-
1
-
-
39849093340
-
Initial severity and antidepressant benefits: A meta-analysis of data submitted to the Food and Drug Administration
-
doi: 10.1371/journal.pmed.0050045
-
Kirsch I, Deacon BJ, Huedo-Medina TB, Scoboria A, Moore TJ, Johnson BT. Initial severity and antidepressant benefits: a meta-analysis of data submitted to the Food and Drug Administration. PLoS Med 2008;5(2):e45 doi: 10.1371/journal.pmed.0050045.
-
(2008)
PLoS Med
, vol.5
, Issue.2
-
-
Kirsch, I.1
Deacon, B.J.2
Huedo-Medina, T.B.3
Scoboria, A.4
Moore, T.J.5
Johnson, B.T.6
-
2
-
-
33846239296
-
Are lipid-lowering guidelines evidence-based?
-
Abramson J, Wright JM. Are lipid-lowering guidelines evidence-based? Lancet 2007;369:168-9.
-
(2007)
Lancet
, vol.369
, pp. 168-169
-
-
Abramson, J.1
Wright, J.M.2
-
3
-
-
20544475947
-
COX 2 inhibitors, traditional NSAIDs, and the heart
-
Jüni P, Reichenbachs, Egger M. COX 2 inhibitors, traditional NSAIDs, and the heart. BMJ 2005;330:1342-3.
-
(2005)
BMJ
, vol.330
, pp. 1342-1343
-
-
Jüni, P.1
Reichenbachs2
Egger, M.3
-
4
-
-
38949168776
-
Mandatory disclosure of trial results for drugs and devices
-
Groves T. Mandatory disclosure of trial results for drugs and devices. BMJ 2008;336:170.
-
(2008)
BMJ
, vol.336
, pp. 170
-
-
Groves, T.1
-
5
-
-
38349049478
-
Selective publication of antidepressant trials and its influence on apparent efficacy
-
Turner EH, Matthews AM, Linardatos E, Tell RA, Rosenthal R. Selective publication of antidepressant trials and its influence on apparent efficacy. N Engl J Med 2008;358:252-60.
-
(2008)
N Engl J Med
, vol.358
, pp. 252-260
-
-
Turner, E.H.1
Matthews, A.M.2
Linardatos, E.3
Tell, R.A.4
Rosenthal, R.5
-
6
-
-
0033620411
-
Accuracy of data in abstracts of published research articles
-
Pitkin RM, Branagan MA, Burmeister LF. Accuracy of data in abstracts of published research articles. JAMA 1999;281:1110-1.
-
(1999)
JAMA
, vol.281
, pp. 1110-1111
-
-
Pitkin, R.M.1
Branagan, M.A.2
Burmeister, L.F.3
-
7
-
-
1642422176
-
Administration of methylprednisolone for 24 or 48 hours or tirilazad mesylate for 48 hours in the treatment of acute spinal cord injury. Results of the third national acute spinal cord injury randomized controlled trial. National acute spinal cord injury study
-
Bracken MB, Shepard MI, Holford TR, Leo-Summers L, Aldrich EF, Fazl M, et al. Administration of methylprednisolone for 24 or 48 hours or tirilazad mesylate for 48 hours in the treatment of acute spinal cord injury. Results of the third national acute spinal cord injury randomized controlled trial. National acute spinal cord injury study. JAMA 1997;277:1597-1604.
-
(1997)
JAMA
, vol.277
, pp. 1597-1604
-
-
Bracken, M.B.1
Shepard, M.I.2
Holford, T.R.3
Leo-Summers, L.4
Aldrich, E.F.5
Fazl, M.6
-
8
-
-
40949098966
-
NIH secrets: Study break
-
Oct 30
-
Lenzer J. NIH secrets: study break. New Republic 2006 Oct 30. www.ahrp.org/cms/index2.php?option=com_content&do_pdf=1&id=398.
-
(2006)
New Republic
-
-
Lenzer, J.1
-
9
-
-
40949091845
-
Drug secrets: What the FDA isn't telling
-
Sep 27
-
Lenzer J. Drug secrets: what the FDA isn't telling. Slate 2005 Sep 27. www.slate.com/id/2126918/.
-
(2005)
Slate
-
-
Lenzer, J.1
-
10
-
-
40949117026
-
Bextra withdrawn from market
-
Apr 7
-
Waknine Y. Bextra withdrawn from market. Medscape Today 2005 Apr 7. www.medscape.com/viewarticle/502642?rss.
-
(2005)
Medscape Today
-
-
Waknine, Y.1
-
11
-
-
40949159187
-
-
Public Citizen Health Research Group versus FDA-complaint 26 Feb
-
Public Citizen Health Research Group versus FDA-complaint (26 Feb 2004). www.citizen.org/documents/ACF5CF.pdf.
-
(2004)
-
-
|