Watchdog Group Threatened Pfizer With Lawsuit Unless They Modified Centrum Vitamin Labels

One major drug manufacturer submitted to the demands of a watchdog group in hopes to deter them from a lawsuit claiming the drugmaker was falsely advertising their products can help prevent breast and colon cancer.

According to ABC news, Pfizer has agreed to remove the “breast health” and “colon health” claims from the labels of its widely used Centrum multivitamin supplements, even though they disagree with the complaints lodged by the nonprofit Center for Science in the Public Interest (CSPI).

The center sent a lengthy letter to Pfizer Chief Executive Ian Read in April alleging that separate Centrum products carried deceptive claims on their labels – that they support “energy and immunity,” “heart health“, “eye health,” “breast health, “bone health” and “colon health.”

The group threatened to sue Pfizer, insisting “those claims of breast and colon health implied that the supplements would prevent breast and colon cancer — disease prevention claims that supplement manufacturers can’t legally make,” CSPI said in a press release, unless the claims were stripped from labels of the products.

Pfizer has agreed to remove the claims related to breast health and colon health from some Centrum product labels over the next six months and to withdraw them from websites and advertising within 30 days, and to modify language relating to heart health and energy.

“The company disagrees with CSPI’s concerns, but has agreed to make these changes in order to fully resolve the issues raised by the organization,” Pfizer said in a statement.

A company spokesperson declined to elaborate when asked about the scientific basis for the various health claims.

Labels for Centrum Ultra Women’s and Centrum Silver Women’s multivitamin supplements stated that those products supported “breast health.” Likewise, labels for Centrum Ultra Men’s and Centrum Silver Ultra Men’s supplements claimed to support “colon health.”

The group said Pfizer partly based the breast and colon claims on the presence of vitamin D in the products, despite inconsistent or inconclusive evidence of vitamin D’s protective role against breast and colon cancer.

Various other Centrum products will continue to claim they foster bone health and eye health, despite CSPI’s earlier objections to the claims.

“A settlement is, by its nature, something where neither side gets all it wants,” said Stephen Gardner, director of litigation for the center. “Once Pfizer agreed to drop the breast and colon cancer claims, we felt that that was too important to let things fall apart over eye and bone health.”

Gardner said the vitamin claims might be interpreted as helping the structure of bone and eyes, a stronger argument than preventing complications.

For Centrum products claiming “heart health,” labels and advertising will now note they are “not a replacement for cholesterol-lowering drugs.” For products promoting “energy,” language will be added to show they do not directly provide an energy boost, but instead support metabolic function, the consumer group said.

Many other companies continue to make unsubstantiated health claims for supplements, Gardner said.

“It’s a tremendous problem. The supplement companies want consumers to buy their supplements instead of FDA-approved actual drugs. So they make claims of disease prevention.”

“For many consumers, a daily multivitamin is an expensive insurance policy to make sure that one’s getting the recommended daily amounts of important vitamins and minerals,” said Gardner.

“But supplement manufacturers must not mislead consumers into thinking that these pills will help ward off cancer.”



,

No comments yet.

Leave a Reply

GET HELP NOW!
  • This field is for validation purposes and should be left unchanged.
Latest Drug Injury News

Underground Railway Dust May Pose Health Risk

Travelling or working on an underground railway for sustained period of time could have health implications due to concentrations of metal-rich microscopic dust particles.

New Study Helps Understand Why Health Care Costs On The Rise

Although many believe is it medical malpractice suites that are causing the increase in the health care costs, it is actually the fear of them that is partly to blame. Doctors are ordering unnecessary tests and procedures for fear of a patient filing a claim down the road

FDA Issues New Warnings Concerning Tolvaptan

The FDA has issued a drug safety communication concerning Tolvaptan, a selective vasopression V2-receptor antagonist used in heart failure patients to treat clinically significant hypervolemic and euvolemic hyponatremia.

New Antiepileptic Drug Causes Blue Discoloration And Vision Trouble

An antiepileptic drug to hit the market has been known to cause vision troubles and skin discoloration. Almost all patients experienced gray/blue skin discoloration who had been taking the pill for two years. More information is needed to better understand the occurrences.

Medical Mattresses Pose Risk Of Infection And Contamination

The FDA warns that medical mattresses may not be as clean as once perceived. Routine checks on mattresses are advised as any rips, tears, or excessive wear alter the efficacy. The medical mattresses as well as the covers have an expected life depending on the manufacturer, which should not go unnoticed.

Latest Medical Device Injury News

Women 30% More Likely To Need Repeat Hip Implant Surgery

Doctors traditionally believed the larger the size of the implant, the more protective it was against failure, according to Sedrakyan. However, he said his study found regardless of size, women had a higher rate of revision occurrence, so some other factor besides the actual implants may be leading to this effect.

Transvaginal Mesh Lawsuits – Who Is At Fault?

For some women a pelvic transvaginal mesh product has been a god sent.  To be able to resume a full active life, without the worry of a leaky bladder, is a true miracle for some women.  And, this only became possible with the help of pelvic mesh. The mesh is most commonly used after pelvic [...]

Metal-on-Metal Hip Implants Cause Soft Tissue Damage Says FDA

Hip joint deterioration can lead to pain, stiffness or difficulty walking. When these symptoms do not respond to conservative treatment, such as physical therapy, patients may be advised to undergo total hip replacement or hip resurfacing. As part of this treatment, they may receive a “metal-on-metal” hip implant in which the “ball and socket” of [...]

Ethicon Recalls Surgical Stapler

The FDA has announced a voluntary global recall of more than 157,000 Ethicon surgical staplers, due to problems with incomplete firing strokes that may cause faulty staple formation, potentially resulting in painful and severe internal complications for the patient. An Ethicon surgical stapler recall was first announced in August, after reports surfaced where surgeons experienced [...]

Another Device Maker Investigated By DOJ

Earlier this month, cardiovascular device maker Abiomed announced that the US Attorney’s Office was investigating the company’s marketing and labeling of the Impella 2.5 circulatory support device. According to Forbes, the announcement confirmed rumors that had been circulating for at least two weeks, though in the press release the company said it had just been [...]