Funny bone symptoms and conditions

I am very glad I found this site. I have been taking Prilosec OTC for 3 years now and it took care of my acid reflux. I woke up 6 months ago feeling like my "funny bone" got hit but never subsided. I then learned it was possibly my ulna nerve. Burning sensation in my left pinky finger and half my ring finger. Anyone experienced this? I switched to a generic Omeprazole at Walgreens a couple of weeks ago and I have experienced the most excruciating sharp, shooting pain in my neck, shoulders and lower back and sometimes other joint areas. Anyone experience this with the generic brand? I am going off of it and see what happens. The pain is intense!!! Thanks for this site!

50 year old male, prescribed Singulair 8 months ago to assist with allergy problems while taken allergy shot treatments. About 2 weeks ago started experiencing numbness/tingling in right foot, then both feet, the spreading up the body to above the waist. The best way to describe the sensation is a combination of the feeling you get when you hit your funny bone and the sensation when you sit or lay in a position that puts one of your limbs to sleep. Had all the blood work tests done at Dr. office to verify no other issues, all blood work is normal, Dr. suggested could be a neuorlogy problem and more tests will be necessary. Receive routine Chiropractic treatments and had him check everything, including new x-rays, nothing there. Read the side effects again for Singulair and realized that this numbness/tingling is just one of the symptoms I have had since starting this drug. The others being unusual weakness, tiredness, which I thought was just part of getting older and severe sinus inflammation, which I had thought was just related to my allergies. Have contacted my allergy doctor that put me on this and he said to stop taking Singulair to see if my side effects go away, since I am near the end of the time that he expected me to take them for anyway.
I will repost after a few weeks or as soon as the side effects go away.

I was taking Levaquin for a sinus infection. After taking the first dose of 750 mg, I noticed that I started having tingling and numbness in my hands and arms. After the second dose, I started feeling the same tingling and numbness in my arms, hands, and legs. Because I had been having severe headaches anyway, I started wondering if I had some kind of neurological problem and my headaches were linked to the strange sensations. However, I noticed that I didn't have any problems with my arms and legs until after I started taking Levaquin. Some of my other symptoms were: tightness in my neck muscles and sore muscles. I also remember seeing a flashing light from the corner of my left eye and floaters. I stopped taking Levaquin after just 2 doses because it began scaring me and I feared what might happen after my third dose. I can't afford to take any chances with my health. That's why I appreciate this post, and I see that I wasn't just imagining these side effects. Since I've stopped taking this medication I still have problems with my arms. They feel heavy like I've been lifting weights and the ache. A couple of times, I've had to take pain medicine for the pain in my arms because they've hurt so bad, it feels kind of like when you hit your funny bone and you try to figure out why they call it a "funny bone" because it's definitely not funny! My arms hurt so bad I couldn't lift them, and I could type or write so I just took some medicine (tremadol) and laid down. It's been weeks since I've taken levaquin, but I still I have sensations and aching and heaviness in my arms. Has anybody been off of Levaquin for a considerable amount of time and found that the symptoms go away? Please give me some hope! :) Thanks.

I have only been on Aciphex for 1 day, and I have tingling/burning in my arms and hands! My stomach feels great, I can actually eat without curling up into a ball on the floor in pain, but I don't like this tinging, almost funny bone, feeling.

I had a severe poison ivy/sumac reaction and slowly the swelling in my face reached the point of affecting my breathing, so I had an emergency treatment with Prednisone. This was my first experience with this drug. (I am not one to use allopathic medicine unless it's an emergency.) The first dose was shots, then I was put on a "med pak" of methylprednisolone, to be used for 5 or 6 days, tapering down the dosages day by day. By the third day, I began to find the side effects increasingly intense. I had had a mild headache, some chest pressure, funny bone aches, stomach/liver aches, as well as sensations of spacy-ness, floating feelings, difficulty focusing my eyes at times, and my attention, etc.; but the chest pressure was what worried me most. It was all on the left side. I eventually called the doctor because the pressure and discomfort was beginning to become severe each time I took a pill. He agreed to let me stop the prednisone. I had about 2 days left of tapering to one a day, but couldn't stand to take anymore. It was beginning to feel like a life or death situation! (My rash is flaring a little now, but not seriously. I am using alternative remedies as well, and things don't seem to be reversing to where they were, thankfully.) I had missed quite a bit of work, and did not feel like myself. Yesterday was my 2nd day off the pills, and I stayed home to work on flushing my system of the prednisone. I felt like I was going through withdrawal. Today I feel much more like myself. I know now that a lot of the "sickness" I was feeling wasn't just an allergic reaction to a plant--I was sick from the medicine as well. In fact, I think it was more the medicine than the poison ivy that kept me out of work. I appreciate the use of something like prednisone in emergency cases...it may have saved my life...but from now on, I'm going to do whatever I can to avoid having to ever use this drug again. It was clearly very damaging to my body. I hope I was able to eradicate it enough, and was not on it long enough to cause any permanent damage. I have not noticed any more pain in my chest since stopping the medicine. (I may, however, insist that my doctor run some tests to make sure there isn't damage, although the damage might not be something they could easily measure at this point. I have no history of heart problems, and a stress test a few years back came out great.) I would seriously encourage anyone who has to use prednisone more than a few days to look for alternatives, or insist (to your doctor) on alternatives (that hopefully won't be worse). This drug is VERY, VERY toxic and dangerous!! I'm very aware of how my body responds to what I put in it. A lot of people aren't as in touch with their body's responses, and may start on a roller coaster of treatments as things come up, not realizing that the problem may have to do with their medicine. I believe this is the case with a lot of the elderly who frequently end up taking pills to remedy the symptoms created by other pills! Good luck to everyone, and God bless us all!!!