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Psychedelic drug MDMA faces FDA panel in bid to become first-of-a-kind PTSD medication

Psychedelic drug MDMA faces FDA panel in bid to become first-of-a-kind PTSD medication
courthousenews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from courthousenews.com Daily Mail and Mail on Sunday newspapers.

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United-states
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Multidisciplinary-association-for-psychedelic
Science-department
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York-university
Educational-media-group
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Drug-administration
Lykos-therapeutics

FDA Hosts Public Psychedelics Discussion, Discloses Major Growth On Number Of New Psychiatric Drugs Filings Post-2000 - Johnson & Johnson (NYSE:JNJ), Mind Medicine (NASDAQ:MNMD)

FDA and Reagan-Udall Foundation are hosting a virtual public meeting on psychedelic research titled Advancing Psychedelic Clinical Study Design, which aims to explore empirical approaches to address issues in drug development.

Michael-bogenschutz
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Patrizia-cavazzoni
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Robert-barrow
Johnson-jnjdr
Johns-hopkins-university
Veterans-administration
Federation-of-state-medical-boards
Neuroscience-office
Udall-foundation

Oral Treatment for Postpartum Depression: What Is It and How Possible Is It?

The US FDA approved the first oral treatment for postpartum depression a month ago. We tell you what is it about and how possible it is.

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Mexico
Tiffanyr-farchione
Drug-administration
Division-of-psychiatry
United-states-food
Statistical-manual
Mental-disorders
Oral-treatment-for-postpartum-depression

The US just approved a new postpartum depression pill. Where does Europe stand on treatment?

The US just approved a new postpartum depression pill. Where does Europe stand on treatment?
euronews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from euronews.com Daily Mail and Mail on Sunday newspapers.

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National-health-service
Sage-therapeutics

FDA approves oral medication treating postpartum depression

SPOKANE — A new drug treating postpartum depression was approved earlier this month by the Food and Drug Administration — possibly filling a gap in care, depending on the drug’s

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Medicine
Harmacology
Sychiatry

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