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FDA is an agency within the Department of Health and Human Services.
The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services.
The brief summary includes all the risk information about a prescription drug and is generally based on the prescribing information. The brief summary may leave out non-risk information, such as the chemical description of the drug, how it works in the body, and directions for using it.
The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nations food supply, cosmetics, and products that emit radiation.
The Brief Summary is a quarterly bulletin intended for all Office of Prescription Drug Promotion (OPDP) stakeholders. The Brief Summary provides news and updates related to OPDP.
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FDA is an agency within the Department of Health and Human Services and consists of nine Center-level organizations and thirteen Headquarter (HQ) Offices.
the consumer brief summary should provide clinically docHub information on the most serious and the most common risks associated with the product and omit less pertinent information. the most frequently occurring Adverse Reactions should be included in the consumer brief summary.

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