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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 Didrex Safety Reports submitted to FDA

Total Didrex reports: 2.
Didrex FDA safety alerts: No.
   Reported hospitalizations: 2.
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FDA Reported Didrex Side Effects: feeling abnormal, depression, constipation, blood cholesterol increased, attention deficit/hyperactivity disorder, apathy, false positive laboratory result, condition aggravated, headache, dyskinesia.
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Didrex Side Effects Report #5284262-7
Consumer or non-health professional from UNITED STATES reported DIDREX problem on Dec 20, 2006. Female patient, weighting 140.0 lb, was diagnosed with depression, attention deficit/hyperactivity disorder, ill-defined disorder and was treated with DIDREX. After drug was administered, patient experienced the following problems/side effects: apathy, attention deficit/hyperactivity disorder, blood cholesterol increased, constipation, depression, dyskinesia, feeling abnormal, headache. DIDREX dosage: unknown. During the same period patient was treated with LEVOXYL, ZOCOR, RESTORIL. Patient was hospitalized. Patient recovered.

Didrex Side Effects Report #5063866-0
DIDREX problem was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2006. Female patient, 32 years of age, weighting 140.0 lb, was diagnosed with attention deficit/hyperactivity disorder, depression, ill-defined disorder and was treated with DIDREX. After drug was administered, patient experienced the following problems/side effects: apathy, attention deficit/hyperactivity disorder, blood cholesterol increased, condition aggravated, constipation, depression, false positive laboratory result, feeling abnormal. DIDREX dosage: 200 MG (50 MG, 1 IN 2 D), ORAL. During the same period patient was treated with LEVOXIL, ZOCOR, RESTORIL. Patient was hospitalized. Patient recovered.

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