Why is it crucial to discuss adverse effects with a patient before prescribing medication?

Discussing adverse effects with a patient prior to prescribing medication is essential to ensure informed consent. Informed consent is a process where a patient understands the risks, benefits, and alternatives associated with a treatment or medication. By openly communicating potential adverse effects, the healthcare provider empowers the patient to make an educated decision regarding their treatment plan.

This process respects the patient's autonomy and right to be actively involved in their health care decisions. Educating patients about adverse effects also helps manage expectations and prepares them to recognize and report any side effects that may arise, leading to better overall treatment adherence and outcomes.

While other factors like regulatory compliance and mitigating legal risks may play a role in the prescription process, the primary focus should be on ensuring that patients are fully informed and involved in their treatment decisions.