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Publications by K.B. Sonawane

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

Value in Health

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

Texas Pharmacists’ Knowledge of Reporting Serious Adverse Drug Events to the Food and Drug Administration

Journal of the American Pharmacists Association : JAPhA

Pharmacology

Pharmacy

2011

English

Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database

Drugs - Real World Outcomes

Pharmacology

2018

English

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

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

Association Between Myocarditis and Other Immune-Related Adverse Events Associated With Immune Checkpoint Inhibitor Use: Analysis of the FDA Adverse Events Reporting System (FAERS)

Journal of Cardiac Failure

Cardiovascular Medicine

Cardiology

2019

English

Prm79 - Weber Effect: An Extended Analysis for Ten Years of Reporting Trends in Fda Adverse Event Reporting System (Faers)

English

Clustering Therapeutic Drugs Using FDA Adverse Event Reporting System

Proceedings for Annual Meeting of The Japanese Pharmacological Society

2020

English

Food and Drug Administration (FDA) Postmarket Reported Side Effects and Adverse Events Associated With Pulmonary Hypertension Therapy in Pediatric Patients

Pediatric Cardiology

Child Health

Pediatrics

Cardiovascular Medicine

Perinatology

Cardiology

2013

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by K.B. Sonawane

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

Related publications

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

Texas Pharmacists’ Knowledge of Reporting Serious Adverse Drug Events to the Food and Drug Administration

Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database

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

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

Association Between Myocarditis and Other Immune-Related Adverse Events Associated With Immune Checkpoint Inhibitor Use: Analysis of the FDA Adverse Events Reporting System (FAERS)

Prm79 - Weber Effect: An Extended Analysis for Ten Years of Reporting Trends in Fda Adverse Event Reporting System (Faers)

Clustering Therapeutic Drugs Using FDA Adverse Event Reporting System

Food and Drug Administration (FDA) Postmarket Reported Side Effects and Adverse Events Associated With Pulmonary Hypertension Therapy in Pediatric Patients