A decade of safety-related regulatory action in the Netherlands: a retrospective analysis of direct healthcare professional communications from 1999 to 2009.
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Inconsistencies among European Union pharmaceutical regulator safety communications: a cross-country comparisonThe role of Periodic Safety Update Reports in the safety management of biopharmaceuticals.Differences between post-authorization adverse drug reactions of biopharmaceuticals and small molecules.Risk management of biosimilars in oncology: each medicine is a work in progress.Prescription behavior for gastroprotective drugs in new users as a result of communications regarding clopidogrel - proton pump inhibitor interaction.Impact of safety-related regulatory action on clinical practice: a systematic review.Additional safety risk to exceptionally approved drugs in Europe?Benefit-Risk Assessment, Communication, and Evaluation (BRACE) throughout the life cycle of therapeutic products: overall perspective and role of the pharmacoepidemiologist.Communication on Safety of Medicines in Europe: Current Practices and General Practitioners' Awareness and Preferences.Changes in prescribing and healthcare resource utilization after FDA Drug Safety Communications involving zolpidem-containing medications.The past, present and perhaps future of pharmacovigilance: homage to Folke Sjoqvist.Benefit-risk reassessment of medicines: a retrospective analysis of all safety-related referral procedures in Europe during 2001-2012.Analysis of safety-related regulatory actions by Japan's pharmaceutical regulatory agency.Postmarketing Safety Events Relating to New Drugs Approved in Brazil Between 2003 and 2013: A Retrospective Cohort Study.Are ECG monitoring recommendations before prescription of QT-prolonging drugs applied in daily practice? The example of haloperidol.Focusing on risk communication about medicines: why now?Prescribing of rosiglitazone and pioglitazone following safety signals: analysis of trends in dispensing patterns in the Netherlands from 1998 to 2008.A cohort study exploring determinants of safety-related regulatory actions for biopharmaceuticals.Post-approval safety issues with innovative drugs: a European cohort study.Impact of safety-related regulatory action on drug use in ambulatory care in the Netherlands.Post-approval appending of CSARs to drug package inserts: an analysis of the types of adverse reactions and time to addition.
P2860
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P2860
A decade of safety-related regulatory action in the Netherlands: a retrospective analysis of direct healthcare professional communications from 1999 to 2009.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
A decade of safety-related reg ...... munications from 1999 to 2009.
@en
A decade of safety-related reg ...... munications from 1999 to 2009.
@nl
type
label
A decade of safety-related reg ...... munications from 1999 to 2009.
@en
A decade of safety-related reg ...... munications from 1999 to 2009.
@nl
prefLabel
A decade of safety-related reg ...... munications from 1999 to 2009.
@en
A decade of safety-related reg ...... munications from 1999 to 2009.
@nl
P2093
P1433
P1476
A decade of safety-related reg ...... mmunications from 1999 to 2009
@en
P2093
Flora M Haaijer-Ruskamp
Jonie T N de Vries
Pieter A de Graeff
Sabine M J M Straus
Sigrid Piening
P2860
P304
P356
10.2165/11532840-000000000-00000
P50
P577
2010-06-01T00:00:00Z
P5875
P6179
1049830764