Month: July 2019

Methenolone & Nandrolone Deca

Metenolone and Nandrolone are actually two different things. Methenolone has nothing to do with Nandrolone. Metenolone is not derived from Nandrolone but derived from dihydrotestosterone (DHT). These two things sound a lot alike, but they are two things.


1. “Nandrolone” category is the safest steroid because Nandrolone has low ability to switch to androgens and to estrogen;
2. Nandrolone Decanoate is what we call Deca. Deca, known as the king of Bulking, is definitely not a name! Deca became famous at the end of the last century, and it can definitely compete with oral drugs like Dianabol and Anadrol in terms of muscle gain;
3. Compared with testosterone, Deca is definitely a crushing grade in terms of protein synthesis ability, and the protein synthesis ability is 130% of testosterone;
4. Compared with Dianabol, Anadrol, etc., Deca is quite gentle and quiet in the muscle gain, Deca’s muscle gain process will not bring blush, chest redness and other characteristics. And you won’t get violent and sweaty because of using Deca.
5. However, Deca can’t be used alone like Dianabol. The biggest risk of using Deca alone is the possibility of “wilting”. This must not be ignored. If you use Deca alone, it must be done with the help of testosterone.


1. Methenolone does not belong to the nandrolone class;
2. Methenolone and testosterone play the same principle, but the anabolic capacity of metoprolol is about 88% of testosterone, there will be no violent bulking like Deca, and its male hormone ability declines more, only the original testosterone 44%;
3. Methenolone is not suitable for non-season weft increase, it is more suitable for long-term use during the preparation period because it has mild nature and does not turn estrogen; no hepatotoxicity, very safe. It effectively protects muscles during fat loss, prevents muscle loss and improves muscle mass. It is suitable for use during fat loss or e preparation;
4. Methenolone often used in conjunction with Stanozolol, Clenbuterol during the preparation period, and finally achieved the effect of increasing lean body mass, dry, and fat reduction.

Therefore, Deca is suitable for the non-season injection cycle, while Methenolone is suitable for the preparation period.

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Trenbolone Enanthate is a long-acting group of trombones, a derivative of Nandrolone that does not convert to estrogen, but it has the side effects of progesterone (similar to the side effects of estrogen). Have certain liver toxicity. Trenbolone can quickly increase muscle strength and circumference and improve muscle mass. Accelerating fat burning is one of the most powerful steroids. Not suitable for beginners, it is ideal for fat loss or preparation.

Trenbolone Acetate does not store water or store fat. Trenbolone is a good choice when it is ready for the game. It works better than when other steroids are used together. Since the Trenbolone Acetate ester chain is relatively short, the half-life is only about 48-72 hours. Its anabolic and androgenic ratio is 500:500. At the same time, Trenbolone Acetate can greatly enhance protein synthesis and nitrogen storage in muscle tissue. More protein means more anabolism of muscle nucleus, which can protect muscles and accelerate body recovery while reducing calories. The more nitrogen storage, the stronger the anabolic environment; the better the muscle tissue is, the better the recovery will be!

Trenbolone Hexahydrobenzyl carbonate / Parabolan is a long-acting injection of trenbolone. The most commonly used is Trenbolone Acetate, which is one of the more rapid effects of Trenbolone. Parabolan’s ester delays the release of Trenbolone, allowing it to be released for more than two weeks. Since the slow release cycle is long and there is no need for frequent injections, it has always been considered more suitable for human use. Trenbolone is about three times more potent than testosterone and is quite strong. In terms of androgenic action, it also exhibits three times the activity, which is a veritable anabolic steroid. Trenbolone’s effect on muscle gain is comparable to testosterone or Dianabol, and there are no estrogen-related side effects. Trenbolone is also a drug that increases lean muscle mass and is popular among athletes who want to quickly increase muscle strength, muscle mass, and lines.

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Testosterone Enanthate is one of the most commonly used drugs to treat low testosterone. It is also very popular in the sports world. It is cheap, available and safe for almost all adult men. This steroid is very effective for beginners and experienced users, side effects are easy to control, and synthetic testosterone is used normally by the body for health benefits.

Testosterone Propionate is a simple form of testosterone ester, which represents the most important form of testosterone. When synthetic testosterone was first introduced, there was no esterification. Since this simple structure has no ester groups attached to it, it works fairly quickly and must be used fairly frequently. In 1937 a German pharmaceutical company first developed the first kind of Testosterone Propionate with ester base, the brand name is called Testoviron.

Testosterone Cypionate is a slow-injection form of the male hormone testosterone. Testosterone is also an anabolic hormone in men and is the basis for other anabolic/androgen steroids. As with all testosterone injections, Testosterone Cypionate is favored by athletes for its ability to increase muscle mass and strength. It’s worth noting that while a number of other steroid compounds have also been injected, they are still considered the main fillers for bodybuilders. There’s no argument that Testosterone Cypionate is one of the most powerful drugs.

Proviron or Provibol(Mesterolone) is the most historically available anabolic steroid on the market. Pharmaceutical giant Schering produced the drug in 1934. Officially known as testosterone, there have been many different brands over the years, but Proviron has long been the most popular.

Halotestin (Fluoxymesterone) in sports is regarded as one of the fastest most effective steroids on the market, its synthetic metabolic rate is very high, but will not let the user increase muscle mass, usually as a pure power drug, bodybuilders use it for the final stages of the competition.

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Nandrolone Phenylpropionate is a kind of protein assimilation hormone. Nandrolone Phenylpropionate can not only increase the synthesis of proteins from amino acids, but also inhibit the decomposition of amino acids into urea, and has the function of promoting the accumulation of calcium in the body. Its assimilation is stronger and more persistent than that of other testosterone derivatives, but its male effects are smaller. Mainly used for protein deficiency diseases, such as severe burns, patients with malignant tumors before and after surgery, the fracture is not easy to heal, severe osteoporosis, premature growth, and development significantly delayed. Welcome to buy Nandrolone Phenylpropionate powder from us.

Nandrolone Phenylpropionate had 12 times the assimilation effect of testosterone propionate and only half the masculinization effect of testosterone propionate. After intramuscular injection of 100mg, the blood concentration reached a peak for 1-2 days.

How long does nandrolone phenylpropionate stay in your system?

They are not active by mouth and must be given by injection into the muscle. The elimination half-life of nandrolone decanoate administered by intramuscular injection is approximately 6 to 12 days.

NPP (Nandrolone Phenylpropionate) vs Deca (Nandrolone Decanoate)

NPP and Deca provide the same benefits of impressive gains in muscle size and strength while recovering more efficiently post-workout. However, there is a difference in how long it will take to start seeing those results depending on which one you use.

Nandrolone is a steroid ester. Wondering how it can be changed slightly to produce different results? Well, in this case, it’s all about the length of the ester chain. NPP is a short-chain ester while Deca is a long-chain ester. The shorter the ester, the more potent it is, and the faster you’ll see results. On average, users of NPP will see size gains within a couple of months, while those taking Deca will have to wait for an extra month or so.

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Methenolone is a medium anabolic but very low androgen steroid. The Methenolone is very versatile. It is often stacked with other (usually stronger) steroids for faster and stronger effects. Metenolone is suitable for both cutting cycles and quality cycles; In both cases, it will restore and grow lean and tight muscle mass faster. Welcome to buy Methenolone powder from us. We have free reship service if your parcel was intercepted.

Methenolone was made in 1960. Squibb began making injectable drugs in 1962. Metenosaurus was originally used for aggressive treatment after surgery for muscle loss, infection, long-term illness, corticosteroids or malnutrition, and in some cases for osteoporosis and breast cancer. Methenolone is often used to promote weight gain, with Methenolone being less than normal and having no side effects.

One notable feature is that it binds firmly to androgen receptors, stronger than testosterone. This quality makes the original brown a good burner.

Methenolone does not convert to estradiol; So you can take it without the risk of estrogen side effects (gynecomastia, water retention).

Methenolone is one of the safest steroids on the market, so women, older athletes, and teenagers often find it the best way to improve their health and avoid side effects.

Overall, Methenolone, one of the safest anabolic steroids available on the market, is a relatively weak compound that takes time to show the best effects. If the drug is used for at least 10 weeks with other steroids, good results will be found.

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Oxandrolone (also known as Anavar) is believed to be a mild oral anabolic steroid. Oxandrolone was first introduced in 1962. Oxandrolone was designed to be as safe as possible for women and children. The same is true in clinical practice, with men, women, and children showing high tolerance. With extensive clinical success, Oxandrolone has been used to promote postoperative lean weight gain, trauma treatment, glucocorticoid disorders, bone mineral density in patients with osteoporosis, and slow development in childhood and adolescence. Welcome to buy Oxandrolone powder from

Oxandrolone is derived from DHT. It is designed to have very strong anabolic and androgen dissociation without significant estrogen or progesterone activity. Oxandrolone is classified as an anabolic steroid of c17-aa, but the effect is not extreme (Oxandrolone was administered at 20mg per day for 12 weeks and no significant effect on liver values was observed). Short-term and low Oxandrolone use does not significantly affect endogenous testosterone production. (the study showed that 80mg per day over 12 weeks inhibited endogenous testosterone production by only 67 percent.)

Most importantly, Oxandrolone increases the ability to retain nitrogen in muscles, reduces sex hormone-binding globulin (SHBG), and inhibits glucocorticoids. An increase in nitrogen retention promotes anabolic capacity, since lowering nitrogen retention levels usually results in catabolic states. A reduction in SHBG will produce higher levels of free testosterone in the body, promoting the free or unbound state of all circulating anabolic steroids. In short, it makes steroid use more effective.

Cortisol is the best known for glucocorticoid suppression. Such a hormone can promote the increase of fat, but also can destroy lean muscle tissue. Oxandrolone also boosts the number of red blood cells, which increases muscle endurance.

Some studies have even shown that Oxandrolone directly promotes fat breakdown. It is thought by many to bind firmly to androgen receptors, reduce the ability of thyroid-binding globulin, and increase the number of thyroxine-binding pro-endogenous proteins. This effect leads to greater utilization of the T3 hormone.

Oxandrolone has been described as a good agent for promoting strength and increasing muscle mass, although the mild nature of the compound makes it less desirable for bloating purposes. Among bodybuilders, the most commonly used is training during the cutting phase. Oxandrolone can be combined with synthetic metabolites such as Methenolone, Stanozolol, and Mesterolone to achieve a stronger, more defined appearance. This combination is very popular.

We cannot call Oxandrolone a very powerful anabolic steroid. However, we can call it a very beneficial anabolic steroid. When we consider its generally good tolerability, it makes it one of the most valuable anabolic steroids of all time. It’s critical that we understand Oxandrolone, know what it can do, and implement it into your plan to get it right.

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Proviron can actually enhance the activity of other steroids by replacing them with a free unbound state, leading to higher use of other steroids. In athletes, Proviron is used primarily to increase androgen levels during dieting or preparation for the competition, and as an anti-estrogen due to its intrinsic ability to antagonize aromatase. Welcome to buy Proviron powder from us.

History of Proviron

Schering developed testosterone in 1934, which is a very old drug for anabolic steroids. It was the first drug to be used in clinical practice to treat “hormone-related diseases”. Proviron has a long history of clinical efficacy and safety and is still widely used today. Men are generally prescribed for the treatment of physical and mental impairment caused by age and subnormal androgen levels, low sexual desire caused by inadequate androgen levels, hypogonadism, and infertility (Proviron improves sperm quality and quantity).

The use of Proviron as a fertility aid may be one of the most controversial indications for the drug. Because it is an effective androgen, it provides minimal inhibition of gonadotropin in normal therapeutic doses, not because it increases LH output. Lacking gonadotropin inhibition, drugs can supplement the androgens necessary for sperm production. Androgen is known to directly stimulate spermatogenesis and to influence sperm transport and maturation through its effects on the epididymis, tubular structures, and seminal vesicles. So the effects of these hormones are not completely inhibited. Proviron appears to have a uniquely positive effect on fertility in some men because its potential stimulation of sperm quantity and quality is not offset by gonadotropin suppression.

The structural characteristics of Proviron

Proviron is a modified form of DHT. The difference is that methyl groups are added to carbon 1, which helps protect the hormone from liver metabolism during oral administration. The same structural modification is also used in oral (methyl phenol) tablets. Alkylation at one site slowed liver metabolism during the first pass of the steroid, although it was much less significant than c-17 alkylation. Although overall bioavailability remains much lower than that of c-17 alpha-alkylated oral steroids, testosterone is resistant enough to achieve therapeutic beneficial blood levels. Proviron also has a very strong binding affinity for sex hormone-binding globulin.


Proviron is not aromatic and is not a measurable estrogen. Anti-estrogen is not required when using this steroid because the drug cannot induce breast development, water retention or other estrogen-related side effects in men.

Proviron is thought to act as an anti-aromatase in the body, preventing or slowing the conversion of steroids to estrogen. The results are somewhat similar to Arimidex, though not as profound. Proviron’s anti-estrogen properties are not unique, and many other steroids have been shown to have similar activity. Dromostanolone, for example, has been successfully used as a treatment for male breast development and breast cancer because of its strong androgen and potential anti-estrogen effect. Proviron can even reduce aromatase activity in peripheral tissues, where it is more resistant to estrogen conversion. The anti-estrogen effect of all these compounds may be caused by their ability to compete with other substrates to bind to aromatase. Because aromatase binds to steroids, it cannot be changed because it is temporarily blocked and does not interact with other hormones to achieve inhibition.


Proviron is classified as an androgen steroid. Androgen side effects are common with this substance, especially at higher doses. This can include oily skin, acne, and episodes of body/facial hair growth. Anabolic/steroids/may also aggravate male pattern hair loss. Women are also warned of the potential masculine effects of anabolic/steroid /. These can include deepening of the voice, irregular periods, changes in skin texture, facial hair growth, and enlargement of the clitoris.


Proviron is not c17-alpha alkylated and no hepatotoxic effects have been reported.


Anabolic steroids/may have harmful effects on serum cholesterol. This includes a tendency to lower HDL (good) cholesterol levels and increase LDL (bad) cholesterol levels, which may shift HDL in favor of a greater risk of atherosclerosis. The relative effects of anabolic/androgen steroids on serum lipids depend on the dose, route of administration (oral or injectable), type of steroid (aromatized or not), and level of resistance to liver metabolism. Proviron is an oral non-aromatic androgen and is expected to have significant negative effects on lipids.

To help reduce cardiovascular stress, it is recommended to maintain an active cardiovascular exercise program throughout active AAS administration and to minimize saturated fat, cholesterol, and simple carbohydrates. Supplementation with fish oil (4 grams per day) and natural cholesterol/antioxidant formula, such as Lipid Stabil or with a similar composition of products is also recommended.

Testosterone inhibition

Proviron has a very weak inhibitory effect on gonadotropin and serum testosterone. Studies have shown that no significant inhibition of testosterone levels occurs when given at moderate doses (150mg/d or less). With higher doses (300 mg/day or more), serum testosterone will be strongly inhibited.

Usage of Proviron

To treat androgen deficiency, Proviron is usually administered three times a day (25mg) at the beginning of treatment. The drug is then continued at a lower maintenance dose, which usually consists of taking one tablet (25mg) once or twice a day. A similar dose is used to support male fertility, usually in conjunction with other fertility drugs such as injectable FSH. The usual dose for male athletes is 50mg to 150mg of testosterone per day, or two to six 25mg tablets. Medications are usually administered in cycles of 6 to 12 weeks, which is usually enough time to notice the benefits of the medication.

While low estrogen and high androgen levels are ideal, many bodybuilders like to use Proviron during the diet or in preparation for competition. When these drugs are relatively low in androgen, this is particularly beneficial if synthetic metabolites such as Methenolone are used alone. Proviron can be used to regulate the ratio of androgens to estrogens, resulting in increased muscle stiffness and density, supporting sexual desire and general well-being and increasing the tendency to burn body fat. When used in combination with Nolvadex, usually 10-20mg per day, it prevents breast development in both men and women. Not recommended for women.

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Nandrolone Phenylpropionate is an injectable form of the anabolic steroid Nandrolone. The properties of this drug are very similar to those of Nandrolone Decanoate. The main difference between the two preparations is the rate at which nandrolone is released into the bloodstream. Nandrolone Decanoate provides about three weeks of Nandrolone release at the injection site, while Nandrolone Phenylpropionate provides only one week. So Nandrolone Decanoate can be given clinically every two or three weeks, while Nandrolone Phenylpropionate is given clinically once a week. On the other hand, the two drugs are actually interchangeable. Like Nandrolone Decanoate, drugs such as Phenylpropionate, which enable athletes and bodybuilders to increase muscle strength and lean muscle mass, are valuable and do not have significant estrogen or androgen side effects.


Nandrolone Phenylpropionate first appeared in 1957. It soon became a prescription drug marketed by the international pharmaceutical giant Organon (now Merck/MSD) under the brand name Nandrolone Phenylpropionate. When first introduced in the United States, Nandrolone Phenylpropionate was used for the retention of sperm quality before and after surgery, osteoporosis, advanced breast cancer, weight loss due to convalescence or disease, geriatric diseases (general weakness and weakness), burns, severe trauma, ulcers, anemia, and developmental retardation in children. In the 1970s, the FDA began to modify the use of the drug, and its use quickly declined significantly. After a while, the drug was used primarily to treat advanced metastatic breast cancer and as an adjunct therapy for postmenopausal osteoporosis in the elderly.

Nandrolone Phenylpropionate has been Organon’s focus for less than a decade. When Nandrolone Decanoate was introduced in the 1960s, drugs with short-term effects, such as Phenylpropionate, were still available but began to decline. At the time, Nandrolone Phenylpropionate had not been abandoned by Organon, in part because some countries had slightly different therapeutic USES and thus remained profitable for some time. As the anabolic steroid market continued to grow in the 1970s and 1980s, it caught the attention of other drug manufacturers, and many drug companies have begun to make their own Nandrolone Phenylpropionate. Today, however, the drug is almost non-existent. The current owners of Organon (Merck/MSD) will sell Nandrolone Phenylpropionate, which is nearing the end of production.


Nandrolone Phenylpropionate is circulating in some human drug markets. The composition and dosage may vary from country to country and manufacturer, but usually contains 25 mg/mL or 50 mg/mL of steroids dissolved in oil.

Structural features:

Nandrolone Phenylpropionate is a modified form of Nandrolone in which a carboxylate (Phenylpropionate) has been attached to a 17-beta-hydroxyl group. Esterified steroids have less polarity than free steroids and are absorbed more slowly in the injection area. Once in the blood, the ester is removed to produce a free (active) nandrolone. Esterified steroids are designed to extend the therapeutic window after administration, allowing less frequent injections than free (unesterified) steroids. Nandrolone Phenylpropionate peaked at release 24 to 48 hours after deep intramuscular injection and dropped to near baseline within a week.

Side effects (estrogen) 

Nandrolone’s estrogen conversion is low, estimated at about 20 percent of testosterone. This is because although the liver converts Nandrolone to estradiol, the estrogen-related side effects of nandrolone are much lower in other, more active, steroid-aromatizing sites, such as adipose tissue. However, elevated estrogen levels at high doses are still noticeable and can cause side effects such as increased hydration, body fat, and breast development in men. Anti-estrogens such as clomiphene or tamoxifen may be necessary to prevent the occurrence of estrogenic side effects. People can also use aromatase inhibitors, such as anastrozole, which control estrogen more effectively by preventing its synthesis. However, compared to anti-estrogen, aromatase inhibitors can be quite expensive and may have negative effects on blood lipids.

It is noteworthy that nandrolone has some progesterone activity in the body. Although progesterone is a c-19 steroid, the removal of this group produces a hormone with a greater binding affinity for its corresponding receptor. Because of this feature, many no-19-anabolic steroids have shown some affinity for progesterone receptors. Progesterone-related side effects are similar to estrogen, including negative feedback inhibition of testosterone and increased fat storage. Progesterone also increases estrogen’s role in stimulating breast tissue growth. There seems to be a strong synergy between the two hormones, so even without excessive estrogen levels, male breast development may even occur under the influence of progesterone. The use of anti-estrogen, which inhibits estrogen, is usually sufficient to reduce the risk of breast dysplasia in men caused by nandrolone.

Side effects (androgen) 

Although classified as anabolic steroids, the substance may still have androgenic side effects, especially at higher doses. These side effects may include oily skin, acne, and episodes of body/facial hair growth. Anabolic/androgen steroids may also aggravate male hair loss. Women are also warned of the potential pathogenic effects of anabolic/androgen steroids. These may include deepening of the voice, irregular periods, changes in skin texture, facial hair growth and clitoral enlargement. Norone is a steroid with relatively low androgen activity relative to its tissue-building effects, so the threshold for androgen side effects is quite high compared to androgen drugs such as testosterone, methyltestosterone. It’s also important to point out that because of its mild androgen properties and ability to suppress endogenous testosterone, nandrolone tends to interfere with sexual desire in males when not using another androgen.

Note that in androgen responsive target tissues such as skin, scalp, and prostate, the relative masculinity of nandrolone is reduced by reduction to DHN. 5- alpha reductase is the main cause of this metabolism. Concurrent use of 5-alpha reductase inhibitors such as finasteride or rasterize interfered with the site-specific effects of nandrolone significantly increasing its tendency to produce androgenic side effects. If low androgen sex is required, use of nandrolone should avoid reductase inhibitors.

Side effects (hepatotoxicity) 

Norone is not c-17 alpha alkylation and does not have hepatotoxic effects. So hepatotoxicity is unlikely.

Side effects (cardiovascular) 

Anabolic/androgen steroids may have harmful effects on serum cholesterol. This includes the tendency to lower HDL (good) cholesterol levels and increase LDL (bad) cholesterol levels, which may convert HDL to LDL, leading to a greater risk of atherosclerosis. The relative effects of anabolic/androgen steroids on serum lipids depend on the dose, the method of administration (oral versus injection), the type of steroid (aromatized or not), and the level of resistance to liver metabolism. Weekly administration of 600mg Deca for 10 weeks showed a 26% reduction in HDL cholesterol levels. This inhibitory effect is slightly higher than that reported by using the same dose of actor Enanthate, which is consistent with earlier research results that Deca has a stronger negative effect on HDL/LDL ratio compared with actor Propionate. The effect of nandrolone on serum lipids was significantly weaker than that of c-17 alpha alkylated. Anabolic/androgen steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and lead to left ventricular hypertrophy, which may increase the risk of cardiovascular disease and myocardial infarction.

To help reduce cardiovascular stress, it is recommended to maintain an active cardiovascular exercise program and to consistently minimize saturated fat, cholesterol, and simple carbohydrates throughout the use of AAS. Also suggested supplementation with fish oil (4 grams per day) and natural cholesterol/antioxidant formula such as Lipid Stabil or products with a similar component.

Side effects (testosterone suppression) :

All anabolic/androgen steroids are expected to inhibit endogenous testosterone production when taken at doses sufficient to promote muscle gain. Studies on 100mg Nandrolone Phenylpropionate have shown that serum testosterone can be rapidly suppressed by a single injection. Testosterone levels dropped to 30% of their initial level on day 3 and remained there for about 13 days. Frequent use can significantly prolong the endogenous hormone recovery window. It is thought that the progestational activity of norone significantly facilitates the inhibition of testosterone synthesis during treatment. Without intervention from testosterone stimulants, testosterone levels should return to normal within 2-6 months of drug disruption. Note that hypogonadism may be secondary to steroid abuse, requiring medical intervention.

In addition to these side effects, for a more detailed discussion of potential side effects, see the steroid side effects section of this book.

Use (male) 

For general anabolic effects, early prescribing guidelines recommend a dose of 25 to 50 mg per week for 12 weeks. Doses commonly used for physical or performance enhancement purposes range from 200 to 400mg per week and are administered over a period of 8 to 12 weeks. This level is enough for most users to see a measurable gain in lean muscle mass and strength. Note that because of the rapidity of phenylpropionate, the weekly dose is usually divided into two doses.

Use (women) 

For general anabolic effects, early prescribing guidelines recommend a dose of 25 to 50 mg per week for 12 weeks. When used for physical or performance enhancement purposes, a dose of 50mg per week (single weekly injection) is the most common, lasting 4 to 6 weeks. Higher doses or longer duration of use are not recommended due to potential androgen side effects. Although only mildly androgenic, women occasionally face viral symptoms when taking the compound. If side effects occur, immediately discontinue phenylpropionate to prevent permanent side effects.