Hi everyone,
I am currently on Endocet 5/325mg. I take 4 to 6 tablets a day. I have Lupus and Sjorgrens Syndrome. It took one full year, before I was diagnosed by a simple blood test. Before that I was taking Endocet for migraines. But, then when I got Lupus I take them even more now. However, I am still in so much pain. I am not sure what else to do. I still feel like the dose is too low. I don't feel that morphine works, either. Endocet does, but when it wears off you feel it! Any suggestions. I will write more, but write now it hurts to type.