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Could cut number of fatal one-vehicle accidents in half10/28/2004ConsumerAffairs
Electronic Stability Control A Lifesaver, Study Finds...
Subaru Outback Tops Crash Tests, Rollover Ratings
Ford Bottoms Out10/28/2004ConsumerAffairs
In rollover testing, the highest rated pickup trucks were the 2005 Dodge Ram 4x2, the Chevrolet Colorado 4x4, and its corporate twin, the GMC Canyon 4x4, e...
The 2005 Subaru Outback sport utility vehicle was the top-rated vehicle in the government's latest frontal and side impact crash tests while the Chrysler 300 topped the passenger car ratings. Ford vehicles got the lowest ratings in two categories.
In fact, the Outback was the only vehicle in the latest group to earn the National Highway Traffic Safety Administration's (NHTSA) top rating of five-stars for all seating positions.
The 2005 Chrysler 300 and its corporate twin, the Dodge Magnum, received the highest scores for a passenger car - five-stars for frontal crash in both seating positions and four-stars and five-stars, respectively, for side impact crash in the driver and rear seating positions.
In rollover testing, the highest rated pickup trucks were the 2005 Dodge Ram 4x2, the Chevrolet Colorado 4x4, and its corporate twin, the GMC Canyon 4x4, each receiving four-stars, a 17.9 percent chance of rollover, if involved in a single-vehicle crash. NHTSA uses both a five-star scale and a percent chance of rollover to rate a vehicle on its likelihood of rollover in a single-vehicle crash.
The two-door Ford Focus and the Ford Ranger 4x4 pickup were the worst performers. NHTSA gave the Focus three out of five stars for driver's side protection and four out of five stars for rear passenger protection. The Ranger 4x4 got two stars in the rollover ratings.
NHTSA's consumer information program uses a one-to-five star rating system, with five being the highest. Star ratings reflect a vehicle's ability to protect the driver and passenger in a crash.
All NHTSA ratings can be found at www.safercar.gov.
Pharmacy Benefit Managers Scrutinized10/28/2004ConsumerAffairsBy James R. Hood
One advocacy group, Taxpayers Against Fraud, predicts the PBMs will collapse in disgrace, just as Enron did, once their inner workings are brought to light...
Selling energy on the open market was one of the bright ideas of the 1990s. The result was Enron. Another was using pharmacy benefit managers (PBM) to act as middlemen for governments and large employers, supplying prescription drugs at reduced prices to their clients' employees.
Three large companies have staked out most of the PBM market since then -- Medco, Caremark and Express Scripts. Together they control the prescriptions dispensed -- and sometimes not dispensed -- to an estimated 200 million Americans.
All are coming under increasing scrutiny by prosecutors and consumer advocates, particularly in light of New York Attorney General Eliot Spitzer's broad assault on fraud in the insurance industry.
Medco Associate U.S. Attorney Jim Sheehan has accused Medco of defrauding federal customers by only partially filling, switching and even destroying their prescriptions.
Express Scripts Spitzer has charged that Express Scripts "Lorraine" by inflating the costs of prescription drugs to New York State's largest employee health plan.
Caremark In a Florida case, Caremark is accused of reselling returned drugs and in Tennessee, a class action suit charges that Caremark violated the Tennessee Consumer Protection Act with its mail order service policy.
The hope was that PBMs would hold down drug prices by negotiating discounts from drug manufacturers but drug prices have soared for individuals and corporate clients alike, causing many to question whether the PBMs are really producing the savings they claim.
One advocacy group, Taxpayers Against Fraud, predicts the PBMs will collapse in disgrace, just as Enron did, once their inner workings are brought to light.
"What happens in these situations is that the public gets a long, hard look inside a very ugly industry and decides to simply do away with it altogether or to regulate it so severely that the game board no longer looks the same," Taxpayers Against Fraud communications director Patrick Burns said in an interview published by TheStreet.com.
The companies claim they have lived up to their promise and cite a recent study which estimated PBMs save their customers as much as 25% off their prescription bill. The PBMs are eagerly awaiting the 2006 Medicare drug benefit, expected to manage hundreds of millions of dollars worth of prescriptions for retirees.
But despite their glowing self-reviews, the companies all face regulatory and litigation challenges, with Medco perhaps most seriously threatened.
Medco faces a whistleblower lawsuit that threatens to lay bare some of the more unattractive aspects of the firm's inner workings. It follows a number of state probes that mostly ended badly for the company.
Associate U.S. Attorney Sheehan is accusing Medco of "active and constructive fraud." He alleges the company violated the False Claims Act by billing for services it did not provide and improperly dodging penalties. Fines under the Act can reach hundreds of millions of dollars.
In a recent hearing, U.S. District Judge Clarence Newcomer described as "well-pleaded" the government's allegation that the company has shorted its customers.
Medco settled an earlier case by agreeing to pay $29 million and adhere to new standards for switching patients' prescriptions. The company agreed to tell patients and doctors if it had financial incentives for suggesting a switch.
In complaints to ConsumerAffairs.com, consumers have complained of lengthy -- sometimes life-threatening -- delays in filling their prescriptions, substituting one drug for another and arbitrarily canceling prescriptions without notifying the patient.
The most frequent complaint, however, is that Medco deceives customers into paying for a 90-day supply of drugs, claiming they will save money, and then delivering only a 30-day supply for the price of 90.
"My plan says that if I go thru Medco, I can get 90 days worth of this drug for $30. So, I tried to save money and do exactly that," said Chris of El Segundo, CA. "But Medco sent me only 15 days of the medication for $30 -- the same price as the 90 day supply."
Caremark has been accused of re-selling prescription drugs that were returned by previous customers and never tested for possible damage or contamination.
Much of the information in the Caremark case has not been made public but the judge has ordered that Caremark CEO Mac Crawford be made available for a deposition no later than Dec. 15. It's highly unusual to require testimony from CEOs and the company says allegations against Crawford are "third-hand hearsay."
The Tennessee suit accuses Caremark of unfairly and deceptively representing to consumers that they must use the companys mail order pharmacy system rather than retail pharmacies.
Attorneys general from 23 states and the District of Columbia have asked for information about the company's business practices.
Sara, a retired nurse in Pasco, Washington complains that the company routinely refuses to fill her prescription for a powerful pain killer needed to keep her Reflex Sympathetic Dystrophy under control.
"They stated (the doctor) is giving me too many doses," Sara said. "One giant, rich company calls the shots as to whether I will be a bit eased of pain or not."
"It all lies in Caremark's hands and there is noting I can do about it. Once again the little man loses," she said. "I only know that I can't and won't tolerate this pain much longer."
As usual, New York's Spitzer minced no words in describing his case against Express Scripts. The company "engaged in a series of deceptive schemes," he said.
"It improperly lined its pockets at the expense of health plans and consumers, driving up the very drug costs it is supposed to lower," Spitzer charged.
Spitzer said the company inflated the cost of generic drugs, diverted millions of dollars in rebates to itself, induced doctors to switch patients' prescriptions to favor manufacturers who paid kickbacks and sold confidential data belonging to the state health plan.
"Express Scripts is successfully expanding its revenue base by adding new clients, striking new alliances, and acquiring selected businesses," according to Fitch Ratings, which has assigned a "stable" rating to the company, which reported $442 million in free cash flow during the twelve months ending June 30, 2004.
Consumers' evaluations are less glowing.
"My 6-year-old diabetic daughter was denied coverage of a potentially life saving medication, Glucose Gel," said Lorraine of Long Island, NY, in a complaint to ConsumerAffairs.com.
"I am an insulin dependant diabetic using a Metronic Insulin Pump," said Kevin of Lancaster, PA. "I have been trying (for 19 days) to get supplies" from Express Scripts, he wrote.
Consumers Happy, PBMs Claim
All the bad news and complaints are news to the pharmacy benefit managers' public relations teams.
"Consumers relying upon the mail-service pharmacy option are overwhelmingly satisfied -- with Medicare beneficiaries reporting the highest levels of satisfaction - and would recommend this option to family and friends," according to a study released earlier this week at the Pharmaceutical Care Management Association's (PCMA) annual meeting in Phoenix.
"Numerous data have shown that mail-service pharmacy is a proven avenue to providing consumers and purchasers with lower prescription drug costs, improved safety, more privacy, and greater drug therapy compliance," said PCMA President Mark Merritt. "With these findings, we now know that mail-service pharmacy consumers are also overwhelmingly satisfied on a wide range of indicators - timeliness of drug delivery, condition and accuracy of drugs received, and ease of reaching a pharmacist.
If the industry's critics agree on one thing, it is that PBMs need more "transparency" -- meaning that consumers and doctors should be able to know when the companies are making decisions because of kickbacks or other incentives offered by drug makers instead of basing them on concerns about their clients' safety and health.
The companies contend that transparency would not necessarily be helpful and might even hinder their ability to get customers the best possible prices on drugs, a stance the Federal Trade Commission (FTC) has endorsed.
Many consumers don't understand what they're signing10/28/2004ConsumerAffairsBy Anne Zieger
Spot Delivery Puts the Dealer in the Driver's Seat...
Work-At-Home Scheme Sued
Promised big payoffs but delivered little10/28/2004ConsumerAffairs
A Chicago woman and her company are charged with advertising a work-at-home job opportunity that promised big payoffs but allegedly ended up costing consum...
A Chicago woman and her company are charged with advertising a work-at-home job opportunity that promised big payoffs but allegedly ended up costing consumers money when start-up fees they paid upfront failed to generate profits.
The complaint filed by Illinois Attorney General Lisa Madigan accuses Paris Hill, doing business as Hill & Associates Consulting Center, of multiple violations of the Illinois Consumer Fraud and Deceptive Business Practices Act.
Hill allegedly advertised openings for employees to prepare bankruptcy petitions as a work-at-home job that required employees to purchase computer software for $139 to prepare the documents.
According to Madigan's complaint, Hill has placed help-wanted ads in the Chicago Tribune since at least July 2004, claiming consumers could earn "$52K/yr with medical & dental benefits after 30 days."
However, consumer complaints received by Madigan's office state otherwise, alleging consumers paid start-up expenses to Hill and then didn't receive the work, or pay, they were promised.
"When Illinoisans look through a newspaper's help-wanted ads, they should expect to find legitimate paying jobs, not consumer fraud," Madigan said. "This case is another reminder that work-at-home opportunities are appealing, but they must be carefully evaluated before any consumer becomes involved."
Madigan's complaint says Hill falsely represented that individuals could earn $52,000 a year, would prepare as many as 50 bankruptcy petitions a month, would be able to work full-time as bankruptcy petition preparers and would be eligible for medical and dental benefits. None of these claims proved to be true.
Hill is also accused of leading individuals to believe they would be employees of her company when in fact they were being hired as independent contractors, and that a call center would generate calls for the petition preparers when in fact they received very few or no calls.
As independent contractors, the individuals allegedly were told they would be paid commissions based on the number of bankruptcy petitions they prepared, earning $20 for one to 25 petitions, and $30 for 25 to 50 petitions and $40 for more than 50 petitions.
According to Madigan's complaint, the work never materialized and the independent contractors prepared few, if any, bankruptcy petitions.
Madigan's complaint seeks to prohibit Hill from committing future acts in violation of Illinois' consumer protection laws and asks the court to assess civil penalties of $50,000 per violation and an additional $50,000 for each violation found to have been committed with the intent to defraud. Madigan's complaint also seeks restitution for the defrauded consumers.
Madigan's Consumer Fraud Bureau warns consumers that many work-at-home schemes are fraudulent and offers consumers tips on how to protect themselves. Before consumers spend money on a work-at-home offer, they should ask the company representative the following questions to determine the truthfulness of the advertisements or literature:
• What does the job involve? What steps will I have to go through? What tasks will I have to complete?
• How and when will I be paid? Who will pay me?
• How much will I have to pay for the work-at-home program, including costs for supplies, equipment, training and other fees?
• What specific standards must my work meet?
GE: Malpractice Caps Don't Work10/27/2004ConsumerAffairs
GE Medical Protective's finding was made in a regulatory filing with the TDI, in a document submitted by GE to explain why the insurer planned to raise phy...
Do caps on medical malpractice damage awards hold down doctors' liability insurance premiums? The nation's largest medical malpractice insurer says they don't.
GE Medical Protective's finding was made in a regulatory filing with the Texas Department of Insurance (TDI),in a document submitted by GE to explain why the insurer planned to raise physicians' premiums 19% a mere six months after Texas enacted caps on medical malpractice awards.
In 2003, Texas lawmakers passed a $250,000 cap on non-economic damage compensation to victims of medical malpractice caps after Medical Protective and other insurers lobbied for the change.
According to the Medical Protective filing: "Non-economic damages are a small percentage of total losses paid. Capping non-economic damages will show loss savings of 1.0%."
The company also notes that a provision in the Texas law allowing for periodic payments of awards would provide a savings of only 1.1%. The insurer did not even provide its doctors that relief and eventually imposed a rate hike on its physician policyholders.
"When the largest malpractice insurer in the nation tells a regulator that caps on damages don't work, every legislator, regulator and voter in the nation should listen," said Douglas Heller, executive director of the Foundation for Taxpayers and Consumer Rights (FTCR).
"Medical Protective's rate increase and this smoking gun document prove that the insurance industry cannot be trusted on the issue of malpractice caps."
Medical Protective and other supporters of medical malpractice caps have repeatedly argued that damage awards are the primary reason for skyrocketing medical malpractice premiums. For example, in a March 2004 report. GE Medical Protective stated that capping non-economic damages is a "critical element [of reform] because in recent years we have seen non-economic damages spiraling out of control."
The Texas rate increase and the actuarial data submitted by the company contradicting the oft-stated importance of caps should lead policymakers to look to insurance regulation, rather than malpractice caps, as a solution to high premiums, according to FTCR.
"While medical malpractice caps limit the rights of injured patients, they do not lower doctors' premiums. If lawmakers and physicians want to reduce costs, they should start fighting to reform insurance companies rather than restrict patients' rights," said Heller.
Wireless Merger Approved - Cingular Will Be Nation's Biggest Carrier
Cingular Becomes Biggest Wireless Carrier10/26/2004ConsumerAffairsBy Truman Lewis
Wireless Merger Approved - Cingular Will Be Nation's Biggest Carrier...
With the blessing of the U.S. Justice Department and the Federal Communications Commission, Cingular today completed its acquisition of AT&T Wireless, creating the nation's largest cellular telephone company.
An immediate advertising blitz is expected as Cingular seeks to bond with AT&T Wireless customers who are being frantically courted by rivals.
In approving the $41 billion deal, the Justice Department said that Cingular and AT&T; Wireless must sell airwave licenses, customer contracts and other assets in 11 states to ensure that rivals can provide competing service.
"Without these divestitures, wireless customers in these markets would have had fewer choices for their wireless telephone service and faced the risk of higher prices, lower-quality service, and fewer choices for the newest high-speed mobile wireless data services," said Hewitt Pate, assistant attorney general in the department's antitrust division.
The government approval permits Cingular and AT&T; Wireless to begin merging operations, which include about 47 million subscribers and licenses to provide service in the top 100 metropolitan areas.
The combined company will replace Verizon Wireless as the leader in the nation's $95 billion wireless industry.
Absent from the celebrations were Consumers Union, the Consumer Federation of America and other consumer organizations, who said the merger could lead to higher prices in some markets. They contended that Cingular has no incentive to compete with its parents, BellSouth and SBC, and thus would be less likely to offer cheaper calling plans in the South.
Cingular says that's absurd. Competition among wireless carriers is "intense" and will remain that way, the company said in a statement.
AT&T Wireless has been practically giving service away lately, trying to hold onto defecting customers. The company has long had the highest customer defection rate of the major wireless carriers.
A Mixed Dowry
Amidst the popping of champagne corks, much remains to be sorted out. Customers of AT&T Wireless, which has had its rocky moments, should see more reliable service and customers of Cingular may expect improved high-speed wireless Web access. AT&T Wireless customers who switch to Cingular's billing plans could enjoy Cingular's rollover minutes, which moves unused minutes to the next month.
But as in any new union, something has to give. While AT&T Wireless customers can stay on their old plans as long as they like, if they want to move to Cingular's plans they'll have to get -- your guessed it -- a new phone.
Cingular's network is largely GSM -- Global System for Mobile Communications -- while AT&T's is mostly TDMA, Time Division Multiple Access. Phones that work on one system won't work on the other and, because of frequency differences, some AT&T Wireless customers with GSM phones will still have to get new phones.
On the other hand, some AT&T Wireless customers have been on both networks for the past several months -- seeing "AT&T" on their phone screens sometimes, "Cingular" at others. In the short term, this will occur in more cities as Cingular allows "home-on-home" roaming as the two networks are reconfigured.
In California and New York City, Cingular service could deteriorate. GSM customers there will be served by the AT&T Wireless network instead of T-Mobile, which has been providing service under contract to AT&T Wireless.
AT&T Wireless customers in parts of Connecticut, Kentucky, Texas and Oklahoma will be sold down the river. As part of the agreement with the Justice Department, subscribers in those areas will be handed off to other carriers. Customers will get a flier in the mail telling them who their new carrier is.
Advice for Consumers
As the happy couple sped off, consumer advisors had a word of caution for customers: pay close attention to your bill until the rice settles and the honeymoon is over. Telephone company billing systems are astonishingly complex and the rough spots in most mergers occur in the attempt to wed two very different systems.
Airbag Fraud Endangers Motorists
About one of every 25 previously damaged vehicles have phony or dummy airbags10/26/2004ConsumerAffairs
Airbag Fraud Endangers Motorists...
About one of every 25 previously damaged vehicles have phony or dummy airbags, but only a handful of states have laws regulating airbag system replacements.
"Airbag systems are expensive to replace so to keep costs down and profits up, scam artists may cut corners," said Larry Gamache, communications director at Carfax, which is offering free airbagchecks in November.
"Victims of airbag fraud have found their airbags stuffed with everything from rags to old shoes or nothing at all. However, most victims of airbag fraud may never know until it's too late."
Airbag fraud is virtually undetectable unless you check the car's computer system.
"If these airbags have been tampered with by improper repair the consumer is buying a vehicle that is not going to offer them any safety at all," said Bruce Strain, an expert in airbag replacement.
Carfax and its affiliated dealers are offering consumers free airbag checks and Carfax Vehicle History Reports during the month of November. To locate a Carfax Dealer, consumers can log on to www.carfax.com click on "find a dealer" and enter their zip code.
"An airbag unit is there to save lives whenever they are needed," said Gamache. "We want to ensure that drivers are made aware of this potentially fatal scam and hopefully help those who may be affected."
Balance Bracelet Settles Lawsuits
Agrees to pay $400,000 to settle claims10/25/2004ConsumerAffairs
The marketers of the Balance Bracelet, a supposed pain relief product, have agreed to pay $400,000 to settle charges that they made deceptive claims about ...
The marketers of the Balance Bracelet, a supposed pain relief product, have agreed to pay $400,000 to settle charges that they made deceptive claims about the bracelet.
In May 2004, the Federal Trade Commission filed a complaint in federal district court in Los Angeles against Media Maverick, Inc., alleging that it violated the FTC Act by deceptively claiming that the Balance Bracelet is a fast-acting, effective treatment for many types of pain.
A class action based on similar allegations was pending in California state court at the time. The settlement announced today is part of a global settlement among the FTC, the defendants, and the class action plaintiffs. The settlement requires the company and its officers to pay $400,000 in monetary relief to a global settlement fund, a significant portion of which will be used by the FTC for consumer redress.
The Balance Bracelet is a C-shaped metal bracelet that allegedly is electro-polarized by an undisclosed process. The defendants marketed the Balance Bracelet through nationally disseminated infomercials and over the Internet with advertising claims that the Balance Bracelet relieves arthritis pain, joint pain, back pain, and injury-related pain, among other things.
Their advertisements also claimed that pain is caused by excess static electricity in the body, which comes from an imbalance of positive and negative energy, and that the Balance Bracelet returns the body to its natural ionic balance. The Commission alleged that the defendants did not have scientific evidence to support their claims.
The FTCs order contains an avalanche clause that requires the defendants to pay $14 million, if the court finds that the defendants misrepresented their financial condition.
The FTCs order prohibits the defendants from misrepresenting that the Balance Bracelet, or any other pain-relief product, relieves pain and from misrepresenting any such products absolute or comparative health benefits, performance, or efficacy. The order also requires the defendants to possess substantiation to support future claims about the absolute or comparative health benefits, performance, or efficacy of any product.
In addition, the defendants must recall all packaging and labeling of the Balance Bracelet that includes the prohibited pain-relief claims.
The order also bars the defendants from selling their customer lists and imposes compliance reporting and record-keeping requirements on the defendants to assist the FTC in monitoring the defendants compliance.
Besides the San Luis Obispo-based Media Maverick, Inc., the actions name the company's officers, Mark Jones and Charles Cody.
Elder Rage - Why Long-Term Care Insurance is Important
Why Long-Term Care Insurance is Important10/25/2004ConsumerAffairs
Elder Rage - Why Long-Term Care Insurance is Important...
When I suddenly had to become a full-time caregiver for my elderly parents, both with health problems and starting to develop dementia (namely Alzheimer's), I had never even heard of Long-Term Care Insurance.
10 Alzheimer's Warning Signs
After we burned through their life savings, and then started chipping away at mine, I was advised to apply for financial assistance for them through the government's Medicaid system -- a program for those at the poverty level. It was quite a long process with mounds of paperwork and numerous investigations, but finally my parents were approved.
I was so happy that monetary help would finally be on the way, until I found out that the financial assistance would only pay to put my parents in a nursing home, not even in assisted living, and with very little help to keep them in their own home.
Since their levels of care were so different (my mother needed everything done for her), there weren't any facilities that would allow them to be together. They'd be across the street from each other in different wings of the home.
After sixty years of marriage, my parents were adamant about staying together in their own home, in their own bed, where they could continue to cuddle and kiss -- as they so frequently did. And, since my father was so "challenging" with quite a long record of manipulative disruptive behaviors, facilities didn't want him anyway.
It was hard, but I committed to keeping my parents together in their own home and attending Adult Day Health Care five days a week. Then, with the help of two marvelous caregivers, after five more years of loving each other, they passed, just a few months apart. Even though caring for every aspect of my parents' last years was the hardest thing I have ever done -- I am proud to say I gave them the best end-of-life I possibly could.
Had I only known to insist that we buy Long-Term Care Insurance for them prior to their illnesses, their in-home care could have been paid for, and I could have saved myself so much misery, not to mention a small fortune. I encourage you to learn from my mistake and look into LTC insurance long before you need it -- for your loved ones as well as yourself. Like fire insurance, hopefully, you'll never have to use it.
Also, call your local Area Agency on Aging, or your Department of Aging, and ask if there are any financial programs, waivers or grants available in your area that you can apply for.
- An estimated 4.5 to 5 million Americans have Alzheimer's disease. In a Gallup poll, 1 in 10 Americans said that they had a family member with Alzheimer's, and 1 in 3 knew someone with the disease.
- Increasing age is the greatest risk factor for Alzheimer's. One in 10 individuals over 65 and nearly half over 85 are affected. Rare, inherited forms of Alzheimer's can even strike individuals in their 30's and 40's.
- A person with Alzheimer's disease will live an average of eight years and as many as 20 years or more from the first onset of symptoms.
- More than 7 out of 10 people with Alzheimer's disease live at home, where family and friends provide 80 percent of their care. The estimated value of this informal care is $257 billion annually.
- One half of the U.S. population has a chronic condition. More than one quarter (26.6%) of the adult population provide care for a chronically ill, disabled or aged family member or friend, which translates to more than 50 million people involved with caregiving.
- 37% of caregivers are living in the same household as the person they care for. 54% are between 35 and 64 years of age. 59% of the adult population either is or expects to be a family caregiver, and 2 million more caregivers will be needed in the next twenty years.
- An estimated 43% of Americans age 65 or older will spend time in a nursing home. By 2012, 75% of Americans over age 65 will require long-term care. Long-term care costs are rising at 6% annually.
- The annual cost of Alzheimer's care in the U.S. is at least $100 billion, and it will soar to at least $375 billion by mid-century, overwhelming our health care system and bankrupting Medicare and Medicaid.
- Alzheimer's disease costs American business $61 billion a year, which is equivalent to the net profits of the top 10 Fortune 500 companies. $24.6 billion covers Alzheimer health care, and $36.5 billion covers costs related to caregivers of individuals with Alzheimer's, including lost productivity, absenteeism and worker replacement.
Three Ways to Pay for Long-Term Care
1. Pay for in-home caregivers and assisted living/nursing homes out of pocket. This is expensive and can often deplete a family's life savings.
2. Meet a very specific poverty level and qualify for government assistance through the Medicaid program. Unfortunately, options are limited, only paying for nursing homes that accept Medicaid.
3. Buy a Comprehensive Long-Term Care Insurance policy. This protects your family's assets from the rising costs of caring for someone who needs full time care. An employer might even pay the tax-deductible premiums. Consider buying it at a younger age, when it is more affordable and accessible. It must be bought before a major chronic illness strikes.
This policy pays for care in the patient's home, assisted living, board & care, and in nursing/dementia care facilities. Medicare and regular health insurance does not pay for long-term care. The average cost for a person who needs long-term care is $40,000 to $70,000 annually, depending on where you live, plus the cost to the family caregiver who may have to leave their job.
Questions to Ask Your Insurance Agent
- Is the coverage comprehensive--meaning it includes all levels of care: in the home, assisted living, board & care, and nursing/dementia facilities?
- What is the daily benefit?
- Is there 5% annually compounded inflation protection?
- What is the elimination period?
- Is it a lifetime benefit period or a limited time benefit policy?
- Is there a spousal discount?
- Can you hire caregivers privately as well as from an agency?
- Is the home care benefit based on a daily, weekly or monthly maximum, and if the benefit is not used, can it be used in the future?
- Does it cover home care coordination of services?
- How many ADL's (Activities of Daily Living) does it take to trigger a claim?
- Is there a time limit for filing a claim?
- Does it cover the cost of Adult Day Care & Adult Day Health Care, hospice and respite programs?
- Is it a tax-qualified plan?
- Is the company highly rated and have they ever raised premiums?
- Can you see the company's published annual audit to check their track record for paying claims?
Long-term care insurance may not be for everyone. But it would have saved our family's entire life savings as well as a fortune in Kleenex. I eventually had to sell my home to provide 24-hour (in their home) care, for 5 years, for 2 parents, both with (misdiagnosed) early stage Alzheimer's disease.
In the beginning, my once-adoring father turned verbally and physically abusive towards me and I was heart-broken to have lost his love. But then, I just couldn't believe it when I'd take him to the doctor -- where he could act completely normal when he needed to. It was an unbelievable nightmare, but with sheer determination I finally solved the endless crisis -- medically and behaviorally.
Once I figured it all out, I was so infuriated that I hadn't gotten the medical help I needed for my father sooner and compelled by the experience that I wrote my first book, Elder Rage, to help the 77 million baby boomers from making the mistakes I made while caring for their aging parents.
Actually written with some laugh-out-loud humor to make a tough subject palatable, Elder Rage has become a guidebook for a generation beginning this difficult phase of their lives. Now an advocate for eldercare awareness and reform, my biggest missions are: funding for, and the importance of, early diagnosis of Alzheimer's; prevention of elder abuse, neglect and exploitation; and funding for Adult Day Cares, which saved my parents' lives as well as my own. More than 5,000 new adult day centers are needed just to cover the current need.
Jacqueline Marcell is an author, publisher, radio host, national speaker, and advocate for eldercare awareness and reform. Her best-selling book, Elder Rage, is a Book-of-the-Month Club selection and being considered for a feature film. Jacqueline hosts an Internet radio program heard worldwide on www.wsRadio.com/CopingWithCaregiving. Jacqueline is also a recent breast cancer survivor who encourages caregivers to reduce stress and get mammograms for early detection.
ATA Files for Bankruptcy
Usual problems -- high fuel prices, intense competition and costly lease payments on its aircraft10/23/2004ConsumerAffairs
ATA Files for Bankruptcy...
ATA Airlines yesterday filed for bankruptcy, beset by a familiar litany of problems -- high fuel prices, intense competition and costly lease payments on its aircraft.
The Indianapolis-based carrier also said it has agreed to sell its hub at Chicago's Midway Airport to AirTran, one of its major competitors, for $87.5 million. That would give Orlando-based AirTran a second hub and strengthen its position against Southwest Airlines.
Like other airlines operating in bankruptcy, AirTran said it will maintain its full flight schedule and honor its frequent-flier commitments. The tenth-largest U.S. airline by traffic, ATA joins United, US Airways and Hawaiian Airlines in bankruptcy. Delta Air Lines is trying to avoid a bankruptcy filing.
ATA is the first major low-cost airline to seek bankruptcy protection. It has long been hobbled by its costly leases, estimated to be about $100 million per year over prevailing market rates. That's one of the things the carrier hopes to fix during its stay in bankruptcy court.
Besides its Midway assets, ATA will turn over its slots at New York's LaGuardia and Washington's Reagan National Airport to AirTran and will fly 15 of its aircraft on AirTran's behalf for six months. ATA and AirTran also say they intend to create a marketing and code-share alliance.
ATA has not arranged financing during bankruptcy but chairman J. George Mikelsons said the AirTran deal would provide an immediate cash infusion while he lines up financing elsewhere.
Taxpayers will be footing some of the bill. Like US Airways, ATA was one of the airlines to receive loan backing from the Air Transportation Stabilization Board after the 9/11 attacks. The board guaranteed a $168 million loan ATA took out in 2002 and will allow ATA to use some of that cash while it works on new financing.
ATA lost $90 million in the first half of this year on revenue of $778 million.
Beefmaster Explorer Outdoor Gas Grill10/21/2004ConsumerAffairs
Beefmaster Explorer Outdoor Gas Grill...
October 21, 2004
Nexgrill Industries is recalling the Beefmaster Explorer Outdoor Gas Grill model number 720-0001 because of a problem with the gas valve.
As consumers adjust the gas pressure regulator (on/off gauge) leading to the propane cylinder, the label on the valve can become positioned in such a manner that it is difficult to read. This can cause consumers to inadvertently leave the gas valve on, posing a fire hazard.
Nexgrill has received two reports of consumers leaving the gas valve on. No injuries or property damage has been reported.
This recall involves the Beefmaster Explorer Outdoor Gas Grill Model Number 720-0001. The table top grill is made of stainless steel and is used with a disposable propane cylinder, which is purchased separately. Each grill has one main burner and a cooking grid that sits over the burner. Model numbers are located on the back panel of the grill. The brand name Nexgrill is on a plate on the grill lid.
The grills were sold at Academy, Bar-B-Que Galore, Crate & Barrel, Home Town and discount department stores nationwide. Crate & Barrel also sold the grills through their catalog and at www.crateandbarrel.com. The grills were sold from January 2002 through June 2003 for about $100.
Consumers should contact Nexgrill to obtain a free replacement gauge. Consumers can also return the product to the company for installation of the replacement gauge at no charge. In addition, Crate & Barrel customers should contact Crate & Barrel to obtain a free replacement gauge or to make arrangements to return the product to the company for installation of the replacement gauge at no charge.
Consumer Contact: Contact Nexgrill toll-free at (800) 913-8999 between 9 a.m. and 5 p.m. PT Monday through Friday or email to firstname.lastname@example.org. Crate & Barrel customers should contact Crate & Barrel toll-free at (800) 451-8217 between 7 a.m. and 9 p.m. CT daily or at www.crateandbarrel.com.
The recall is being conducted in cooperation with the U.S. Consumer Product Safety Commission (CPSC).
Florida Sues 12 Leasing Companies In NorVergence Case
The leasing companies demanded payments from consumers for services they knew were not being provided10/21/2004ConsumerAffairs
Florida Sues 12 Leasing Companies In NorVergence Case...
Florida Attorney General Charlie Crist has filed a civil complaint against 12 leasing companies, accusing them of violating Florida's deceptive and unfair trade practices statute. The leasing companies demanded payments from consumers for services despite knowing that services were not being provided, Crist charged.
The leasing companies purchased contracts from NorVergence beginning in 2003 after NorVergence had entered into agreements with approximately 700 small Florida businesses to provide local telephone, mobile phone and high-speed Internet services at reduced rates.
NorVergence allegedly used high-pressure sales tactics, including claims that the offer was for a limited duration and available only to a few select companies, in order to finalize contracts that cost consumers as much as $1,000 per month.
"Small businesses were hurt by the false, deceptive, misleading and unfair sales tactics used by NorVergence," said Crist. "The leasing companies knew the scheme and compounded the harm by making intolerable demands to be paid for services that were unconscionably priced and never provided."
NorVergence targeted small businesses that had good credit ratings and that were owned by persons who were age 60 or older but lacked in-house legal and technology personnel to protect them. The small business owners agreed to sign contracts with NorVergence with an understanding of the following terms:
• They were obtaining telephone services directly from NorVergence;
• NorVergence would provide the consumers with unlimited long distance, cell phone and high-speed Internet at greatly reduced rates; and
• In order to use the NorVergence services, customers would have to rent a "Matrix" box.
These business terms were later found to be inaccurate. Many consumers never received telecommunication service, and in any event NorVergence terminated service when it went into bankruptcy. The company failed to install the Matrix box for consumers who had entered the agreement and thus failed to deliver the promised reduced rates.
Additionally, it was found that the Matrix was nothing more than a commercial router that sells for $500 to $1,200, creating an unconscionably large disparity between the value of the box and the $1,000-per-month lease payments due under the rental agreement.
In further violation of the agreement, the leasing companies then began demanding payments for services that were never provided. When customers missed their monthly bills, the leasing companies accelerated payments and demanded payment in full, in sums ranging from $10,000 to more than $90,000.
After receiving subpoenas from the Attorney General, three leasing companies CIT Technology Financial Services, Inc., Northland Capital Financial Services and BB&T; Leasing Company agreed to a moratorium of the payment demands and are not currently facing charges.
The 12 leasing companies that the Attorney General is suing are: Wells Fargo, Commerce Commercial Leasing, LLC, Court Square Leasing Corporation, Dolphin Capital Corporation, IFC Credit Corporation, National City Commercial Capital Corporation (formerly known as Information Leasing Corporation), Irwin Business Finance, Liberty Bank Leasing, Patriot Leasing Co. Inc., Popular Leasing U.S.A., Inc., Preferred Leasing, LLC and Sterling National Bank.
Each is charged with two counts of violating Florida's unfair and deceptive trade practices statute. If convicted of the charges, the companies face a $10,000 fine for each violation of the statute and a $15,000 fine for each violation involving a senior citizen, as well as consumer restitution and attorney fees and costs.
The Attorney General is also seeking an injunction to prevent the leasing companies from making further efforts to collect on these unconscionable agreements.
Colorado Attorney General Ken Salazar is urging Colorado business customers of NorVergence to file a written complaint with supporting documents with his office, after businesses complained that the state was not helping them in their struggle with the leasing companies.
The NorVergence bankruptcy has created significant financial problems for several thousands of businesses nationally, Salazar said. Because NorVergence entered into telecom leases with Colorado companies, most of which did not receive the promised equipment or services, my office has been working with other state and federal law enforcement agencies on investigative and legal options to assist them.
One major issue in this matter concerns the legal enforceability of the equipment leases signed by NorVergence customers. The equipment leases in question obligate the business customers to pay the leasing companies regardless of whether the equipment and services were ever provided by NorVergence. The leases also require the customers to waive all rights, claims and warranties.
The leases also stipulate that any legal disputes must be litigated in the home state of the leasing or finance company holding the assigned lease contract. The leasing and finance companies that purchased the leases from NorVergence are now seeking payment under the lease terms, and in some cases have filed collection lawsuits against the business customers for full payment.
Salazars office has also been in contact with the Federal Trade Commission regarding possible combined or separate legal action by the federal government, Salazar said.
Texas Mother Loses Malpractice Case10/20/2004ConsumerAffairs
A jury in Harris County, Texas rejected a woman's claim that a vaginal delivery done by Dr. Reiter caused nerve damage to her nine pound newborn daughter....
October 20, 2004
A jury in Harris County, Texas rejected a woman's claim that a vaginal delivery caused nerve damage to her newborn daughter.
In November 1998, Lisa Holm received prenatal care from Dr. Alexander Reiter and delivered Vencenza Robles on Jan. 17, 1999. Holm had previously had a large baby and her newborn weighed almost nine pounds.
Holm and Vencenza's father sued Dr. Reiter for negligence and medical malpractice, claiming that he promised to deliver the baby by cesarean section, but then chose not to do so. Dr. Reiter argued that he followed Holm's development closely and concluded that the fetus would not be dangerously large. He also argued that he employed all necessary procedures during vaginal delivery to ensure the safety of the child.
Enough Vaccine, Medicine, Thompson Says
Help is on the way, says Health and Human Services Secretary Tommy G. Thompson10/20/2004ConsumerAffairs
Enough Vaccine, Medicine, Thompson Says...
Help is on the way, says Health and Human Services Secretary Tommy G. Thompson, who says that about 60 million doses of influenza vaccine combined with an ample supply of antiviral medicines -- potentially enough for more than 40 million people during the flu season -- puts America in a strong position during the upcoming flu season.
Thompson said the nation's cache of vaccine and medicines includes an additional 2.6 million doses of influenza vaccine that Aventis will make available in January.
The Centers for Disease Control and Prevention (CDC),meanwhile, issued interim guidance on the use of antiviral medicines for preventing and treating the flu. In addition, the formalization of a federal government task force will help ensure an ongoing coordinated effort to manage the supply of medicine and prevent price gouging.
"In addition to the 60 million doses of influenza vaccine, we have healthy supplies of antiviral medicines to help keep you safe from the flu," Thompson said. "While we don't have as much flu vaccine as we planned for, the combination of existing vaccine and antiviral medicines gives us the ability to stave off any harsh effects of the flu."
Thompson said the combined supply of influenza vaccine and antiviral medications precludes the need for seniors and others to stand in long lines waiting for vaccine. In addition, about 24 million doses of this influenza vaccine supply has yet to be distributed and will be steered toward the people and places who need it the most. He advised seniors seeking vaccine to be patient and persistent, keeping in contact with their doctors and public health departments.
"We are still in the early stages of the flu season, and millions more doses of the vaccine will be shipped in coming weeks, so there is still time to get vaccinated," Secretary Thompson said. "We understand the public's concerns about the loss of the Chiron flu vaccine, but they should know we have a healthy supply of vaccines and medicines to cope with flu season."
Thompson said the government is exploring every option to replace some of the lost vaccine from other sources, and said the Bush administration has made unprecedented investments to protect against the flu.
Federal Task Force
Thompson also announced the formalization of a federal task force that will coordinate our nation's efforts to ensure that the flu vaccine and treatment medication goes to those who need it most and without any price gouging.
Thompson said marshalling all the resources of the federal government -- including the health agencies, Department of Justice, Federal Trade Commission, Homeland Security and Veterans Affairs -- will help ensure that all aspects of flu season are being addressed for the American public.
The Flu Action Task Force will also continue ongoing partnerships with the private sector in addressing challenges of the flu season, including the public health community, physicians, law enforcement and prosecutors, trade associations and advocacy groups.
"From the time we learned about our loss of the Chiron vaccine, a strong partnership between federal agencies, the private sector and the public health and law enforcement communities has helped us rapidly and effectively address the challenges before us," Secretary Thompson said. "It's important that we keep these partnerships strong during flu season, this year and beyond."
In 1994, there were five injectable influenza vaccine manufacturers: Wyeth, Evans (now part of Chiron), Connaught (now part of Aventis), Parke Davis and Lederle; today there are two - Aventis and Chiron.
The high risks of complex vaccine production, unpredictable consumer demand and low profit margins, coupled with the lack of liability protection from costly lawsuits, drove many manufacturers out of the flu vaccine business during the 1990s.
Getting manufacturers back into the marketplace is further complicated by the length of time for a new manufacturing facility to come on-line - five years or more. The FDA has high standards for flu vaccine production, including good manufacturing processes, which ensure the safety and efficacy of vaccines. These high standards helped keep 46 million doses of contaminated vaccine produced by Chiron from making it into the arms of Americans this year.
This administration is the first to create stockpiles of both influenza vaccine and antiviral medications, Thompson said. The department invested $40 million in 2004, and seeks another $40 million in 2005, to stockpile influenza vaccine through the Vaccines for Children Program. It invested $87.1 million to stockpile 2.3 million doses of Tamiflu. And it invested $34 million on Rimantadine capsules to treat 4.25 million adults and Rimantadine syrup to treat 750,000 kids.
These stockpiles give the government new ability to protect the most vulnerable, and respond effectively when there is a shortage of vaccine.
In August, Thompson unveiled the department's draft Pandemic Influenza Response and Preparedness Plan. This plan outlines a coordinated national strategy to prepare for and respond to a flu pandemic. One of the first internal committees the Secretary created when he came to HHS was on the pandemic flu.
Privacy Issues in Google Desktop
It could expose users' private information10/20/2004ConsumerAffairs
Google points out that the initial release was a beta test, and that refinements are being made. One of those refinements may be advanced features like pas...
When Internet search engine company Google introduced a new desktop search engine for computers October 14, it was seen as just the latest audacious move by this technological David, going up against the Goliath of Microsoft.
But in recent days the Internet buzz, from chat rooms to expert forums, has been less about Google's bold move and more about the potential loss of privacy associated with this new tool.
Experts say the new search engine, which is downloaded and installed on individual computers, could expose users' private information if they use shared computers. If, for example, you check your email on a computer at the library or at an Internet caf - and that computer has the desktop search engine, whoever uses the computer after you could pull out private information from emails you sent or received or Web sites you visited.
That becomes a real problem, for example, if you just accessed a site that requires a password, experts say.
The desktop search engine automatically records email that downloaded and read through Microsoft Outlook products and pages pulled up in Microsoft's Internet Explorer browser. It can also track files stored in Word, Excel and PowerPoint.
Google points out that the initial release was a beta test, and that refinements are being made. One of those refinements may be advanced features like password protection and multiuser support, a company official said.
Google says users of shared computers can look for an indicator in the system tray at the lower fight corner of the computer screen. If there is a multicolored swirl visible, it means the software is loaded and running. The company said its software can be disabled to prevent the user's movements from being tracked.
The procedures were performed at Nyack Hospital. Mr. Carey began experiencing headaches after the first part of the procedure -- the septoplasty. ...
Consumers Sue AstraZeneca Over Nexium Ad Campaign
Charges company used a massive and misleading advertising and promotional campaign to deceive consumers10/19/2004ConsumerAffairs
Consumers of the heartburn medication Nexium are suing the drug's distributor, AstraZeneca, alleging the pharmaceutical company sought to preserve market s...
Consumers of the heartburn medication Nexium are suing the drug's distributor, AstraZeneca, alleging the pharmaceutical company sought to preserve market share and profits as the patent on their blockbuster drug, Prilosec, was set to expire, by initiating a massive and misleading advertising and promotional campaign to deceive consumers into purchasing Nexium, a nearly identical new drug.
Filed in U.S. Superior Court in Los Angeles, the suit contends that the core of AstraZeneca's scheme was to use misleading information to convince consumers that Nexium was a significantly better drug than Prilosec.
The pharmaceutical planned to redirect consumer loyalty from the flagship drug Prilosec to Nexium before the expiration of Prilosec's U.S. patent and the onslaught of competition from generic manufacturers that would deprive AstraZeneca of significant profits, the suit charges.
"AstraZeneca knew that with the expiration of their Prilosec patent, they would lose market share and profits. We intend to show that they initiated a plan to deceive consumers and recoup those lost revenues," said Steve Berman, lead attorney for the plaintiffs. "This suit is a response to their deception and is a message to AstraZeneca and all pharmaceutical companies that they will be accountable to consumers for their actions."
The suit is brought by the AFL-CIO, the Congress of California Seniors, and the California Alliance for Retired Americans and seeks to be classified as a class action on behalf of consumers nationwide who purchased Nexium. All three of the organizations are members of the Prescription Access Litigation Project (PAL), a national coalition of 100 consumer organizations dedicated to fighting illegal pharmaceutical price inflation through class-action litigation.
"More and more workers cannot get the healthcare they need, and out-of-control drug prices are a huge factor," said Gerry Shea, AFL-CIO's director of governmental affairs. "The AFL-CIO is joining the Prescription Access Litigation Project and the suit against AstraZeneca because it's high time that drug companies were held accountable for deceiving American consumers into buying 'new' drugs they don't need at prices they can't afford."
Prilosec (also known as Losec) is a proton-pump inhibitor (PPI) used to treat heartburn and was AstraZeneca's most profitable drug. By 2000, Prilosec was the most prescribed drug in the world, with global sales reaching $6 billion. But with Prilosec's patent set to expire in 2001, its loss of brand name protection and assured competition from generic drug manufacturers posed a financial vulnerability to the pharmaceutical company.
According to the suit, AstraZeneca responded to this financial threat by launching a massive advertising campaign to overshadow the perceived effectiveness of Prilosec, and persuade consumers that Nexium was a new and improved PPI.
"AstraZeneca pulled a massive 'bait and switch' on the American public," said Nan Brasmer, President of the California Alliance for Retired Americans. "Rather than looking for new drugs that would be real improvements for patients, they poured millions of dollars into promoting a drug that was far more expensive but no better than equally effective generic drugs."
The ads claimed that Nexium was proven more effective at acid inhibition than comparable drugs, the suit states. However, the clinical trials alluded to in these ads only compared Nexium at dosage levels twice those of Prilosec (40 mg to 20 mg respectively). No tests were done to compare 40 mg of Nexium to 40 mg of Prilosec.
Not Enough Malpractice Suits, Researcher Claims10/18/2004ConsumerAffairs
Not Enough Malpractice Suits, Researcher Claims...
Medical malpractice has become a political football, one that's been kicked around in the presidential campaigns and debates. For the Republicans, curbing medical malpractice and other "frivolous" suits is a key theme of the campaign. Four states will vote Nov. 2 on whether to enact legislation limiting such lawsuits.
The American Medical Association warns that million-dollar jury awards and a flood of frivolous lawsuits are increasing the cost of doctors' insurance and creating a "full-blown liability crisis."
But not everyone agrees that there are too many malpractice lawsuits and few studies support the arguments used by the damage caps' proponents. In fact, Amitai Etzioni, who teaches sociology at George Washington University, says flatly there are too few lawsuits.
For every patient who sues, there are several who should but don't, says Etzioni.
Etzioni quotes a 1990 Harvard University study which found that only one out of eight patients who had a valid medical malpractice claim actually filed a suit. The study examined the records of more than 30,000 patients in New York -- one of the nation's most litigious states -- and discovered that in 1984 nearly 13,000 cases supported by "strong or certain evidence of negligence" were never pursued in court.
The Harvard study found that 3.7% of all patients suffered from complications caused by doctors. Later studies have found that number to be as high as 17.7%. Among the complications cited: the surgical removal of the wrong leg or kidney, brain damage to newborns and transplant procedures that didn't properly match donor and recipient.
In 2000, the National Academy of Sciences' Institute of Medicine found that between 44,000 and 98,000 patients died every year because of mistakes made by doctors and other healthcare personnel.
Why so few suits? As Etzioni sees it, many patients didn't know that it was negligence that caused their new problem. Others refuse to sue because they consider it human to err, or are grateful to a physician of many years for past care, or are fearful that they will be refused treatment if they file suit.
But even if there aren't too many malpractice suits, aren't the high jury awards associated with those that are filed wreaking havoc?
As it turns out, says Etzioni, more than two-thirds of malpractice lawsuits are either dismissed or dropped before they can be settled or brought to trial, so no massive awards result. And when plaintiffs do prevail in malpractice, really large jury awards are rare and are often scaled back on appeal, Etzioni said.
Frivolous suits can be dealt with without punishing those who deserve compensation, Etzioni argued. Louisiana, for instance, has malpractice review panels made up of three doctors and an attorney who are responsible for ruling on the merit of claims. Patients who wish to file a suit first have to submit their cases to these panels. If a panel rules that the case is without merit, a plaintiff still may bring his or her suit, but the panel's report can be filed with the court.
Lawyers reject claims that they are too quick to accept malpractice cases.
"As attorneys, our job is to protect the injured whose lives are ruined by physicians who don't appear to care enough about the patient to exercise reasonable care, or who have not kept up with their studies," said Chicago attorney Clifford Horwitz. "Thanks to malpractice suits, many of these physicians have lost their surgical privileges because they have butchered and ruined so many people."
Horwitz also argues that the $250,000 cap for pain and suffering damages is a red herring.
"If $250,000.00 is the cap on damages, will insurance carriers pay $250,000.00? Ever? No, they won't. Why should they? Since that is their maximum payout on their case, they will instruct their attorney to get the plaintiff to accept less or to try the case," Horwitz said.
In many states, supporters of damage caps have argued that malpractice suits drive doctors out of state, limitiing access to medical care by the state's residents. But a 2003 report from the General Accounting Office (GAO) found that malpractice suits do not appear to significantly limit access to health care.
GAO examined the experiences in five states with reported malpractice-related problems (Florida, Nevada, Pennsylvania, Mississippi, and West Virginia) and four states without reported problems (California, Colorado, Minnesota, and Montana) and analyzed growth in malpractice premiums and claims payments across all states and the District of Columbia.
But the GAO said that, although some physicians reported reducing certain services they consider to be high risk in terms of potential litigation, such as spinal surgeries and mammograms, GAO did not find access to these services widely affected, based on a review of Medicare data and contacts with providers that have reportedly been affected.
Nor is it a certainty that damage caps reduce doctors' insurance costs, a recent Texas survey found.
Texas enacted damage caps last year and the number of lawsuits filed has been declining. But more than half the state's doctors have yet to see a decrease in their liability insurance premiums, the Dallas Morning News reported.
Pfizer Warns of Bextra Risks
Safety of All COX-2 Inhibitors Questioned10/16/2004ConsumerAffairs
Pfizer Warns of Bextra Risks...
Pfizer has issued a warning that its popular pain killer Bextra could increase the risk of heart attack or stroke in patients who have undergone heart bypass surgery.
Bextra is a COX-2 inhibitor, as is Vioxx, withdrawn by Merck earlier this month after studies showed it increased the risk of heart attack or stroke in patients who took it longer than 18 months.
In its warning to doctors, Pfizer said a clinical study of 1,500 patients showed that those who had undergone coronary bypass surgery and taken Bextra intravenously and orally were at high risk for heart attacks. A similar study last year reached the same conclusion.
Vioxx, Bextra and other popular COX-2 inhibitors, including Pfizer's Celebrex, are widely prescribed for patients suffering from arthritis and other painful conditions. Celebrex is the best-selling COX-2 drug. Bextra is a newer, faster-acting version of Celebrex.
Pfizer said it is now conducting tests to determine whether Bextra increases heart attack risk in patients who take it for chronic pain.
The latest warnings contradict Pfizer's earlier assurances that its COX-2 drugs are safe. On October 7, the company said clinical trails had shown that Celebrex does not pose the same risks as Vioxx and said patients have no reason to be concerned.
In fact, the study that demonstrates the Bextra problem was conducted last spring.
Pfizer repeated its contention yesterday that Bextra and Celebrex are chemically different from Vioxx and do not carry the same risks.
The U. S. Food and Drug Administration (FDA) said it will convene a meeting of experts in January to consider safety concerns involving Bextra and Celebrex.
Feds OK Internet Service Over Power Lines
Consumers will be able to tap into the Internet by simply plugging into any electrical outlet10/14/2004ConsumerAffairs
Feds OK Internet Service Over Power Lines...
The Federal Communications Commission (FCC) has cleared the way for electric utility companies to provide consumers with high-speed Internet service over existing power lines. Consumers will be able to tap into the Internet by simply plugging into any electrical outlet.
Known as Broadband over Power Lines (BPL), this method of connecting consumers to the fast lane of the information highway may also help utilities gather critical intelligence to enhance the security, reliability and efficiency of the U.S. electric power grid. It can more quickly detect power outages, automatically read meters and power down non-essential devices in an emergency.
In a formal meeting, the five FCC commissioners affirmed the application of existing technical rules to BPL deployments and implemented additional rules to facilitate continued BPL roll-outs, marking the conclusion of a nearly two-year rulemaking process.
How quickly can consumers expect to see this service offered? Even before the official rulemaking, some companies have been setting up these systems around the country, mainly in areas where traditional high-speed internet service is spotty.
Current Communications Group has formed two joint ventures with Cinergy, a diversified energy company. The first venture will provide a bundle of broadband and voice services to Cinergy's 1.5 million customers in Ohio, Indiana and Kentucky. The second venture will deploy BPL to smaller municipal and cooperatively owned power companies covering 24 million customers across the United States.
"Today's FCC decision is as significant as the Commission's decision a decade ago to foster competition in the mobile telephone and video programming businesses, through PCS and direct broadcast satellite licensing," said William Berkman, Chairman of Currcent Communications Group.
"BPL is a high-quality alternative that transforms every in-home power outlet into a broadband outlet and will help bridge the gap in services to America's underserved communities. Furthermore, it enables electric utilities to enhance their systems' reliability and broaden their service offerings efficiently through a single general communications network built on their existing infrastructure," Berkman added.
Study Links Tumors to Cell Phone Use
People who have used cell phones for at least 10 years may have an increased risk of developing a rare brain tumor10/14/2004ConsumerAffairs
Study Links Tumors to Cell Phone Use...
A study in the international journal Epidemiologyfinds that people who have used cell phones for at least 10 years may have an increased risk of developing a rare brain tumor.
A research team from the Institute of Environmental Medicine at the Karolinska Institute in Stockholm, Sweden, found that using a cell phone for a decade or more quadrupled the risk of developing acoustic neuromas. The rare tumors generally occurred on the side of the head where the phone was most often held.
"We were surprised by the results," said Anders Ahlbom, professor of epidemiology at the institute and leader of the research team. "We think this is relatively strong data that is not down to chance."
The World Health Organization sponsored the research and medical and technology experts say it's likely to renew concerns about cell phone safety. They say it will be much harder for the industry to stonewall further medical research in this area.
In May 2000, an expert British panel concluded that the weight of available evidence indicated no adverse health effects from the use of cell phones but cautioned that children should only use them in emergencies.
For their part, industry spokesmen downplayed the study, saying it's only one piece of research and that no conclusions can be drawn from it.
The study involved 150 acoustic neuroma patients and 600 healthy people. At least five other studies are said to be underway into a possible acoustic neuromas-cell phone link.
Acoustic neuromas are slow-growing noncancerous tumors that develop on a nerve linking the brain and the inner ear. They can cause hearing loss and can be life-threatening if untreated. They're not very common, occurring in about one person per 100,000 in the general population.
The research team said it found no association between the tumors and heavy cell phone use, but rather on the length of time those in the study had been regular cell phone users.
Rainier Mountain Bicycles10/13/2004ConsumerAffairs
Rainier Mountain Bicycles...
October 13, 2004
Giant Bicycle Inc. is recalling about 160 Rainier Mountain Bicycles. The front brake mounting tabs can break, causing the brakes to fail and the rider to lose control of the bicycle.
The company has received six reports of the tabs breaking. No injuries have been reported.
The recall involves only 2004 Rainier model mountain bicycles with Marzocchi EXR Comp front forks. Model numbers included in the recall are 333502, 333503, 333504 and 333505. The bicycle is blue and silver and is made of aluminum. The names Giant and Rainier are printed on the frame of the bicycle. Earlier models of this bicycle are not included in this recall.
The bikes were sold by authorized Giant Bicycle dealers nationwide from February 2004 through March 2004 for about $850.
Consumers should contact Giant Bicycle to determine whether their bicycle is included in this recall. Authorized dealers who sold these bicycles will schedule an inspection and free repair.
Consumer Contact: Contact Giant Bicycle at (866) 458-2555 between 9 a.m. and 5 p.m. PT Monday through Friday, or go to the firms Web site at www.giantbicycle.com
The recall is being conducted in cooperation with the U.S. Consumer Product Safety Commission (CPSC).
Biggest takedown ever, feds say10/06/2004ConsumerAffairs
Ashcroft announced the arrest of 135 individuals worldwide in what he said was the most extensive multinational enforcement operation ever directed at tele...
Scams include bogus weight-loss products, deceptive credit card offers, work-at-home scams, and a scam involving English-language and auto mechanic courses10/06/2004ConsumerAffairs
FTC Continues Crackdown on Scams Aimed at Hispanic Consumers...
Lawsuits, Investigations Bug Orkin
Pest exterminator Orkin is swatting some pests of its own10/05/2004ConsumerAffairs
A consumer lawsuit seeks to represent 65,000 Florida customers and the state's attorney general is reported to be investigating racketeering allegations ag...
Pest exterminator Orkin is swatting some pests of its own. A consumer lawsuit seeks to represent 65,000 Florida customers and the state's attorney general is reported to be investigating racketeering allegations against the company.
To make matters worse, a federal judge also recently upheld a multimillion-dollar arbitration judgment in favor of an Orkin customer from Ponte Vedra, Fla., and it's reported the firm has been the target of 15,000 complaints in Florida over the last four years.
Florida Attorney General Charlie Crist has issued a subpoena for Orkin's records and documents, but won't discuss the case. The Orlando Sentinel reported that complaints include hard-to-decipher guarantees, inadequate termite treatment and inspection, routine denial of claims and failing to require subcontractors to get required building permits for termite repairs.
The consumer lawsuit accuses Orkin of deceptive and unfair trade practices. An Oct. 14 hearing in Hillsborough County Circuit Court will hear the plaintiffs' argument that the suit should be a class action representing 65,000 Orkin customers in Florida.
Just last year, Orkin settled a $6.7 million lawsuit involving a termite-damaged apartment complex in Hillsborough County. Terms of the settlement are confidential.
In the arbitration case, customer Collier Black presented evidence that in making termite repairs to his home, subcontractors had not obtained the required building permits. He won a $4.25 million judgment at a 2003 arbitration hearing, which a federal judge later reduced to $2 million.
The arbitration panel ruled in Black's favor after Black's attorneys uncovered hundreds of similar cases in north and central Florida.
It was apparently Black's case that caught Crist's attention. He opened a racketeering investigation in April, issuing a subpoena requesting company records and documents.
Nursing Home Cost Hits $70,000 Per Year
Inflation may be under control, but nursing home costs continue to skyrocket10/04/2004ConsumerAffairs
Nursing Home Cost Hits $70,000 Per Year...
Inflation may be under control, but nursing home costs continue to skyrocket. A major insurance company says the average daily cost of a private room in a nursing home in the United States is $70,080 per year, or $192 per day.
The highest rates were reported in the state of Alaska where the cost is $204,765 per year or $561 per day on average. The lowest rates were found in Shreveport, Louisiana at $36,135 per year or $99 per day.
The average length of stay in a nursing home for current residents is 2.4 years, which makes the average cost of a nursing home stay approximately $168,192. The data is contained in the 2004 MetLife Market Survey of Nursing Home and Home Care Costs.
The study also found that the cost of a home health care aide averaged $18 per hour nationally. Home health care is most expensive in Hartford, Connecticut at $28 per hour and least expensive in Shreveport, Louisiana and Jackson, Mississippi where rates are $13 per hour on average.
According to the 2003 MetLife Market Survey of Nursing Home and Home Care Costs the average daily rate for a private room in a nursing home was $181 per day or $66,065 annually. The hourly rate in 2003 for a home health aide was $18.
"The cost of long-term care continues to rise," said Sandra Timmermann, Ed.D., director of the MetLife Mature Market Institute. "Whether one chooses care at home or care in a nursing home, the costs can be exorbitant. As people prepare for their retirement and assess their asset and income requirements, it is also essential that they plan for the possibility that they will need assistance with day-to-day living. Unanticipated long-term care costs can derail an individual's financial plan; long-term care insurance may be a solution," said Timmermann.
People are living longer, but long life may not be accompanied by good health. In 1940, a 65-year-old woman could expect to live an additional 14.7 years; by 2000 a 65-year-old woman could expect to live another 19.5 years, and by 2040 women are expected to live an additional 22 years.
Chances increase that as people age they will develop a chronic condition or physical or cognitive disability for which they will require assistance. For example, almost 38% of people aged 65 and over are diagnosed with a severe disability, and 47% of those aged 85 and older have Alzheimer's Disease or another form of dementia.
Approximately 1.6 million people reside in 18,000 nursing homes in the United States with just under 10% of the residents people aged less than 65 years old and 46.5% aged 85 years and over, according to the National Center for Health Statistics. Most residents (72%) are women and three-quarters require assistance with three or more activities of daily living.
More than 1.3 million patients received home health care services from 7,200 agencies in 2000, with more than half receiving help with at least one activity of daily living. Seven in ten patients were ages 65 and older, and 65% were women, according to the National Center for Health Statistics.
British Study Finds Vitamin Supplements May Increase Cancer Risk
Not only do vitamin supplements not protect against gastro-intestinal cancer, they may slightly increase the risk of cancer10/01/2004ConsumerAffairs
British Study Finds Vitamin Supplements May Increase Cancer Risk...
Not only do vitamin supplements not protect against gastro-intestinal cancer, they may slightly increase the risk of cancer, according to a systematic review and meta-analysis of previously published randomised trials in this weeks issue of THE LANCET, a leading British medical journal.
If the findings are correct, 9,000 in every million users of such vitamin supplements will die prematurely as a result of taking something they think is good for them.
"The prospect that vitamin pills may not only do no good but also kill their consumers is a scary speculation given the vast quantities that are used in certain communities, David Forman of the University of Leeds and Douglas Altman, Cancer Research UK, said in an accompanying commentary.
The researchers cautioned that the findings are preliminary and "(do) not offer convincing proof of hazard," pending further studies.
The mortality analysis in Bjelakovic and colleagues review is work in progress, and does not offer convincing proof of hazard. In the event that a hazard is established from a complete review, these researchers will need to identify which specific interventions are associated with any risk. It is unlikely that all supplements will exert a similar effect and it will be vital to establish the safety profile for those with demonstrated benefits.
"The human diet is a complex mix of oxidants and antioxidants. Excess oxidants can cause cancer by inducing gene mutations," said Goran Bjelakovic, a professor at several European university, the study's lead investigator.
The investigators identified 14 randomised trials totalling over 170,000 participants. Overall, the results did not show any protective effect of supplementation with beta-carotene, vitamins A, C, E, and selenium (alone or in combination) compared with placebo on oesophageal, gastric, colorectal, pancreatic, and liver cancer incidences.
In half the trials, there was a small but statistically significant increase in mortality among people taking antioxidants compared with placebos. The results also showed that two combinations of supplements were associated with increased mortality risk: beta-carotene and vitamin A, and the combination of beta-carotene and vitamin E.
Four of the trials suggested that selenium was associated with a reduction in gastro-intestinal cancer risk.
We could not find evidence that antioxidant supplements can prevent gastrointestinal cancers; on the contrary, they seem to increase overall mortality. The potential preventive effect of selenium should be studied in adequate randomised trials," Dr. Bjelakovic said.
Previous studies have failed to demonstrate that antioxidant vitamin supplements reduced the risk of heart disease among people at high risk of vascular disease.