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With the shortage resolved, the regulatory framework simply returns to its usual conditions: compounding justified by individual clinical need, with a prescription and a clear reason why the standard commercial product does not work for that patient

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We have previously demonstrated that the common use of the drug in babies and children without oxidative stress (and thus not at risk for APAP-associated neurodevelopmental problems) interferes with multivariate analyses, such as the one performed by Alemany et al