FDA report: eculizumab (Soliris) for the treatment of patients with paroxysmal nocturnal hemoglobinuria (Q28293514)
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English | FDA report: eculizumab (Soliris) for the treatment of patients with paroxysmal nocturnal hemoglobinuria |
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FDA report: eculizumab (Soliris) for the treatment of patients with paroxysmal nocturnal hemoglobinuria (English)
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September 2008
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13
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9
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993-1000
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