U.S. FDA issues Emergency Use Authorisation for Merck’s molnupiravir
The authorization provides an additional treatment option against the Covid-19 virus in the form of a pill that can be taken orally
The authorization provides an additional treatment option against the Covid-19 virus in the form of a pill that can be taken orally
Only antibody authorised in the US for pre-exposure prophylaxis of COVID-19
First Emergency Use Listing granted by WHO for a protein-based Covid-19 vaccine
The study was performed independently by investigators at the US Food and Drug Administration (FDA), Center for Biologics Evaluation and Research
Orencia is the first FDA-approved therapy to prevent acute graft versus host disease following hematopoietic stem cell transplant
Evusheld is a combination of two long-acting monoclonal antibodies and is the only antibody therapy authorised in the US to prevent Covid-19
Philips Patient Monitors IntelliVue MX750 and IntelliVue MX850 pair with advanced software and services to offer clinical decision support, continuous, scalable patient management and enhanced infection control
Organised by the Indian Stroke Association, it has attracted over 800 doctors from India and overseas
Expanded EUA includes both treatment of patients with Covid-19 and post-exposure prophylaxis (PEP) in high-risk pediatric and infant patients
Transaction adds to Sanofi pipeline a potential first-in-class vaccine candidate in acne vulgaris, a condition affecting millions of people worldwide
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