Acting FDA Commissioner Calls For Independent Investigation Into Approval Of Alzheimer's DrugUS Food and Drug Administration Acting Commissioner Dr. Janet Woodcock on Friday requested an investigation by the US Department of Health and Human Services Office of Inspector General into the controversial approval of the Alzheimer's disease drug Aduhelm.
Additional Batch Of Johnson & Johnson Vaccine Authorized For Emergency Use By FDAThe U.S. Food And Drug Administration announced Tuesday that they are authorizing additional batches of the Johnson & Johnson coronavirus vaccine produced at Emergent BioSolutions.
FDA Orders J&J Vaccines Made At Baltimore Emergent Plant To Be TossedThe Food and Drug Administration is forcing Johnson & Johnson to throw out millions of vaccine doses made at a plant here in Baltimore. The FDA, for months, had been reviewing and testing the doses manufactured at the Emergent Biosolutions facility here in Baltimore.
FDA Clears 10M Johnson & Johnson COVID Vaccine Doses From Baltimore's Emergent BioSolutionsU.S. regulators are allowing for the release of 10 million doses of Johnson & Johnson's COVID-19 vaccine from a troubled Baltimore factory
FDA Says To Avoid Eating Cicadas 'If You're Allergic To Seafood'Cicadas might seem like a crispy, protein-packed snack, but people with seafood allergies should think twice about eating them, according to the US Food and Drug Administration.
Maryland Health Officials Prepared To Vaccinate Children Ages 12 To 15 After CDC Advisors Recommend PfizerUS Centers for Disease Control and Prevention advisers voted unanimously Wednesday to recommend giving Pfizer/BioNTech's Covid-19 vaccine to kids as young as 12.
Maryland Resumes Johnson & Johnson COVID Vaccinations After CDC, FDA Lift PauseMaryland has begun to administer the Johnson & Johnson vaccine again after the Food & Drug Administration, along with the U.S. Centers for Disease Control & Prevention, lifted the pause on the one-shot covid-19 vaccine on Friday.
FDA Completes Inspection Of J&J Vaccine Maker Emergent BioSolutions, Cites Concerns Over Cross-Contamination, SanitationThe U.S. Food and Drug Administration has completed its inspection of the Baltimore-based Johnson & Johnson vaccine maker Emergent BioSolutions Tuesday and "cited a number of observations concerning whether the facility’s processes met our requirements and standards."
Johnson & Johnson COVID Vaccine Maker Emergent BioSolutions Asked To Stop Making Doses While FDA Investigation UnderwayEmergent BioSolutions, the Baltimore, Maryland-based company manufacturing the Johnson & Johnson coronavirus vaccines, was asked to stop manufacturing COVID-19 related products, while the Food & Drug Administration continues its investigation into quality control issues at the plant that ruined 15 million potential doses of the vaccine.
FDA, CDC Recommend ‘Pause’ For Johnson & Johnson COVID-19 Vaccine Over Clot ReportsThe U.S. is recommending a “pause” in administration of the single-dose Johnson & Johnson COVID-19 vaccine to investigate reports of potentially dangerous blood clots.
FDA Advisory Committee Votes To Recommend Authorizing Johnson & Johnson's New COVID-19 VaccineAn FDA advisory committee voted Friday to recommend authorizing Johnson & Johnson's new COVID-19 vaccine.
CDC Shares Distribution, Messaging Advice On Johnson & Johnson's New COVID-19 VaccineThe Centers for Disease Control and Prevention on Friday updated state and local partners on distribution plans for Johnson & Johnson's new COVID-19 vaccine which is expected to be made available for ordering on Sunday, CBS News reports.
'Game-Changing' Johnson & Johnson Single-Dose Covid-19 Vaccine Meets Requirements For Emergency Use Authorization, FDA SaysJohnson and Johnson’s new Baltimore-made vaccine is safe and effective at fighting COVID-19 according to a new analysis from the Food and Drug Administration, which is likely to vote Friday to allow emergency use by the public.
FDA Approves Moderna's COVID-19 Vaccine For Emergency Use, Baltimore Hospital Among Those To Work On Vaccine TrialsThe FDA on Friday approved Moderna's COVID-19 vaccine for emergency use.
Drugs Recalled After 'Mix-Up' Packages Depression Medication, Erectile Dysfunction Drug TogetherPharmaceutical distributor AvKare is voluntarily recalling 100mg sildenafil tablets and 100mg trazodone tablets due to a "product mix-up," the company announced Wednesday.