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Popular Steroids:
Anadrol (oxymetholone)
Anadur (nandrolone hexylphenylpropionate)
Anavar (oxandrolone)
Andriol (testosterone undecanoate)
AndroGel (testosterone)
Arimidex (anastrozole)
Aromasin (exemestane)
Clomid (clomiphene citrate)
Cytomel (liothyronine sodium)
Deca Durabolin (nandrolone decanoate)
Dianabol (methandrostenolone)
Dynabolan (nandrolone undecanoate)
Ephedrine Hydrochloride
Equipoise (boldenone undecylenate)
Erythropoietin (EPO)
Femara (Letrozole)
Finaplix (trenbolone acetate)
Halotestin (fluoxymesterone)
HCG (human chorionic gonadotropin)
HGH (human growth hormone)
Masteron (drostanolone propionate)
Nilevar (norethandrolone)
Nolvadex (tamoxifen citrate)
Omnadren 250
Primobolan (methenolone acetate)
Primobolan Depot (methenolone enanthate)
Primoteston Depot
Stenox (Halotestin)
Sustanon 250
Teslac (testolactone)
Testosterone (various esters)
Testosterone Cypionate
Testosterone Propionate
Testosterone Enanthate
Trenbolone Acetate
Winstrol (stanozolol)
Winstrol Depot (stanozolol)

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Drug Profiles


 Name  Manufacturer  Volume   Price $   Price €   Quantity / Order 
   Halotestex 10mg (Fluoxymesterone)   British Dragon 50 tabs $95   €74 

You may experience any of the following side


effects from Phentermine, dry mouth, drowsiness, constipation and difficulty sleeping fluoxymesterone may occur. If side effects persist after a few days or get worse, notify your doctor. Side effects fluoxymesterone will generally go away after a couple of days of use.

Consider giving this paper to the person who is going to be fluoxymesterone 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. fluoxymesterone 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.


to enanthate and cypionate, propionate is a very short ester and is released quite fast. That meanss fluoxymesterone injections are needed more frequently. Levels will peak after 24-36 hours and begin tapering from there on out, making the longest possible time-span fluoxymesterone between injections about 3 days. Most athletes will opt to inject 50-100 mg every day to every other day. As we said before, results fluoxymesterone are seen very fast.

The dosages observed are normally 100mg every 4-5 days. fluoxymesterone Masteron is not hepatoxic so liver damage is quite unlikely. High blood pressure and gynecomastia are not a problem since neither water nor salt retention occurs and the estrogen level remains

low. The main problem are acne and a possible accelerated hair loss since dihydrotestosterone is highly affinitive to the skin's androgen receptors, fluoxymesterone in particular, to those on the scalp. Since Masteron. in most cases, is not administered in excessively high dosages and fluoxymesterone the intake, at the same time, is limited to a few weeks, the compatibility for the athlete is usually very good.

fluoxymesterone by Damian Bachs

Anastrozole (Arimidex)

Noting the hypothesis fluoxymesterone that an elevated blood insulin level may be of some advantage to bodybuilders, Fahey and his colleagues fluoxymesterone (1993) undertook an experiment in which they fed athletes a liquid meal of "Metabolol",


which consisted of 13.0g protein, 31.9g carbohydrate and 2.6g fat per 100ml and provided 825kJ of energy.

Proviron fluoxymesterone has four distinct uses in the world of bodybuilding. The first being the result of its structure. It is 5-alpha fluoxymesterone reduced and not capable of forming estrogen, yet it nonetheless has a much higher affinity for the aromatase enzyme (which converts fluoxymesterone testosterone to estrogen) than testosterone does. That means in administering it with testosterone or another aromatizable compound, fluoxymesterone it prevents estrogen build-up because it binds to the aromatase enzyme very strongly, thereby preventing these steroids from interacting with


it and forming estrogen. So Mesterolone use has the extreme benefit of reducing estrogenic fluoxymesterone side-effects and water retention noted with other steroids, and as such still help to provide mostly lean gains. Its also fluoxymesterone been suggested that it may actually downgrade the actual estrogen receptor making it doubly effective at reducing circulating estrogen levels. fluoxymesterone

Propecia is indicated for the treatment of male pattern hair loss (androgenetic alopecia) in adult men only.

Danabol / Dianabol fluoxymesterone is an orally applicable steroid with a great effect on the protein metabolism. Danabol / Dianabol has a very strong anabolic and androgenic effect giving a

great buildup of strength and muscle mass in its users. The additional body weight consists of a true increase in tissue and, in fluoxymesterone particular, in a noticeable retention of fluids.

• It improves sexual performance- (75%)

In a mass stack fluoxymesterone Winny makes a good match for Deca and Nilevar. Whether or not its anti-progestagenic effects are for real or not, lets just say it can't hurt. In any fluoxymesterone stack with Deca the use of 25-50 mg a day for the first 6-8 weeks of the stack can kickstart it and add some strength. With Nilevar there is a practical objection because it is also 17-alpha alkylated and more toxic than Winny, so your stack would


be limited to 6 weeks, which is not overly productive.

Formula (base): C18 H22 O2

Andropen 275 is fluoxymesterone a five-ester blend of testosterone produced by British Dragon, and is clearly an attempt to profit off fluoxymesterone of the popularity of Sustanon. Actually, if you are inclined to use blended products such as this (and personally, fluoxymesterone I´m not anymore), then I think you´ll find this to be a product far superior to Sustanon. fluoxymesterone

As far as adding products, no ancillaries are needed, but its highly recommended that this is only used when anabolic/androgenic steroids are also being used. First of all the extra free calories work with the

steroids to enhance results, but also because an increased level of thyroid hormones can be extremely catabolic and the fluoxymesterone use of anabolic compounds to counter muscle loss is a requirement here.

STH (somatotropic fluoxymesterone hormone) has a strong anabolic effect and causes an increased protein synthesis which manifests itself in a muscular hypertrophy (enlargement of fluoxymesterone muscle cells) and in a muscular hyperplasia (increase of muscle cells). The latter is very interesting since this increase cannot be fluoxymesterone obtained by the intake of steroids. This is probably also the reason why STH is called the strongest anabolic hormone.

Dianabol has always been one of


the most popular anabolic steroids available. Dianabol's popularity stems from it's fluoxymesterone almost immediate and very strong anabolic effects. 4-5 tablets a day is enough to give almost anybody dramatic results. fluoxymesterone It is usually stacked with deca durabolin and testosterone enanthate. Along with strong anabolic effects comes the usual androgen side effects, fluoxymesterone users often report an overall sense of well being. Dianabol is a strong anabolic and fluoxymesterone androgenic product. It most often produced dramatic gains in size and strength. Dianabol fluoxymesterone was also shown to increase endurance and glycogen retention.

Decrease HPTA function: Yes, extreme

Average Dose: Men 15-50


mg/day......Women 5-10 mg/day

Ephedrine is similar in structure to amphetamines, because of this. fluoxymesterone It mimics some of the effects of "speed" such as dampening the appetite and raising fluoxymesterone blood pressure. It Is however, much weaker and far less toxic than amphetamines (although It is banned as a stimulant by most athletic organizatlons). fluoxymesterone The effect of ephedrine Is called a "futile energy cycle." Ephedrine stimulates the conversion of thyroid fluoxymesterone into Its most active form. T-3 in peripheral tissue. This stimulates the metabolism and burns up calories quicker. Caffeine and aspirin stimulate the thermogenic effects of ephedrine. In fact


It has recently become quite commonplace for pre-contest bodybullders to forgo the use fluoxymesterone of dangerous thyroid drugs and instead use a combination of ephedrine, aspirin and caffeine for cutting fluoxymesterone up. A usual dose for fat loss has been in the area of 100 mg caffeine. 50 mg ephedrine fluoxymesterone and one aspirin tablet, three times dally. I've seen athletes get totally shredded on this fluoxymesterone stack without losing any muscle! Recent studies on humans found that combining ephedrine fluoxymesterone with caffeine and aspirin enhances calorie-dissipating. Caffeine and aspirin are thought to help by suppressing agents that would normally further block release of norepinephrine. The long term effects of


combining these three OTC drugs Is largely untested though. While It appears they fluoxymesterone are safe, in large dosages they could be dangerous, particularly the ephedrine.

Testosterone is also a relatively safe fluoxymesterone steroid to use, with some studies showing no adverse effects from 20weeks at 600mgs/week! (3)Personally, I have used fluoxymesterone up to 2 grams per week of various testosterones but now I prefer to keep my dose of it around ½ a gram.


by Bill Roberts - This drug appears to be comparable to nandrolone in its potency. It lacks nandrolone's advantage of being metabolically deactivated by 5 a -reductase. It is only slightly estrogenic, and only after


conversion to estrogen. I cannot at the moment comment on whether the effect it does produce is owed fluoxymesterone to strong binding at the AR or to effectiveness in promoting non-AR-mediated mechanisms fluoxymesterone for growth. I wouldn't expect much results with less than 400 mg/week. With that dose I would expect to see some noticeable but fluoxymesterone not dramatic results by the third week. Below 200 mg/week I would expect to see essentially nothing. fluoxymesterone

Release and action of GH and IGF-1: GHRH (growth hormone releasing hormone) and SST (somatostatin) fluoxymesterone are released by the hypothalamus to stimulate or inhibit the output of GH by the pituitary. GH has direct effects on many tissues, as

well as indirect effects via the production of IGF-1. IGF-1 also causes negative feedback inhibition at the pituitary and hypothalamus. fluoxymesterone Heightened release of somatostatin affects not only the release of GH, but insulin and thyroid hormones as well.

Primobolan fluoxymesterone depot is a registered trademark of Schering A/G avaiable in 50 mg/cc from Mexico and 100 mg/cc from Europe. It is is the \"Cleanest and Gentles\" fluoxymesterone anabolic steroid, will not aromatize, non-toxic, low in androgens.

Active Life: 14-16 days.


DNP accomplishes the astounding boost in metabolic rate via inhibition of the F0F1 ATP synthase molecule, located in the

inner wall of each mitochondrion. While the electron transport chain still functions to pump hydrogen ions into the intermembrane space, fluoxymesterone the coupling of the proton gradient to ATP production is rendered impossible by DNP. As a result, ATP production is dramatically reduced, and the fluoxymesterone energy is instead thrown off as heat. This results in an astounding production of heat; when using dinitrophenol, the fluoxymesterone athlete will radiate so much heat that it is uncomfortable to be within any proximity of them. Luckily, fluoxymesterone this heat does not fully contribute to body temperature increases, and is instead thrown off from the entire body surface, particularly the head. As a result,
adequate doses of DNP will usually only elevate body temperature by about 1-1.5?C. This is a good thing for your central nervous fluoxymesterone system and other delicate tissues; if the heat produced by ATP contributed in a more direct matter to body temperature, effective fluoxymesterone doses for fat loss would cause supraphysiological body temperature increases on a level unwitnessed at this time. Nonetheless, fluoxymesterone overheating is a very real danger; this and other side effects shall now be addressed.

HCG:Human fluoxymesterone Chorionic Gonadotropin is a drug used to jump start the body's production of testosterone after the end of a steroid cycle. It act in the body by imitating the action


of LH (a hormone that regulated testosterone production).

The recommended dosage is 1 mg once a day to be fluoxymesterone administrated with or without meals.

Day 14: 60 mcg

Roaccutane is teratogenic which means it is likely to damage an unborn fluoxymesterone baby. It may also increase the risk of miscarriage.

The drug is moderately effective at doses of 400 mg/week. fluoxymesterone The long half-life of nandrolone decanoate makes it unsuited to short alternating cycles, but suitable for more traditional cycles, with a built-in fluoxymesterone self-tapering effect in the weeks following the last injection.

If overdose of anadrol is suspected, contact your local

poison control center or emergency room immediately.

CIALIS is not for everyone. If you take nitrates, often used for chest pain (also known fluoxymesterone as angina), or alpha-blockers (other than Flomax 0.4 mg once daily), prescribed for prostate problems or high blood pressure, do not take fluoxymesterone CIALIS. Such combinations could cause a sudden, unsafe drop in blood pressure. Don't drink alcohol in excess (to a level of intoxication) with CIALIS. fluoxymesterone This combination may increase your chances of getting dizzy or lowering your blood pressure. CIALIS fluoxymesterone does not protect a man or his partner from sexually transmitted diseases, including HIV.

Food intake: the

type and timing of food consumed, its glycemic index (the glucose elevating effect) and the amount fluoxymesterone consumed;

It is not correct that Nolvadex reduces levels of estrogen: rather, it blocks fluoxymesterone estrogen from estrogen receptors and, in those tissues where it is an antagonist, causes the receptor to do nothing.

Benzodiazepines fluoxymesterone may be habit-forming (causing mental or physical dependence), especially when taken for fluoxymesterone a long time or in high doses.


Anapolon is the U.S. brand name for oxymetholone. Anapolon it is a very potent oral androgen. Anapolon 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 admittedly characteristic of nearly all fluoxymesterone anabolic/androgenic steroids), showed particular promise in treating cases of severe anemia. For this purpose it fluoxymesterone turned out to be well suited, and Anapolon was popular for quite some time.

Effective Dose: fluoxymesterone 50-100 mg a day.

Keep Androgel / Cernos Gel in a cool dry place where the temperature stays below 25°C fluoxymesterone (77°F).

Similar to testosterone and Anadrol 50R, Anabol is a potent steroid, but also one which brings about noticeable side effects. For starters methandrostenolone is quite


estrogenic. Gynecomastia is likewise often a concern during treatment, and may present itself quite early into a cycle (particularly fluoxymesterone when higher doses are used). At the same time water retention can become a pronounced problem, causing a notable fluoxymesterone loss of muscle definition as both subcutaneous water and fat build. Sensitive individuals may therefore want to keep the estrogen under control fluoxymesterone with the addition of an antiestrogen such as NolvadexR and/or ProvironR. The stronger drug ArimidexR fluoxymesterone (antiaromatase) would be a better choice, but can also be quite expensive in comparison to standard estrogen maintenance therapies.

 - Your dermatologist will


also measure your liver enzymes with the blood tests because roaccutane also increases fluoxymesterone these enzyme levels. If your liver enzymes remain high then your dermatologist can lower your dose or stop your fluoxymesterone treatment.

Propecia tablets. Each Propecia film-coated tablet contains 1 mg finasteride. Propecia, comes in packs of 28 tablets fluoxymesterone and is manufactured by Merck Sharp & Dohme.

Nolvadex C&K / Tamoxifen Nolvadex C&K tablets. Each Nolvadex C&K tablet fluoxymesterone contains 20mg tamoxifen. Nolvadex C&K comes in packs of 30 tablets and is manufactured by AstraZeneca.

Nitrates are also found in recreational drugs such as amyl

nitrate or nitrite ("poppers"). If you are not sure if any of your medications contain nitrates, or fluoxymesterone if you do not understand what nitrates are, ask your healthcare provider or pharmacist. fluoxymesterone

HGH Basics

As with all testosterone injectables, one can expect a considerable fluoxymesterone gain in muscle mass and strength during a cycle. Since testosterone has a notably high affinity for estrogen conversion, the mass gained from fluoxymesterone this drug is likely to be accompanied by a discernible level of water retention. The resulting loss of definition of course makes Testosterone cypionate a very poor choice for dieting or cutting phases. The excess level of

estrogen brought about by this drug can also cause one to develop gynecomastia rather fluoxymesterone quickly. Should the user notice an uncomfortable soreness, swelling or lump under the nipple, an ancillary drug like Proviron fluoxymesterone and/or Nolvadex should probably be added. This will minimize the effect of estrogen greatly, making the steroid much more tolerable to fluoxymesterone use. The powerful antiaromatase Arimidex is yet a better choice, but the high price tag prevents it from being more popularly used. Those who have fluoxymesterone a known sensitivity to estrogen may find it more beneficial to use ancillary drugs like Nolvadex and Proviron from the onset of the cycle, in order to prevent estrogen


related side effects before they become apparent.

All the talk about IGF-1's half-life is UTTER BULLSHIT. It is fluoxymesterone technicality without any real-world applicability. Yes rhIGF-1 has a "short half-life". But what does it mean? It means that fluoxymesterone it is either taken up by a cell receptor or bound up by a binding protein in short order. Does it mean that 20 minutes after the IGF-1 is fluoxymesterone pinned you should pin more because "blood levels are low"? Not by any means. Once it's activated a cell fluoxymesterone receptor, that's where it initiates a cellular response that will take about 72 hours to be complete and which will consume lots of energy. So the half-life



Miller suggests that an athlete who fluoxymesterone is engaged in a prolonged strenuous event should consume between 30 and 60 grams of carbohydrate per hour during fluoxymesterone the event.

Liver Toxic: Yes,debatable

Trenbolone promotes red blood cell production and increases the rate of glycogen fluoxymesterone replenishment, significantly improving recovery (13). Like almost all steroids, trenbolones effects are dose dependant with higher dosages having the greatest effects on body composition and strength. Mental changes are a notorious side effect of trenbolone use (15), androgens

increase chemicals in the brain that promote aggressive behavior (16), which can be beneficial for some athletes wanting to improve speed fluoxymesterone and power.

Like all medications, KAMAGRA can cause some side effects. These are usually mild and don't fluoxymesterone last longer than a few hours. Some of these side effects are more likely to occur with fluoxymesterone higher doses of KAMAGRA. With KAMAGRA, the most common side effects are headache, facial flushing, and upset stomach. KAMAGRA may also fluoxymesterone briefly cause bluish or blurred vision or sensitivity to light. In the rare event of an erection lasting more than 4 hours, seek immediate medical help.

Bonavar Cycles



Water Retention: Yes, high

In the human body fluoxymesterone growth hormone is produced by the pituitary gland. It exists at especially high levels during adolescence when it promotes fluoxymesterone the growth of tissues, protein deposition and the breakdown of subcutaneous fat stores. Upon maturation fluoxymesterone endogenous levels of GH decrease, but remain present in the body at a substantially lower level. In fluoxymesterone the body the actual structure of growth hormone is a sequence of 191 amino acids. Once scientists isolated this hormone, many became fluoxymesterone convinced it would exhibit exceptional therapeutic properties. It would be especially effective in cases of


pituitary deficient dwarfism, the drug perhaps restoring much linear growth if administered during adolescence. fluoxymesterone

In the U.S.A. dianabol was introduced in the 1960s by Ciba Giegy. The patent expired on the fluoxymesterone product and this is how a number of rival brands emerged with the same chemical constituents. fluoxymesterone Dianabol is a brand name and not a chemical name, therefore any product containing methandrostenolone, is now called dianabol (including fluoxymesterone Anabol).

Oxymetholone easily converts into estrogen which causes signs of feminization and fluoxymesterone the already mentioned water retention, which in turn requires the intake of antiestrogens. The increased water retention,

in addition to the aesthetical problems, can be further detrimental since it may cause high blood pressure. In extreme cases fluoxymesterone the intake of an anti-hypertensive drug may be necessary.

Anabolic steroids such as Stanabol fluoxymesterone are synthetic derivatives of the male hormone testosterone. Stanozolol has a pronounced anabolic effect with fewer fluoxymesterone masculinizing side effects than testosterone and some other synthetic anabolic steroids. fluoxymesterone Anabolic steroids are used in stimulating appetite and increasing weight gain, strength, and vigor. They should be fluoxymesterone used as a part of an overall program with other supportive and nutritional therapies.


Testo LA (Australia) - 100 mg/ml

World wide Deca is one of the most popular injectable fluoxymesterone steroids. It's popularity is likely due to the fact that Deca exhibits significant anabolic effects with minimal androgenic side fluoxymesterone effects.

For fat loss, clenbuterol seems to stay effective for 3-6 weeks, then it's thermogenic properties seem to subside. This is noticed fluoxymesterone when the body temperature drops back to normal. It's anabolic properties subside much quicker, somewhere around 18 days.

Phentermine Directions fluoxymesterone

Testosterone 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, fluoxymesterone and remain markedly elevated for approximately two weeks. It may actually take three weeks for the action of this drug to fully diminish. fluoxymesterone For medical purposes this is the most widely prescribed testosterone, used regularly to fluoxymesterone treat cases of hypogonadism and other disorders related to androgen deficiency. Since patients generally do not selfadminister fluoxymesterone 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.


Proviron© is also not a c17 alpha alkylated compound, an alteration commonly used with oral anabolic/androgenic fluoxymesterone steroids. Not using this structure in the case of Proviron© removes the notable risk of liver toxicity we fluoxymesterone normally associate with oral dosing. We therefore consider this a "safe" oral, the fluoxymesterone user having no need to worry about serious complications with use. This steroid in fact utilizes the same 1-methylation we see present on Primobolan© fluoxymesterone (methenolone), another well tolerated orally active compound. Alkylation at the one position fluoxymesterone also slows metabolism of the steroid during the first pass, although much less profoundly than 17 alpha alkylation.

Likewise Proviron© and Primobolan© are resistant enough to breakdown to allow therapeutically beneficial blood fluoxymesterone levels to be achieved, although the overall bioavailability of these compounds is still much lower than methylated oral fluoxymesterone steroids.

Brand Names:

Abuse Potential

Description 4: Stanabol 50 (Winstrol fluoxymesterone Depot) (stanozolol)


Each 10ml multidose vial contains 75mg per ml. Beginning in May, 2005, new flip-off tops are purple fluoxymesterone coloured and have Trenabol stamped on them. Older vials have a white coloured generic flip-off top.

Tamoxifen cycle and dosage

The normal daily

dosage taken by athletes is 10-30 mg/day. To prevent estrogenic side effects normally 10 mg/day fluoxymesterone is sufficient, a dosage which also keeps low the risk of reducing the effect of simultaneously taken fluoxymesterone steroids. Often it is sufficient if the athlete begins this preventive intake of Nolvadex C&K three to four weeks after the fluoxymesterone first intake of anabolic steroids. Athletes who have tendencies toward gynecomastia, strong water retention, and increased fluoxymesterone fat deposits with steroids such as Dianabol, Testosterone, Anadrol 50, and Deca-Durabolin usually take 20-30 mg/day The combined application of Nolvadex C&K 20-30 mg/day and Proviron 25-50 mg/day in these cases
leads to excellent results. The same is true for athletes who are in competition, and for women. Women, however, should do without the intake of fluoxymesterone Proviron or at least reduce the dose to one 25 mg tablet per day.

Additional monitoring of your dose fluoxymesterone or condition may be needed if you are taking other medicines for impotence, azole antifungals (e.g., itraconazole, fluoxymesterone ketoconazole), cimetidine, erythromycin, mibefradil, rifamycins (e.g., rifampin), high blood pressure medicines, fluoxymesterone or delavirdine. If you are taking an HIV protease inhibitor (e.g., ritonavir, saquinavir), do not take more than a 25 mg dose of sildenafil in a 48-hour period. If you are taking


more than a 25 mg dose of sildenafil and are also taking an alpha-blocker medicine (e.g., doxazosin, fluoxymesterone prazosin, terazosin) for various conditions (e.g., enlarged prostate), separate the time between taking these medicines by more fluoxymesterone than 4 hours. See How To Use section for drug-food interaction information.

This drug is not toxic nor have any side effects been fluoxymesterone seen in athletes who used the drug\' as an anti-estrogen. This drug is the most popular fluoxymesterone anti- estrogen amongst steroid users.

Testosterone propionate is a commonly manufactured, oil-based injectable testosterone compound. The added propionate ester will slow the rate in which the


steroid is released from the injection site, but only for a few days. Testosterone propionate is therefore comparatively much faster acting than other fluoxymesterone testosterone esters such as cypionate or enanthate, and requires a much more frequent dosing schedule. While cypionate fluoxymesterone and enanthate are injected on a weekly basis, propionate is generally administered (at least) every third day. Figure one illustrates fluoxymesterone a typical release pattern after injection. As you can see, levels peak and begin declining quickly with this fluoxymesterone ester of testosterone. To make Testosterone Propionate even more uncomfortable to use, the propionate ester can be very irritating to the site of injection.


In fact, many sensitive individuals choose to stay away from Testosterone Propionate completely, their body reacting with a pronounced fluoxymesterone soreness and low-grade fever that may last for a few days. Even the mild soreness that is experienced by most users can be quite uncomfortable, fluoxymesterone especially when taking multiple injections each week. The standard esters like enanthate and cypionate, which fluoxymesterone are clearly easier to use, are therefore much more popular among athletes.

by Bill Roberts - One obvious fluoxymesterone difference between Winstrol Depot and other injectables is that it is not esterified, being sold as aqueous stanozolol suspension. (It should not be

called water-soluble: virtually none of it is dissolved in the water.) This means that it does not have a classical half-life, where fluoxymesterone at time x the level is Ѕ the starting level, at time 2 x the level is ј, at time 3 x the level is 1/8, etc. Instead, fluoxymesterone the microcrystals slowly dissolve, and when they have all dissolved levels of the drug then fall very rapidly. fluoxymesterone

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. fluoxymesterone

Common uses and directions for Nolvadex

For example, one might use the HCG for two to three weeks in the middle of a cycle, and for two


or three weeks at the end of a cycle. It has been speculated that the prolonged use of HCG could repress fluoxymesterone the body’s own production of gonadotropins permanently. This is why the short cycles are the best way to go.

fluoxymesterone Not a rapid mass builder, instead Equipoise® will be looked at to provide a slow but steady gain of strength and fluoxymesterone quality muscle mass. The most positive effects of this drug are seen when it is used for longer cycles, usually lasting more fluoxymesterone than 8-10 weeks in duration. The muscle gained should not be the smooth bulk seen with androgens, but very defined and solid. Since water bloat is not contributing greatly to the diameter of the

muscle, much of the size gained on a cycle of Equipoise® can be retained after the drug has been discontinued. It is interesting to note that structurally fluoxymesterone Equipoise® and the classic bulking drug Dianabol are almost identical. In the case fluoxymesterone of Equipoise® the compound uses a l7beta ester (undecylenate), while Dianabol is 17 alpha fluoxymesterone alkylated. Aside from this the molecules are the same. Of course they act quite differently in the body, which goes to show the 17-methylation effects fluoxymesterone more than just the oral efficacy of a steroid.

Roche Valium (Diazepam) is an antianxiety agent (benzodiazepine), used primarily for short-term relief of mild to


moderate anxiety. It may also be used to treat symptoms of acute alcohol withdrawals, to help control epilepsy, or to relieve muscle spasms.


Effective Dose (Men): 50-150mg ED

Xenical may cause some side effects that are usually mild to moderate and decrease fluoxymesterone after the first week of the treatment. The most common side effects are fatty/oily stool, fluoxymesterone oily spotting, intestinal gas with discharge, bowel movement urgency, poor bowel control, or headaches may occur. If these fluoxymesterone effects persist or worsen, notify your doctor promptly. Intestinal side effects (e.g., oily stool) may increase in intensity if you exceed your daily dietary fat allowance.

If you notice other effects not listed above, contact your doctor.

It is interesting fluoxymesterone to note that Anadrol 50 does exhibit some tendency to convert to dihydrotestosterone, although fluoxymesterone this does not occur via the 5-alpha reductase enzyme (responsible for altering testosterone to fluoxymesterone form DHT) as it is already a dihydrotestosterone based steroid. Aside from the added c-17 fluoxymesterone alpha alkylation, oxymetholone differs from DHT only by the addition of a 2-hydroxymethylene group. This fluoxymesterone 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 fluoxymesterone 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 fluoxymesterone the reductase inhibitor finasteride (Proscar) to reduce the androgenic nature of testosterone, it would be of no benefit with Anadrol 50 as this enzyme fluoxymesterone is not involved.

In his book, Anabolics 2002, Bill Llewellyn says that Cytomel is not a drug to start off on, and that use of milder drugs like T4 (Synthroid) or triacana can help ease a person into the use of T3. I'm

inclined to disagree here however. Triacana is weak compound and I find of little use. Its fluoxymesterone not easily found anymore and not cheap either. T4 is basically similar to Cytomel except that fluoxymesterone its weaker. Something that users normally compensate with higher doses and sends them down a similar lane as simply using cytomel. Agreed, cytomel fluoxymesterone is NOT a drug for beginners, but with adequate research, experience with diet and some fluoxymesterone self-control, I don't see why cytomel shouldn't be the first thyoid compound used. But for recreational users looking for a fatburner, I still suggest using clenbuterol over cytomel for all intents and purposes. Cytomel is much more powerful,


but clenbuterol is a lot safer for use. The results are easier to maintain with clenbuterol as well. Negative feedback in the thyroid fluoxymesterone may decrease natural levels of T3 in the body, causing a decrease of metabolic rate after coming off a cycle of T3. That can cause a rebound effect during fluoxymesterone which a lot of weight is gained back.

VIAGRA does not cure erectile dysfunction. fluoxymesterone It is a treatment for erectile dysfunction. VIAGRA does not protect you or your partner from fluoxymesterone getting sexually transmitted diseases, including HIV-the virus that causes AIDS. VIAGRA is not a hormone or an aphrodisiac.

Danabol / Dianabol (Methandienone) additional information


What are the side effects of KAMAGRA?

HCG Pregnyl information and description

Rohypnol is a short-acting fluoxymesterone benzodiazepine with general properties similar to those of Valium. It is used in the short-term fluoxymesterone treatment of insomnia, as a pre-medication in surgical procedures and for inducing anaesthesia.


Day fluoxymesterone 2: 80 mcg

Benzodiazepines may also have other actions. For example, diazepam has been fluoxymesterone shown to counteract the cardiovascular toxicity of chloroquine. It is thought that diazepam increases the urinary clearance of chloroquine by improving electrocardiographic and hemodynamic




Delivery: 50 tabs (10mg/tab)
Substance: Fluoxymesterone
Halotestin is an oral steroid which was introduced on the market by Upjohn Company in 1957. Fluoxymesterone substance is precursor of methyltestosterone. Through its changes in the chemical structure, was made much more androgenic than testosterone. The anabolic component is only slightly pronounced. Based on its characteristics Halotestin is used mainly when the athlete is more interested in a strength build up rather than in a muscle gain. Powerlifters and weightlifters who must stay within a certain weight class often use this drug because they are primarily interested in a strength gain without adding body weight.
In bodybuilding Halotestin is almost exclusively taken during preparation for a competition. Since its substance is strongly androgenic while at the same time aromatizing very poorly, this substance helps the athlete obtain an elevated androgen level while keeping the estrogen concentration low.
With a low body fat content Halotestin gives the bodybuilder a distinctive muscle hardness and sharpness. Although the muscle diameter does not increase, it appears more massive since the muscle density is improved. The fact that daily dose of up to 20 mg does not cause water and salt retention makes it even more desirable. During a diet, it helps the athlete get through difficult, intense training while increasing the aggressiveness of many users. This is another reason why Halotestin (fluoxymesterone) is so popular among powerlifters, weightlifters, football players, and, in particular, boxers. The generally observed dose is normally 20-40 mg/day. Bodybuilders are usually satisfied with 20-30 mg/day while powerlifters often take 40 mg/day or more. The daily dosage of Halotestin (fluoxymesterone) is usually split into two equal amounts and taken mornings and evenings with plenty of fluids. Since the tablets are l7-alpha alkylated, they can be taken during meals without any loss in effect. Those who are tired of taking Dianabol (methandrostenolone) tablets will find fluoxymesterone an interesting alternative. In the meantime we know several bodybuilders who have combined this steroid with injectable, mostly anabolic, steroid preparations such as Anadrol, Deca-Durabolin, Primobolan Depot, or Equipoise. The quick strength gain induced by Halotestin can usually be turned into solid, high-quality muscle tissue by taking the above steroids. This is an especially welcome change for athletes who easily retain water and have to fight against swollen breast glands. Many will be surprised at what progress can be achieved by a simple combination of 30 mg/day and 700 mg Equipoise every two days over a four week period. Halotestin side effects Besides Anadrol (oxymetholone) and Methyltestostcrone it is the oral steroid with the most side effects. Those who would like to try Halotestin should limit the intake to 4- 6 weeks and take no more than 20-30 mg daily. Fluoxymesterone puts extremely high stress on the liver and is thus potentially liver damaging. Other frequently-observed side effects are increased production of the sebaceous gland (which goes hand in hand with acne), nasal bleeding, headaches, gastrointestinal pain, and reduced production of the body's own hormones. Men who tries this steroid become easily irritable and aggressive. Gynecomastia and high blood pressure caused by edemas do not occur with Halotestin.

Halotestex (fluoxymesterone) is an oral derivative of the male hormone testosterone. Unlike testosterone, halotestex does not convert to estrogen. Therefore, estrogen-related side effects such as fat deposition, water retention, and gynecomastia do not occur. Halotestex has powerful androgenic properties. It is particularly noted for increased strength without significant additional weight gain. Side effects include aggression, oily skin, and virilization. Halotestex is considered to be very toxic to the liver, and thus must be used with caution and for short durations only.

The strong androgen component will generate good strength increases with little body weight gain.

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Aldactone (Spironolactone)
Arimidex (Anastrozole)
Clomid (Nolvadex)
Nolvadex (Clomid)
Omnadren 250
How to Order
Oxandrin (Oxandrolone)
Side Effects
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Sustanon 250
Testosterone Cypionate
Testosterone Enanthate
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Winstrol Depot (Stromba)
Erythropoietin (Epogen, EPO)
HCG (Pregnyl)
Aldactone (spironolactone)
ANADROL (A50) - Oxymethylone
ANDRIOL- testosterone undecanoate
Androgel - Testosterone Gel
Arimidex - Anastrozole - Liquidex
Aromasin - exemestane
Catapres - Clonidine hydrochloride
Cheque Drops
CLOMID- clomiphene citrate
CYTADREN - aminoglutethimide
DANOCRINE- danazol
DECA Durabolin - nandrolone decanoate
DNP - (2,4-Dinitrophenol)
Durabolin - Nandrolone phenylpropionate
Erythropoietin - EPO, Epogen
ESCICLINE - formebolone
  ANADUR - (nandrolone hexyloxyphenylpropionate)
DIANABOL - Dbol - methandrostenlone / methandienone
EQUIPOISE - EQ - boldenone undecylenate
HGH (Human Growth Hormone)
How To Inject Steroids
Femara - Letozole
FINAPLIX - trenbolone acetate
HALOTESTIN - fluoxymesteron
Human Chorionic Gonadotropin (HCG)
L-THYROXINE-T-4/liothyronine sodium
LASIX - Furosemide
LAURABOLIN - nandrolone laurate
Megagrisevit Mono - Clostebol acetate
MENT - MENT, 7 MENT, Trestolone acetate
METHANDRIOL - methylandrostenediol dipropionate
MIOTOLAN - furazabol
NAXEN - naproxen
NELIVAR - norethandrolone
NOLVADEX - tamoxifen citrate
PARABOLAN - trenbolone hexahydrobencylcarbonate
Primobolan Acetate
Primobolan Depot
Primoteston Depot
Steroid Side Effects
Steroid Terms
WINSTROL - stanazolol (oral)
Anabolicurn Vister (quinbolone)
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