Medical assistance symptoms and conditions

I have only been on Budeprion for a week so I don't know if I am experiencing side effects or not. Yesterday I had hot flashes and dizzy spells, but I attributed them to the warm weather. I've had chronic dry mouth/throat which I heard is a side effect. I've also noticed that my hands have been cold and kinda sweaty, and today they feel pretty numb. I started taking this because I have been battling depression, smoking, and social anxiety for a long time and decided it was time to seek medical assistance. Yesterday I went out and had a good time, but afterwards I had a big panic attack...the first one in months! I think it's too soon to attribute this to the Budeprion XL. They said it could take over a month for it to build up in my system/take effect. Has anyone else had similar experiences?

I am a professional nurse with extreme allergies; however, please for you own benefit consult your physician but do not stop taking it unless he or she states adverse or of course, you have some reaction requiring emergency medical assistance (911).

Yes I am dizzy, weak, very nauseated (and with my emaciated body frame due to other health issues cannot afford to not eat), and the first 2 days of therapy got a whopper headache. However, I had a UTI that likely moved into the kidneys and also look to have stones and after 8 days am passing urine properly and not up every hour not passing urine; hence it is killing an infection that might kill me.

Early on with this drug we did prescribe higher dosages then perhaps necessary they have now cut back quantity and instead of doing BID dosing do QD dosing. You might require a lower dosage at my body weight they prescribed only 250 mg. a day and this has given me some side effects but is treating an infection that could be fatal...

K. BS,RN,UM,QC,DON

Question...I have had migraines for most of my life, the first one I remember was when I was 7. I cannot stomach narcotic pain relievers and was thrilled when Imitrex came out. I took it for years. The only side effects I had were a warm rush, like an alcohol buzz, and sleepiness. Then, 5 years ago I was diagnosed with severe mitral regurgitation. My doctor took me off Imitrex right away and switched me to Maxalt, which I also love. It works great. I had open heart in 2001 to fix the mitral valve, then early in 2005 discovered I have tricuspid regurgitation. No surgery as of yet, thank God. I am on disability for the first heart problem and medicare and medical assistance will no longer cover the Maxalt, only the Imitrex. I took one the other day and almost had to go to the ER. I could barely move, breathe, or speak. Thankfully, after an hour or so, the symptoms subsided. But it really scared me. Now my doctor is giving me all the samples he can of Maxalt that they get in the office.
I am wondering if there is a connection between vavular disease and Imitrex? Has anyone had any of these problems?