Tingling in hands symptoms and conditions

I took my daughter (14yrs old) off of Singulair 2 nights ago after being in the ER. She's been taking this drug for 3 years off and on. We were told she had asthma 3yrs ago and now yesterday after taking the Methacholine challenge test, she doesn't have asthma. Talk about being confused and angry. Over the last three years my daughter changed into a very anxious person, couldn't sleep at nights, very vivid dreams that made her surround herself with pillows thinking her dreams were real, sadness, chest pains, tingling in hands, arms & legs, knee pain (could be sport related?) and a very short fuse. I came across another website and then this one about the side effects of this drug and immediately took her off. She has slept better the last two nights but still has a little chest pain (indigestion), which I hope subsides soon. This has been a terrible stress for her and the whole family and I'm praying being off this drug will help my daughter restore her self confidence and happiness in her life.
A.

hello again ladies. i'm 3 weeks 4 days post removal of mirena and i'm just having my first proper period. it is heavier than normal, but bearable. i was just wondering if anyone else has really bad headaches after removal. i'm not usually a headache sufferer, i was wondering if it could be hormone related.
the heartburn i was previously experiencing has completely cleared up, (so far) the pregnancy feeling has gone and i'm no where near as agitated or moody. i'm so glad i had the evil device removed i do feel better but not completely yet.

also i don't know if anyone else has the the same problem, but i've been having blood tests because i was feeling ill and having joint pain. i had blood tests which showed a raised esr level. i had the test repeated 3 weeks post removal and its the level has dropped quite a lot. it was 20 which is the lowest result i've had so far. i've been tested for lupus arthritis etc, could mirena have been the culprit all along? hmmmmmm..........

Hi all! Well I got my mirena taken out on Wednesday. The Dr. was very sweet I told her my symptoms and she said lets take this out then! While she was down there she said " Hmm I'm going to look at a swab under the scope." She came back in and said that the mirena gave me a bad infection! I had to take some strong one time antibiotic that killed my stomach! I can't wait to start to feel better. I did notice I can see a lot better then I did, no more blurry eyes. The last 3 1/2 years have been utter hell for me. I've been in and out of different Dr. offices not finding anything. I was dizzy all the time, I started out small after I delivered my baby and gained 60 lbs since it was put in. I had a shooting pain on my right side, horrible anxiety attacks, blurred vision, fuzzy mind, head aches, ovarian cysts, lower back pain and bloated belly. I am so relieved I got this disgusting thing out of my body!!! I hope my life will go back to normal now.

I lasted a whole week with Topamax! Side effects I experienced were flat, bitter tasting soft drinks, minor tingling in hands and forearms, some dizziness, and some decreased sensation during sex. But on day 6, shortness of breath set in. I wasn't aware that this was a side effect of topamax until I searched the internet. I'm so grateful for all of the posts here. On day 7, I took my last 25mg topamax and expected my breath to return to me. That was 6 days ago and I'm still waiting.... I've read that it takes 6 days for topamax to clear your system, but I'm eager to hear of accounts as to how long it took for side effects to disappear. Can anyone throw me a bone?? I keep telling myself that tomorrow it will be better, but "tomorrow" hasn't come. All other side effects are gone.

I have pitting edema in my lower legs that will not go away with diuretics, two teeth broke off, enlarge abdomen, pain and tingling in hands, pain in my left knee, one sore throat after another, and I get a foul taste in my mouth without warning.

IF YOU FEEL/EXPERIENCE ANYTHING ABNORMAL FOR YOU OR DO NOT FEEL QUITE YOURSELF SEE YOUR G.P./NURSE AND SERIOUSLY CONSIDER GETTING THE MIRENA COIL REMOVED
This medication may be suitable for some people but if you experience any of the following, I urge you please, please please, 'demand' that you want the Mirena removed. My symptoms were noticeably worse around my time of ovulation. I've also found out that people previously treated for/suffering from depression should not be prescribed this medication. (I've been on Prozac in the past). I had it fitted in Aug 2007 to combat very heavy periods and severe PMT at the recommendation of my G.P.and had it removed Sept 2008. Symptoms I experienced :-

Dry/furry mouth
Headaches (over time these became migraines)
No concentration
Poor memory
Lethargy (constantly tired and drained)
Smelly discharge (still noticeable straight after washing)
Very heavy legs
Numbness in my legs
Joint pain and clicking (mainly in my shoulders and knees)
Developed facial hair (mainly under chin and jawline)
Hair loss
Weight gain around my stomach (without increasing my food intake)
Feeling constantly bloated.
Spotting randomly for duration of Mirena being fitted. (Brown spotting)

Panic Attacks ( awoken in the middle of the night with them) escalating to the following:-
Palpitations (for no apparent reason)
Clammy/sweating palms and feet
Aggitation ( during an episode if someone was talking to me I wanted to really yell at them 'Just shut the **** up! You're doing my head in!)
Feelings of madness (actually wanted to run away from my own mind)
Pins and needles/Tingling in my hands and feet
Electric shock like surges going through my body (my nerve endings were obviously suffering)
Muscle tremours/shaking (mainly arms and legs)
Eyes became extremely light sensitive
Heightened awareness of sound

Insomnia
Terrible nightmares
Depression
Feelings of detachment from the real world.
Visual disturbances
Episodes of blurred vision

These symptoms did not appear straight away but appeared gradually and with more veangance the longer I had the coil. The more concerning episodes I experienced happened after about 3 months and very erratically. I could not predict when or what time of day I was going to have an episode or pinpoint any reason for bringing on an attack. I had no control over the effects, was absolutely petrified when I experienced a panic attack and just had to ride it out.
All my G.P. did was prescribe me anti-depressants to which I reacted badly. Blood tests also failed to show anything abnormal.
I even tried herbal medicines as an alternative and experienced similar reactions to the prescription drugs. I've now become very pill-phobic and would rather ride out and get over symptoms myself. Paracetamol & Ibuprofen being the only medicine I trust to take now. I had a horrendous year and everyone suffered. Not only my family, but I was signed off of work for 3 months. It was a very worrying time for my husband and my children, who all had to keep an eye on me and witness the effects of my symptoms. On looking back now, I don't know how I managed to function at all and even do my job. Most of the time my energies were spent concentrating on trying to appear normal and held-together to the outside world.
Although I feel 100% better in myself, I noticeably experience more migraines and headaches than I ever did in the past, along with palpitations, usually during my week before. Two days before it I often really feeI like I'm losing the plot! I also really bloat up now a week before my period, feel sick and have a feeling of being ' very full', so am hungry but don't really want to eat. One of my big toe-nails has gone black over the past few months and not through injury. This has just been sent away for analysis. The one on the other foot is raised/ridged/thick/yellow, but normal growth has resumed half-way up now, which I feel co-incides with the state of my health on having Mirena removed. The nurse I saw recently explained that it is true that nails and hair show the history of our health so, for me, this would seem true.
I wish I'd been made fully aware of all possible side-effects of this medication and am now actually concerned that the effects I've suffered may have left some permanent damage.
In spite of all this, it's so good to be me.

I am so happy I found this web site i literally thought I was loosing my mind
for the last six months to a year since being prescribed omerprazole I have been to neurologist for tingling in hands, arms, feet,face,head and arms . I have been to the rheumatologist for unexplained pain in my feet, back,stomach.I have made numerous trips to the emergency room for chest pain, lightheadedness only to be told by all of these health care professionals that nothing was wrong with me. I feel so relieved to know that I am not crazy
because that was my next stop the mental hospital

I took it for 3 days with extreme nausea, some heart racing, palpitations, headache, restless leg and insomnia. Then 4th day, I was afraid I needed to go to the ER - extreme heart racing, palpitations, numbness in left arm, tingling in hands and feet and feeling like I was about to faint. I waited it out for an hour and a half and is slowed down. But now after about 18 hours, my fingers are still tingly and feeling heartbeat in my neck.

My dermatologist prescribed it for an infection after a derma-filler injection. The side effects were not discussed. My ENT agreed that the med was best for my infection but did not seem concerned over the initial symptoms.

I have a heart murmur and cannot take anything containing pseudoephrine - this med acts like a mega dose of it!

March 3, 2009
I returned to the doctor today to get a different antibiotic because Avelox made me worse off than the sinus infection I had. I stopped taking it about two weeks ago and still have side effects from the drug. My doctor had given it to me about two other times. The last time I recall was in November. I didn't finish taking my prescription then either.
I thought maybe I was having flu symptoms also, but it was the drug making me more ill. RASH, HIVES, RED HANDS, SWOLLEN TONGUE THRUSH, BUMPS ON MY TONGUE, TINGLING IN MY BACK, VOMITING,HEADACHES, PAIN IN MY STOMACH NOT LONG AFTER TAKING A DOSAGE. FREEZING HANDS, THROAT FEELS LIKE IT'S CLOSING UP AND DIFFICULTY SWALLOWING, COULDN'T GET OUT OF BED, MUSCLE FATIGUE, ACHES WEAKNESS, JOINTS HURT, TINGLING IN HANDS, ANXIETY,CRYING SPELLS, NIGHTMARES, SKIN SENSITIVITY, INSOMNIA, THEN EXTREME FATIGUE, DIZZINESS AND LIGHT HEADED UPON STANDING AND/OR GETTING UP FROM A SITTING OR SQUATING POSITION. EVERYTHING HURTS ALL THE TIME IN EVERY MUSCLE...... I BASICALLY FEEL LIKE I AM DYING.
My fiance thought I was totally losing my mind. I was moody, aggressive, irritable, depressed etc... I felt like like a different person.. My fiance of course got sick also and his doctor prescribed it to him. His side effects included muscle aches and pains and extreme fatigue and mood swings. I looked up some side effects when I was started taking it a few weeks ago, but didn't pursue the research until the side effects got worse. I took it for 7 days this time. My fiance took it for three days. I called him at work after seeing this website and told him to stop taking the medication immediately. I am still sick with a sinus infection, and a whole slew of other crap going on. I called the doctors office and went in right away to get a different medication. To no avail, when I went to my doctors office there was a rep from Avelox there. I said don't give that Avelox to anyone sarcastically. I then saw his tag on his shirt and his bag full of Avelox samples. He asked what type of symptoms I had and I told him.. He said he would report it to the company.... What do you think they will do about it? MOST LIKELY NOTHING. I am an educated person with the capability and time to research anything I need to and I will do my best to dig up the most dirt I possibly can about this horrible medication. They need to stop pushing these meds on doctors to give us and make us more ill than we were to begin with. I JUST HOPE MY AILMENTS AREN'T PERMANENT. People try to make light of the situation because they don't want to be sued. I think the FDA needs to be revamped and the Government should stop letting these pharmaceutical companies poison us. I AM NOT EXAGGERATING EITHER! DO NOT TAKE IT.
I have been going to my doctor for about fifteen years and she never gave me any medication that had made me this ill. I get samples a lot because I have no insurance. Sometimes she gives me scripts. Today I got Zithromax which always worked well for me in the past. Very little side effects. I realize that everyone reacts differently to certain meds, but come on now! It isn't just a coincidence that all of us commenting and complaining here are imagining these horrible side effects! Today I got Zithromax which always worked well for me in the past. (Very little side effects).Then why did I ever have to take Avelox if there are other antibiotics that will make me better not worse. They push these meds on doctors to give to us that's why! I always trusted and admired my doctor. She always treats me well and does right by me. What is going on with these medical companies?! SOMETHING HAS TO BE DONE ABOUT THIS!

First I want to say, after reading several posts, that it seems a lot of you are taking Topamax without food, which may be causing your "spaciness." My doctor suggested always taking it with food, even though it says with or without food, and I only experienced spaciness the few times I took it at bedtime without food. Once I started taking it with breakfast and dinner, that never happened again.

I am a 48 year old woman, prescribed Topamax in September of 08 for migraine associated vertigo without headaches, with facial numbness. The first thing I noticed was I immediately had headaches, which to me indicated it was dehydrating me as that is the only time I get a "normal" headache. So I knew I had to drink a lot of water. Soon after starting Topamax I developed a dry cough that lasted the entire time I was on the med. I did not relate it to the drug at the time, however. It never even occurred to me. After about two months on the drug I started having trouble breathing with extreme dryness in my airways. I was prescribed an albuterol inhaler which did not help. I was then prescribed a corticosteroid inhaler which also did not help. I thought the trouble breathing was from taking Nadolol which I was prescribed for occasional heart fluttering - the neurologist said this was a normal side effect of Topamax. I stopped taking the Nadolol but the trouble breathing continued. I also had more migraines with vertigo and facial numbness than before I started taking the drug. I hoped it would eventually stop and the drug would kick in to help the vertigo, so I stayed on the drug. I had very minor tingling in my feet, but it was tolerable. I became very stressed out, had trouble sleeping, depression, my face started breaking out in November (and still is), I lost interest in everything that I normally enjoy - reading, photography, following politics in the news (sort of an obsession of mine). In December I was so depressed that for the first time in my 11 year career I started canceling appointments and eventually took three weeks off from work to "re-group." In January the neurologist decided that we would increase the dose from 100 mg to 150 mg for one more month, and if it did not get rid of my migraines with vertigo, we would discontinue the drug. The first day on the increased dose I had a killer headache, and I drank 150 ounces of water before it went away. That night I did not have to go to the bathroom during the night, unheard of for me. That's a lot of water to drink and not have to pee. Within two days of increasing the dose, my cough became much worse, and within three days, the breathing became more difficult. Within five days, I was having trouble speaking because my airways felt so dry. I called the doctor the next morning and he said it was not the drug, but if I wanted to, stop taking it. So I went off it cold turkey, per his instructions. I had rebound migraines every day for a week or two and my heart was pounding, sometimes for three or four hours at a time. Eventually the cough and trouble breathing went away, however, I had to continue drinking lots of water or I would notice that I didn't have to urinate, sometimes not at all. Again, unheard of for me. I saw a cardiologist at the neurologist's urging and they said the heart pounding was just anxiety. I disagree, as did another doctor of mine. We both believe it was withdrawal. I have now found out (by getting copies of my medical records) that the neurologist is now attributing all of my side effects from the Topamax to "somatization." In other words, psychosomatic - not a side effect, but just a way of getting medical attention. I am seeing a few people on this board who have also experienced a dry cough and trouble breathing. Can I have the same side effects as other people and have them still be psychosomatic, even though I had no idea those side effects could occur? I don't think so.

I have a theory that Topamax interferes with hormones which causes a lot of the side effects like lack of concentration, memory loss, anxiety, depression, insomnia, acne, and hair loss - all symptoms of peri-menopause and menopause. Ask any woman in her 40's or 50's if she has these symptoms and most of them will say yes. My face has not been this broken out since high school! My hair is falling out at a rapid rate. I won't even bother mentioning these to the neurologist. He'll just say it's not the drug.

I'm very frustrated and not sure what to do at this point. The neurologist has me taking a supplement called Migrelief now, but I think it takes three months to kick in, so I have no relief at this point.

Has anyone else experienced the trouble breathing with dry cough? I don't believe for a moment that it was psychosomatic.

I've been on Lamictal 150mg for 2 years. recently I have been having tingling in my feet and arms/hands. I'm wondering if anyone else has had anything similar.

Hi-I am a 59 year old female have been taking 20mg Simvastatin for 3 months for a cholesterol level of 238 and have noticed significant symptoms that cannot be from any other origin than this medication-dry skin, change of hair texture, psoriasis and bulging in thumb joints, stomach flu, shoulder pain and tingling in hands, vision problems. I am a healthy flight attendant except for all these things that have happened in the last 3 MONTHS!!! I am seeing my doctor tomorrow to discuss a change. I want to take a natural medication to lower my cholesterol.

Same here. Pretty much like a zombie. Numbness and tingling in hands and feet. Spaced out. Stoned like in high school.

I have taken Simvastatin for several years. Just recently noticing tingling in hands and feet. Also, some leg weakness and some dizziness. Take other medications that also have dizziness as side effect and also battle sinus problems. Could the sinus problems also be a side effect? Doctor says I may have case of neuropathy. That is also a side effect of Simvastatin. My dosage reduced several months ago but just stopped totally about a week ago. Hoping for good results from the stoppage. Could it be months before I notice a difference if it is truly side effects?

I stumbled onto this website just today looking for information on another drug. Little did I know what I was going to find and so happy I did. I have been taking Zocor for nearly 5 yrs. now. My health has taken a spiral downhill. I too, have been experiencing almost every symptom that has been mentioned. Rt. shoulder pain, hand pain, pain and tingling in hands and feet, leg cramps, muscle weakness, numbness, memory loss, itching, fuzzy headed at time, can't concentrate, and trouble breathing. My doctor has told me my cholesterol is just fine the last two times I've had my checkup, but has never suggested I come off it. I guess I will be calling him tomorrow.

Hi
My husband has been prescribed 2 different blood pressure meds Lisionpril and metoprolol back in June. Come mid July he started to have trouble sleeping and slight tingling in hands and feet. Then it progressed to the arms and legs and then the face and chest. We have seen cardiologist, neurologist, sleep apnea doctors, Had EKG, MRI, Heart sonograms, Nerve test done due to the symptoms. Everything came back normal. He is miserable. The burning and pain is unbearable to wear he wants to cut his feet off and the only thing we keep hearing is well LETS DO ANOTHER TEST or TRY THIS MED. So now he is taking a a sleep med for insomnia and some seizure med for the nerve pain, thinking he may have neuropathy. This is going on 2 months now of trial and error and after reading 20 minutes of experiences, I THINK ITS THE MED!!!!!!!
What do we do then? He had high blood pressure so what meds are good with no side affects of burning or insomnia? Any suggestions or help would be of great appreciation. Thank you!!!

I have been taking Topomax for migraines for about 3 years now. Staying at the 75mg at night dosage. Going to 100mg just does not work for me. GI disturbances too severe. Diarrhea mostly. Early on same as a lot of the other reports, tingling in hands, bad tasting soda, some hair loss, and intermittent upset stomach and diarrhea. Memory not as good as without the med and balance a little off. All of these have diminished in intensity and frequency. Up side, weekly headaches that forced me to go to bed gone. Being an irritable wretch because my head hurt, was about to begin to hurt, or just got over hurting gone. At this point in my life the pros still outweigh the cons and as long as that is true I will continue with the regimine.

My 6th time for Botox and ten days after the injections, I ended up in the ER with flu like symptoms, nausea, tingling in hands and feet, dry mouth, and extreme anxiety. After multiple, and expensive tests, the physician said that I was experiencing an adverse reaction to Botox. I cannot get the Dermatologist to call me back and my Family Practitioner isn't familiar with this condition. I am reaching out in the hopes of finding someone who can relate to this and welcome any feedback or referrals to help me.

August 5, 2008

Thank you for this website. These testimonies has confirmed by suspicions of Advair's side effects.

I am 52 years old and was diagnosed with adult onset asthma 10 months ago. My physician prescribed Advair (500) and Albuterol inhaler. I was instructed to take the Advair 2 times/day and Albuterol 3 times/day. During the last few months, I have noticed a slight weight gain, fatigue, hoarseness, dry mouth and occasional insomnia. The hoarseness has resulted in 2.5 weeks of losing my voice. Also, I have noticed that my recovery from a prior illness, such as cold, was very slow.

As a result, I discontinued the Advair and use the albuterol as needed. My voice began to returned to normal in two days and I am feeling much better.

Now I am wondering if I am experiencing drug withdrawal symptoms due to discontinuing Advair five day ago. The following symptoms are: dizziness, and needle-like tingling in hands, feet and side.

Again, thank you gals for sharing you'll experience with Advair.

Hi I've been on topamax for 4 years . Had all the side effects...weight loss,tingling in hands and feet,no memory and speech problems! I was taking 600mgs a day! I take it for epilepsy! I was on the highest dose. my doc then weened me from top. to zonegran 600mgs. It's very similar to topamax. For me it is not helping me as much as the topamax. I think it's a great drug!!!! I did not loose hair, no constipation, no rapid heartbeat for me! I am going back on it . Yes sometimes I would get in a hostel mood and can't spell shit , but for me it's all GOOD !

I've been on Zocor 40 mg. for 9 months. After being on it 4 months I began to have symptoms. Dizziness, vertigo, tingling in hands and on scalp, stabbing pains in head and chest, eyelid and finger twitching, throbbing of arteries above each ear and head tremors. Went to ER when vertigo and tremor got unbearable, they found nothing. Been to several doctors and not one of mentioned that these symptoms could be from Zocor.
Internet research enlightened me and I stopped taking it yesterday. Will advise if symptoms decrease.

Here is my Mirena Story.

I was 6 weeks post partum....I had mirena inserted...it was very painful and I was not warned about that.
About a week later I noticed yellowing in the whites of my eyes which I thought could be coming from a iron def. since I just gave birth. So I made sure I was eating well and taking vitamins. I also had severe itching at night especially on my ankles and legs. Oh and sex drive was gone. It was fine the 6 weeks after birth but as soon as mirena was in it was gone!!! I went to the doctor about a month after insertion and asked to have it removed, of course my doc said it couldn't be iud causing my problems...come back in a month...So I did....within this month I started having severe anxiety, insomnia and panic attacks, to the point were I actually thought I was loosing my mind. Of course again the doc told me that it wasn't iud and prescribed me an antidepressant which I reluctantly excepted. I'm not depressed...my life was perfect before mirena!!! I finally went back for the third time and decided I wasn't leaving until somebody took this thing out of me!

Here is a list of other side effects that I had/still have!!

acne
migraines
extreme lower back pain
numbness and tingling in hands and feet
vision problems
fogginess
An ADHD type feeling
inability to focus or concentrate
extreme fatigue
feeling of throat closing up
heart racing and palpitations
night sweats
sinusitus
dizziness and light headiness
headache

The problem here is that the doctors don't even know how extreme these side effects can be and they keep telling us that it's not the mirena. PLEASE trust your instinct.....I wanted to trust my doctor but I knew in my heart what was causing my problems...I am only 1 week post mirena and I am still having a lot of my problems but I can tell a difference. DON'T LET IT GET OUT OF HAND....TAKE IT OUT!!!!

DON'T GET MIRENA...IT MAY WORK WELL FOR SOME...BUT IN MY OPINION IT IS NOT WORTH THE CHANCE THAT THESE HORRIBLE SIDE EFFECTS COULD HAPPEN.....HAD I BEEN INFORMED PROPERLY I WOULD HAVE NEVER HAD MIRENA INSERTED!!

Good Luck Ladies!!

I've been on Topamax since Sept 2007 and the only side effects I have had were at the beginning were the tingling in the hands and feet when I was brining my dosage up. Soda tastes awful but I no longer drink it and that is a godsend after being a heavy drinker of it for years. I do find there are time when I can't find the right word to say, or I forget what I was doing, but I deal with it. I have lost 20 pounds since being on the medication. After being on it for 6 months the tingling is gone, I usually counteracted it by drinking plenty of water in the morning, that got rid of it. The drug has taken away the migraines, and regular headaches I have suffered from for years. It has also stabilized my moods and taken away my anxiety issues. I'm 36 and have never felt better. Topamax is definitely not for everyone. For those that are suffering, please do contact your doctors and try to get off the medication.

I don't know if this is a side effect or not but on two occasions I have experienced some numbing or tingling in hands and forearms. The feeling was so different that it alamed me but it wore off later that day. I believe this type of feeling has happened twice and it has coincided with the use of Scalpicin on my scalp.

i started taking simvastatin about 6 months ago and i am getting double vision and pins and needles in my hands i also am getting cramp in my legs and backache