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Why Taking The Brand Name Version of a Drug Is So Important To Injury Prevention While purchasing a generic version of a drug may be a cost effective way to get the medications you need, doing so may present some serious risks. This is because generic drugs are not held to the same manufacturing standards as brand name versions of medications. The U.S. Food and Drug Administration has a stringent (more...)

FDA Proposes Social Media Rules For Drug And Medical Device Manufacturers In order to protect United States consumers from the dangers of suffering a drug injury, the U.S. Food and Drug Administration (FDA) strictly regulates the way medications are marketed. Now, the FDA is stretching its coverage of this field of the medical industry by creating a set of guidelines drug manufacturers should adhere to when (more...)

FDA Recalls Hemodialysis Drug Due To Deadly Contamination It’s important that certain safety and sanitation standards are practiced during the manufacturing process of medications in order to ensure the product will be safe for consumption. When and if these standards are not met, patients may be put at a serious risk of suffering a drug injury. A fine example of the risks was (more...)

FDA Releases Online Version of The Orange Book Finding a reliable source of information about medications can be extremely difficult. This lack of detailed medication data often leads to errors in the distribution and administration of a medication, causing serious Drug Injuries. This leaves many citizens wondering where to find answers to questions about medications. The Drug Injury Attorneys with Ferrer Poirot Feller (more...)