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Evusheld: EMA recommends authorisation of COVID-19 medicine

European Medicines Agency (EMA) has recommended granting a marketing authorisation for Evusheld, developed by AstraZeneca, for the prevention of COVID-19 in adults and adolescents...

EU drug regulator OKs Pfizer COVID pill for high-risk patients

The European Union's drug regulator- EMA- on Thursday approved Pfizer's antiviral COVID-19 pill for treating adults at risk of severe illness, as the region...

EU looking into new possible side-effects of mRNA COVID-19 vaccines

Three new conditions reported by a small number of people after vaccination with COVID-19 shots from Pfizer and Moderna are being studied to assess...

Two jabs ‘vital’ to battle Delta variant: EMA

The EU's medicines watchdog said on Wednesday two jabs by approved vaccine makers were "vital" to provide maximum protection against the highly infectious coronavirus...

AstraZeneca shots should be halted for over-60s too: EMA official

Countries should avoid giving the AstraZeneca coronavirus vaccine to people over 60 in addition to younger age groups

EU approves Pfizer-BioNTech vaccine for 12- to 15-year-olds

The vaccine was "well tolerated" in children and there were no "major concerns" in terms of side effects, the Amsterdam-based European Medicines Agency said.

EU watchdog expects first application for COVID-19 vaccine in days

EMA did not name the company it expects to file the application, but Pfizer and BioNTEch are the most advanced in the regulatory process among the three companies

Pharma gets nod for first ever Ebola vaccine

EMA’s human medicines committee (CHMP) has recommended granting a conditional marketing authorisation in the European Union for Ervebo, the first vaccine for Ebola virus

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