Pinched nerve symptoms and conditions

I have had 2 cortizone injections in my neck for pain down my arm caused by pinched nerve. I have had hot flashes since day 1 and they haven't subsided. I have them all day and all night long. I actually think I have them more than I don't. Doctor said that the hotflashes might have at first been caused by the injection but now he says it must be menopausal. To me it seems too coincidental. And my increased appetite is winning the battle. I can't seem to get enough to eat, but it did help my pain.

I am a 35 year old male in perfect health. last week i received two Kenalog injections in my trap muscles to to treat muscle spasms{trigger points) from a pinched nerve in my back. When I went home later that day as I layed down I begin having severe heart palpitations. I went to my doctor and my blood pressure was very high 169/94 with a heart rate of 127. For the last week I have been experiencing anxiety attacks, insomnia, hot flashes, sweating, nervousness jittery, very emotional. I had my heart checked out and had bloodwork drawn all normal. I was put on lopressor 50 mg 2times per day and xanax to help me sleep at night. I am crawling out of my skin! I can feel my heart beating all hours of the day and night! It is driving me crazy!! I regret getting the injection!!! The doctor told me it could take 2 months before the steroid leaves my body. I hope I will not have any lasting affects of the drug! I am very nervous these symptoms will not go away! I also am experiencing headaches and burning in my stomach. I am also always hungry and yet I am losing weight.Im thinking about seeing an endocrinologist. Im scared!!

I had a bulging disk and a pinched nerve and was put on PREDNISONE - 60mg for 5 days, then 40 mg for 5 days and then 20 for 5 days. I had a round face to begin with, which I always hated, but now, my face just looks like a balloon that someone painted a face onto. I have a huge face, a double chin, huge stomach, I look 5 months pregnant and I absolutely HATE myself on this drug. I've been off now for a week and nothing has subsided except the sweats -- very embarrassing! I work and in the middle of a meeting, I sweat so badly that it rolls off my giant red face in rivulets. I'm just miserable. Does anyone know how long it takes to get rid of the side effects of this demon-drug?? I want to stay in the house and hide.

My 62 year old husband has had Parkinson's for about 10 years now. The other day he was prescribed Prednisone (20 mg tablets, twice a day) for 5 days. After the first day his pinched nerve problem was greatly improved, and as a side effect, his Parkinson's symptoms disappeared completely and he was like normal again! This is a miracle to us and we are looking for medical research to help prescribe Prednisone for Parkinson's', or some agent similar. Did the Prednisone make the other Parkinson's drugs more effective; or did the Prednisone fix the Parkinson's on its own. We don't know. For 5 days, it was bliss; I hope we can get someone to weigh the side effects against the miracle of being normal without any Parkinson's symptoms!

Hi I am 31, have been put on prednisone for a pinched nerve in my shoulder blade. Iv taken two pills of 10 mil. For two days. one pill a day for two days. I'm stopping now. I feel so tired weak and unable to exercise. My chest is so heavy and heart flutters. I'm a smoker so it seems worse after a cigarette. I also have a few glasses of wine a day. I'm so frightened at these feelings. My tummy is now bigger in just that short of time. I really wish I knew all this first. Can any one tell me how long before I'm normal from the short usage. Please this really sucks and very scary. Also the smoking and alcohol how does it effect this? Please

I took Zocor for 9 months after I had a heart attack. After about 8 months I began having sever muscle spasm in my legs. I had a couple of episodes where when walking I couldn't pick up my feet and thought I was having a stroke and had to sit down and rest before walking on. I had to do this several times to get where I was going. I told my cardiologist and he had me stop the Zocor. The spasms stopped but I never regained the strength in my legs. Today I have had to put ramps in at home cannot climb steps. The ramp is difficult because of the incline but it is better than crawling up my steps to get in the house. I can only walk about 50 steps before my legs give out on me. I cannot walk on uneven ground without holding on to something or someone. I have now had 2 back surgeries because I have been told over and over it is my back with no relief for the legs. This last surgery my left foot drags and my big toe hangs down and I cannot pull it up. Now I fall a lot because of that and have to wear an AFO to keep my foot and toe up so it doesn't drag and trip me. The back doctor thinks it another pinched nerve and wants to open back up again. I am so tired of them trying to convenience me it is my back when I know it was the Zocor and the damage apparently is irreversible but no one wants to agree with me. I am sick of it and just wish they would say yes it was the Zocor and get you a scooter and live the best you can. I know I am headed for that road I use a walker and cane when I don't have someone with me to hold on to. Because I am so unstable on my legs.

I had Mirena inserted into my cervix in March 2009. Almost one month later, I started having lower back pains and also pain in the left side of my pelvic. After going through 3 weeks of physiotherapy, the pain has reduced but it is not yet gone. Also, I've gained almost 10lbs during the past two months even though there is no change in my diet. Are these side-effects of Mirena?

Less than 2 months after taking Lipitor I have been experiencing intense weakness of the legs, especially the hip area. A normally avid walker, last week really woke me up when I was unable to walk over 40 feet without having to stop from sheer leg exhaustion. I'd have to actually lean on my partner until I could manage to shuffle again- a shuffling gait is what I had to resort to just to make it back to the car.
This is bullshit because even though I've had some angina symptoms, right up until I went to the hospital I was able to hike; was still relatively strong.
So today I have spent hours researching side effects and have seen on this site alone many mentions of intense leg weakness and pain with Lipitor.
This, along with simultaneously educating myself on the truth about high cholesterol has convinced me to gradually cease taking this medication.

Instead I will replace with sufficient quantities of VitC, buckwheat combined with gingko, and of course I can never stop with the garlic because it is delicious.

I am 72 years old and in 1995 I had an artery blockage and had angioplasty.Upon my release from the hospital I was put on several prescriptions, beta blockers, cholesterol, Aspirin, Vitamins, etc. which I had been taking regularly for 13 years without any problems. In 2008 after having chest pain and going to the hospital my heart doctor advised me I had Atrial Defibrillation and put me on Warfarin and also told me to stop taking all the vitamins I was using along with my daily aspirin dose and one of my prescriptions. Since then I have had constant shoulder and muscle pain in my arm and leg. I have had several treatments by a chiropractor and several physical therapy treatments and the pain has not subsided. My memory has gotten worse also however I thought that was due to my age until I read some of the above side effects of Warfarin. I definitely have a lack of energy and also changed my diet due to the Warfarin. I have informed my heart doctor about the problems and he advised it is not due to the Warfarin. I don't agree with him after reading all the posts, but I am not a doctor. I will continue my prescribed dosage and Pt/Inr tests as schedule for a while, but if my pain etc doesn't get better I will probably do like the lady's posting and stop the warfarin on my own.

My 90 year old, very mentally sound, grandmother was admitted to the hospital 2 days ago after complaining of severe pain in her back. While in the emergency room, after being diagnosed with a pinched nerve, her blood pressure rose and the staff doctor decided to admit her and put her on this horrible drug! He started her out with 100mg 2 times a day. My grandmother went from her usual calm perfectly sane self to a combative, babbling, lunatic within 6 hours of her first dose! It scared my aunt so bad that she started calling everyone to come say goodbye while there was still a chance that grandma would recognize us! I just knew that there was no way my completely lucid grandmother could go into dementia overnight so I told her to find out if the doctors had administered a new medication since they admitted her. They had and it was toprol XL. The stupid doctor tried to tell us that her behavior was related to a very low dose of prednisone that she taking for 2 years. We immediately demanded that the toprol be stopped and within 8 hours she started to return to us. She had spastic tremors, severe dementia, hallucinations, shallow breathing, agitation(went from laughing to combative in the space of 10 minutes!), dehydration, very frequent urination, extreme mood swings, brain fog/confusion, eyesight and hearing loss, her tongue swelled up, and her eyes were rolling back. It has been 36 hours since her last 100 mg dose and she is still fading in and out. We pulled her out of the hospital and brought her home today where the side effects have decreased but continue none the less. Since 11 this morning she has had bouts of not recognizing her own home and asking us to do things like take things out of the oven that she said she put in it, which of course she had not. I am praying to God that this medicine does not leave permanent damage. My grandmother is an unusual case for mental soundness at her age and it would be so unfair for that to be stolen away from her because of some stupid medicine that she was not only forced to take but over dosed with as well! DO NOT TAKE THIS MEDICINE WITHOUT RESEARCHING IT THOROUGHLY!

I have had the mirena in for about 17 months. The first 10 months I was nursing and didn't think much of it. The last 7 months I have been a little depressed. Just recently, I have had tingling in my hands and feet and lower back pain. I have been treated by my MD who I love for a pinched nerve. He has done complete x-rays and back/spine MRI and everything has come back fine. I am a healthy 35 year old who wonders if it could be the Mirena causing my symptoms?? Just interested is anyone feeling the same?? Please respond :)
I have read so many experiences on this website and I have an apt. next week to get it OUT!

I thought i was going nuts in a matter of days. i figured i was just stressed out from work and how my lifestyles changed throughout this new year, but i'm only 18 life shouldn't be this way. I Started taking Doxy on March 4th for my acne, and for the first week i was fine, no side affects except for the feeling like there was something in my throat. but then as I continued into the second week, i would wake up fatigued and dehydrated; which stayed with me throughout the day. I started getting neck aches and in the lower back, all on top of a migraine that would come and go. All day i'd feel dizzy, fatigued, tired, disoriented, and thoughts that i'll never be healthy and i'd always feel this way would constantly go through my mind. I even went to my family physician because I thought had a pinched nerve in my neck which was giving me all this pain in my neck and the headaches. my doctor confirmed that i didn't have a pinched nerve so i continued to tell myself that im alright.... right? no news is good news.....right? It wasn't until today(march 17th) that i considered doxycycline hyclate to be a possible culprit. I realized something was very wrong when i couldn't even tell my dad what i was experiencing w/o getting emotional... for NO REASON!!!!! my dad looked up this "Doxy" and we stumbled across this helpful site filled with blogs about people taking the exact same medication with the exact same side affects. As much as i'd love to have a clear face, it's not worth messing up your mind. i took my morning dose today, but will not continue to take anymore of this "Doxycycling Hyclate" hopefully, with time, my mindset will return back to it's normal functioning. just THINK POSITIVE!!!!!!!

I had Mirena put in the end of November and was thrilled with it. I instantly regained my sex drive. I had a lot of spotting for the first few weeks but hardly any bleeding since then. About two weeks ago I noticed that the right side of my body was numb but brushed it off as I have previous neck problems and thought it might be a pinched nerve or something. The numbness is constant, from just below my ribs down to my toes, worst in the hip/groin area. I now have very little sensation during intercourse. My doctor has run blood tests and was mentioning testing for MS but after reading these posts I think it may be the Mirena. I have also had painful joints and started seeing a counselor as I have been feeling very depressed (she has recommended anti depressants). I have also had a lot of bruising, not sure if this is related, and am sick more often (have spent a total of 38 days on antibiotics since I got it put in, hadn't needed any for years before this). Making an appt today to talk to doctor!!!

Just took this for the first time, for some back pain related to a pinched nerve. Within about half an hour I started to feel loopy and then it knocked me out completely for a few hours. My back feels pretty good though.

OH MY GOSH! I thought I was crazy until I found this site. Ok, I had my Mirena inserted January of 2007, and IMMEDIATELY experienced joint pain, pain in my hands and feet, and it's 22 months later.. the pain NEVER went away. I thought because I was a very hardcore athlete when I was younger, that this was par for the course, that I will be getting arthritis. I'm 34 years old. Crazy to say arthritis at 34? I think so. Well, I have been researching my symptoms for months and months online and gone to a few different doctors over this. My symptoms include chronic fatigue, headaches (on a good week 4 days out of the week), joint pain in my hands and feet, sensations in my hands and feet that feel like they are swollen (but they aren't), upper and lower back pain, heart palpitations, leg cramps, hair loss, ABSOLUTELY NO SEX DRIVE AT ALL, muscle fatigue, and I've gained 40 lbs since I had it put in... OUCH. NONE of this (except for headaches and some depression) was experienced before the Mirena. Funny, I never linked it to the Mirena. I've had my thyroid checked, been diagnosed with carpal tunnel (lol what about my feet? Good doc!) had blood sugar checked (nope, not diabetes!), well, now I'm on to getting checked for fibromyalgia. Kinda wondering though, if there is a link to fibromyalgia and Mirena, like it could induce it? Sounds like so many of you have the same symptoms, and many have thought the same things... fibro, diabetes, lupus, ms, hell, I even though lyme disease at one point. This is ridiculous... I'm having it out this week.

Extreme Weakness, extreme excessive sweating, nausea, dizziness, itching, terrible headaches.In addition, I seemed to have contacted a moderate case of the flu. At least I had what seemed like the flu. However it is possible that it was just more of the same from the prednisone. My doctor gave me prednisone for a pinched nerve in my neck and a herniated disk in the same #7vertebrea. He gave me 12 days. As soon as I started taking it, I began to feel very weak, I had headaches, terrible exploding headaches. I found that I began to itch on my arm for no apparent reason, except for a bracelet in the area.In addition, I began to have excessive sweating, extreme sweating, the water would be pouring down my face. At that time, I would feel my heart pounding have some dizziness, and just overall bad feeling. It was debilitating, I spent a lot of time on the couch because I could not function in my daily activities. I went from exercising for 90 minutes to barely being able to get through 15 minutes. My question is will I go back to "normal" when this medicine gets out of my system. What is the half life of this drug? Should I do a detox of some sort. Worst of all, the problem with my neck has not really resolved and I will probably need some other sort of intervention. I never got that burst of energy that other people experienced with this medication.

I had a chronic sinus infection and my doctor put me on Levaguin and 80 mg of prednisone. I am 62 and I take only synthroid as a prescribe. drug. I told my doctor I was a borderline diabetic. She told me the side effect were bone weakening in the hip and pelvis and stomach upset. At first I had a lot of energy and sleep a lot less. I just thought I was getting better. I tapered down to 1 1/2 . After taking them for 11 days I was not able to function. My body was under extreme distress, I have very excellent blood pressure and I am in very good health. I have been off the drug for 4 days. I am still experiencing sweating, hypertension, extreme muscle spasms. I am unable to wear my contacts, I am short tempered and I am normally the opposite. I have horrible headaches and I very seldom ever get headaches. I told my doc and she said it would go away in time.
My body is fatigued I am have trouble focusing,sleeplessness. I don't know where to turn at this point. Sometimes I feel like I should go to er because of the hyperventilating and rapid heart beat. I am afraid to exercise. I am eating a lot of high protein foods, I am not gaining weight, I have lost 7 lbs in two weeks. PLEASE EVALUATE THE RISKS OF THIS DRUG IT HAS BEEN A NIGHTMARE FOR ME. DOCTORS DON'T ALWAYS TELL YOU THE WHOLE TRUTH AND THEY NEED TO BE HELD ACCOUNTABLE FOR THIS.

So I finally had the Mirena taken out. Feel a little better, but am having the "Mirena crash". Lost a couple of pounds already (two weeks), but started bleeding two days after removal and haven't stopped since. Heavy at first with huge clots and now still clotting just not as bad. Seems to be dying down finally. Mirena is the absolute worst thing I have ever done to my body. Oh and when I went in to get Mirena removed I felt like I had a pinched nerve in my back that miraculously went away the minute it was taken out! My doctor denies any symptoms were from Mirena. I almost think the drug company that produces this is paying all doctors a kickback for using it. Don't listen when they tell you it's great. I have read pages and pages of women with the same complaints I have about Mirena. If your reading this and thinking of getting it I say: DON'T DO IT!!!!!!!!!!!!!!!!

Yes, at my second Remicade infusion, I got a stiff neck and severe pain, like a pinched nerve around cervical 4. The pain radiates down my right arm. It hurts 24/7. I also got this when I took Cipro! Today is my 3rd infusion and the pain is still there. The doctor says it is just arthritis, but this is not arthritis. It is a Remicade side effect. Analgesics so not help the pain.

I have stomach pains and increased vaginal itching. This is my second day of a sixth day dose. I'm wondering if ithe steroid is causing a yeast infection. I'm taking the medication for a pinched nerve in my neck.

Hi all, I have had the Mirena since May of 08. I had twins in Feb of this year and was given the little plastic ring for birth control. That gave me TERRIBLE migraines. i hardly ever even have headaches let alone migraines. It was impossible to take care of twin infants along w/migraine pain. I really shouldn't be on estrogen anyway because of a clotting problem in my family. So my doctor recommended the Mirena. I wanted it anyway because I can't remember to take pills now, (I'm a little busy.) Since I had it put in I have been losing my hair in unbelievable amounts which my doctor attributed to my just having twins. My depression and anxiety meds are NOT working anymore. My fourth and fifth toes on my right foot are completely numb and stiff, almost like I have arthritis or something. I have NO interest in having sex w/my husband. But after taking care of twins, who does?? Just kidding. I am not very happy with this IUD, but have decided the alternative (being pregnant) is not a better option at this time. So, for now I will continue to be a bitchy, balding, arthritic, celbate mother of two. Good luck to everyone else

I am a 57 year old man, who has been suffering from asthma several years. This spring my doctor put me on Singulair as an additional medicine to my cortisone-inhalator. after one month I feel symptoms of depression an mood-changing, severe ups and downs.
AND - as an additional symptom i have partially lost my feeling in some fingertips, and now parts of my left thumb and even a feeling of "cold2, mostly in my left hand.
anyone who share that symptom?
M.

I have been taking Neurontin since January 2008 with a gradual increase from 300 mg to 900mg daily.
I am having several of the side effects especially since the increase to the 900mg.
Sleepy, constipation, burning eyes, pain on my left side, probably the kidney area.
I was put on the medicine for a pinched nerve in my back which was causing pain in my left leg. It seems to be easing but I don't like the side effects. Will they gradually go away?
Hope to receive some response from others.
J

I am a 25 year old, who was perfectly healthy prior to recently when I was diagnosed with Nephritic Syndrome and Minimal Change Disease and possibly FSGS (kidney diseases) I was put on 60 mg of Prednisone for 1 month then I was lowered to 40 mg for one month and I am then dropping to 30 mg. I am also taking Fosamax for my bones and a Vitamin D pill because my last lab test showed low vitamin D levels.

I am dizzy constantly and can not live a normal life, I can not drive or do any activities that I had previously done. My chest is so tight and constricted all of the time, my heart rate is so fast and pounds at my chest. I have no energy to do anything, I can barely open a door at times. I am beginning to grow unwanted hair on my face. My abdomen is always bloated. I have pain in my rib cage, and shoulders. I feel very sore throughout my entire body. I do not really sleep at night, so I look very tired all the time.

I have actually lost weight, I have no appetite at all. I am down 10-15lbs.

Now for the Pro- my Kidney Diseases are currently in remission and this has happened much faster than the Nephrologist had thought.

I am very anxious to getting my life back to normal and getting off the Prednisone.

Has any one else experienced increased heart rate, chest tightness, or rib pain?

I wish everyone the best in their roads to recovery!!

hello all,
I had my Mirena put in on October of 07. due to heavy bleeding which caused severe Enemia. I have since had problems with very Low potassium, re-occurring yeast and bacterial infections and some heart palpitations. The latest symptom I have been experiencing is numbness in my left leg and foot. sometimes totally numb. My dr. told me that it could be a pinched nerve in my back but I have not done anything to strain or stress it. after reading this website i am convinced that these symptoms are caused by my IUD.
I am going to call my OBGYN tomorrow and have this IUD removed!!!!!