EMA fast-tracks review of AstraZeneca’s sipavibart to stop Covid
Pharmaceutical Technology - 02 Jul 2024EMA fast-tracks review of AstraZeneca’s sipavibart to stop Covid ...
ema astrazeneca
EMA fast-tracks review of AstraZeneca’s sipavibart to stop Covid ...
At request of AstraZeneca, Europe withdraws marketing authorization of COVID vaccine Vaxzevria
FiercePharma - 08 May 2024At request of AstraZeneca, Europe withdraws marketing authorization of COVID vaccine Vaxzevria ...
European Medicines Agency pulls authorization for AstraZeneca's COVID shot, at company's request
The Independent - 08 May 2024European Medicines Agency pulls authorization for AstraZeneca's COVID shot, at company's request ...
EMA accepts AstraZeneca’s regulatory submission for sipavibart for COVID-19 prevention
Pharmafile - 01 Jul 2024EMA accepts AstraZeneca’s regulatory submission for sipavibart for COVID-19 prevention ...
AstraZeneca's COVID prevention drug application gets EU fast-track assessment
Reuters - 30 Jun 2024AstraZeneca's COVID prevention drug application gets EU fast-track assessment ...
EMA receives application for conditional marketing authorisation of COVID-19 Vaccine AstraZeneca
European Medicines Agency | - 13 Nov 2020EMA receives application for conditional marketing authorisation of COVID-19 Vaccine AstraZeneca ...
EMA: Benefits of AstraZeneca significantly outweigh side effects
Telegrafi - 11 Nov 2024EMA: Benefits of AstraZeneca significantly outweigh side effects ...
AstraZeneca's COVID-19 Prevention Drug For Patients With Weak Immune Systems - European Medicines Agency Accepts Marketing Application Under Accelerated Assessment
Yahoo Finance - 01 Jul 2024AstraZeneca's COVID-19 Prevention Drug For Patients With Weak Immune Systems - European Medicines Agency Accepts Marketing Application Under Accelerated Assessment ...
EMA CHMP recommends AstraZeneca’s Fasenra to treat EGPA
Pharmaceutical Technology - 24 Sep 2024EMA CHMP recommends AstraZeneca’s Fasenra to treat EGPA ...
AstraZeneca’s Tagrisso combination receives CHMP recommendation for advanced lung cancer
PMLiVE - 06 Jun 2024AstraZeneca’s Tagrisso combination receives CHMP recommendation for advanced lung cancer ...
Sanofi & Regeneron Drug Dupixent Gets EMA Approval as the First Biologic COPD Med
MedCity News - 07 Jul 2024Sanofi & Regeneron Drug Dupixent Gets EMA Approval as the First Biologic COPD Med ...
EMA Finds No Link Between GLP-1 Drugs and Suicidal Thoughts, Self-Harm
BioSpace - 12 Apr 2024EMA Finds No Link Between GLP-1 Drugs and Suicidal Thoughts, Self-Harm ...
Misleading Claims on Well-Known Rare Risk of AstraZeneca COVID-19 Vaccine
FactCheck.org - 23 May 2024Misleading Claims on Well-Known Rare Risk of AstraZeneca COVID-19 Vaccine ...
Covid-19: EU states to resume AstraZeneca vaccine rollout
BBC.com - 18 Mar 2021Covid-19: EU states to resume AstraZeneca vaccine rollout ...
EU says 'no evidence' to restrict AstraZeneca jab use
FRANCE 24 English - 31 Mar 2021EU says 'no evidence' to restrict AstraZeneca jab use ...
EMA awards double validation for Daiichi Sankyo and AstraZeneca’s cancer ADC
Pharmaceutical Technology - 04 Mar 2024EMA awards double validation for Daiichi Sankyo and AstraZeneca’s cancer ADC ...
EU drug regulator: Unusual blood clot is 'very rare AstraZeneca side effect'
BBC.com - 07 Apr 2021EU drug regulator: Unusual blood clot is 'very rare AstraZeneca side effect' ...
European Medicines Agency: There is no indication that AstraZeneca's vaccine causes blood clots
Telegrafi - 25 Oct 2024European Medicines Agency: There is no indication that AstraZeneca's vaccine causes blood clots ...
EMA: Women and young people are not at higher risk of developing rare blood clots because of AstraZeneca
Telegrafi - 26 Oct 2024EMA: Women and young people are not at higher risk of developing rare blood clots because of AstraZeneca ...
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