Allergies Bacteria FDA Approval 
The Pharma Data
DECEMBER 13, 2020
Food and Drug Administration (FDA) approved a first-of-its-kind intentional genomic alteration (IGA) in a line of domestic pigs, referred to as GalSafe pigs, which may be used for food or human therapeutics. SILVER SPRING, Md. , 14, 2020 /PRNewswire/ — Today, the U.S. In the U.S.,
The Pharma Data
JULY 29, 2021
BOTOX ® was first approved by the FDA in 1989 for two rare eye muscle disorders – blepharospasm and strabismus in adults. In children being treated for urinary incontinence, other side effects include urinary tract infection and bacteria in the urine. About BOTOX ®.
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XTalks
AUGUST 2, 2023
Paxlovid was first authorized under the FDA Emergency Use Authorization in December 2021 ; however, it has received FDA approval on May 25, 2023. pneumoniae serotypes) replaced the company’s first pneumococcal conjugate vaccine Prevnar (PCV7, approved by the FDA in February 2000) in a February 2010 FDA approval.
The Pharma Data
SEPTEMBER 10, 2021
About BOTOX ® BOTOX ® was first approved by the FDA in 1989 for two rare eye muscle disorders – blepharospasm and strabismus in adults. In children being treated for urinary incontinence, other side effects include urinary tract infection and bacteria in the urine.
The Pharma Data
SEPTEMBER 8, 2021
About BOTOX ® BOTOX ® was first approved by the FDA in 1989 for two rare eye muscle disorders – blepharospasm and strabismus in adults. In children being treated for urinary incontinence, other side effects include urinary tract infection and bacteria in the urine. Atogepant is currently under review by the U.S.
XTalks
DECEMBER 24, 2020
Several saliva-based tests also received FDA approvals and authorizations, making sample collection easier and less invasive compared with traditional nasopharyngeal swabbing. However, regulators are warning people with allergies to polyethylene glycol (PEG), an excipient in Pfizer’s vaccine, not to get vaccinated just yet.
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