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List of works by Monica A Muñoz

An Evaluation of "Drug Ineffective" Postmarketing Reports in Drug Safety Surveillance.

scientific article

An Evaluation of Postmarketing Reports with an Outcome of Death in the US FDA Adverse Event Reporting System

scientific article published on 24 January 2020

Complementary Use of U.S. FDA's Adverse Event Reporting System and Sentinel System to Characterize Direct Oral Anticoagulants-Associated Cutaneous Small Vessel Vasculitis

scientific article published on 08 October 2020

Discontinuation of Direct Oral Anticoagulants in Response to Attorney Advertisements: Data From the FDA Adverse Event Reporting System

scientific article published on 05 May 2019

Drug Interaction Between Febuxostat and Thiopurine Antimetabolites: A Review of the FDA Adverse Event Reporting System and Medical Literature

scientific article published on 20 January 2020

Evaluation of Postmarketing Reports from Industry-Sponsored Programs in Drug Safety Surveillance

scientific article published on 01 May 2019

Impact of a New Consumer Form on the Quantity and Quality of Adverse Event Reports Submitted to the United States Food and Drug Administration

scientific article published on 11 October 2019

Liver injury associated with dimethyl fumarate in multiple sclerosis patients

scientific article published on January 2017

Patterns in spontaneous adverse event reporting among branded and generic antiepileptic drugs.

scientific article

Pravastatin versus simvastatin for prevention of contrast-induced nephropathy.

scientific article published on 08 March 2011

Predicting medication-associated altered mental status in hospitalized patients: Development and validation of a risk model

scientific article published on 01 June 2019

Regarding "Retrograde administration of ultrasound-guided endovenous microfoam chemical ablation for the treatment of superficial venous insufficiency"

scientific article published on 01 March 2019

Serious Liver Injury Associated with Macitentan: A Case Report.

scientific article published on 29 December 2017

The Impact of Litigation-Associated Reports on Signal Identification in the US FDA's Adverse Event Reporting System

scientific article published on 01 October 2019

Towards Automating Adverse Event Review: A Prediction Model for Case Report Utility

scientific article published on 01 April 2020

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