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FAERS Data: Three Ways the FDA Makes it Available to the Public

FAERS Data: Three Ways the FDA Makes it Available to the Public

FAERS is the database that houses reports submitted to FDA on adverse events and medication errors. This database is used by the FDA’s drug and biologic post-marketing safety surveillance program. FDA Drug Info Rounds pharmacists review the three ways FAERS data is made available to the public.”Learn more of the FDA Drug Info Rounds.

reachmd.comJul 3, 2017

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Food and Drug Administration News

U.S. Food and Drug Administration Approves Bristol Myers Squibb’s COBENFY™ (xanomeline and trospium chloride), a First-In-Class Muscarinic Agonist for the Treatment of Schizophrenia in Adults

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Food and Drug Administration FDA Approval Process

Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is too easy and, as a result, too many drugs are approved that are later found to be unsafe. On the other hand, a number of industry lobbyists have pushed for a more lenient approval process so that pharmaceutical companies can get new drugs approved more easily and quickly. Consider a null hypothesis that a new, unapproved drug is unsafe and an alternative hypothesis that a new, unapproved drug is s

Many consumer groups feel that the U.S. Food and Drug

Drug Administration Approval Process

Drug Administration Approval Process

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📣 BIG NEWS!! The U.S.... - Food Allergy Research & Education

📣 BIG NEWS!! The U.S.... - Food Allergy Research & Education

FacebookFood Allergy Research

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