This almanac discusses prescription and over-the-counter drugs, and examines the research, testing and marketing procedures, and FDA approval process. Post-market surveillance of prescription drugs is also explored, including voluntary and mandatory adverse reaction reporting requirements, and the most commonly reported medication errors. This almanac also discusses Food and Drug Administration (FDA) regulation of prescription drug marketing, internet pharmacies, and sets forth steps the consumer can take to research prescribed drugs. Prescription drug litigation is also examined. The Appendix provides sample forms, applicable statutes, and other pertinent information and data. The Glossary contains definitions of many of the terms used throughout the almanac.
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