2022

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2022
EMA completes review of anxiety medicine Stresam (etifoxine)

The Committee for Medicinal Products for Human Use of the European Medicines Agency (CHMP EMA) has completed its safety review of the medicinal product Stresam (etifoxine) and made…

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Start of the review concerning studies conducted at Synchron Research Services, India

The European Medicines Agency (EMA) has started a review of medicinal products studied by Synchron Research Services, a contract research organization (CRO) located in…

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Updated safety information on COVID-19 vaccines

On 17 February 2022, the Pharmacovigilance Risk Assessment Committee (PRAC) of the European Medicines Agency (EMA) published an update of safety information…

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Hydroxychloroquine: increased risk of cardiovascular complications when used with macrolide antibiotics; reminder about psychiatric reactions

Before prescribing systemic azithromycin or other systemic macrolide antibiotics (erythromycin or clarithromycin) to patients receiving hydroxychloroquine, carefully weigh the benefit and…

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Regarding amendments to the package leaflet of the COVID-19 mRNA vaccine (nucleoside-modified) (Spikevax)

Taking into account the report of the Pharmacovigilance Risk Assessment Committee (PRAC) based on the assessment of the analysis of Periodic Safety Update Reports (PSURs)…

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Regarding amendments to the instructions for medical use of medicinal products containing nadroparin (nadroparin)

The Pharmacovigilance Risk Assessment Committee (PRAC), based on the assessment of the analysis of Periodic Safety Update Reports (PSURs) for medicinal products,…

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Updated safety information on COVID-19 vaccines

On 20 January 2022, the Pharmacovigilance Risk Assessment Committee (PRAC) of the European Medicines Agency (EMA) published an update of safety information…

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Regarding amendments to the package insert for medicinal products containing quinapril/hydrochlorothiazide (quinapril/ hydrochlorothiazide)

The Pharmacovigilance Risk Assessment Committee (PRAC), based on the assessment of the analysis of Periodic Safety Update Reports (PSURs) for medicinal products,…

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Regarding amendments to the instructions for medical use of medicinal products containing quinapril (quinapril)

The Pharmacovigilance Risk Assessment Committee (PRAC), based on the assessment of the analysis of Periodic Safety Update Reports (PSURs) for medicinal products,…

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Regarding amendments to the instructions for medical use of medicinal products containing pregabalin (pregabalin)

Having considered the available data from preclinical and clinical studies, EudraVigilance, and the literature, and also taking into account the pathophysiological mechanism and clinical characteristics of toxic epidermal necrolysis…

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