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New psych ward to open on California's death row : report

Under pressure to improve mental health treatment for inmates in California's massive prison system, officials plan to build a new psychiatric ward to provide inpatient mental health care for prisoners on death row, according to a court-ordered report. The new ward, set to open on Oct. 1, will serve severely mentally ill prisoners on death row at the San Quentin prison near San Francisco, said the report filed late Tuesday. Matthew Lopes, a special master overseeing mental health care in California's prisons, found that 37 severely mentally ill death row inmates at San Quentin prison near San Francisco were entitled to 24-hour inpatient care in a hospital but were not getting it. Lopes, assigned to develop the report by federal Judge Lawrence K. Karlton last December, said he had worked with state officials and lawyers representing inmates to draft plans for a new ward. "They were refusing to transfer them (to a mental hospital) because they said it was too dangerous

FDA aims to develop e-cigarette standards; nicotine policy

The U.S. Food and Drug Administration is working to develop strong product standards for electronic cigarettes and other nicotine delivery devices that will protect public health and enable the agency to withstand legal challenges, its class="mandelbrot_refrag"> tobacco chief said on Wednesday. Mitchell Zeller, director of the FDA's Center for class="mandelbrot_refrag"> Tobacco Products, said the agency is exploring potential product standards in the areas of addiction, toxicity and product appeal as it prepares to gain regulatory authority over electronic cigarettes and other nicotine-delivery devices. The establishment of product standards is one of five priorities for the division over the next few years, Zeller said, outlining them publicly in the most comprehensive manner to date. They include putting in place regulations for approving new products and monitoring them after they reach the market, ensuring that the agency has in place a strong

Saudi MERS response hobbled by institutional failings

When class="mandelbrot_refrag"> Saudi Arabia announced last week it had found 113 more cases of the deadly Middle East Respiratory Syndrome (MERS), it didn't just force a rethink of the threat the virus poses, it exposed institutional failings.     Saudi health sources and international virologists said poor communication and a lack of accountability in government departments, inadequate state oversight and a failure to learn from past mistakes have all hindered Saudi Arabia's battle against the SARS-like virus.     They say it is too soon to tell if reforms introduced by a new acting health minister can overcome what they see as underlying problems.     Some top Saudi health officials say they accept that delays in reporting MERS cases were caused by poor communication between hospitals, laboratories and government departments, but they stress things have improved significantly since the appointment of the new minister in late April.     The health ministr

FDA lifts partial hold on study testing Geron's only drug

class="mandelbrot_refrag"> Geron Corp said the U.S. Food and Drug Administration had lifted a partial clinical hold on a study testing its sole drug as a treatment for myelofibrosis, a rare form of blood cancer, sending the company's shares soaring in morning trading. Enrollment in the early-stage trial, sponsored by the Mayo Clinic, was halted in March over concerns about liver toxicity pending followup data from Mayo's investigator on the possible reversibility of the liver damage. Enrollment for the study ceased in January, and about 20 of the 79 patients dropped out. Geron, whose shares rose as much as 33 percent on Thursday, did not then disclose the reason behind the dropouts, but said the remaining enrolled patients would continue to receive the drug, imetelstat.   true       However, in March the FDA also imposed a halt on separate company-sponsored trials evaluating the use of the drug in thrombocythemia and multiple myeloma, citing similar concern

Weight gain differs with various antidepressants

People who take antidepressants tend to put on a few pounds, a new study confirms, and some of the drugs are linked to more weight gain than others. Using health records from one New England healthcare system, researchers studied 19,244 adults treated with antidepressants, recording their weights over the course of a year. The results showed that people taking citalopram (Celexa), from a class of antidepressants known as selective serotonin reuptake inhibitors, or SSRIs, gained more than two and a half pounds, on average. Other SSRIs were associated with weight gain similar to citalopram, with people taking fluoxetine (Prozac) gaining on average a pound and a half and those taking sertraline (Zoloft) gaining nearly two pounds, the authors write in JAMA Psychiatry. On the other hand, people taking bupropion (Wellbutrin) lost on average nearly half a pound. The tricyclic antidepressants nortriptyline and amitriptyline were also linked with significantly less weight gain than th

Shire to test its ADHD drug in 4 to 5-year olds in U.S.

Shire Plc SHP.L has agreed to a U.S. Food and Drug Administration request to study its stimulant Vyvanse in preschool children as concern rises over the diagnosis and treatment of attention deficit hyperactivity disorder, the drugmaker said on Thursday. _0"> A report last year by the Centers for Disease Control and Prevention found that the number of children diagnosed with ADHD increased 41 percent from 2003 to 2011 and that 6.4 million children, or 11 percent of those aged 4 to 17, have been diagnosed with that condition. Drugs treatments include Ritalin, Adderall and Vyvanse. Only Adderall, which is also made by Shire, is approved to treat children under the age of 6. Yet children much younger are taking the drugs and the FDA wants additional information to ensure they are safe in this very young population.   true       Gwen Fisher, a spokeswoman for U.K.-based Shire, said the company is designing three clinical trials for children aged 4 to 5. One will examine how the

Ackman seeks court ruling on Allergan special meeting

William Ackman's Pershing Square Capital Management said it had filed a lawsuit seeking confirmation that its request to hold a special shareholder meeting of class="mandelbrot_refrag"> Allergan Inc would not trigger Allergan's poison pill takeover defense. _0"> Ackman, who owns nearly 10 percent of Allergan, last week filed documents with the Securities and Exchange Commission to call a shareholder meeting to elect new directors to the company's board. The Botox maker has rejected a $53 billion joint offer from Ackman and Canadian drugmaker class="mandelbrot_refrag"> Valeant Pharmaceuticals International . An Allergan spokeswoman declined to comment immediately. Allergan adopted the one-year shareholder rights plan on April 22, the day Valeant and Ackman made the offer, saying it needed time to consider takeover proposals.   true       Allergan's shareholder rights plan, or poison pill, will be triggered if a person or gro