UN refugee agency says Turkish asylumseekers at sea deserve hearings

“Returning an asylum-seeker to his country of origin without hearing his or her claim is against the fundamental principles of international refugee law and may amount to refoulement,” the refugee agency’s spokesman, Rupert Colville, said, referring to the illegal eviction of a refugee. The spokesman for the UN High Commissioner for Refugees (UNHCR) said that under European Union (EU) law, Italy would appear to be responsible for assessing the claims of the asylum-seekers, thought to be 11 men and two boys. Under the terms of the EU Dublin Regulation, the 13 should be able to disembark from the Antigua and Barbuda-registered Lydia Oldendorff in Malta and then be transferred to Italy, Mr. Colville added. Alternatively, the owner, who flew to Malta, has said that he would be prepared to send his ship back to Italy, providing he received clear assurances within the next 36 hours from the Italian authorities that the 13 can disembark. Mr. Colville said the situation aboard the vessel is “extremely tense” because of the limited quarters for the 13 asylum-seekers, 16 crew members and four newly hired security guards. At least one of the men reportedly has attempted suicide. He urged Malta and Italy “to act in accordance with their responsibilities under international law without further delay.” read more

Pfizer will ask FDA to remove black box suicide warning from its

by Matthew Perrone, The Associated Press Posted Sep 24, 2014 9:53 am MDT AddThis Sharing ButtonsShare to TwitterTwitterShare to FacebookFacebookShare to RedditRedditShare to 電子郵件Email Pfizer will ask FDA to remove “black box” suicide warning from its anti-smoking medication WASHINGTON – New government-approved labeling on Pfizer’s drug Chantix suggests that the anti-smoking medication may not carry the risks of suicidal behaviour that first earned it the Food and Drug Administration’s strongest warning more than five years ago.The FDA updated the drug’s label Monday to include data from a number of recent studies that found little to no evidence of psychiatric problems or suicidal tendencies in patients taking the twice-a-day tablet.The new labeling represents a victory for Pfizer Inc., which requested the update. Company executives say they will now ask the FDA to completely remove the drug’s so-called “black box” label — the strongest type — which warns prescribers of links to hostility, agitation, depression and suicidal behaviour.“Based on all this new information, a boxed warning is not supported,” said Pfizer senior vice-president, Steve Romano, in an interview with The Associated Press. “The bottom line is that the label needs to reflect the most current understanding of the product’s benefits and risks.”The FDA is convening a panel of its outside experts next month to review the latest data on Chantix’s safety — prompted by Pfizer’s request to update the label. The meeting comes more than a year after New York-based Pfizer paid $275 million to settle some 2,000 lawsuits alleging Chantix caused various psychiatric problems, injuries and suicides.The FDA originally added the boxed warning about suicide in 2009, after receiving dozens of reports of suicide and hundreds of reports of suicidal behaviour among patients taking the smoking-cessation drug.At that time, the FDA also required Pfizer to conduct additional studies to determine the extent of the drug’s psychiatric side effects.The new drug labeling includes results of five Pfizer studies enrolling nearly 2,000 patients which showed no increase in suicidal tendencies based on a medical questionnaire. The FDA also updated the label with results from four large independent studies of between 10,000 and 30,000 Chantix users. Those studies found no difference in self-injury, hospitalization and other serious adverse events between people taking Chantix and those using other quit-smoking aids, including nicotine patches and the medication bupropion.There were several limitations to these larger studies. First, they only recorded problems that resulted in hospitalization, meaning many issues likely went unreported. Additionally, the studies were conducted after news of Chantix’s side effects had been widely reported, which means doctors may have steered patients with a history of psychiatric issues toward the alternate therapies.The new FDA label isn’t all positive. It also contains new information about risks of seizure and interactions with alcohol among Chantix patients.Pfizer’s drug works by binding to the same spots in the brain that are activated by nicotine when people smoke. The drug, known chemically as varenicline, blocks nicotine from binding to those spots and prevents the release of “feel-good” brain chemicals that make smoking so addictive.The FDA first began investigating potential side effects with Chantix in 2007, the year after it hit the market.The drug’s labeling tells patients to stop taking Chantix immediately if they experience agitation, depressed mood, suicidal thinking and other behavioural changes. Doctors are advised to weigh the drug’s risks against its potential benefit of helping patients quit smoking.Chantix had global sales of $648 million last year. That was down about 26 per cent from the drug’s peak sales of $883 million in 2007.Pfizer shares rose 26 cents to $30.31. It shares had slipped almost 2 per cent through Tuesday’s close since the start of the year. read more