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It is common sense
Clinical experience strongly supports its use for the indications below but we're working with promising preclinical data, not robust human RCTs
We dont expect that the reevaluation will take long but the result could cause the Agency headaches down the road whenever the FDA declares a drug shortage resolved
Always report unexpected or concerning symptoms to your healthcare provider, and utilise the Yellow Card Scheme (yellowcard.mhra.gov.uk) to report suspected side effects directly to the MHRA, contributing to ongoing medication safety surveillance
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