Adverse drug reactions can emerge at various points during treatment – immediately upon starting, after dosage adjustments, or even following discontinuation. It’s crucial for patients to be aware of potential symptoms requiring attention and to understand the process for reporting these effects. These reactions aren’t always predictable, highlighting the importance of vigilant monitoring. Symptoms warranting concern should be promptly discussed with a healthcare professional. Additionally, reporting these incidents to the National Organization for Medicines (EOF) is vital for pharmacovigilance. This reporting helps authorities track and assess medication safety, protecting public health. Knowing when and how to report side effects empowers patients to actively participate in their healthcare and contribute to safer medication use.