Category: Products

Cipla (India)
30 Caps x 15mg Total 450mg

Leptos 15 (Sibutramine Hydrochloride), Generic Meridia/Reductil

General Information

Leptos (Generic Meridia) 15 mg capsules are sibutramine hydrochloride.

Sibutramine Hydrochloride is being sold in Europe under the brand name Reductil and under the brand name Meridia in the US. Leptos (Generic Meridia) 15 mg is manufactred in India. Even though it contains the exact same chemical as Reductil / Meridia its cost is significantly less than that of Reductil / Meridia. Indian patent law allow Indian Drug manufacturers to make drugs that are patented by other companies internationally as the law protects only the processes by which drugs are made, and not the drugs themselves. Under current Indian law, which recognizes patents on ways to make drugs but not the drugs themselves. This means Indian companies can make drugs under patent in the West, provided they use a process that is different from the original. Manufacturers are able to produce and sell medicines here at a tiny fraction of the prices charged in the United States. In some cases, though, the generic makers have been blocked from selling their wares in other developing countries that have Western-style patent laws. Sibutramine is also sold in India under brand names Obestat, Sibutrex, Sibutrim and Slenfig and Leptos (Generic Meridia – Reductil) is an oral prescription medication that is used for the medical management of obesity, including weight loss and the maintenance of weight loss.

How does Leptos (Generic Meridia – Reductil) work?

Leptos (Generic Meridia – Reductil) works by affecting appetite control centers in the brain. In medical studies in overweight people, along with a reduced calorie diet, it produced significant reductions in body weight. Leptos (Generic Meridia – Reductil) should be used as part of a comprehensive weight loss program supervised by your doctor, that includes a reduced calorie diet and appropriate physical activity.

How long does it take to work?

Every person will respond differently to Leptos (Generic Meridia – Reductil) when used as part of a comprehensive weight loss program. You may be able to lose 4 or more pounds of body weight in the first month you take it . If you find that you do not lose at least 4 pounds during the first month, you should notify your doctor so he or she can re-evaluate your situation. Your doctor may wish to change your dose of Leptos (Generic Meridia – Reductil). Most people who lose weight on Leptos (Generic Meridia – Reductil) lose it in the first 6 months of treatment. Scientific studies that lasted one year have shown that many people who lost weight and remained on Leptos (Generic Meridia – Reductil) therapy maintained their weight loss.

Who should take it?

A weight loss program that includes a reduced calorie diet and appropriate physical activity may be adequate in some patients. You should discuss with your doctor whether Leptos (Generic Meridia – Reductil) should be added to such a program. Leptos (Generic Meridia – Reductil) is recommended for overweight people with an initial body mass index (BMI) of 30 or higher, or for overweight people with a BMI of 27 or higher if they have medical risk factors such as high blood pressure, diabetes, or high cholesterol. Your doctor can determine our BMI and will decide if you meet these criteria.

How and when should I take Leptos (Generic Meridia – Reductil)?

Follow your doctor’s instructions on how and when to take it. Your doctor will recommend that you take one (1) Leptos (Generic Meridia – Reductil) capsule a day. You can take on an empty stomach or after a meal.

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• Cheap weight loss product
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Viagra generic [Cenforce-100] (Sildenafil citrate) – Centurion Laboratories (India)	Ajanta House (India) Pack :: 4 Sachets x 100mg Total 400mg

Kamagra / Kamagra Oral Jelly (Sildenafil Citrate – Generic Viagra)

General information

Kamagra 100mg Tablets and Jellies are an effective treatment for Male Erectile Dysfunction (E.D). It is a generic Sildenafil Citrate and is produced by company Ajanta Pharma. Kamagra tablets and jelly contain the same ingredients and perform in a similar way to Viagra produced by Plizer but it is a much cheaper alternative. It takes approximately 45 minutes for Kamagra tablets and jellies to start working and is effective for 4-6 hours.

Some patients struggle to swallow medicine in tablet form. A new popular form of Kamagra is now available in Oral Jelly sachets. The Kamagra jelly comes in 5 flavours. Users simply squeeze the sachet onto a spoon to take orally. Lower side effects are often reported and many users claim the treatment starts to work quicker than conventional tablet form although this is circumstancial. It is more expensive than the cost of tablets but this reflects supplier costs and increased weight in postage.

Users already taking or planning to take Nitrate based medications must not use this product. (See our list below or consult your doctor if you are unsure about medicine you are already taking).

Why Kamagra is like Viagra

The active component in both drugs is Sildenafil Citrate. The FDA first approved it’s use in treating Erectile Dysfunction in 1998. In the same way that Ibuprofen is the generic equivalent of Nurofen, Kamagra is the generic equivalent of Viagra. Pretty much all the generic viagra substances are made of sildenafil citrate like Viagra. The main difference between Kamagra and Viagra is the price, with Kamagra being a much cheaper alternative.

Why Kamagra is cheaper

Many people buy Kamagra to save money. It can be sold at prices much cheaper than Viagra. Why? The company that produces Kamagra (Ajanta Pharmaceutical) did not incur the cost that it took Pfizer to do research on the erectile dysfunction drug. Kamagra is just as effective as its brand name alternative drug Viagra. They contain the same active ingredient and produce the same desired effect. Savings are passed on to the customer and the competition makes producers of erectile dysfunction drugs maintain high quality. This benefits the consumer.

How to take this medicine

• Always take this medicine with a large glass of water
• Avoid large or fatty meals close to when you intend to take the medicine
• Allow 1 hour for the treatment to become most effective
• This treatment is not designed to be taken with alcohol or while heavily under the influence of effectiveness of treatment will diminish if these steps are not followed

Warning

Users taking the following should not take Kamagra Oral Jelly 100 mg sachets.

This list is not comprehensive.

Nitroglycerin, isosorbide dinitrate, nitroprusside (any “nitric oxide donor” medicines), cimetidine, erythromycin, azole antifungals (e.g., itraconazole, ketoconazole), mibefradil, rifamycins (e.g., rifampin) or high blood pressure medicines. Also the use of poppers (Amyl Nitrate, Amyl Butrate etc) is dangerous whilst using Kamagra 100mg tablets.

Side Effects

From time to time patients taking this treatment experience the following side effects. These can be minimised by following the instructions above carefully.

• Mild de-hydration
• Headache
• Blocked nose
• Mild Nausea
• Slight stinging in eyes

Most of these side effects go away upon drinking a sensible amount of water.

Advantages

• World’s No.1 sexual enhancer
• Much cheaper than Viagra
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Long R3 IGF-1 (Insulin-like Growth Factor)

General information

IGF-1 is the abbreviation for Insulin-Like Growth Factor 1. This is a naturally occurred long-chain polypeptide protein hormone and not a dangerous steroid. IGF-1 has molecular structure, which is quite similar to insulin. IGF-1 plays a vital role in childhood growth, especially bones and stimulates anabolic effects (muscle growth) in adults. IGF-1 greatly boosts muscle mass by inducing a state of muscle hyperplasia (increase in number of new muscle cells) in the body

Long R3 IGF-1 is a more potent version of IGF-1. It’s chemically altered to prevent deactivation by IGF-1 binding proteins in the bloodstream. This results in a longer half-life of 20-30 hours instead of 20 min.

There are 70 inter-connected amino acids that make up a single chain of IGF-1. This hormone is produced when the liver is stimulated by HGH. When levels of HGH rise in the blood, the liver responds by producing more IGF -1. These higher “bursts” spur growth and regeneration by the body’s cells, especially in muscle cells. Increases in IGF-1 levels have shown positive effects on increases in muscle strength, size, and efficiency. When you do not have enough IGF-1 in your body, whether caused by disease, malnutrition or a hormone imbalance, your growth can be stunted.

The primary purpose of IGF-1 is to stimulate cell growth. Every cell in the human body can be affected by IGF -1, but cells in muscle, cartilage, bone, liver, kidney, skin tissue, lungs, and nerves tend to be most positively affected.

Products which increase IGF-1 can help improve muscularity and healing and recovery times. IGF-1 can also stimulate a decrease in body fat, an increase in lean muscle mass, improved skin tone and restful sleep. IGF -1 has also been documented to increase the rate and extent of muscle repair after injuries or strains. Not only do muscles recover more quickly, they also tend to return stronger and healthier than ever when levels of IGF -1 in the bloodstream are at their highest.

IGF-1 also has a positive affect in the aging process. It can prevent age-related degeneration of muscles, skin tissue and bones. Because IGF-1 levels tend to level off and fall rapidly when the liver is not stimulated by HGH production, these benefits are greatest when consistently high HGH levels are maintained.

Combined with other supplements and monitored responsibly, IGF -1 can be beneficial for those individuals who suffer from stunted growth or growth hormone deficiencies as well as those individuals who strive to be in the best physical shape possible. Athletes, bodybuilders and physical competitors around the world are learning all about the benefits of IGF-1 and implementing the growth hormone into their daily regimented workouts. Whether you are an athlete yourself, or you prefer to workout more than a few times a week, IGF-1 can be beneficial for you. Even if you aren’t an athlete at all, but are looking to get as healthy and fit as possible for your own reasons, IGF -1 can be beneficial for you.

IGF-1 dosages and length of cycle

IGF-1 novices will be able to use a smaller dose than a more advanced user. For your first IGF-1 cycle, you need to remember that less is more, meaning that you donӴ have to use a lot to get great results. This is not like testosterone where you need big doses for big muscles. For your first or second cycle with IGF-1, you will use 50mcg per injection day, 3 days per week (or 20-25 mcg daily), and split into two daily injections. For LONG R3 IGF-1 you can inject less frequent. for advanced users dosages may grow but never exceed 120 mcg daily.

The same is true for the length of cycle. IGF -1 effectiveness falls rapidly after prolonged use. Some users report 40 days, some 60 days, but our advice is to limit IGF-1 cycle for 4-5 weeks to get maximum effect then take rest. Some advanced users may do 50 days but only if they know what they’re doing. Too much IGF-1 will result in deregulation of IGF -1 receptors on the surface of muscle cells. This will jeopardize any gains from the injected IGF -1 since very little receptors means very little response! Time gap between cycles should be 20-40 days.

IGF-1 is also best taken either subcutaneously (preferably) or IM, having more direct effects on the body when injected. It’s also recommended to be taken during the morning/evening only (novice) or after work out only  (novice) or morning/evening plus after weight training sessions (advanced user). So advanced user makes from two to four injections daily.

IGF-1 usage

Assuming that we use the lyophilized form (dry powder) of Long R3 IGF-1, equivalent to a 1000 mcg vial, it is best prepared by using 1ml or 2ml of acetic acid. Let the acetic acid seep into the vile after removing the vacuum from the container. Then, let the mixture in the vial sit for a while. Put it in the fridge where the IGF -1 mixture can dissolve without accidentally knocking the vial or shaking its contents. Then afterwards, it’s all about diluting your Long R3 IGF-1 in NaCl or bacteriostatic water before intra-muscular or subcutaneous entry.

In most cases you have 1mg (1000mcg) bottle of substance, with 1 ml of pre-made acid. Since we want to use 25mcg for our injection, you need to use an insulin syringe (29 gauge 50 IU for easier measuring) and withdraw to the 2.5 tick mark on the syringe. Yes, that is a very, very small amount to withdraw which is why we recommend the 1/2cc or even 30 IU syringes. Now using acetic acid can be very painful, and it is almost impossible to inject such a small amount so you will now use bacteriostatic water or NaCL water to add more volume to the syringe. This will also help reduce the pain of the acid injection. After you withdraw your small 2.5 IU on the slin pin, just finish filling the syringe with the water.

But what to do if IGF -1 comes in powder and there’s no acid supplied (generic brands)?
That’s not easy subject to answer 🙁

If you dissolve in bacteriostatic water lifetime will be too short. Some users claim it’s just 2-3 days under +4C, so in this case you have to dissolve TOO small dosages, which is very difficult. However, in special acid solution it lives up to 4 weeks. Put 4 ml solution into 1 mg IGF-1. 1 mg = 1000mcg

How to prepare acid solution? You need bacteriostatic water, acetic acid, syringe 10 ml, and filter 0.22 mm or better 0.11mm

Take 1 ml 99% acetic acid then 7ml sterile water, shake well then leak out 7 ml out of total 8ml. Add 7ml of water AGAIN, so finally we receive 1,5% acetic acid solution.

Preferably put filter onto the syringe and put 4 ml of solution into 1mg IGF1 vial.

Insulin syringe has 40 IU for 1 ml (when measuring insulin and IGF). Thus 4 ml of solution contains 250 mcg per ml.

1000mcg/4mL:

• 31 mcg per 5 IU
• 40 IU = 250 mcg
• 20 IU = 125 mcg
• 10 IU = 62,5 mcg

So, if your dosage is 30 mcg utilize 5 IU, if dosage is 25 mcg, utilize ~4.5 IU

It’s not advisable to freeze liquid but if there’s no other way – do it no more than 1 time

Stacking IGF-1

The IGF-1 that’s produced from the use of fast acting Nandrolone or Trenbolone is nothing significant when you compare to the amount that’s contained in a single 10mcg Long R3 injection. Having said that, it’s safe to inject exogenous IGF-1 while taking either one of these compounds.

IGF-1 and Human Growth Hormone?

Long R3 IGF-1 can directly stimulate muscle growth when compared to HGH. This is because HGH indirectly results in growth and repair by first inducing IGF-1 release in the liver. If you don’t have to worry about IGF-1 release in the liver (because your directly injecting the IGF-1), new growth will be optimized.

Usage of IGF-1 brings more faster results than HGH because HGH acts indirectly and process is slower.

If stacking with HGH after workout you can do for example like this: 5 IU HGH then 50 mcg IGF after 20 minutes (or smaller dosages if you make more frequent injections).

Is there a benefit to using both of these substances together?

Many research studies have shown that GH and IGF -1 act synergistically to augment the effect of either hormone taken individually. So, the greatest results will take place when effective dosages of both hormones are injected. Usually 10-20mcg of IGF-1 (post workout) and 4-8 IU HGH EOD (with breakfast and at 1 p.m.) is the ideal stack for optimal results and minimal side effects.

Medical usage

Tissue build up is one of the main features of IGF -1, so I’d say it’s of greater value. IGF -1 can genetically change muscular and cellular counts within the body; it can also enhance the body’s ability to regenerate damaged tissue. In fact, IGF -1 is now under intensive research for its potential to repair tissue in burn patients, and for its regenerative effects on AIDS patients suffering from muscular wasting. Immediate effects are, of course, impossible to observe since it takes a respectable amount of time to see any visible changes in muscular repair.

There’s no known lethal risk of administering IGF -1 to diabetic patients. In fact, IGF -1 can reduce the body’s need for insulin, and according to one short study, it can reduce insulin dependence of the body by as high as 45%. This may bring very promising results if we are allowed to study this matter further. If anyone experiences any uncomfortable side effects, stop it’s usage and see if the side effect disappear.

Side effects of IGF-1

IGF -1 is commonly known to cause feelings of fatigue. Some people feel very tired quickly when using this compound. It can, however, be looked at in a more positive light since more sleep means better growth. Other side effects include muscular stiffness, headaches, occasional nausea, and some also claim that it’s sometimes responsible for hypoglycemia or low blood sugar.

Advantages

• IGF -1 greatly promotes cell growth
• IGF -1 has anti-aging effect
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Massone S.A. (Argentina)
6 X 75 IU vials with water solution

Human menopausal gonadotropin (hMG)

HMG is a mixture of luteinizing hormone (LH) and follicle-stimulating hormone (FSH)
It is used for stimulating hormones by triggering FSH, and also LH production in the body. This drug was originally designed for use in women where it stimulates the ovaries to produce multiple follicles, thus making their fertile abilities more viable.

HMG is a drug very similar to HCG and posesses some of its functions, but also it has additional benefit of FSH stimulation, while HCG (human chorionic gonadotropin) is known mainly for its LH stimulation. HM Gonadotropin injection was originally designed as a fertility drug. FSH (follicle stimulating hormone)  effect can greatly induce higher sperm count production by the men’s body.

HM Gonadotropin hormone can be most effective when ran along with HCG and other LH stimulating drugs.

HMG vs HCG

How HMG aka Human Menopausal Gonadotropin differs from HCG and why it may be a better alternative to this mainstay of post cycle therapy.

Post Cycle Therapy or PCT for short is a must after you have finished a steroid cycle. If you want to keep the strength and muscle gains you worked so hard for when you were on the juice, you need to help return your own body’s hormonal levels back to normal – or all you hard work will be wasted. Many great PCT protocols have been outlined over the years, and many individuals have had success following them. Nevertheless, what works can always work better.

For years, bodybuilders used HCG to kick-start their HPTA after a cycle. There’s still a lot of debate as to how it should be used, but for simplicities sake it’s fair to say it should be administered once the testes show sign of atrophy. This makes sense since, contrary to popular belief, HCG (and HMG) do not “cure” or “recover” anything. They do not return testosterone levels permanently and they do not assure that production will return to normal. They simply give a temporary boost that can be extremely helpful when one’s hormonal system is suppressed and attempted to return to normal. It’s a little bit of a “head start” on recovery, but at some point, the body must produce hormones all on its own – otherwise, it really isn’t recovery, its just substituting one drug for another. This is why supplementation is also recommended at this time.

Now that we’re established exactly how these drugs work, let’s examine the differences.

The most significant disparity is in the fact that HCG mimics LH (luteinized hormone). It gives the body a false signal that LH is present and everything else responds accordingly. HMG actually elevates natural LH. Now to some, there’s little difference, but it’s always better when the body reacts in the most natural manner. There’s also less of a chance of building up a tolerance when this occurs. And in the case of HCG, tolerance is developed pretty quickly. That’s why excessive HCG use is not recommend. Use too much, too often, and it won’t work at all.

Exactly how much LESS suppressive HMG is appears to still remain speculative. But it’s a good guess that it’s less so.

There’s another, still empirical, opinion that HMG causes less of an estrogen spike. The use of HMG for bodybuilding purposes is so new there’s no way of proving this one-way or the other. Yet. But again, it stands to reason this is so.

One absolute difference between the two compounds is the fact that HMG raises FSH (Follicle Stimulating Hormone) and HCG does not. Again, this is due to the fact that HCG works synthetically and HMG stimulates the entire feedback loop. This is especially appealing since an increase in FSH means higher sperm count and ejaculate volume.

HMG dosage and usage

A typical dose of 75 Units a day for 2 weeks is sufficient for restoring normal testicular function and sperm count in males. If necessary, the dose of menotropins may be increased by 75 to 150 Units FSH and 75 to 150 Units LH every four or five days

Note: Dosage regimen may vary according to physician preference or patient response. f the ovaries are abnormally enlarged or the serum estradiol concentration is excessively elevated on the last day of menotropins therapy, human chorionic gonadotropin should not be given for that cycle.

Although HMG is relatively new to the steroid community there are already misconceptions surrounding its use. People fail to realize that recommended dosages in the enclosed literature are for the original purpose of drug – that of a fertility stimulant in women. For men’s purposes, a much lower dose is needed. A single shot of 75 i.u.’s may be all that’s necessary. You can even try spitting that up into two half shots over two days. Using more, will not do more. It will not elevate testosterone higher, or give you bigger balls so don’t even think about it.

To be used

immediately after the cycle, max two weeks long. Must be followed by clomiphene

Conclusion

Anecdotal feedback on HMG has been very positive. It seems to work at least as well as HCG and most users feel it’s superior. Until more is known  it may be best to alternate between HCG and HMG. This may also have an additional benefit of lessening the desensitizing effects of HCG.

As mentioned, any LH stimulation is temporary so while you’re recovering it’s best to have every advantage. Supplements such as unleashed and POST CYCLE can make the most of natural hormone production and get you on the road to recovery faster.

HMG and HCG may be related but it looks like HMG is the bigger brother.

Length of treatment

You’ll start receiving hMG or pure FSH shots three days into your monthly menstrual cycle and continue taking them for seven to 12 days each month, depending on how long it takes your eggs to mature. Your doctor will train you or your partner to give the shots. She’ll also monitor you closely to see whether you’re responding to the medication — frequent trans-vaginal ultrasounds and blood tests are often necessary. When your eggs are mature, you’ll be given an hCG injection. You’ll most likely ovulate 24 to 36 hours later. You’ll either be sent home to have sex, or your doctor will schedule an intrauterine insemination for a day or two later.

Most women will go through a maximum of three to six drug cycles. Success rates don’t improve if you take the drugs longer, so if you try three or more times and don’t get pregnant, your doctor may increase the dosage or suggest another kind of treatment.

Side effects of HMG

You may notice abdominal tenderness, bloating, fluid retention, and weight gain, or have a hard time giving yourself an injection. The newer, purer gonadotropins such as Gonal F and Follistim cause fewer side effects and can be injected using smaller needles subcutaneously (under your skin). Repronex can also be injected subcutaneously.

You’ll also have a 10 to 40 percent chance of conceiving twins or more with these fertility drugs. Though many couples consider this a blessing, multiple fetuses increase your risk of miscarriage and other complications.

Original female usage

ovarian syndrome, luteal phase defects, or an unexplained fertility problem. If you’re undergoing an assisted reproductive technology (ART) treatment such as in vitro fertilization (IVF), gonadotropins can help you produce several eggs for the procedure.

Gonadotropins can also help men who have a hormonal imbalance (that originates in the pituitary gland or hypothalamus) linked to a low sperm count, or poor sperm quality or motility (its ability to move). (See more information about fertility drugs for men.)

Treatment: What to expect

HMG consist of FSH and LH, while urofollitropin or recombinant FSH are made purely of FSH. Whichever you choose to be injected with for seven to 12 days will translate into a dose of FSH that’ll prompt your ovaries to produce several eggs, whereas you normally produce only one a month.

After you receive those shots, you’ll be injected with another substance called HCG, which will tell your ovaries to release your mature eggs into your fallopian tubes. If an egg meets up with a healthy sperm on its way to your uterus, you’ll have a chance to conceive.

This treatment can be a very hands-on, emotionally intense process, too, since you’ll have to go the doctor’s office for frequent monitoring. Find a willing friend, support group, or professional to talk to before, during, and after your treatment. (See therapists’ top ten tips for coping with a fertility problem. Also, visit the BabyCenter Community to discuss Clomid and similar fertility drugs with others.)

Women who take fertility drugs sometimes develop ovarian hyperstimulation syndrome (OHSS), a condition signaled by weight gain and a full, bloated feeling. Some patients also have shortness of breath, dizziness, pelvic pain, nausea, and vomiting. OHSS occurs when you respond too well to the drugs and produce too many eggs; your ovaries rapidly swell to several times their size and leak fluid into your abdominal cavity. Normally this resolves itself with careful monitoring by your physician. But in rare cases it can be life threatening, and you have to be hospitalized for more intense monitoring.

On the bright side, researchers who recently examined the results of eight different studies conducted between 1989 and 1999 found that fertility drugs don’t increase a woman’s risk of developing ovarian cancer, even if she takes them for more than a year. Previously this issue was a major source of controversy and concern.

Success rates

Between 20 and 60 percent of women who use this treatment conceive (the wide range is due to all the other factors affecting pregnancy, from the time you have sex and your age to the speed and agility of your partner’s sperm). Very little information is available on the live birth rate for fertility drugs, but a few studies put the number at 70 to 85 percent.

Form

• Intramuscular injection
• Humegon, Pergonal & Repronex;
• Subcutaneous injection
• Repronex
• Indications

Demonstrated ovulatory dysfunction with:

• No current pregnancy
• No evidence of primary ovarian failure
• No uncontrolled thyroid or adrenal dysfunction
• No ovarian cysts (except in case of PCOS)
• Used in conjunction with hCG

In women, inducing ovarian follicular growth and maturation. In men, used to treat hypogonadotropic hypogonadism, and to induce spermatogenesis (sperm production).

How does it work?

Possesses hormonal activities of FSH and LH.

• Suggested Evaluations
• Pre-RX
• thyroid disease
• ovarian enlargement or cyst formation
• uterine fibroid tumors
• undiagnosed unusual vaginal bleeding
• estrogen levels
• primary pituitary or ovarian failure or enlargement
• evidence of prostate cancer in men
• testicular failure
• renal and hepatic functions
• During RX
• mid-cycle urine LH test (OPK)
• estrogen levels
• progesterone levels
• mid-cycle ultrasound to detect follicle development

Usual Dosage

Dosage must be carefully determined for each patient, and may be changed during treatment cycle. During a fertility treatment cycle in women, from a ratio of 75 units FSH:75 LH to 150 units FSH:150 LH injected once daily for 5 days or more. For male treatment, 75 units FSH:75 LH units three times weekly for several months.

Instructions

Keep refrigerated. Maintain BBT chart or other recommended cycle charting methods throughout treatment cycle. If self-injecting and miss a dose, take as soon as remember, but not as late as the following day. Do not double doses. Use prepared/mixed solution immediately and discard any unused medication.

Common side effects

• Injection site pain
• Lower abdomen tenderness
• Fluid retention
• Headache
• Emotional irritability
• Breast discomfort
• Fatigue
• Multiple births
• Side effects to report to your doctor
• Severe pain or swelling in lower abdomen or extremities
• Shortness of breath
• Vomiting or diarrhea
• Precautions
• Pregnancy Category X: May cause birth defects if used during pregnancy.
• Exercise caution if patient is breastfeeding.
• May result in ovarian hyperstimulation.
• May result in multiple births.
• Drug interactions or incompatibility

Packaging and storage

Store below 40 °C (104 °F), preferably between 15 and 30 °C (59 and 86 °F), unless otherwise specified by manufacturer.

Advantages

• HMG increases the testosterone production in the testes very quickly and reliably, even more than HCG. Ideal for PCT.
• You can buy HMG (Human Menopausal Gonadotropin) here

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Buy Humulin NPH (Insulin) – Lilly (France) 5 Cartriges x 3ml. [100 IU/ml.] Total 1500IU	Buy Humulin Regular (Insulin) – Lilly (France) 5 Cartriges x 3ml. [100 IU/ml.] Total 1500IU

Humulin (Insulin Human Biosynthetic Antidiabetic Agent)

Action And Clinical Pharmacology

Humulin is a polypeptide hormone consisting of a 21 amino acid A-chain and a 30 amino acid B-chain linked by two disulfide bonds.

Humulin is found to be chemically, physically, biologically and immunologically equivalent to pancreatic human insulin which differs slightly from porcine or bovine insulin in amino acid composition.

Studies indicate immunogenic problems with biosynthetic human insulin (BHI) produced by recombinant DNA technology are less likely than with insulin derived from animal origin. Biosynthetic human insulin is devoid of all protein contaminants of pancreatic origin normally present in trace amounts in all insulin of pancreatic origin. The purification procedures used in the manufacture of biosynthetic human insulin result in a product which contains an insufficient quantity of E. coli polypeptides to be antigenic in deliberately sensitized animals. No antibodies to E. coli polypeptides have been detected in specifically designed radioimmunoassay methods examining patient serum samples.

The administration of suitable doses of insulin to patients with diabetes mellitus, along with controlled diet and exercise, temporarily restores their ability to metabolize carbohydrates, fats and proteins; to store glycogen in the liver; and to convert glucose to fat. When given in suitable doses at regular intervals to a patient with diabetes mellitus, the blood sugar is maintained within a reasonable range, the urine remains relatively free of sugar and ketone bodies, and diabetic acidosis and coma are prevented.

Insulin preparations differ in onset, peak and duration of action. The addition of protamine to insulin, in the presence of zinc, produces a stable complex with less intense and more prolonged action, due to its slow dissolution.

Types of Humulin

Humulin-R

Regular, Insulin Injection, Human Biosynthetic, is a rapidly acting insulin with a relatively short duration of activity (6 to 8 hours).

Humulin-N

NPH, Insulin Isophane, Human Biosynthetic, is an intermediate-acting insulin with a slower onset of action than Regular insulin and a longer duration of activity of up to 24 hours.

Humulin-L

Lente, Insulin Zinc Suspension Medium, Human Biosynthetic, is an intermediate-acting insulin with a slower onset of action than Regular insulin and a longer duration of activity of up to 24 hours.

Humulin-U

Ultralente, Insulin Zinc Suspension Prolonged, Human Biosynthetic, is a long-acting insulin with a slower onset of action than Regular insulin and a longer duration of activity (of at least 24 hours or more).

Humulin Mixtures

Humulin Mixtures (10/90, 20/80, 30/70, 40/60 and 50/50 Insulin Injection, Human Biosynthetic and Insulin Isophane, Human Biosynthetic) are intermediate-acting insulins with a more rapid onset of action than NPH alone and a duration of activity of up to 24 hours.

Humulin-N, Humulin-L or Humulin-U may be mixed with Humulin-R to meet individual metabolic requirements of the patient as determined by the physician.

Indications And Clinical Uses

For the treatment of insulin-requiring diabetic patients.

Humulin-R only should be used for the treatment of emergencies such as diabetic coma and pre-coma, in diabetics undergoing surgery, but not Humulin-N, Humulin-L, Humulin-U or Humulin Mixtures.

In switching patients from animal source insulins to Humulin, it is possible that the patients will require a change in dosage; the adjustment may be made with the first dose or over a period of several weeks. Any change of insulin should be made cautiously and only under medical supervision.

Changes in refinement, purity, strength, brand, type and/or method of manufacture (recombinant DNA versus animal source insulin) may result in the need of a change in dosage.

Contra-Indications

Hypoglycemia (see Hypoglycemia in Overdose).

Humulin-N, Humulin Mixtures, Humulin-L and Humulin-U should not be given i.v. or used for treatment of diabetic coma.

Manufacturers’ Warnings In Clinical States

A few patients who experienced hypoglycemic reactions after being transferred to Humulin have reported that these early warning symptoms were less pronounced than they were with animal-source insulin.

Under no circumstances should any Humulin Mixture be given i.v.

Do not use the Humulin-N, Humulin-L, Humulin-U or Humulin Mixtures if you see lumps that float or that stick to the sides of the vial, or if the contents of the vial are clear and remain clear after the bottle is shaken or rotated. Note: The contents of the vial of Humulin-R should be clear. Do not use if cloudy.

Precautions

Visual disturbances in uncontrolled diabetes due to refractive changes are reversed during the early phase of effective management. However, since alteration in osmotic equilibrium between the lens and ocular fluids may not stabilize for a few weeks after initiating therapy, it is wise to postpone prescribing new corrective lenses for 3 to 6 weeks.

Insulin requirements may be increased during illness or emotional disturbances or if the patient is receiving concurrent administration of drugs with hyperglycemic activity, e.g. oral contraceptives, corticosteroids or thyroid replacement therapy.

Insulin requirements may be reduced in the presence of renal or hepatic impairment or if the patient is receiving concurrent administration of drugs with hypoglycemic activity, e.g. monoamine oxidase inhibitors and beta-adrenergic blockers.

The number and size of daily doses and the time of administration, as well as diet and exercise, are problems that require direct and continuous medical supervision. Usually, the most satisfactory injection time is before breakfast.

Prompt recognition and appropriate management of the allergic complications of insulin therapy are essential for the safe and effective control of diabetes mellitus.

Transferring from Other Insulin: A small number of patients transferring from insulin of animal source to insulin of recombinant DNA origin may require a reduced dosage, especially if they are tightly controlled and bordering on hypoglycemia. The dosage reduction may occur with the first dose or over a period of several weeks. There is a risk of hypoglycemia if the insulin requirement is decreased, and both the physician and the patient should be aware of this possibility. The risk can be considered to be minimal if the daily dose is less than 40 units.

Pregnancy

It is essential to maintain good control of the insulin-diabetic patient throughout pregnancy. Insulin requirements usually decrease during the first trimester and increase during the second and third trimesters.

Lactation

Diabetic patients who are nursing may require adjustments in insulin dose and/or diet.

Drug Interactions: Hormones that tend to counteract the hypoglycemic effects of insulin include growth hormone, corticotropin, glucocorticoids, thyroid hormone and glucagon. Epinephrine not only inhibits the secretion of insulin, but also stimulates glycogen breakdown to glucose. Thus, the presence of such diseases as acromegaly, Cushing’s syndrome, hyperthyroidism, and pheochromocytoma complicate the control of diabetes.

The hypoglycemic action of insulin may also be antagonized by phenytoin. Insulin’s hypoglycemic action can be increased in some patients by concomitant administration of anabolic steroids, MAO inhibitors, guanethidine, alcohol, propranolol (masking effect) or other drugs affecting beta-adrenergic receptors, or by daily doses of 1.5 to 6 g of salicylates.

Insulin requirements can be increased, decreased, or unchanged in patients receiving diuretics. Concomitant administration of oral contraceptives can cause a decrease in glucose tolerance in diabetic women possibly resulting in increased daily insulin requirements.

Adverse Reactions

Since Humulin has been available worldwide, reports of local and systemic allergic reactions in patients receiving it have been received. As with all insulins, local inflammatory responses may result from improper cleansing of the skin, contamination of the injection site with alcohol, use of an antiseptic containing impurities or accidental intracutaneous rather than s.c. injection. Local reactions that result in skin sensitivity phenomena usually subside spontaneously.

Insulin lipohypertrophy has been reported with Humulin. This complication has been ascribed to the local pharmacologic effects of the s.c. injection of insulin. A few cases of lipoatrophy and serum sickness have also been reported.

Symptoms And Treatment Of Overdose

Hypoglycemia

Cause Hypoglycemia (low blood glucose, also called ‘insulin reaction’) can occur if the patient takes too much insulin, misses meals, exercises or works too hard just before a meal, or has an infection or becomes ill (especially with diarrhea or vomiting). Or if his/her body’s need for insulin changes for other reasons.

Symptoms

Hypoglycemia may occur in any patient receiving insulin and is most commonly manifested by hunger, nervousness, warmth and sweating, and palpitations. Patients also may experience headache, confusion, drowsiness, fatigue, anxiety, blurred vision, diplopia, or numbness of the lips, nose or fingers. The clinical manifestations of hypoglycemia can be masked by the concomitant administration of propranolol or other beta-adrenergic blockers.

Symptoms are likely to appear anytime when the blood sugar concentration falls below 2.2 mmol/L (40 mg/100 mL) but may occur with a sudden drop in blood glucose even when the value remains above 2.2 mmol/L (40 mg/100 mL).

Treatment

If a patient is unable to take soluble carbohydrate or fruit juice orally, hypoglycemia is treated with 10 to 20 g of dextrose i.v. or glucagon may be given s.c. or i.m.

Dosage And Administration

The dosage should be determined by the physician, according to the requirements of the patient.

New Patients

Patients receiving insulin for the first time can be started on Humulin in the same manner as they would be on animal-source insulin.

Patients should be monitored closely during the adjustment period.

Transfer Patients

When transferring patients from animal-source insulin to Humulin, use the same dose and dosage schedule.

Some patients transferring to Humulin will require a change in dosage from that used with animal-source insulin. If an adjustment is needed, it may be made with the first dose or over a period of several weeks.

Changes in total daily dosage, the number of injections per day, and/or timing of injections may be necessary to achieve maximum glycemic control.

When a patient on high doses of animal insulin is switched to Humulin, it may be appropriate to reduce the starting dosage and monitor the patient carefully.

Patients who have systemic allergy to pork or beef insulin may also react to human insulin. In such patients, appropriate procedures (intradermal testing and, if necessary, desensitization) should be undertaken before therapeutic doses of human insulin are administered.

A few patients who experienced hypoglycemic reactions after being transferred to Humulin have reported that the early warning symptoms, i.e., nervousness, sweating and palpitations, were less pronounced than they were with animal-source insulin.

Formulations of Humulin appear to produce a slightly faster onset and slightly shorter duration of action than the corresponding forms of animal-source insulins.

Humulin-R is a clear, colorless solution. It may be administered by s.c., i.m. or i.v. injection.

Humulin-N, Humulin Mixtures, Humulin-L and Humulin-U are suspensions. They should be administered by s.c. injection only.

S.C. administration, preferably by the patient, should be in the upper arms, thighs, buttocks or abdomen. Injection sites should be rotated so that the same site is not used more than approximately once a month.

Care should be taken to ensure that a blood vessel has not been entered. The injection site should not be massaged.

Mixing Instructions

The rapid action of Humulin-R is preserved when mixed with Humulin-N; independent of the time lag between mixing and administration, and independent of the proportion of regular insulin incorporated in the mixture.

Humulin-L and Humulin-R bind immediately after mixing resulting in a delay in the onset of the regular insulin action, reduction in peak activity magnitude, and prolonged total duration of activity.

Mixing Humulin-R and Humulin-U results in reduction of the quick-acting effect of regular insulin.

The effects of mixing Humulin with animal-source insulins have not been studied. This practice is not recommended.

Stability and Storage

Insulin should be stored in a cold place (2 to 10°C), preferably in a refrigerator, but not in a freezer. Do not let it freeze or leave it in direct sunlight. Expiration dates are stated on the labels.

When in use, vials and cartridges may be kept at room temperatue for up to 28 days.

Availability And Storage

Humulin-R

Each mL contains 100 units of Regular insulin. Nonmedicinal ingredients: glycerol and m-cresol. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Cartridges of 1.5 and 3 mL, boxes of 5. Vials of 10 mL.

Humulin-N

Each mL contains 100 units of NPH insulin. Nonmedicinal ingredients: dibasic sodium phosphate, glycerol, m-cresol, phenol, protamine sulfate and zinc. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Cartridges of 1.5 and 3 mL, boxes of 5. Vials of 10 mL.

Humulin-L

Each mL contains 100 units of Lente insulin. Nonmedicinal ingredients: methyl paraben, sodium acetate, sodium chloride and zinc. May contain dimethicone, hydrochloric acid and sodium hydroxide. Vials of 10 mL.

Humulin-U

Each mL contains 100 units of Ultralente insulin. Nonmedicinal ingredients: methyl paraben, sodium acetate, sodium chloride and zinc. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Vials of 10 mL.

Humulin 10/90

Each mL contains 10 units of Regular insulin and 90 units of NPH insulin. Nonmedicinal ingredients: dibasic sodium phosphate, glycerol, m-cresol, phenol, protamine sulfate and zinc. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Cartridges of 1.5 and 3 mL, boxes of 5. Vials of 10 mL.

Humulin 20/80

Each mL contains 20 units of Regular insulin and 80 units of NPH insulin. Nonmedicinal ingredients: dibasic sodium phosphate, glycerol, m-cresol, phenol, protamine sulfate and zinc. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Cartridges of 1.5 and 3 mL, boxes of 5. Vials of 10 mL.

Humulin 30/70

Each mL contains 30 units Regular insulin and 70 units of NPH insulin. Nonmedicinal ingredients: dibasic sodium phosphate, glycerol, m-cresol, phenol, protamine sulfate and zinc. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Cartridges of 1.5 and 3 mL, boxes of 5. Vials of 10 mL.

Humulin 40/60

Each mL contains 40 units of Regular insulin and 60 units of NPH insulin. Nonmedicinal ingredients: dibasic sodium phosphate, glycerol, m-cresol, phenol, protamine sulfate and zinc. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Cartridges of 1.5 and 3 mL, boxes of 5. Vials of 10 mL.

Humulin 50/50

Each mL contains 50 units of Regular insulin and 50 units of NPH insulin. Nonmedicinal ingredients: dibasic sodium phosphate, glycerol, m-cresol, phenol, protamine sulfate and zinc. May contain: dimethicone, hydrochloric acid and sodium hydroxide. Cartridges of 1.5 and 3 mL, boxes of 5. Vials of 10 mL.

Humulin cartridges are designed for use with the B-D Pen, B-D Pen Ultra Cartridge System, or future Lilly injector systems.

Advantages

• Non-anabolic steroid alternative to muscle growth
• You can buy Humulin here

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British Dragon (Thailand)
50 Tabs x 10mg Total 500mg

Halotestin halotestex (fluoxymesterone)

Halotestin (fluoxymesterone substance) is precursor of methyltestosterone, which is more androgenic by nature than plain testosterone. Anabolic properties of halotestin are not very strong thus it’s mostly used for increasing strength rather than muscle gains. This is especially interesting for powerlifters, who need to increase strength without increasing own mass and moving to higher weight class.

In bodybuilding, Halotestin is mostly used in pre-competition stacks thanks to it’s strong androgenic effect, low aromatization and maintaining low estrogen levels. This leads to decent improvement in muscle hardness and shape, especially if athlete has low body fat. Dosages like 20 mg/ED does not cause water retention.

Halotestin increases recovery, allowing more intense training. In addition, users report increased aggressiveness, which makes it useful not only to bodybuilders or weight lifters but especially to football and hockey players and fighters of all kinds.

Halotestin (fluoxymesterone) dosage and usage

Dosage for bodybuilders normally range between 20 and 30 mg/ED. Powerlifters should go with 40 mg/ED, sometimes more.

Split daily dosage on two equal parts and take mornings and evenings with substantial amount of water. Could be taken along with meal.

Stacking

Since this is mostly androgenic steroid it requires anabolic component to increase cycle effectiveness.
For pre-competition cycle it best stacks with primobolan in order to avoid water retention and “puffy” muscles.

For more gaining Tables of Cycles and even contest preparations it could be well stacked with Nandrolone Decanoate, (deca), oxymetholone (Anadrol/Anapolon (Oxymetholone)) or Boldabol (Equipoise).

Great progress could be achieved by taking 600 mg Boldabol (Equipoise) / week and halotestin 30 mg/ED for 4 weeks

Improved strength induced by Halotestin could be turned into solid, quality muscle gains by taking the above mentioned gear. This is extremely beneficial to the athletes who are prone to estrogen-related sides such as water retention and swollen breast glands.

Detection time

3 months

Halotestin (fluoxymesterone) side effects and PCT

Maybe only Anadrol (Anadrol 50 / Anapolon 50)  (oxymetholone) produces more side effects than Halotestin (fluoxymesterone). Usage of this product within the cycle should not exceed 4-6 weeks with 20-30 mg/ED in most cases. Halotestin is highly liver-toxic and thus using of liver protectors such as Liv-52 or Essentiale Forte is highly desirable. Also it may cause gastrointestinal pain.

Other possible sides are:

• acne
• nasal bleeding
• headaches

And, of course, it suppresses endogenous hormonal production, so proper PCT is required. Athlete should at least use clomiphene to restore afterwards. Also increased aggressiveness in males reported.

Gynecomastia and high blood pressure are not the case with it.

Female usage

In bodybuilding – NO. There are some medical (anti-cancer) usages, but this is beyond the scope of current article

Advantages

• Low aromatization
• Good for pre-competition cycle
• You can buy Halotestin here

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Merck & Co., Inc. (Greece)
14 Tabs x 5mg Total 70mg

Fincar, Finasteride, Generic Proscar/Propecia

Active Ingredient: Finasteride

Generic Names: Proscar, Propecia, Finast, Fincar

Proscar or more known brand Propecia is a hair growth medication for the management of significant hair loss. Propecia is a medical breakthrough-the first pill that effectively treats male pattern hair loss on the vertex (at top of head) and anterior mid-scalp area.

By all measures, the clinical results of Propecia in men are impressive:

• 83% maintained their hair based on hair count (vs. 28% with placebo).
• 66% had visible re-growth as rated by independent dermatologists (vs. 7% with placebo).

Importantly Propecia helps grow natural hair-not just peach fuzz and is as convenient to take as a vitamin: one pill / 1mg a day.

Advantages

• Effectively treats male pattern hair loss
• You can buy Fincar, Proscar (Finasteride, Propecia) here

There are several reliable sources where you can buy anabolic steroids:

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Nandrolone Decanoate (Deca-Durabolin)

Nandrolone Decanoate (Deca-Durabolin) is a favorite to thousands of steroid users. In our recent survey, it was revealed that Deca is the most widely used anabolic steroid. It is easy on the liver and promotes good size and strength gains while reducing body fat.

Although Nandrolone Decanoate is still contained in many generic compounds, almost every athlete connects this substance with Deca-Durabolin. Organon introduced Deca-Durabolin during the early 1960’s as an injectable steroid available in various strengths. Most common are 50 mg/ml and 100 mg/ml. Deca-Durabolin is the most widespread and most commonly used injectable steroid. Deca’s large popularity can be attributed to its numerous possible applications and, for its mostly positive results. The distinct anabolic effect of Nandrolone Decanoate is mirrorred in the positive nitrogen balance.” Nitrogen, in bonded form. is part of protein. Deca Durabolin causes the muscle cell to store more nitrogen than it releases so that a positive nitrogen balance is achieved. A positive nitrogen balance is synonymous with muscle growth since the muscle cell, in this phase, assimilates (accumulates) a larger amount of protein than usual. The same manufacturer, however, points out on the package insert that a positive nitrogen balance and the protein building effect that accompany it will occur only if enough calories and proteins are supplied. One should know this since, otherwise, satisfying results with Nandrolone Decanoate cannot be obtained.

The highly anabolic effect of Nandrolone Decanoate is linked to a moderately androgenic component, so that a good gain in muscle mass and strength is obtained. At the same time, most athletes notice considerable water retention which, no doubt, is not as distinct as that with injectable testosterones but which in high doses can also cause a smooth and watery appearance. Since Deca-Durabolin also stores more water in the connective tissues, it can temporarily ease or even cure existing pain in joints. This is especially good for those athletes who complain about pain in the shoulder, elbow, and knee; they can often enjoy pain-free workouts during treatment while using Nandrolone Decanoate. Another reason for this is that it blocks the cortisone receptors thus allowing less cortisone to reach the muscle cells and the connective tissue cells. Athletes use Nandrolone Decanoate, depending on their needs, for muscle buildup and in preparation for a competition. Deca-Durabolin is suitable, even above average, to develop muscle mass since it promotes the protein synthesis and simultaneously leads to water retention. The optimal dose for this purpose lies between 200 and 600 mg/week. Scientific research has shown that best results can be obtained by the intake of 2 mg/pound body weight. Those who take a dose of less than 200 mg/week will usually feel only a very light anabolic effect which, however, increases with a higher dosage. The anabolic and consequent buildup effect of Nandrolone Decanoate, up to a certain degree, depends on the dosage. In the range of approx. 200 to 600 mg/week, the anabolic effect increases almost proportionately to the dosage increase.  If more than 600 mg/week are administered, the relationship of the positive to the negative effects shifts in favor of the latter.In addition, at a dosage level above 600 mg/week, the anabolic effect no longer increases proportionately to the dosage increase, so that 1000 mg/week do not guarantee significantly better results than 600 mg/week.

Most male athletes experience good results by taking 400 mg/week. Steroid novices usually need only 200 mg/week. Deca Durabolin works very well for muscle buildup when combined with Dianabol (D-bol) and Testoviron Depot. The famous Dianabol (D-bol)/Deca stack results in a a fast and strong gain in muscle mass. Most athletes usually take 15-40 mg Dianabol (D-bol)/day and 200-400 mg Deca/week. Even faster results can be achieved with 400 mg Deca/week and 500 mg Sustanon/week. Athletes report an enormous gain in strength and muscle mass when taking 400 mg Deca/week, 500 mg Sustanon/week, and 30 mg Dianabol (D-bol)/day. Deca is a good basic steroid which, for muscle buildup, can be combined with many other steroids. Although Nandrolone Decanoate is not an optimal steroid when preparing for a competition, many athletes also achieve good results during this phase. Since Deca Durabolin is a long-term anabolic, there is risk that with a higher dosage, the competing athlete will retain too much water. A conversion into estrogen, that means an aromatizing process, is possible with deca durabolin but usually occurs only at a dose of 400 mg/week.

During competitions with doping tests Nandrolone Decanoate must not be taken since the metabolites in the body can be proven in a urine analysis up to 18 months later. Those who do not fear testing can use Deca as a high-anabolic basic compound in a dosage of 400 mg/week. The androgens contained in 400 mg/week also help to accelerate the body’s regeneration. The risk of potential water retention and aromatizing to estrogen can be successfully prevented by combining the use of Proviron with Nolvadex. A preparatory stack often observed in competing athletes includes 400 mg/week Deca-Durabolin, 50 mg/day Winstrol, 228 mg/week Parabolan, and 25 mg/day Anavar. Although the side effects with Deca-Durabolin are relatively low with dosages of 400 mg/week, androgenic-caused side effects can occur. Most problems manifest themselves in high blood pressure and a prolonged time for blood clotting, which can cause frequent nasal bleeding and prolonged bleeding of cuts, as well as increased production of the sebaceous gland and occasional acne. Some athletes also report headaches and sexual overstimulation. When very high dosages are taken over a prolonged period, spermatogencsis can be inhibited in men, i.e the testes produce less testosterone. The reason is that Deca Durabolin, like almost all steroids, inhibits the release of gonadotropin from the hypophysis.

Women with a dosage of up to 100 mg/week usually experience no major problems with Deca Durabolin. At higher dosages androgenic-caused virilization symptoms can occur, including deep voice (irreversible), increased growth of body hair, acne, increased libido, and possibly clitorishypertrophy. Since most female athletes get on well with Deca-Durabolin a dose of Deca 50 mg+/week is usually combined with Anavar 10 mg+/day. Both compounds, when taken in a low dosage, are only slightly androgenic so that masculinizing side effects only rarely occur. Deca, through its increased protein synthesis, also leads to a net muscle gain and Anavar, based on the increased phosphocreatine synthesis, leads to a measurable strength gain with very low water retention.

Other variations of administration used by female athletes are Nandrolone Decanoate and Winstrol tablets, as well as Deca-Durabolin and Primobolan’s tablets. Since Nandrolone Decanoate has no negative effects on the liver it can even be used by persons with liver diseases. Exams have shown that a combined application of Dianabol / Deca-Durabolin increases the liver values which, however, return to normal upon discontinuance of the 17-alpha alkylated Dianabol and continued administration of Deca-Durabolin. Even a treatment period with Deca-Durabolin over several years could not reveal a damage to the liver. For this reason Nandrolone Decanoate combines well with Andriol (240-280 mg/day) since Andriol is not broken down through the liver and thus the liver function is not influenced either. Older and more cautious steroid users, in particular, like this combination.

Dosage and usage

See Deca-Durabolin

Stacking

See Deca-Durabolin

 

Detection times

Injectable Nandrolone Decanoate stays in your system for more than one year, in certain occasions even up to 18 months, probably due to oil’s ability to remain in tissues.

We do not know scientifically proven period for oral Nandrolone Decanoate. Our suggestion (just suggestion) is that it might be approximately four times lower, i.e. from 2 to 4 months.

Side effects and PCT with Dianabol

See Deca-Durabolin

Female usage

Not recommended

Advantages

• Highly anabolic effect
• Liver-friendly
• The most popular injectable anabolic steroid worldwide
• You can buy Deca Durabolin here

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