Share

E D E X (Alprostadil)

2015-06-17
Download E D E X (Alprostadil) PDF Online Free

Author :
Release : 2015-06-17
Genre :
Kind : eBook
Book Rating : 456/5 ( reviews)

GET EBOOK


Book Synopsis E D E X (Alprostadil) by : James Lee Anderson

Download or read book E D E X (Alprostadil) written by James Lee Anderson. This book was released on 2015-06-17. Available in PDF, EPUB and Kindle. Book excerpt: "Although, your health condition may impact your everyday life, do not let it define who you are." EDEX (alprostadil) injection and suppositories are used to treat certain types of erectile dysfunction (sexual impotence; inability to get or keep an erection) in men due to neurogenic, vasculogenic, psychogenic, or mixed etiology. EDEX injection is also sometimes used in combination with other tests to diagnose erectile dysfunction. Alprostadil is in a class of medications called vasodilators. It works by relaxing the muscles and blood vessels in the penis to keep enough blood in the penis so that an erection can occur. Alprostadil does not prevent pregnancy or the spread of sexually transmitted diseases such as human immunodeficiency virus (HIV). This medicine is available only with your doctor's prescription.Thanks and may you have a good understanding about this drug-EDEX. You may want to share this book with your family and friends who may be in need of help and would want to use this medicine. Take care, and as always, be well!

Approved Drug Products with Therapeutic Equivalence Evaluations

1999-04
Download Approved Drug Products with Therapeutic Equivalence Evaluations PDF Online Free

Author :
Release : 1999-04
Genre :
Kind : eBook
Book Rating : 243/5 ( reviews)

GET EBOOK


Book Synopsis Approved Drug Products with Therapeutic Equivalence Evaluations by : Barry Leonard

Download or read book Approved Drug Products with Therapeutic Equivalence Evaluations written by Barry Leonard. This book was released on 1999-04. Available in PDF, EPUB and Kindle. Book excerpt: Identifies drug products approved on the basis of safety and effectiveness by the FDA under the Federal Food, Drug, and Cosmetic Act. Drugs on the market approved only on the basis of safety (covered by the ongoing Drug Efficacy Study Implementation review) or pre-1938 drugs are not included in this publication. The main criterion for the inclusion of any product is that the product is the subject of an application with an effective approval that has not been withdrawn for safety or efficacy reasons. Contains therapeutic equivalence evaluations for approved multisource prescription drug products.

Lehne’s Pharmacotherapeutics for Advanced Practice Nurses and Physician Assistants - E-Book

2020-02-28 Medical
Download Lehne’s Pharmacotherapeutics for Advanced Practice Nurses and Physician Assistants - E-Book PDF Online Free

Author :
Release : 2020-02-28
Genre : Medical
Kind : eBook
Book Rating : 129/5 ( reviews)

GET EBOOK


Book Synopsis Lehne’s Pharmacotherapeutics for Advanced Practice Nurses and Physician Assistants - E-Book by : Laura Rosenthal

Download or read book Lehne’s Pharmacotherapeutics for Advanced Practice Nurses and Physician Assistants - E-Book written by Laura Rosenthal. This book was released on 2020-02-28. Available in PDF, EPUB and Kindle. Book excerpt: Lehne's Pharmacotherapeutics for Advanced Practice Nurses and Physician Assistants, 2nd Edition builds on the same foundation of clearly explained, up-to-date, and clinically current content as the trusted Lehne undergraduate text, while focusing on the information that advanced practice nurses and Physician Assistants specifically need for safe and effective prescribing. Three introductory chapters provide foundational content for new prescribers in the areas of prescriptive authority, rational drug selection, prescription writing, and promoting positive outcomes of drug therapy. Core drug chapters are focused on the drugs that prescribers will most commonly see in clinical practice. A sharp focus is also placed on pharmacotherapeutic decision-making, with Black Box Warnings and new bulleted Key Prescribing Considerations features. The second edition features completely new chapters on Genetic and Genomic Considerations, Muscarinic Antagonists and Immunomodulators, and updated content throughout. It’s everything advanced practice nursing and Physician Assistant students need to be safe and effective prescribers! Introductory chapters tailored to the specific needs of prescribers cover topics such as prescriptive authority, rational drug selection and prescription writing, and promoting positive outcomes of drug therapy. Carefully focused pharmacotherapeutic content reflects the drugs most commonly seen and used by prescribers, with emphasis not on the first drug discovered or developed in each class but on the agents most often used today. Primary care drugs are addressed first in each chapter as appropriate, followed by acute care drugs. UNIQUE! Prescriber-focused pedagogical aids further reinforce the most important information for prescribers. Integrated coverage of Canadian trade names appears throughout the text and is highlighted with a familiar maple-leaf icon. Integrated coverage of interprofessional collaboration addresses the growing global interest in interprofessional collaboration and incorporates opportunities for interprofessional collaborative practice throughout.

Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

2019-12-09 Medical
Download Handbook of Pharmaceutical Manufacturing Formulations, Third Edition PDF Online Free

Author :
Release : 2019-12-09
Genre : Medical
Kind : eBook
Book Rating : 238/5 ( reviews)

GET EBOOK


Book Synopsis Handbook of Pharmaceutical Manufacturing Formulations, Third Edition by : Sarfaraz K. Niazi

Download or read book Handbook of Pharmaceutical Manufacturing Formulations, Third Edition written by Sarfaraz K. Niazi. This book was released on 2019-12-09. Available in PDF, EPUB and Kindle. Book excerpt: The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Six, Sterile Products is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this sixth volume of a six-volume set, compiles data from FDA and EMA new drug applications, patents and patent applications, and other sources of generic and proprietary formulations including author’s own experience, to cover the broad spectrum of cGMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent. Features: Largest source of authoritative and practical formulations, cGMP compliance guidance and self-audit suggestions Differs from other publications on formulation science in that it focuses on readily scalable commercial formulations that can be adopted for cGMP manufacturing Tackles common difficulties in formulating drugs and presents details on stability testing, bioequivalence testing, and full compliance with drug product safety elements Written by a well-recognized authority on drug and dosage form development including biological drugs and alternative medicines

Approved Drug Products with Therapeutic Equivalence Evaluations, 1999

2000-03
Download Approved Drug Products with Therapeutic Equivalence Evaluations, 1999 PDF Online Free

Author :
Release : 2000-03
Genre :
Kind : eBook
Book Rating : 795/5 ( reviews)

GET EBOOK


Book Synopsis Approved Drug Products with Therapeutic Equivalence Evaluations, 1999 by : Barry Leonard

Download or read book Approved Drug Products with Therapeutic Equivalence Evaluations, 1999 written by Barry Leonard. This book was released on 2000-03. Available in PDF, EPUB and Kindle. Book excerpt: Identifies drug products approved on the basis of safety & effectiveness by the FDA under the Federal Food, Drug, & Cosmetic Act. Drugs on the market approved only on the basis of safety (covered by the ongoing Drug Efficacy Study Implementation review) or pre-1938 drugs are not included in this publication. The main criterion for the inclusion of any product is that the product is the subject of an application with an effective approval that has not been withdrawn for safety or efficacy reasons. Contains therapeutic equivalence evaluations for approved multisource prescription drug products.

You may also like...