A fuzzy recognition-primed decision model-based causal association mining algorithm for detecting adverse drug reactions in postmarketing surveillance

2010 ◽  
Author(s):  
Yanqing Ji ◽  
Hao Ying ◽  
Peter Dews ◽  
Margo S. Farber ◽  
Ayman Mansour ◽  
...  
Keyword(s):  
Adverse Drug Reactions ◽  
Decision Model ◽  
Association Mining ◽  
Postmarketing Surveillance ◽  
Causal Association ◽  
Drug Reactions ◽  
Model Based ◽  
Mining Algorithm ◽  
Fuzzy Recognition

Postmarketing Surveillance and Adverse Drug Reactions

JAMA ◽  
1999 ◽  
Vol 281 (9) ◽  
pp. 824 ◽  
Author(s):  
Timothy Brewer ◽  
Graham A. Colditz
Keyword(s):  
Adverse Drug Reactions ◽  
Postmarketing Surveillance ◽  
Drug Reactions

scholarly journals Postmarketing surveillance of adverse drug reactions.

BMJ ◽  
1984 ◽  
Vol 288 (6428) ◽  
pp. 1458-1459 ◽  
Author(s):  
W M Castle ◽  
J A Lewis
Keyword(s):  
Adverse Drug Reactions ◽  
Postmarketing Surveillance ◽  
Drug Reactions

scholarly journals Safety and Antihypertensive Effect of Selara® (Eplerenone): Results from a Postmarketing Surveillance in Japan

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Shoko Takahashi ◽  
Megumi Hiramatsu ◽  
Shinichi Hotta ◽  
Yukie Watanabe ◽  
Osamu Suga ◽  
...  
Keyword(s):  
Blood Pressure ◽  
Adverse Drug Reactions ◽  
Antihypertensive Effect ◽  
Antihypertensive Drugs ◽  
Postmarketing Surveillance ◽  
Drug Reactions ◽  
Surveillance Period ◽  
Mineralocorticoid Receptor Antagonist ◽  
New Findings ◽  
The Mean

Prospective postmarketing surveillance of Selara (eplerenone), a selective mineralocorticoid receptor antagonist, was performed to confirm its safety and efficacy for hypertension treatment in Japan. The change in blood pressure after initiation of eplerenone treatment was also examined. Patients with essential hypertension who were eplerenone-naïve were recruited regardless of the use of other antihypertensive drugs. For examination of changes in blood pressure, patients were excluded if eplerenone was contraindicated or used off-label. Patients received 50–100 mg of eplerenone once daily and were observed for 12 weeks. No treatments including antihypertensive drugs were restricted during the surveillance period. Across Japan, 3,166 patients were included for safety analysis. The incidence of adverse drug reactions was 2.4%. The major adverse drug reactions observed were hyperkalemia (0.6%), dizziness, renal impairment, and increased serum potassium (0.2% each). The mean systolic blood pressure decreased from 152.1±19.0 mmHg to 134.8±15.2 mmHg at week 12, and the mean diastolic blood pressure decreased from 85.8±13.7 mmHg to 77.7±11.4 mmHg. There were no significant new findings regarding the type or incidence of adverse reactions, and eplerenone had a clinically significant antihypertensive effect, leading to favorable blood pressure control.

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