Nerve endings symptoms and conditions

Wow, I thought I was going crazy. I've been so sick the last week but didn't think it would be this new medication. I'm taking 150 mg once a day for 15 days. I have three left of which are going in the garbage. I missed a family reunion today because I'm so tired I can't function. It's like someone gave me a sleeping pill. I've taken three pregnancy tests of which they were all negative thinking I was pregnant. The nausea is horrible. Just talking about food makes me vomit. I have stomach cramps, severe lower back pain, my heart feels like it's doing flip flops at night. My face feels very hot at times. My hands feel like raw nerve endings when put in cold water or wind blows over them. My arms tingle and hurt when exposed to the sun. I just want to lay in bed and not face the world. I've been dieting and lost 15 pounds prior to starting the medication. Boom, all that stopped. Still doing all the workouts and carefully eating but have gained 4 pounds back. Very disappointing. I am so glad I found this site. You won't find this information on the manufactures website.

I've been on doxy for about 10 days. I've never had problems with "photosensitivty" when it had been listed as a side effect on other medications. Totally disregarded the warning. I was put on it for some problems that might arise with acne due to a hormonal injection. I was going to the Florida keys in a few days and thought I should go to a tanning bed to get a little color so I wouldn't burn down in the Keys. Within a couple of days my hands began to tingle, burn with warm water, freeze with cool water. It was like my skin was burnt off and my nerve endings were exposed to the elements. While in Florida with my feet and hands in bandages to keep the heat/sun from causing pain I noticed blistering and still have them. I thought I had shingles, even though I had it on both sides of my body! Had an increased heart rate and 2t pitting edema in my feet and calves when flying home and increased itching on feet and hands. Very nervous at this point! I massaged my calves to increase the flow back towards my heart and it seemed to help. I am also experiencing GiI problems as well, severe heartburn and bloating. My son said I looked like I was pregnant! I can't wait to talk to my Dr. tomorrow and will stop taking this medicine. Thanks to all of you for your information. I'm relieved to find out what is causing all of this. I only hope my symptoms will go away sooner than later!

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 started using lipitor from my doctor, it lowered my cholesterol all around but I started to have lower back pains. At first I thought it might be prostate cancer, but after having to MRI's done they found no cancer, thank god. But I went to an orthopedic surgeon to see what the problem was. He looked at the mri's and saw lower dics hitting my nerve endings. He also thought that it might be muscle problems so he gave me 3 epidurals and that helped for a while took away about 50% of my pain, but I still have the pain, It is hard for me to get comfortable when I sit or even when I am sleeping. I don't want to think that it is the lipitor that is doing it to me but after talking with others I feel it is time to talk to my doctor about it. My doctor said that lipitor is the safest one that will do very little harm to my liver. I am not a doctor so I would not know.. My cholesterol level was 246 at one time now it is 175. I am now facing possible spine fusion to help correct my disc problem. But will also ask doctor to prescribe something else.

Alan

Hello: I am so sorry that all of us are suffering since taking this pill. My experience with Yasmin was brutal and 3 years later I know am told that I have developed b12 deficiency or a very serious, but treatable condition called pernicious anemia. I never had it before then pill. I took Yasmin for only 5 months and felt sick the whole time. Headaches, strange moods, even a popping sound in my head some times, bizarre symptoms. I called my OBGYN and told he I was stopping. She said the pill did not cause this, but if I felt it was related to stop. AND IT WAS! She now admits to feeling bad for this. She did not mean it. Doctors only know what they read from the literature of a drug. I stopped taking it and was in the hospital within three days. I was in shock. Night sweats, tingling skin, no energy, stomach problems of every kind. Severe pain in my left ovary, suicidal depression and on and on. The worst part is that I began to get sicker and sicker. 3 years later of still being sick. The only thing that has helped my system is acupuncture and a serious diet change to aid my system, I find out that I have a serious b12 deficiency, which I never had. They call it an autoimmune disease which impedes you from processing b12 and all this starts in the tummy! I lost a baby during this time while pregnant, now we know it was this! The Yasmin pill has been pulled off the social medicine of some European countries due to such severe side effects. Their is a girl on this blog getting names together to start a class action suit. I am in. No one can get me my three years of suffering back, or my lost baby or my lost work. I am a professional flamenco dancer and let me tell you it is not easy to perform with a serious b12 deficiency which affects nerve endings, heart tissue and neurology! And the cure for this is b12 injections for life! If you want me to forward your name to the girl with the attorney you can write me at:****** Well I am going to keep trying to be well. I am young and have a whole life ahead of me.

I am 47 and have been on Lipitor now for about 7 months. For the last week or so, I have been experiencing upper shoulder, neck, and elbow pain. I passed it off as possibly the way that I sit at my computer. 1 week ago I went to the doctor to have the normal liver blood tests and she (the PA) asked if I had been experiencing any pain in my legs. At the time I didn't, and I didn't think anything of asking about my upper shoulder and neck problems, so I said "No, I feel fine".
Now today, I have been experiencing a constant twitch (for the lack of a better term) in my left foot. It's not like a normal twitch, in fact when my husband asked me to describe the sensation, I said that it felt like my nerve endings were twitching. I have also had a lot of dull headaches lately (which is very uncommon for me). I decided to search for Lipitor side effects and found this site. The thing that worries me more than anything is that my mom (which is 80 years old) has been on Lipitor now for approximately 4 years. She complained of her knees hurting but, chalked it up to her age. She contacted the doctor and he said that it wouldn't cause the kind of pain she was describing. It was most likely due to her age. I am so thankful I found this site and that everyone has taken the time to share their story. I am hoping that there is a healthier alternative. I read somewhere (maybe this site) to start taking CoQ10 and Vitamin C to reduce your cholesterol naturally. Hope this helps. Also, your natural CoQ10 is reduced considerably when taking statins. Thank you to everyone that has posted here. If I hear anything new I will let you know. God Bless and best wishes to everyone.

I take tramodol and phentermine for pain related to neurofibromatosis a genetic dixsorder that impacts nerve endings. I am experiencing increased body aches and muscle soreness.
The best site http://www.phentermine.com.md
Thanks

I take tramodol for pain related to neurofibromatosis a genetic dixsorder that impacts nerve endings. I am experiencing increased body aches and muscle soreness.
The best site TRAMADOL pharmacy.com.md
Thanks

I take tramodol for pain related to neurofibromatosis a genetic dixsorder that impacts nerve endings. I am experiencing increased body aches and muscle soreness.
The best site TRAMADOL www.pharmacy.com.md
Thanks

I have been on Toprol for 10 months now. I have never felt this awful in my life. (I have an appointment with a Cardiologist next month to get off of it.) My BP is currently 180/120 which is ridiculous. The anxiety is so awful that now I have to be medicated for that. I have also experienced incredible itching from the nerve endings in my skin and am medicated for that as well. I was wondering if anyone has experienced that side effect.

I received kenalog and novacaine inj. in my scalp for over two years. From surgery for bellspalsy I had and my eyes and face did not go back. My scalp startid itching 2 mnths later. I went to at least 10 different doctors to find out what was wrong. The doctor new all the time it was from the cut nerve endings in my scalp. A neurologist finally told me the bad news. Nothing can be done. Belive me I know your pain. This has been going on for 10 years. Somtimes I wish I would not wake up. My famly is at the end of their ropes and I've pushed all my friends away. I just went to the emergency room with upper respitory problems and heart , panic, palpatatins, can' sleep you name it I have it I just made 59 and went through Katrina and my whole family lost their homes and lives they new. Nine grandchildren and 4 married children, I can't enjoy life at all. Right now i',m going from hot and cold sweats and this has been going on for years. (I have every side effect that everyone has posted. Ruined life from La to Mississippi

Bad sinus infection which almost cauesd my eardrum to burst. I took my first pill(500mg) of Levaquin on a Monday afternoon and the 2nd on Tuesday morning. That Tuesday night I noticed my hands were ver hot as I rested them on my stomach...thought I had fever so didn't think much about it. I woke up in the middle of the night and my feet were feeling funny and my left shoulder was starting to hurt. Took my 3rd pill on Wednesday morning as I lie in bed. When I got up my feet felt as if they on on fire. I could hardly walk. Both hands and feet feel as though the nerve endings are exposed. About midday, my shoulder pain had grown to feel like it had been dis-jointed(left-shoulder only). I have absolutely NO movement of my left shoulder. My knees also feel like they could give way at any moment. I cannot walk barefoot on anything. imagine yourself in the summer, about 110 degrees, walking on rough concrete....that would be mild. Wednesday was the last pill. It is now Friday and all pain is still there. Waiting on call from Doctor. I would NOT advise anyone to take this stuff!

A horrible itchy rash, that is on all parts of my skin that is exposed to the sun. Body tingles at night. Seems like all my nerve endings are jumping, or getting bit by misquitoes.

I have been a diabetic for 42 yrs. I had been experiencing severe pain in my toes, feet, and legs where the nerve endings twitched and ached so bad, I would be up all night soaking and massaging my feet and legs. I was diagnosed with Neuropathy and was prescribed Doxepin at bedtime. It has helped tremendously.

My eyes were dilated with Neosynephrine and it caused me to syncope (faint). The opthamologist sent me to the hospital for tests and it was discovered that the nerve endings around my heart are very sensitive to Neosynephrine and Nitroglycerine. They cause my already low blood pressure to drop and cause syncope. Not a common accurrence.

I was on ortho-triclyclen for 5 years and LOVED it. About a year ago, I started to get a "period" every 2 weeks. I was mainly on the pill to control acne, but now I use it for birth control now that I have finally found a good guy! I tried a few pills, but still had the early bleeding. I read about Yasmin and had heard good things about it. It helped w/the early bleeding a little bit, but not completely. My doc had to add 10 mg of progestrin the week before I was supposed to get my period, but I'm STILL getting it one week early which adds up to 2 weeks of "supplies" and as you know, they aren't cheap! Since I started taking Yasmin 8 months ago, every few months, on the Sunday prior to my period, I get horrible nausea, vomiting, dizziness, tingling throughout my nerve endings and it knocks me out for about 2 days. It's the most horrible feeling! Sleeplessness as well. Therefore, my body is only trying to tell me 'something' and I'm going to give the birth control pills a break. I'm going to give my body some time to readjust itself hormonely and physically. Luckily, my boyfriend is understanding and only wants me to get back on track. I have made an appt w/my OB/GYN to discuss other options. Finding the right BCP has been a challenge for me for the past year...if only the docs could give us little pin prick and tell us what pill would be best for us with the least side effects. We are all so different!

I was taking 500mgs of Neurontin for about 5 months. I am
very sensitive to meds, so my psych decided I should "try" this for my anxiety disorder.
I was wonderful until my hair started to fall out..and I mean
FALL OUT. I also gained about 8 lbs--facial swelling also.

Well, if I thought that was bad, I am into 5 weeks of withdrawal and I have NEVER been through anything like it. My anxiety is so bad that I am never at peace unless I take
prescribed tranquilizers..1and 1/2 mgs of clonazepam and .75mgs of xanax. My digestive tract is completely off-
balance..horrible indigestion. Sometimes I feel that my nerve endings are exposed. My knee joints ache also. I have never felt more miserable in my life. My psych is on sabbatical and never returned my emergency calls even though he is still legally my psych with no backup psych.

Please tell me, are these side effects permanent? I can take it if it's temporary....

I take tramodol for pain related to neurofibromatosis a genetic dixsorder that impacts nerve endings. I am experiencing increased body aches and muscle soreness. Could this be a side affect of the drug?

I have been seriously ill for 8 months now after taking 3 500 mg. doses of Levaquin for a simple uncomplicated UTI. My doctor assured me that the antibiotic was perfectly safe. I trusted him, to my regret. I have been plagued with Severe Central Nervous System neurotoxicity. I also have severe tenonitis in both wrists and both ankles. My veins bulge. I have blurred vision, visual distortions, headache, muscle spasms through my whole body, abdominal pain with indigestion,,nausea, acid reflux, memory loss, confusion, agitation, abnormal dreams, tingling in my feet, toes, legs, arms, head and back. Severe back pain. Lumpy large muscule tissue in lower back. Pain upon walking. Difficulty concentrating, sensitivity to light and sound. Ringing in ears. Neuromuscular pain in chest, underarms,legs, arms, shoulders, all over body. This nightmare is ongoing and getting worse. I hope that I can help others with these problems. I flew to Indianapolis, Indiana to see Dr. David A. Flockhart, Chief of Clinical Pharmacology at IU School of Medicine. He was the only person that I read about that had background and experience in fluoroquinolone antibiotic adverse drug reations. He told me that this class of drugs, when not eliminated from the body, binds to the nerve endings/gaba receeptors in the brain. He stated that the drug does not metabolize much and sits in the brain and causes events to happen. He also stated that the drug binds to the nerve endings throughout the body including the stomach and also binds to the ends of the bone. He stated that it would take time for me to get better. He stated it would take three years if everything went ok. He prescribed Valium in as low a dose as possible to control tremors,seizures, and muscle spasms. If that did not work he recommended the gabapentin/Neurontin that my current neurologist had me on. The valium does help with the muscle spasms and nausea. The Neurontin helps me to sleep better and helps with the nerve pain. I still need further testing to determine the possibility of front temporal lobe partial epilepsy. I have already experienced two episodes of full body convulsions. Don't let your doctors tell you that its all in your head or dismiss your syptoms. If you have tendon problems, refrain from strenous exercise and lifting heavy objects as you are at risk for tendon rupture. I take low dose valium and 1 Neurontin at bedtime to help with nerve pain. The set back to these types of drugs are that your body builds up a tolerance and you eventually need to increase dosage. They are hard to come off of and can cause increased seizures if withdrawn too quickly. Dr. Flockhart told me that I would need to check in to a drug rehab center to come off of valium after prolonged use. I think that all victims of fluoroquinolone antibiotics should come together and work to get these drugs removed from the market. That's what it will take. The FDA cannot ignore publicity in numbers. Thanks to all for listening. Jessica/adrvictim