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New insight on how neural dynamics vary during spontaneous behavior

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FDA Approves Rybrevant

21/05/2021 approves, FDA, Rybrevant

FDA Approves Rybrevant (amivantamab-vmjw) as the First Targeted Treatment for Patients with Non-Small Cell Lung Cancer with EGFR Exon 20

This Is Why The FDA Hasn’t Authorized The COVID Vaccines

05/05/2021 Aut, FDA, Hasn't, is, the, this, Why

The first doses of the COVID-19 vaccine were administered back in December 2020, according to The Washington Post, but that

FDA approves higher-dose naloxone hydrochloride nasal spray

04/05/2021 approves, FDA, higher-dose, nalox

(HealthDay)—The U.S. Food and Drug Administration approved use of a higher dose of naloxone hydrochloride nasal spray for treating opioid

The FDA Plans to Ban Menthol Cigarettes and Flavored Cigars-Here's Why

30/04/2021 ban, c, FDA, Menthol, plans, the, to

The US Food and Drug Administration (FDA) announced today that it plans on taking steps within the next year to ban

FDA: N95 masks, now plentiful, should no longer be reused

23/04/2021 FDA, masks, N95, Now, plentiful

The Biden administration has taken the first step toward ending an emergency exception that allowed hospitals to ration and reuse

U.S. FDA Grants Accelerated Approval to Trodelvy for the Treatment of Metastatic Urothelial Cancer

16/04/2021 Accelerated, Approval, cancer, FDA, for, Grants, metastatic, of, the, to, treatment, Trodelvy, U.S., Urothelial

FOSTER CITY, Calif.–(BUSINESS WIRE)–Apr. 13, 2021– Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the U.S. Food and Drug Administration

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12/04/2021 2019 Novel Coronavirus, 2019-nCoV, adverse effects, coronavirus, Coronavirus vaccine, covid 19 vaccine, drug development, experimental drug, FDA, HCoV-229E, HCoV-OC43, hospitals, Human coronavirus 229E, Human coronavirus HKU1, Human coronavirus OC43, inpatient care, patient safety, side effect, T-cell, 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. Dozens of Americans are rolling up

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12/04/2021 Arrhythmia, biv, biventricular pacing, bradycardia, cardiac resynchronization therapy, crt, defibrillator, device safety, FDA, Heart Failure, icd, implantable cardioverter defibrillator, sudden death, u.s. food and drug administration, united states food and drug administration

The US Food and Drug Administration has declared Medtronic’s recall of seven models of defibrillating cardiac rhythm devices, due to

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07/04/2021 (isatuximab-irfc), and, approves, Carfilzomib, combination, dexamethasone, FDA, for, in, multiple, myeloma, or, patients, Refractory, Relapsed, Sarclisa, With

PARIS, March 31, 2021 /PRNewswire/ — The U.S. Food and Drug Administration (FDA) has approved Sarclisa (isatuximab-irfc) in combination with

FDA Approves Myrbetriq to Treat Pediatric NDO

03/04/2021 adverse effe, angioneurotic edema, antigens, biologic therapy, bladder infection, Child, childhood, children, FDA, headache, hypertension, increased blood pressure, kids, oab (overactive bladder), overactive bladder (oab), pediatrics, Spinal cord injury, u.s. food and drug administration, united states food and drug administration, urinary frequency, Urinary Tract Infection, urinary tract infection (uti), UTI

The US Food and Drug Administration (FDA) has expanded the indication for Mirabegron (Myrbetriq/Myrbetriq Granules) to treat neurogenic detrusor overactivity

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Bake Off desserts are a recipe for success when it comes to health benefits
Benidipine calcium channel blocker improves cigarette smoke-induced lung emphysema: Study
WHO declares JN.1 a COVID variant of interest as it spreads widely
thioridazine action
New insight on how neural dynamics vary during spontaneous behavior

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