wilbert martin (147 risultati)

Soft cover. Condizione: Very Good -. Journal Offprint. 7 page reprint (NO. 151) from the Public Health Reports, November 14, 1913. "A discussion of the need for restriction of the sale and distribution of bichloride of mercury tablets." Top edge has wear. Paper.

PAP. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

Soft Cover. Condizione: Good. 1st Edition. First Edition. Good copy. No jcaket. In burgundy cloth soft covers with gilt lettering on front cover and spine. Burgundy stained edges. Square copy. No writing on any inner text pages. Previous owners' name on front endpapers and title page. Bumping and rubbing of ends of spine, corners and edges. Crease on page 409. Two small closed tears on page 251. Moderate shelf rubbing and wear. Thank you for your patronage. Size: 12mo - over 6¾" - 7¾" tall.

Soft cover. Condizione: Fair. No Jacket. n/a (illustratore). Soft Cover. Fair/N/a. 8vo - over 7¾" - 9¾" tall. There are 16 chapters in the book. It is a softbound red with gold embossed title on the front cover. The edges show some wear around the edges, but the inside doesn't look like it has ever been used. I don't find any writing on the inside of the book, not even the former owner's name. I know it is very difficult to purchase a vintage book without holding, so I'll try to provide pictures if you would like them.

PAP. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

PAP. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

Paperback. Condizione: New.

PAP. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

Condizione: As New. Unread book in perfect condition.

HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

Condizione: As New. Unread book in perfect condition.

Condizione: New.

Hardcover. Condizione: Near Fine. Condizione sovraccoperta: Near Fine. 1st Edition. hardback book and dust jacket in near fine condition.

Hardcover. Condizione: Good. Pages slightly tanned. Tear at the bottom of the front end page. Book plate on inside of front cover. Contents are clean. Good.

Condizione: New.

Paperback. Condizione: New. Print on Demand. This book provides a historical look at revisions of two landmark pharmaceutical texts, the United States Pharmacopoeia (USP) and the National Formulary (NF). The USP and NF are essential standards for drugs, and the book presents the history of their development as well as the latest revisions. It offers a critical review of the general principles to be followed in revising the USP and the NF, with insights into the deliberations of the committees responsible for updating these vital references. The author provides a detailed account of the changes implemented in the 9th revision of the USP and the 4th edition of the NF. With the evolution of medicine, pharmaceuticals, and scientific understanding, their latest revisions incorporate significant changes in requirements, standards, and testing methods to ensure the continued quality and safety of drugs used in the United States. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This book is a comprehensive guide to the pharmacology, therapeutics, dosage, and major medicinal uses of common, essential medications. The author presents information on the physiologic actions of drugs, their therapeutic uses, and appropriate dosages, which can be straightforward for the professional but overwhelming to the average individual seeking a basic understanding of prescription drugs. By examining various drug classifications and their mechanisms, this book provides a better understanding of safe and effective medication use. By exploring synergistic actions of drugs and offering insight into the avoidance of side effects, the author helps readers make wise choices about their healthcare. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This book analyzes the U.S. Pharmacopoeia, a crucial text in regulating the identity and purity of drugs in the United States. The author provides historical context for the development of the Pharmacopoeia, and a deep examination of its impact on the field of medicine and the pharmaceutical trade generally. The book explores the various revisions and changes made to the Pharmacopoeia over time, the challenges and controversies involved in its creation and usage, and its overall importance in safeguarding public health. The author illuminates how the Pharmacopoeia's requirements have shaped drug manufacturing practices and the evolution of the pharmaceutical industry. Through this analysis, the book sheds light on the intricate relationship between scientific advancement, government regulation, and the availability of safe and effective medications. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. Unveiling the vast therapeutic potential of the present-day United States Pharmacopeia, this indispensable guide delves into the multifaceted uses of official remedies and time-honored agents. Drawing upon the wealth of knowledge accumulated over centuries, the author explores the practical applications and limitations of a wide range of medicinal substances. Beyond the celebrated remedies, this book sheds light on the often-overlooked therapeutic value of extrapharmacopeial substances, arming practitioners with a comprehensive understanding of both traditional and contemporary treatment options. It underscores the crucial distinction between genuine discoveries and mere repackaging, empowering readers to navigate the complex landscape of proprietary and generic medications. The author's meticulous analysis of disinfectant agents empowers readers to confidently select and employ the most effective substances for preventing the spread of infectious diseases. From the potent action of chemical disinfectants to the natural efficacy of sunlight and heat, this book provides a thorough understanding of the principles and practices of disinfection. With its unwavering focus on the convergence of pharmacology and medicine, this book offers invaluable insights into the dynamic relationship between therapeutic agents and the human body. It challenges the notion of therapeutic nihilism, asserting that a deep understanding of pharmacology can unlock a world of effective and safe treatment options that have been meticulously tested and proven over time. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This book, including contributions from leading medical minds of the early 20th century, offers a comprehensive catalog of therapeutic remedies available at the time of its publication. It is an invaluable resource for scholars and medical practitioners seeking to understand and appreciate the evolution of pharmacology, particularly the shift away from nostrums and towards scientifically validated medications. The author seeks to lay bare the shortcomings of popular remedies and patented medicines, while simultaneously illuminating the wide range of applications and limitations of established, official remedies. The book provides an overview of the history of the US Pharmacopoeia and offers practical advice on the appropriate use and limitations of medications, making it an indispensable tool for understanding the history of medicine, assessing the present state of pharmacology, and predicting its future directions. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This book collects and summarizes criticisms and comments that medical doctors and pharmacists have made about the eighth edition of the Pharmacopoeia of the United States, as well as the third edition of the National Formulary, both published in 1905. The book's author provides a retrospective look at the evolution of laws governing the production and sale of drugs in the United States, offering commentary on legal standards, definitions of poisons, international standards for potent medications, and more. The contents of this book have been arranged to serve as a reference for popularly discussed substances, providing a reflection of trends in current medical thought and the requirements of medical practitioners. It provides a balanced overview of the challenges faced by early 20th-century medical professionals in regulating and standardizing the medications available to them, and highlights the progress that has been made in the field of drug regulation since that time. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This book is an extensive and updated index of available literature relating to the nature, object, or content of the Pharmacopoeia of the United States of America and the National Formulary, two books recognized by statute as authoritative standards of the purity and strength of drugs and their preparations. In addition to the descriptions from the official texts, the volume offers a rich collection of comments on actions and uses of drugs and commentary on unusual, toxic, or secondary effects of official drugs and preparations. Moreover, this book captures the state of drug regulation as it was at a specific time period, providing essential historical context for the evolution of modern-day standards. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This book is a compilation of comments and abstracts on the 8th edition of the United States Pharmacopoeia (U.S.P.), authored by the United States Public Health Service. It provides an overview of the pharmacopoeia's significance and relevance, as well as its incorporation of standards from foreign pharmacopeias. The author presents diverse perspectives on the U.S.P., highlighting its role in defining drug purity and strength, and explores the need for ongoing revisions and updates to align with evolving medical knowledge and therapeutic practices. The book also covers related topics such as the National Formulary (N.F.), biological products, and analytical methodology. The insights in this book offer valuable context for researchers, medical professionals, and policymakers seeking to understand the development, interpretation, and impact of the U.S.P. in shaping the landscape of medicine and public health. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New.

Paperback. Condizione: New. Print on Demand. This book examines the Parmacopoeia of the United States (U.S.P.), a legal standard for drug quality since 1820. The latest edition includes monographs on over 1,000 drugs. Its standards are adopted by the U.S. Food and Drug Administration for regulating the drug industry. The author, a pharmacist and pharmacognosist, traveled extensively to compile data on medicinal plants and created monographs on many drugs that had no previous official standards. This book is an essential tool for understanding the history and significance of the U.S.P. and its role in ensuring the quality of drugs. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This book explores revisions to the Pharmacopoeia of the United States of America over time. It places particular focus on the Eighth Edition (1905) and the National Formulary Third Edition (1906). The author examines the legal, social, and medical factors which influenced the revisions of these texts. Among the topics analyzed are narcotics, antidotes, and the establishment of drug standards. The author also reviews attempts to establish a limited materia medica and includes a discussion of the work of the Committee on Revision. The book concludes by reflecting on the significance and the possible future of the US Pharmacopoeia. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.

Paperback. Condizione: New. Print on Demand. This publication provides comprehensive information on official drug standards as defined in the United States Pharmacopoeia and the National Formulary. In 1906, the Pure Food and Drugs Act transformed the Pharmacopoeia into a legal standard and, since then, the book has become a trusted source for pharmaceutical standards, aiding in prosecutions related to the quality and authenticity of drugs. This summary analyzes the latest revisions of the Pharmacopoeia and the Formulary, discussing their implications for pharmacists, physicians, and the general public. The author explores the legal status and development of drug standards, the scope and nature of the Pharmacopoeia and Formulary, and analytical data related to official drug articles. The book also examines ongoing debates about the inclusion of new drugs and the exclusion of existing ones and discusses the broader historical and medical context of these decisions. Ultimately, this book serves as a valuable resource for understanding the evolution and significance of drug standards in the United States. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item.