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Adancor FDA adverse reports: 1. View All Adancor FDA Adverse Reports

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Adancor Side Effects Report: 5488953-4,Anaemia Macrocytic, Blood Iron Decreased, Erythema Multiforme, Lymphopenia, Oral Herpes, Thrombocytopenia, Toxic Skin Eruption
on Oct 01, 2007 Male patient from FRANCE, , 88 years of age, was diagnosed with angina pectoris, hypertension, hypercholesterolaemia, atrial fibrillation (What is atrial fibrillation?) and was treated with Adancor. After Adancor was administered, patient had the following side effects: Adancor and anaemia macrocytic, Adancor and blood iron decreased, Adancor and erythema multiforme, Adancor and lymphopenia, Adancor and oral herpes, Adancor and thrombocytopenia, Adancor and 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.


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Adancor Side Effects
Adancor and Anaemia macrocytic
Adancor and Blood iron decreased
Adancor and Erythema multiforme
Adancor and Lymphopenia
Adancor and Oral herpes
Adancor and Thrombocytopenia
Adancor and Toxic skin eruption

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