Topic: Adverse event reporting

Adverse event reporting is the process of identifying, documenting, and communicating any undesirable experiences associated with the use of a medical product.

More on: Adverse event reporting

The importance of adhering to established clinical trial guidelines for reporting serious adverse events, including potential vaccine injuries, is a key topic discussed in the podcast episodes.

The first episode Dr. Hazan on Ivermectin, COVID, and MRNA Vaccines discusses the potential detrimental effects of mRNA vaccines on the microbiome and the need for scientific integrity, transparency, and independent research to advance public health.

The second episode Ecstasy Therapy: Bad trip features an interview with a participant in an MDMA-assisted therapy trial for PTSD who experienced significant distress and questions the reliability of the data collected, highlighting the importance of comprehensive reporting of adverse events in clinical trials.

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