Study identification

EU PAS number

EUPAS5568

Study ID

48174

Official title and acronym

PRJ2215: Assessment of Bupropion Misuse/Abuse 2004-2011 (201235)

DARWIN EU® study

No

Study countries

United States

Study description

The objective of this study is to examine the degree of misuse and abuse of bupropion using the Drug Abuse Warning Network Database. Objectives are as follows: 1. To examine the number of bupropion reports over time within the DAWN database and to draw a comparison against the number of all DAWN reports for prescription drugs. 2. To examine the number of reports for bupropion, stratified by demographics, route of administration, and disposition of the patient.

Study status

Finalised
Research institutions and networks

Institutions

Contact details

GSK Clinical Disclosure Advisor GSK Clinical Disclosure Advisor Pharma.CDR@gsk.com

Study contact

GSK Clinical Disclosure Advisor GSK Clinical Disclosure Advisor

Primary lead investigator
Study timelines

Date when funding contract was signed

Planned:
Actual:

Study start date

Planned:
Actual:

Data analysis start date

Planned:
Actual:

Date of final study report

Planned:
Actual:
Sources of funding
Pharmaceutical company and other private sector 

More details on funding

GlaxoSmithKline
Regulatory

Was the study required by a regulatory body?

No

Is the study required by a Risk Management Plan (RMP)?

EU RMP category 3 (required)