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8 juin 2017 - FDA requested that Endo Pharmaceuticals remove its opioid pain medication, reformulated Opana ER (oxymorphone hydrochloride), from the market based on its concern that the benefits of the drug may no longer outweigh its risks.
Ajouté au bande de temps:
Opioids and the FDA
By
Anastasia
13 nov. 2018
0
0
521
Date:
8 juin 2017
Maintenaint
~ Il y a 8 ans et 4 mois
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