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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Strokes can change the way a
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Health Experts answered these questions:
My wife has arthritis,quite severe. if she sustains a bruise or a cut the results last for weeks or even months. she bruises badly with the slightest...
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Do You Have a Health Question about Probucol? Ask a Health Expert!
Vaccine Safety
Community-reported Probucol side effects:
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Review Probucol Safety Reports submitted to FDA
Total
Probucol reports: 2.
Probucol FDA safety alerts: No.
Reported deaths: 2 Reported hospitalizations: 2.
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Probucol Side Effects Survey,
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FDA Reported Probucol Side Effects: renal impairment, platelet count decreased, hepatic function abnormal, haemolytic anaemia, depressed level of consciousness.
More About Probucol.
If you have questions about Probucol, you can ask
a Health Expert or
Ask Patient Community about Probucol.
Probucol Side Effects Report #5471301-3
Health Professional from JAPAN reported PROBUCOL problem on Sept 18, 2007. Male patient, weighting 123.5 lb, was diagnosed with hyperlipidaemia, insomnia, back pain, dyspepsia, cerebrovascular disorder, gastritis prophylaxis and was treated with PROBUCOL. After drug was administered, patient experienced the following problems/side effects:
depressed level of consciousness, haemolytic anaemia, hepatic function abnormal, platelet count decreased, renal impairment. PROBUCOL dosage: 250 MG. During the same period patient was treated with
DEPAS, DICLOFENAC, ISALON, SOLETON, CLOPIDOGREL, OMEPRAL. Patient was
hospitalized. Patient died on 02/18/2007.
Probucol Side Effects Report #5407297-X
PROBUCOL problem was reported by a Health Professional from JAPAN on July 30, 2007. Male patient, weighting 123.5 lb, was diagnosed with hyperlipidaemia, insomnia, back pain, dyspepsia, cerebrovascular disorder, gastritis prophylaxis and was treated with PROBUCOL. After drug was administered, patient experienced the following problems/side effects:
depressed level of consciousness, haemolytic anaemia, hepatic function abnormal, platelet count decreased, renal impairment. PROBUCOL dosage: 250 MG. During the same period patient was treated with
DEPAS, DICLOFENAC, ISALON, SOLETON, CLOPIDOGREL, OMEPRAZOLE. Patient was
hospitalized. Patient died on 02/18/2007.
