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Donald S. Fong

Simon K. Law

Ursula Schmidt-Erfurth

Editors

Drugs in Ophthalmology

Donald S. Fong

Simon K. Law

Ursula Schmidt-Erfurth

Editors

Drugs in

Ophthalmology

1 3

Donald S. Fong, MD, MPH

Ursula Schmidt-Erfurth, MD

Director

Professor and Chair

Clinical Trials

Department of Ophthalmology

Department of Research and Evaluation

Medical University of Vienna

Kaiser Permanente Southern California

Währinger Gürtel 18–20

100 S. Los Robles

A-1090 Vienna, Austria

Pasadena

 

CA 91101, USA

 

Simon K. Law, MD, PharmD

 

Jules Stein Eye Institute

 

100 Stein Plaza 2-235

 

Los Angeles

 

CA 90095, USA

 

ISBN-10 3-540-23435-7 Springer-Verlag Berlin Heidelberg New York ISBN-13 978-3-540-23435-7 Springer-Verlag Berlin Heidelberg New York

Library of Congress Control Number: 2005933261

This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilm or in any other way, and storage in data banks. Duplication of this publication or parts thereof is permitted only under the provisions of the German Copyright Law of September 9, 1965, in its current version, and permission for use must always be obtained from Springer. Violations are liable to prosecution under the German Copyright Law.

Springer is a part of Springer Science+Business Media springeronline.com

© Springer-Verlag Berlin Heidelberg 2006 Printed in Germany

The use of general descriptive names, registered names, trademarks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use.

Product liability: the publishers cannot guarantee the accuracy of any information about dosage and application contained in this book. In every individual case the user must check such information by consulting the relevant literature.

Editor: Marion Philipp, Heidelberg, Germany

Desk Editor: Martina Himberger, Heidelberg, Germany

Production: ProEdit GmbH, Heidelberg, Germany

Cover: Frido Steinen-Broo, EStudio Calamar, Spain

Typesetting: Stürtz GmbH, Würzburg, Germany

Printed on acid-free paper 24/3151 Re 5 4 3 2 1 0

Disclaimer

The nature of drug information is that it is constantly changing because of continuing research and clinical experience and is often subject to ongoing evaluation. While significant care has been taken to ensure the accuracy of the information, the reader is advised that the authors, editors, reviewers, contributors, and publishers cannot be responsible for the continued currency of the information, for any errors or omissions in this book, or for any consequences arising therefrom. Because of the changing nature of drug information, readers are advised that decisions regarding drug therapy must be based on the independent judgment of the ophthalmologist, changing information (literature and manufacturer‘s information), and changing medical practice.

List of Contributors

Amani A. Fawzi, MD

University of Southern California

Keck School of Medicine

Doheny Eye Institute

San Pablo Street 1450

Los Angeles

CA 90033, USA

Donald S. Fong, MD, MPH

Director

Clinical Trials

Department of Research and Evaluation

Kaiser Permanente Southern California

100 S. Los Robles

Pasadena

CA 91101, USA

Simon K. Law, MD, PharmD

Jules Stein Eye Institute

100 Stein Plaza 2-235

Los Angeles

CA 90095, USA

Rike Michels

Department of Ophthalmology

Medical University of Vienna

Währinger Gürtel 18–20

A-1090 Vienna, Austria

Ursula Schmidt-Erfurth, MD

Professor and Chair

Department of Ophthalmology

Medical University of Vienna

Währinger Gürtel 18–20

A-1090 Vienna, Austria

Hasan Syed, MD, Stanford University

Medical Center

General Surgery

Welch Road 1170

Palo Alto

CA 94304, USA

Table of Contents

I Alphabetical Listing of Drugs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

1

II Dosage Summary for Anti-infectives . . . . . . . . . . . . . . . . . . . . . . . . . . . 221

Introduction

This drug handbook is divided into two sections:

Alphabetical Listing of Drugs

Entries in this section are listed by generic name. Information for each drug is arranged in a consistent format for easy reference. If one or more of the following categories is not applicable to a certain drug, it will not be listed. If Pregnancy Category is not listed for an individual drug, then it is either listed under the first drug in a group of drugs, or safety and efficacy in pregnancy have not been established.

Summary of Anti-infectives

This section summarizes the common doses of antibiotics, antifungals, and antivirals. For each drug, the dose for each route of administration is included.

Generic name

Brand names

Common trade names

 

 

Class of drug

Therapeutic class

 

 

Indications

Common uses of the drug

 

 

Dosage form

Common forms of the drug

 

 

Dose

The amount of drug to be given or taken during therapy.

 

The dosage is to be taken as a guideline and does not

 

preclude other dosage regimens

 

 

Contraindications

Information pertaining to inappropriate use of the drug

 

 

Warnings

Hazardous conditions related to use of the drug and disease

 

states or patient populations in which the drug should be

 

used cautiously

 

 

Adverse reactions

Considerations to be taken into account

 

 

Pregnancy category

FDA categories that indicate the potential for causing birth

 

defects

A

Controlled studies in pregnant women have failed to

demonstrate a risk to the fetus in the first trimester with no

 

 

evidence of risk in later trimesters. The possibility of fetal

 

harm appears remote

B

Either animal-reproduction studies have not demonstrated

a fetal risk but there are no controlled studies in pregnant

 

 

women, or animal-reproduction studies have shown an

 

adverse e ect that was not confirmed in controlled studies

 

in women in the first trimester and there was no evidence

 

of a risk in later trimesters

C

Either studies in animals have revealed adverse e ects on the

fetus (teratogenic, embryocidal e ects, or other) and there

 

 

are no controlled studies in women, or studies in women and

 

animals are not available. Drugs should be given only if the

 

potential benefits justify the potential risk to the fetus

D

There is positive evidence of human fetal risk, but the

benefits from use in pregnant women may be acceptable

 

 

despite the risk (e.g., if the drug is needed in a life-threate-

 

ning situation or for a serious disease for which safer drugs

 

cannot be used or are ine ective)

6

 

Generic name

X

Studies in animals or humans have demonstrated fetal

 

abnormalities or there is evidence of fetal risk based on

 

human experience, or both, and the risk of the use of the

 

drug in pregnant women clearly outweighs any possible

 

benefit. The drug is contraindicated in women who are or

 

may become pregnant

 

 

Drug interactions

Only clinically important interactions are listed

I

Alphabetical Listing of Drugs

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