Bottoms symptoms and conditions

I have had electrical feelings in my body since the first day of the first shot.
The first one was a shooting of electricity almost like I stuck my finger in an outlet. I was vacuuming the floor and I threw the vacuum out of my hand it was so intense. I thought that was weird since the handle is all plastic. Then I got another one brushing my teeth and they just kept happening. Now I have electric tingly sensations on the tops of my hands, in the bottoms of my feet, in the crease of my arms and down my forearms, and behind my knee and on the backs of my legs. It sometimes feels like a bug is crawling on me. I slapp it realizing nothing is there. Also have the sensation of an itch that I can't seem to find. I have these sensations all the time.. my face itches and my head itches.

I am also really glad I have found this website. I had my mirena placed in March 2006. I loved it, told all my friends thought it was a miracle. I have completely changed my mind. I have dizziness, headaches, joint pain and my PCP put on Lexapro for anxiety and mild depression in September 09.
I have a 3 and 4 year old, but am so fatigued at times I don't want to do anything but sit around. I can not lose any weight. I tried nutrisystem and
that didn't help. I am also having having a symptom that hasn't been mentioned on the site. I have done some research and noticed that the mirena can also cause blood vessels to constrict. In December 08 after having some (quite a few) drinks and smoking cigaretts at my husbands
Christmas Party the next morning my forearms and hands were a dusty blue color. I have had this happen one time since. A couple of times the bottoms of my feet were a purple/ bluish color looked as if they were badly bruised. After researching the cause of this, the only thing I can find is that the mirena can also cause constriction of the blood vessels. Has anyone else had this happen???? I had and echocardiogram done, that was fine all my blood work has come back normal. Am seeing a neurologist, he has me scheduled for a nerve condition test, but he thinks
I may need to see a vascular doctor.

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

I've been on this med for 6 years. It was not until I started reading this site that I figured out that my problems might be related to Advair use. I've had sore joints/muscles for years. Terrible insomnia, in fact my doctor has me on prescription sleeping pills, but I still can't sleep. I've gained 50 lbs in five years. My eyes bother me continuously. I feel depressed for no good reason. The bottoms of my feel are so sore in the morning that I can hardly walk. I can't exercise - just too tired. (and I used to all the time).

I've recently quit taking advair - cold turkey, but I'm not sure if that's wise. It's been two weeks and today is the first day that I haven't felt very well. I'm wondering how long the body stores this stuff and if I should have weaned off more slowly.

Thanks for all your comments and for this site. What a blessing!

35, male, athletic: i took 3x 500mg and immediately got sore joints and severe flu-like symptoms. i was completely bedridden, loss of balance, sore from head to toe, major bloating and cramping... MISERABLE. this was near the beginning of November. while most side effects have lessened, i have had tendon issues as recently as last week. basically, any "strenuous" exertion will injure the tendons, although i haven't ruptured anything yet. bottoms of feet were sore for a couple weeks for no apparent reason. having trouble remembering words, finishing sentences, etc... digestion seems to be "off", and there is a bitter taste in my mouth that has been there since the beginning. also, "phantom itch" deep in both ears that comes and goes, and earwax production seems to have ceased... weird. oh, and D-R-Y eyes, nose and mouth upon waking. very dry skin as well. it did kill the infection though. i guess i'll be back to normal again someday. i hope.

I have been taking Bupropion XL 150mg ("generic" Wellbutrin) once a day as a mood stabilizer everyday for exactly 2 weeks. I suddenly developed severe itching in random different areas on my body. My lower scalp, palms of my hands, and ankles were the first areas that itched but did not have any obvious marks on the skin as to what was causing it. About 3 hours later it became progressively worse and started showing tiny red raised areas in the previously stated places on my body and started to spread to my neck, wrists, mid-chest below my breasts, behind my knees, and upper thighs near the front panty lines, but even worse on my lower back.

I was becoming a bit scared and annoyed by the constant itching and the hives that were forming in those areas. I had never in my life had hives before. The bottoms of my feet were so itchy but they did not have any hives on them, they just itched! I took 2 benadryl and tried to sleep but woke up quite a bit during the night because of itching.

By morning, the hives were worse and especially on the back of my neck where it was swollen and red and I could not even bend my head back. My face was slightly swollen and my eyes were puffy as well. My right palm was so swollen and painful and I could not make a fist.

I called my doctor but he was on vacation, so I had to talk to a message service he had set up in his absence!
I went to the emergency walk-in care center near my home and was evaluated by a physician who concluded that all this was actually due to the Wellbutrin which I myself found hard to believe and wanted to deny it in my mind. He ordered me to stop taking it and prescribed all sorts of drugs to counteract the hives and itching.

I am writing this only about 9 hours after seeing the emergency physician and have had some rest and taken my prescribed medicines, Medrol ( a steroid-type drug) to treat the swelling, Hydroxyz hcl for the itching, Allegra for allergy, and Zantac for the side effects (stomach pain) of all these drugs I now have to take for a while!
The swelling has gone down a bit and itching has subsided somewhat. In conclusion I must note, that it was the pharmacy's decision to substitute the Wellbutrin my doctor had prescribed with a "generic" version (bupropion) that is still so new to the market and is still undergoing studies on human subjects. We are the guinea pigs and did not even know it.

I have been trying to figure out what is wrong with me since I already suffer with anxiety. On New Year's Day I went to Emerg believing again that I was having a heart attack, as my left hand was so light I couldn't squeeze it closed. After test they determined my heart was fine, but the only way I can find relief is by hanging my left hand (and right hand) over the bed for the blood to flow back. My MD thought I might have carpel tunnel syndrome and I went to see a nerve specialist. They determined I was fine and anxious - of course! To date I'm still waking up in the middle of the night with tingling hands and pains in the bottoms of my feet that shoots upwards. I went on this site, by fluke, I never thought the IUD could do this. I "googled" Mirena tingling hands and feet and 2 pages of symptoms have come up. I realize that I am anxious, and that anxiety manifests itself in many ways, but these symptoms are real. I called my gyno and asked to have it removed. I believe that he won't believe me, as when I told him about the emerg visit, he said "well that has nothing to do with me". Meaning, the Mirena that was inserted. I am going to ask him though to take it out ASAP and also if other's have complained of the same symptoms as I am hoping that this truly is the reason for my discomfort. I'm only 40, eat well, work out 4 times a week and in good shape. Hope this is helpful in determining if this is also a situation for others.

My only problem with Advair, but believe me it was a doozy, was pain in my feet - on the bottoms of my feet. I mean, this pain was so terrible that when I woke up in the morning I could barely walk because the bottoms of my feet hurt that much. All day long I would have to put up with the pain. This went on for almost two years before I decided to quit the Advair. After I quit it the pain in my feet was completely gone within two months. The problem isn't the Flovent in the Advair. The problem is the Serevent in it. I know this because after quitting the Advair I still continued with a Flovent HFA inhaler for my asthma and the pain still went away.

I am on 300mgs of topamax a day for epilepsy, and my side effects are the flat tasting carbonated beverages. But the worst side effects is the feeling in the bottoms of my feet. They feel as if my sox are all bunched up and stuffed between my toes, and knotted up under the balls of my feet. It is a miserable feeling. I get the tingling feelings as well. My wife and I love hiking and I a try to stay in shape by doing 4 miles a day on my treadmill. I am 60 years old. I have to really push myself mentally. I hate this feeling. I don't mind the flat tasted, as I can do without the carbonation anyway, but the feet stuff has got to go.

I had a hip replacement in June, then contracted a staph infection after that (non-MRSA, thank goodness!), for which I have been on a 12 week antibiotic protocol, in addition to having the hip opened again for cleaning and replacement. For the first 6 weeks, I had a PICC line in my arm, which was infusing Oxacillin every four hours 24/7, as well as two oral doses per day of Rifampin. After the removal of the PICC line, I was put on a daily dose of 750 mg of Levaquin (I was also on Levaquin in the hospital, and couldn't sleep for weeks after coming home from the hospital). I have now been on Levaquin for 4 weeks and have incredible pain. The first symptom and most annoying was insomnia, as well as EXTREME rotator ruff pain, stiff fingers, tendor pain in my left elbow, and right knee. I can't walk well, the bottoms of my feet hurt (what's up with that?), and I can't even put on my bra by myself, my shoulders hurt so much. I thought I could take the pain because I just DO NOT want to have the staph infection come back and have another hip replacement, but I think I will actually have to go off of it. It's just too much pain. And I'm worried about long term damage.

I have had trouble with eczema/psoriasis for several years and it has spread to most of my body. Hands, arms, elbows, back, chest and stomach, hips, back-side of my thighs, knees, bottoms of my feet, scalp, inside my ears, forehead, what haven't I mentioned? So far, Prednisone is the only medication I can take that clears it up. Trouble is, the doc won't let me take it long enough to completely clear the rash before I'm tapered off. After reading some of the other posts, I've got to say that I've never noticed any adverse reaction. My appetite is up a little, but my energy level is also up and I burn off any extra calories. I sleep better (no itching) and for longer periods, wake feeling better, have a better outlook for the day and am ready to go. I'm a salesman, so my mental attitude is important, and my wife and family all agree that I'm less moody and in a generally better frame of mind while taking Prednisone. I've noticed no stomach or bowel distress except for being a little less regular than normal. But no constipation and no diarrhea. I'm 61 so a few muscular aches and pains and joint stiffness are to be expected, but I've noticed no unusual incidents. While I don't advocate taking large doses (define large doses???) for long periods, I've read that taking Prednisone on an every-other-day basis can be effective while greatly reducing the risk of side-effects. I think Prednisone has been a real "miracle drug" for me and just wish there was something as effective without the side-effects.

OMG- I wish I had read this before I had this thing put in. Its been in about 4 months, I bled for 6 weeks after having it put in (which was painful), my cramps during that time felt like someone was stabbing me (worse then labor pains) I lost so much of my hair, which is coming back ( I thought the hair loss was from the after pregnancy) that I still have a receding hairline. The bottoms of my feet always hurt, my stomach always looks bloated and I cant loose the extra 10 pounds (which I gained after having it put in) I have absolute NO DRIVE, feel depressed all the time, feel no pleasure in anything that I cant even enjoy my infant son. My boyfriend calls me crazy and unstable because I am so moody. WOW, I am calling to make an appointment to have this taken out ASAP

I'm a 44 year old female, and I have been taking 40mg. of lisinopril for over a year now. I also take omeprazole 20 mg. (a sub for prilosec) every day. Before taking lisinopril, I did have high blood pressure, but since taking this medication, I have had more problems than that. I have an irritating cough all the time and phlegm in my throat so thick that I feel as if I am chocking to death. I also have a severe rash all over my body and on the bottoms of my feet, and on my hands. I am depressed all the time, have no interest in sex whatsoever, and basically feel like crap all the time. I have a very bad pain in the left side of my neck that I know is not a result of sleeping the wrong way. I have to say, I never felt this way before taking this medication, but today I got to the point that I wanted to look up side effects to see if what I'm taking is hurting me. After reading some of these posts, I believe I know what my problem is. My husband was also on lisinopril, but 20mg and had such a terrible cough that we thought he had pneumonia. He is off the medication now, and his cough had disappeared. For me, the rash, and depression is the biggest thing. I have decided to take myself off this medication on my own, and try to find another way to deal with my high blood pressure. If you know of any herbs, and/or foods that help with blood pressure, I would love to hear about them. Thank you all for the information you have posted here. I'm sure it will help others think about what the doctors and pharmaceutical companies are trying to do to us. Seems the more medications they prescribe, the worse side effects we endure. Thanks again everyone!

I am a very healthy 21 yr old. I have always had a slight problem with urinary tract infections, nothing major tho. Doctors in the past always prescribed an antibiotic, usually Macrobid. I went in to see a doctor at MEA that gave me 3 samples of LEVAQUIN. They were each 750 mg. Within 3 days of taking the pills I was unable to get out of bed. My stomach pains were so severe I had to constantly bend over to relieve some of the pain. I had no appetite. My chest hurt so bad I couldn't talk loud, laugh or cough without crying from the pain. My fingers began to swell and became numb. I could barely sleep and when I did it was a very restless sleep. I woke up during the night one night and couldn't feel anything in my left shoulder. It has been close to 8 months since I took LEVAQUIN. I still have problems with my joints hurting horribly. I see spots like you would see after a camera flash in my eyes all day everyday. The bottoms of my feet still hurt if I stand still for a long time. LEVAQUIN is so dangerous. PLEASE BE CAREFUL!!!

In my case, Cipro tablets were prescribed for a potential prostate infection. The first dose was taken on 12/12/07. While taking this medication, I experienced "pens and needles" and shooting pains all over my body, leg pains behind my knees, right groin swelling to the point I could barely walk, and chest discomfort just below the sternum. The chest discomfort started after the second dose. My use of this drug was discontinued on about 12/17/07 (after 6 doses). I threw it away. Read the label BEFORE you start this medication. It's quite alarming after the fact.

I let my physician know about my problems with the Cipro and he then prescribed Levaquin, 500 mg, which is the same class of antibiotic. This was confusing to me later since I told them about the problems with Cipro. The doctor knows best...right- so I took 1 Levaquin per day from 12/21/07 until 12/26/07, again about 6 doses. My symptoms re-appeared after about the third day. Pen and needle pains re-occurred although they never entirely went away from the Cipro, severe swelling and tendon pain behind knees- especially the left knee, some chest discomfort, swelling in the armpits, and groin area. Swelling sensations were most prevalent behind both knees and the armpits. Shooting pains also occurred everywhere in my body, especially in the arms and legs. Shooting pains also occurred in my head and jaw with no warning but were less severe. The bottoms of my feet also hurt at times. Sleep was difficult to come by so extreme fatigue set in. I have been off the Levaquin now since 12/26/07 (5 days) and still have some shooting pains but some of the swelling has subsided. The symptoms have reduced but not disappeared entirely. I will never take a quinolone antibiotic again. My suggestion to others is to file an Adverse Drug Reaction report with FDA on their Medwatch website.

I again saw the physician on 12/27/07 and he said that it's "possible" I could be having a rare side effect. Another physician I know said I was having some type of hypersensitivity to the medication but that he had never come across such a case in his practice. Just my luck.

Struggling with a sinus infection that threatened to bore into my brain, resulting, ultimately, in seizures and death, I've been taking Levaquin now for three days. I'm experiencing anxiety and sleeplessness, however, it's not from the medication. It's from all the hyperbole on the internet.

Look, I understand that many have had adverse reactions to this medication. One dose of penicillin can kill you without warning. At anytime. No warning. I suspect that few of those labellings Levaquin "poison" would ever bother to consider that - or anything else. All wrapped up in your misery, you spout off with rhetoric that is really better left to lawyers and politicians.

If you were uninformed of the possible side-effects of this medication, blame your doctor. I see that the last post here is dated November 2007, and the bottom of this first page takes us to October 2006. Perhaps one could take a bit of responsibility for oneself and do some research on one's own before popping a pill handed out by a disinterested physician. This information is out there - and yes, your doctor could have seen it, too. But he didn't bother, did he? Neither did you.

So, yes, with my first dose, and despite the impact drill driving through my eye-socket, I waited for the seizures, swelling and signs of imminent demise. Nothing. Sorry. Oh, my sinuses feel better, I don't have a brain infection, and so I won't die frothing at the mouth on my living room floor.

I'm sorry you feel bad - and if you hadn't run off at the mouth calling what may be one of the last effective antibiotics "poison", I might mean that with some sincerity. Oh, and lest you forget, antibiotics are poison by definition - the idea being that they affect/poison/kill the source more than they do the host.

So let's stop the hyperbole, and simply say you had a bad reaction to this medication. Not everyone does. Your option might have been to skip the doctor and the meds altogether, and see how you'd fare. But that would leave the responsibility, and the blame, all on you, then, wouldn't it? Far better to spread it around some.

Very bad rash that a week later has not gone away. Nexium actually burned my skin! I look like I have color like I just came from the beach. This is a dangerous drug. it works for the reflux, but the side effects arent worth it. I also develiped hip pain, like it was sucking the calcium out of the bone! The hip pain is gone, but i still have burning, itchy skin, and red all over, less than a week later after stopping, about 5 days off it now. Be careful if you are sensitive to hives, this medicine brought me to the emergency room with swollen hands and feet. it is dangerous!

I am having tingling burning sensation in my feet, legs and hands and arms. My blood pressure was not improving on 5 mg so I upped it to 10 and those symptoms are much worse. The tingling sensation goes all the way up my left arm and up above my knees on my legs.

I have tried to take the Lisinipril before and stopped for these same reasons. My doctor does not seem to think that it is due to the Lisinipril. so I tried it again and the burning, burning sensation is driving me crazy and keeping me awake. I have to get up and stand in cold water for a while to get some relief.

I have not read about anyone with the same symptoms. Does anyone out there have these symptoms??

I am taking 5 mg of lisinopril daily. When I sit for more than 5 minutes or so and get up, it is extremely painful to walk. The bottoms of my feet hurt for about a minute, then slowly the pain goes away. I halved the pill and noticed that the pain diminished. Has anyone had similar problems?