Hands and fingers symptoms and conditions

After being on Fosamax for 6 years, my yearly bone scan didn't show much difference in my bone loss. I started wondering about the pain in my knees, right hip, hands and fingers. It wasn't until I started noticing my index and little fingers starting to grow in the opposite positions and hardening around the first joint, and shooting pains that I started looking up side effects of Fosamax. I have taken myself off this medication since reading that it can cause joint pain. I'm not sure this is the problem with my fingers, but time will tell. Who wants crooked fingers caused by Fosamax.

I was given Avelox by my Allergist three weeks ago because I had yet another sinus infection, she had me come in and pick up some samples she had with 5 days worth of 400 strength Avelox.
The night of the third dose I was awakened by numbing and tingling and pain in my right arm from the elbow down to my hand, I had never had this before. I called the nurse the next day and she said to stop taking the drug which I did. I figured now that I stopped taking the drug the symptoms would go away.
A few days later I was out shopping and within a few hours of walking around I began to have so much pain in my right foot/ankle/heel that I had to come home, I could not put my foot down.
Then within the next few days my knees began to hurt, behind the knee and in the side. It has been 3 weeks now and the foot pain is better but my hand,elbow and knees are bothering me so much I can't sleep. The other symptom feels like nerve pain in my legs, hands and fingers. I am really troubled by this, I am a very active healthy 62 year old Woman, I have not been able to exercise all of this time.
I went to see my Allergist who prescribed the Avelox and informed her of all of these symptoms. She said that this was a rare side effect and that I was particularly sensitive. I asked her if the symptoms would go away soon and she gently said that it would take time.
Then she said that she had prescribed Avelox to her husband a few months ago, she said he had the same reaction as me (how does this translate to a rare occurrence?) and that he was slowly improving. She thought I should go to a Physical Therapist or a Rheumatologist, I told her I can't afford that.
At this point I am scared I won't get back to how I was before. I have had knee surgery in the past but my knees were doing fine until this.
Have other people slowly recovered as my doc has suggested will happen?
I don;t know what I should be doing at this point. Help!
S.

I am a 29 y/o male.this month i got a terrible sinus infection, probably due to a month's struggle with allergies. I was initially prescribed Augmenting but after just 1 pill i was up all night with stomach cramps & diarrhea. I was scared to take another dose so my dr. prescribed me Levaquin as an alternative. After reading the warnings I became very worried due to the fact that I already have lower back/hip and joint pain issues. I also work evening freight at Home Depot. After 1 Levaquin yesterday morning, I went to work ready to take it easy and not hurt my body more than it already does... after about 30 minute of simply opening small boxes and putting light-weight merchandise on the shelves, i began to feel extreme tension/aching in my hands and fingers.I was being very careful with my back & neck, but never even thought this might effect my hands??? I woke up this morning hoping it would be gone... no such luck, even after a full night's rest they still feel like i have arthritis, and no my hips (S.I. joints)are popping out like crazy. i am about to take the 2nd dose, only b/c my ears nose and throat do feel much better. I am just glad I picked up paperwork/and can afford to take a few days of LOA if this gets any worse. It is hard for me just to type this now : (. I'm scared.

Has anyone had the experience of previously taking Levaquin without side effects, then when taking it again, developed severe headaches, joint aches, muscle pain and weakness, etc? I am currently going through this. I've taken Levaquin before probably 2 or 3 times due to upper respiratory problems and not noticed any side effect but this time, I've taken 5 days worth, 3 in hospital 2 as outpatient dose and can hardly move. I had the same experience in 2004 with zithromax. Had taken it without side effects, then suddenly when taking it again developed such bad chest pain, I thought as did my doctor, that I was having heart attack and spent a week in hospital before figuring that one out.

I had a prostate infection and a sinus infection. Was given Levaquin 750 MG for three weeks once a day. Started having hand and finger pain two weeks in out of the blue. Did a little research and stopped medication. What I found was that Levaquin can cause skeletal fluorosis or just fluorosis in some people. Considering the internet response and the number of other medications that react with Levaquin I would guess this is a pretty common side effect. I started a body purge the day I stopped and have experienced a dramatic decrease in pain. I also have Fibro so a slight pain is manageable though my pain has never been in my hands and fingers. If you have taken this off and on for different infections through the years or any of its cousins, like Cipro, I'm sure you will wonder if it could have contributed to joint pain and reduced activity levels caused by the pain for many years. Good luck to us all.

I have been on Toprol -XL Metoprolol ER 100 MG, I have been on for about 2 mos. Not quite sure have to check dr records. I have had Weight gain about 20 lbs, headaches, swelling of ankles and feet,shortness of Breath, a horrible feeling of not being able to catch or take my breath, fear anxiety, stomach pains, depression, vivid dreams, waking up and not being able to sleep, tossng and turning until 4am. could feel heart beating fast but subtle. numbing in my hands and fingers lack of motivation. I have been going to a nurse practioner who is helping me to wean off of this drug. It has changed me I ave never been ill in my life except for the common cold. and having babies. There is really nothing wrong with my heart according to tests they have run, My Blood pressure was high and they were trying to get it under control, tried other meds and then went to this. It has been a horrible experience especially when you just learned you have HBP and then you get all these terrible side effects from the medicine that is suppose to be saving your life or help save it. I do not know how I will do with weaning But i will sure try and keep you posted. I am a little nervous about being weaned off, but hopefully I can find something natural to help me out. This is literally been poison to my Body ******

I have been taking Lotrel for about 3 years and I have a tingling and burning sensation in my hands and fingers, especially when lying down at night. When this occurs I usually wake up after 2 or 3 hours of sleep. I also experience pain in both shoulders.

I think that since I have started the Advair, if anybody has had this symptom and I do not find it in the regular side effects, I have numbness from my waist all the way down to my feet. I have not felt my toes since about 3 weeks ago. I have already had the MRI of the spine and was told nothing to worry about, I have the best looking spine any radiologist had seen. My doctor took labs and they were all negative and normal and now she is going to send me to a neurologists because she is stumped. I believe I am going to stop taking the Advair, because it is the only NEW drug I have started since this began and see if that is the problem and if so. My problem is solved. If anybody else has had this problem let me know. Also numbness has began in my hands and fingers.

My daughter is 15 she has always been healthy. After her 3rd Gardasil shot on 10/14/2008 she began having headaches, nausea, vomiting, dizziness tingleing in her hands and fingers (this happened in the next few days after the shot), tiredness, chest pain, stomach pain, face rash, eye itchiness and hot/cold flashes. I am really upset that I allowed my daughter to get this shot. The doctor says she doesn't feel this is from the shot but there is no other explanation since she had none of these problems before! As a mother I feel terribly guilty for letting her get the shot. I haven't seen anything about how long people are having these side effects. Do the side effects go away in time?

My 13 year old sister is a normal active teenager. She received the first Gardasil shot last October with Hep B. In November, she received the second Gardasil shot with the meningitis vaccine. Right before Christmas, she started experiencing tingling in her hands and fingers. Two days before the New Year, her knees swelled three times their normal size and were extremely painful. It took two weeks for her knees to become only slightly swollen. Several doctors and a specialist in pediatric arthritis later, she was diagnosed with chronic arthritis. She had no previous joints issue at all. She has been on medication for a year. We can only hope she has juvenile arthritis and that it will go in remission. Unfortunately, her wrists have started to hurt recently.

After much research by my mom and myself, we have come to the conclusion her spontaneous arthritis was a result of Gardasil. Most likely the combination of Gardasil and the meningitis vaccine was the cause. It should be noted that the FDA allowed Merck to fast-track Gardasil for approval. The Gardasil vaccine was never tested with the meningitis vaccine; however, most physicians give multiple vaccines at one time.

I get some stomach cramping from the Z-Pak, but the most disturbing side effect would be the chest pain. I have swollen glands right now and I had vertigo and the doctor told me it was probably a bacterial infection because the gland under my chin is the one that is swollen. Every time I take this medication the side effects are different. I also had the agitation the last time I took Z-Pak. Sometimes I have had the lose bowels, especially after taking the two pills together the first day. Well, I guess it is better than having an infection so I will continue to take it. There are other medications that are worse for me. At least I am not getting a rash and I cannot take penicillin.

I started Levaquin 500 MG on Thursday Aug. 29, 2008. I did not have any problem the first night. But the second day at about 3:00 PM I was working on my computer when my finger joints started to get stiff and my hands and arms started to shake. I just thought I was tired and forgot about it. At 1:30 AM August 30, I was awakened by someone shouting in my ear , You are going to die. I woke up in a sweat and my heart pounding. My hand were stiff and my knee joints were very tight. I also was in a very bad panic attack.
I went to my desk and wrote my wife a letter telling her how much I loved her and my dog Abby. I then proceeded to give her funeral instructions as to which funeral home church and buriel plot.. This writing was 3 pages long. I called my doctor and they as much told me this could not happen. My blood pressure was 240 over 120 when I took it. I took a valium and this calmed me down in 10 minutes. They gave me a new antibiotic for my Bronchitis. So I thought the nightmares and pain was over. Not so quick last night at 2:20 AM I was awake by the screaming in my ears you are going to die. I tried to call my wife but I could not get the word out for help. I tried to move my hands and fingers they would not move. Finally I rolled off the bed and yelled my wifes name she did not hear me.
This drug has set back my recovery from my panic attacks. This drug should be badded by the FDA. But as usual the government does nothing to help the public only big business.

I began taking Aromasin 1 year ago for advanced (Stage 4) BC with mets to the bones. I have increasingly had severe joiont aches, my hands and fingers ache so badly at times, I feel I can barely hold a book, or type, etc. My hands and fingers tingle and feel numb. I also have severe wrist pain so much so that I sometimes use a heating pad for some relief. I do not wish to discontinue it because it seems to be working and my Oncologist says the side effects are more tolerable than chemo, which I have already had before. I feel like my Dr. sometimes thinks I am exaggerating my pain levels, but I struggle with daily activities. I am on Fentanyl patches and even have to resort to Hydrocodone when it becomes to intolerable.

Hello folks - thought I would post here as well.........I am on 20MG of LISINOPRIL 1 time daily. I notice during regimented times of the day I get the side effects. I take it when I wake up in the morning. I have been on this for about a year now...........it has lowered by HBP from 150's/80's to about 130/80..............regular........I am a 37 year old Male

Problem is the multiple side affects:

1. Tiredness - comes and goes all throughout the day - almost like I could just close my eyes and go to sleep anywhere.........feels like someone threw sand in my eyes.......
2. Shortness of breath
3. Sore Muscles - everywhere - it doesn't discriminate!!!!
4. Pain in the chest mostly the left side but sometimes the right
5. Headache in one spot in the head - doesn't last long
6. Wake up often in the middle of the night with dead hands or legs
7. Sometimes I just have a total memory blank on things I should know right away - usually only occurs when I'm getting tired.
8 Of course the panic from thinking something is wrong with me!!!

Anyone else with these set of symptoms????

Drop me a note!!!!

I quit Lipitor (40mg) five weeks ago. I believe I was on a trajectory to disabilty within a year.
The unbelievable left elbow pain has gone (maybe the cortisone worked!). My left knee feels "normal" again, not perfect but nearly like it used to be. Within a couple of days of quitting I had severe pain in my right thumb along the bone, then in the middle of my right hand, then between the first and second fingers in my right hand. I currently have minor pain in my right wrist (this is new) on the pinkie side and minor pain in my left shoulder where the arm joins (this has been intermittent for a couple of months). I am feeling much better - but would not be at all surprised if pain appears in another part of my body before this is all history! There is also plenty of joint clicking going on.
I believe I first reported pain to the assistant doctor to the heart surgeon two weeks after I had the stent put in and was put on Lipitor. I was also on various other medications. I had tingling on the ends of my fingers and toes at random - hard to describe but it was as if a fairly sharp object (like a ball point pen, say) was being pressed progressively harder from the end of the finger/toe and towards the rest of that finger/toe: and as the pressure increased it would suddenly become painful. It was not a tingling/numb sensation but more a tingling which increased sufficiently that it hurt.
I am only being so specific because when I described these "symptoms" the doctor shrugged. If anyone has had similar - and I have seen tingling mentioned here - please make contact with me as I do want to report my experience back into the medical community but find, an exact description difficult. Things never needed to have got so bad if this was the first warning.
I since asked my family doctor if my knee problem was Lipitor related and she thought not: I was referred to Physical Therapy. I also told the physical therapists (who thought my knee should recover much sooner, and were surprised that I had zero mobility pain) that I also had serious elbow pain.
The orthopedic surgeon I saw did not connect the elbow problem to Lipitor.
The heart surgeon (stent insert) could perhaps be the only person who I did not tell of the pains - I don't remember - but I may be so grateful to be alive - that he may be someone to whom I did not voice a complaint!
On the positive - five weeks later I am feeling significantly better.

I was wondering if any of you are experiencing tingling in your hands and feet, which increases during sleep. I have been on this medication for two months and have just started noticing this sensation.

My ENT prescribed Levaquin 500mg per day for 12 days for an unusual bacterial sinus infection. Within four days I was feeling horrible. I have been off the medication for four days now but my symptoms haven't improved much.

My biggest complaint is that I can hardly walk due to terrible ankle and foot pain. All of the joints in my feet hurt but particularly both ankle and big toe joints. I can’t find a pair of shoes or even slippers that are comfortable. Every joint in my entire body aches. My shoulders and my arm muscles are so sore that it hurts to do anything. My wrists and my hands and fingers hurt and feel swollen. I can’t open jars or similar tasks. My knees and hips are sore so walking is painful. My lower back hurts if I walk much. Joints that I've had problems with in the past hurt even worse including my neck (cervical spine). My skin is very sensitive to touch even to my clothes, bed sheets and slippers. I’m miserable. I already had dry eyes but this drug has made them MUCH worse. My eyes are so dry, they both hurt and they are both bloodshot. My eyes are now even more sensitive to light so I wear sunglasses to reduce pain causing glare. Cognitively, I feel like I am in a fog; it’s kind of a spacey, surreal feeling. I feel like jumping out of my skin. I have had chest pain twice. My heart races at times. I have an intermittent, frequent knife like pain in between my shoulder blades (on the left side) and it is worse when I breathe deeply. I have tingling in my hands and they usually feel cold. I feel queasy at times. In general I feel ill and I have no energy. I fatigue easily. I don't know whether to cry or to scream but I feel like doing both. I've always had headaches but they are more frequent now. On top of it all I still have intermittent burning in my sinuses so I don't know if the drug has even cleared up the infection or not. I was re cultured today.

I have taken Cipro (similar to Levaquin) in the past so I did not make the connection between the Levaquin and my symptoms until two days after I had completed the drug. It was Christmas Day. I was too sick to join in the festivities. As I sat alone I started to think about my symptoms and I went online to research my symptoms. To my shock I discovered that there are thousands suffering as I am with similar symptoms due to this drug. I now fear that I may suffer permanent damage as a result of this drug. I was never warned regarding ANY of the dangers. The common adverse problems associated with this drug is NOT common knowledge in the health care setting but it should be. I printed out pages and pages of postings of sufferers and brought them to my ENT. I provided him with a list of sufferers web sites. He sat in stunned silence and it was obvious that he had been painfully unaware of the suffering that this drug was causing.

I blame the pharmaceutical companies and the FDA for allowing this tragedy to continue. I would like the name of a competent, experienced attorney with a proven track record against pharmaceutical companies. If any of you can provide me with the name of an attorney I will be in your debt.

I thank you all for your postings because at least I know that I am not alone. My heart goes out to you all.

Chris

Brain zaps, tingling in hands and fingers. I take 300 mg, 150mg AM and 150mg PM. Sometimes before I take my PM dose I get the electrical sensation, I call brain zaps in my ears and tingling in my hands and fingers. I have had about a 12 pound weight gain and still going. The weight gain is depressing in itself. I also have the excessive sweating. YUK!

I was recently diagnosed with Hoshimotos Thyroiditis. It's only been three days since I have been on the Levoxyl (100 mcg), but I am feeling slight chest pain and tingling in my face. My heart isn't racing though; it's just a dull pain! I am nervous that it will continue to increase and that other symptoms will come about. Just reading about people's experienced on this site has made me nervous too! Has anyone ever experienced this and if so, did other symptoms follow?

Thanks for your feedback!!!

Hi there... I have just found this site and I'm very grateful to everyone who has taken the time to sit down and tell us their story mine is very similar. BELIEAVE me I feel like I am pushing my family away and I'm losing my relationship with the one person who used to make me feel like I was the most beautiful woman in the world.
I'm a 40 yr female have or maybe had a great job that I loved... On April 12 I noticed a small red rash on my lower right leg no big deal went to the Dr. gave me some cream and sent me home well I went to work and by the afternoon things just seem to get bad my legs began to swell and little blisters started to pop up so I went to the E.R. they had no Idea what was wrong with me got me an appointment to see a skin DR. so I went home but the pain from the swelling was so bad I could not walk any longer went back to the E.R. they gave me some pain meds and called in some other DR. things had gone from bad to worse my feet had gotten to big I could not put on shoes and I had bruised completely across the bottoms of my feet they put me on 30mg of PRED. and it seem to be under control sent me home after 3 day in the hospital things were good for about a day or so I thought I would go back to work well that was not a very good idea.... My sister had to come and take me back to the ER where they did 2 biopsies and still have no idea what is wrong with me. so now they put me on 60mg of PRED the rash has gone, lots of scaring on my feet because of the blisters once they broke and dried out but I can live with that....
It's the side effects that they don’t tell you about,
MOON FACE I can't look at myself cause really that’s not me anymore,
WEIGHT GAIN I have always been thick but I can't handle the extra 30lbs I've gained,
MOOD SWINGS are unbearable,
PAINFUL JOINTS, CAMEL HUMP, BLOODY NOSE, BRUSING, SORE TEETH/GUMS, DRY EYES, FAITIGE, and worsted of all
I don’t have a support systems in my life so I'm fighting this by myself everyday, I have 3 kids that I have tried to explain all this to but they don't get it and well my boyfriend he tells me he understands that its the meds pushing him away but if I can't figure away to control this I will lose every thing including my job. I cant even get the energy together half the time to make it up and down the stairs which also comes with the pain of just trying to lift each leg up to climb the stairs, I also have the camel hump which I find very painful, The acne and the hair growth that I have to get wax off once a month cause I feel like a man I feel like a loser and as of the last couple of days I just want to give up I am now down to 20mg per day but I find that I am feeling so sick I cant think straight I hope and pray for each and every person out there that has to take this MED that you get better and I do hope that my symptoms wont come back. Thanks for being here and I’m glad I found this site. I know now that I’m not losing my mind completely. Elizabeth.

I was diagnosed with asthma 8 months ago at 45 years old. It was quite a shock considering I never had sympthoms untill recently. The doctors thought that abulterol would be enough to control it but unfortunately the events become too frequent. They then swictched me to Singular. Wow, what a mistake that wa! Yes, my breathing improved but the side effects were frightening and painful. After only two or three days my arms, hands and fingers were numb and tingling...constant pins and needles...and virtually useless. At night I had the worst most vivid nightmares I've ever had. And I was unable to fall asleep because my mind was constantly racing. It's almost enough to make one psychotic. Plus I had sudden, very painful ear and tooth aches.

All this cleared up a few days after stopping Singualr.

This drugs is suppose to interfere with your body's signals to produce inflammation but it has to be doing so much more, and most of that not good. It seems clear based on my side effects and others I've read about it has a huge impact on the central nervous system too.

This is not a safe drug. I wouldn't be surprised if someone, some day uses it as an excuse for some really bad behaviour. In fact, I'm shocked that this is given to kids at all. If I had to take this for months I would go insane.

BTW, months later, on advice of my doctor, I tried it again with the intent of taking it every other day to limit dose. Nice idea, but no cigar. After just one dose I was once again "flipping out" in bed.

If you have really bad asthma and singular works for you without side effects that's great news. But I'd still ask myself what kind of impact is it having on your body if it does so much damage to so many other people. How safe can it really be?

If you have kids, and they're taking it, please keep a close eye on them. Sometimes kids don't have the communication tools to explain to parents what they're experiencing. Don't make them suffer...and don't let them be punished at school because their behaviour is uncontrollable. It could very well be this med.

i recieved 3 kenalog epidural injections for herniated disc, 2 weeks apart, followed by a decompression nucleoplasty, also with Kenalog injection. after the first epidual. i began having extreme irritablity which i reported to the pain management doc. he said he couldn't prescribe anything but could refer me to a psychologist, which i declined , realizing i was having a reaction to something. after the 3rd epidural, my irritabilty had increased to the point where i was shouting and screaming, and had completely lost my patience. my face had blown up, and cheeks were hard to the touch, and my neck skin was swollen and hanging down. i described my appearance as "looking like a blowfish".

on the day of the nucleoplasty, i agreed that the doc should go ahead and use it again, since it was important for the procedure, and it was not a "true (anaphalctic) type reaction.

after this last injection of Kenalog, i had a terrible terrible reaction. my face became even larger, with big dark circles under my eyes, and my eyes partially closed, appeared like slits. i was frightened by my reflection in the mirror.

my feet, ankles and legs swelled up to the point where it was painful and difficult to walk.

i also i developed insomnia.

at the same time i was "off the wall" with irritability, anger, impatience, and could not stop crying.

during the day i had a general ill and sleepy feeling, and fell asleep driving, without notice.

throughout this period of Kenalog adminstration, i also had flu like symptoms every morning. sore throat, laryngitis, loose cough, muscle pains. i noticed black and blue marks on my extremities as well.

now i have a full blown flu and full blown bronchitis, and i feel so very very ill.

my feet and calves, hands and fingers are experiencing very painful cramping, intermittantly throughout the day and night. it's happening right now in my left hand, so i have to stop typing. i wait for one minute and try to continue typing, but that causes the painful spasm to return. i try again 2 more times, waiting a minute in between spasms. finally it stops and i can continue typing.

there are probably more symptoms, like the irregular heart beat, and these little bumps on the skin of my right cheek, but i need to rest now.

generally, i feel sicker probably than i can ever recall feeling in my life.

would appreciate hearing from anyone with similar symptoms, and especially how long before my face returns to normal. i live with the fear of what will i do if it does not?

Why is mobic better then save advil or aleve? I have a prescription but haven't started it yet. I have fibromyalgia and osteo arthritis in neck, shoulders, back, hips, knees and most recently my hands and fingers.
I have a long history of irregular heart beats(pvc's ) and I am reluctent to complicate them with added comlications from mobic. If soemone has info that would help I would appreciate it.

Until I read some of these stories, I didn't know it might be the Levaquin tearing my whole body to pieces. I have been on 750mg. once daily for 2 weeks now for a severe sinus infection. I have 9 more days of it, but I'm calling my doctor in the am. I've had diarrhea for 2 weeks, and increasing muscle and bone pain that started in my lower back, now down through my legs, hands and fingers swollen and going to sleep all the time, tho this seems to have stopped...not the pain in every joint in my body is excrutiating. I really can't walk anymore, can't pick up my legs, have tremors in my hands, fingers, unbelievable pain in every bone in my body! I also have an active infection in my gall bladder and now a gall baldder attack. My gall bladder has to be removed asap. My potassium dropped to critical, 2.4 and my Internal Medicine Dr. can't seem to get it back up. I take blood tests every day to check my potassium level.

My sinus specialist prescribed this med for me. My hips and legs keep locking up and I'm afraid of what's happening to me. I have to have surgery now, and my body won't function. I will talk to both doctors tomorrow...and to my cardiologist. This medicine shouldn't be on the market. I hope there's a lawsuit...My neice went into kidney failure from Levaquin a few years ago. I didn't have any idea it was the meds until I found this site.
Is this reversible or permanent?

I've been taking Toprol XL for PVC's for about a year now. At first they also took away constant headaches, yeah!!! But as of late, i've noticed that I'm EXTREMELY fatigued all of the time, i've gained at least 10 pounds since taking this and my circulation is horrible in my hands and fingers. I still have the PVC's anyway. I went off the meds 3 days ago, without DR's ok and kind of feel dizzy and yucky, i have to go see the Doc tomorrow cuz he's miffed that i stopped taking it. Anyway...that's about it