Tag Archives: FDA

Benzodiazepine Use Linked to Miscarriage; Stopping the Drugs After Long-Term Use Increased Risk of Fatality, New Research Finds

Mental health watchdog CCHR presses for DEA reclassification of benzodiazepines due to risks of physical dependency and addiction. Continue reading

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Despite Claims of Safety, Electroshock Caused Memory Loss in Majority of Teens in New Study, CCHR Warns

Researcher says study failed to show the safety or efficacy of electroconvulsive therapy. Continue reading

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Heart Disease Risk Increases the Longer ADHD Drugs are Taken, Study Finds

Researchers advise prescribers to keep monitoring patients on ADHD drugs for symptoms of heart disease. Continue reading

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World Health Organization Calls Involuntary Electroshock Treatment a Human Rights Abuse

New guidance from World Health Organization and UN High Commissioner for Human Rights also calls for laws banning electroconvulsive therapy (ECT) for children. Continue reading

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Antipsychotics Overprescribed to Seniors with Dementia in Home Health Care, Despite Serious Risks, Study Indicates

Antipsychotic use by elderly with dementia was also linked to worse outcomes in performing their activities of daily living after home health care ended. Continue reading

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ADHD Drugs Do Not Enhance Performance, Worsen Cognitive Ability in Some People, Study Indicates

High potential for abuse and overdose of prescription stimulants prompts U.S. Food and Drug Administration to research alternative treatments. Continue reading

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Foster Children Prescribed Psychiatric Drugs At Four Times the Rate of Non-Foster Children, New Study Finds

Previous government recommendations for improved oversight of psychotropics in foster care have not resolved the overdrugging problem. Continue reading

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Antidepressants Increase Risk of Suicidal Behavior in Children and Young Adults, Don’t Reduce Risk in Adults, Study Says

Other recent research has found antidepressants double the risk of suicidal thoughts and actions in adults. Continue reading

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Electroshock’s Serious Risks, Ineffectiveness Not Adequately Disclosed to Patients, Audit of Information Pamphlets Finds

Patients are not given enough information about the drawbacks of electroshock to give true informed consent for the procedure, researcher says. Continue reading

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FDA Updates Warning on Stimulants Prescribed for ADHD, Now Lists Risks of Misuse, Addiction, Diversion and Overdose

FDA Updates Warning on Stimulants Prescribed for ADHD. Now Lists Risks of Misuse, Addiction, Diversion and Overdose. Continue reading

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