235 related articles for article (PubMed ID: 32020439)
1. The quality assessment of the Japanese Adverse Drug Event Report database using vigiGrade.
Tsuchiya M; Obara T; Miyazaki M; Noda A; Takamura C; Mano N
Int J Clin Pharm; 2020 Apr; 42(2):728-736. PubMed ID: 32020439
[TBL] [Abstract][Full Text] [Related]
2. Quality evaluation of the Japanese Adverse Drug Event Report database (JADER).
Tsuchiya M; Obara T; Sakai T; Nomura K; Takamura C; Mano N
Pharmacoepidemiol Drug Saf; 2020 Feb; 29(2):173-181. PubMed ID: 31823506
[TBL] [Abstract][Full Text] [Related]
3. vigiGrade: a tool to identify well-documented individual case reports and highlight systematic data quality issues.
Bergvall T; Norén GN; Lindquist M
Drug Saf; 2014 Jan; 37(1):65-77. PubMed ID: 24343765
[TBL] [Abstract][Full Text] [Related]
4. Completeness of Spontaneous Adverse Drug Reaction Reports Sent by General Practitioners to a Regional Pharmacovigilance Centre: A Descriptive Study.
Durrieu G; Jacquot J; Mège M; Bondon-Guitton E; Rousseau V; Montastruc F; Montastruc JL
Drug Saf; 2016 Dec; 39(12):1189-1195. PubMed ID: 27688025
[TBL] [Abstract][Full Text] [Related]
5. Exploring Completeness of Adverse Event Reports as a Tool for Signal Detection in Pharmacovigilance.
Lee I; Jokinen JD; Crawford SY; Calip GS; Kilpatrick RD; Lee TA
Ther Innov Regul Sci; 2021 Jan; 55(1):142-151. PubMed ID: 32720297
[TBL] [Abstract][Full Text] [Related]
6. Evaluation of completeness of suspected adverse drug reaction reports submitted to the mexican national pharmacovigilance centre: a cross-sectional period-prevalence study.
Sánchez-Sánchez B; Altagracia-Martínez M; Kravzov-Jinich J; Moreno-Bonett C; Vázquez-Moreno E; Martínez-Núñez JM
Drug Saf; 2012 Oct; 35(10):837-44. PubMed ID: 22924896
[TBL] [Abstract][Full Text] [Related]
7. Characteristics of pediatric adverse drug reaction reports in the Japanese Adverse Drug Event Report Database.
Noda A; Sakai T; Obara T; Miyazaki M; Tsuchiya M; Oyanagi G; Murai Y; Mano N
BMC Pharmacol Toxicol; 2020 May; 21(1):36. PubMed ID: 32448369
[TBL] [Abstract][Full Text] [Related]
8. Analysis of Adverse Drug Reaction Risk in Elderly Patients Using the Japanese Adverse Drug Event Report (JADER) Database.
Chisaki Y; Aoji S; Yano Y
Biol Pharm Bull; 2017; 40(6):824-829. PubMed ID: 28566626
[TBL] [Abstract][Full Text] [Related]
9. Differential completeness of spontaneous adverse event reports among hospitals/clinics, pharmacies, consumers, and pharmaceutical companies in South Korea.
Oh IS; Baek YH; Kim HJ; Lee M; Shin JY
PLoS One; 2019; 14(2):e0212336. PubMed ID: 30763386
[TBL] [Abstract][Full Text] [Related]
10. Data-Driven Identification of Adverse Event Reporting Patterns for Japan in VigiBase, the WHO Global Database of Individual Case Safety Reports.
Wakao R; Taavola H; Sandberg L; Iwasa E; Soejima S; Chandler R; Norén GN
Drug Saf; 2019 Dec; 42(12):1487-1498. PubMed ID: 31559542
[TBL] [Abstract][Full Text] [Related]
11. Quantity is not enough: completeness of suspected adverse drug reaction reports in Spain-differences between regional pharmacovigilance centres and pharmaceutical industry.
Fernandez-Fernandez C; Lázaro-Bengoa E; Fernández-Antón E; Quiroga-González L; Montero Corominas D
Eur J Clin Pharmacol; 2020 Aug; 76(8):1175-1181. PubMed ID: 32447435
[TBL] [Abstract][Full Text] [Related]
12. Lack of essential information in spontaneous reports of adverse drug reactions in Catalonia-a restraint to the potentiality for signal detection.
Plessis L; Gómez A; García N; Cereza G; Figueras A
Eur J Clin Pharmacol; 2017 Jun; 73(6):751-758. PubMed ID: 28251276
[TBL] [Abstract][Full Text] [Related]
13. Completeness of published case reports on suspected adverse drug reactions: evaluation of 100 reports from a company safety database.
Impicciatore P; Mucci M
Drug Saf; 2010 Sep; 33(9):765-73. PubMed ID: 20701409
[TBL] [Abstract][Full Text] [Related]
14. Safety of Memantine in Combination with Potentially Interactive Drugs in the Real World: A Pharmacovigilance Study Using the Japanese Adverse Drug Event Report (JADER) Database.
Sato K; Mano T; Iwata A; Toda T
J Alzheimers Dis; 2021; 82(3):1333-1344. PubMed ID: 34151816
[TBL] [Abstract][Full Text] [Related]
15. Adverse drug reaction reporting in institutions across six Chinese provinces: a cross-sectional study.
Zhang X; Niu R; Feng B; Guo J; Liu Y; Liu X
Expert Opin Drug Saf; 2019 Jan; 18(1):59-68. PubMed ID: 29883236
[TBL] [Abstract][Full Text] [Related]
16. [Completeness of pharmacovigilance reporting in general medicine in France.].
Humbert X; Jacquot J; Alexandre J; Sassier M; Robin N; Pageot C; Kheloufi F; Joyau C; Coquerel A; Durrieu G; Fedrizzi S
Sante Publique; 2019; Vol. 31(4):561-566. PubMed ID: 31959257
[TBL] [Abstract][Full Text] [Related]
17. [Role and Applicability of Spontaneous Reporting Databases in Medical Big Data].
Sakai T
Yakugaku Zasshi; 2021; 141(2):165-168. PubMed ID: 33518634
[TBL] [Abstract][Full Text] [Related]
18. Filling quality of the reports of adverse drug reactions received at the Pharmacovigilance Centre of São Paulo (Brazil): missing information hinders the analysis of suspected associations.
Ribeiro A; Lima S; Zampieri ME; Peinado M; Figueras A
Expert Opin Drug Saf; 2017 Dec; 16(12):1329-1334. PubMed ID: 28817316
[TBL] [Abstract][Full Text] [Related]
19. Disproportionality Analysis of Safety Signals for a Wide Variety of Opioid-Related Adverse Events in Elderly Patients Using the Japanese Adverse Drug Event Report (JADER) Database.
Omoto T; Asaka J; Sakai T; Sato F; Goto N; Kudo K
Biol Pharm Bull; 2021; 44(5):627-634. PubMed ID: 33952819
[TBL] [Abstract][Full Text] [Related]
20. Pharmacovigilance Assessment of Drug-Induced Acute Pancreatitis Using a Spontaneous Reporting Database.
Niinomi I; Hosohata K; Oyama S; Inada A; Wakabayashi T; Iwanaga K
Int J Toxicol; 2019; 38(6):487-492. PubMed ID: 31470743
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]