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Moxonidine Side Effects summary

Total Moxonidine reports: 6.
Moxonidine FDA safety alerts: No.
   Reported hospitalizations: 5.
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Moxonidine Poll Results

Have you experienced Moxonidine side effects?

Yes, Severe	50%
Yes, Mild	20%
Yes, Minor	20%
No	10%

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Moxonidine Side Effects reported on Patientsville.com

None reported at this time.

Moxonidine FDA reported side effects and reactions

2008

2007

2006

Moxonidine Side Effects reported to FDA

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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.



Moxonidine Side Effects Report #5757807-8
MOXONIDINE problem was reported by a Consumer or non-health professional from GERMANY on May 14, 2008. Male patient, 84 years of age, was diagnosed with intentional overdose and was treated with MOXONIDINE. After drug was administered, patient experienced the following problems/side effects: hypotension, intentional overdose, somnolence. MOXONIDINE dosage: unknown. During the same period patient was treated with AMLODIPINE, LISINOPRIL, VENLAFAXINE. Patient recovered.