Durogesic Patch – Informed Consent
We represent a lady who has experienced brain damage as the result of inappropriate prescription of a Durogesic Patch. She had one day surgery and was sent home wearing a Durogesic Patch. The...
It seems like U.S healthcare is more concerned about profits than patients these days. Now is the time to learn more about the latest legal battles patients face with conditions from head to toe and how to be your own best healthcare advocate, so you receive the care you deserve.
We represent a lady who has experienced brain damage as the result of inappropriate prescription of a Durogesic Patch. She had one day surgery and was sent home wearing a Durogesic Patch. The...
Desipramine is a dangerous drug which has been associated with sudden deaths in children and adolescents.
On Monday, Baxter announced they are temporarily suspending the production of the drug Heprin, after 350 negative reactions have been reported in conjunction with the drug. The active ingredient in Heprin, a blood-thinning medication, was reportedly made at a Chinese facility that the U.S. Food and Drug Administration (FDA) failed to inspect, according to a report in the Wall Street...
The U.S. Food and Drug Administration (FDA) has approved revisions to the current Ortho Evra Contraceptive Patch label. The updated labels will reflect results from a new study that found users of the patch were at an increased risk of developing serious blood clots (also known as (VTE - venous thromboembolism), than those women who use birth control pills.The study was conducted by Boston...
The FDA has sent warning letters to seven pharmacies ,within the last week regarding false or misleading claims about their made-to-order products, commonly marketed as bio-identical hormone replacement therapy (BHRT).The FDA has also agreed to create public-awareness campaigns designed to dispel myths about "bio-identicals."Some pharmacies that make "bio-identicals" say they are all-natural and...
Merck & Co., a popular drug manufacturer, announced a recall of more than one million vaccines due to a contamination risk. U.S. Health officials say the recall is not a health threat. Dr. Julie Gerberding, head of the Centers for Disease Control and Prevention, echoed that in a news conference.The recalled vaccine, HIB, is used to protect babies and children from meningitis and pneumonia. Merck...
Chantix, a prescription drug aide to help adults quit smoking, is being evaluated by the FDA for adverse health effects.Pfizer Inc., the manufacturer, recently submitted reports to the FDA describing suicidal ideation (thoughts). In the aftermath of a recent case that reported erratic behavior while taking Chantix, the FDA also requested any additonal information on cases with any...
Today, the U.S. Food and Drug Administration announced - GlaxoSmithKline (GSK), manufacturer of the popular type 2 diabetes drug, Avandia, has agreed to add new warning information to the existing boxed warning about the potential risk for heart attacks.People who suffer from type 2 diabetes that have heart disease or who are at high risk of heart attack should talk with their medical doctor...
The FDA has announced that it is going to add a label to include the risk of hearing loss for the erectile dysfunction (ED) drugs Cialis, Levitra, and Viagra and to Revatio, which is used to treat pulmonary arterial hypertension (PAH). The new labeling will display more prominently the potential risk of sudden hearing loss, and a guide for consumers on what to do if they experience sudden...
The federal government is planning on requiring warnings for certain contrast agents used with ultrasound technology. These contrast agents are used to improve diagnoses of heart problems in patients evaluated with ultrasound imaging equipment.The contrast agents are sold under the brand name Definity, by Bristol-Myers Squibb, and Optison, of General Electric. Physicians inject the imaging...