jack3d ve hyper ac..mass impact.

slm ataberkim birsey danısmak ıstıyorum bnde suan jack3d universal creatin mega forte mussletech nitrotech ve ast bcaa 4500 var snce bunları nasıl kombıne etmelıyım ve diger sorum dark matterden ck fayda gordunmu sımdıden tesekkurler.
birde jack 3 d yle beraber creatin kullanılırmı acaba yasım 21 kılom 72 boy 1 77

 

jack3 ile creatin kulllandim ve iyi sonuc almistim tabii ki supplement isi kisiden kisiye degisik sonuclar verebiliyor, denemen de bir zarar yok bence...Dark matter bence piyasada ki en iyi antreman sonrasi bir urun....

 

Ck Tesekkurler yardimin icin pki dark matterdeki az proteini gun icinde nasil karsiliyorsun acaba supplement olarak yani dark matterin yannda wheyi nasil kombine etmeliyim

 

DARK MATTER is your ultimate post workout muscle growth accelerator designed to be taken immediately after your workout before you consume any other shake or meal. All other substances will only slow down the precise nutrient infusion of the high velocity nano-physic particles in DARK MATTER, shorten your anabolic window and impede maximum muscle growth and recovery.

workout dan hemen sonra yaklasik 1 saat sonra yemek veya shake....

 

jack3d

ilk kutuda duzenli aldim bir sorun yoktu ikinci kutunun ortasindayken,yaklasik iki hafta once tatli kasigiyla 3 kasik aldim,(kendi kucuk kasigiyla 4-5 yada daha fazla)spor salonunda super energie geldi ama kalp atislarim hizlandi kalp krizi geciriyorum sandim,birde felc olacam korksu geldi,korku yuzunden panik atak oldum kaldirdigim agirliklarin 2 kat fazlasini kaldirdim,ama , yuzumde leke cikti sonra, kafanim arkasinda yag bezesi olustu ,(jack3d kaynaklamiyordur belkide) korkudan 100%whey i ve jack3d yide biraktim,kullananlar dozunda kullansin,fazlasi bunyeniz guclu degilse sorun yaratabilir,, daha cok bilgisi varsada paylasirsa sevinirim,jack3d ile ilgili....

 

jack3d

Kutunun ustunde yazan neyse onu kullanacaksin... o zaman kutunun ustune 5 kasik kullanin yazarlardi...Acemice bir tecrube yasamissiniz...2.5 veya 3 kasik bile fazla jack3d icin...5 kutunun ustunde tuketimim oldu uzun zaman dilimin de hic bir zaman 2.5 kasigi gecmedim gecmem de... Jack3dnin forumunda bu kullanim tozlari ile forumcularin tecrubeleri var, oradan da bilgi edinebilirsiniz.. Tesekkurler...

 

Büyük cesaret

 

Bence de (

 

jack3d Nisan ayi sonu itibari ile Amerika'da satisi yasaklanmistir....Icindeki DMAA maddesi yuzunden... Bununla birlikte asagidaki urunler de dahil... Limitleri sinirin da bir jack3d kullanici olarak uzuldum....


FDA NEWS RELEASE

For Immediate Release: April 27, 2012
Media Inquiries: Tamara Ward, 301-796-7567, [email protected]
Trade Press Inquiries: Sebastian Cianci, 240-402-2291, [email protected]
Consumer Inquiries: 888-INFO-FDA

FDA challenges marketing of DMAA products for lack of safety evidence
Agency cites ten companies in warning letters

The U.S. Food and Drug Administration today issued warning letters to ten manufacturers and distributors of dietary supplements containing dimethylamylamine, more popularly known as DMAA, for marketing products for which evidence of the safety of the product had not been submitted to FDA.

Also referred to as 1,3-dimethylamylamine, methylhexanamine, or geranium extract, the ingredient is in dietary supplements and is often touted as a "natural" stimulant.

The companies receiving warning letters and their product names are:


Company Product(s)
Exclusive Supplements Biorhythm SSIN Juice
Fahrenheit Nutrition Lean Efx
Gaspari Nutrition Spirodex
iSatori Global Technologies, LLC PWR
Muscle Warfare, Inc. Napalm
MuscleMeds Performance Technologies Code Red
Nutrex Research Hemo Rage Black
Lipo-6 Black Ultra Concentrate
Lipo-6 Black
Lipo-6 Black Hers Ultra Concentrate
Lipo-6 Black Hers
SEI Pharmaceuticals MethylHex 4,2
SNI LLC Nitric Blast
USP Labs, LLC Oxy Elite Pro
Jack3D
"Before marketing products containing DMAA, manufacturers and distributors have a responsibility under the law to provide evidence of the safety of their products. They haven’t done that and that makes the products adulterated," said Daniel Fabricant, Ph.D., Director of FDA’s Dietary Supplement Program.

Specifically, the warning letters cite the companies for marketing products for which a notification had not been submitted for the use of DMAA as a New Dietary Ingredient (NDI). Under current law, dietary supplement manufacturers or distributors who use certain dietary ingredients not marketed in a dietary supplement prior to October 15, 1994, are responsible for notifying the FDA of evidence to support their conclusion that their dietary supplements containing NDIs are safe. Manufacturers or distributors must submit notification at least 75 days before marketing their products. The companies warned today were marketing products for which this requirement had not been met.

The FDA warning letters also advised the companies that the agency is not aware of evidence or history of use to indicate that DMAA is safe. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), manufacturers, marketers and distributors of dietary supplements are responsible for ensuring that they are marketing a safe product.

The FDA letters noted that DMAA is known to narrow the blood vessels and arteries, which can elevate blood pressure and may lead to cardiovascular events ranging from shortness of breath and tightening in the chest to heart attack. The agency has received 42 adverse event reports on products containing DMAA. While the complaints do not establish that DMAA was the cause of the incidents, some of the reports have included cardiac disorders, nervous system disorders, psychiatric disorders, and death.

The agency additionally warned the companies that synthetically-produced DMAA is not a “dietary ingredient” and, therefore, is not eligible to be used as an active ingredient in a dietary supplement. DSHEA defines a dietary ingredient as a vitamin, mineral, amino acid, herb or other botanical, a dietary substance for use by man to supplement the diet, or a concentrate, metabolite, constituent, extract, or combination of these substances.

The companies have 15 business days to respond to the FDA with the specific steps they will take to address the issues in the warning letters.

For more information:

How dietary supplements are regulated
Dietary Supplement Health and Education Act of 1994
New Dietary Ingredient notification process
Reporting adverse events associated with FDA regulated products
#

The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.


Read our Blog: FDA Voice

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Yeni Jack3d yi deneyen var mı ?

 

Amerika'da raflarda yerini aldi, eski ambalajinin yarisi kadar.. Ama henuz kullanmadim....

 

Cok yakinda tekrar donuyorum...

 

nereden sıparıs edebılırız jack3d