Arimidex is generally well

tolerated and the most common adverse effects include asthenia, headache, hot flushes, back pain, dyspnea, vomiting, diarrhea, constipation, abdominal pain, anorexia, bone pain, pharyngitis, dizziness, rash, dry mouth, peripheral edema, pelvic pain, depression, chest pain.

Brand Names: Broncodil, Broncoterol, Cesbron, Clenasma, Clenbuter, Pharmachim, Contrasmina, Contraspasmina, Monores, Novegam, Oxyflux, Prontovent, Spiropent, Ventolase, Ventapulmin... Is available in 10-20 mcg tablets. Clenbuterol is known as a sympathomimetic. These hormones are taken to mimic adrenaline and noradrenaline in the human body. Clenbuterol is a selective

beta-2 agonist that is used to stimulate the beta-receptors in fat and muscle tissue in the body.

American athletes have a long a fond relationship with Testosterone cypionate. While testosterone enanthate is manufactured widely throughout the world, cypionate seems to be almost exclusively an American item. It is therefore not surprising that American athletes particularly favor this testosterone ester. But many claim this is not just a matter of simple pride, often swearing cypionate to be a superior product, providing a bit more of a "kick" than enanthate. At the same time it is said that Testosterone cypionate produces

a slightly higher level of water retention, but not enough for it to be easily discerned. Of course when we look at the situation objectively, we see these two steroids are really interchangeable, and cypionate is not at all superior. Both are long acting oil-based injectables, which will keep tesosterone levels sufficiently elevated for approximately two weeks. Enanthate may be slightly better in terms of testosterone release, as this ester is one carbon atom lighter than cypionate (remember the ester is calculated in the steroids total milligram weight). The difference is so insignificant however that no one can rightly claim it to

be noticeable (we are maybe talking a few milligrams per shot).

by Bill Roberts - This substance, used in some Australian veterinary products, is to be avoided by male bodybuilders. It is highly estrogenic, and has no redeeming properties. It is a poor anabolic and the mythical "receptor-cleaning" properties that have been claimed for it are pure fantasy.

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.

Testosteron 10 mg/ml; Sopharma BG

Testosterone Prop. (o.c.) 50 mg/ml; Quad U.S., Lilly U.S.

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

Water Retention: None

Clenbuterol is attractive for its pronounced thermogenic effects as well as mild anabolic properties.

Our body must always produce HGH or we would not be able to function. However, as we age, our body produces less and less HGH. By age 60 we will probably have lost 75% of the HGH that our body produced.

Molecular Weight (ester): 74.0792

Sharper vision

The Crucial Role of the Friend or Peer Observer:

The presence of the acetate ester allows TRI-TRENBOLA 150 to display a rapid initial physiological response. The other two esters, hexahydrobenzylcarbonate and enanthate, which release at slower rates, prolong the physiological response with a relatively flat absorption curve over the duation of the injection life-cycle. Trenbolone has a great effect on promoting protein synthesis, as well as creating a positive nitrogen balance. It is an appetite stimulant and improves the conversion of proteins. In laboratory tests,

it has been demonstrated that trenbolone increases protein and decreases fat deposition. It has proven to be an excellent product for promoting size and strength in the presence of adequate protein and calories, promotes body tissue building processes, and can reverse catabolism.

Clenbuterol is used post cycle to aid in recovery. It allows people to keep eating large amounts of foot without adding excess adipose tissue (fat).

stay calm, squeeze earlobe/ press on fingernail of person in an effort to arouse them if person responds, try to walk them around if no response, check person's breathing and pulse if unconscious but

breathing, place in lateral or coma position call an ambulance by dialing 911.

Each 10 ml multidose vial contains either 100 mg per ml. Beginning in July, 2005, new flip-off tops are dark green coloured and have Durabol stamped on 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.

Clenbuterol is a widely used bronchodilator in many parts of the world. It is most often prepared in 20mcg tablets (see: Spiropent), but Clenbuterol is also available in syrup and injectable form (see: Spasmobronchal). This drug belongs to a broad group of drugs knows as sympathomimetics. Clenbuterol affect that sympathetic nervous system in a wide number of ways, largely mediated by the distribution of adrenoceptors.

The drug trenbolone acetate is, without a doubt, the most powerful injectable anabolic steroid

used by members to gain muscle. However the full properties of the drug are not always fully understood. This profile will separate fact from fiction and help steroid.com members decide if trenbolone is right for them.

Guideline dosage is 50mg of the injectable every 2 to 3 days and around 20 to 50mg of the oral per day.

Arimidex is indicated for the treatment of advanced breast cancer in post-menopausal women with disease progression following tamoxifen therapy.

Primobol is a mild oral anabolic with extremely low androgenic activity, meaning that there is only a minimal chance of typical steroid side-effects.

It does not convert to estrogen and, therefore, estrogen-caused water retention and fat deposition will not occur from using it. Methenolone increases the conversion of protein to lean muscle tissue through its anabolic activity. Because primobol has virtually no androgen (i.e., masculinizing) effects, it can generally be used safely by women.

Insulin is used in a wide variety of ways. Most athletes choose to use it immediately after a workout. Dosages used are usually 1 IU per 10-20 pounds of lean bodyweight. First-time users should start at a low dosage and gradually work up. For example, first begin with 2 IU and then

increase the dosage by 1 IU every consecutive workout. This will allow the athlete to safely determine a dosage. Insulin dosages can vary significantly among athletes and are dependent upon insulin sensitivity and the use of other drugs. Athletes using growth hormone and thyroid will have higher insulin requirements, and therefore, will be able to handle higher dosages.

Cautions:

Testosterone enanthate cycle

Sustanon effects

Dianabol is simply a mass building steroid that works quickly and reliably.

Keep oxandrolone in a tightly closed container and out of reach of children. Store oxandrolone

at room temperature and away from excess heat and moisture (not in the bathroom).

Phentermine Side Effects

Deca is not known as a very "fast" builder. The muscle building effect of this drug is quite noticeable, but not dramatic. The slow onset and mild properties of this steroid therefore make it more suited for cycles with a longer duration. In general one can expect to gain muscle weight at about half the rate of that with an equal amount of testosterone. A cycle lasting eight to twelve weeks seems to make the most sense, expecting to elicit a slow, even gain of quality mass. Although active in the body for much

longer, Deca is usually injected once or twice per week. The dosage for men is usually in the range of 300-600mg/week. If looking to be specific, it is believed that Deca will exhibit its optimal effect (best gain/side effect ratio) at around 2mg per pound of lean bodyweight/weekly. Deca is also a popular steroid among female bodybuilders. They take a much lower dosage on average than men of course, usually around 50mg weekly.

Brain function

Xenical (Orlistat)

    Melting Point: 235  238 Celcius

Response - This is false.

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.

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

Clenbuterol is a selective beta-2 agonist that is used to stimulate the beta-receptors in fat and muscle tissue in the body.

Diazepam is a long-acting oral and parenteral benzodiazepine. Diazepam is similar to chlordiazepoxide and clorazepate in that all three generate the same active metabolite. Diazepam is used orally for the short-term management of anxiety disorders and acute alcohol withdrawal, and as a skeletal muscle relaxant. Parenterally, it is indicated as an antianxiety agent, sedative, amnestic, anticonvulsant, skeletal muscle relaxant, anesthetic adjunct, and as a treatment for alcohol withdrawal. In addition to treating status epilepticus, diazepam has recently been shown effective in preventing recurrence of febrile seizures.I Although

diazepam has been the benzodiazepine of choice for status epilepticus, recent evidence indicates that lorazepam may be more beneficial because it provides longer control of seizures and produces less cardiorespiratory depression. Diazepam was approved by the FDA in November 1963. Phase III data for a rectal formulation of diazepam in the treatment of acute repetitive seizures was completed April 1995. The NDA for the rectal formulation (Diastat) is expected to be filed in 1995. Diazepam is a schedule IV controlled substance.

Aromatization: No, but it will raise testosterone levels and increased aromatization may occur.

It

is best to use some kind of birth control while you are taking tamoxifen and for about 2 months after you stop taking Nolvadex C&K. However, do not use oral contraceptives since they may interfere with tamoxifene. Tell your doctor right away if you think you have become pregnant while taking Nolvadex C&K.

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.

It takes 60 minutes before KAMAGRA starts to work and stays to work for up to 4 hours.

Additional description: ProvironŠ (Mesterolone)

Nolvadex is also useful during a diet since it helps in the burning of fat. Although tamoxifen has no direct fatburning effect its antiestrogenic effect contributes to keeping the estrogen level as low as possible. Nolvadex should especially be taken together with the strong androgenic steroids

Dianabol and Anadrol, and the various testosterone compounds.

Ephedrine information and description

The above information is intended to supplement, not substitute for, the expertise and judgment of your physician, or other healthcare professional. It should not be construed to indicate that use of Propecia is safe, appropriate, or effective for you. Consult your healthcare professional before using Propecia.

References:

1. Anat Histol Embryol. 2003 Apr;32(2):70-9.
2. J Lab Clin Med. 1995 Mar;125(3):326-33.
3. Zhonghua Nan Ke Xue. 2003;9(4):248-51
4. J Clin Endocrinol Metab. 2003 Apr;88(4):1478-85

5. J Clin Endocrinol Metab. 2004 Feb;89(2):718-26.
6. Am J Physiol. 1998 Jun;274(6 Pt 1):C1645-52.
7. Biochim Biophys Acta. 1995 May 11;1244(1):117-20.
8. Am J Physiol Endocrinol Metab. 2001 Dec;281(6):E1172-81.
9. Health Psychol. 1990;9(6):774-91.
10. Fertility and Sterility 33.

Women should normally avoid its intake since it could result in unpleasant androgen-linked side effects. Changes in voice and alopecia must be classified as irreversible, hirsutism and clitorial hypertropy as in part reversible." Women who are not afraid of this are found at many competition scenes. In our opinion, 250 mg is the maximum quantity

of Testosterone enanthate that a female athlete should take each 7-10 days. However in competition bodybuilding and especially in powerlifting much higher dosages and shorter injection intervals have been observed in women.

Reductil is mild in nature and produces fewer side effects compared to other appetite suppressants on the market. In clinical studies, the most common side effects were increased blood pressure and/or heart rate, headache, dry mouth, constipation, and sleeplessness.

In addition, androgenic side effects are common with this substance, and may include bouts of oily skin, acne and body/facial hair growth.

Aggression may also be increased with a potent steroid such as this, so it would be wise not to let your disposition change for the worse during a cycle. With Dianabol there is also the possibility of aggravating a male pattern baldness condition. Sensitive individuals may therefore wish to avoid this drug and opt for a milder anabolic such as Deca-Durabolin. While Dianabol does convert to a more potent steroid via interaction with the 5-alpha reductase anzyme (the same enzyme responsible for converting testosterone to dihydrotestosterone), it has extremely little affinity to do so in the human body's. The androgenic metabolite 5alpha dihydromethandrostenolone

is therefore produced only in trace amounts at best. Therefore the use of Proscar/Propecia would serve no real purpose.

Formula (base): C19 H28 O2

Trenabol Depot is a strong, androgenic steroid which also has a high anabolic effect. Whether a novice, hard gainer, power lifter, or pro bodybuilder, everyone who uses Trenabol Depot is enthusiastic about the results: a fast gain in solid, high-quality muscle mass accompanied by a considerable strength increase in the basic exercises. in addition, the regular application over a number of weeks results in a well visible increased muscle hardness over the

entire body without dieting at the same time. Frequently the following scenario takes place: bodybuilders who use steroids and for some time have been stagnate in their development suddenly make new progress with Trenabol Depot. Another characteristic is that Trenabol Depot, unlike most highly-androgenic steroids, does not aromatize. The substance trenbolone does not convert into estrogens so that the athlete does not have to fight a higher estrogen level or feminization symptoms. Those who use Trenabol Depot will also notice that there is no water retention in the tissue. To say it very clearly: Parbolan is the number one competition

steroid. When a low fat content has been achieved by a low calorie diet, Trenabol Depot gives a dramatic increase in muscle hardness. In combination with a protein rich diet it becomes espe-cially effective in this phase since Trenabol Depot speeds up the metabolism and accelerates the burning of fat. The high androgenic effect prevents a possible overtraining syndrome, accelerates the regeneration, and gives the muscles a full, vascular appearance but, at the same time, a ripped and shredded look.

Agovirin inj. 25 mg/ml; Leciva CZ

There is no need for an anti-estrogen as Winny may have such a property of its own and does

not aromatize at any rate. The only counter-indication with Winny would perhaps be an anti-hypertensive if you use for a longer stack. Be sure to get liver values checked if you use for longer than 6 weeks on end. There is no real use for Clomid or Nolva post-cycle for Winny specifically since there is no post-cycle aromatisation to cause negative feedback. That makes whatever gains you made on Winny quite easy to maintain.

There is no evidence in the literature, nor I think practical evidence, that trenbolone acetate has a "special role" in burning fat. Rather, it is an extraordinarily potent AAS, being about three times as effective

per milligram as testosterone esters. For this reason, any property which anabolic steroids have, trenbolone acetate will demonstrate more strongly per milligram.

Harifin dosage

Trenbolone promotes red blood cell production and increases the rate of glycogen 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 and power.

Dosage:

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 testosterone esters such as cypionate or enanthate, and requires a much more frequent dosing schedule. While cypionate and enanthate are injected on a weekly basis, propionate is generally administered (at least) every third day. Figure one illustrates

a typical release pattern after injection. As you can see, levels peak and begin declining quickly with this 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 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, especially when taking multiple injections each week. The standard esters like enanthate and cypionate,

which are clearly easier to use, are therefore much more popular among athletes.

Normally, blood glucose and blood insulin levels are not both elevated for any extended period of time as these two chemicals influence each other through a feedback system in the body. In the post-absorptive state, the blood insulin concentration tends to decrease during exercise, allowing the blood glucose to be maintained at or above resting levels and to provide increased energy supplies (fuel) to muscle cells. Following a meal, the blood glucose and amino acid levels rise (the absorptive state) and this triggers an increase in insulin release from

the pancreas, driving glucose and amino acids from the blood into cells and maintaining the blood glucose level within a certain physiological (operating) range.

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.

Bodybuilders and powerlifters, in particutar, like Oxandrolone for three reasons. First, Oxandrolone causes a strong strength gain by stimulating the phosphocreatine synthesis in the muscle cell without depositing liquid (water) in the

joints and the muscles. Powerlifters and weightlifters who do not want to end up in a higher weight class take advantage of this since it allows them to get stronger without gaining body weight at the same time. The combination of Oxandrolone and 20-30 mg Holotestin daily has proven to be very effective since the muscles also look harder. Similarly good results can be achieved by a simultaneous intake of Oxandrolone and 120-140 mcg Clenbuterol per day. Although Oxandrolone itself does not cause a noticeable muscle growth it can clearly improve the muscle-developing effect of many steroids. Deca Durabolin, Dianabol (D-bol), and the various

testosterone compounds, in particular, combine well with Oxandrolone to achieve a "mass buildup" because the strength gain caused by the intake of these highly tissue-developing and liquid-retaining substances results in an additional muscle mass. A stack of 200 mg Deca Durabolin/week, 500 mg Testoviron Depot (e.g. Testoviron Ethanate 250)/week, and 25 mg Oxandrolone/day leads to a good gain in strength and mass in most athletes. Deca Durabolin has a distinct anabolic effect and stimulates the synthesis of protein; Oxandrolone improves the strength by a higher phosphocreatine synthesis; and Testoviron Depot inereases the aggressiveness

for the workout and accelerates regeneration.

Testosterone: Description

This is another one of the popular ones. Next to Deca and D-bol the third most abused substance among athletes is stanozolol, as documented by the many positive drug tests. Among them the case sprinter Ben Johnson, who was stripped of his Gold Medal in the 100 meter dash in the 1988 Olympics. But since then the number of positives has grown exponentially. In bodybuilding Shawn Ray's positive in the 1990 Arnold Schwarzenegger Classic (a brief stint the IFBB had with drug testing). Ray was the winner of that event, but Canadion pro Nimrod King was also

shown to have stanazolol metabolites in his urine.

Rohypnol Street Names

Methenolone is available as an injection or as an oral. The injection is naturally regarded as better. Its an enanthate ester which is quite long-acting and only needs to be injected once a week in doses of 300-600 mg. Because it by-passes hepatic breakdown on the first pass, it also has a higher survival rate. The orals are a lot less handy, but often preferred by bodybuilders who are afraid of needles or who are already taking one or more injectable compounds. The tabs are in a short-lived acetate form, meaning that doses of 100-150 mg per day are

needed, split over 2 or 3 doses, making the tabs quite inconvenient for use. The reason doses need to be split up, unlike most oral steroids, is because Methenolone is not 17-alpha-alkylated, but 1-methylated for oral bio-availability. This reduces the liver stress, but also the availability, hence the multiple and high doses needed daily.

The side effects of Omnadren are similar to those of other testosterone compounds. Next to the high water retention other negative effects that are noticed are a sometimes strong acne and a distinctly increased aggressiveness in some users. An aggressive behavior can mostly be explained by the

fact that athletes simply use too high a dosage of Omnadren and too low a dosage of the other (and more expensive) testosterones. The very severe acne, however, is only caused by Omnadren. Often no purulent pustules but many small pimples appear so that the athlete looks as if he has an allergy. This is not intended to discourage anyone but it is a fact that many athletes after a brief time develop an acne on their lower arm, upper arm, shoulder, chest, back, and also in their face which, during an earlier intake of Sustanon or Testosterone enanthate, did not manifest itself.

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 3. 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. In speaking with chemist Patrick Arnold about my thoughts on this, I was afforded very believable support for my suspected explanation. According to Pat:

"I share your thoughts on this. Anadrol has an acidic hydrogen in the A-ring at a vicinity that is approximate to where the acidic phenolic hydrogen of estradiol is. I suspect it is a potent estrogen agonist". Clearly 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 Cytadren and Arimidex would similarly prove to be totally useless with this steroid, as aromatase is uninvolved.

Or if you observe that they have become: confused, disorientated, sweaty, drowsy.

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. Now that anabolics are controlled, this is an almost impossible find. In general, the only versions you\'ll find on the black market are Sten from Mexico, which contains 75mg cyp with 25mg propionate along with some DHEA, and Testex from Leo in Spain which contains 250mg cypionate is a light resistant

ampule. 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. Real Steris products have the inking STAMPED into the box and the labels cannot be removed from the bottle. Any variation of that is definitely counterfeit. A running dosage of test cypionate is generally in the range of 200-600mg per week. When this was available for $20 per10ml bottle, many users would take a whopping 2000mg per week. This kind of dosage however, is unsafe, generally not needed and in today's day and age too costly.