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Pulmonary hypertension (PH) is a clinical and pathophysiological syndrome caused by changes in pulmonary vascular structure or function that results in increased pulmonary vascular resistance and pulmonary arterial pressure, and it is characterized by pulmonary endothelial dysfunction, pulmonary artery media thickening, pulmonary vascular remodeling, and right ventricular hypertrophy, all of which are driven by an imbalance between the growth and death of pulmonary vascular cells

Highly bioavailable and ideal for those needing enzyme cofactor support.

Use before moisturiser as part of your morning or evening skincare routine

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This teaching aid will enhance intramuscular injection skills teaching and training