Acta Haematologica
Original Paper
Safety of Intravenous Immunoglobulin for Treatment of Auto-Immune ThrombocytopeniaGutteridge C.N. · Veys P. · Newland A.C.Department of Haematology, The London Hospital, London, UK
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Article / Publication Details
Received: April 07, 1987
Accepted: July 09, 1987
Published online: February 24, 2009
Issue release date: 1988
Number of Print Pages: 3
Number of Figures: 0
Number of Tables: 0
ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)
For additional information: https://www.karger.com/AHA
Abstract
The incidence of hepatitis and HIV seroconversion has been examined in 64 patients receiving intravenous immunoglobulin (pepsin-treated at pH 4.0) for auto-immune thrombocytopenia. No evidence of HIV seroconversion has been detected. Five patients developed abnormal liver function following treatment. However, in no case could this be directly attributed to the treatment and no patient has developed chronic liver disease.
© 1988 S. Karger AG, Basel
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Article / Publication Details
Received: April 07, 1987
Accepted: July 09, 1987
Published online: February 24, 2009
Issue release date: 1988
Number of Print Pages: 3
Number of Figures: 0
Number of Tables: 0
ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)
For additional information: https://www.karger.com/AHA
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
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