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MHRA - Reporting adverse reactions Report suspected side effects to medicines, vaccines, e-cigarettes, medical device incidents, defective or falsified (fake) products to the Medicines and Healthcare products Regulatory Agency to ensure safe and effective use

In addition, our clinical trials must be conducted with product produced under current Good Manufacturing Practices (cGMP) regulations

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Your healthcare provider will monitor your progress and adjust your treatment plan as needed

Then for the next dose, we have to find a different pharmacy carrying that dose. If a patient cant get their next escalated dose, they either have to stay on the low dose without full benefits, or stop and restart the whole process from the beginning