Homozygous familial hypercholesterolaemia

Homozygous familial hypercholesterolaemia is a rare life-threatening disease characterized by the difficulty of your body to remove LDL “bad” cholesterol from your blood. The condition raises the chance of a heart attack at an early age, but some treatments can lower your risk.

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PCSK9
Monoclonal Antibody
Repatha®
140 mg/mL
3,5 mg
-80 °C
06/2025
135,00 
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