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Serious, ‘Unexpected’ Adverse Events From Nasal Esketamine

04/16/2021 affective disorders, anxiety disorder, benzodiazepines, Depression, Europe, European, FDA, Mood Disorder, panic attack, psychophysiologic disorder, psychophysiologic illness, psychosomatic, psychosomatic disorder, psychosomatic illness, Psychotherapy, sedation, Suicide, U.S. Food and Drug Administration, united states food and drug administration

Patients who receive esketamine for treatment-resistant depression (TRD) are at increased risk for serious and unexpected adverse events (AEs), new

Health News

US Government Directs Johnson & Johnson to Run Vaccine Plant

04/05/2021 2019 Novel Coronavirus, 2019-nCoV, coronavirus, coronavirus vaccine, covid 19 vaccine, FDA, HCoV-229E, HCoV-OC43, Human coronavirus 229E, Human coronavirus HKU1, Human coronavirus OC43, leadership, pandemic, professional development, quality control, U.S. Food and Drug Administration, united states food and drug administration, vaccine, wuhan coronavirus

Editor’s note: Find the latest COVID-19 news and guidance in Medscape’s Coronavirus Resource Center. Federal health officials on Saturday put

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US Plans to Use Real World, Trial Data to Determine When Vaccines Need to Be Updated

03/18/2021 2019 Novel Coronavirus, 2019-nCoV, clinical research, clinical studies, clinical trials, Corona Virus, coronavirus vaccine, covid 19, covid 19 vaccine, covid19, FDA, HCoV-229E, HCoV-OC43, Human coronavirus 229E, Human coronavirus HKU1, Human coronavirus OC43, novel coronavirus, U.S. Food and Drug Administration, united states food and drug administration, vaccine, Vaccines, wuhan coronavirus

CHICAGO (Reuters) – U.S. officials plan to use data gathered from people who have already been vaccinated against COVID-19 as

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Insider Alleges Eli Lilly Blocked Her Efforts to Sound Alarms About US Drug Factory

03/12/2021 diabetes mellitus type 2, diabetes mellitus type ii, drug safety, drug/treatment safety, ED, Erectile Dysfunction, Ethics, FDA, headache (migraine), Impotence, Migraine, migraine headache, patient safety, quality control, treatment safety, Type 2 Diabetes, U.S. Food and Drug Administration, united states food and drug administration

(Reuters) – On a chilly spring morning in 2019, Amrit Mula arrived in her office at pharmaceutical giant Eli Lilly

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Promising Treatments for Molluscum Contagiosum and Acne

02/26/2021 Acne, acne vulgaris, Activism, activist, alopecia androgenetica, androgenetic alopecia, androgenic alopecia, child, Childhood, children, FDA, Kids, molluscum contagiosum, New York, Pediatrics, retinoids, skin and soft tissue infection, skin care, Social Issues, U.S. Food and Drug Administration, united states food and drug administration

No Food and Drug Administration–approved treatment currently exists for molluscum contagiosum, which affects an estimated 6 million people in the

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FDA to Allow Pfizer-BioNTech Vaccine to Be Stored at Higher Temps: NYT

02/24/2021 coronavirus vaccine, covid 19 vaccine, FDA, U.S. Food and Drug Administration, united states food and drug administration, vaccine, Vaccines

(Reuters) – The U.S. Food & Drug Administration plans to approve Pfizer Inc and BioNTech SE’s request to store their

Medications

FDA Approves Libtayo (cemiplimab-rwlc) Monotherapy for Patients with First-line Advanced Non-Small Cell Lung Cancer with PD-L1 Expression of ≥50%

02/22/2021 (cemiplimab-rwlc), ≥50%, advanced, Approves, cancer, Cell, expression, FDA, First-line, for, Libtayo, lung, Monotherapy, Non-Small, of, Patients, PD-L1, with

TARRYTOWN, N.Y. and PARIS, Feb. 22, 2021 /PRNewswire/ — Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Sanofi today announced that the U.S. Food and Drug Administration

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FDA approves genetically engineered pigs for food and transplants

12/15/2020 and, Approves, engineered, FDA, Food, for, genetically, pigs, transplants

Pigs that have been genetically engineered to be free of a molecule that triggers meat allergies have been approved by

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FDA panel endorses Pfizer coronavirus vaccine for emergency use

12/11/2020 coro, endorses, FDA, panel, Pfizer

Infectious disease doctor on Pfizer coronavirus vaccine: You could inject me today Infectious disease doctor Matt McCarthy praises the Pfizer

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FDA approves first COVID-19 drug: antiviral remdesivir

10/23/2020 antiviral, Approves, covid 19, Drug, FDA, first, remdesivir

U.S. regulators on Thursday approved the first drug to treat COVID-19: remdesivir, an antiviral medicine given to hospitalized patients through

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