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                             87 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Access to medicines in low-income countries Marthe Everard
2003
1-2 p. 137-149
artikel
2 Affordably priced new drugs for poor populations: Approaches for a global solution Elias Mossialos
2002
1-2 p. 1-29
artikel
3 Amodiaquine-induced dystonic reactions: Case reports and implications for policy change in Ghana A.K. Akpalu, Jr.
2005
1-2 p. 1-4
artikel
4 Antidepressants and suicide among young women in Sweden 1999–2013 Larsson, Jan
2017
1-2 p. 101-106
artikel
5 Antidepressants and violence: Problems at the interface of medicine and law Healy, David
2007
1-2 p. 17-33
artikel
6 Are there safety concerns for biosimilars? Lekkerkerker, Frits
2009
1-2 p. 47-52
artikel
7 A survey of issues regarding ADR and ADR reporting amongst doctors in Delhi Ashima Bhatia
2005
1-2 p. 39-46
artikel
8 Attainment of target blood pressure and patterns of antihypertensive therapy in type 2 diabetic hypertensive Asian Indians Singh, Nitesh
2008
1-2 p. 45-50
artikel
9 Attitudes to pharmaceutical promotion techniques among healthcare professionals in the Republic of Tatarstan, Russia Burashnikova, Irene S.
2008
1-2 p. 57-71
artikel
10 Atypical antipsychotic agents for the schizophrenia prodrome: Not a clear first choice Kruszewski, Stefan P.
2008
1-2 p. 37-44
artikel
11 Biologicals van Boxtel, Chris J.
2009
1-2 p. 1-3
artikel
12 Biologicals in Japan Hama, Rokuro
2009
1-2 p. 59-68
artikel
13 Biopharmaceuticals in the Russian Federation: A snapshot of policies for registration, reimbursement and use Ziganshina, Lilia E.
2009
1-2 p. 75-88
artikel
14 Biosimilar medicines and safety: New challenges for pharmacovigilance Rägo, Lembit
2009
1-2 p. 5-11
artikel
15 Biosimilars: The French policy Schück, Stéphane
2009
1-2 p. 41-45
artikel
16 Book Review Dukes, Graham
2008
1-2 p. 107-108
artikel
17 Book Review Edwards, I. Ralph
2007
1-2 p. 109-110
artikel
18 British diplomat cleared of drunk flying charges: Paroxetine was involved Herxheimer, Andrew
2007
1-2 p. 35-40
artikel
19 Claim and counterclaim: The treatment of Attention Deficit Hyperactivity Disorder (ADHD) – Preventing or contributing to the development of Substance Use Disorder (SUD)? Kean, Brian
2007
1-2 p. 65-74
artikel
20 Clinical trials and drug promotion: Selective reporting of study 329 Jureidini, Jon N.
2008
1-2 p. 73-81
artikel
21 Communicating with patients about harms and risks Andrew Herxheimer
2005
1-2 p. 23-26
artikel
22 Compensation for drug injury: A novel solution for diethylstilbestrol? Dukes, M.N. Graham
2007
1-2 p. 87-91
artikel
23 Conflicts of interest in medical research in Germany and USA: A scrutiny of legal and ethical guidelines for reviewers and investigators Ritlewski, Kristoff M.
2007
1-2 p. 41-56
artikel
24 Continuing medical education and pharmaceutical industry involvement: An evaluation of policies adopted by Canadian professional medical associations Shnier, Adrienne
2017
1-2 p. 1-16
artikel
25 Contribution of clinical pharmacology to improve the use of medicines in developing countries Sri Suryawati
2005
1-2 p. 57-64
artikel
26 Counterfeit medicines: An intent to deceive Reggi, Valerio
2007
1-2 p. 105-108
artikel
27 Data needed for developing and monitoring policies Elias Mossialos
2003
1-2 p. 15-27
artikel
28 Drugs and Money
2003
1-2 p. 1-3
artikel
29 Dutch Health NGO granted Official Relations with World Health Organisation 2008
1-2 p. 109
artikel
30 Editorial van Boxtel, Chris J.
2007
1-2 p. 1-2
artikel
31 Editorial van Boxtel, Chris J.
2008
1-2 p. 1-3
artikel
32 Experiences with budgets Christine Huttin
2003
1-2 p. 81-84
artikel
33 Experiences with generics Kees de Joncheere
2003
1-2 p. 101-109
artikel
34 Experiences with patient charges Flora M. Haaijer-Ruskamp
2003
1-2 p. 93-96
artikel
35 Experiences with pharmacy benefit management programmes in the USA Helene L. Lipton
2003
1-2 p. 111-118
artikel
36 Experiences with professional education Stephen Chapman
2003
1-2 p. 119-125
artikel
37 Experiences with reference pricing Christine Huttin
2003
1-2 p. 85-91
artikel
38 Fatal neuropsychiatric adverse reactions to oseltamivir: Case series and overview of causal relationships Hama, Rokuro
2008
1-2 p. 5-36
artikel
39 Four decades of European medicines regulation: What have they brought us? John A. Lisman
2005
1-2 p. 73-79
artikel
40 Homicidal ideation causally related to therapeutic medications Marks, Donald H.
2009
1-2 p. 119
artikel
41 How the European Union reviews and approves ‘follow-on biologics’ or biosimilar products Rossignol, Nicolas
2009
1-2 p. 105-109
artikel
42 “If nothing goes wrong, is everything alright?” in reverse van Boxtel, C.J.
2007
1-2 p. 99-103
artikel
43 Impaired reproduction after exposure to ADHD drugs: Systematic review of animal studies Danborg, Pia Brandt
2017
1-2 p. 107-124
artikel
44 IMS Health reports global biotech sales grew 12.5 percent in 2007, exceeding $75 billionIMS news releases 2009
1-2 p. 111-113
artikel
45 Informed consent by cancer patients in Japanese case law Kiyomi Tomita
2002
1-2 p. 59-65
artikel
46 Intoxication anosognosia: The spellbinding effect of psychiatric drugs Breggin, Peter R.
2007
1-2 p. 3-15
artikel
47 Legal issues in dementia Kapp, Marshall B.
2008
1-2 p. 91-103
artikel
48 Making use of economic evaluation David McDaid
2003
1-2 p. 67-74
artikel
49 Managing the aftermath of iatrogenic injury Charles Vincent
2005
1-2 p. 5-11
artikel
50 Measures relating to use of drug subsidy lists and to regulation A.S. Mitchell
2003
1-2 p. 77-79
artikel
51 Meeting highlights from the Committee for Medicinal Products for Human Use, 18–21 February 2008 2008
1-2 p. 111
artikel
52 Methods for monitoring and evaluating processes and outcomes Monique F. Mrazek
2003
1-2 p. 55-66
artikel
53 Monitoring the quality of primary care: Use of hospital-based audit studies Phil Hider
2005
1-2 p. 81-89
artikel
54 Off-label use of medicines: The need for good practice guidelines Dooms, Marc
2017
1-2 p. 17-23
artikel
55 Opinions of Maltese doctors and pharmacists on medication errors Tanti, Amy
2017
1-2 p. 81-99
artikel
56 Overview of safety monitoring of biologicals in China Chen, Yixin
2008
1-2 p. 69-74
artikel
57 Patient-risk due to negligence by Locum General Practitioners outside of office hours J.J. Visser
2002
1-2 p. 41-49
artikel
58 Pharmacovigilance of biosimilars from a regulatory point of view: Is there a need for a specific approach? Giezen, Thijs J.
2009
1-2 p. 53-58
artikel
59 Policy options for cost containment of pharmaceuticals Ad H. Rietveld
2003
1-2 p. 29-54
artikel
60 Preliminary safety assessment of sulphadoxine-pyrimethamine during intermittent presumptive treatment of pregnant women in a region with high prevalence of G6PD deficiency A.N.O. Dodoo
2005
1-2 p. 13-18
artikel
61 Prescription audit of NSAIDs and gastroprotective strategy in elderly in primary care Al Khaja, Khalid Ahmed Jassim
2017
1-2 p. 57-68
artikel
62 Priority medicines for the citizens of Europe and the world: A research and development agenda Bart Wijnberg
2005
1-2 p. 27-37
artikel
63 Providing affordable medicines in transitional countries Kees de Joncheere
2003
1-2 p. 127-135
artikel
64 Psychosocial consequences of screening for albuminuria and certain other risk factors Tymstra, Tjeerd
2002
1-2 p. 51-57
artikel
65 Quality and safety considerations for recombinant biological medicines: A regulatory perspective Barnes, Henry J.
2009
1-2 p. 13-22
artikel
66 Recognition of possible risk factors for clinically significant drug-drug interactions among Indian people living with HIV receiving highly active antiretroviral therapy and concomitant medications Priyanka, Poka Siva Sai Lakshmi
2017
1-2 p. 25-55
artikel
67 Regional pharmacovigilance practice in China Yue, Wang
2008
1-2 p. 51-56
artikel
68 Risky procedures: Experiences and views of psychiatrists and views of management of mental health care institutions J. de Bie
2005
1-2 p. 47-56
artikel
69 Sandoz receives European Commission approval for biosimilar filgrastimNovartis Media releases 2009
1-2 p. 117
artikel
70 “Scalpel safety”: Modeling the effectiveness of different safety devices' ability to reduce scalpel blade injuries Fuentes, Hector
2008
1-2 p. 83-89
artikel
71 Scope of the problem Kees de Joncheere
2003
1-2 p. 7-13
artikel
72 Switching to non-prescription status Peter R. Noyce
2003
1-2 p. 97-99
artikel
73 Tainted blood in Canada: An extraordinary history Dukes, M.N. Graham
2009
1-2 p. 89-92
artikel
74 The business case for medical informed consent Kapp, Marshall B.
2007
1-2 p. 57-64
artikel
75 The doctor as expert witness in court: Observations and lessons from the Philippines Hartigan-Go, Kenneth Y.
2007
1-2 p. 93-97
artikel
76 The establishment of the Drug Naming Committee to restrict look-alike medication names in Iran: A qualitative study Abolhassani, Nazanin
2017
1-2 p. 69-79
artikel
77 The First Meeting of Hand Hygiene Campaigning Nations: WHO World Alliance for Patient Safety, August 2007 2008
1-2 p. 105-106
artikel
78 The global biopharma industry and the rise of Indian drug multinationals: Implications for Australian generics policy Löfgren, Hans
2009
1-2 p. 31-40
artikel
79 The Heparin Story Usdin, Steve
2009
1-2 p. 93-103
artikel
80 The pharmaceutical industry in discredit: Mercury or Aesculapius? L. Offerhaus
2005
1-2 p. 19-22
artikel
81 The role of drug donations on hospital use of antibiotics during the war and postwar period Ranko Škrbić
2002
1-2 p. 31-40
artikel
82 Title Unavailable
2002
1-2 p. 67-70
artikel
83 Tort, error and talk: What can we learn from the litigation crisis? Hugman, Bruce
2007
1-2 p. 75-86
artikel
84 UK biotech seeks bail out 2009
1-2 p. 115-116
artikel
85 Unfinished business: Clinical Pharmacology and World Health Anthony J. Smith
2005
1-2 p. 65-71
artikel
86 Vaccine policy, regulations and safety in India Gogtay, N.J.
2009
1-2 p. 23-30
artikel
87 WHO News
2005
1-2 p. 91-92
artikel
                             87 gevonden resultaten
 
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