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The field requires urgent Phase I/II human trials before any clinical recommendations can be made

Alison Cave, the MHRAs Chief Safety Officer, emphasized the importance of informed decision-making: The decision to start, continue, or stop treatments should be made jointly by patients and their doctor, based on full consideration of benefits and risks. This statement underscores a key point: while the numbers are concerning, they must be contextualized within the millions of prescriptions issued and the complex health profiles of the patients taking these drugs