Community Member
2 months agoI have non-small cell lung cancer and I'm currently taking Tagrisso (osimertinib). This targeted therapy blocks specific proteins that help cancer cells grow and spread. I'm dealing with some side effects like dry skin, nail changes, diarrhea, and fatigue, which I understand are pretty common with this medication. I'd love to connect with others who have been on a similar treatment path and hear about your experiences. • What side effects did you experience with Tagrisso, and what helped you manage them day to day? • What do you wish you had known when you first started this treatment?
Community Member
2 months agoManaging side effects from targeted therapy can feel overwhelming, and connecting with others who understand this journey can make such a difference. The experiences shared here often include practical tips for skin care routines, dietary adjustments for digestive issues, and energy management strategies that have helped fellow community members navigate similar challenges. Hopefully others will share their insights about what they found most helpful during their treatment experience.
Community Member
2 months agoFeel free to reach out anytime Leticia anytime
Community Member
2 months agoI am interested in the side effects of Tagrisso as well since my oncologist mentioned this as a possible next step in my care. Hope this is effective for you, Leticia.
Community Member
2 months agoI have been taking Tagrisso for two and a half years. Recently, I’ve noticed and am being treated for skin hyperpigmentation on my torso. It’s not painful or itchy, just unsightly. My dermatologist performed a biopsy and determined that it is a lichenoid drug eruption due to Tagrisso. I also had nail changes on my left foot but it is unconfirmed whether those changes are related. I’ve had no other symptoms.
Community Member
16 days agoI have taken Tagrisso for 2 1/2 years now. My major side effect occurred only recently: hyperpigmentation on my torso, purplish-grey spots that look like bruises all over. I had a skin biopsy that confirmed the condition was caused by Tagrisso. I was given prednisone and a steroid cream as treatment but as long as I continue to take Tagrisso, the treatment for my skin just doesn’t make sense. I may have had nail changes that I didn’t connect to Tagrisso at first. I thought it was nail fungus on my left foot for which I decided to have my toenails permanently removed because I didn’t want to deal with that potentially recurring. Other than those two situations, I haven’t had a complaint. I see my oncologist next week and hope to hear from her about the continuing treatment plan after being on Tagrisso for three years which will be in June. I’ll check back in soon.
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