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Results: 1 to 20 of 90

1.

Standardizing drug adverse event reporting data.

Wang L, Jiang G, Li D, Liu H.

Stud Health Technol Inform. 2013;192:1101.

PMID:
23920875
[PubMed - in process]
2.

Standardizing adverse drug event reporting data.

Wang L, Jiang G, Li D, Liu H.

J Biomed Semantics. 2014 Aug 12;5:36. doi: 10.1186/2041-1480-5-36. eCollection 2014.

PMID:
25157320
[PubMed]
Free PMC Article
3.

Adverse event profiles of 5-fluorouracil and capecitabine: data mining of the public version of the FDA Adverse Event Reporting System, AERS, and reproducibility of clinical observations.

Kadoyama K, Miki I, Tamura T, Brown JB, Sakaeda T, Okuno Y.

Int J Med Sci. 2012;9(1):33-9. Epub 2011 Nov 17.

PMID:
22211087
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Hypersensitivity reactions to anticancer agents: data mining of the public version of the FDA adverse event reporting system, AERS.

Kadoyama K, Kuwahara A, Yamamori M, Brown JB, Sakaeda T, Okuno Y.

J Exp Clin Cancer Res. 2011 Oct 5;30:93. doi: 10.1186/1756-9966-30-93.

PMID:
21970649
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Building a knowledge base of severe adverse drug events based on AERS reporting data using semantic web technologies.

Jiang G, Wang L, Liu H, Solbrig HR, Chute CG.

Stud Health Technol Inform. 2013;192:496-500.

PMID:
23920604
[PubMed - in process]
6.

Drug-versus-drug adverse event rate comparisons: a pilot study based on data from the US FDA Adverse Event Reporting System.

Hochberg AM, Pearson RK, O'Hara DJ, Reisinger SJ.

Drug Saf. 2009;32(2):137-46. doi: 10.2165/00002018-200932020-00006.

PMID:
19236120
[PubMed - indexed for MEDLINE]
7.

Influence of the MedDRA hierarchy on pharmacovigilance data mining results.

Pearson RK, Hauben M, Goldsmith DI, Gould AL, Madigan D, O'Hara DJ, Reisinger SJ, Hochberg AM.

Int J Med Inform. 2009 Dec;78(12):e97-e103. doi: 10.1016/j.ijmedinf.2009.01.001. Epub 2009 Feb 18.

PMID:
19230751
[PubMed - indexed for MEDLINE]
8.
9.

AERS spider: an online interactive tool to mine statistical associations in Adverse Event Reporting System.

Grigoriev I, zu Castell W, Tsvetkov P, Antonov AV.

Pharmacoepidemiol Drug Saf. 2014 Aug;23(8):795-801. doi: 10.1002/pds.3561. Epub 2014 Feb 12.

PMID:
24677538
[PubMed - in process]
10.

Facilitating adverse drug event detection in pharmacovigilance databases using molecular structure similarity: application to rhabdomyolysis.

Vilar S, Harpaz R, Chase HS, Costanzi S, Rabadan R, Friedman C.

J Am Med Inform Assoc. 2011 Dec;18 Suppl 1:i73-80. doi: 10.1136/amiajnl-2011-000417. Epub 2011 Sep 21.

PMID:
21946238
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Thrombotic events associated with C1 esterase inhibitor products in patients with hereditary angioedema: investigation from the United States Food and Drug Administration adverse event reporting system database.

Gandhi PK, Gentry WM, Bottorff MB.

Pharmacotherapy. 2012 Oct;32(10):902-9. doi: 10.1002/j.1875-9114.2012.01126.

PMID:
23033229
[PubMed - indexed for MEDLINE]
12.

Antipsychotics, glycemic disorders, and life-threatening diabetic events: a Bayesian data-mining analysis of the FDA adverse event reporting system (1968-2004).

DuMouchel W, Fram D, Yang X, Mahmoud RA, Grogg AL, Engelhart L, Ramaswamy K.

Ann Clin Psychiatry. 2008 Jan-Mar;20(1):21-31. doi: 10.1080/10401230701844612.

PMID:
18297583
[PubMed - indexed for MEDLINE]
13.

Prospective data mining of six products in the US FDA Adverse Event Reporting System: disposition of events identified and impact on product safety profiles.

Bailey S, Singh A, Azadian R, Huber P, Blum M.

Drug Saf. 2010 Feb 1;33(2):139-46. doi: 10.2165/11319000-000000000-00000.

PMID:
20082540
[PubMed - indexed for MEDLINE]
14.

Aspirin- and clopidogrel-associated bleeding complications: data mining of the public version of the FDA adverse event reporting system, AERS.

Tamura T, Sakaeda T, Kadoyama K, Okuno Y.

Int J Med Sci. 2012;9(6):441-6. doi: 10.7150/ijms.4549. Epub 2012 Jul 25.

PMID:
22859904
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Data mining for signal detection of adverse event safety data.

Chen HC, Tsong Y, Chen JJ.

J Biopharm Stat. 2013;23(1):146-60. doi: 10.1080/10543406.2013.735780.

PMID:
23331228
[PubMed - indexed for MEDLINE]
16.

Statin-associated muscular and renal adverse events: data mining of the public version of the FDA adverse event reporting system.

Sakaeda T, Kadoyama K, Okuno Y.

PLoS One. 2011;6(12):e28124. doi: 10.1371/journal.pone.0028124. Epub 2011 Dec 20.

PMID:
22205938
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Platinum agent-induced hypersensitivity reactions: data mining of the public version of the FDA adverse event reporting system, AERS.

Sakaeda T, Kadoyama K, Yabuuchi H, Niijima S, Seki K, Shiraishi Y, Okuno Y.

Int J Med Sci. 2011;8(4):332-8. Epub 2011 May 21.

PMID:
21611115
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Antimicrobials and the risk of torsades de pointes: the contribution from data mining of the US FDA Adverse Event Reporting System.

Poluzzi E, Raschi E, Motola D, Moretti U, De Ponti F.

Drug Saf. 2010 Apr 1;33(4):303-14. doi: 10.2165/11531850-000000000-00000.

PMID:
20297862
[PubMed - indexed for MEDLINE]
19.

Profiling structured product labeling with NDF-RT and RxNorm.

Zhu Q, Jiang G, Chute CG.

J Biomed Semantics. 2012 Dec 20;3(1):16. doi: 10.1186/2041-1480-3-16.

PMID:
23256517
[PubMed]
Free PMC Article
20.

Adverse event profile of tigecycline: data mining of the public version of the U.S. Food and Drug Administration adverse event reporting system.

Kadoyama K, Sakaeda T, Tamon A, Okuno Y.

Biol Pharm Bull. 2012;35(6):967-70.

PMID:
22687540
[PubMed - indexed for MEDLINE]
Free Article

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