The chemical name of Stanozolol is 17-methyl-2′ H -5(alpha)-androst-2-eno [3,2- c  ]pyrazol-17(beta)-ol and it has the molecular weight of 344.5392 g/mol at the base. The anabolic-androgenic ratio of this steroid compound is 320:30 and it has the molecular formula of C22H36N2O. The active life of oral Winstrol is 8-9 hours, while the active life of injectable Winstrol is 36-48 hours. The active ingredient of Winstrol tablets is 2 mg of stanozolol and inactive ingredients include Dibasic Calcium Phosphate, D&C Red #28, FD&C Red #40, Lactose, Magnesium Stearate, and Starch.

It is generally believed that the injectable version of Winny is superior to oral version in the context of nitrogen retention, which means that injectable Winstrol users enjoy preservation and buildup of lean body mass in a better way than oral Winstrol users. Moreover, injectable Winstrol negates the first pass of the compound to pass easily through the liver and is less toxic. However, the injectable version may cause pain at the injection site when administered. Injectable Winstrol can be taken orally as well because of unique structure of the compound.

One of the biggest benefits of Winstrol is that users admiring it can expect a dry look to physique if the body fat is relatively low. Commonly used as a cutting cycle drug, Stanozolol has the unique potential of improving nitrogen retention and protein synthesis to a significant extent. Use of this performance enhancing drug is also associated with strengthened tendons and ligaments. Winny has a significant effect on sex hormone-binding globulin levels in the body and can temporarily prevent steroid hormones from exerting their activities, primarily because of its plasma-binding characteristics. By doing this, Winstrol leads to an improved percentage of free testosterone circulating in the body that may further enhance the potency of concurrently used anabolic steroids.

Classified as a controlled substance under the Anabolic Steroids Control Act of 1990 and assigned to Schedule III, Winstrol can reduce the level of high-density lipoproteins and raise the level of low-density lipoproteins. Winny use is associated with increased low-density lipoproteins and decreased high-density lipoproteins and effective in controlling the frequency and severity of attacks of angioedema and in increasing serum levels of C1 INH and C4. Winstrol effects on improving serum levels of C1 INH and C4 are attributed to an increase in protein anabolism.

The weight and fat loss drug is popular with women and beginners as well because of its anabolic nature and very few androgenic side effects. When used in doses of 25-100 mg per day by men and 5-15 mg per day by women, Winstrol can lead to dramatic gains and the best part is that these gains are nearly permanent. Use of this performance enhancing drug should not be made for a period exceeding six weeks at a stretch. In case the duration has to be extended, users should emphasize on monitoring the liver values through blood tests to avoid permanent damage.

When abused or of a low grade, Winstrol may lead to side effects such as elevated liver values, liver toxicity, negative effects on cholesterol levels, acne, prostate enlargement, aggravation of male pattern baldness, deepening of the voice, body/facial hair growth, and enlargement of the clitoris. Medically, this anabolic steroid is recommended prophylactically to decrease the frequency and severity of attacks of angioedema.

The abuse of Winstrol may cause increased bromsulphalein (BSP) retention, and increases in serum bilirubin, glutamic oxaloacetic transaminase (SGOT), and alkaline phosphatase. Winstrol abuse may even lead to cholestatic jaundice with, rarely, hepatic necrosis and death. It may even cause inhibition of testicular function, testicular atrophy and oligospermia, impotence, chronic priapism, epididymitis and bladder irritability, edema, retention of serum electrolytes (sodium, chloride, potassium, phosphate, and calcium).

Use of this anabolic steroid and performance enhancing drug is not recommended to females with breast cancer and hypercalcemia, male patients with breast cancer or those examined for or suffering from prostate cancer. The drug is not recommended to pregnant or lactating women or those who may get pregnant while using Winstrol. It is also not advised to children or those having allergy to Stanozolol or its ingredients. Medical advice should be sought immediately if side effects such as abdominal pain, light colored stools, dark colored urine, unusual fatigue, nausea or vomiting, or yellowing of the skin or eyes are experienced as these may be early signs of liver complications. Use of Winstrol is not recommended to those suffering from health problems like testicular atrophy, testicular cancer, prostate cancer, breast cancer, liver damage, kidney damage, stroke, high blood pressure, and respiratory problems. Stanozolol abuse may even lead to health complications such as increased or decreased libido, habituation, excitation, insomnia, depression, bleeding in patients on concomitant anticoagulant therapy, premature closure of epiphyses in children, nausea, vomiting, and diarrhea.

Men using this steroid may even experience coughs, insomnia, night sweats and cardiac irregularities. Two dosages of Winstrol should not be taken together at the same time, even if the first dose was missed accidentally. In case the first Winstrol dosage was missed, it should be skipped and the next dose should be taken at the scheduled time.

In case of expired Winstrol tablets or if the tablets or injections are not to be used any more, the same should be discarded after having consulting a pharmacist or local waste disposal company on how to safely discard Winstrol. It is highly recommended that Winstrol should not be flushed down the toilet or poured into a drain, unless specifically recommended by a qualified authority. Winstrol tablets or injections should be properly discarded, when expired or no longer needed. Winstrol must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and kept away from unauthorized use, pets, sunlight, moisture, heat, sources of ignition, and children.

The chemical name of Trenbolone is 17β-Hydroxyestra-4, 9, 11-trien-3-one and it has a half life of nearly 2-3 days. The molecular weight of Tren is 270.37 g/mol at the base and its molecular formula is C18H22O2.

It is believed by many sportsmen that use of Trenbolone is associated with dramatic increases in terms of body mass, more effectively than with weight training alone. Classified as a Schedule II drug by the DEA, Trenbolone has a binding affinity for the androgen receptor five times as high as that of testosterone. Use of Tren is also associated with an increase in nitrogen uptake by muscles, which further translates into improvements in the rate of protein synthesis, which stimulates appetite and reduces the rate of catabolism. Trenbolone use is also associated with an increase in male secondary sex characteristics, without the requirement to convert to DHT. The steroid leaves the body as beta-glucuronides or sulfates as Tren as well as 17epi-trenbolone are both excreted in urine. If that was not all, this steroid can enhance “feed efficiency” in quick time and without leading to side effects. This means that Tren users can expect efficient processing and use of food while reaping the complete benefits of ingested vitamins and minerals at a very high rate.

The difference between trenbolone acetate and trenbolone enanthate lies in the esters. While the acetate version has two esters, the enanthate version has seven esters attached to it. Moreover, the esters of trenbolone acetate are more potent than trenbolone enanthate when compared milligram to milligram.

Trenbolone Acetate (Finaplix)

Trenbolone Acetate or Finaplix is one of the best anabolic steroids and muscle-building compounds. Also known as Finaject and Finajet, Trenbolone acetate is required to be administered frequently because of its short life. One of the biggest reasons why this performance enhancing drug is popular among sportsmen is because it does not lead to estrogen formation and therefore can even be used by sportsmen and others who are prone to excess estrogen formation.

It has the molecular formula of C20H24O3 and has an anabolic-androgenic ratio of 500:500. It has an active life of 2-3 days and has the molecular weight of 270.3706 g/mol at the base.

With strong androgenic properties and no estrogenic activity, it is a 19-nor steroid and derived from the compound nandrolone. The difference between trenbolone acetate and nandrolone are the C9 and C11 double bonds. The reason Tren does not have estrogenic activity is because of the C9-10 double bond, which is important for aromatization of the A ring to be possible and no aromatization can happen by occupying this bond.

The anabolic steroid can have effects on muscle growth in limitless ways, which is what makes it one of the best drugs for maintaining as well as adding quality muscle mass. Moreover, Tren has the potential of significantly enhancing the IGF-1 levels that promote muscle satellite cells, which are important to repair damaged muscle fibers. Use of this steroid is also associated with a significant enhancement in the context of the amount of DNA per muscle cell.

The ideal dose of Tren acetate is 50-150 mg every day for men and the steroid is not usually recommended to girls and women. It is best to use Bromocriptine, Vitamin B6, or Cabergoline with Tren acetate to control prolactin levels while Letrozole may be used for reducing lower progesterone levels. Since use of Tren acetate may reduce thyroid levels to increase prolactin levels, use of the compound T3 is highly recommended.

Trenbolone Enanthate

Due to the androgenic nature of trenbolone enanthate, sportsmen and others can expect dramatic enhancements in terms of muscle mass, nitrogen retention, protein synthesis, muscle function, and body strength. These benefits make Tren enanthate a popular drug with strength athletes and those into body building. The steroid can be made a part of both a bulking steroid cycle as well as a cutting steroid cycle. Since the steroid has a strong cortisol-reducing effect along with the ability to bind to the glucocorticoid receptor, it can quickly and smoothly lead to the reduction of body fat.

The active metabolite of Tren, 17beta-trenbolone has a binding affinity to the progesterone receptor (PgR), which is actually greater than progesterone itself but Letrozole use can be made to prevent this side effect. Trenbolone users are always advised to keep a close check on their cholesterol levels, liver enzymes, and kidney function as the steroid could negatively influence all of these functions.

The recommended dose of Trenbolone enanthate is 300-600 mg every week for men; the steroid is not indicated to girls and women, especially pregnant or lactating women or those who may get pregnant while using Tren.

Oral trenbolone

Oral Trenbolone shows almost no binding for sex-hormone binding proteins that makes it an extremely good choice in androgen receptor studies. This is because Oral Tren would demonstrate equal binding in all tissues irrespective of the amount and presence of the proteins, which makes it a good choice as far as supposed binding capacity, is concerned. However, use of oral trenbolone may lead to liver toxicity in some cases and therefore the use of Milk Thistle is recommended. Moreover, users of oral Tren are advised to consume seven to nine glasses of water every day.

The steroid is extremely anabolic since compounds are able to activate the mechanisms of anabolics dependent upon the androgen receptors, which is one of the many ways in which muscle growth is facilitated through anabolic steroids and performance enhancing drugs. This steroid is admired globally for its anti-catabolic abilities and inhibiting cortisol and some other catabolic hormones in the body.

The abuse of Trenbolone can lead to side effects such as deepening of the voice, body/facial hair growth, clitoris enlargement, male pattern baldness, oily skin, acne, prostate enlargement, water retention, breast growth and lactation in men, anxiety, increased aggression, and complications of kidney and liver function.

The primary male sex hormone, testosterone, is produced naturally in males and required for promoting growth and maintenance of male sexual characteristics. However, the level of naturally-producing testosterone may decline with passing age and this is where derivatives of the hormone (such as testosterone cypionate, testosterone enanthate, testosterone phenylpropionate, testosterone propionate, and testosterone suspension) come into the picture.

It is worthwhile to note that testosterone is also important to promote the development of prostate and seminal vesicles besides promoting deepening of the voice, widened shoulders, rib cage expansion, growth of chest and facial hair, reductions in subcutaneous fat, and growth of spermatogenesis tissue in testes. The natural production of testosterone may decline because of chronic kidney failure, genetic abnormalities, pituitary gland dysfunction, radiation treatment for cancer, inflammatory diseases, drugs for treating prostate cancer and corticosteroid drugs, and alcoholism.

By using testosterone derivatives, men with low testosterone levels can expect reduced risk of dementia and improvements in terms of blood sugar control, energy levels, sexual function, and muscle mass.

Testosterone Enanthate: This derivative of testosterone is commonly used by sportsmen to deliver dramatic on-field performances and benefit from improved muscle mass, muscle function, body strength, and muscle size. The anabolic steroid is equally effective in recovering quickly from extreme body building and intense workouts. In addition to this, testosterone enanthate is also beneficial in improving the count of red blood cells and promoting protein synthesis and nitrogen retention. The recommended dose of testosterone enanthate is 250-500 mg per week when administered in an intramuscular way through a 22-23 gauge needle with a 1 or 2ml syringe. This steroid is generally stacked with Anavar, Clenbuterol, Dianabol, Deca Durabolin, Equipoise, and Primobolan. Abuse of testosterone enanthate can lead to side effects, including painful penile erections, vomiting, nausea, increased serum cholesterol, irregular menstrual cycles, and virilizing effects.

Testosterone Propionate: Considered to be one of the most popular derivatives of testosterone, testosterone propionate is highly popular among professional cyclists, body builders, power lifters, athletes, and MMA fighters. It has an active life of two to three days and the levels of water based gains and water retention on a testosterone propionate cycle are lower compared to that of the enanthate or cypionate versions of testosterone. Use of this anabolic steroid is related to a slight increase in red blood cell count and oxygen carrying capacity of the body. It is also used by sportsmen to lose body fat and gain muscle mass at the same time. The recommended dosage of testosterone propionate is 500 mg per week when administered intramuscularly via a 22-23 gauge needle with a 1 or 2ml syringe usually about 1″ length. The steroid is commonly stacked with Anadrol, Deca Durabolin, Dianabol, and Equipoise. Abuse of the steroid can lead to side effects like headache, anxiety, depression, painful penile erections, hair loss, oily skin, and jaundice.

Testosterone Cypionate: The anabolic steroid and derivative of testosterone, the male sex hormone, is recommended by practitioners for treating deficiency of endogenous testosterone. The steroid is best used in doses of 200-1000 mg by first-time users and 500-1000 mg weekly by regular steroid users. Common injection sites for administering intramuscular testosterone cypionate injections are dorsogluteal site (buttock), ventrogluteal part of the gluteus, deltoid (shoulder), hands and muscle (arms), or pectorals (chest region). It is classified as the oil-soluble 17β-cyclopentylpropionate ester of the androgenic hormone (testosterone). Its chemical name is androst-4-en-3-one, 17-(3-cyclopentyl-1-oxopropoxy)-, (17β)- and the molecular weight is 412.61 and its molecular formula is C27H40O3. It has an anabolic/androgenic ratio of 100:100 and best used for promoting performance, strength, stamina, muscle mass, and muscle definition improvements. Testosterone cypionate abuse may lead to side effects such as acne, change in sex drive, irritation, gum pain, hair loss, and headache.

Testosterone Suspension: Considered to be one of the best anabolic steroids and testosterone compounds, testosterone suspension is best admired by sportsmen for promoting new muscle tissues and repair broken muscle tissues in as short as six to eight weeks. With no connected esters and an active life of two to three days, this derivative of the primary male sex hormone is one of the best drugs for promotion of IGF-1 (insulin like growth factor-1) and red blood cells. It has the molecular bodyweight of 288.429 g/mol at the base and its molecular formula is C27H40O3. This testosterone derivative is also useful in promoting nitrogen storage and protein synthesis besides securing muscle tissue against catabolic (muscle wasting) glucocorticoid testosterone that is employed by the body for maintenance of the ability of homeostasis in the wake of variations in regards to weather and outside environment. The ideal dose of this steroid for men is 350-1000 mg per week in oral form and 50-100 mg per day in injectable form. The testosterone compound is generally stacked with Equipoise and Deca Durabolin during a bulking cycle and abuse of this steroid can cause side effects such as acne, greasy skin, liquid storage, and gynecomastia. The steroid is not indicated to pregnant and lactating women and children.

Testosterone Phenylpropionate: This derivative of testosterone, the male sex hormone, has an active life of nearly 4-5 weeks and its release time is 1-3 weeks. The long-acting anabolic is best admired for its unique ability to dramatically improve immunity, growth and development of male sexual organs, energy, endurance, and maintenance of secondary sexual characteristics. In addition to this, Testosterone Phenylpropionate is also admired for promoting weight loss and protecting the body against heart diseases and improving the levels of protein synthesis and nitrogen retention. The recommended dose of this anabolic steroid for men is 350-1000 mg per week for a period of six to eight weeks. It is highly recommended that users of the steroid should consume at least eight to ten glasses of water for preventing dehydration and balance out the water ratio. When abused, Testosterone Phenylpropionate can cause fluid retention, gynecomastia, hair loss, and enlarged prostate. Pregnant and breastfeeding women or those suffering from prostate or breast cancer or liver dysfunction and heart ailments and children should avoid using this steroid.

The molecular formula of Sustanon is C19H28O2 and it can be detected over a period of 2-3 months. It has the chemical name of 17ß-hydroxyandrost-4-en-3-one and an active life of approximately 2-3 weeks. A blend of four components of testosterone–testosterone propionate 30 mg, testosterone decanoate 100 mg, testosterone phenylpropionate 60 mg, and testosterone isocaproate 60 mg (the total amount of testosterone per mL is 176mg); It includes 100 mg benzyl alcohol per mL solution and should never be given to premature babies or neonates.

Sustanon is useful in developing and maintaining reproductive tissues such as prostate, epididymis, seminal vesicles, testes, and penis even at low dosages. Each of the four compounds of testosterone is released gradually at different time intervals and reacts in a very positive manner together. This means that users admiring the anabolic steroids are relieved from pain at injection sites and the associated swelling. Medically, Sustanon 250 is recommended to patients opting for testosterone replacement therapy and treating medical complications wherein oxygen carrying capacity of the body is to be enhanced. Sportsmen admire this drug for its unique abilities to promote muscle function, muscle size, body strength, protein synthesis, performance, stamina, red blood cell production, and nitrogen retention besides promoting the count of red blood cells and well being. It is medically recommended to treat hypogonadal men and helps them by improving plasma concentrations of testosterone, dihydrotestosterone, oestradiol (estrogen hormone), and androstenedione.

Sustanon use is also associated with decrease of SHBG (sex hormone binding globulin). With use of the steroid, the levels of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) are restored to the normal range and hypogonadal men get benefited through improvement of testosterone deficiency symptoms and administration of the steroid is also associated with dramatic increases in terms of lean body mass and bone mineral density and reductions in the level of body fat mass. If that was not all, Sustanon users also report improvements in the level of sexual function, such as libido and erectile function. Male users also report reductions in serum LDL-C, HDL-C, and triglycerides besides experiencing improvements in levels of hemoglobin and Hematocrit, with no reported clinically relevant changes in liver enzymes and PSA.

One of the biggest advantages of this anabolic steroid is that its use does not cause formation of excess estrogens, which means that it can even be used by those having a history of excess estrogen formation after using anabolic steroids and performance enhancing drugs, especially harsh and aromatizable drugs. A single dose of the anabolic steroid results in an increase of total plasma testosterone with peak levels of approximately 70 nmol/l (Cmax) that are reached nearly 24-48hrs (tmax) after administration. On the other hand, plasma testosterone levels return to the lower limit of the normal range in males in nearly three weeks.

The recommended dose of Sustanon is 250 mg per week though some sportsmen even use this steroid in doses of 1000 mg per week. It should be administered by deep intramuscular injection. This anabolic compound is generally stacked with Anadrol, Trenbolone, and Winstrol or with Growth Hormone or Thyroxin during an anabolic steroid cycle of six to eight weeks. A post cycle therapy with Clomiphene, Tamoxifen, or Arimidex is highly recommended to restore the natural production of hormones. The elimination of Sustanon 250 usually takes place through the urine as conjugates of etiocholanolone and androsterone.

Sustanon doses should be adjusted after medical approval if the user is also being administered with enzyme-inducing agents or enzyme-inhibiting drugs as that may decrease or increase testosterone levels.

The steroid is not indicated to pregnant or lactating women or those who may become pregnant while using Sustanon. It is also not suggested to those with breast or prostate cancer or having an existing allergy to Sustanon’s active ingredient or any of its excipients, including arachis oil and should not be used by those allergic to soya or peanuts.

The abuse of Sustanon may cause fluid retention, hypertension, nausea, acne, gynecomastia, prostatic disorder, priapism (prolonged and painful erections), polycythemia, myalgia, pruritus, Depression, nervousness, mood disturbances, libido increase, and reduced libido. Sustanon 250 abuse may even cause migraine, epilepsy, high blood pressure, hypercalcaemia, depression, hair loss, impotency, testicular atrophy, kidney disorders, or heart problems. Long-term abuse of the steroid may result in health complications such as infertility, reduced sperm count, oily skin, acne, heart damage, fluid retention, shrinking of the testicles, and increased risk for breast and prostate cancer. When used or abused by women, it may cause virilization, harm to the fetus, clitoral enlargement, growth and development of male secondary sexual characteristics, and oily skin.

It is also contraindicated to people suffering with medical complications such as kidney disorders, migraine, epilepsy, high blood pressure, hypercalcaemia, or heart problems.

Sustanon is a prescription drug and should only be bought with a medical prescription though it can be purchased online with or without a prescription in different forms such as capsules, tablets, syrups, and injections. However, the significance of medical advice and prescription should never be disputed or neglected or delayed at any point of time.

Sustanon must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and kept away from unauthorized use, pets, sunlight, moisture, and children. It should not be refrigerated or freezed and must preferably be stored in the original package. In case of expired Sustanon tablets or if the tablets or injections are not to be used any more, the same should be discarded after having a word with a pharmacist or local waste disposal company on how to safely discard Sustanon. It is highly recommended that Sustanon should not be flushed down the toilet or poured into a drain, unless specifically recommended by a qualified authority. Sustanon tablets or injections should be properly discarded when it is expired or no longer needed.

Originally developed as a drug for treating depression in men, Proviron or Mesterolone is an orally applicable androgen and derivative of Dihydrotestosterone (DHT). The IUPAC name of Proviron is 1 alpha-methyl-17 beta-hydroxy-5 alpha-androstan-3-one and the molecular mass of this prescription drug is 304.467 g/mol at the base. It has the molecular formula of C20H32O2 and has an active life of eight to twelve hours though its effects can be experienced up to 24 hours. The drug has an anabolic-androgenic ratio of 100-150: 30-40 and can be detected over a period of 5-6 weeks.

One of the biggest advantages associated with use of Proviron is its unique ability to promote the count and quality of sperm and is also indicated to treat serious wellness problems such as low libido and erectile malfunction. The drug is even recommended to male patients struggling with impotency or lack of testosterone. In addition to these advantages, use of Mesterolone is also associated with improved release of luteinizing hormone and follicle-stimulating hormone for stimulating testes so that more testosterone can be produced.

Since it is not a 17 alpha alkylated compound, it can be used for a long period of time. The drug can even enhance potency of testosterone when used in an anabolic steroid cycle with it. The fact that Proviron can attach itself to SHBG (sex hormone-binding globulin) and albumin means that a large percentage of testosterone (free) is made available to conduct anabolic actions. Furthermore, the performance enhancing drug can also be used as an anti-aromatase and this characteristic proves to be beneficial when the drug is stacked with other anabolic steroids and performance enhancing drugs that may convert to estrogen to some extent. Since this steroid can bind to the aromatase enzyme, it does not allow steroids that are made a part of the cycle (with Proviron) to interact with enzymes and lead to formation of estrogens. Some sportsmen even use Mesterolone in an anabolic steroid cycle in place of testosterone that can have a negative effect on the libido since Proviron can enhance the level of libido to some extent because of the dihydrotestosterone effects of Mesterolone. A combined therapy with gonadotrophic hormone exhibiting follicle-stimulating hormone activity may be advised for initiating treatment and treatment with Proviron may be repeated after an interval of several weeks.

It is important to note that use of Proviron is meant only for male patients though a medical practitioner may recommend its use to some female patients. When advised, individuals administered with it should undergo regular prostate examinations prophylactically.

The increased level of free testosterone can then be utilized by the body for promoting protein synthesis that in turn stimulates muscle gain. Moreover, the steroid also has the ability to reduce the amount of free estrogen in the body by minimizing estrogen receptors’ ability to bind to estrogen. The drug is medically recommended to individuals suffering with potency disturbances due to androgen-deficiency, easy fatigability, lack of concentration, weak memory, disturbances of libido, depressive moods, general vegetative complaints, irritability, and declining physical activity and mental alertness in middle- and old-aged men. It may even be indicated for promoting the development of secondary male sex characteristics in cases of prepuberal hypogonadism and increasing fructose concentration up to normal values to enhance the chances of procreation.

The ideal dose of Mesterolone is 25-100 mg per day for men and 25 mg every day for women though some sportsmen, male as well as female, increase the doses to 50-125 mg every day and 40-60 mg per day, respectively.  Tablets of Proviron should not be chewed and must always be swallowed with a full glass of water.

Medical advice should always be sought before you use or purchase the drug, especially if you are suffering from heart complications, epilepsy, diabetes, porphyria (a rare metabolizing disorder), migraine, impaired kidney function, or high blood pressure. The drug should not be taken by users suffering from previous or existing liver tumor or high blood calcium levels. Few drugs (such as Phenytoin and Phenobarbital) may interfere with the absorption of Proviron and Proviron may interfere with absorption of drugs like Thyroxine, Anti-diabetics, Cyclosporine, and Anticoagulants like warfarin.

Overdosing or abuse of this drug can lead to health complications such as oily skin, acne, exacerbation of male pattern baldness, growth of body/facial hair, deepening of the voice, and menstrual irregularities. The use of Mesterolone is not recommended to patients with carcinoma of the prostate or those who are undergoing androgen therapy of any kind, including the use of Proviron. In case a dose of this drug has been missed and it is almost time for the next dose, the first dose should be ignored and the next dose should be taken at the designated time. Under no circumstances, two doses of the drug should be taken together for the dose that was missed. Medical advice should be sought without any delay and use of Proviron should be stopped immediately if side effects such as pain in liver area, headache, loss of appetite, depression, unexplained weight loss, aggression, symptoms of an enlarged prostate (change in urination), acne, or hirsutism are experienced.

The tablets of Proviron should be kept in the original packaging unless it is time to use them. The tablets should be stored in a cool, dry place and they should never be stored in the bathroom or car. Mesterolone is also not be to be pregnant and lactating women or women who may get pregnant while using the drug and those suffering from liver, kidney, and heart complications or having an existing allergy to the drug or any of its ingredients. It must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and kept away from unauthorized use, pets, sunlight, moisture, and children.

Primobolan has the chemical name of 17ß-hydroxy-1-methyl-5a-androst-1-en-3-one acetate and its anabolic/androgenic ratio is 88:44-57. The molecular weight of Primobolan is 344.488 g/mol at the base and its molecular formula is C22H32O3. The active life of oral Primobolan is 4-6 hours and active life of liquid (injectable) Primobolan is 10-14 days. This steroid can be detected over a period of 4-5 weeks and its anabolic/androgenic ratio is 88:44-57. It is available both as an injectable (enanthate) and oral (acetate).

The steroid is a long acting anabolic with mild anabolic effects and extremely low androgenic properties. Its potency is considered slightly lower than Deca Durabolin, on a milligram for milligram basis. The injectable version of Primo has a long ester attached to it, which facilitates slow absorption of the active Methenolone compound while offering steady blood concentrations. The steroid is best used during a cutting cycle (in oral or injectable form) for maintaining muscles while the users are on a low-calorie diet. This dihydrotestosterone (DHT) based anabolic steroid is mostly admired by people who are very susceptible to side effects of estrogens such as oily skin, acne, gynecomastia, and bloating. The steroid is not 17-alpha-alkylated but 1-methylated for oral bioavailability and is considered to be one of the safest anabolic steroids. This steroid is commonly used between anabolic steroid cycles during “off-time” for maintaining muscle mass and body strength gains.

Since this rare androgen-based steroid is a mild steroid, it can be used by women as well as beginners. The use of Primo, even at high doses, does not lead to formation of excess estrogens and the steroid is medically recommended to reduce breast tumors. The anabolic steroid is also advised to HIV/AIDS patients as it has the potential of enhancing immunity of the body to a significant extent. Sportsmen, especially those into body building and weight-related sports, use it for gaining and maintaining lean tissue.

The drug causes less inhibition than Testosterone or Deca Durabolin in the context of anabolic effects, due to lack of conversion to DHT, low CNS activity, and lack of aromatization to estrogen. Moreover, Primo is not metabolically deactivated by 5a-reductase.

One of the biggest advantages associated with use of Primo is that it does not lead to aromatization like other performance improving drugs. Moreover, the anabolic steroid is one of the best drugs to reduce female estrogen and androgenic DHT levels. In addition to this, Primo use is also associated with significant improvements in terms of active and total testosterone by promoting sex hormone-binding globulin (SHBG) and luteinizing hormone (LH). Furthermore, gains made with Methenolone are smooth and nearly permanent rather than fast but short-term in nature.

Since use of Methenolone is not related to interferences in the context of endogenous testosterone as much as injectable nandrolone or testosterone, sportsmen admiring it can be relieved of estrogenic side effects like oily skin, acne, and gynecomastia as the steroid is not converted into estrogen and is low in androgens. Moreover, this steroid is extremely potent in nature and can be easily purchased online with just a few clicks using secured payment options like VISA and MasterCard debit and credit cards. Well-known for its comparative safety and low incidence of side effects, Primobolan is best admired for its potential of helping users preserve muscle mass while losing body fat.

Usually, the recommended dose of legal Primobolan is 200-400 mg/week for men and 50-100 mg/week for women and the dosages can be taken with or without meals. The ideal dose of Primo tablets for men is 50-100 mg every day and 10-25 mg every day for women while the dose of injectable Primo is 350-650 mg every week for men and 100 mg every week for women. The anabolic steroid is commonly stacked with Deca Durabolin, Testosterone, Dianabol, Clenbuterol, T3, and Anadrol and is also used by some sportsmen with Sustanon 250 for bulking cycles though most sportsmen use Primo for cutting cycles.

The drug is not recommended to those suffering from health complications such as testicular atrophy, testicular cancer, prostate cancer, breast cancer, liver damage, kidney damage, stroke, high blood pressure, and respiratory problems. It is also not suggested to pregnant and lactating women or women who may get pregnant while using Primo. The steroid is also not suggested to children or those having an existing allergy to Primobolan or any of its active or inactive ingredients. Individuals making use of drugs such as Prasterone, Tamoxifen, DHEA, and Androstenedione should avoid using Primobolan unless the same is specifically approved by a qualified medical practitioner. Furthermore, two dosages of the drug cannot be taken together at the same time, even if the first dose was missed accidentally. In case the first dose was missed, it should be skipped and the next dosage should be taken at the scheduled time.

In order to ensure that you do not abuse Primobolan, it is best to buy it after getting a medical prescription (after complete evaluation of medical reports and history) and the purchase should always be made from a reputed steroid store or pharmacy.

Primobolan must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and kept away from unauthorized use, pets, sunlight, moisture, and children. In case of expired Primobolan tablets or if the tablets or injections are not to be used any more, the same should be discarded after having a word with a pharmacist or local waste disposal company on how to safely discard Primobolan. It is highly recommended that Primobolan should not be flushed down the toilet or poured into a drain, unless specifically recommended by a qualified authority. Primobolan tablets or injections should be properly discarded when it is expired or no longer needed.

One of the biggest advantages of Parabolan is that it binds well to the androgen receptors, which makes it easy for sportsmen using it to benefit from lean hard muscles and a rapid gain in terms of body strength and muscle mass. The fast acting and long lasting steroid is commonly used as a pre-contest drug and is one of the best fat burning drugs. If that was not all, Parabolan use is as effective for a bulking steroid cycle as it is for a cutting steroid cycle. Since it binds strongly with glucocorticoid receptor, it is helpful in promoting catabolism that is the process of protein conversion into muscles. Use of this steroid is also associated with avoiding possible overtraining symptoms and gaining a lean appearance with refined muscle tissue and performance improvements.

Users can also expect no water retention or storage of extra fat in subcutaneous tissues after using this steroid and gain leaner, more refined, and much-harder muscles with Parabolan than with other anabolic steroids and performance enhancing drugs. Moreover, users of this steroid are relieved from concerns related to systemic problems such as hypertension because of an increase in fluid volume and atherosclerosis (because of fat deposition).

The chemical name of Parabolan is 17beta-Hydroxyestra-4, 9, 11-trien-3-one and its molecular formula is C20H242O. It has an active life of 5-7 days and can be detected for 4-5 weeks.

Furthermore, Parabolan has the unique potential of making nutritional partitioning possible and users can expect conversion of food to muscles and not to fat. This potent anabolic androgenic steroid is a progestin and binds strongly to the female hormone progesterone. It is a part of the Trenbolone family and derived from 19-Nor-Testosterone. Use of this anabolic steroid is also related to enhancements in terms of IGF-1 and an increase in the satellite cells that are beneficial for repairing damage muscle tissue. The steroid is also admired by budding as well as professional sportsmen since it can enhance regenerative properties of muscle tissues via inhibition of protein mobilization and muscle breakdown in gluconeogenesis, which means that users of this anabolic steroid can expect promotes extra skeletal muscle gains leading to dramatic physical strength gains.

After an anabolic steroid cycle with Parabolan, most steroid users take Letrozole as the post cycle therapy drug. This is because the aromatase inhibitor Letrozole can reduce the progesterone levels considerably. Some users even add 25 mcg of T3 every day to control the level of prolactin in the body as Parabolan may reduce the thyroid level to some extent and this may cause a rise in prolactin levels. For men, the ideal dosage of Parabolan is 300-500 mg per week.  Use of this steroid should not be made for a period exceeding eight weeks at a stretch. Since use of the steroid can cause liver toxicity in some cases, it is best to consume seven to nine glasses of water every day throughout an anabolic steroid cycle involving Parabolan or Parabolan only cycle. The steroid can be stacked with Methenolone during cutting steroid cycles and with Nandrolone during bulking steroid cycles. It may be stacked with Boldenone during both cutting as well as bulking cycles. Some sportsmen even use it in a cycle with Winstrol with Nolvadex as the post cycle therapy drug.

Use of this performance enhancing drug should not be made by children or those having an existing allergy to the drug or any of its ingredients. Use of Parabolan is not recommended to those suffering from health problems like testicular atrophy, testicular cancer, prostate cancer, breast cancer, liver damage, kidney damage, stroke, high blood pressure, and respiratory problems.

The steroid is not recommended to girls and women, especially pregnant or breastfeeding women or women who may get pregnant while using the drug. This is primarily because Parabolan is a very potent androgen and the female body has very minimal levels of androgens. Any increase in androgen levels may lead to development of male sexual characteristics such as deepening of the voice, increase of body hair or hirsutism, menstrual disturbances and clitoral enlargement. The worst part is that some of the side effects in women may be permanent in nature even after use of the steroid has been discontinued.

The abuse or use of low grade Parabolan may lead to health complications such as sexual dysfunction, gynecomastia, low thyroid levels, high prolactin levels, increase of body hair or hirsutism, menstrual disturbances, deepening of the voice, and clitoral enlargement. In men, use of this anabolic steroid may lead to side effects such as formation of abnormal breast tissue (gynecomastia) and the suppression of normal testosterone production due to the negative feedback effect Parabolan has on the HPTA (hypothalamic pituitary testicular axis). Men using this steroid may even experience coughs, insomnia, night sweats and cardiac irregularities. Two dosages of Parabolan should not be taken together at the same time, even if the first dose was missed accidentally. In case the first Parabolan dose was missed, it should be skipped and the next dosage should be taken at the scheduled time.

In case of expired Parabolan tablets or if the tablets or injections are not to be used any more, the same should be discarded after having consulting a pharmacist or local waste disposal company on how to safely discard Parabolan. It is highly recommended that Parabolan should not be flushed down the toilet or poured into a drain, unless specifically recommended by a qualified authority. Parabolan tablets or injections should be properly discarded, when expired or no longer needed. Parabolan must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and kept away from unauthorized use, pets, sunlight, moisture, and children.

Since Nolvadex has the ability of inhibiting the growth of tumors that respond to estrogens, it is one of the most popular drugs for treating node-positive breast cancer in women following total mastectomy or segmental mastectomy, axillary dissection, and breast irradiation. The antiestrogen is also recommended for treating metastatic breast cancer in women and men and Nolvadex is an alternative to oophorectomy or ovarian irradiation in premenopausal women with metastatic breast cancer. Medically, it is advised for the treatment of breast cancer that has spread to other parts of the body (metastatic breast cancer) and is also advised to treat breast cancer in certain patients after surgery and radiation therapy and may even be suggested to minimize the chances of breast cancer in high-risk patients.

Each Nolvadex tablet includes 30.4 mg of tamoxifen citrate that s equivalent to 20 mg of tamoxifen and the list of inactive ingredients includes carboxymethylcellulose calcium, magnesium stearate, mannitol, and starch. The drug is the trans-isomer of a triphenylethylene derivative and has the chemical name of (Z)2-[4-(1,2-diphenyl-1-butenyl) phenoxy]-N, N-dimethylethanamine 2 hydroxy-1,2,3- propanetricarboxylate (1:1). The molecular weight of Tamoxifen citrate is 563.62 g/mol at the base and its molecular formula is C32H37NO8. The pKa’ is 8.85, the equilibrium solubility in water at 37°C is 0.5 mg/mL and in 0.02 N HCl at 37°C, it is 0.2 mg/mL.

One of the biggest advantages of this antiestrogen is that patients whose tumors are estrogen receptor positive are more likely to benefit from it. In addition to that, it can minimize the occurrence of contralateral breast cancer in patients receiving adjuvant therapy for breast cancer. In women with Ductal Carcinoma in Situ (DCIS) after breast surgery and radiation, Nolvadex can minimize the risk of invasive breast cancer. It is worthwhile to note that Tamoxifen citrate is well tolerated in males with breast cancer and safety profile of the drug in males is similar to that noticed in women.

Sportsmen using anabolic steroids and performance enhancing drugs like Dianabol, Anadrol, and Testosterone derivatives often make use of Nolvadex and medical studies in the past have suggested that use of this antiestrogen is associated with dramatic improvements in levels of luteinizing hormone, follicle-stimulating hormone, testosterone, and estrogen control.  Since use of Nolvadex is featured by its mild yet highly effective properties, it is often preferred compared to Arimidex, Femara, and Aromasin since it does not prevent aromatization but plays the role of an estrogen antagonist, which is also useful in burning fat.

The recommended dose of Nolvadex for patients with Ductal Carcinoma in Situ (DCIS) is 20 mg daily for 5 years while sportsmen on steroids use it in doses of 20-45 mg per day, with or without food.

Nolvadex is not recommended to those having a history of blood clots (e.g., deep vein thrombosis, pulmonary embolism, stroke) or health conditions that require treatment with a “blood thinner” (like warfarin) or bupropion, estrogens, hormonal forms of birth control (e.g., birth control pills, patches, implants), phenobarbital, rifamycins (e.g., rifampin), St John’s wort. The drug is also not advised to those suffering from kidney damage, liver damage, high blood pressure, and stroke. The drug is contraindicated in women requiring concomitant coumarin-type anticoagulant therapy or in women with a history of deep vein thrombosis or pulmonary embolus. Before seeking medical advice, it is important to communicate medical history, especially if the same is characterized by high cholesterol/triglycerides, limited or no ability to walk (immobility), diabetes, high blood pressure, smoking, cataracts, and liver disease.

Nolvadex abuse can lead to side effects, which may be mild or severe, including hypercalcemia, peripheral edema, distaste for food, pruritus vulvae, depression, dizziness, light-headedness, headache, hair thinning and/or partial hair loss, and vaginal dryness. In very rare cases, side effects like erythema multiforme, Stevens-Johnson syndrome, bullous pemphigoid, interstitial pneumonitis, and rare reports of hypersensitivity reactions including angioedema may happen.

Women keen to use Tamoxifen citrate should avoid getting pregnant for two months after last stopping its use and others should best use birth control methods that don’t use hormones like diaphragms with spermicide or plain intrauterine devices (IUDs). Moreover, breast-feeding is not recommended while using this drug as it is unknown of Nolvadex passes into breast milk or may cause potential risk to the infant. Nolvadex is not recommended to individuals suffering with high amount of calcium in the blood, severely decreased platelets, decreased white blood cells, cataracts, problems with eyesight, blood clot in lung, stroke, obstruction of a blood vessel by a blood clot, blood clot in a deep vein, pregnancy, or a mother who is producing milk and breastfeeding. A loss of sexual ability or interest may occur in men making use of Nolvadex

Medical advice should be sought on an immediate basis after stopping use of Nolvadex if side effects such as pain or pressure in pelvis, vaginal bleeding, changes in the amount or timing of bleeding or increased clotting, sudden chest pain, shortness of breath, coughing up blood, pain, tenderness, or swelling in one or both of your legs , sudden trouble seeing in one or both eyes , sudden severe headache with no known cause, sudden trouble walking, dizziness, loss of balance or coordination, or lack of appetite and yellowing of your skin or whites of eyes is noticed after making use of the antiestrogen.

To maintain its efficacy and shelf life, Nolvadex is required to be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and must be kept in a well-closed and light-resistant container. It must be protected against unauthorized use, pets, sunlight, moisture, and children. In case of expired Nolvadex tablets, the same should be discarded after having a word with a pharmacist or local waste disposal company on how to safely discard Nolvadex.

The drug was originally developed as an antiestrogen to treat breast cancer with SERM (Selective Estrogen Receptor Modulator) Tamoxifen (Nolvadex). This anabolic steroid is very popular among budding as well as professional sportsmen who want to retain strength while losing mass. It is also used as a muscle defining drug and some sportsmen even use Masteron as a diuretic. Classified as a Schedule III drug under the Anabolic Steroids Control Act of 1990, Masteron has a half life of 2-3 days. It has the chemical name of 2 alpha-methyl-17 beta-hydroxy-5 alpha-androstan-3-one and anabolic-androgenic ratio of 62:25. It has the molecular weight of 360.5356 g/mol at the base, can be detected over a period of three weeks, and its molecular formula is C23H36O3.

Being 5-alpha reduced, this anabolic steroid cannot lead to estrogen upon interaction with the aromatase enzyme. Still, Masteron demonstrates a very high affinity for the aromatase enzyme. The best part is that this anabolic steroid can even reduce the amount of estrogens created by other steroids in an anabolic steroid cycle as other steroids may use less aromatase enzymes.

Masteron is even admired for its ability to promote dramatic enhancements in the terms of body strength and muscle function while helping users maintain body fat or even reducing it that is helpful in inhibiting loss of muscles while dieting. Considered a pre-contest drug for bodybuilders, Masteron is best used in dosages of 50-100 mg every day or every other day or 300-350 mg per week though some sportsmen and steroid users even use Masteron in doses of 400-500 mg every week. It is commonly stacked with Equipoise or Deca Durabolin or even Dianabol or an injectable testosterone. Cutting cycle with Masteron may include Winstrol, Primobolan, or Oxandrolone.

Masteron is available in steroid stores and pharmacies in two forms: Masteron propionate and Masteron enanthate. The primary difference between Masteron propionate and Masteron enanthate is that while the enanthate version is slow but long acting, the propionate version is slow and is required to be injected every other day.

Masteron enanthate

Masteron enanthate, which is also known as Drostanolone enanthate, has the chemical name of 17beta-Hydroxy-2alpha-methyl-5alpha-androstan-3-one Enanthate. It has an active life of nearly eight to nine days and can be detected up to three weeks. Masteron enanthate has an anabolic androgenic rate of 62:25. Recommended dosage of Masteron enanthate is 400-600 mg weekly for men and 100 mg weekly for women and can be stacked with Trenbolone Enanthate, Clenbuterol, Ephedrine, T3, IGF, and Testosterone.

The steroid is second to none for promoting muscle function and definition and has the ability to inhibit the transformation of free testosterone to estrogen and thereby enhances the rate of free testosterone circulating in the body.

Use of Masteron enanthate should not be made by children or those having an existing allergy to the drug or any of its ingredients. Use of Drostanolone enanthate is also not recommended to those suffering from health problems like testicular atrophy, testicular cancer, prostate cancer, breast cancer, liver damage, kidney damage, stroke, high blood pressure, and respiratory problems.

Two doses of this steroid should never be taken together even if the first dose was missed unknowingly. In such a case, the first dose should be skipped and the next dosage should be taken at the scheduled time.

Masteron Propionate

Also known as Drostanolone Propionate, this anabolic steroid is effective for inhibiting estrogens from making an interaction with the aromatase enzyme and is considered by sportsmen as a performance enhancing drug that prevents estrogenic side effects and has anabolic and androgenic properties.

A powerful anabolic/androgenic steroid derived from DHT, it can be used as a bulking and cutting agent for promoting an improved look of density and hardness to the muscles. Commonly used as a cutting or pre-contest drug, Masteron Propionate is often associated with improvements in terms of aggression, performance, stamina, muscle size, and muscle function and is useful in giving a new and improved meaning to loss of body fat and weight. Since use of this steroid is characterized by low levels of water retention, Masteron users can expect distinct muscle lines.

The recommended dosage for Drostanolone propionate is 50-150 mg/ml or 350 mg/week (or 100mgs every other day) to 500 mg/week while the ideal dose for women is 25-50 mg every other day to every third day. It is usually stacked with anabolic steroids such as testosterone propionate, trenbolone acetate, Anavar, Winstrol, and Equipoise. A commonly followed cycle involving the propionate version of Masteron is 150 mg Masteron propionate and 150 mg Testosterone propionate each (EOD – every other day), 50-100 mg Trenbolone acetate every day, and 50 mg of Winstrol every day (only during last 4 weeks of the cycle).

Water retention and gynecomastia are rare with use of this steroid. This steroid also does not result in aromatization and exhibits anti-estrogenic capabilities. Sportsmen can even run Masteron for lengthy cycles without worrying about damage to the liver. However, abuse of Masteron can lead to side effects, which may be mild or severe. This may include oily skin, acne, body/facial hair growth, deepening of the voice, and hair loss.

In case of Masteron tablets have expired or if the tablets or injections are not to be used any more, the same should be discarded after having consulting a pharmacist or local waste disposal company on how to safely discard Masteron. It is highly recommended that Masteron should not be flushed down the toilet or poured into a drain, unless specifically recommended by a qualified authority. Masteron tablets or injections should be properly discarded, when expired or no longer needed. Masteron must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and kept away from unauthorized use, pets, sunlight, moisture, and children.

The chemical name of Letrozole is 4,4′-(1H-1,2,4-Triazol-1ylmethylene)dibenzonitrile and its molecular formula is C17H11N5. The antiestrogen has the molecular weight of 285.31 g/mol at the base. The active ingredient in Femara tablets is letrozole, a non-steroidal aromatase inhibitor while the list of inactive ingredients in Femara tablets includes colloidal silicon dioxide, ferric oxide, hydroxypropyl methylcellulose, lactose monohydrate, magnesium stearate, maize starch, microcrystalline cellulose, polyethylene glycol, sodium starch glycolate, talc, and titanium dioxide.

Letrozole is considered as one of the most potent drugs for stimulating metabolic rate of the body and promoting burning of fat. It is also useful in reducing the levels of LDL (bad) cholesterol and promoting the level of spermatogenesis in male patients suffering from non-obstructive azoospermia and treat endometriosis. The third-generation selective oral aromatase inhibitor, Letrozole, is also used to stimulating dramatic enhancements in terms of growth hormone, cortisol, SHBG, hepatic production of binding proteins, HDL, and growth and development of sexual characteristics. If that was not all, Femara also has the ability to promote healthy immune function, healthy cholesterol levels, joint health, cognitive function, and muscle growth while reducing or even eliminating estrogenic side effects such as oily skin, gynecomastia, and fluid retention.

The medication may even be recommended by medical practitioners to treat certain types of breast cancer (such as hormone-receptor-positive breast cancer) in women after menopause or preventing the cancer from making a return. By reducing the amount of estrogens in the body, Letrozole helps in slowing or reversing the growth of these breast cancers.

The use of Letrozole, for a period of three to six weeks, is also associated with restoration of natural products of hormones, like testosterone. If that was not all, one 2.5 mg tablet of Femara is good enough to inhibit side effects of estrogens by as much as 80 percent.

The ideal dosage of Letrozole is 2.5 mg once a day for treating patients with breast cancer. Sportsmen use Letrozole in dosages of 0.5-1.0 mg every day, with or without meals. It is very important to note that this is a prescription drug and must be used and purchased only with a prescription. Moreover, its use should always be followed by a medical recommendation for the same after careful and complete evaluation of medical reports and history. At no point of time, two dosages of the drug can be taken together, even if missed accidentally. In case the first dose has been missed, it should be skipped and the next dose should be taken at its scheduled time.

Letrozole use is not recommended to pregnant and breastfeeding women and children or those having allergies to the drug or any of its ingredients. Those suffering with prostate, breast, or testicular cancer or treated for high blood pressure, liver damage, stroke, and kidney damage should avoid using the drug. Patients making use of drugs such as Prasterone, Tamoxifen, DHEA, and Androstenedione should avoid using Letrozole unless the same is specifically approved by a qualified medical practitioner.

The abuse of Letrozole can lead to side effects and thus best avoided. When abused or of a low grade, it can lead to side effects such as hot flushes, night sweats, vomiting, bone pain, loss of appetite, headache, stomach pain, cough, and breast pain. Use of Letrozole should not be made by individuals treated for high blood fats (cholesterol), bone problems (such as osteopenia, osteoporosis), stroke or blood clots, heart disease (such as chest pain, heart attack, heart failure), high blood pressure, kidney problems, and liver problems.

In rare cases, Femara use may cause severe health complications such as chest/jaw/left arm pain, confusion, coughing up blood, sudden dizziness/fainting, pain/swelling/warmth in the groin/calf, tingling/weakness/numbness in the arms/legs, weakness on one side of the body, vision changes, sudden/severe headache, slurred speech, bone fractures, mental/mood changes (such as depression, anxiety), swelling of arms/legs, and blurred vision. Drugs such as estrogens (such as ethinyl estradiol, conjugated estrogens), estrogen blockers (such as anastrozole, tamoxifen) may interfere with functioning and action mechanism of Letrozole and this may cause serious side effects or may cause the medications not to work correctly. The consumption of alcoholic beverages should be reduced, if the same cannot be completely eliminated, while Letrozole is being used.

The drug should not be handled by women who are pregnant or who may become pregnant as breathing the dust from Femara tablets or handling this medication as this drug can be absorbed through the skin and lungs. The doses of this drug should be based on medical conditions and response to treatment and the doses should preferably be taken at the same time each day. Medical advice should be sought on an immediate basis if side effects such as persistent nausea/vomiting, unusual tiredness, dark urine, and yellowing eyes/skin are experienced after making use of Femara tablets or injections.

In order to maintain its shelf life and potency, Letrozole (Femara) is best stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F). It should be protected against unauthorized use, pets, sunlight, moisture, and children and should never be kept in the bathroom since moisture could minimize or even nullify its efficacy. In case of expired Letrozole tablets, the same should be discarded after having a word with a pharmacist or local waste disposal company on how to safely discard Letrozole. It is highly recommended that Femara should not be flushed down the toilet or poured into a drain, unless specifically recommended by a qualified authority. Femara tablets or injections should be properly discarded when it is expired or no longer needed.