Risultati per: La FDA approva il sistema di riabilitazione dell’ictus

Funziona in modo diverso dagli adulti, ma efficiente

‘Non approvati e pericolosi per diabetici’

Esperto Imperial College: ‘Piani qualità dell’aria più radicali’

The US Food and Drug Administration (FDA) has approved Florida’s program to import certain prescription medications from Canada, the agency announced. But before Florida can import the medications, the state will need to submit additional information about the drugs to the FDA, test them to make sure they are up to the agency’s standards, and replace the drugs’ labels with FDA-approved ones.

Assessore a inaugurazione sale operatorie del Policlinico

New England Journal of Medicine, Ahead of Print.

This cross-sectional study characterizes the frequency and degree of innovation of new dermatologic drugs approved by the US Food and Drug Administration (FDA) from 2012 to 2022.

Caccia nei prodotti bellezza ai Pfas, ‘gli inquinanti eterni’

‘Colonna vertebrale del Ssn, salva migliaia di vite al giorno’

‘Colonna vertebrale del Ssn, salva migliaia di vite al giorno’

New England Journal of Medicine, Ahead of Print.

In Reply We appreciate the Letter by Drs Leavens and Wagener in response to our Viewpoint that raised issues for the US Food and Drug Administration (FDA) to consider as it strives to regulate e-cigarettes.

To the Editor The proposal to cap nicotine concentrations in combustible cigarettes is based on sound scientific evidence that cigarettes with very low levels of nicotine will significantly reduce smoking- and tobacco-related harm. However, we believe that a proposal presented in a recent Viewpoint for a federal nicotine cap on e-cigarettes is misguided and runs contrary to current evidence. The focus on e-liquid nicotine concentrations alone is problematic because these restrictions fail to consider that e-cigarettes, unlike cigarettes, offer users ways beyond nicotine concentrations to control nicotine delivery, including manipulating device power and compensatory puffing. In fact, the best evidence suggests that this proposed policy would lead to a product that is as addictive as e-cigarettes with higher nicotine concentrations, which may be more appealing to young people, and more harmful.

This Viewpoint examines how US states are reforming legislation to allow access to psychedelics for therapeutic use, but federal laws consider these agents to be Schedule I drugs, and the discordance between state and federal law may create confusion and conflict.

In 2021, the US saw an estimated 1.6 million chlamydia cases and more than 700 000 gonorrhea cases.