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Determining Whether a Definitive Causal Relationship Exists Between Aripiprazole and Tardive Dyskinesia and/or Dystonia in Patients With Major Depressive Disorder, Part 4: Case Report Data.
タグ:
FAERS
2016/4/29
Systematic Analysis of Adverse Event Reports for Sex Differences in Adverse Drug Events.
タグ:
FAERS
2016/04/23
[Validation of an adverse event reporting system in primary care].
タグ:
FAERS
2016/4/23
Post-licensure safety surveillance of 23-valent pneumococcal polysaccharide vaccine in the Vaccine Adverse Event Reporting System (VAERS), 1990-2013.
タグ:
VAERS
FAERS
2016/4/19
Ischemic Colitis as a Complication of Medication Use: An Analysis of the Federal Adverse Event Reporting System.
タグ:
FAERS
2016/04/14
Dipeptidyl peptidase-4 inhibitors and heart failure: Analysis of spontaneous reports submitted to the FDA Adverse Event Reporting System.
タグ:
FAERS
2016/04/14
Can the vaccine adverse event reporting system be used to increase vaccine acceptance and trust?
タグ:
VAERS
2016/4/7
Opportunities for Web-based Drug Repositioning: Searching for Potential Antihypertensive Agents with Hypotension Adverse Events.
タグ:
FAERS
2016/4/3
Post-licensure surveillance of quadrivalent inactivated influenza (IIV4) vaccine in the United States, Vaccine Adverse Event Reporting System (VAERS), July 1, 2013-May 31, 2015.
タグ:
VAERS
FAERS
2016/3/27
Enhanced surveillance of tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) vaccines in pregnancy in the Vaccine Adverse Event Reporting System (VAERS), 2011-2015.
タグ:
VAERS
2016/3/26
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