I had four rounds of docetaxal. The shortness of breath and tachycardia only happened on rounds 2, 3 and 4. My dose wasn't altered but I think that was because I changed oncologists half way through and I convinced the second doctor to continue AFTER they did all the tests to rule out anything nasty like blood clot and heart probelms. My LVEF heart levels went down but that was because I was HER2+ and on herceptin which has a direct effect on the heart. That did cause delays to some of my treatments but from memory I think (?????) I had finished docetaxal by then. I also got excruciating bone pain but this they put down to neulasta injection. I got neutropenic after round 1 and was admitted to hospital in isolation for a week. After that I had neulasta for rounds 2, 3 and 4. Bone pain was severe. They gave me panadeine forte then endone but didn't work. I got the pain in my femurs and sternum which again made the ER doctors think I was having a heart attack thanks to severe chest pain, shortness of breath and tachycardia!!!! That's when they rang me husband at work and told him to get to emergency ASAP. The only thing that eased the bone pain from the neulasta was period pain tablets with naprosyn that you get over the counter at the chemist. One doctor said it was fine to take this, then the pharmacist at the hospital said not to take them. I took them anyway. We have to be guided by our doctors but it was reassuring to me that other women were going through the same 'weird' side effect. Even so, it's important to have all the tests to rule out anything. It's only after they rule every out that they then say to you "Oh we think it is a side effect from the treatment." Better to be safe than sorry.
Good luck