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Nisis Safety Reports
Total Nisis reports: 3.Nisis FDA safety alerts: No.
Reported deaths: 1 Reported hospitalizations: 3.
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Reported Nisis Side Effects: haemoglobin decreased, suicide attempt, multi-organ failure, circulatory collapse, blood pressure decreased, jaundice, haemolytic anaemia, chromaturia, asthenia, serum ferritin decreased, red blood cell count decreased.
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Nisis Side Effects Report #5309348-X
Consumer or non-health professional from FRANCE reported NISIS problem on Apr 16, 2007. Female patient, 79 years of age, weighting 94.80 lb, was diagnosed with hypertension and was treated with NISIS. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, gastritis atrophic, gastrointestinal haemorrhage, haematocrit decreased, haemoglobin decreased, iron deficiency anaemia, red blood cell count decreased, serum ferritin decreased. NISIS dosage: 160 MG, QD. During the same period patient was treated with CORDARONE, HYPERIUM, DAFALGAN, ESOMEPRAZOLE MAGNESIUM. Patient recovered.
Nisis Side Effects Report #5079487-X
NISIS problem was reported by a Physician from FRANCE on June 14, 2006. Male patient, 60 years of age, was diagnosed with hypertension and was treated with NISIS. After drug was administered, patient experienced the following problems/side effects: asthenia, chromaturia, haemoglobin decreased, haemolytic anaemia, jaundice. NISIS dosage: 40 MG, QD. During the same period patient was treated with FERVEX. Patient was hospitalized. Patient recovered.
Nisis Side Effects Report #5176710-8
Physician from FRANCE reported NISIS problem on Dec 14, 2006. Male patient, 69 years of age, was treated with NISIS. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, circulatory collapse, multi-organ failure, suicide attempt. NISIS dosage: unknown. During the same period patient was treated with ZOLPIDEM TARTRATE, TRICYCLIC ANTIDEPRESSANTS. Patient was hospitalized. Patient died.