FDA Restricts Hydrocodones
This just plain pisses me off. I’ve never gotten a bottle of any schedule II medicine with a refill on it. I know not a single doctor that will call it in to the pharmacy for you. You either pick up the script from the doctor’s office as a monthly refill (I had a doctor that wouldn’t even mail it across town to me, because he’d had patients “lose” the scripts too many times or tell him they never received it in the mail. I didn’t feel I should have been treated that way because of other patients, but I let it slide since he took my pain seriously.), or they demand to see you every single month. I don’t have that kind of time. I don’t take Vicodin because it doesn’t work for me, but I know a lot of people that rely on this drug during the worst of their Fibro pain, or other forms of Chronic pain. This is completely unfair to them and even worse, it adds to the stigma that pain patients are drug addicts when generally, that is NOT the case. I’ve been treated like this in the emergency room over a migraine (I did not ask for anything for pain, and yet the nurses were whispering that I “seemed like I was angling for something”. All I asked was for them to call my doctor and have him treat me since he was on staff there, nothing else. He was furious when I told him how they treated me and actually said that they should have given me a shot of morphine and sent me home, especially since I had a history and was a patient being treated year-round for migraines.), and it enraged me, so I only see more irritation in the future if a doctor messes with my medication again.