Does Perjeta cause watery eyes, and how can I manage it?

Where can I find that medicine water eye s

Where do I find the eye drops

Nothing helped me except finishing. My eyes just poured tears all day long. Gosh I have actually forgotten about that.

My eyes did the same thing, I walked around with a tissue in hand all day. My oncologist recommended putting a heat pack on eyes (amazon - just for eyes) or warm wash cloth will work. Do that daily, I am not sure if it helped but it felts good. Once treatment is over, it will all get better.

Yes, I actually woke up almost blind in one eye. I’m on cyclosporine eye drops. Had plugs put in and 2 yrs later had a laser treatment. Still on eye drops and had more plugs a month ago. I see my opthamologist every 6 months now.

A nurse told me about "Retain" eye drops. It was so bad out shopping with my husband one day, people thought I was really crying!! I was laughing so hard.

I have that due to Docetaxel. I apply warm compress for about 10 mins (dry or wet) should do that at least 2/3 times a day. I also apply Refresh Tears one drop about 2/3 times a day. As someone said it will gradually subside once the chemo is out of the system.

I had watery eyes and itching from Perjeta. Recently switched from phesgo to hylecta and both side effects have improved.

Yes, whenever I stand up my eyes water so bad I have to have a tissue ready or I leave a trail of tears. Wasn’t sure which chemo was causing it but if it’s the Perjeta then unfortunately I have infusions for another 6 months. Ugh! I’ve tried drops, warm compresses and Genteal tears but nothing seems to help. Also Aquaphor around my eyes at night to reduce the redness helps with that

My opthamologist prescribed cyclosporine drops and put plugs in my eyes. It helped. They still water in wind or when snow skiing, but has diminished significantly. I am 2 years post cancer treatment.

Eye docs can put plugs in your tear ducts. That is painless stays a long time and can stop dry-eye caused running of tears.

Watery eyes can be a frustrating side effect that some patients experience with certain treatments. It's great that you're reaching out to connect with others who might have similar experiences - this community is such a valuable resource for sharing practical tips and support. Hopefully, other members will share what has worked for them, and it's always worth discussing any bothersome symptoms with your care team to explore the best management options for your specific situation.