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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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Total Wytens reports: 3.
Wytens FDA safety alerts: No.
   Reported hospitalizations: 1.
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FDA Reported Wytens Side Effects: systemic lupus erythematosus, hyperproteinaemia, double stranded dna antibody, cytolytic hepatitis, coombs positive haemolytic anaemia, antiphospholipid syndrome, anaemia haemolytic autoimmune, fatigue, diabetes mellitus, condition aggravated, road traffic accident.
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Wytens Side Effects Report #5275636-9
Health Professional from JAPAN reported WYTENS problem on Mar 14, 2007. Male patient, 56 years of age, was diagnosed with insomnia and was treated with WYTENS. After drug was administered, patient experienced the following problems/side effects: amnesia, delirium, memory impairment, road traffic accident. WYTENS dosage: 2 MG. During the same period patient was treated with DIOVAN, MYSLEE. Patient recovered.

Wytens Side Effects Report #5343410-0
WYTENS problem was reported by a Consumer or non-health professional from FRANCE on May 21, 2007. Female patient, 65 years of age, was diagnosed with hypertension and was treated with WYTENS. After drug was administered, patient experienced the following problems/side effects: condition aggravated, diabetes mellitus, fatigue, systemic lupus erythematosus. WYTENS dosage: unknown. Patient recovered.

Wytens Side Effects Report #5414920-2
Consumer or non-health professional from FRANCE reported WYTENS problem on July 26, 2007. Female patient, 71 years of age, was diagnosed with hypertension and was treated with WYTENS. After drug was administered, patient experienced the following problems/side effects: anaemia haemolytic autoimmune, antiphospholipid syndrome, coombs positive haemolytic anaemia, cytolytic hepatitis, double stranded dna antibody, hyperproteinaemia, systemic lupus erythematosus. WYTENS dosage: unknown. During the same period patient was treated with RABEPRAZOLE, XANAX. Patient was hospitalized. Patient recovered.


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Thank you for visiting Patientsville.com. We hope you found our information about prescription drug side effects helpful. The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Thank you for visiting Patientsville.net. Hope you enjoyed finding Wytens safety information and found answers to Your Questions about Wytens side effects

amnesia, delirium, memory impairment, road traffic accident condition aggravated, diabetes mellitus, fatigue, systemic lupus erythematosus, was diagnosed with insomnia and was diagnosed with hypertension and was diagnosed with hypertension and