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Total Adancor reports: 1.
Adancor FDA safety alerts: 2004 .
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Adancor Side Effects Report #5488953-4
Consumer or non-health professional from FRANCE reported ADANCOR problem on Oct 01, 2007. Male patient, 88 years of age, was diagnosed with angina pectoris, hypertension, hypercholesterolaemia, atrial fibrillation and was treated with ADANCOR. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, blood iron decreased, erythema multiforme, lymphopenia, oral herpes, thrombocytopenia, toxic skin eruption. ADANCOR dosage: 40 MG (20 MG, 2 IN 1 D); LONG-TERM. During the same period patient was treated with FUROSEMIDE, RAMIPRIL, PRAVASTATIN, PREVISCAN. Patient was hospitalized. Patient recovered.


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anaemia macrocytic, blood iron decreased, erythema multiforme, lymphopenia, oral herpes, thrombocytopenia, toxic skin eruption, , was diagnosed with angina pectoris, hypertension, hypercholesterolaemia, atrial fibrillation and