Clinical features of adverse reactions associated with telbivudine

AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of e...

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Published inWorld journal of gastroenterology : WJG Vol. 14; no. 22; pp. 3549 - 3553
Main Authors Zhang, Xue-Song, Jin, Rui, Zhang, Shi-Bin, Tao, Ming-Ling
Format Journal Article
LanguageEnglish
Published United States Department of GI and Hepatology, Beijing Youan Hospital affiliated to Capital Medical University, Beijing 100069, China 14.06.2008
The WJG Press and Baishideng
Subjects
Online AccessGet full text
ISSN1007-9327
2219-2840
DOI10.3748/wjg.14.3549

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Abstract AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis. RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high. CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.
AbstractList AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis. RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high. CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.
To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.AIMTo analyze the clinical features and risk factors of adverse reactions associated with telbivudine.Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.METHODSClinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.RESULTSOut of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.CONCLUSIONThe adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.
R5; AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.
AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis. RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high. CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.
To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis. Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high. The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.
Author Xue-Song Zhang Rui Jin Shi-Bin Zhang Ming-Ling Tao
AuthorAffiliation Department of GI and Hepatology, Beijing Youan Hospital affiliated to Capital Medical University, Beijing 100069, China
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Keywords Mitochondria
Nucleoside analogue
Adverse drug reaction
Telbivudine
Hepatitis B
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Adverse drug reaction; Hepatitis B;Mitochondria; Nucleoside analogue; Telbivudine
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Adverse drug reaction
Telbivudine
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Fax: +86-10-63395319
Correspondence to: Rui Jin, Professor, Department of GI and Hepatology, Beijing Youan Hospital Affiliated to Capital Medical University, Beijing 100069, China. jinrui@public.bta.net.cn
Telephone: +86-10-83997117
Author contributions: Jin R designed the research; Zhang SB, Tao ML and Zhang XS performed the research; Zhang SB and Tao ML collected and analyzed the data; and Zhang SB wrote the paper.
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Snippet AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that...
To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. Clinical data were collected from cases that presented with...
To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.AIMTo analyze the clinical features and risk factors of...
R5; AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.METHODS: Clinical data were collected from cases...
AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that...
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StartPage 3549
SubjectTerms Adult
Arrhythmias, Cardiac - chemically induced
Creatine Kinase - blood
Drug Synergism
Hepatitis B, Chronic - blood
Hepatitis B, Chronic - drug therapy
Humans
Interferons - adverse effects
Interferons - therapeutic use
Male
Middle Aged
Muscle Weakness - chemically induced
Neuralgia - chemically induced
Nucleosides - adverse effects
Nucleosides - therapeutic use
Pyrimidinones - adverse effects
Pyrimidinones - therapeutic use
Rapid Communication
Retrospective Studies
Risk Factors
Telbivudine
Thymidine - analogs & derivatives
替比夫定
线粒体
药物反应
Title Clinical features of adverse reactions associated with telbivudine
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