99%+ Purity Oral Pill & Tablet Exemestane (Aromasin) Pure Powder

Product Details:

 

Aromasin Powder Information
Aromasin Price100gAccording to your needs
500gAccording to your needs
1000gAccording to your needs
Steroid packagingSpecial stealth packaging through Customs
Delivery timeAbout 7 days
ShippingEMS, Hongkong Post, DHL, TNT, Fedex
Payment termsWU, MG, Bitcoin, T/T
Minimum order10g
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99%+ Purity Oral Pill & Tablet Exemestane (Aromasin) Pure Powder

Product Name:   Exemestane (Aromasin) Powder

CAS #:   107868-30-4

Purity:   ≥99%

Exemestane Price:   According to your needs

Exemestane Half Life:   Around 24hrs

Exemestane dosage:   12.5mg-25mg daily

Exemestane Detection time:   2 weeks 

Exemestane Side Effect:   Hoarseness,ankle swelling acne,vomiting,nausea,more hair on the face changes in menstrual periods,changes in skin color

Exemestane Results:   Weight loss and muscle growth for bodybuilder and athletes

 

Exemestane (Aromasin) Specifications:

COA

TEST ITEMSSPECIFICATIONRESULTS
Description: White Crystalline PowderWhite Powder
Identification: PositivePositive
Assay(by HPLC): 98.0~102.0%98.64%
Absorbance(E1cm): 465~495482.5
Melting Point: 191~195°C193.5~195.0°C
Loss On Drying: 0.5%max0.19%
Specific Rotation: +288°~ +298°+290.2°
Residue On Ignition: 0.1%max0.03%
Related Substances: Total:1.5%max<1.3%
 Single:0.5%max<0.4%
Residue Solvents: 0.2%max0.10%
Heavy Metals: 20PPm max<10PPm

 

Exemestane (Aromasin) Descriptions:

Aromasin, as it is most commonly called, is a very potent AI which works by blocking the aromatase enzyme in the body. This drug was originally developed to help fight breast cancer in women by reducing estrogen which some believe to aid in cancer cell growth. While not quite as strong as Letrozole, Exemestane is considerably stronger than Anastrozole.

Studies done with this substance typically show around an 85% reduction in estrogen levels in the body. This can be very useful to bodybuilders who are using aromatizing compounds such as testosterone. Typically, one will begin the use of Exemestane the same day they begin their cycle.

It is also important to note that Aromasin has shown to be very effective at increasing testosterone and IGF levels in the body. Because of this, this drug is also very useful during PCT regime when one is trying to restore natural testosterone levels in order to avoid a post cycle "crash".

It is important to keep doses of Exemestane reasonable, as too much estrogen suppression can result in hindered muscle gains and loss of sex drive. One 25mg tablet a day should be sufficient for effectively keeping estrogen related sides out of the picture, or for effectively raising natural testosterone levels during PCT.

 

Exemestane (Aromasin) Medical Uses:

Exemestane is indicated for the adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to it for completion of a total of five consecutive years of adjuvant hormonal therapy. US FDA approval was in October 2005.

Exemestane is also indicated for the treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy.

 

Exemestane (Aromasin) Contraindications:

The drug is contraindicated in premenopausal women, which of course includes pregnant and lactating women.

 

Exemestane (Aromasin) Adverse effects:

The most common side effects (more than 10% of patients) are hot flashes and sweating, which are typical of estrogen deficiency as caused by exemestane, and also insomnia, headache, and joint pain. Nausea and fatigue are mainly observed in patients with advanced breast cancer.

 

Exemestane (Aromasin) Overdose:

Single doses of up to at least 32-fold (800 mg), as well as continuous therapy with 24-fold (600 mg) the usual daily dose are well tolerated. No life-threatening overdosing is known in humans, but only in animal studies with 2000- to 4000-fold doses (adjusted to body surface area).

 

Exemestane (Aromasin) Interactions:

Exemestane is metabolized by the liver enzyme CYP3A4. While the CYP3A4 inhibitor ketoconazole had no significant effect on exemestane levels in a clinical trial, the strong CYP3A4 inductor rifampicin significantly cut exemenstane levels about in half (AUC −54%, Cmax −41% for a single dose), potentially compromising its effectiveness. Other 3A4 inductors such as carbamazepine and St John's Wort are expected to have similar effects. The clinical relevance of this effect has not been investigated.

Estrogens probably reduce exemestane effectiveness: It would usually be counter-productive to reduce the body's estrogen synthesis with exemestane and then substitute estrogen with pharmaceuticals.

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