast, women who are or may become pregnant; ipatients with nephrosis or the nephrotic phase of nephritis; patients with hypersensitivity to the drug or with severe hepatic dysfunction.
Anadrol (Oxydrol) is the U.S. brand name for oxymetholone, a very potent oral androgen. This compound was first made available in 1960, by the international drug firm Syntex. Since oxymetholone is quite reliable in its ability to increase red blood cell production (and effect characteristic of most anabolic/androgenic steroids), it showed great promise in treating cases of severe anemia. It turned out to be well suited for this purpose, and was popular for quite some time. But recent years have brought fourth a number of new treatments, most notably the non-steroidal hormone Epogen (erythropoietin). This drug is shown to have a much more direct effect on the red blood cell count, without the side effects of a strong androgen. Syntex stopped in the U.S. in 1993, which was around the same time they decided to drop this item in a number of foreign countries as well. Plenastril from Switzerland and Austria was dropped; following soon was Oxitosona from Spain. Many Athletes feared Anadrol 50 might be on the way out for good. But new HIV/AIDS studies have shown a new light on oxymetholone. These studies are finding (big surprise) exceptional anti-wasting properties to the compound and believe it can be used safely in many such cases. Interest has been peaked, and as of 1998 Anadrol 50 is again being sold in the United States. This time we see the same Anadrol 50 brand name, but the manufacturer is the drug firm Unimed. Syntex continues to market & license this drug in a number of countries however (under a few different brand names).
Anadrol (Oxydrol) is considered by many to be the most powerful steroid available, with results of this compound being extremely dramatic. A steroid novice experimenting with oxymetholone is likely to gain 20 to 30 pounds of massive bulk, and it can often be accomplished in less than 6 weeks, with only 50-100mg a day. This steroid produces a lot of trouble with water retention, so let there be little doubt that much of this gain is simply bloat. But for the user this is often little consequence, feeling bigger and stronger on Anadrol 50 than any steroid they are likely to cross. Although the smooth look that results from water retention is often not attractive, it can aid quite a bit to the level of size and strength gained. The muscle is fuller, will contract better and is provided a level of protection in the form of "lubrication" to the joints as some of this extra water is held into and around connective tissues. This will allow for more elasticity, and will hopefully decrease the chance for injury when lifting heavy. It should be noted however, that on the other hand the very rapid gain in mass might place too much stress on your connective tissues for this to compensate. The tearing of pectoral and biceps tissue is commonly associated with heavy lifting while massing up on heavy androgens. There is such a thing as gaining too fast. Pronounced estrogen trouble also puts the user at risk for developing gynecomastia. Individuals sensitive to the effects of estrogen, or looking to retain a more quality look, will therefore often add Nolvadex to each cycle.
It is important to note however, that this drug does not directly convert to estrogen in the body. Oxymetholone is a derivative of dihydrotestosterone, which gives it a structure that cannot be aromatized. As such, many have speculated as to what makes this hormone so troublesome in terms of estrogenic side effects. Some have suggested that it has progestational activity, similar to nandrolone, and is not actually estrogenic at all. Since the obvious side effects of both estrogens and progestins are very similar, this explanation might be a plausible one. However we do find medical studies looking at this possibility. One such tested the progestational activity of various steroids including nandrolone, norethandrolone, methandrostenolone, testosterone and oxymetholone. It reported no significant progestational effect inherent in oxymetholone or methandrostenolone, slight activity with testosterone and strong progestational effect inherent in nandrolone and norethandrolone. With such findings it starts to seem much more likely that oxymetholone can intrinsically activate the estrogen receptor itself, similar to but more profoundly than the estrogenic androgen methAndriol. If this is the case we can only combat the estrogenic side effects of oxymetholone with estrogen receptor antagonists such as Nolvadex or Clomid, and not with an aromatase inhibitor. The strong anti-aromatase compounds such as Arimidex, Femara, or Aromasin would prove to be totally useless with this steroid, as aromatase is not involved.
Anadrol (Oxydrol) is also a very potent androgen. This factor tends to produce many pronounced, unwanted androgenic side effects. Oily skin, acne and body/facial hair growth can be seen very quickly with this drug. Many individuals respond with severe acne, often requiring medication to keep it under control. Some of these individuals find that Accutaine works well, which is a strong prescription drug that acts on the sebaceous glands to reduce the release of oils. Those with a predisposition for male pattern baldness may want to stay away from Anadrol 50 completely, as this is certainly a possible side effect during therapy. And while some very adventurous female athletes do experiment with this compound, it is much too androgenic to recommend. Irreversible virilization symptoms can be the result and may occur very quickly, possibly before you have a chance to take action.
It is interesting to note that Anadrol 50 does exhibit some tendency to convert to dihydrotestosterone, although this does not occur via the 5-alpha reductase enzyme (responsible for altering testosterone to form DHT) as it is already a dihydrotestosterone based steroid. Aside from the added c-17 alpha alkylation, oxymetholone differs from DHT only by the addition of a 2-hydroxymethylene group. This grouping can be removed metabolically however, reducing oxymetholone to the potent androgen l7alpha-methyl dihydrotestosterone (mesterolone; methyldihydrotestosterone). There is little doubt that this biotransformation contributes at least at some level to the androgenic nature of this steroid, especially when we note that in its initial state Anadrol 50 has a notably low binding affinity for the androgen receptor. So although we have the option of using the reductase inhibitor finasteride (Proscar) to reduce the androgenic nature of testosterone, it would be of no benefit with Anadrol 50 as this enzyme is not involved.
The principle drawback to Anadrol 50 (Oxydrol) is that it is a 17alpha alkylated compound. Although this design gives it the ability to withstand oral administration, it can be very stressful to the liver. Anadrol (Oxydrol) is particularly dubious because we require such a high milligram amount per dosage. The difference is great when comparing it to other oral steroids like Dianabol or Winstrol, which have the same chemical alteration. Since they have a slightly higher affinity for the androgen receptor, they are effective in much smaller doses. Anadrol 50 has a lower affinity, which may be why we have a 50mg tablet dosage. When looking at the medical requirements, the recommended dosage for all ages has been 1 - 5 mg/kg of body weight. This would give a 220lb person a dosage as high as 10 Anadrol 50 tablets (500mg) per day. There should be little wonder why when liver cancer has been linked to steroid use, Anadrol 50 (Oxydrol) is generally the culprit. Athletes actually never need such a high dosage and will take in the range of only 1-3 tablets per day. Many happily find that one tablet is all they need for exceptional results, and avoid higher amounts. Cautious users will also limit the intake of this compound to no longer than 4-6 weeks and have their liver enzymes checked regularly with a doctor. Kidney functions may also need to be looked after during longer use, as water retention/high blood pressure can take a toll on the body. Before starting a cycle, one should know to give Anadrol 50 the respect it is due. It is a very powerful drug, but not always a friendly one.
When discontinuing Anadrol 50, the crash can be equally powerful. To begin with, the level of water retention will quickly diminish, dropping the user's body weight dramatically. This should be expected, and not of much concern. What is of great concern is restoring endogenous testosterone production. Anadrol 50 will quickly and effectively lower natural levels during a cycle, so HCG and Clomid/Nolvadex are a must when discontinuing a cycle.
The old practice of slowly tapering off your dosage is totally ineffective at raising testosterone levels. Without ancillary drugs, run away cortisol levels will likely strip much of the muscle that was gained during the cycle. If HCG and Clomid/Nolvadex are used properly, the person should be able to maintain a considerable amount of new muscle mass. Before going off, some alternately choose to first switch over to a milder injectable like Deca-Durabolin. This is in an effort to harden up the new mass, and can prove to be an effective practice. Although a drop of weight due to water loss is likely when making the switch, the end result should be the retention of more (quality) muscle mass with a less pronounced crash. Remember ancillaries though, as testosterone production will not be rebounding during Deca therapy.