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1.5 million people annually are harmed from drug errors. Don't Risk Your Health! Ask a Health Expert Now

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 Manidon Safety Reports submitted to FDA

Total Manidon reports: 3.
Manidon FDA safety alerts: No.
   Reported hospitalizations: 2.
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FDA Reported Manidon Side Effects: syncope, renal failure acute, hypotension, hyperkalaemia, hypokinesia, hypertonia, hyperglycaemia, hepatitis, hepatic necrosis.
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Manidon Side Effects Report #5293457-8
Health Professional from SPAIN reported MANIDON problem on Mar 29, 2007. Female patient, 71 years of age, was diagnosed with essential hypertension, dementia alzheimer's type, atrial fibrillation, diabetes mellitus and was treated with MANIDON. After drug was administered, patient experienced the following problems/side effects: hepatic necrosis, hepatitis, hyperglycaemia. MANIDON dosage: unknown. During the same period patient was treated with ARICEPT, DIGOXIN, DIANBEN, DEPRAX, ISCOVER, NOVODORM. Patient was hospitalized. Patient recovered.

Manidon Side Effects Report #5091353-2
MANIDON problem was reported by a Consumer or non-health professional from SPAIN on Aug 08, 2006. Female patient, 82 years of age, was diagnosed with hypertension, dyspepsia, depression and was treated with MANIDON. After drug was administered, patient experienced the following problems/side effects: hypertonia, hypokinesia. MANIDON dosage: 120 MG PO. During the same period patient was treated with FLATORIL, SEROXAT, ACECLOFENAC, LEKOVIT CA. Patient recovered.

Manidon Side Effects Report #5397279-9
Consumer or non-health professional from SPAIN reported MANIDON problem on July 11, 2007. Male patient, 78 years of age, was treated with MANIDON. After drug was administered, patient experienced the following problems/side effects: hyperkalaemia, hypotension, renal failure acute, syncope. MANIDON dosage: 240 MG QD ORAL. During the same period patient was treated with ENALAPRIL, CLOPIDOGREL BISULPHATE, ZOCOR. Patient was hospitalized. Patient recovered.

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