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Category: Defective Drugs

Amylin Held Back Safety Data from FDA on Diabetes Drug

06/30/2012
Articles
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Documents recently posted to the FDA’s website say pharmaceutical company, Amylin, has not been completely forthcoming about its diabetes drug, Byetta, and related drug Bydureon, concerning their potential for cardiovascular complications. The active ingredient is the same in the two drugs which are both used to treat type 2 diabetes. However, Bydureon […]

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Yet Another DePuy Lawsuit Filed

06/27/2012
Announcement
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  Another DePuy ASR hip implant lawsuit was filed this week against DePuy Orthopaedics and its parent company, Johnson & Johnson.  This lawsuit was filed on behalf of a 61 year old woman who lives on a farm near Gainesville, Florida.  She had the misfortune of being implanted with not […]

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Pradaxa Tops FDA’s List for Serious Adverse Events

06/26/2012
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According to an analysis by the Institute for Safe Medication Practices, Pradaxa drug (Dabigatran) topped the list of direct reports to the FDA for serious adverse drug events in 2011.  Pradaxa took the lead with 817 direct reports, followed by Coumadin (Warfarin) with 490 direct reports, Levaquin (Levofloxacin) with 393, […]

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Avandia and Actos Linked to Macular Edema Vision Problems

06/13/2012
Actos
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According to a study published June 11, the users of Actos (pioglitazone) or Avandia (rosiglitazone) may face an increased risk of developing macular edema.  Published in the Archives of Internal Medicine, British researchers collected data on more than 100,000 patients with type 2 diabetes who were enrolled in the British […]

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Azithromycin & Sudden Cardiac Death

05/21/2012
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A study published in the New England Journal of Medicine on May 17, 2012, suggests that the popular antibiotic azithromycin may increase the risk of sudden cardiovascular death, especially among patients who are already at risk for cardiovascular disease.  Different patient groups were treated with azithromycin (Zithromax), amoxicillin, ciprofloxacin (Cipro), […]

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FDA Cautions Against Long Term Fosamax Use

05/17/2012
Articles
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The U.S. Food and Drug Administration (FDA) announced on Wednesday, May 9, that patients taking the osteoporosis drug, Fosamax, or any of the bone-building class of drugs known as bisphosphonates, should be reevaluated every three to five years to determine if it is safe for them to remain on the […]

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