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Tamoxifen blocks the actions of estrogen, a female hormone. Certain types of breast cancer require estrogen to grow.

Tamoxifen is used to treat some types of breast cancer in men and women. It is also used to lower a woman’s chance of developing breast cancer if she has a high risk (such as a family history of breast cancer).

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99%+ Purity Methyl Tadalafil (Methyltadalafil) CAS :171488-11-2

Product name:Methyl Tadalafil
CAS NO.:171596-29-5
Assay:99%
Molecular Formula:C22H19N3O4
Molecular Weight:389.341
Description:White Crystalline Powder
Storage Confined Preservation

Methyl Tadalafil Description:

Methyl Tadalafil is a phosphodiesterase type 5 inhibitor, is used to treat erectile dysfunction (ED) and decreased libido in males. Methyl Tadalafil works by aiding relaxation of blood vessels and increasing blood flow in the penis during sexual arousal, resulting in improved erectile function. Methyl Tadalafil is much longer lasting. Effects can be felt anywhere between 36-48 hours.

Methyl Tadalafil improves erectile function significantly, possibly increased sexual activity, and is very safe.
There are limited side effects associated with its use. The most common side effects are headache, upset stomach, back pain, and muscle aches, and usually subside with in a few hours.
Methyl Tadalafil was also found to be significantly higher at the end of the month, due to increased sexual activity.

Methyl Tadalafil Application:

Methyl Tadalafil is a PDE5 inhibitor marketed in pill form for treating erectile dysfunction (ED) under the name Methyl Tadalafil, and under the name Adcirca for the treatment of pulmonary arterial hypertension.

Methyl Tadalafill’s pharmacologic distinction is its longer half-life (17.50 hours) resulting in longer duration of action, and so partly responsible for “The Weekend Pill” sobriquet. Furthermore, the longer half-life is the basis for current investigation of Methyl Tadalafil’s daily therapeutic use in relieving pulmonary arterial hypertension.

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Product Name:   Finasteride Powder

CAS #:   98319-26-7

Purity:   ≥99%

Finasteride Price:   According to your needs

Finasteride Half Life:   Around 1 month

Finasteride dosage:   0.5 mg once daily

Finasteride Detection time:   Unknown

Finasteride Side Effect:   Decreased libido (sex drive);decreased amount of semen released during sex;impotence (trouble getting or keeping an erection); or breast tenderness or enlargement.

Finasteride Results:   Prostate enlargement;Pattern hair loss

Dutasteride (Avodart) Specifications:

COA

Test Items Specification Test Results
Description White or almost white powder Complies
Identification Meet the requirements Complies
Loss on drying ≤0.5% 0.2%
Melting range 246℃~252℃ 246℃~248℃
Heavy metals ≤20ppm Complies
Residue on ignition ≤0.1% Complies
Related substances Biggest Impurities≤0.5% 0.36%
Total Impurity≤1.0% 0.7%
Assay 97.0%~103.0% 99.5%

Dutasteride (Avodart) Descriptions:

Avodart (dutasteride) prevents the conversion of testosterone to dihydrotestosterone (DHT) in the body. DHT is involved in the development of benign prostatic hyperplasia (BPH).

Avodart is used to treat benign prostatic hyperplasia (BPH) in men with an enlarged prostate. It helps improve urinary flow and may also reduce your need for prostate surgery later on.

Avodart is sometimes given with another medication called tamsulosin (Flomax). Be sure to read the medication guide or patient instructions provided with each of your medications.

Avodart may also be used for purposes not listed in this medication guide.

Dutasteride (Avodart) Effects:

Dutasteride belongs to a class of drugs called 5 alpha-reductase inhibitors. A class of drugs refers to medications that work similarly. They’re often used to treat similar conditions.

There is a hormone in your blood called dihydrotestoterone (DHT), which causes your prostate to grow. Drugs like dutasteride prevent the formation of DHT in your body, causing an enlarged prostate to shrink.

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Progesterone

Progesterone Details:

Product Name: Progesterone
Synonyms: PROGESTERONE-WATER SOLUBLE;progestin;PROGESTERONE;PRIMOLUT;17alpha-Hydroxy-6alpha-methylpregn-4-ene-3,20-dione;17alpha-Progesterone;3,20-Pregnene-4;4-Pregnen-3,20-dion
CAS: 57-83-0
MF: C21H30O2
MW: 314.46
EINECS: 200-350-6
Product Categories: MI;FINISHED MEDICINE;Steroids;ketone;Biochemistry;Steroids (Others);Intermediates & Fine Chemicals;Pharmaceuticals;Intracellular receptor;Steroid and Hormone;API;ENDOMETRIN;Plant extract;Pharma material;Inhibitors
Mol File: 57-83-0.mol

Progesterone Specifications:

COA

TEST ITEMS SPECIFICATION RESULTS
Description : White or Almost White Crystalline Powder white powder
Identification : A.B. Positive
Assay : 97.0~103.0% 99.3%
Specific Rotation : +101°~+105° +102.6°
Loss On Drying : 1.0%max 0.27%
Melting Point : 153~157°C 153.0~155.0°C
Organic Volatile Impurities : meets the requirement. Conforms
Related Substances : meets the requirement. Conforms
Residual Solvents : meets the requirement. Conforms
Particle Size : 100% ≤ 20 microns Conforms
Conclusion The specification conform with USP30 standard

Progesterone Descriptions:

Progesterone (abbreviated as P4), also known as pregn-4-ene-3,20-dione,is an endogenous steroid and progestogen sex hormone involved in the menstrual cycle, pregnancy, and embryogenesis of humans and other species.It belongs to a group of steroid hormones called the progestogens,and is the major progestogen in the body. Progesterone is also a crucial metabolic intermediate in the production of other endogenous steroids, including the sex hormones and the corticosteroids, and plays an important role in brain function as a neurosteroid.

Progesterone Effects:

The use of progesterone and its analogues have many medical applications, both to address acute situations and to address the long-term decline of natural progesterone levels. Because of the poor bioavailability of progesterone when taken orally, many synthetic progestins have been designed with improved oral bioavailability and have been used long before progesterone formulations became available.

Progesterone is a female Progesterone Hormones important for the regulation of ovulation and menstruation.
Women take progesterone by mouth for inducing menstrual periods who have not yet reached menopause but are not having periods due to a lack of progesterone in the body; and treating abnormal uterine bleeding associated with hormonal imbalance, and severe symptoms of premenstrual syndrome (PMS). progesterone is also used to prevent overgrowth in the lining of the uterus in postmenopausal women who are receiving estrogen hormone replacement therapy. Progesterone is also used in combination with the hormone estrogen to “oppose estrogen” as part of hormone replacement therapy. If estrogen is given without progesterone, estrogen increases the risk of uterine cancer.

Buy Tibolone (Livial) CAS :5630-53-5

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Tibolone

Tibolone Details:

Product name:Tibolone,Livial
Assay:99.5% min
Packing:foil bag or tin
Delivery:Express courier.
Character:White powder.
Categories:Pharmaceutical; Active Pharmaceutical Ingredients; Biochemistry; Steroids

Tibolone Specifications:

COA

Tibolone SPECIFICATION RESULTS
Description : White Or Almost White Crystalline Powder White Powder
Identification : Infrared Absorption Positive
Assay : 97.0~103.0% 99.15%
Melting Point : 33~37°C 34.5~36.5°C
Loss On Drying : 0.5%max 0.30%
Specific Rotation : +32°~ +36°(C=1 in dioxane) +33.5°
Organic Volatile Impurities : 2500PPm max <1000PPm
Residual Solvents : Meet the requirements.(USP29) Confirms
Chromatographic purity : sum of impurities:3.0%max <3.0%
Conclusion The specification conform with USP32 standard

Tibolone Descriptions:

Tibolone is a synthetic hormone-type drug which is used mainly for hormone replacement therapy in post-menopausal women. It is a synthetic steroid that has the same activity as the female sex hormones estrogen and progesterone and the androgen testosterone. Tibolone helps restore hormonal balance in the body.

When estrogen levels are low tissues can slowly degenerate, as is experienced during menopause. In addition, low levels of estrogen can cause distressing symptoms such as hot flushes, night sweats, mood swings, reduced sex drive and vaginal dryness.

Tibolone is broken down into three compounds which act in a similar way to the natural estrogen and progesterone found in the body. It restores plasma endorphin level in post-menopausal women and acts centrally to affect the thermo-regulatory system.

Tibolone Usages:

Tibolone is used to mimic the activity of the naturally occurring female sex hormones oestrogen and progestogen in the body. It helps to restore the natural balance of these hormones.

Tibolone is a female sex hormone, sometimes known as a hormone replacement therapy (HRT). Tibolone is broken down in the body to make hormones and it then has an effect similar to combined HRT (a type of HRT containing the female hormones oestrogen and progestogen).

Tibolone is used to relieve symptoms that start to occur when the female body no longer produces certain hormones such as oestrogen. This may occur after the menopause, also known as the change of life, or after surgery to remove the ovaries. Tibolone may also be used to stop your bones from becoming brittle.
In general this drug is used to treat symptoms associated with a lack of oestrogen in women who have gone through the menopause (change of life) more than one year ago.

Benefits of being on this drug can include replacement of lost hormones leading to an improvement in a number of symptoms including hot flushes, night sweats, dryness or irritation of the vagina and reduced sex drive. Tibolone can also reduce the likelihood of your bones becomes brittle and breaking by preventing the bone disease osteoporosis.

Here are ypical uses of tibolone.

Prevention of bone fractures in women
Treatment of symptoms associated with low levels of the hormone oestrogen in women.

Tibolone Dosage:

Take Tibolone by mouth usually once a day, with or without food. Swallow the Tibolone whole with some water.

It is important that you see your doctor for regular check-ups (at least once a year) whilst you are taking tibolone. You should also go for regular breast screening and cervical smear tests and check yourself regularly for any breast changes such as dimpling of the skin, changes in the nipples and lumps. If you have started the menopause you should not take tibolone until 12 months after your last natural period.
Use this medication regularly in order to get the most benefit from it.

Remember to use Tibolone at the same time each day – unless specifically told otherwise by your doctor.
It may take up to a few weeks before the full benefit of this drug takes effect.

Certain medical conditions may require different dosage instructions as directed by your doctor.

Dosage is based on your age, medical condition, response to therapy, and use of certain interacting medicines.

Take Special Care with Tibolone:

Before starting tibolone treatment, you should inform your doctor about your personal and family medical history. Your doctor will perform a thorough physical and gynecological examination before beginning treatment and periodically along its duration, especially breast.

Should see your doctor immediately if any of these conditions worse or appear while taking tibolone:

– Gynecological disorders of any kind
– Changes or alterations in the breast
– High levels of fat (triglycerides) in the blood or a family history of this
– Hypertension, particularly if it worsens or does not improve with antihypertensive therapy
– Disorders of the liver or kidney
– Diabetes
– Functional disorders of the gallbladder
– Headaches (migraines) intense and repetitive
– An immune disease called systemic lupus erythematosus
– Epilepsy
– Asthma
– Jaundice (yellowing of the skin and whites of the eyes)
– Pruritus (itching)

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Product Name:   Dutasteride Powder

CAS #:   164656-23-9

Purity:   ≥99%

Dutasteride Price:   According to your needs

Dutasteride Half Life:   Around 1 month

Dutasteride dosage:   0.5 mg once daily

Dutasteride Detection time:   2-3 hours

Dutasteride Side Effect:   Decreased libido (sex drive);decreased amount of semen released during sex;impotence (trouble getting or keeping an erection); or breast tenderness or enlargement.

Dutasteride Results:   Hair Growth

Dutasteride (Avodart) Specifications:

COA

Test Items Specification Test Results
Description White or almost white powder Complies
Identification Meet the requirements Complies
Loss on drying ≤0.5% 0.2%
Melting range 246℃~252℃ 246℃~248℃
Heavy metals ≤20ppm Complies
Residue on ignition ≤0.1% Complies
Related substances Biggest Impurities≤0.5% 0.36%
Total Impurity≤1.0% 0.7%
Assay 97.0%~103.0% 99.5%

Dutasteride (Avodart) Descriptions:

Avodart (dutasteride) prevents the conversion of testosterone to dihydrotestosterone (DHT) in the body. DHT is involved in the development of benign prostatic hyperplasia (BPH).

Avodart is used to treat benign prostatic hyperplasia (BPH) in men with an enlarged prostate. It helps improve urinary flow and may also reduce your need for prostate surgery later on.

Avodart is sometimes given with another medication called tamsulosin (Flomax). Be sure to read the medication guide or patient instructions provided with each of your medications.

Avodart may also be used for purposes not listed in this medication guide.

Dutasteride (Avodart) Effects:

Dutasteride belongs to a class of drugs called 5 alpha-reductase inhibitors. A class of drugs refers to medications that work similarly. They’re often used to treat similar conditions.

There is a hormone in your blood called dihydrotestoterone (DHT), which causes your prostate to grow. Drugs like dutasteride prevent the formation of DHT in your body, causing an enlarged prostate to shrink.

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JinYang Assay: 99%
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JinYang Appearance: The product is yellow or light yellow crystalline powder, odorless, tasteless, soluble in water and alcohol

JinYang Usage: For the treatment of erectile dysfunction (ED), the use of antidepressants, antipsychotics and anti-hypertensive drugs cause impotence, and after surgery or trauma caused by impotence are valid.
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COA

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Loss on drying ≤2.0% 1.15%
Heavy metals PPM <30ppm Complies
Microbiology
Total Plate Count <1000cfu/g 800cfu/g
Yeast & Mold <100cfu/g 90cfu/g
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High quality plant extract Maca Extract Macamide Powder/Red maca powder

Product name: Peruvian Maca Root Extract Powder
Latin name: Lepidium meyenii
Active ingredients: Beta Ecdysone
Appearance: Brownish Yellow Powder
Origin: Root
Specification: Ratio Extract: 4:1 10:1 20:1
Test Method: TLC

Peruvian Maca Root Extract Powder Description:

Maca extract is taken from the root of the maca plant. It is consumed as a root vegetable and it grows naturally in Peru. This extract is thought to have many health benefits and healing properties. There are many ways to prepare maca extract, including drying the roots and grinding them into a fine powder or boiling the roots to extract the natural oils. The extract typically is sold in a liquid or a gel-like capsule.

Maca is a cruciferous plant Lepidium in the shape of radish-like hypertrophy of the roots, originating in Peru and Central’s (Jinin) and Pasco (Pasco) near the Andes above 4,000 meters, the area cold, strong winds, eco- harsh conditions unsuitable for other crops, and thus Mame a source of food for Inca.. Maca can increase with physical, energetic, eliminate anxiety and improve sexual function. Its fresh roots can eat with meat and vegetables , also be dried food cooked with water or milk.

Body builders or people who are trying to lose weight can sometimes benefit by taking maca extract. It contains many vitamins and minerals as well as amino acids, which help to boost themetabolism and this makes the body run more efficiently. Amino acids can also help to improve muscle structure. Maca extract is sometimes used as an alternative to dangerous anabolic steroids used by body builders to improve muscle mass.

Peruvian Maca Root Extract Powder Application:

The nutritional value of dried maca root is high, similar to cereal grains such as rice and wheat. The average composition is 60-75% carbohydrates, 10-14% protein, 8.5% dietary fiber, and 2.2% fats. Maca is rich in the dietary minerals calcium and potassium (with low content of sodium), and contains the essential trace elementsiron, iodine, copper, manganese, and zinc as well as fatty acids including linolenic acid, palmitic acid, andoleic acids, and 19 amino acids.

Maca is consumed as food for humans and livestock, suggesting any risk from consumption is rather minimal. It is considered as safe to eat as any other vegetable food. However, maca does contain glucosinolates, which can causegoiters when high consumption is combined with a diet low in iodine. This being said, darker colored maca roots (red, purple, black) contain significant amounts of natural iodine, a 10-gram serving of dried maca generally containing 52 µg of iodine. Though this is common in other foods with high levels of glucosinolate, it is uncertain if maca consumption can cause or worsen a goiter.

Small-scale clinical trials performed in men have suggested that maca extracts can improve semen quality, and boost libido. A small double-blind, randomized, parallel group dose-finding pilot study has shown that Maca root may alleviate SSRI-induced sexual dysfunction.A 12-week randomized, double-blind, placebo-controlled study in 56 subjects found that Maca has no effect on sex hormone levels in men, including LH, FSH,prolactin, 17-OH progesterone, testosterone or estradiol.

A recent review states “Randomized clinical trials have shown that maca has favorable effects on energy and mood, may decrease anxiety and improve sexual desire. Maca has also been shown to improve sperm production, sperm motility, and semen volume.” In total over 160 studies into the health effect of Maca have been indexed by the United States National Library of Medicine,National Institutes of Health.However, a 2010 review of the extant evidence for the effect of Maca on libido found only tentative support for its aphrodisiac claims.

Peruvian Maca Root Extract Powder Function:

Adaptogenic Properties

Maca root considered an adaptogenic herb. Adaptogenic herbs help increase the bodies resistance to stress whether the stress is a physical or emotional ailment it doesn’t matter. Adaptogens helps normalize body functions one in particular is to restore proper adrenal gland and endocrine functions.
Balance Hormones

One of the best benefits to using maca is its ability to balance hormones naturally. It makes Maca great for a variety of hormonal disorders such as PMS( Pre-menstrual syndrome), menopause, andropause and various other conditions which involve unbalanced hormones. Maca does not stimulate production or directly work any particular hormone, its hormone balancing effects come from its adaptogenic properties which aid the adrenal glands and support the endocrine system.

Increase Energy

Much like other adaptogenic herbs, maca provides a non central nervous stimulating and adrenal gland friendly way to naturally increase energy. Adaptogenic herbs support the adrenal glands and don’t cause burn out like various other CNS stimulants such as caffeine. Maca has also been shown to increase stamina and endurance.

Increase Libido/Sex Drive

Another of maca most prized benefits is its ability to increase libido and boost sex drove. Studies have shown maca can heighten libido and sexual desire and may alleviate SSRI induced erectile dysfunction. If that wasn’t enough maca has shown in studies to boost fertility by increasing sperm quality, volume, motility and production.

Rich Source of Nutrients

Maca is a source of nutrients such as amino acids, fatty acids, sterols, vitamins, minerals such as selenium, calcium, magnesium, and iron. Maca is also rich in over 60 health boosting phyto-chemicals/compounds which are where a lot of its benefits stem from also.

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Product name:Flibanserin hydrochloride
Synonyms:Flibanserin; Flibanserin HCl
CAS NO:147359-76-0
Molecular formula:C20H21F3N4O・ClH
Appearance:white crystalline powder
Assay 99%

Flibanserin Hydrochloride Description:

Flibansetrin HCL has high affinity for serotonin receptors in the brain: it acts as an agonist on 5-HT1A and an antagonist on 5-HT2A. In vivo, flibanserin binds equally to 5-HT1A and 5-HT2A receptors.

However, under higher levels of brain 5-HT (i.e., under stress), flibanserin may occupy 5-HT2A receptors in higher proportion than 5-HT(1A) receptors. It may also moderately antagonize D4 (dopamine) receptors and 5-HT2B and 5-HTB2C. Its action on neurotransmitter receptors may contribute to reduction in serotonin levels and increase in dopamine and norepinephrine levels, all of which may play part in reward processing.

Flibanserin Hydrochloride Application:

Flibansetrin hcl has high affinity for serotonin receptors in the brain: it acts as an agonist on 5-HT1A and an antagonist on 5-HT2A. In vivo, flibanserin binds equally to 5-HT1A and 5-HT2A receptors. However, under higher levels of brain 5-HT (i.e., under stress), flibanserin may occupy 5-HT2A receptors in higher proportion than 5-HT(1A) receptors. It may also moderately antagonize D4 (dopamine) receptors and 5-HT2B and 5-HTB2C. Its action on neurotransmitter receptors may contribute to reduction in serotonin levels and increase in dopamine and norepinephrine levels, all of which may play part in reward processing.

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Flibanserin

Product Name:Flibanserin
Another Name:Addyi,Flibanserin Powder,Bimt 17,167933-07-5,Sex Enhancement Powders
CAS: 167933-07-5
Assay:99.86%
Molecular formula: C20H21F3N4O
Molecular weight: 390.4021
InChI: InChI = 1 / C20H21F3N4O / c21-20 (22,23) 15-4-3-5-16 (14-15) 26-11-8-25 (9-12-26) 10-13-27- 18-7-2-1-6-17 (18) 24-19 (27) 28 / h1-7,14H, 8-13H2, (H, 24,28)
Density: 1.292 g / cm3
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Flibanserin is called ,known as the “female Viagra”, is a prescription medication used to enhance sexual desire and decrease emotional distress in premenopausal women with hypoactive sexual desire disorder (HSDD).

A new drug designed to boost sexual desire in women is controversial for some and eagerly awaited by others, but it’s hit a potentially serious snag. The drug didn’t boost women’s desire any more than a placebo in two clinical trials. The Food and Drug Administration posted the clinical trial results on its website today in advance of a committee meeting on Friday, when a panel of experts will vote whether or not to recommend approval of the drug called flibanserin. (The FDA usually follows the recommendations of its expert panels. ) Although there was a slight increase in the number of sexually satisfying events flibanserin users had each month, the FDA staff who reviewed the results said the so-called response rate isn’t “particularly compelling. ”
It’s called the “little pink pill, ” a tiny tablet that could have a huge impact on treating female sexual dysfunction. If it’s approved, it would become the first drug of its kind on the market.

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