Hi, has anyone ever had a Paclitaxel induced seizure? It happened to me today and was very scary! This was my 6th chemo round, already completed 4 rounds of EC and one round of Paclitaxel 2 weekly. Didn’t have any reaction to the first Paclitaxel round other than the usual bone pain and stomach cramps. I was only ten minutes in to the second round today and my face suddenly  felt really hot, back pain then dizziness and feeling sick and then the next thing I knew I was surrounded by the crash team and was told I had a seizure! They stopped it and my oncologist has switched me to Nabpaclitaxel which I’m starting this Friday. 

Thanks for reading grateful to hear your experiences x