Left hand symptoms and conditions

I took Zocor for 25 days when I suddenly had such pain at night in my upper arms that I couldn't raise my arms up at all. It's been 2 full weeks since I stopped taking Zocor, and every single night around 7 I develop severe pain somewhere in my body, usually in my hands, knees or feet. It's in a different place almost every night. Tonight it's in my left hand across the whole top of my hand, below the wrist. Can Zocor cause this kind of pain so long after stopping taking it? And I only took it for 25 days! Please help - this really hurts and I hope it will improve.

I took my 2nd Avelox pill at 10am this morning, by lunch time I felt very jittery and anxious, and had isolated tingling in my left hand and foot. Tonight I had severe abdominal pain and then the subsequent emptying of the bowels (ok, that's gross!). I am a healthy 39-year old woman who has never had any side effects from medication. This was prescribed for a sinus infection. Thank you all for your posts about your experience with this horrible stuff. I feel better knowing that I'm not going crazy. Unfortunately, because this is a once-a-day pill, this stuff is still in my system. For those of you who are posting on this site saying you've had no side effects and this medicine worked great, you probably work for Bayer in their PR department....if not and you really did not have any side effects, this site is for those of us who HAVE had side effects.

ok, i have been on lisinopril 10mg hctz for about a year now. sometimes i feel the cough, sometimes my throat fells tight , but one thing that scared the hell out of me just in the last few weeks was a sudden bald spot on the top of my head, granted i am 50, but i have a reasonable head of hair, i also, to my surprise found a little bald spot usually where a man does not go bald down toward the back of the head. I just walked by my haircut lady to ask her if i had this bald spot two months ago and she said no way and to hurry and see a dermatologist, i am truly thinking its this dam drug, anyone else experience sudden hair loss in strange places on the head? thanks.

I have had rheumatoid arthritis for 20 years,controlled reasonably well with a combo of methotrexate, naproxen and enbrel. I do a 10 day course of prednisone several times a year for bad flares. I absolutely hate taking prednisone because it turns me into a crabby, edgy, insomniac who can't stop eating. It makes me bloat and that REALLY makes me nuts because I've done so well at weight watcher's, I don't need that nasty, upset stomach over full bloat feeling. And the "roid head" headache thing ? I'm on the phone all day at work so that's bad, too. The insomnia is the worst, really, because I just lie there awake. When I stop taking it I return to normal within 2 days. I only do it when I am absolutely desperate - I already lost some tendons in my left hand to arthritis related damage so I tend to use the prednisone when the fluid builds up in the right hand or if I'm really too sore. I'm also aware that long term prednisone usage is a one way ticket to osteoporosis / osteoarthritis, so I really have to feel like I cannot deal before I take it. It's a hate/hate relationship.

I don't know if the lisinopril is the cause but I have had may things going on and something caused them. My feet and legs itch until they feel like there on fire. My hair seems to have just died. It's crisp and breaks off when I comb it. I have used all kinds of products trying to strengthen my hair but no luck. My pinky finger and the ring finger on my left hand have been nump for several months. When I comb through my hair I hit a spot that shoots pain to my right ear. My doc said the numb fingers was from proping my elbo on my desk. He said it would go away if I propped it on something padded. So for several months now I have used a foam pad about an inch thick to prop it on. There still numb. And the muscle in that had has weakened. In Aug. I was rushed to the hospital. my potassium was very low. My colon was infected. My kidneys were infected. My temp was 104. My whole body was shutting down. Im still taking the lisinopril 20/25. I am calling my doctor tomorrow and tell him im not taking it anymore. Im so glad I found this site. Now I at least have an idea why im falling apart.

I'm 54, started taking lisinopril in jan 09. I took for about 3 months and noticed a decrease in libido. My pressure was pretty much in control, so I stopped taking it. I started again around 1st of Aug 09. Approx 3-4 weeks later, I began to experience severe pain in my left shoulder and arm. It began to move into my neck and back. I went in for an EKG to ensure I wasn't having a stroke. It was normal. I experience dizziness and headaches. I wake in the night and my 2 left fingers on the left hand are completely numb. The pain in my neck is now moving to the right side and some shoulder pain seems to be apparent. I noticed pain in other joints as well. I'm unable to work out at the gym as I usually do due to the pain my my left arm. I highly suspect these symptoms to be caused by lisinopril. I've been taking 20mg and was just switched to 20 mgm Hct. a week ago. X-Rays were taken of my neck and shoulder last week. Haven't' heard from the doctor as of yet. I was on Diovan before I lost my job and health benefits. As a vet, the VA put me on the Lisinopril. The Diovan worked fine for me, too expensive for us vets I guess. I am discontinuing the Lisinopril as of today 10/24/09. I feel like I imagine a ninety year old would feel with these aches and all. I havent' admitted it, but I believe I'm feeling mildly depressed as well. Let's see what a week of purging this from my system does. f. D.

I was in the hospital for a gall bladder surgery 2 weeks ago and found out while in there I had a UTI. The doctor's at the hospital put me on Clarithromycin the first day. Then my family Dr. came in and changed it to Levaquin via IV drip for another 6 days. I was then prescribed 2 pills for when I got home to take. The first 2 days in the hospital I had pain in my shoulder and I know that was from the air they blew into me for the surgery. BUT, after that, I have had continued shoulder, neck pain and now has spread into my wrists, my legs, virtually I feel like one big ache. Last night, I had to take my shirt off because it was hurting my skin for the shirt to touch it. My sense of taste is weird too. I have Ehlers Danlos Syndrome but I know that my pain right now is a direct result from Levaquin. I went in to fix one problem and came out with another one. Like I need that! I feel for all of you. I identify with most all of your complaints. I was on the drug for 10 days. I can barely grasp anything without pain in my left hand. I don't know what to do. Does this go away? Or is this permanent?

Within 5 days after beginning Tri-Clor treatment, I began developing very bad indigestion and panic attacks similar to the feelings I had while recovering from Gall Bladder and liver drain surgery.
The second effect was the sudden arthritic swelling and pain in the fingers of my left hand which is my dominate use hand. I stopped immediately taking the Tri-Clor The indigestion went away in one day. The pain and swelling in the hand mostly the palm and fingers, has persisted for almost a month and does not respond to the usual treatments of Chondroitin and Glucosamine.

I have been taking Doxycycline Hyclate 100mg twice a day for 6 days for a tick bite infection. I've developed a rash on the palm of my left hand. It doesn't itch, but burns a little. My doctor says it's not an allergic reaction. I need to get rid of my illness, and the rash really doesn't bother me that much. What I fear are what internal side effects I might be having from reacting to the medicine.

I take lithium, 1350mg/day, for 5 years now, and about 2 years ago I started getting tremors but worse in my left hand, so it was actually painful and for a while the doctor thought it was carpal tunnel but it turned out not to be and he didnt know what caused it-now ever since then my left hand has gotten worse & typing with it is a little problematic, its like the nerves are messed up in that hand, it won't always hit the right numbers. Its starting to freak me out a little, but in the last year I've started having episodes where my entire left side goes tingly like its asleep, my vision blurs, I get shaky all over and have such rapid heart palpitations it feels like my entire body is in shock. This lasts for about half an hour usually, has landed me in the ER twice, & they claimed each time not to know what caused it and looked at me like I was making it up, and didn't give me anything for it. I also get the typical symptoms- mild hair loss, memory loss, speech impairment, weight gain (I was 120 now I'm 160- luckily it distributed so its not too obvious), & it does not stop depressive episodes, just shortens them, and I still get anger episodes fairly often, usually as a split second reaction to something very small. I'm definitely looking into getting off of this as it is worrying me, more about the episodes and my left arm/hand issues than anything else, especially that now I have trouble with coordination in my left hand,which sucks because my desk jobs always involve a LOT of typing.

I have been taking Eltroxin for over 8 years due to treatment for Hodgkins Disease (cancer of the Lymph nodes, glands) the side effects I have noticed are headaches, blurred vision, lack of energy, sore joints especially knees, weight fluctuations, stomach cramps, heart rhythm increase, numbness in my left shoulder & arm and sometimes my little finger on my left hand is completely numb, sleep irregularity, night sweats. I cant seem to find any specialist who will listen to me. I have stopped taking them from time to time and most of the symptoms disappear but my metabolism slows down so much that I have no alternative but to resume taking them.

i am 29 yrs old and i had mirena put in about 7 weeks ago. For the past 2 weeks i have experienced anxiety and feelings of hopelessness. I have always been very optimistic and now I just feel kind of blah or flat. My mood can change instantly and I have been definitely taking my anger out on my poor family. I feel lightheaded all of the time and have had heart palpitations. I have had the cords cut 3times and my husband can still feel them which makes sex horrible. My back has been hurting and i have been experiencing sharp pain in my left hand. My hair has been oily lately. Thank God for these blogs bc i thought i was losing it or maybe just stressed with 2 kids but this is definitely not normal for me. I used to have a lot of patience and now I feel like i can not tolerate anything. I am having my mirena removed today and i cannot wait to feel like myself again. I would not recommend this to my worst enemy.

I am so relieved to read all of this. Now I know I'm not crazy. My hair is falling out, I have flutters in my tummy. Thought I was pregnant for a minute there. I had Mirena put in 09/2008 two months after my daughter was born and I CAN NOT shake my baby weight. I am a mother of 4 and have never had this problem. My left hand is in pain, I have off and on numbness. Sooooo my appt. to have it removed is scheduled for 07/28/2009. Thank God for this site because I truly thought was was loosing my mind.

To everyone out there that has issues with doxycycline...
Now i fully understand the old saying that nothing is free in life.

I got it for lyme disease 7 days ago, and it was one of the free prescripts from my grocery store (great i thought). Little did i know how powerful this stuff can be. For the last week i have basically had severe headaches and wanted to give up on life. I didn't want to work out, didn't want to go to work, had chest pains, muscle spasms, and DEEP DEPRESSION....
now i know why this is free, because after it gets you so depressed, they figure your doctor will put you on something to get you out of depression, a money making drug. This is probably the meds talking still (i stopped yesterday after what felt like a complete and utter mental breakdown). Regardless of my silly conspiracy theory, i am glad i stopped taking it, and i hope that i start feeling like myself again.

i have inserted mirena in jan'2007 to control excess bleeding. but now i am 44 years i feel numbness in fingers of left hand. get depressed quickly is it due to mirena or something else. let me know

roopa anto

Has anyone had side effects pop up after 3 years? Yes, you heard me. Three years. Hair falling out. Joint pain. "Foggy headedness." Chest discomfort. Gotta be that. Please share.

Been on Wellbutrin for almost 6 weeks now. Last week I started having a really itchy scalp, no flakes, just itchy and then bumps would appear where I had itched. My vaginal area was also itchy and I treated myself for a yeast infection unknowingly. This past weekend I broke out in what I now know was hives (urticaria angioedema). First my left ankle swelled (3 inches) and looked like it was sprained, but instead it was super itchy and then became achy and painful. Within 24 hours that ankle went down but the other side swelled up so badly that I had pitting edema in my ankle and could leave dents in it. The third day, still with constant scalp and ear itching, i developed hives and large welts on my inner thighs as well as a large welt on my shoulder. I have been taking benadryl, which seems to help the itching for a little, but not for long enough. Yesterday I was at work and my butt started to itch so badly I had to leave. I had developed huge welts in the creases between my leg and butt right were one sits on a chair! Huge 3-4 inches. I was so uncomfortable. My thumb also had swelled up and I could not move my left hand without burning itch and pain. I finally called the doctor and set up an appointment.
I was told to take benadryl 25-50mg, zantac 150mg twice a day, and Zyrtec once a day to control the hives. This has helped a bit.
When I saw the doctor today and we went over everything, the ONLY change in months has been the addition of the Wellbutrin. I am going to stop taking it today and since my story sounds much like the ones below hopefully this will improve before my eyes or throat swell! Thanks for all your posts.

I took Avelox for 4 days and stopped for various reasons. My left hand became numb, I experienced bouts of anxiety and persistent nausea. Fortunately my sinus infection cleared up, but I wouldn't take this medication again.

My doctor had me on a 10-day course of amoxicillin for a sinus infection. By the last day, I had contracted pneumonia and the sinus infection had rebounded until it was worse than ever. So, like many others who have posted here, my doctor prescribed Avelox. Fortunately I read the entire printout from the pharmacy, including all warnings of potential side-effects, both minor and serious. I grew concerned on day three when I had numbness and tingling all down my right arm, and following the warnings, called my doctor. Fortunately, my doc is a smart guy: he told me to stop the course of Avelox immediately, and if the nerve symptoms returned, I should go to the ER.

Some of the symptoms others here have mentioned -- many far, far more serious than mine -- seem neurological, as if the drug is also messing with brain function rather than just causing an allergic reaction (especially the seriously altered mental states).

A symptom that has occurred occasionally during the past weeks since I stopped the Avelox is an odd tremor in my eyes when I'm tired. My eyeballs shake quickly and sharply from side to side for about 10 seconds at a time. I had a similar reaction many years ago, when my doctor at the time prescribed a high dose of Paxil (anti-anxiety). The difference was that then the eye tremors stopped two days after I stopped the drug; the symptoms now started long after the Avelox was out of my system.

I linked to this webpage specifically because I was wondering how common adverse reactions to Avelox are. God knows we need some new antibiotics to fight the increasingly more resistant strains of bacteria. But if our bad experiences are as common as I fear, even though some people experience wonderful results, this is one drug that should be prescribed with extreme care. Not only that, but both the physician and the pharmacist should be especially diligent in explaining the more dangerous adverse effects so that patients (who don't always have a half hour to read through hundreds of single-spaced lines of instructions on drug sheets) are well-informed enough to participate in our own care. If that just means telling our doctors that the risks outweigh the benefits, please prescribe something else, so be it.

Hi my name is Chistopher.
I just have a bad experience with this medicament, my reaction is wired
my peanus start eaching realy bad it feels like is burning and then my left
hand start turning red and burning until it got black purple. I didn't know I was alergic to sulfamethoxazole, as soon as this happened I just stop taking this medicine, then I eate a lot of garlics and cactus nopales and all my allergic reaction go away like ten minutes after I eate that.

I have been on 10 MG of Lipitor for almost 3 years. Since I began taking it I have had recurring issues with an anxious feelings, my lower GI is constantly churning and I feel like I am stressed out. I have a low stress job, a stable happy family life and yet I feel nervous all the time. I sleep for 3-4 hours and then wake up and am unable to get back to sleep. I have been forced to take a nap ever day after lunch just to get through the day. Additionally, I developed tremors in my hands and was diagnosed with something called Benign Essential Tremor and put on another medication to control the shaking.

Yesterday I decided I had enough of this and went to see my cardiologist to discuss the symptoms. I stopped taking the Lipitor on my own 2 days before. The doctor told me that none of my symptoms were related to Lipitor! I replied that I was convinced that they were all in fact caused by this drug. He suggested I stop taking the statin for 2 weeks and see if the symptoms stop. I am now on day 4 without lipitor and am already feeling less anxious.

I went to the Nuerologist 2 weeks ago and got her to discontinue the anti-tremor medication. I am going to get all this crap out of my system and hopefully get my life back.

My dear daughter age 10 with history of EhlersDanlos Syndrome and Asthma, Has always been on her regular treatment of QVAR and Albuterol from the time she was a baby ,Today I took her for a recheck of her pneumonia,found out she lost three pounds in a week and he started her on a Nebulizer machine first dose today went find .Second dose half way through we stopped her machine to see how much she had used and her left hand was curled up and she could not control it ,She had the jitters to go with this . Her hand was weak and at bedtime was still week. Dear husband says she wont take that again and we are following up first thing in morning with doctor. I am doing my praying tonight!!!!!
Double check with doctor about side effects .

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.

I was giving prednisone for only 5 days (not sure about dose, but it tapered to one pill on the last day) for a bronchitis induced severe asthma attack. I have only had asthma twice in my 50 years, both times associated with a bad case of bronchitis. The "doc in the box" reduced his original dosage due to the 3 corisone injections I recently had in my spine. After reading these posts I feel grateful I wasn't on a higher, longer term dose. I have some of the same side effects listed here including uncontrollable appetite, fat gain around the middle, water weight gain, constantly having to urinate, superhuman energy, heart palpitations, and approximately two weeks after finishing, I began to get a mustache (hairs that were previously white became brown over a two week period). I have read on the internet and been told by my pharmacist that this is temporary. I have also read and been told that the 2mg estradiol I take every day since my hysterectomy causes the body to retain and not rid itself of the steroids as it normally would (estrogen is actually listed as drug interaction with prednisone). The doctor in the box apparently just ignored this interaction and prescribed it anyway. However the main reason I am posting is a very strange possible side effect that occurred approximately 1 week after my final dose. I was awakened in the middle of the night with SEVERE pain (felt like bone pain, not muscle) in my right knee that lasted until morning. By mid morning it was gone. The next night I had the same experience but in both knees. It lasted about 5 more days, gradually tapering in intensity, and then just went away. I do have severe arthritis in my lumbar and cervical spine, having had surgeries to repair injuries from a snowmobiling accident. I have normal arthritis elsewhere for a 50 year old, but have NEVER had issues with my knees. Has anyone had this strange symptom? None of my doctors (internist, rheumatologist, physiatrist - who gave me the injections and prescribed physical therapy for my spine) had any explanation. The only explanation I have is the prednisone because I had taken the Z-pac (antibiotic) with no side effects several times in the past. Weird!

Incidentally, I am off the prednisone for about 5 weeks, am still hungry all the time, still fat, still bloated. Unfortunately the extra energy is gone. Best of luck to everyone on this strange drug. My heart sincerely goes out to all of you on long term therapy. God bless.

Thanx for this site. I took Doxy for 3 days (100mg twice a day) and i woke up with a terrible headache on my right forehead. I took ibuprofen then my left hand started shaking and my heart was beating so fast. I ended up calling 911 thinking something was more serious with me but by the time the paramedics came my pulse and heart beat were normal. Almost 48 hours later i still had the headache and now was having shortness of breath, feeling tired, back ache, panic attack and light headedness. I called my DR and she said i probably just needed some rest. No mention of some possible side effect to doxy so i used my initiative and googled this stupid doxy drug..Wow the results were very helpful and now i know its the doxy doing this to me for sure. I stopped taking it right away which is after only 3 days after but my body hasn't gone back to normal. No more shortness of breath but still have back ache, Oh and for some reason i cant sleep..its 5 am right now and am on my computer..so i think i'll add insomnia to the list of side effects..NEVER AGAIN WILL I TAKE DOXY