Archive for March, 2008

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27
Mar

Blue Steel and Hero products may cause defective product injuries

March 27, 2008

The FDA reported that diet products labeled “Blue Steel” and “Hero” may cause defective product injuries, including dangerous affects on blood pressure.

These products are marketed as diet products but may have undeclared ingredients, have not been proven safe or effective by the FDA, and may cause defective product injuries.

The undeclared ingredients may interact with some prescription medications, possibly lowering blood pressure to dangerous levels, and causing defective product injuries.

These unapproved diet products could cause Texas defective product injuries.

Read more: http://www.fda.gov/bbs/topics/NEWS/2008/NEW01809.html

Popularity: 51% [?]

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25
Mar

Cantaloupes may be source of salmonella, defective product injuries

March 25, 2008

The FDA reports that cantaloupes from a Honduran grower and packer appear to be the source of defective product injuries in the United States.

The defective product injuries resulting from the cantaloupes include salmonella and 50 people in 16 states have suffered defective product injuries because of the grower’s cantaloupes.

The FDA has asked that all cantaloupes from the company be detained to limit further defective product injuries.

Contaminated cantaloupes could cause Texas defective product injuries.

Read more: http://www.fda.gov/bbs/topics/NEWS/2008/NEW01808.html

Popularity: 45% [?]

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19
Mar

Reebok to pay $1 million for recalled lead bracelets which caused the defective product related death of a child in 2006

March 20, 2008

USA Today reported that Reebok will pay a $1 million fine for recalled bracelets that contained toxic levels of lead which caused the death of a 4-year-old child.

Reebok imported and distributed lead charm bracelets, giving them away with children’s shoes purchases.

A heart-shaped charm from the defective product caused a fatal defective product injury in the child who swallowed the charm.

The bracelets were recalled and no other defective product injuries were reported. Lead toxicity in cases like this could cause Texas defective product injuries.

Read more: http://www.usatoday.com/money/industries/retail/2008-03-18-reebok-fine-cpsc_N.htm?csp=34

Popularity: 43% [?]

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18
Mar

FDA issues drug injury alert on Tussionex

March 18, 2008

The United States Food and Drug Administration has issued an alert on Tussionex Pennkinetic Extended Release Suspension due to recent reports of drug injuries, including death, as a result of misuse and inappropriate use of the prescription cough medicine.

Risk of drug injury is associated with patients who may be taking more Tussionex, or doctors who may be prescribing more Tussionex than is recommended or prescribing Tussionex more frequently than every 12 hours.

Children under 6 years old who take Tussionex against recommendations could also be at risk of drug injury

Misuse and inappropriate use of Tussionex could also cause Texas drug injuries.

Read more: http://www.fda.gov/bbs/topics/NEWS/2008/NEW01805.html

Popularity: 29% [?]

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13
Mar

FDA Issues Alert on Tussionex

The Food and Drug Administration has released a warning on the cough medication Tussionex, which contains hydrocodone. Cases of serious adverse events, including death, have been reported in people and children using the product.

Tussionex is a prescription cough medicine that is used by both adults and children. It contains the potent narcotic hydrocodone and has the potential for overdose if used improperly. The warning issued by the FDA includes the following language:

  • Tussionex should not be used (is contraindicated) in patients less than 6 years old. FDA has received reports of death in children less than 6 years of age who have been prescribed Tussionex.
  • Consult the prescribing information to determine the correct dose and dosing frequency of Tussionex. Tussionex is an extended-release formulation that should not be prescribed at an interval less than 12 hours.
  • Discuss with the patient the amount of and frequency of Tussionex to be given. Instruct patients not to take, and parents not to administer Tussionex more frequently than every 12 hours.

Be sure to follow dosing instructions to avoid a potential Texas drug injury or death.

Click here to read more http://www.fda.gov/bbs/topics/NEWS/2008/NEW01805.html

Popularity: 31% [?]

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13
Mar

Pharmaceutical levels found in drinking water could cause drug injuries

March 13, 2008

Yahoo News reports that many water agencies are saying that the quality of their drinking water is well above Environmental Protection Agency (EPA) standards when confronted with the results of an Associated Press investigation, which showed the national environmental effect of improper disposal of pharmaceuticals on water.

However, many water agencies say their water has not been tested for pharmaceuticals.

The Associated Press investigation found trace amounts of pharmaceuticals in the water of 24 metropolitan areas across the nation.

Councilman James G. Gennaro says he is very concerned about the presence of drugs in drinking water.

Sen. Bob Menendez agrees that it is of national environmental concern if drinking water contains pharmaceuticals and that the government should be working to correct the problem.

While the human risks of consuming low levels of pharmaceuticals in drinking water over a long period of time are unknown, studies have shown alarming environmental effects on human cells and wildlife and could suggest potential for drug injuries over the long term.

According the study, trace amounts of drugs were found in large metropolitan areas cross the nation, and could have national environmental effects, including Texas environmental injuries.

Read more: http://news.yahoo.com/s/ap/20080312/ap_on_re_us/pharmawater_reax;_ylt=Ai_aQpOkkMncseRcl0itqrhvzwcF

Popularity: 39% [?]

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7
Mar

Supreme Court ruling could have serious consequences for injured victims

The Supreme Court recently handed down a ruling regarding defective medical devices that may have serious ramification for the victims of Texas defective medical product injuries. A Texas defective medical device injury can be life-altering and extremely painful; injuries suffered from devices that were negligently manufactured—such as an artificial hip implant laden with bacteria or a painkiller patch that leaks and exposes users to harmful levels of dangerous drugs—can even result in death.

The Supreme Court ruled that a medical device manufacturer, despite if one of their devices is later proven to be defective, is not liable for damages to a harmed individual if the device was originally approved by the Food and Drug Administration (FDA). This ruling comes as a huge surprise to most Americans, who expect our courts to be able to help us if we fall victim to a Texas defective medical device injury.

Click here to read more http://www.tennessean.com/apps/pbcs.dll/article?AID=/20080227/BUSINESS/802270409

Popularity: 37% [?]