Should You “Do Your Own Research” on Prescription Medications?
These days, it’s common to hear people say they “did their own research” on a medical issue. However, what that often means is a quick Google search that can lead to a rabbit hole of misinformation. While the internet provides vast amounts of information, not all of it is reliable. When it comes to prescription medications and pharmaceuticals, relying on unverified sources can lead to confusion, fear, or even dangerous decisions.
That said, it’s not wrong to want to better understand the treatments your doctor recommends. In fact, reading about the medications prescribed to you or a loved one can help you feel more informed. It’s a good way to prepare for discussions with your healthcare provider. But it’s important to remember that your doctor is the expert in this field, with years of training and experience that no online article can replace. If you ever feel uncertain or uncomfortable with their advice, the best course of action is to seek a second opinion from another medical professional, not from “Dr. Google.”
There are reputable sources available online that can help you ask the right questions and make more informed decisions. With the right research, you can enter your doctor’s office ready to ask specific, intelligent questions and have a more productive conversation.
Stay Informed with FDA Drug Safety Communications
When researching a drug or medical device, a source of information is the FDA’s Drug Safety and Availability page. This resource provides up-to-date information about new safety issues related to approved medications. As drugs are used more widely by the public, side effects or risks that were not identified during clinical trials may emerge. To keep patients and healthcare professionals informed, the FDA monitors the ongoing safety of drugs and issues alerts when new concerns arise.
The FDA’s physicians and scientists continuously review data from clinical trials, case reports, and medical literature to assess potential risks. If a new safety concern is identified, the FDA may require changes to the prescribing information, patient medication guides, or issue a public Drug Safety Communication to alert patients and healthcare providers. These alerts are invaluable for making more informed decisions about treatment options. You can also sign up for email alerts on the website for specific medications.
The FDA emphasizes that every medicine has both benefits and risks, whether it’s a prescription drug or an over-the-counter remedy. Understanding these risks, which can include potential interactions with other substances or the possibility that the medicine might not work as expected, can help you make informed decisions. The FDA’s Think It Through: Managing the Benefits and Risks of Medicines page offers practical advice on how to weigh these factors.
Ultimately, doing your own research should empower you to have more meaningful conversations with your doctor, not replace their expertise. By combining what you learn from reputable sources like the FDA with your doctor’s professional advice, you can make well-informed decisions about your health.
Please note this article is for informational purposes and is not a substitute for legal advice.
Mikal C. Watts is Board-Certified in Personal Injury Trial Law by the Texas Board of Legal Specialization and is a Martindale-Hubbel AV Rated Lawyer.