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Pharmacists' Roles in Addressing Oncology Biosimilar Challenges

Pharmacists' Roles in Addressing Oncology Biosimilar Challenges
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Moderna COVID vaccine authorized by FDA for emergency use in US

CAMBRIDGE, Mass. Americans will soon have access to a second COVID-19 vaccine.
Stephen Hahn, commissioner of the U.S. Food and Drug Administration, granted emergency authorization Friday to a vaccine made by Moderna, a week after giving similar clearance to one made by Pfizer and its German collaborator, BioNTech.
His is authorizing rather than approving the vaccine, because longer-term research is needed to meet the full standards for approval, which officials don t want to wait for during the public health emergency.
The speedy path to authorization was possible because the agency “cut through regulatory red tape,” Hahn said at a Friday night press conference. We worked quickly based on the urgency of this global pandemic . we have not cut corners. ....

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Pfizer COVID vaccine vials may hold extra doses, adding to US supply

The U.S. might have more doses of Pfizer-BioNTech s COVID-19 vaccine than it thought.
While each vial is supposed to hold five doses of the first vaccine authorized for emergency use by the Food and Drug Administration, Politico was first to report on Wednesday that pharmacists have discovered some vials may have extra doses, potentially adding to the country s supply.
The amount of vaccine remaining in the multidose vial after removal of 5 doses can vary, depending on the type of needles and syringes used, a Pfizer spokesperson told USA TODAY in a statement. At this time, we cannot provide a recommendation on the use of the remaining amount of vaccine from each vial. Vaccinators need to consult their institution’s policies for the use of multidose vials. ....

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