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The FDA announced this week that the drug Onfi (clobazam), manufactured by Lundbeck, Inc. “can cause rare but serious skin reactions that can result in permanent harm and death.” All cases known by the FDA have resulted in hospitalization, including one patient who became blind and another who died. Several lawsuits have been filed on… Continue reading
by Eric Fredrickson, Esq., Harman Law LLC A bipartisan group of lawmakers in the U.S. House of Representatives pushed for H.R. 3309, ironically titled the “Innovation Act,” that drastically curtails the ability of patent holders to enforce their intellectual property rights. The bill passed the House today, December 5 with a 325-91 vote. The bill… Continue reading
A Trial Lawyer’s Playbook. When one football team goes up against another, both the teams may be very evenly matched on paper. What tips the balance in favor of one team over another? A good coach will consider factors beyond the team’s wins and losses. Where is the game being played, is your team the… Continue reading
The FDA has republished a Class 1 recall, the most serious, for the Hospira Inc. GemStar Infusion System. The GemStar pump by Hospira is designed to deliver fluids via IV, to lower back or spinal areas, and in other parts of the body. It is small, lightweight and can be portable when using battery power.… Continue reading
Many Americans will be driving long distances to see their loved ones this holiday season. Unfortunately, the holidays are among the most dangerous times to be on the road. The number of injuries and deaths from automobile crashes increases substantially in the time period between Thanksgiving and New Year’s. The following tips can help you… Continue reading
The FDA has classified the Medtronic cardiac “guidewires” recall as a Class 1, the most serious category. Medtronic issued a voluntary recall of the “guidewires,” the wire connectors used to connect cardiac devices that help regulate heartbeat and other functions and facilitate heart surgery because the coating on the wire may disintegrate causing the wire… Continue reading
The leukemia drug Icusig that was given rapid approval by the FDA in December 2012 is now off the market and clinical trials are halted. The FDA received an alarming number of reports of more than a dozen deaths and a still-to-be-counted tally of serious injury from blood clots, heart attack, stroke, lack of blood… Continue reading
A South Dakota jury sided with a woman claiming her ovarian cancer was linked to her use of Johnson & Johnson talc-based body powder. After a two week trial and nearly twelve hours of deliberations, the jury said J&J should have warned consumers of the risks. According to the Sioux Falls, South Dakota newspaper the… Continue reading
The Harman Law Firm has filed a complaint against the manufacturer of the Medtronic MiniMed Paradigm MMT 722 Insulin Pump following the death of a young woman who was using the device The MiniMed Insulin Pump is designed to deliver insulin continuously into the body, making multiple injections per day unnecessary. The young college student… Continue reading
This week, ProPublica in conjunction with the radio program “This American Life” released a Tylenol investigation, a blistering report on the popular over the counter drug and the manufacturer’s failure to adequately warn of the serious, deadly risks despite long-held concerns of the FDA and the medical community. New warnings are being placed on Tylenol… Continue reading
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