Pensacola Personal Injury Lawyer articles in category: FDA & Prescription Drugs

Finally a beautiful and succinctstatement from a Federal Judge on the real nature of the move to preempt state courts from having pharmaceutical liability lawsuits The two pageOrder is making the...

Democrats have now subpoenaed workers in the FDA to determine how in the world they approved Ketek despite scientific concerns over its safety. The new antibiotic ended up killing people from liver damage. Turns out the clinical trials were falsified and at least one doctor has gone to prison. Still no one at Aventis or the FDA has yet to be punished, so well intentioned lawmakers are at least...

On the heals of the newly expanded recall of Am2Pat pre-filled hepain syringes for bacterial contamination, another manufacturer (Baxter) has annnounced a recall nearly 10% of its yearly heparin production. The press is implying a link to the case filed by actor Dennis Quaid over the overdosing of his two infant children by poorly labeled heparin, but the vials involved are actually different....

Judge Brier has just ruled in the Celebrex cases that the 200 milligram daily dosagethat was common for Celebrex has not been scientifically shown to cause heart attacks and strokes. You may recall that Celebrex is the Cox-2 inhibitor drug just like Vioxx that hasbeen subject to allegations that its use causes heart attacks and strokes, very much like Vioxx.This may sound like very good news...

I watched in amazement as Neil Covuto failed to conceal his anguish and outrage as he interviewed a Vioxx trial lawyer about the recent announced settlement of Vioxx case litigation. Neil had no concern about the horrible things that the drug company was willing to do to make a profit, including hiding and distorting important safety data from the medical community and the FDA. Nor was Neil...

If you are soon to receive a heart bypass, at least you won't face the propsect ohf being given the medication known as Trasylol. After consultation with agencies in the U.S., Canada, and Germany, the drug manufacturer has announced that it is wiithdrawing the drug worldwide. See Article. The FDA approved the drug in 1993 and started re-evaluating the drug's side effects after the publication ...

An FDA panel took a vote last week to ban cough and cold products for children under six years of age. According to the experts who testified before the panel, these cough and cold medicines are wholly ineffective in the treatment of cough and colds and have far more risks than benefits.This recommendation comes just a few weeks after drug companies pulled pediatric formulations of cough and...

One way the big manufacturers were going to avoid any liability for their actions was to stack the courts to rule that State courts could not interfere (with jury verdicts) in areas where the Feds have regulated. Unfortunately for their diabolic plans, some of the conservatives put on the Supreme Court actually believe in keeping the Feds out where the States can do a better job of protecting...

A more hellish scenario is hard to imagine: you go in for cosmetic Botox injections and find yourself unable to speak or breathe. Eric Kaplan spent months trapped in his own body after the couple were injected with a "homemade brew" of Botox. The selling of phony and low grade Botox is not an isolated problem, there are reports of low grade Botox being for as little as 10$ for an injection size...

As we looked at injury cases from the Bosch and Lomb Renu with MoisturLoc contact lens solution, we noticed a number of cases of Acanthamoeba infection. This is different from the fusarium fungal infection that had been most widely cited in relation to the Renu product, so predictably Bosch and Lomb denied any relationship between its product an Acanthamoeba infections. As if it it just couldn't...

It has been over 9 months since Dr. David Graham, an FDA safety official stated in his June 16, 2006 memo that Ketek should be withdrawn. He said approval of the drug was a "mistake" and contended that "every principle concerning the review and approval of new drugs was abandoned or suspended where [Ketek] is concerned."Dr. Graham believes the benefits of Ketek are outweighed by the risk of...

Despite the recent FDA warning about Sleep Aid medications like Ambien and Lunesta causing hypnotic and potentially dangerous sleep walking behavior, attorneys have been slow to take on these cases. An ongoing theme of the calls to the lawyers' offices invariably involve someone driving while in this hypnotic state. When arrested, the hapless driver is charged with driving under the influence,...

As the debate heats up over the HPV vaccination for young girls (pushed heavily by Merck), it should be mentioned that the normal tort laws for injuries from the product do not apply to vaccines. They can injure and kill and there is no liability. There is a federal compensation system, however, and the whole scheme is designed to promote vaccinations. That's ok as long as vaccinations are...

The suits against the makers of Vioxx, Celebrex, PPA and Ortho Evra all include claims that the medication could cause strokes. Strokes a re complicated injuries and can be very severe. The difficulty in proving such claims arises from the variety of other factoors that can lead to a stroke. Some understanding of the different knds of strokes is helpful. Strokes that involve a bleeding in the...

According to a new study, for suicidal patients who had taken antidepressants, fluoxetine (Prosac) was associated with the lowest risk for causing suicidal tendencies, as opposed to venlafaxine (Effexor) which had the highest risk, as published in the December issue of the Archives of General Psychiatry. The aim of this study was to investigate, in a nationwide series of suicidal subjects, how...