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1.5 million people annually are harmed from drug errors.
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From simple mix-ups to fatal overdoses, medication mistakes happen, on average, once a day to every hospital patient, a new report says. Nationwide, at least 1.5 million people annually are harmed from drug errors, more than half of them in nursing homes.
Many Unfavorable Drug Studies Aren’t Published. Nearly a third of antidepressant drug studies are never published in the medical literature, and nearly all of those happen to show that the drug being tests failed to work.
Only Drugs That are Safe Should be put on the Market. Drug developers are just beginning to come to grips with recent FDA oversight reforms and how they will affect drug safety. But, it appears that industry and consumer advocates are not together on how well the overhaul will be able to prevent future drug safety scandals.

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Review Menesit Safety Reports submitted to FDA

Total Menesit reports: 2.
Menesit FDA safety alerts: No.
Reported deaths: 2    Reported hospitalizations: 2.
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FDA Reported Menesit Side Effects: myeloblast count increased, monocyte count decreased, mean cell volume abnormal, lymphocyte count increased, haemoglobin decreased, haematocrit decreased, brain natriuretic peptide increased, acute myeloid leukaemia, condition aggravated, myelocyte count decreased.
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Menesit Side Effects Report #5236935-X
Pharmacist from JAPAN reported MENESIT problem on Feb 07, 2007. Female patient, 86 years of age, was diagnosed with parkinsonism, hypokalaemia and was treated with MENESIT. After drug was administered, patient experienced the following problems/side effects: acute myeloid leukaemia, brain natriuretic peptide increased, haematocrit decreased, haemoglobin decreased, lymphocyte count increased, mean cell volume abnormal, monocyte count decreased, myeloblast count increased, myelocyte count decreased. MENESIT dosage: 600 MG/DAY. During the same period patient was treated with ASPARA K, PARLODEL. Patient was hospitalized. Patient died on 01/14/2007.

Menesit Side Effects Report #5254101-9
MENESIT problem was reported by a Pharmacist from JAPAN on Feb 26, 2007. Female patient, 86 years of age, was diagnosed with parkinsonism, hypokalaemia and was treated with MENESIT. After drug was administered, patient experienced the following problems/side effects: acute myeloid leukaemia, brain natriuretic peptide increased, condition aggravated, haematocrit decreased, haemoglobin decreased, lymphocyte count increased, mean cell volume abnormal, monocyte count decreased, myeloblast count increased. MENESIT dosage: 600 MG/DAY. During the same period patient was treated with ASPARA K, PARLODEL. Patient was hospitalized. Patient died on 01/14/2007.


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acute myeloid leukaemia, brain natriuretic peptide increased, haematocrit decreased, haemoglobin decreased, lymphocyte count increased, mean cell volume abnormal, monocyte count decreased, myeloblast count increased, myelocyte count decreased, was diagnosed with parkinsonism, hypokalaemia and was diagnosed with parkinsonism, hypokalaemia and