137,000,000,000 square feet: total US drywall use, 2004-2007 (WSJ online, 4/17/09)
550,000,000 pounds of drywall imported to US since 2006—enough to build 60,000 homes(heraldtribune.com, 2/18/09)
309,000,000 square feet: amount of drywall imported from China, 2004-2007—enough to build 35,000 homes (WSJ online, 4/17/009)
100,000 minimum number of homes estimated to be affected by Chinese drywall (msn.com, 6/5/09)
75,000 estimate of how many potential Chinese drywall cases could develop nationwide by Coral Gables lawyer Ervin Gonzalez (news-press.com, 5/11/09)
…and losing out bigtime. While the lawsuits from homeowners who’ve been affected by the Chinese drywall debacle continue to mount nation-wide, what happens to the contractors, like this one in Norfolk, VA who threw out over $1,000,000 in Chinese drywall inventory? They’re caught in the middle of one big mess.
This week, journalist Philip Dawdy reported on the popular website Furious Seasons that Wyeth’s Effexor me-too drug Pristiq, FDA approved in early 2008, had already generated 1,272 adverse event reports in the FDA’s MedWatch system through the end of 2008, and wrote with live links to the reports:
“It’s discouraging that 17 of those reports involve completed suicides through the end of 2008. There are also 48 reports of suicidal ideation through the end of 2008.”
“That’s a lot in such a short period of time, especially considering that this drug isn’t exactly widely used,” Dawdy points out. Read the rest of this entry »
On May 19, 2009, researchers presented a study that found children who received the trivalent inactivated influenza vaccine [TIV] had a three times greater risk of hospitalization for the flu than kids who were not vaccinated at the International Conference of the American Thoracic Society in San Diego.
To determine whether the vaccine was effective in reducing the number of hospitalizations over consecutive flu seasons for 8 years, the researchers conducted a study of 263 children between the ages of 6 months and 18, evaluated at the Mayo Clinic between 1996 and 2006, with laboratory-confirmed influenza and reviewed records to determine which kids had received a flu shot before the illness and hospitalization. Read the rest of this entry »
On May 12, 2009, the House Energy and Commerce Subcommittee on Health held a hearing on the Medical Device Safety Act of 2009. HR 1346 would overturn the February 2008 Supreme Court decision that, for the first time, denied patients the right to sue device makers for compensation when injured by certain medical devices.
In the case of Riegel v Medtronic, the court ruled that a device maker cannot be sued under state law by patients alleging injury from a device that received marketing approval from the FDA.
“The Court’s decision has left consumers without any ability to seek compensation for their injuries, medical expenses and lost wages resulting from injuries caused by defective premarket approval (PMA) devices or inadequate safety warnings,” according to a March 5, 2009 press release by Representatives Frank Pallone, Jr (D-NJ), Chairman of the Energy and Commerce Subcommittee on Health, and Henry Waxman (D-CA), Chairman of the Energy and Commerce Committee, issued when introducing the Medical Device Safety Act of 2009. Read the rest of this entry »