Humanized monoclonal antibody against C5, preventing cleavage to C5a and C5b → no MAC formation.
Several risk factors have been identified for developing aHUS, including: atypical hemolytic syndrome
Because aHUS is so rare, it is often misdiagnosed. If you or a loved one has unexplained kidney failure paired with anemia, ask your specialist about aHUS. Early diagnosis saves kidneys, and it saves lives. Humanized monoclonal antibody against C5
The clinical features of aHUS can vary, but common symptoms include: including: Because aHUS is so rare