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Find medically-focused summaries describing herbal, vitamin, and supplement products. Patient-focused information includes side effects and uses. Health care professional-focused information includes mechanism of action, interactions, and scientific references.

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AccessPharmacy

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Textbooks, drug monographs, quizzes, flashcards, videos, cases, and calculators, selected for relevance to Pharmacy education.

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AGELINE

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Content focus on social gerontology, which is the study of aging in psychological, health-related, social, and economic contexts. Includes abstracts of over 200 academic journals, books, book chapters, and dissertations from 1978 to present.

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Government resource including broad coverage of: health topics, Evidence-based Practice Center reports, US government programs, research tools, data and statistics, grants, consumer health.

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Alt HealthWatch

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Includes academic journal and magazine articles, reports, association and consumer proceedings, and book excerpts covering alternative and complementary therapies, including homeopathy, herbalism, nutrition, and traditional Chinese medicine from 1990 to the present.

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Some drugs could be dangerous if not dispensed, stored, or used properly. The FDA requires that pharmacists must use approved strategies to reduce these risks. This database includes the full text of all required risk evaluation and mitigation strategies for US-approved drug products.

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Online access to current and past United States Food and Drug Administration-approved labels for prescription and over-the-counter drugs.

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Houses documents (legal reports, presentation files, emails, memos, etc.) from the pharmaceutical industry, regulatory agencies, universities, and funding agencies regarding drug and pharmacy-related lawsuits. Hosted by the University of California San Francisco.

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Combines chemical, pharmacological and pharmaceutical data with comprehensive drug targeting information.

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Search for prescription and over the counter drugs approved for sale in the United States; find approved labels, original application documents as submitted by the drug company, and replies from the Food and Drug Administration.

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