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Adverse drug reactions to antibiotics collected by a pharmacovigilance center in Korea: an eight-year retrospective study

Journal of allergy and clinical immunology, 2018-02, Vol.141 (2), p.AB87-AB87

2018

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Serious bradycardia and remdesivir for coronavirus 2019 (COVID-19): a new safety concerns

Clinical microbiology and infection, 2021-05, Vol.27 (5), p.791.e5-791.e8

2021

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The drugs that mostly frequently induce acute kidney injury: a case − noncase study of a pharmacovigilance database

British journal of clinical pharmacology, 2017-06, Vol.83 (6), p.1341-1349

2017

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Hubungan Pengetahuan Tenaga Kesehatan Tentang Pharmacovigilance Terhadap Sikap Pelaporan ADR di Kota Semarang

Journal of pharmaceutical science and clinical research, 2023-08, Vol.8 (2), p.218-225

2023

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GLP-1 receptor agonist-associated tumor adverse events: A real-world study from 2004 to 2021 based on FAERS

Frontiers in pharmacology, 2022-10, Vol.13, p.925377-925377

2022

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Fatal adverse drug reactions: A worldwide perspective in the World Health Organization pharmacovigilance database

British journal of clinical pharmacology, 2021-11, Vol.87 (11), p.4334-4340

2021

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Knowledge, Attitudes and Practices of Dentists Regarding Pharmacovigilance and Reporting of Adverse Drug Reactions in Northwestern Turkiye: A Cross-Sectional Study

Cumhuriyet Üniversitesi Dişhekimliği Fakültesi dergisi = Journal of Cumhuriyet University Dental Faculty, 2023-03, Vol.26 (1), p.69-76

2023

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Veterinary Pharmacovigilance in Algeria: Situation and Prospects

Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca. Veterinary Medicine, 2021-05, Vol.78 (1), p.68

2021

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The safety of JAK-1 inhibitors

Rheumatology (Oxford, England), 2021-05, Vol.60 (Supplement_2), p.ii24-ii30

2021

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INVOLVING PHARMACIES IN PHARMACOVIGILANCE – A COMPARISON BETWEEN FRANCE AND ROMANIA

Farmacia (București), 2023-06, Vol.71 (3), p.648-654

TOMA , ALEXANDRA

2023

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Postmarket safety profile of suicide/self-injury for GLP-1 receptor agonist: a real-world pharmacovigilance analysis

European psychiatry, 2023-11, Vol.66 (1), p.e99-e99, Article e99

2023

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COVID-19 vaccine post-marketing surveillance: Cardiovascular doctors have a role to play

Archives of cardiovascular diseases, 2021-08, Vol.114 (8-9), p.521-523

2021

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A real-world study of adverse drug reactions of two isocitrate dehydrogenase inhibitor based on the US FDA adverse event reporting system and VigiAccess databases

Frontiers in pharmacology, 2024-11, Vol.15

2024

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Active‐comparator restricted disproportionality analysis for pharmacovigilance signal detection studies of chronic disease medications: An example using sodium/glucose cotransporter 2 inhibitors

British journal of clinical pharmacology, 2023-02, Vol.89 (2), p.431-439

2023

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Adverse drug reaction signals mining comparison of amiodarone and dronedarone: a pharmacovigilance study based on FAERS

Frontiers in pharmacology, 2024-10, Vol.15, p.1438292

2024

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Comparative analysis of semaglutide induced adverse reactions: Insights from FAERS database and social media reviews with a focus on oral vs subcutaneous administration

Frontiers in pharmacology, 2024-10, Vol.15, p.1471615

2024

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Disproportionality analysis of drug-induced dry mouth using data from the United States food and drug administration adverse event reporting system database

Heliyon, 2024-10, Vol.10 (19), p.e38561, Article e38561

2024

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Evaluation of Kosovo pharmacists’ knowledge of tamoxifen-induced psychiatric disorders in comparison with reported side effects in the WHO pharmacovigilance database

Pharmacy practice : official journal of the GRIPP (Global Research Institute of Pharmacy Practice), 2024, Vol.22 (1)

2024

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Disponibilité de l’information médicale requise pour la déclaration d’une réaction indésirable médicamenteuse à Santé Canada: une étude exploratoire

Canadian journal of hospital pharmacy, 2024-02, Vol.77 (1)

2024

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Neurological Adverse Events Associated With Esketamine: A Disproportionality Analysis for Signal Detection Leveraging the FDA Adverse Event Reporting System

Frontiers in pharmacology, 2022-04, Vol.13, p.849758-849758

2022

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Neki čimbenici utjecaja na nedovoljno prijavljivanje sumnji na nuspojave cjepiva

Paediatria Croatica, 2024-07, Vol.67 (3-4), p.65-70

2024

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Updated insights into adverse events associated with mepolizumab: a disproportionality analysis from the FDA adverse event reporting system database

Frontiers in medicine, 2024-10, Vol.11

2024

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Antihypertensive drugs as factors that induct, aggravate and imitate psoriasis

Farmacja Polska, 2020-10, Vol.76 (9), p.519-526

Demczuk, Karolina

2020

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Fulminant Myocarditis with Combination Immune Checkpoint Blockade

The New England journal of medicine, 2016-11, Vol.375 (18), p.1749-1755

2016

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COVID-19 vaccines and myocarditis

Archives of cardiovascular diseases, 2021-06, Vol.114 (6-7), p.515-517

2021

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Adverse drug reactions to antibiotics collected by a pharmacovigilance center in Korea: an eight-year retrospective study

Serious bradycardia and remdesivir for coronavirus 2019 (COVID-19): a new safety concerns

The drugs that mostly frequently induce acute kidney injury: a case − noncase study of a pharmacovigilance database

Hubungan Pengetahuan Tenaga Kesehatan Tentang Pharmacovigilance Terhadap Sikap Pelaporan ADR di Kota Semarang

GLP-1 receptor agonist-associated tumor adverse events: A real-world study from 2004 to 2021 based on FAERS

Fatal adverse drug reactions: A worldwide perspective in the World Health Organization pharmacovigilance database

Knowledge, Attitudes and Practices of Dentists Regarding Pharmacovigilance and Reporting of Adverse Drug Reactions in Northwestern Turkiye: A Cross-Sectional Study

Veterinary Pharmacovigilance in Algeria: Situation and Prospects

The safety of JAK-1 inhibitors

INVOLVING PHARMACIES IN PHARMACOVIGILANCE – A COMPARISON BETWEEN FRANCE AND ROMANIA

Postmarket safety profile of suicide/self-injury for GLP-1 receptor agonist: a real-world pharmacovigilance analysis

COVID-19 vaccine post-marketing surveillance: Cardiovascular doctors have a role to play

A real-world study of adverse drug reactions of two isocitrate dehydrogenase inhibitor based on the US FDA adverse event reporting system and VigiAccess databases

Active‐comparator restricted disproportionality analysis for pharmacovigilance signal detection studies of chronic disease medications: An example using sodium/glucose cotransporter 2 inhibitors

Adverse drug reaction signals mining comparison of amiodarone and dronedarone: a pharmacovigilance study based on FAERS

Comparative analysis of semaglutide induced adverse reactions: Insights from FAERS database and social media reviews with a focus on oral vs subcutaneous administration

Disproportionality analysis of drug-induced dry mouth using data from the United States food and drug administration adverse event reporting system database

Evaluation of Kosovo pharmacists’ knowledge of tamoxifen-induced psychiatric disorders in comparison with reported side effects in the WHO pharmacovigilance database

Disponibilité de l’information médicale requise pour la déclaration d’une réaction indésirable médicamenteuse à Santé Canada: une étude exploratoire

Neurological Adverse Events Associated With Esketamine: A Disproportionality Analysis for Signal Detection Leveraging the FDA Adverse Event Reporting System

Neki čimbenici utjecaja na nedovoljno prijavljivanje sumnji na nuspojave cjepiva

Updated insights into adverse events associated with mepolizumab: a disproportionality analysis from the FDA adverse event reporting system database

Antihypertensive drugs as factors that induct, aggravate and imitate psoriasis

Fulminant Myocarditis with Combination Immune Checkpoint Blockade

COVID-19 vaccines and myocarditis

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