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Publications by Robert L. Levin

Adverse Event Detection Using the FDA Post-Marketing Drug Safety Surveillance System: Cardiotoxicity Associated With Loperamide Abuse and Misuse

Journal of the American Pharmacists Association : JAPhA

Pharmacology

Pharmacy

2017

English

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Adverse Events Associated With Colchicine Drug Interactions: Analysis of the Public Version of the Fda Adverse Event Reporting System

English

Clustering Therapeutic Drugs Using FDA Adverse Event Reporting System

Proceedings for Annual Meeting of The Japanese Pharmacological Society

2020

English

Serious Adverse Drug Events Reported to the Food and Drug Administration (FDA): Analysis of the FDA Adverse Event Reporting System (FAERS) 2006-2011 Database

English

Adverse Events Associated With Pediatric Use of Proton Pump Inhibitors: Analysis of the Fda Adverse Event Reporting System

English

Performance of Pharmacovigilance Signal-Detection Algorithms for the FDA Adverse Event Reporting System

Clinical Pharmacology and Therapeutics

Pharmacology

2013

English

Three-Component Mixture Model-Based Adverse Drug Event Signal Detection for the Adverse Event Reporting System

CPT: Pharmacometrics and Systems Pharmacology

Modeling

Simulation

Cardiovascular Medicine

Pharmacology

Cardiology

2018

English

Bisphosphonates and Nonhealing Femoral Fractures: Analysis of the FDA Adverse Event Reporting System (FAERS) and International Safety Efforts

Journal of Bone and Joint Surgery - Series A

English

Loperamide Cardiotoxicity: “A Brief Review”

Annals of Noninvasive Electrocardiology

Medicine

Cardiovascular Medicine

Physiology

Cardiology

2017

English

Towards Early Detection of Adverse Drug Reactions: Combining Pre-Clinical Drug Structures and Post-Market Safety Reports

BMC Medical Informatics and Decision Making

Health Policy

Health Informatics

2019

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Robert L. Levin

Adverse Event Detection Using the FDA Post-Marketing Drug Safety Surveillance System: Cardiotoxicity Associated With Loperamide Abuse and Misuse

Related publications

Adverse Events Associated With Colchicine Drug Interactions: Analysis of the Public Version of the Fda Adverse Event Reporting System

Clustering Therapeutic Drugs Using FDA Adverse Event Reporting System

Serious Adverse Drug Events Reported to the Food and Drug Administration (FDA): Analysis of the FDA Adverse Event Reporting System (FAERS) 2006-2011 Database

Adverse Events Associated With Pediatric Use of Proton Pump Inhibitors: Analysis of the Fda Adverse Event Reporting System

Performance of Pharmacovigilance Signal-Detection Algorithms for the FDA Adverse Event Reporting System

Three-Component Mixture Model-Based Adverse Drug Event Signal Detection for the Adverse Event Reporting System

Bisphosphonates and Nonhealing Femoral Fractures: Analysis of the FDA Adverse Event Reporting System (FAERS) and International Safety Efforts

Loperamide Cardiotoxicity: “A Brief Review”

Towards Early Detection of Adverse Drug Reactions: Combining Pre-Clinical Drug Structures and Post-Market Safety Reports