The FDA tracks “adverse events” related to drugs in its Adverse Event Reporting System (AERS).  Potential safety issues revealed in this manner may lead the agency’s Center for Drug Evaluation and Research (CDER) to require the manufacturer to make changes in the drug’s labeling in one or more places: boxed warnings, contraindications, precautions, adverse reactions, and patient package insert/medication guide.

While the FDA at least attempts to keep up with newly emerging risks, harm has usually been done by the time the problem is discovered. Is it too much to ask for medications to be proven safe before they are prescribed and sold?

If you believe you have been harmed by an unsafe drug, contact Hodes Milman for a free case evaluation. We’re aggressive personal injury and medical malpractice lawyers based in Los Angeles, serving all of California. We have the experience to take on the legal teams of pharmaceutical companies and have achieved multi-million dollar verdicts for our clients. Call us toll-free at (949) 640-8222 or submit the contact form via our website, www.hodesmilman.com.

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When you work with us, you’ll see the difference. A lot of firms are quick to show you numbers, and it is absolutely true that your lawyer should have experience and a strong track record in the area that you require. However, we’ll take it one step further. We also believe that your attorney should put your needs, cares and desires first. Because you deserve more than just compensation for your losses - you deserve a true advocate.

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