Pharmacokinetics of Orally Administered Oseltamivir in Healthy Obese and Nonobese Thai Subjects

OA  Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Com...

Full description

Saved in:
Bibliographic Details
Published inAntimicrobial Agents and Chemotherapy Vol. 58; no. 3; pp. 1615 - 1621
Main Authors Jittamala, Podjanee, Pukrittayakamee, Sasithon, Tarning, Joel, Lindegardh, Niklas, Hanpithakpong, Warunee, Taylor, Walter Robert John, Lawpoolsri, Saranath, Charunwattana, Prakaykaew, Panapipat, Salwaluk, White, Nicholas J., Day, Nicholas P. J.
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for Microbiology 01.03.2014
Subjects
Online AccessGet full text
ISSN0066-4804
1098-6596
1098-6596
DOI10.1128/AAC.01786-13

Cover

Abstract OA  Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to AAC .asm.org, visit: AAC       
AbstractList Oseltamivir is the most widely used anti-influenza drug. In the 2009 H1N1 pandemic, in which the influenza viruses were oseltamivir sensitive, obesity was identified as a risk factor for severe disease and unfavorable outcomes. The aim of this study was to investigate the pharmacokinetic properties of oseltamivir and its active metabolite, oseltamivir carboxylate, in obese and nonobese healthy subjects. A single-dose, randomized, two-sequence crossover study was conducted in 12 obese and 12 nonobese healthy Thai volunteers. Each volunteer was given 75 mg and 150 mg oseltamivir orally with an intervening washout period of more than 3 days. The pharmacokinetic properties of oseltamivir and oseltamivir carboxylate were evaluated using a noncompartmental approach. The median (range) body mass indexes (BMIs) for obese subjects were 33.8 kg/m(2) (30.8 to 43.2) and 22.2 (18.8 to 24.2) for nonobese subjects. The pharmacokinetic parameters of oseltamivir carboxylate, the active metabolite of oseltamivir, were not significantly different between obese and nonobese subjects for both 75-mg and 150-mg doses. Both doses were well tolerated. Despite the lower dose per kilogram body weight in obese subjects, there was no significant difference in the exposure of oseltamivir carboxylate between the obese and nonobese groups. Standard dosing is appropriate for obese subjects. (The study was registered at ClinicalTrials.gov under registration no. NCT 01049763.).
Oseltamivir is the most widely used anti-influenza drug. In the 2009 H1N1 pandemic, in which the influenza viruses were oseltamivir sensitive, obesity was identified as a risk factor for severe disease and unfavorable outcomes. The aim of this study was to investigate the pharmacokinetic properties of oseltamivir and its active metabolite, oseltamivir carboxylate, in obese and nonobese healthy subjects. A single-dose, randomized, two-sequence crossover study was conducted in 12 obese and 12 nonobese healthy Thai volunteers. Each volunteer was given 75 mg and 150 mg oseltamivir orally with an intervening washout period of more than 3 days. The pharmacokinetic properties of oseltamivir and oseltamivir carboxylate were evaluated using a noncompartmental approach. The median (range) body mass indexes (BMIs) for obese subjects were 33.8 kg/m 2 (30.8 to 43.2) and 22.2 (18.8 to 24.2) for nonobese subjects. The pharmacokinetic parameters of oseltamivir carboxylate, the active metabolite of oseltamivir, were not significantly different between obese and nonobese subjects for both 75-mg and 150-mg doses. Both doses were well tolerated. Despite the lower dose per kilogram body weight in obese subjects, there was no significant difference in the exposure of oseltamivir carboxylate between the obese and nonobese groups. Standard dosing is appropriate for obese subjects. (The study was registered at ClinicalTrials.gov under registration no. NCT 01049763.)
OA  Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to AAC .asm.org, visit: AAC       
Oseltamivir is the most widely used anti-influenza drug. In the 2009 H1N1 pandemic, in which the influenza viruses were oseltamivir sensitive, obesity was identified as a risk factor for severe disease and unfavorable outcomes. The aim of this study was to investigate the pharmacokinetic properties of oseltamivir and its active metabolite, oseltamivir carboxylate, in obese and nonobese healthy subjects. A single-dose, randomized, two-sequence crossover study was conducted in 12 obese and 12 nonobese healthy Thai volunteers. Each volunteer was given 75 mg and 150 mg oseltamivir orally with an intervening washout period of more than 3 days. The pharmacokinetic properties of oseltamivir and oseltamivir carboxylate were evaluated using a noncompartmental approach. The median (range) body mass indexes (BMIs) for obese subjects were 33.8 kg/m2 (30.8 to 43.2) and 22.2 (18.8 to 24.2) for nonobese subjects. The pharmacokinetic parameters of oseltamivir carboxylate, the active metabolite of oseltamivir, were not significantly different between obese and nonobese subjects for both 75-mg and 150-mg doses. Both doses were well tolerated. Despite the lower dose per kilogram body weight in obese subjects, there was no significant difference in the exposure of oseltamivir carboxylate between the obese and nonobese groups. Standard dosing is appropriate for obese subjects. (The study was registered at ClinicalTrials.gov under registration no. NCT 01049763.)
Oseltamivir is the most widely used anti-influenza drug. In the 2009 H1N1 pandemic, in which the influenza viruses were oseltamivir sensitive, obesity was identified as a risk factor for severe disease and unfavorable outcomes. The aim of this study was to investigate the pharmacokinetic properties of oseltamivir and its active metabolite, oseltamivir carboxylate, in obese and nonobese healthy subjects. A single-dose, randomized, two-sequence crossover study was conducted in 12 obese and 12 nonobese healthy Thai volunteers. Each volunteer was given 75 mg and 150 mg oseltamivir orally with an intervening washout period of more than 3 days. The pharmacokinetic properties of oseltamivir and oseltamivir carboxylate were evaluated using a noncompartmental approach. The median (range) body mass indexes (BMIs) for obese subjects were 33.8 kg/m(2) (30.8 to 43.2) and 22.2 (18.8 to 24.2) for nonobese subjects. The pharmacokinetic parameters of oseltamivir carboxylate, the active metabolite of oseltamivir, were not significantly different between obese and nonobese subjects for both 75-mg and 150-mg doses. Both doses were well tolerated. Despite the lower dose per kilogram body weight in obese subjects, there was no significant difference in the exposure of oseltamivir carboxylate between the obese and nonobese groups. Standard dosing is appropriate for obese subjects. (The study was registered at ClinicalTrials.gov under registration no. NCT 01049763.).Oseltamivir is the most widely used anti-influenza drug. In the 2009 H1N1 pandemic, in which the influenza viruses were oseltamivir sensitive, obesity was identified as a risk factor for severe disease and unfavorable outcomes. The aim of this study was to investigate the pharmacokinetic properties of oseltamivir and its active metabolite, oseltamivir carboxylate, in obese and nonobese healthy subjects. A single-dose, randomized, two-sequence crossover study was conducted in 12 obese and 12 nonobese healthy Thai volunteers. Each volunteer was given 75 mg and 150 mg oseltamivir orally with an intervening washout period of more than 3 days. The pharmacokinetic properties of oseltamivir and oseltamivir carboxylate were evaluated using a noncompartmental approach. The median (range) body mass indexes (BMIs) for obese subjects were 33.8 kg/m(2) (30.8 to 43.2) and 22.2 (18.8 to 24.2) for nonobese subjects. The pharmacokinetic parameters of oseltamivir carboxylate, the active metabolite of oseltamivir, were not significantly different between obese and nonobese subjects for both 75-mg and 150-mg doses. Both doses were well tolerated. Despite the lower dose per kilogram body weight in obese subjects, there was no significant difference in the exposure of oseltamivir carboxylate between the obese and nonobese groups. Standard dosing is appropriate for obese subjects. (The study was registered at ClinicalTrials.gov under registration no. NCT 01049763.).
Author Sasithon Pukrittayakamee
Saranath Lawpoolsri
Nicholas J. White
Walter Robert John Taylor
Nicholas P. J. Day
Podjanee Jittamala
Prakaykaew Charunwattana
Warunee Hanpithakpong
Joel Tarning
Salwaluk Panapipat
Niklas Lindegardh
Author_xml – sequence: 1
  givenname: Podjanee
  surname: Jittamala
  fullname: Jittamala, Podjanee
  organization: Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
– sequence: 2
  givenname: Sasithon
  surname: Pukrittayakamee
  fullname: Pukrittayakamee, Sasithon
  organization: Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
– sequence: 3
  givenname: Joel
  surname: Tarning
  fullname: Tarning, Joel
  organization: Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand, Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
– sequence: 4
  givenname: Niklas
  surname: Lindegardh
  fullname: Lindegardh, Niklas
  organization: Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand, Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
– sequence: 5
  givenname: Warunee
  surname: Hanpithakpong
  fullname: Hanpithakpong, Warunee
  organization: Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
– sequence: 6
  givenname: Walter Robert John
  surname: Taylor
  fullname: Taylor, Walter Robert John
  organization: Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
– sequence: 7
  givenname: Saranath
  surname: Lawpoolsri
  fullname: Lawpoolsri, Saranath
  organization: Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
– sequence: 8
  givenname: Prakaykaew
  surname: Charunwattana
  fullname: Charunwattana, Prakaykaew
  organization: Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
– sequence: 9
  givenname: Salwaluk
  surname: Panapipat
  fullname: Panapipat, Salwaluk
  organization: Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
– sequence: 10
  givenname: Nicholas J.
  surname: White
  fullname: White, Nicholas J.
  organization: Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand, Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
– sequence: 11
  givenname: Nicholas P. J.
  surname: Day
  fullname: Day, Nicholas P. J.
  organization: Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand, Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28269052$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/24366750$$D View this record in MEDLINE/PubMed
BookMark eNqNkc1v1DAQxS3Uim4LN84oHJBAaortxE5yQVqtgCJVLBLlbE3sSeMlsYudFO1_j9vd8iVV4mSN_Js38-YdkwPnHRLyjNEzxnj9ZrlcnVFW1TJnxSOyYLSpcykaeUAWlEqZlzUtj8hxjBuaatHQx-SIl4WUlaALoj73EEbQ_pt1OFkdM99l6wDDsM2WZrTOxgkDmmwdcZhgtDc2ZNZl5wjD1G-zdYsRM3Am--Sdvysue7DZl7ndoJ7iE3LYwRDx6f49IV_fv7tcnecX6w8fV8uLHAStphxRFLzkDKA0smsbNBTbUjQV7Yxo064AAjhjrOUGwYCUHWrGu1JyrdHUxQl5u9O9ntsRjUY3JRPqOtgRwlZ5sOrvH2d7deVvVNGIdLsqCbzaCwT_fcY4qdFGjcMADv0cFRNUFKUUov4flBVV2dQ0oa93KMSRq42fg0tXUIyq2-xUyk7dZadYkdjnf1r4tft9WAl4uQcgahi6AE7b-JuruWyo4InjO04HH2PATmk7wWT9rXM7PDT99J-me90H8Bc7vLdX_Q8bUCWHCkArUatCMclE8RM3584P
CODEN AACHAX
CitedBy_id crossref_primary_10_1002_jcph_2326
crossref_primary_10_3390_pharmaceutics16020234
crossref_primary_10_1080_17425255_2018_1440287
crossref_primary_10_3389_fimmu_2019_01071
crossref_primary_10_1093_jtm_taz020
crossref_primary_10_1080_14656566_2024_2376660
crossref_primary_10_1055_a_2369_8680
crossref_primary_10_1007_s40266_024_01169_y
crossref_primary_10_1111_bcp_12892
crossref_primary_10_1080_17425255_2022_2132931
crossref_primary_10_1002_phar_4621
crossref_primary_10_1080_17512433_2017_1255550
crossref_primary_10_1111_obr_12320
crossref_primary_10_1002_btm2_10196
crossref_primary_10_1128_aac_01719_23
crossref_primary_10_1097_MJT_0000000000000401
crossref_primary_10_1128_mbio_00887_23
crossref_primary_10_1586_14787210_2015_1043890
Cites_doi 10.1056/NEJMp068177
10.1093/epirev/mxm012
10.1378/chest.10-1160
10.1128/AAC.45.10.2723-2732.2001
10.1503/cmaj.092127
10.2165/00003088-199937060-00003
10.1093/jac/dkq013
10.1016/j.jchromb.2007.09.018
10.1093/cid/ciq152
10.1086/656316
10.1177/0091270007299761
10.1093/jac/dkq158
10.1093/epirev/mxm007
10.1345/aph.1H174
10.1128/AAC.45.4.1162-1167.2001
10.1093/jac/dkq015
10.1128/AAC.00422-11
10.1093/jac/dkr257
10.1111/j.1365-2125.2005.02340.x
10.1093/jac/dki018
10.3949/ccjm.77a.10135
10.1002/jps.22627
10.1378/chest.09-2517
10.1016/S0166-3542(00)00123-6
10.1093/jac/dkq511
10.1016/j.ijantimicag.2009.12.023
10.1046/j.1365-2125.2002.01678.x
10.1056/NEJMra1000449
10.1177/0091270012440280
10.47102/annals-acadmedsg.V36N4p285
10.1128/AAC.00588-08
10.1038/ijo.2008.102
10.1046/j.1440-6047.11.s8.12.x
10.1001/jama.2009.1536
ContentType Journal Article
Copyright 2015 INIST-CNRS
Copyright © 2014 Jittamala et al.
Copyright © 2014 Jittamala et al. 2014 Jittamala et al.
Copyright_xml – notice: 2015 INIST-CNRS
– notice: Copyright © 2014 Jittamala et al.
– notice: Copyright © 2014 Jittamala et al. 2014 Jittamala et al.
DBID AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7T2
7T7
7U1
8FD
C1K
FR3
P64
5PM
DOI 10.1128/AAC.01786-13
DatabaseName CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
Health and Safety Science Abstracts (Full archive)
Industrial and Applied Microbiology Abstracts (Microbiology A)
Risk Abstracts
Technology Research Database
Environmental Sciences and Pollution Management
Engineering Research Database
Biotechnology and BioEngineering Abstracts
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
Risk Abstracts
Technology Research Database
Health & Safety Science Abstracts
Engineering Research Database
Industrial and Applied Microbiology Abstracts (Microbiology A)
Biotechnology and BioEngineering Abstracts
Environmental Sciences and Pollution Management
DatabaseTitleList MEDLINE
CrossRef



Risk Abstracts
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Pharmacy, Therapeutics, & Pharmacology
Biology
EISSN 1098-6596
EndPage 1621
ExternalDocumentID PMC3957867
01786-13
24366750
28269052
10_1128_AAC_01786_13
aac_58_3_1615
Genre Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations Thailand
Asia
GrantInformation_xml – fundername: Wellcome Trust
  grantid: 093956
GroupedDBID ---
.55
.GJ
0R~
23M
2WC
39C
3O-
4.4
53G
5GY
5RE
5VS
6J9
AAGFI
AAYXX
ACGFO
ADBBV
AENEX
AGNAY
AGVNZ
AI.
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BTFSW
C1A
CITATION
CS3
DIK
E3Z
EBS
EJD
F5P
FRP
GX1
H13
HH5
HYE
HZ~
H~9
J5H
K-O
KQ8
L7B
LSO
MVM
NEJ
O9-
OK1
P2P
RHI
RNS
RPM
RSF
TR2
UHB
VH1
W2D
W8F
WH7
WHG
WOQ
X7M
X7N
XOL
Y6R
ZGI
ZXP
~A~
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
-
0R
55
AAPBV
ABFLS
ADACO
BXI
HZ
RHF
ZA5
7X8
7T2
7T7
7U1
8FD
C1K
FR3
P64
5PM
ID FETCH-LOGICAL-a507t-ee532421aa4d6fb9ed0eb45970fd5b667aa5a2111b2deada66fec12f462cced83
ISSN 0066-4804
1098-6596
IngestDate Thu Aug 21 14:02:42 EDT 2025
Fri Sep 05 08:54:50 EDT 2025
Thu Sep 04 23:34:41 EDT 2025
Tue Dec 28 13:58:53 EST 2021
Sat May 31 02:12:52 EDT 2025
Wed Apr 02 07:28:55 EDT 2025
Tue Jul 01 04:32:21 EDT 2025
Thu Apr 24 22:55:12 EDT 2025
Wed May 18 15:26:31 EDT 2016
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords Human
Obesity
Neuraminidase inhibitor
Enzyme
Nutrition disorder
Oral administration
Enzyme inhibitor
Glycosylases
Oseltamivir
Exo-α-sialidase
Glycosidases
Hydrolases
Antiviral
Pharmacokinetics
Nutritional status
Language English
License CC BY 4.0
This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license. http://creativecommons.org/licenses/by/3.0
This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-a507t-ee532421aa4d6fb9ed0eb45970fd5b667aa5a2111b2deada66fec12f462cced83
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Undefined-3
ObjectType-Article-2
ObjectType-Feature-1
OpenAccessLink https://pubmed.ncbi.nlm.nih.gov/PMC3957867
PMID 24366750
PQID 1501374980
PQPubID 23479
PageCount 7
ParticipantIDs proquest_miscellaneous_1501374980
pubmedcentral_primary_oai_pubmedcentral_nih_gov_3957867
pascalfrancis_primary_28269052
asm2_journals_10_1128_AAC_01786_13
pubmed_primary_24366750
crossref_primary_10_1128_AAC_01786_13
proquest_miscellaneous_1505346558
highwire_asm_aac_58_3_1615
crossref_citationtrail_10_1128_AAC_01786_13
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2014-03-01
PublicationDateYYYYMMDD 2014-03-01
PublicationDate_xml – month: 03
  year: 2014
  text: 2014-03-01
  day: 01
PublicationDecade 2010
PublicationPlace Washington, DC
PublicationPlace_xml – name: Washington, DC
– name: United States
– name: 1752 N St., N.W., Washington, DC
PublicationTitle Antimicrobial Agents and Chemotherapy
PublicationTitleAbbrev Antimicrob Agents Chemother
PublicationTitleAlternate Antimicrob Agents Chemother
PublicationYear 2014
Publisher American Society for Microbiology
Publisher_xml – name: American Society for Microbiology
References e_1_3_2_26_2
e_1_3_2_27_2
WHO (e_1_3_2_2_2) 2006
e_1_3_2_29_2
Roche Laboratories Inc (e_1_3_2_35_2) 2010
e_1_3_2_41_2
e_1_3_2_40_2
e_1_3_2_20_2
e_1_3_2_43_2
e_1_3_2_21_2
e_1_3_2_42_2
Lye DCB (e_1_3_2_13_2) 2007; 36
e_1_3_2_22_2
e_1_3_2_23_2
e_1_3_2_24_2
e_1_3_2_25_2
e_1_3_2_9_2
e_1_3_2_15_2
e_1_3_2_38_2
e_1_3_2_8_2
e_1_3_2_16_2
e_1_3_2_37_2
e_1_3_2_7_2
e_1_3_2_17_2
e_1_3_2_6_2
e_1_3_2_18_2
e_1_3_2_39_2
e_1_3_2_19_2
e_1_3_2_30_2
CDC (e_1_3_2_4_2) 2011
e_1_3_2_10_2
e_1_3_2_31_2
e_1_3_2_5_2
e_1_3_2_11_2
e_1_3_2_34_2
e_1_3_2_12_2
e_1_3_2_33_2
e_1_3_2_36_2
e_1_3_2_14_2
Aekplakorn W (e_1_3_2_32_2) 2004; 87
NIH (e_1_3_2_28_2) 2009
WHO (e_1_3_2_3_2) 2009
References_xml – ident: e_1_3_2_26_2
  doi: 10.1056/NEJMp068177
– ident: e_1_3_2_23_2
– ident: e_1_3_2_27_2
  doi: 10.1093/epirev/mxm012
– volume-title: Division of AIDS table for grading the severity of adult and pediatric adverse events
  year: 2009
  ident: e_1_3_2_28_2
– ident: e_1_3_2_15_2
  doi: 10.1378/chest.10-1160
– ident: e_1_3_2_43_2
  doi: 10.1128/AAC.45.10.2723-2732.2001
– ident: e_1_3_2_11_2
  doi: 10.1503/cmaj.092127
– volume: 87
  start-page: 685
  year: 2004
  ident: e_1_3_2_32_2
  article-title: Prevalence and determinants of overweight and obesity in Thai adults: results of the second national health examination survey
  publication-title: J. Med. Assoc. Thai.
– ident: e_1_3_2_7_2
  doi: 10.2165/00003088-199937060-00003
– ident: e_1_3_2_9_2
  doi: 10.1093/jac/dkq013
– ident: e_1_3_2_30_2
  doi: 10.1016/j.jchromb.2007.09.018
– ident: e_1_3_2_17_2
  doi: 10.1093/cid/ciq152
– ident: e_1_3_2_12_2
  doi: 10.1086/656316
– ident: e_1_3_2_40_2
  doi: 10.1177/0091270007299761
– ident: e_1_3_2_22_2
– volume-title: Tamiflu (oseltamivir phosphate) package insert
  year: 2010
  ident: e_1_3_2_35_2
– volume-title: Pharmacological management of pandemic influenza A (H1N1) 2009 and other influenza viruses
  year: 2009
  ident: e_1_3_2_3_2
– ident: e_1_3_2_5_2
  doi: 10.1093/jac/dkq158
– ident: e_1_3_2_24_2
  doi: 10.1093/epirev/mxm007
– ident: e_1_3_2_37_2
  doi: 10.1345/aph.1H174
– ident: e_1_3_2_42_2
  doi: 10.1128/AAC.45.4.1162-1167.2001
– ident: e_1_3_2_6_2
  doi: 10.1093/jac/dkq015
– ident: e_1_3_2_20_2
  doi: 10.1128/AAC.00422-11
– ident: e_1_3_2_21_2
  doi: 10.1093/jac/dkr257
– ident: e_1_3_2_36_2
  doi: 10.1111/j.1365-2125.2005.02340.x
– ident: e_1_3_2_8_2
  doi: 10.1093/jac/dki018
– ident: e_1_3_2_14_2
  doi: 10.3949/ccjm.77a.10135
– ident: e_1_3_2_31_2
  doi: 10.1002/jps.22627
– ident: e_1_3_2_16_2
  doi: 10.1378/chest.09-2517
– ident: e_1_3_2_41_2
  doi: 10.1016/S0166-3542(00)00123-6
– ident: e_1_3_2_18_2
  doi: 10.1093/jac/dkq511
– ident: e_1_3_2_34_2
  doi: 10.1016/j.ijantimicag.2009.12.023
– ident: e_1_3_2_38_2
  doi: 10.1046/j.1365-2125.2002.01678.x
– volume-title: Rapid advice guidelines on pharmacological management of human infected with avian influenza A (H5N1) virus
  year: 2006
  ident: e_1_3_2_2_2
– volume-title: Antiviral agents for the treatment and chemoprophylaxis of influenza. Recommendations of advisory committee on immunization practice (ACIP)
  year: 2011
  ident: e_1_3_2_4_2
– ident: e_1_3_2_10_2
  doi: 10.1056/NEJMra1000449
– ident: e_1_3_2_39_2
  doi: 10.1177/0091270012440280
– volume: 36
  start-page: 285
  year: 2007
  ident: e_1_3_2_13_2
  article-title: Review of human infections with avian influenza H5N1 and proposed local clinical management guideline
  publication-title: Ann. Acad. Med. Singapore
  doi: 10.47102/annals-acadmedsg.V36N4p285
– ident: e_1_3_2_29_2
  doi: 10.1128/AAC.00588-08
– ident: e_1_3_2_25_2
  doi: 10.1038/ijo.2008.102
– ident: e_1_3_2_33_2
  doi: 10.1046/j.1440-6047.11.s8.12.x
– ident: e_1_3_2_19_2
  doi: 10.1001/jama.2009.1536
SSID ssj0006590
Score 2.2459495
Snippet OA  Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
Oseltamivir is the most widely used anti-influenza drug. In the 2009 H1N1 pandemic, in which the influenza viruses were oseltamivir sensitive, obesity was...
SourceID pubmedcentral
proquest
asm2
pubmed
pascalfrancis
crossref
highwire
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1615
SubjectTerms Administration, Oral
Adult
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antiviral Agents
Antiviral Agents - administration & dosage
Antiviral Agents - blood
Antiviral Agents - pharmacokinetics
Biological and medical sciences
Body Mass Index
Cross-Over Studies
Dose-Response Relationship, Drug
Female
Humans
Male
Medical sciences
Metabolic diseases
Middle Aged
Obesity
Obesity - metabolism
Oseltamivir
Oseltamivir - administration & dosage
Oseltamivir - analogs & derivatives
Oseltamivir - blood
Oseltamivir - pharmacokinetics
Pharmacology
Pharmacology. Drug treatments
Thailand
Young Adult
Title Pharmacokinetics of Orally Administered Oseltamivir in Healthy Obese and Nonobese Thai Subjects
URI http://aac.asm.org/content/58/3/1615.abstract
https://www.ncbi.nlm.nih.gov/pubmed/24366750
https://journals.asm.org/doi/10.1128/AAC.01786-13
https://www.proquest.com/docview/1501374980
https://www.proquest.com/docview/1505346558
https://pubmed.ncbi.nlm.nih.gov/PMC3957867
Volume 58
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fb9MwELbGEIgXBANGB0wGwV66lNSx0_SxmkDTpG1FdNLeLCd2ttA2nZYUqfyV_EncJc6PTtsEvERt4sZO78v5zr77jpCPYNJrEw-1owZCO1yxgaOigXI0zHVhzBkPh5gofHziH57xo3NxvrHxuxW1tMzDXvTr1ryS_5EqnAO5YpbsP0i2vimcgM8gXziChOH4VzIeW97pKZiKBd0yWH6n12o2W9WkuFiKs3uamVmu5snPBIPPberRqotFAcrdg5NFuii-TC5VgsoEV2eytuE6SvNknhSsTSjUiyIxDn-KjAM2i6tenR8v9A-VGtM9SnLoV81q3f9dZQmyFXTHy-k1XlypqZqbGl1HGGk7KVdrmi2TKZj4xeqBuQBAX7ZXKvq8CdVqJQeg1mrFox4nDd9UW0_7vsODsjBxz5SqGZlPfVHWv610twhaGPVaihgN2dtnCIZZD6PRQQ90UYAcjO1mIN-reYEWxj0fnCm3mSer2IAb02cd1KhUJEUgPYl9PyAP2QCsOQwT-Nbw18P4y6Qo-3xVKgYLPreHhBTVtn8wFVQ2Z-tmU0VljZG8KoOXOS6rsNzmJt2M9m2ZT5Nn5Kn1e-ioBPFzsmHSLfKorIS62iKPj22MxxbZs6he7dNJkxyY7dM9Om541lcviLwJf7qIaQl_2oY_bcGfJim18KcF_ClgmFbwpwh_WsH_JTn7-mVycOjYeiGOAq8md4wR6B70leLaj0HJaNeEHDxmN9YihH9TKaEYTO4h06BAle_HJuqzmPssiowOvFdkM12k5jWhAY9C7UWB0JxzsHhDV7OhiL2YcxYOhdshH1Aq0iqDTBa-NAskSFEWUpR9r0O6lcxkZBn3sfDL7I7Wn-rWVyXTzB3tdirxSxiDXINdh-yuAaK-EwuYP3QF65D3FUIkTCS4Owj6YLGEJxDIPsqHgXtvG-Eh42LQIdslqpoeLGA7ZLCGt7oBEtmvX0mTy4LQHmMFAn-wc9-TvSFPGp3ylmzm10vzDvyBPNwtXrE_G5gPaA
linkProvider Colorado Alliance of Research Libraries
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Pharmacokinetics+of+Orally+Administered+Oseltamivir+in+Healthy+Obese+and+Nonobese+Thai+Subjects&rft.jtitle=Antimicrobial+Agents+and+Chemotherapy&rft.au=Podjanee+Jittamala&rft.au=Sasithon+Pukrittayakamee&rft.au=Joel+Tarning&rft.au=Niklas+Lindegardh&rft.date=2014-03-01&rft.pub=American+Society+for+Microbiology&rft.issn=0066-4804&rft.eissn=1098-6596&rft.volume=58&rft.issue=3&rft.spage=1615&rft_id=info:doi/10.1128%2FAAC.01786-13&rft_id=info%3Apmid%2F24366750&rft.externalDBID=n%2Fa&rft.externalDocID=aac_58_3_1615
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0066-4804&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0066-4804&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0066-4804&client=summon