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Ventolin (Salbutamol Sulfate (Albuterol))

Ventolin
Ventolin
Active Ingredient: Salbutamol Sulfate (Albuterol)
Manufacturer: GlaxoSmithKline ™
Salbutamol (Albuterol) and Clenbuterol belong to the same medicine class called Beta-2 Andrenergic Receptor Agonist/Antagonist. Both medicines share the same properties and both have been used for same conditions in many medical trials. Typically used to treat Asthma, it stimulates beta-2 receptors, which medical studies have shown to extremely beneficial for Asthma as well as fat loss and strength gain. Salbutamol is thermogenic, it will increase metabolism. Some studies may suggest Salbutamol may be more effective in humans than Clenbuterol which has been studied mostly in animals. Please note that the inhaler version of the medicine is potent for asthma only, since it's dose is too small and is rapidly absorbed.

Extracts from the Medical Press:

"Salbutamol has been proven just as efficient as clenbutrol and in fact has been proven anabolic even in humans, while clenbuterol has been proven anabolic in animals only. "
Journal of Sport Medicine 1997 Dec
Clarkson PM, Thompson HS
Department of Exercise Science, School of Public Health and Health Sciences, University of Massachusetts, Amherst, USA.

"Salbutamol (2.7 ppm) fed to pigs between weaning and slaughter increased ADG (5%), dressing percentage (2%) and cross-sectional area of the longissimus (LD) muscle (14%). In fatter, White-line-sired pigs, but not in leaner, Meat-line-sired animals, it reduced backfat thickness (25%)." (This means increased muscle mass by 14% and fat decrease by 25%)
Journal Animal Science 1990 Jan
Warriss PD, Brown SN, Rolph TP, Kestin SC.
AFRC Institute of Food Research, Bristol Laboratory, Langford, UK.

"The data demonstrate that the chronic administration of therapeutic levels of salbutamol increases maximal anaerobic power in man, irrespective of the subjects' training status"
International Sports Medicine 2005 Sep
Le Panse B, Collomp K, Portier H, Lecoq AM, Jaffre C, Beaupied H, Richard O, Benhamou L, De Ceaurriz J, Courteix D.
LPM-IPROS, Faculte des Sports, Orleans, France.

"..in response to salbutamol administration (DeltaAIx-Salb) were determined before and after weight reduction. After a 12-week weight reduction program, the average weight loss was 7.96 +/- 3.47 kg, with losses of 21.88 +/- 20.39 cm2 in visceral fat areas.."
Yonsei Med J. 2005 Aug
Park SH, Shim KW.
Department of Cardiology and Ewha Medical Research Institute


"The beta-adrenergic system is involved in the control of energy metabolism and expenditure...The beta2-AR was stimulated with two doses of salbutamol...the findings support a role for this polymorphism in the development and maintenance of overweight and obesity"
Journal of Clinical Endocrinology Metabolism 2005 Apr.
Park SH, Shim KW.
Department of Cardiology and Ewha Medical Research Institute


"Isoproterenol and salbutamol elicited strong lipolytic responses in adipocytes isolated from horse and pony subcutaneous adipose tissue..."
Comp Biochem Physiology 2003 Oct
Carrington EF, Desautels M, Naylor JM.

University of Saskatchewan, Western College of Veterinary Medicine

"A 65-year-old Kenyan Asian developed rapidly progressive multiple symmetrical lipomatosis over 8 years.... A clinical trial of oral salbutamol, a beta 2-agonist, was performed with significant therapeutic effect. The body fat mass showed a reversal of the rapid progression while on the treatment, associated with an increase in the resting metabolic rate."
Clinical Endocrinology 1987 Nov
Leung NW, Gaer J, Beggs D, Kark AE, Holloway B, Peters TJ.
Division of Clinical Cell Biology, MRC Clinical Research Centre, Harrow, Middlesex, UK

"...Furthermore, continuous infusion of salbutamol (1.15 mg.kg body wt-1.day-1) via miniosmotic pumps did cause significant increases in muscle mass, protein..."
American Journal of Physiology
Choo JJ, Horan MA, Little RA, Rothwell NJ.
Department of Physiological Sciences, University of Manchester Medical School, United Kingdom
"Eight normal male subjects received single oral doses of BRL 35135 (8 mg) or the selective beta 2-adrenoceptor agonist salbutamol (8 mg)... BRL 35135 and salbutamol produced a significant fall in serum potassium concentration compared with placebo, in keeping with beta 2-adrenoceptor stimulation...A significant increase in basal metabolic rate occurred with both BRL 35135 and salbutamol. In the case of salbutamol, this effect appeared to be mediated solely by beta 2-adrenoceptors."
Clinical Science (London)
Wheeldon NM, McDevitt DG, McFarlane LC, Lipworth BJ.
Department of Clinical Pharmacology, Ninewells Hospital and Medical School, Dundee, Scotland, U.K.

"One group of animals (T-I) was fed salbutamol at a dose of 2 mg x kg-1 diet x day-1 for 38 days, while in another group (T-II) the beta-adrenergic agonist was discontinued in the diet 5 days before slaughter on the 43rd day. The semitendinosus muscle protein content increased (p < 0.05), while fat and collagen content decreased (p < 0.05) in the T-I group. These differences were not apparent in the group from which salbutamol was withdrawn. The data show that salbutamol is able to increase muscle content at the expense of fat stores in productive animals..."
An. Nutrition & Metabolism
del Barrio AS, Garcia-Calonge MA, Fernandez-Quintela A, Simon E, Portillo MP, Astiasaran I, Martinez JA.
Department of Nutrition and Food Science, University of Pais Vasco, Vitoria, Spain.


We do not encourage of the use of Salbutamol for any other uses than strict therapeutical under a licensed physician care. Salbutamol is a potent medicine, use with care.


Buy Salbutamol (Ventolin) 4mg (100 tablets)   $ 59    
Buy Salbutamol (Ventolin) 4mg (200 tablets)   $ 99    
Buy Salbutamol (Ventolin) 4mg (300 tablets)   $ 139    

We sell the original Ventolin (Salbutamol) tablets.

Tablets and infusion are the only valid methods used in the above medical studies. The inhaler version of Salbutamol will NOT produce the same results as described in the medical studies above, the inhaler is only good for selected asthma conditions.

  

Information presented is not medically approved, may be inaccurate and is unreliable. It can not and must not serve as any basis of decision making regarding any health concern or issue.



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