Pinched nerve symptoms and conditions

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.

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!!!!!

Been off this medication now for 4 months and have realized I don't have the unexplainable anxiety I use to have. This was over odd things like driving, which I have done for years quite happily. Also seem to take life in a more relaxed way all round. One side effect still to go(I hope) is neck pain with headache, though these aren't so frequent now. Weight too has remained stable.

I wish I would have found this sight two years ago!! I started taking Yasmin, seen the commercials saying reduces pms, so I thought I would try it. The week before I went on it I had a pinched nerve in my back. I mention the back because I thought at first it was my problem. So I had a shooting pain going down the back of my leg and then all of a sudden my foot started tingling. I went back to the doctor, he gave me predisone, gained 20 pounds in a month. I was miserable, I was going to the doctor every two weeks, with pain. I went through serveral MRIs, CT scans, blood work for everything you could imagine (metal poisoning, vitamin deficiency, etc..) I had four epidurals trying to figure out where the pain and tingling was coming from. I was on percocet, taking it every 4 hours. I went to two different neurologist, three orthopedic doctors, Chiropractors, acupuncture. Nothing helped. I took Lyrica, for the tingling, nothing, I started taking Cymbalta, because I thought I would be miserable forever. I felt like I had restless leg syndrome.(RLS). Finally after 7 miserable months, not thinking it could possibly be the Yasmin, I have been on the pill before (Ortho-Tri Cyclen) I went off the pill in June. I almost immediately started feeling better. By the end of August I was feeling GREAT!! My Husband and I decided to have another baby (#3) I had a great pregnancy, and other than needing to loose a little weight couldn't be happier.

I have been taking warfarin for over a year now. I'm not sure if my symptoms are from the meds or not. I have a very itchy scalp, and I occassionly have difficulty swallowing. Right now I have a pinched nerve and right shoulder pain, have had it on and off for 6 months, my right index finger was numb and tingly for a month. I am currently seeing different doctors to see what the problem is, so far nothing. I'm hoping to go off Warfarin soon, against my hematologist's advice. Has anyone had any similiar symptoms while taking warfarin?

My doctor prescribed Armour Thyroid to me to help me lose weight; he did this without taking a blood test. My thyroid was perfectly fine when I began taking it. I took it for three weeks, but didn't like the palpitations and weird things happening to my heart so I stopped. Since then, about two weeks ago, I have had horrible muscle cramps in my upper back, neck and shoulders. I also have pain in my right arm which I am assuming is a pinched nerve from the muscles. Any ideas what to do?? I can't take the pain much longer.

I would like to stop taking paxil, I have been on it for 3 yrs. When I skip my medicine I get what feels like electrical shocks in my neck & head. I wasnt sure if I had a pinched nerve at 1st but began to associate this with the event that I had not taken my meds. I also have onset of panic attacks & rapid heart, & terrible terrible forgetfulness, as to even what cabinet I would like to open, I open the wrong one, go into the wrong doorway, wrong driveway. I am very concerned. I have told my Dr. that I would like to get off this Paxil but Ive been told that it would be best since I was suffering from anxiety attacks in past. I would like to be committed to be able to handle the withdrawls. If anyone has been successful in stopping Paxil and now feels pretty back to normal, please let me know. Thanks

I too have been taking Aciphex for acid reflux for about three weeks and although it seems to have helped with the burning and nausea, I have just recently (four days ago) been experiencing a slew of symptoms. They include headache, blurred vision in my left eye, facial numbness, both forearms numbness, leg (knee down) numbness, and tingling sensation in head. I went to the ER yesterday due to the left arm and left side facial numbness. They ruled out heart attack, blod clot, stroke, bleeding in brain, and brain tumor via a CT scan and a host of other neurological examinations. Doctors have suggested an MRI to rule out something else neurological (MS, neurofibromatosis, etc.) that a CT scan might not pick up. Also, will do a neck MRI to rule out a bulging disc or pinched nerve. I am hoping that it is just the Aciphex.

Hi all,

I am on my 30th day of this crap. Now, I haven't had the complications a lot of people have, but I have had an ache in my legs just above my knees for probably 3 of the four weeks and in the last week of this an ache in my shoulders and neck area.

I too had the night sweats problem and a LOT of anxiety when i was taking this at first, but I read somewhere else that you're not supposed to have caffeine while on this drug. So, I quit all caffeine, except chocolate, this past two weeks and all my night sweats, anxiety, and sleeplessness went away.

I do however, still have a terrible tiredness each day after taking it and it typically lasts till about 8-9 at night before it starts to lessen.

Funny thing is, i don't think this 500mg of it each day has fixed this supposed prostititus problem i allegedly have. I still think its a pinched nerve in my spinal cord, but the doctors think I'm nuts.

Anyways...good luck and I hope my aches go away after today since I am done taking this.

Phil
p.s. 35 years old...in good shape and I was doing karate before starting this, but been too tired while on it to want to do anything and the karate never made my legs constantly ache.

I am a slender, athletic woman who is now potentially scarred for life by this horrible drug. In July 2006 I was given kenalog injections bilaterally for bursitis by a rheumatologist. In early October I noticed the development of a large indentation on my right hip. During a consultation with another doctor regarding my ongoing hip pain, I was told that this dent was caused by kenalog and would likely never go away. I confronted the rheumatologist who administered the injections and she pretended to be unaware of this as a result of injections and ordered an mri claiming that my horribly disfigured hip could be caused by a pinched nerve (said with a straight face). Well, the MRI confirmed the kenalog caused my dent, and I read on Bristol Myers Squibb's kenalog information site that local fat atrophy is caused by improper administration of the injection. Rheumatologist claims a plastic surgeon can fix this. I am consulting an attorney because this screams negligence.

I had been taking Zocor for about five years when I developed a tingling in my feet & toes. I went to my Doctor
and he said I probably had a pinched nerve that was causing the problem. So I went t a chiropractor for about a month, but the problem got worse. Went back to my doctor and he immediately said that I had neuropathy. I went to a neurogolist had tests taken and sure enough I had nerve damage to my feet & legs with severe shooting pains and tight
muscles. I asked the neurologist what caused the problem, he said it was the statins in the Zocor I was taking. I stopped
the Zocor the immediately but the damage was done. The neurologist told me the statin break down the fatty tissue covering the nerves and could take months even years to heal. Now I was a very active 70 year ald man went to the ymca three times a week walked 3-4 miles a day, worked the weights even played golf 2-3 days a week. Well, all that has stopped. walking has become a chore. because the pads of my feet feel like they have big knots in them. But the good news is I wont give up and let this rule my life. I still work the weights and still struggle thru the pain of walking that 1 mile a day. oh yes I have started taking vitamin C for my cholesterol

I started taking Lisinopril 2.5 weeks ago and I have been having severe muscle cramps in both calf muscles and started yesterday in both forearm muscles. Dr wants me to have an MRI to check for pinched nerve but after reading the side effects and seeing muscle cramps on the list, I think it would be a waste of time and money. They never look at the side effects before scheduling new tests. Be careful.

Taking 25mg of TROPOL.
Lower back pain; all tests negative; MD feels it's pinched nerve. Numbness in both legs with tingling and needle like feeling in toes of both feet. Both legs feel like someone is squeezing front and back of legs. Legs are not swollen

I have been taking Lipitor for 3 years; I started having problems with my finger and thumb on my left hand. I passed it off as arthritis. Not being aware of the side effects of Lipitor. Then I started having numbness in my finger tips. My Dr said it could be a pinched nerve in my neck. However, tests are expensive with no insurance, so I bypassed the MRI. In the last 6 months I have been getting weaker in my legs, I can hardly walk a block without my legs starting to shake. Yesterday I was at work and went to walk down a flight of stairs and almost fell. I had to do a lot of walking and my knees started giving out on me. I was so embarrassed. I had to stop and rest, and let the rest go on. My husband saw a Lipitor commercial and heard the side effects one being Muscle weakness. I have stopped Lipitor affective today. I will be sending my Dr an e-mail immediately after this to let her know I am discontinuing Lipitor. I am afraid of what I have done to meself. I just hope I can get my health back.

I went to the dr in sept about a pinched nerve in the right side of my neck and was given a shot in my left upper arm(which didnt help). A month or so later i noticed a dent in that area so i called the dr that gave me the shot and was told "yea that can happen but its not common"!!! so what i wanna know WHY AND THE HECK WASNT I TOLD THAT BEFORE!!! Im sure i would have opted out for the shot that didnt even help but left a nasty dent in my arm. The area feels hot and like a bruise but no other side effects that I noticed......and people wonder why we have no faith in drs!!!

hi im a 19 year old girl and i've been on tramadol for at least a year. i was given it because of a pinched nerve in my lower back. and what is worse than the back pain is the addiction. my doctor told me since it is no-narcotic there will be no addiction so i took as perscribed. 2 every 6 hours.. well that didn't help so i bumped it up to three.. well here i am a year later and im trying like hell to get off.. i have horrible withdrawels.. i tried to get off them about a month ago but the withdrawels were so terrible i couldn't so tomorrow i am trying to again.. luckily i have a little smirinoff to help me when im at my worst.. you know just to take the edge off.. not to get drunk or anything.. but i love my tramadol.. but hate these withdrawels.. why is it that im having them? could it all be in my mind.. could i just be building up the idea of not having them so much that i put my self in a state of anxiety.. please help.. tell me if anyone has had withdrawels from these wolf in sheeps clothing pills

I'm 44 and my cardiologist placed me on 40mg of Lipitor last year. I have been pretty diligent about taking the prescribed dosage. But in the last 6 months or so, I had been dealing with severe muscle spasms, extreme muscular twitching, neck pain, arm pain, and muscle cramps in my arms and fingers. At first I thought I had a pinched nerve in my neck or ALS because of the muscular twitching. Then I had to deal with the HUGE memory lapses. I thought I was going crazy. I recently stopped taking the Lipitor because I kept forgetting to get my re-fill and voila... no more cramping, very little twitching and my arm and neck pain is improving. The memory issue hads gotten better and I notice that I have more energy.

I hate that I din't read this forum sooner. This stuff needs to be taken off the market. I would like to take the Res Q 1250, but you have to give your first born to pay for it. Any other suggestions?

Mish

WED, 29 JUL BY BETTY
63 YRS OLD - HAVE BEEN ON MED SINCE THE 60'S. FIRST WAS EUTHROID THEN SYNTHROID BOTH WORKED VERY WELL. SINCE MAR '05 DR CHANGED ME OVER TO LEVOTHYROXINE (BAD IDEA). HAVE THE FOLLOWING SYMPTOMS: FATIGUE, TINGLING IN THE LEGS, NUMBNESS IN HANDS BUT THE MOST UNBEARABLE WAS THE CRAMPS IN MY LEFT ANKLE & CALF. THOUGHT I HAD A PINCHED NERVE. WENT TO A CHIROPRACTOR WITH NO PAIN RELIEF, THEN A ACUPUNCTURIST (SOME RELIEF) THEN IT HIT ME...SIDE EFFECTS FROM THIS DRUG. QUIT TAKING IT & WILL SEE MY DR TOMORROW AFTERNOON AND INSIST ON GOING BACK TO SYNTHROID. I HAVE A HARD TIME COPING WITH THIS PAIN AND WILL NOT LIVE THIS WAY. EVERY STEP I TOOK WAS EXCRUCIATING ESP WHEN I HAD TO WALK FR THE PARKING LOT TO MY JOB. I EVEN HAD TO SIT IN THE BATHTUB TO TAKE A BATH MY LEG HURT SO MUCH. I THREW AWAY THE POISON (PILLS) THAT CAUSED ME SO MUCH PAIN.
THE CRAMPING COMES AND THEN SUBSIDES BUT NOT FOR LONG. TRIED USING THE HEATING PAD, MASSAGES BUT IT KEPT RETURNING. HOPE THIS HELPS ALL THAT READS THIS.
WOULD LIKE TO HEAR MORE FEEDBACK ON OTHERS EXPERIENCES. THOSE THAT HAD THE LEG CRAMPS CAN YOU RELATE HOW IT AFFECTED YOU AND TO WHAT EXTENT.
THANKS TO ALL OF YOU FOR SHARING YOUR STORIES , WHICH CONFIRMED MY SUSPICION ABOUT THIS HORRIBLE DRUG.