Moxonidine Side Effects
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Moxonidine Safety Reports reported to FDA
Total Moxonidine reports: 5.Moxonidine FDA safety alerts: No.
Reported hospitalizations: 5.
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Reported Moxonidine Side Effects: blood iron increased, blood creatinine increased, blood cholinesterase decreased, blood bilirubin increased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, blast cell count increased, basophil count increased, anisocytosis, blood count abnormal, aortic arteriosclerosis.
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Moxonidine Side Effects Report #5196605-3
Consumer or non-health professional from GERMANY reported MOXONIDINE problem on Dec 20, 2006. Female patient, 84 years of age, was diagnosed with hypertension and was treated with MOXONIDINE. After drug was administered, patient experienced the following problems/side effects: anti-erythrocyte antibody, antinuclear antibody positive, aortic arteriosclerosis, aspartate aminotransferase increased, blood bilirubin increased, blood cholinesterase decreased, blood count abnormal, blood creatinine increased, blood iron increased. MOXONIDINE dosage: unknown. During the same period patient was treated with ISOPTIN, MARCUMAR. Patient was hospitalized. Patient recovered.
Moxonidine Side Effects Report #5141111-5
MOXONIDINE problem was reported by a Physician from GERMANY on Oct 19, 2006. Female patient, 84 years of age, was diagnosed with hypertensive heart disease and was treated with MOXONIDINE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, ill-defined disorder, leukopenia, neutropenia, normochromic normocytic anaemia. MOXONIDINE dosage: unknown. During the same period patient was treated with ISOPTIN, MARCUMAR, DIOVAN. Patient was hospitalized. Patient recovered.
Moxonidine Side Effects Report #5169691-4
Consumer or non-health professional from GERMANY reported MOXONIDINE problem on Oct 19, 2006. Female patient, 84 years of age, was diagnosed with hypertensive heart disease and was treated with MOXONIDINE. After drug was administered, patient experienced the following problems/side effects: anisocytosis, aspartate aminotransferase increased, basophil count increased, blast cell count increased, blood bilirubin increased, blood cholinesterase decreased, blood creatinine increased, blood iron increased, blood lactate dehydrogenase increased. MOXONIDINE dosage: unknown. During the same period patient was treated with ISOPTIN, MARCUMAR, DIOVAN. Patient was hospitalized. Patient recovered.
Moxonidine Side Effects Report #5181072-6
MOXONIDINE problem was reported by a Consumer or non-health professional from GERMANY on Oct 19, 2006. Female patient, 84 years of age, was diagnosed with hypertension and was treated with MOXONIDINE. After drug was administered, patient experienced the following problems/side effects: anisocytosis, aspartate aminotransferase increased, basophil count increased, blast cell count increased, blood bilirubin increased, blood cholinesterase decreased, blood creatinine increased, blood iron increased, blood lactate dehydrogenase increased. MOXONIDINE dosage: unknown. During the same period patient was treated with ISOPTIN, MARCUMAR. Patient was hospitalized. Patient recovered.
Moxonidine Side Effects Report #5194726-2
Consumer or non-health professional from GERMANY reported MOXONIDINE problem on Oct 19, 2006. Female patient, 84 years of age, was diagnosed with hypertension and was treated with MOXONIDINE. After drug was administered, patient experienced the following problems/side effects: anti-erythrocyte antibody, antinuclear antibody positive, aortic arteriosclerosis, aspartate aminotransferase increased, blood bilirubin increased, blood cholinesterase decreased, blood count abnormal, blood creatinine increased, blood iron increased. MOXONIDINE dosage: unknown. During the same period patient was treated with ISOPTIN, MARCUMAR. Patient was hospitalized. Patient recovered.