Back to: Just the Inserts Training Course

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By now, you’ve seen that informed consent isn’t just about signing a form. It’s about having a full picture: the diagnosis, the plan, the benefits, the risks, the options, and your right to speak up. But here’s the truth: In most medical settings, you won’t be handed that full picture.

And that’s where the manufacturer insert comes in. It’s not perfect. It’s not warm or personalized. It’s not a sales pitch. But it is one of the only legal documents that:

• Discloses the known side effects and adverse events before and after a medical product was made available to the public
• Explains what studies were (and weren’t) done
• Lists ingredients and contraindications (medical conditions that increase your risk for an adverse reaction)
• Reveals the manufacturer’s own legal disclaimers

Inserts give you the pieces we’re often missing in healthcare. They are pieces of communication between you, the manufacturer, and the government. They also give you something the system rarely does: a place to start asking better questions no matter if you accept, delay, or decline any or all medical products.

Whether you’re a patient or a parent, reading the insert puts you back in the driver’s seat. It helps you bridge the gap between what’s marketed and what’s actually written.

Let’s show you how to read one, step by step. By the end of this training, you will be well-equipped to find and read any insert for any medical product on the market!