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How People Can Report Adverse Drug Reactions to the FDA MedWatch Program

February 23, 2022 By Law Offices of Thomas J. Lamb, P.A.

MedWatch is an FDA program for reporting “serious reactions” resulting from a prescription medication. The FDA is particularly interested in those drug injury events which resulted in any of the following outcomes: Patient's Death: an adverse reaction to a drug is the suspected cause of death Life-Threatening Condition: a serious … [Read more...]

Filed Under: Unsafe Drugs Tagged With: FDA MedWatch reporting system

Osteoarthritis “Medical Food” Limbrel Tied to Life-Threatening Events

November 28, 2017 By Law Offices of Thomas J. Lamb, P.A.

What is Limbrel? Limbrel is marketed by Primus Pharmaceuticals Inc., and is classified as a "medical food," which the FDA defines as: A food which is formulated to be consumed or administered enterally under the supervision of a physician and which is intended for the specific dietary management of a disease or condition for which distinctive … [Read more...]

Filed Under: Unsafe Drugs Tagged With: baicalin, catechin, drug safety communication, FDA, FDA investigation, FDA MedWatch reporting system, flavonoid capsule, limbrel, medical food, osteoarthritis, osteoarthritis drugs, Primus Pharmaceuticals

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