CDER highlights key Web sites. A searchable, web-based tool for this database is not currently available. This database can be reviewed by downloading raw data sets. This database includes: medical device manufacturers registered with FDA and; medical devices listed with FDA; Note: Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by FDA. 10903 New Hampshire Avenue Silver Spring, MD 20993 Ph. Facts and Comparisons eAnswers Drug Database [On-site Access Only] Faculty Opinions (formerly, F1000Prime) [On-site Access Only] FASTATS A to Z; FDA Adverse Event Reporting System: FAERS; FDA Approved Animal Drug Products (Green Book) Animal Drugs @ FDA; FDA Drug Approvals and Databases; FDA Approved Drugs by Medical Condition, CenterWatch Since January 2017, it may also include correction or removal actions initiated by a firm prior to review by the FDA. Now in the NCBI Bookshelf It is essential to anyone interested in keeping abreast of today's health-related drug literature. ... Search the FDA's Medical Device Adverse Events Database (MAUDE) Download Sample Report . Facts and Comparisons eAnswers Drug Database [On-site Access Only] FDA Adverse Event Reporting System: FAERS; FDA Drug Approvals and Databases; FDA Approved Drugs by Medical Condition, CenterWatch; FDA Post-Approval Database; Index Nominum - Micromedex [On-site Access Only] LactMed - Drugs and Lactation Database, NIH: NLM. Search FDA MedWatch Drug and Medical Device Adverse Event Data ☎ (860) 368-0332 Search FDA Adverse Events Databases. The status is updated if the FDA identifies a violation and classifies the action as a recall and again when the recall is terminated. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. It should be noted that there are limitations to this data. Web page provides quick links to everything from acronyms to wholesale distributor and third-party logistics providers reporting. Plus: Thousands of medical device types are still eligible for reporting outside the FDA’s public database. Data sources include IBM Watson Micromedex (updated 7 Dec 2020), Cerner Multum™ (updated 4 Dec 2020), ASHP (updated 3 Dec … Produced by the Web of Science Group, this comprehensive database provides indexing and abstracts for pharmaceutical and medical journals published worldwide. These FDA databases can be useful tools in finding adverse events with drugs, medical devices, vaccines, food, cosmetics, and dietary supplements. Search Vaccine Adverse Events. This database contains Medical Device Recalls classified since November 2002. Drugs marked "unapproved medical gas", "unapproved homeopathic" or "unapproved drug other" on this Web site have not been evaluated by FDA for safety and efficacy and their labeling has not been approved. 1-888-INFO-FDA (1-888-463-6332) Contact FDA In addition, FDA is not aware of scientific evidence to support homeopathy as effective. Databases Premarket approval (PMA) is the FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class III medical devices. Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Abstracts for pharmaceutical and medical journals published worldwide for educational purposes only and is not aware fda medical databases... Searchable, web-based tool for this database can be reviewed by downloading raw sets... Initiated by a firm prior to review by the web of Science,. 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