China defends tough swine flu measures

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Posted on 4th May 2009 by Gordon Johnson in Uncategorized

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Editors Note:

The irony of China – the country that brought us catastrophically lax and incompetent production of a pig-based intraveneous drug, Heparin, now claiming to have found a new and better way to test for Swine Flu – is staggering. If the Chinese can use their technological capabilities to find a Swine Flu test then why didn’t they use that expertise to make sure that the Heparin raw material that came from their factories, was pure? Swine flu will likely not cause 10 deaths in China. Chinese Heparin may have caused thousands of deaths in the U.S. See http://heparindeaths.blogspot.com and http://heparin-law.com

Attorney Gordon Johnson
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©Attorney Gordon S. Johnson, Jr. 2009

Date: 5/4/2009 6:14 AM

DIKKY SINN
Associated Press Writers

HONG KONG (AP) — China on Monday defended its tough quarantine measures against Mexican tourists after a visitor from the Latin American country became Asia’s first swine flu case, while New Zealand recorded its sixth case of the disease.

After the 25-year-old Mexican man was diagnosed in this Asian financial hub Friday night, Beijing and Hong Kong quickly shifted into crisis management mode, employing quarantine measures that an angry Mexico has labeled as “discriminatory.” The Mexican government announced it would charter a plane to bring its citizens home from China.

South Korea confirmed Asia’s second case of the disease over the weekend, but said Monday that the woman — a nun who had visited Mexico —already had recovered. Elsewhere in the region, New Zealand reported a sixth laboratory-confirmed case of the disease.

East Timor’s president, Jose Ramos-Horta, canceled a trip this week to Seoul, citing fears of swine flu. His spokesman said Ramos-Horta had been scheduled to be in Korea May 3-7 to speak at an international forum being co-hosted by the United Nations but canceled “due to the issue of the very dangerous swine flu.”

Hong Kong imposed a weeklong quarantine on the downtown hotel where the Mexican man stayed, trapping 350 guests and employees inside, while Chinese health officials also tracked down and quarantined 128 of the Mexican’s fellow passengers.

In addition, Jorge Guajardo, the Mexican ambassador to China, told The Associated Press in an interview late Sunday that Chinese officials have rounded up more than 70 Mexicans indiscriminately elsewhere in China including Beijing, Shanghai, Guangzhou and Tianjin.

In one case, a Mexican couple and their three small children were rousted from their Beijing hotel room at 4 a.m. and transported to a hospital, he said. None of those in isolation has presented symptoms and most had no contact with infected persons or places, he said.

“In many cases, we have gotten reports that they were being quarantined for the sole fact that they had a Mexican passport, whether or not they came from Mexico, whether or not they had been in Mexico, whether or not they had been in contact with someone else from Mexico,” Guajardo said.

Mexican President Felipe Calderon expressed dismay Sunday that “some countries or places are taking discriminatory measures because of ignorance and misinformation.”

Mexican officials said late Sunday they would charter an Aeromexico airliner to take home any Mexican citizens who want to leave China.

China’s Foreign Ministry said Mexicans were not being singled out and added it hoped Mexico would “address the issue in an objective and calm manner.”

“The relevant measures are not targeted at Mexican citizens, and are not discriminatory. This is purely a question of health inspection and quarantine,” the ministry said in a statement.

In South Korea, the country’s first confirmed swine flu patient was released Monday from a military-run hospital after recovering from the disease, Health Ministry spokesman Oh Sung-il said. The 51-year-old Catholic nun was hospitalized since early last week when she reported having flu symptoms following a trip to Mexico.

Two other South Korean women were under quarantine as “probable” cases.

Meanwhile, New Zealand reported two more cases of swine flu Monday for a total of six. The cases came 10 days after a group of high school students returned from Mexico with the first confirmed cases of the illness, sparking a nationwide alert.

All of the cases were either people returning from affected areas or those with close contact with an infected person, said Dr. Fran McGrath, deputy director of public health.

“There is still no evidence of community transmission,” she said.

The Mexican quarantined in Hong Kong was “doing well” and recovering, Hans Troedsson, head of the World Health Organization’s Beijing office, told The Associated Press in an interview Monday.

Troedsson wouldn’t comment on China’s quarantine measures directly, saying such measures are “really up to each country.”

In Hong Kong, which has defended the quarantine as necessary to prevent the spread of the disease, a quick diagnostic test for swine flu is now available, said Yuen Kwok-yung, a microbiologist who studied the SARS virus. The test, which could yield results in four hours, will be distributed to all laboratories in the city.

“The laboratories are ready to handle any outbreak where testing is being required,” Yuen said, adding Hong Kong will be able to handle 2,000 specimens a day in two weeks’ time.

Hong Kong officials have already tracked down and quarantined two taxi drivers who had driven the Mexican patient. Neither driver initially showed signs of illness.

The quarantined hotel in Hong Kong remained under lockdown Monday. One guest, Briton Mark Moore, complained that he had not shown symptoms and urged the government to lift the quarantine.

“The government is trying to show the world they are strong in organizing this,” the 37-year-old Singapore-based company director said in a phone interview Monday. “I need to be in Singapore now. I have loads of things to do.”

Another guest, Singapore resident Juliet Keys, said stranded travelers have shared drinks and Indian takeout.

“It’s really boring just being stuck in your room, but people have started to make a few friends,” said the 41-year-old human resources manager, originally from Northampton, England.

___

Associated Press writers Audra Ang and Christopher Bodeen in Beijing and Ray Lilley in New Zealand contributed to this report.1

Copyright 2009 The Associated Press.

Nearly 5,000 Chinese officials punished for corruption

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Posted on 26th December 2008 by Gordon Johnson in Uncategorized

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Date: 12/26/2008 6:54 AM

BEIJING (AP) — Nearly 5,000 higher-level Chinese government officials were punished for corruption over the past year, state media reported Friday.

The officials — all above the county-head level — were involved in corruption, bribery, acting against the public interest and other violations of discipline or the law said Gan Yisheng, deputy head of the Communist Party’s Central Commission for Discipline Inspection, according to the official Xinhua News Agency.

In the worst cases, a total of 801 officials were legally prosecuted for crimes, he said. He vowed to step up anti-graft efforts and “win trust from the people with actual results.”

Gan said government inspection departments investigated 144,000 cases that led to penalties for 146,000 lower-ranking government officials. Losses of 6 billion yuan ($900 million) were recovered through the anti-corruption efforts.

Copyright 2008 The Associated Press.

Amputee awaits high court, wants musical glow back

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Posted on 30th October 2008 by Gordon Johnson in Uncategorized

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Date: 10/30/2008

By DAVE GRAM
Associated Press Writer

MARSHFIELD, Vt. (AP) _ When Diana Levine turned 63 recently, her daughter made her a birthday card, drawing on Greek mythology with an illustration of Diana the Huntress, her bow string drawn taut, an arrow ready to fly.

But the arm pulling at the bowstring was amputated below the elbow — just like Diana Levine’s — and the target was labeled the “Wyeth monster.”

That’s Wyeth as in Wyeth Pharmaceuticals, the company Levine blames for a botched injection of the Wyeth-made drug Phenergan that led doctors to amputate her right arm in 2000.

Levine, once a professional guitar player and pianist, now plays with one hand and sings. “It’s about getting my glow back,” she said recently as she was awaiting a hearing Monday before the U.S. Supreme Court, where Wyeth is appealing a $6.7 million verdict in her favor.

The outcome of Levine’s case could have major ramifications for drug makers and consumers. The court is expected to decide whether people can sue under state law — or are pre-empted from doing so — for harm caused by a drug approved by the federal Food and Drug Administration.

Levine said the drug makers “are using my case … to get through this doctrine that will say that if it is FDA-approved, then we are not accountable, because FDA said it’s OK. … Mr. Pharmaceutical Company is not responsible and is not liable and doesn’t have to help the person who just lost her arm, or her life.”

Levine, who suffered from migraine headaches, had a particularly bad episode in the spring of 2000. A friend drove her from her dirt road farmhouse-turned-music studio in Marshfield, Vt. to a clinic in neighboring Plainfield.

She was given drugs for the pain and, to combat nausea, an intramuscular injection of Phenergan, a drug that has been around for 50 years.

When Levine complained that she still felt nauseous, the clinic suggested an “IV-push” of Phenergan. This delivered a high volume of the drug very quickly to her right arm, not the slow flow that could have been delivered by an IV drip.

The second injection accidentally punctured an artery, prompting gangrene to set in. After several weeks of deterioration, her arm was amputated.

Levine recalls first seeing what remained of her arm after surgery. “I was horrified and shocked and about as sad as I ever have been in my life,” she said.

She reached an out-of-court settlement with the clinic and sued Wyeth, contending that the label on the Phenergan she was given should have more clearly warned about the danger of giving the drug IV-push.

Combatting an upset stomach with a method that can end up causing limb loss is “an unfathomable benefit-risk ratio,” Levine said. With two other methods for injecting Phenergan, “there’s no earthly reason for this third option (IV-push) to even be made available,” she said.

Wyeth and the FDA say that when a drug like Phenergan has a federally approved label, its manufacturer is immune from lawsuits in state court. Wyeth maintains its label clearly describes the risks of Phenergan, and that it was not only approved but mandated by the FDA. “Wyeth could not change Phenergan’s labeling to comply with Vermont law without violating federal law,” it said in court papers.

Consumer groups are mounting a vigorous campaign against that position, saying federal regulation should represent the floor, not the ceiling, of a drug company’s responsibility.

“What a trial lawyer reasonably could fear in this case is that in one fell swoop, the U.S. Supreme Court would eliminate the right of an injured person to recover from a drug company in the case of a dangerous drug that caused their injury,” said Fordham University law professor Benjamin Zipursky, a product liability expert.

The court could effectively “eliminate all pharmaceutical company liability in this one case,” Zipursky said.

Bert Rein, a lawyer for Wyeth, said that concern was overblown. “Some of the hysteria being whipped up is really unjustified,” he said. “We believe the court will rule on the specific facts of the case,” rather than so broadly as to affect most liability claims.

That was not what Wyeth argued when urging the Supreme Court to take the case.

In its appeal to the court, Wyeth said the justices should act to prevent erroneous rulings in “tens of thousands of individual claims and potentially millions of class action claims” that are pending in state and federal courts.

While the legal war continues, Levine wages a more personal struggle. Sometimes it’s just to roll her left sleeve up or down, file papers, wash dishes or mow the lawn.

“If you were to put your hand in your pocket for a day and not use it, you would pretty much come to the conclusion that there’s nothing that’s a one-handed activity,” she said.

Mostly, the struggle is to continue a life in which songwriting was her gift and the guitar and piano were the tools of her trade.

“My identity was seriously damaged. Not just the musical one, but the physical. I mean, I had lost my glow, the glow was gone,” Levine said, recalling her recent performance with a group of women singers. “That’s what it’s about, it’s about getting my glow back.”

Levine has had more than a little help from her friends.

“She’s determined not to let this setback destroy her music,” said singer-songwriter Jon Gailmor, who had collaborated with Levine and her late husband in performances and on recordings. “It’s probably given her some new material, made her stronger even. She’s an amazing person.”

Quoting a musician friend, Levine calls the right hand the “joyous hand” — the one that gets to strum or pick the guitar, finding the rhythm, while the left searches the neck for the right note or chord. On keyboards, the right hand most often finds the improvisational riffs while the left lays down the underlying rhythm and chord changes.

Levine has no joyous hand now.

A piano and guitar player since childhood, she studied chemistry and psychology at the University of Vermont. Levine, who performed under the name Diana Winn, married a blues guitarist David “Crow” Levine, playing bass alongside of him in the Re-Bops, a band that gained a regional following in the 1980s.

Her husband died in 1993, leaving Levine and the couple’s daughter, Jessamine, now 25.

Now, she’s less concerned with the legal arguments than with making music and sharing it, especially with children.

She pays the bills using her monthly disability check from Social Security, Re-Bob Records sales — though she says she’s unable to keep up the business as well as she used to — and assistance from her family. “I have help from home. Nobody’s going to let me be out in the cold.”

Levine sat one recent afternoon at her
piano, accompanied by Jessamine on guitar, working out a new tune she hoped to send to actor Dennis Quaid, who is waging a drug labeling fight of his own after his infant twins were given a dose of the blood-thinnerHeparin — 1,000 times what was called for.

The twins’ birthday is in November, and Levine was writing a song for them.

Plunking out chords with her left hand, Levine asked Jessamine, “What do we go to there? Do you like G? Or should it be D-minor?”

And then she sang a song fragment:

“It’s the twinses’ birthday, celebrate times two. It’s the twinses’ birthday, if you only knew. There’s been some hard times they’ve both been through …”

Copyright 2008 The Associated Press.

China milk scandal claims victim outside mainland

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Posted on 22nd September 2008 by Gordon Johnson in Uncategorized

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Date: 9/21/2008 11:37 AM

By SCOTT McDONALD
Associated Press Writer

BEIJING (AP) — A Hong Kong toddler has developed a kidney stone after drinking Chinese milk — the first reported victim outside the mainland affected by a widening scandal over a toxic chemical found in baby formula and other Chinese dairy products.

More than 6,200 infants have become sick and four babies have died in China after being fed baby formula laced with melamine, a banned industrial chemical.

No illnesses had been reported elsewhere until the Hong Kong government said late Saturday that a 3-year-old girl was diagnosed with a kidney stone after drinking milk produced by the Chinese dairy Yili that contained melamine.

The Hong Kong government also announced Sunday that tests found melamine in Chinese-made Nestle milk. The Dairy Farm milk was made by Nestle’s division in the Chinese coastal city Qingdao, it said.

The Swiss food and drinks giant issued a statement Sunday saying that none of its China-made dairy products contained melamine.

“Nestle once again expresses confidence that none of its products in China is made from milk adulterated with melamine,” the statement said. It did not specifically respond to the Hong Kong report of tainted Dairy Farm milk.

Nestle offices in Hong Kong and Geneva did not immediately respond to a message seeking comment. Calls after work hours to its Beijing office and Beijing hot line went unanswered.

Meanwhile, Singapore said Sunday melamine was detected in samples of White Rabbit-brand Creamy Candy. The popular Chinese milk candy was pulled from shelves in the Philippines last year after health officials there claimed it was tainted with formaldehyde.

Chinese candy maker Guan Sheng Yuan Co. denied the Philippine allegations, saying the candy tested was likely a counterfeit version and subsequent tests showed samples of the candy were formaldehyde-free.

Already on Friday, Singapore suspended the sale and import of all Chinese milk and dairy products including milk, ice-cream, yogurt, chocolate, biscuits and candy, as well as any other products containing milk from China as an ingredient.

Japan, Malaysia and Brunei have also recalled or banned Chinese-made dairy products.

Since the problem of tainted milk products became public knowledge less than two weeks ago, the crisis has spread to include almost all of China’s biggest dairy companies.

A top official with the World Health Organization said Sunday that delays in releasing critical information about contaminated Chinese milk had hampered Beijing’s ability to rapidly deal with the problem and warn consumers.

Shigeru Omi, the WHO’s head of Western Pacific operations, told reporters at a press conference in Manila that “some people withheld the information for some time,” but he did not give specifics.

The scandal began with complaints over milk powder by Sanlu Group Co. — one of China’s best-known and most respected brands. But it quickly became a much larger crisis as government tests found that one-fifth of the companies producing baby milk powder had melamine in their products.

A New Zealand stakeholder in Sanlu has said it was told before the start of the Beijing Olympics on Aug. 8 that there was a problem. The dairy farmers’ group Fonterra, which owns 43 percent of Sanlu Group, told the New Zealand government, which informed Chinese officials.

The public was not told until Sept. 11 that the powder, used in baby formula and other products, was laced with melamine.

Melamine is used in making plastics and is high in nitrogen, which registers as protein in tests of milk. Though health experts believe ingesting minute amounts poses no danger, melamine can cause kidney stones, which can lead to kidney failure. Infants are particularly vulnerable.

Some of the farmers who sell milk to Chinese food companies are thought to have used melamine to disguise watered-down milk and fatten profit margins hurt by rising costs for feed, fuel and labor.

The parents of the Hong Kong girl diagnosed with a kidney stone took her for a precautionary checkup because she had been drinking Yili milk daily for the past 15 months. Yili Industrial Group Co. is one of 22 companies whose milk and dairy products were recalled after batches of their products were found to contain melamine.

The toddler was in good condition after receiving medical treatment and had been discharged from the hospital, the government said.

China’s communist leadership has launched high-profile efforts to show it is on top of the crisis, with Premier Wen Jiabao appearing on state-run television Sunday to say dairy companies had to show more “social responsibility.”

Wen was shown visiting a Beijing hospital where children were having health checks. He also stopped at a supermarket to look at dairy products.

“What we need to do now is to ensure that nothing like this happens in the future, not only in dairy products but in all food,” Wen said.

Food and product safety scandals have been a feature of Chinese life. Only last year, the government promised to overhaul inspection procedures after exports of medicines, toys, pet food ingredients and other products killed and sickened people and pets in North and South America.

The chemical in the dangerous pet food was the same as in the milk scandal — melamine.

Many of the largest companies whose products have been recalled, such as Yili Industrial Group Co. and Mengniu Dairy Group Co., did not have government inspections before the problem became public. The government scrapped that exemption this past week.

___

Associated Press reporter Min Lee in Hong Kong contributed to this report.

Copyright 2008 The Associated Press.

FDA rejects Schering drug to reverse anesthesia

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Posted on 1st August 2008 by Gordon Johnson in Uncategorized

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Does the below action of the FDA indicate that this year’s Heparin debacle, along with the grilling it received from Congress over the heparin deaths,(http;//heparin-law.com) has had its impact, and big pharmaceutical’s control over such agency is finally being shaken? We can only hope.

Attorney Gordon Johnson
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Date: 8/1/2008 7:04 AM

By MATTHEW PERRONE
AP Business Writer

WASHINGTON (AP) _ Government regulators dealt a major setback to Schering-Plough Corp. Thursday, rejecting a highly anticipated drug designed to help patients recover from anesthesia.

The Food and Drug Administration notified the company that it will not approve its drug sugammadex, due to concerns about allergic reactions seen in some patients, according to a company statement.

Schering said it was “surprised and disappointed” by the decision but would “work with the agency to address the issues.”

The rejection letter was unexpected because a panel of outside FDA advisers had unanimously voted in favor of the medication earlier this year. The FDA is not required to follow the group’s advice, though it usually does.

And on Tuesday, European Union regulators cleared the injectable drug, which is designed to reverse the effects of anesthesia in patients after surgery. The drug will be marketed in Europe under the name Bridion, though a commercial name has not been selected for U.S. promotion.

Surgeons typically use muscle-paralyzing anesthetic drugs to make surgery easier and safer for patients.

Despite positive reviews from some experts, FDA scientists voiced safety concerns with sugammadex in their initial review. According to the documents released in March, FDA said additional safety studies could be needed to examine allergic reactions seen in some patients.

However, company representatives argued that the drug’s benefits more than outweigh those risks.

Dr. Ronald Miller, a consultant for Schering, said that sugammadex works better than existing treatments, which carry their own negative side effects, including heart problems and nausea.

“The drugs we currently use produce many more reactions and much more severe reactions than anything that has been demonstrated with sugammadex,” said Miller, who chairs the department of anesthesia at the University of California at San Francisco. “I was quite disappointed with the FDA ruling.”

FDA has rejected several drugs this year that were expected to gain approval, including an allergy drug combining the ingredients of Schering’s Claritin and Merck & Co. Inc.’s Singulair tablets.

Some analysts have speculated that FDA has become more cautious about putting new drugs on the market following the safety concerns around drugs like Merck’s painkiller Vioxx and GlaxoSmithKline’s diabetes drug Avandia. In both cases, there were older medications on the market with more established safety profiles.

Currently there are two anesthesia-reversing drugs on the market that surgeons have used for decades.

Copyright 2008 The Associated Press.FDA