Skin sensations symptoms and conditions

I just went to the Dr. for my second Lupron injection and to get some help with the side effects. Menopausal/emotional me, started crying!!! Gawd! I went in with my list of side effects from the last 3 months (and it was long!) and wondered what was worse, the pain of endometriosis or the life changing side effects of Lupron. My Dr. is wonderful and spent an hour with me; he decided to put me on Provera (progesterone or add-back therapy) for a week to see if the side effects improve. If they do, I get my second dose of Lupron in a week. If not, we stop it all and let my body slowly try to get back to normal (although I have never known what "normal" is since endometriosis) and see how the "therapy" worked. He is strongly encouraging me to follow through with the 6 month course as that is the recommended length of time for the best results. I'm 5'8" and have lost 10 lbs. in the last three months, I'm down to 107 lbs. He told me to try and eat more if I could (although my nausea is constant 24hrs. a day) and make sure to take a daily vitamin and calcium for bone loss. He said that he has never heard of blurred vision to be a side effect of Lupron, "But every woman is effected differently." I'm really hoping the Provera works - any kind of relief is better than this! I'm still having 3-4 hotflashes every hour with extreme exhaustion/fatigue, night sweats, daily migraine headaches, nausea 24hrs. a day, life changing mood swings, and shaky hands. He kept reminding me that this only 6 months out of my life - it's not forever ... forever feels like an awful long time when you can barely get out of bed!

I started taking Singulair only three days ago. I normally am very "body sensitive" and am extremely in touch with how new drugs interact with me. The first day I noticed my heart racing and I had a hard time going to sleep. The second and third day I've felt strange pin prick itching sensations all over my body. I don't want to even imagine how I would feel taking this every day for over a week! Yes, my sinuses are better, but I most certainly feel more anxious and the skin sensations are downright irritating - as if there are small insects crawling in my scalp and all over my body! Yuck!

I experienced a hike in b/p after taking benedryl. I was placed on Lisonpril. After two weeks, I experienced extreme difficulty walking, weakness and fatigue, vertigo, persistent cough, panic attacks and anxiety. My skin felt like I was bathed in menthol or vicks vapor rub. I am not sure if it is the same "tingling" or "burning" that has been reported by others. E/r visits, ekg, cat scans, blood tests came back normal. I received inconsistent medical advice from e/r docs, cardiologist and internist (i.e. stay on the med, but change it, take it only if your b/p is high, get off of it completely- you dont have high b/p and dont need it). I decided to get off of it. Its been three weeks off the Lisinopril. I have improved daily; however, I am not back to normal. Anxiety and "menthol-like" skin sensations still remain. This web site has helped tremendously with jsut knowing that I am not crazy or alone. Thanks.

i started on 25mg/day for first week. worst side effect was severe jaw tension which caused headaches and insomnia, also slight nausea and weird skin sensations (very much like coming down from acid/e). went up to 50mg for month or so, then 75mg, now on 100mg - this seems to be the right dose for me at the moment. planning to go back to 50mg in about a year. side effects seem to last for a week after changing dose. but the very first week was worst. i noticed benefits after about two weeks. i was really worried that i would feel zombied and have no libido - not the case at all. thats what i was like before cause i was so depressed. very glad i started on small dose, and changed gradually, i can imagine doing otherwise would suck big time. my most important message - ZOLOFT IS ONLY PART OF MY TREATMENT. my doctor helped to develop a treatment plan which involves yoga, affirmations, identifying negative thoughts and behaviours and changing them, seeking help from other sources (university counsellor), eating well, maintaining more regular sleeping patterns, getting out in sunlight and fresh air etc. if your doctor won't help you with this, or doesn't care about your side effects, or whether you're on the right dose - FIND ANOTHER DOCTOR!! there are also good websites like depressionnet, beyondblue and anu.edu.au/moodgym

I was given Levaquin 500 mg a few days ago to treat 2 conditions: a sinus infection and an infection in my foot. Within a day, I had a horrible rash on my arms and legs, and I felt terrible. Unfortunately, I had taken the 2nd dose, so a total of 1000 mg. I was also developing stiffness in my joints. I had taken Levaquin several times before, prescribed by an ENT, for stubborn sinus problems, and didn't seem to react to the drug. But this time I certainly did. I was taken off Levaquin and put on another antibiotic. But the side effects have been awful. The rash is pretty much gone, tho I still have some prickly skin sensations. The joint stiffness in my hips is much better, but my fingers, wrists and forearms are still sore and stiff. I was told Levaquin has a 3 day half life, so I am at about day 5. I am just hoping all these symptoms subside, but I am not expecting it to be a quick deal. I think Levaquin is extremely toxic. I am a 56 year old active healthy woman with an 11 year old daughter still being raised. I am grateful my side effects weren't any worse. I am going to register a complaint with the FDA and I wish there were a class action suit against the manufacturer's of this awful drug.