Shoulder blades symptoms and conditions

11 days ago I had indigestion and following that I had continuous heartburn. Doctor said it was gastritis and prescribed me gaviscon and omeprazole. I took one omeprazole pill in the morning after breakfast everyday for 5 days when I started to have the following symptoms: bad cramps/aches on left shoulder blades/neck, cramps/pins and needles in left arm, numbing of hands at times, nausea, tightening of the chest, sweaty cold hands and feet and lastly the most painful of all, numbing of my throat! The doctor checked my throat many times and said that it is not swollen yet I am positive there is something wrong with it. It is actually not sore when I swallow, just feels numb and cloudy? Sometimes I can't yawn fully because my throat closes up when I do and I cannot speak too much as I get breathless. I see that people here have started getting these symptoms via a long term use of this medication and not mere 5 days. Either way, I stopped taking it since today however symptoms are still present and stronger than ever tonight. I cannot sleep as I am too afraid to, as I have also been getting very vivid nightmares. I have started taking Ranitidine (twice a day)from today and I am a bit nervous about whether it is going to bring me nasty side effects too or not. I really just want the omeprazole's side effects to go away first but it seems as though it may actually take some time.... anyone had this numb throat which has caused difficulties in breathing? I also couldn't go to sleep before because when I would lie down my chest and throat felt like they were closing up even more and if I tried to sleep I would feel as though I couldn't breathe. Does Randitine cause nightmares!?

I hate this thing and can not wait to have it removed!!! I'm 45 and thought this was a great choice for me with menopause on the horizon. NOT! I had the very painful insert on Aug 4th 09 and have been bleeding ever since. 2 weeks of bleeding straight, I'd rather give birth to a razor blade! Then spotted for two weeks. Went back to have a recheck on Sept. 3rd and have had a tampon in all day and night for a month! I 'm now worried about TSS and I'm now also 10 pounds heavier, have experienced tingling in my arms, pain across my shoulder blades and I cry, a lot! I called my Dr. and she said this was normal and would subside! WHAT? Sex is not even an issue because who wants to be down in the red zone! I'm having it expelled on Tues. the 6th and can't wait to lose the symptoms and be back to normal. I look forward to having sex again without towels down like I'm house training a puppy. Good Luck to all of us and yes I think we should sue!

I am a 34 year old woman in Texas.My daughter got sick at School and so it spread and we all got it.I have a problem with my spit glands backing up.I don't know the medical term,anyway.I went to my ear nose and throat specialist and he said I had fluid in my ears and had a bad sinus infection so he prescribed me Avelox.This is my fourth day on it.I have noticed every since I started taking it I have a nasty taste in my mouth.My mouth is dry most of the time.But it seemed i felt a little better.I was on the computer talking to my Mother and BAM! Immediately my lymph nodes are very swollen,My neck,there is a huge bump on the right side of my neck,A bump where my wind pipe,I am dizzy,I was trying to write down everything and I kept misspelling everything,It feels at times I am out of my body if that makes any since,The pain is like someone beat the crap out of me and I am bruised all over randomly on different parts of my Body,I keep getting what feels like vibrations in my hands,My eyes at times feel like they are going out and in really fast,I still have extreme whizzing even after using the inhaler,When I cough you can hear stuff in there but it will not come out,I feel like I can't catch my breath,My back feels bruised at my shoulder blades..If I would have seen this site before I took Avalox I would have never taken them.
I feel like we are all just experiments to see what the drug does to different people.There's gotta be something we can do about this.This is not right.We need answers like,What are the long term effects.????
Now I am tired I feel like it has made me so tired but I am to afraid to go to sleep in fear that I won't wake up.I have 3 kids and I am not ready to die.I am suppose to be going to a pep rally tomorrow at my Kids School but instead I will have to spend my time in a Hospital.This is B.S.
I am so happy I found this web site.I thought it was just me.About a year and a half ago they found a mass in my lymph node and the doctor said after I get better he will set me up with another ct scan to see if it has gotten any bigger.It is 2 x the size since I was at the doctor's 4 days ago.This is ridiculous!
Thank You,A.

Vertigo, weakness, fatigue, exhaustion, aching numbness in arms, numbness in face arms and legs, extreme pressure in head and neck, burning feeling radiating from the base of my neck through shoulder blades to arms, foggy brain, waking up feeling (for no reason) like I have a major hang over, chills, aching feet, weight gain, feeling very fearful of my symptoms because they feel like nothing I have ever experienced.
THESE LAST 4 WEEKS HAVE BEEN HELL!
I had my Mirena inserted on June 30 2008. I experienced mild discomfort for the first 4-6 weeks. The spotting was the worst of it and that was no more than an inconvenience. I was happy with my choice of birth control.
Then this hell began about three months after insertion.
During the last week of September the symptoms listed above started. They were mild at first but by within a week and a half I felt HORRIBLE. I suspected that it may be the Mirena, but at the same time I thought I was dying.
October 1 or 2nd (it is all a blur) I was home by myself when I started feeling the numbness and head pressure coming on again (my symptoms were coming and going, not constant) so I laid down on the couch to get off my feet. All of a sudden I felt like I was losing consciousness. I grabbed the phone and called my husband to get me to the ER. I thought I was dying. A blood clot or something. Once there, they did blood test after blood test, an EKG, urine tests, and basically I was told that there were no major system problems. I know this sounds a like classic anxiety, but I know it is not. I have to say they were very good there and encouraged me to see my family physician (whom I had already been to earlier that week) again.
I called to make an appointment to have the Mirena removed the very next day. My GYN kind of shrugged off what I was going through saying that it was anxiety and asked if I still wanted the thing removed!!! of course I did. Having that thing removed was very empowering. I was feeling so helpless and it was the one thing that I could do to possibly help my situation. The feeling of relief was amazing.
I did see my family physician again who agrees that what I am going though is related to the Mirena. She did ordered a CAT scan (came back negative) just in case.
Post removal (It has been 17 days) I have been slowly getting better. My "episodes" are getting more and more diminished and further apart. I have noticed that I am flooded with exhaustion after each of these "episodes". I also never know when there going to strike making it hard to make plans. My husband has been very supportive through out and was convinced before I was that it was the IUD. He has volunteered to get a vasectomy.
GOOD LUCK TO ALL YOU LADIES.
If you have stumbled across this because you are desperately searching for answers, all I can tell you is that I believe that the Mirena IUD has had devastating effects on many, many women, but hang in there you are not alone and you are not insane. What you are experiencing is very real. Have it removed ASAP!!!!!!!!!!

I began taking Levaquin for a kidney infection. After the first pill (500mg) I had insomnia, joint pain and a little under the weather. I thought maybe it was a combination of the pill and still having the kidney infection. I figured the infection wasn't gone because the first med, Sulfameth/trimethoprim 800/160 I had a reaction too also. That was prescribed for 10day when I only was 4days into it with that pill. So I went from Friday to Monday without any medications. I felt that the kidney infection was still there because I was still hurting, not as bad as when I went to ER but knew it wasn't gone. So Monday night I started taking the Levaquin. Felt bad after the first pill but after taking the 2nd pill I became very weak, had ringing in my ears, eyes started to swell,had sweats nausea, stomach hurt and became very bloated, neck pain so bad I could hardly turn my neck. Pain running down into my shoulder blades, jaw pain, sore throat, nausea, felt like someone was squeezing muscle in left arm and squeezing muscle on left side of neck Started to have some muscle pain in right calf. Call Dr. on call and he said STOP taking the medicine, take some Benadryl and if gets worse go to the ER. Well, I took some Benadryl which made it seem a little better, but this is the day after and my muscles by my shoulder blades are so sore and have a burning sensation. I still feel somewhat weak but not as bad as last night. Seems I tired out real quick. This medicine made me feel like I was on the way out. I was prescribed it for 7 days and only took it for 2. Now I am very hesitant about taking anything as I have had reactions now to 2 different meds. Still don't know if kidney infection is gone or not. Does anyone know of any natural ways to rid yourself of kidney infection? I would appreciate any advice anyone has. All I know this has been 2weeks of @@@@ since I was diagnosed with this kidney infection.

I was given the medication to prevent a tooth infection. I tried taking it several times for it but every time I take it I get pain between my shoulder blades and it hurts to swallow. It is worse trying to swallow liquids. I am done. I don't know for sure if it's the med or if I am having a heart attack.
J.

I have been taking 20 mg. for two weeks and I have developed a dry cough, pain in the middle of my shoulder blades and my left arm. I tried to cut my grass and felt like I was going to die. I am 48 year old male with BP of 140/90. Lisinopril has lowered my BP as low as 90/60 so I cut the dosage in half. Now I feel like my throat has been ripped out and I'm hurting all over. I will never take Lisinopril again. I was on Benicar, but it was expensive and didn't really work. I am going to start exercising more and try the health food stores.

Sorry to post again, but NO ONE REPLIED TO MY POST!

I am 5 days post removal and need reassurance. Unlike everyone else, I have NOT felt better right away. I am just as tired (if not more), more irritable, and JUST GOT ACNE on my face and arms 2 days AFTER removal! I'm still dizzy and the brain fog is just as bad. Have not bled a drop at all.

I know everyone is different, but my removal experience has been completely different... don't feel better, no bleeding/clots, no immediate improvement. IS SOMETHING WRONG WITH ME??? Was it not the Mirena after all???

I took Levaquin on multiple occasions for a severe prostate infection. I took a 15 day supply...then off for 1 week...another 15 day supply...off for two weeks...and then a 30 day supply. I took another 30 day supply when the infection resurfaced about a year later. During the time I was on it I experienced extreme "arthritis like" pain in my ankles, wrists, shoulders, and especially my back. The infection was over 3 years ago and I have not taken Levaguin since. However, the joint pain has never went away. I can barely climb stairs as my right knee feels like it is going to pop out of socket. The bone pain in my neck and between my shoulder blades is horrible. I visited a doctor (I never even considered the Levaguin as a possible antagonist) and was told that I had spinal degeneration and needed physical therapy. Protect yourself and your family from this drug.

I was recently put on Yasmin, I've just finished up my first pack. Some of my friends told me to read the blogs on it cause it's not all that it's cracked up to be. I was originally put on it due to PMDD. I get hellacious PMS and i was told that this pill can help. I also take antidepressants to treat mild depression, so the low/single dose hormone is essential for me. Throughout the past month I've had two migraine headaches which is unusual. I do get headaches but not like these. I can't even open my eyes, eat, or have any noise or light around. It's really awful. I do have the dizzy spells and some gnarly pain in my lower abdomen and in between my shoulder blades. It feels like cramps but I'm not having a period yet. I'm hoping these side effects will go away as my body adjusts but frankly, from these blogs I'm really leery to keep taking this pill. Any recommendations for a girl who needs a monophasic pill and need extra help staying sane during PMS? Any news helps. Thanks and best of luck to us all.

I just spent the night in th ER for chest pains due to Yasmin.

I had been on it for a month and since the beginning I felt something was wrong.. My leg started to spasm and I got these sharp pains in my chest that moved to the back between my shoulder blades. Was told that it was acid reflux and to take tums. Didn't help. Eventually the spasms moved to my upper body (back, arms and head). My EKG, blood test and chest x rays were normal, but I still feel headaches and a weird tingling in my arms and ears are painful sometimes. All these things pains come and go so I have no clue what it can be. Stopped taking it 2 days ago and I'm hoping that it will go away on it's own without doing permanent damage.

Has anyone had similar problems that resolved on it own after stopping?

Back in October last year i was having really bad pain behind my eyes - they hurt on movement. I went to my doctors 8 times within two weeks - he kept giving me pain killers saying it was a tension headache. The last appointment i had with him id lost the vision in my right eye - they eventually referred me to the hospital. After loads of tests and questions they finally put me on Steroids and strong antibiotics via drip and i had MRI scans but by then i had lost my sight completed and was told i would never regain my sight as my nerves were severely damage. After a week or so on Prednisone my sight was getting slightly better in the left eye which was great i could think about seeing my son again. I have been taking Prednisone along with loads of other tables one for my bones and nerves and folic acid and very strong painkillers etc for months. I tried to reduce my dose as directed and my condition got worse the pain behind my eyes came back and they they said i had C.R.I.O.N so now im back on a high dose and im also taking azathioprine. I have experienced all the side affects of this drug - Round Face (moon face) server muscle cramp - i was unable to walk for 8 hours a few weeks ago i was in so much pain. Terrible bad back - shoulder blades hurts. Terrible spots. Really bad heaches. Eye pain. Water retention. Sleeping problems. Mood swings. Theres to many to list. This drug helped me regain my sight but i cant wait for the azathioprine to get into my system so i can start to reduce the steroid and start loosing some weight and get rid of all the other side affects.

I'm so glad I found this web site because I did think there was something seriously wrong with me, I took Prevacid for years without any side effects, switched to Nexium because it was cheaper and never had any problems with it, I was just at my doctors in Dec. 08 asked the doctor if there was a generic brand for Nexium because the cost has risen on that also so he prescribed 40mg of Omeprazole, took my 1st dose on Dec 31st, I thought I was having a heart attack, had severe pain between my shoulder blades, alot of burping, sick to my stomach, when I would eat it felt like my food was stuck in my chest, and also had a very nervous feeling, my husband suggested, that I stop taking the Omeprazole until I could talk with the dr. I only took it for 4 days and had these effects, I can only imagine what long term would do, I am feeling better still slight effects, but nothing like before, I will never take this drug again, I guess I will go back to forking out more money for the Nexium, it is just crazy the price we have to pay for meds.

I used to take Atenolol and had side effects. Unfortunately, all doctors know is to push drugs, instead alternatives. I am taking a natural product now with no side effects.

Vertigo, weakness, fatigue, exhaustion, aching numbness in arms, numbness in face arms and legs, extreme pressure in head and neck, burning feeling radiating from the base of my neck through shoulder blades to arms, foggy brain, waking up feeling (for no reason) like I have a major hang over, chills, aching feet, weight gain, feeling very fearful of my symptoms because they feel like nothing I have ever experienced.
THESE LAST 4 WEEKS HAVE BEEN HELL!
I had my Mirena inserted on June 30 2008. I experienced mild discomfort for the first 4-6 weeks. The spotting was the worst of it and that was no more than an inconvenience. I was happy with my choice of birth control.
Then this hell began about three months after insertion.
During the last week of September the symptoms listed above started. They were mild at first but by within a week and a half I felt HORRIBLE. I suspected that it may be the Mirena, but at the same time I thought I was dying.
October 1 or 2nd (it is all a blur) I was home by myself when I started feeling the numbness and head pressure coming on again (my symptoms were coming and going, not constant) so I laid down on the couch to get off my feet. All of a sudden I felt like I was losing consciousness. I grabbed the phone and called my husband to get me to the ER. I thought I was dying. A blood clot or something. Once there, they did blood test after blood test, an EKG, urine tests, and basically I was told that there were no major system problems. I know this sounds a like classic anxiety, but I know it is not. I have to say they were very good there and encouraged me to see my family physician (whom I had already been to earlier that week) again.
I called to make an appointment to have the Mirena removed the very next day. My GYN kind of shrugged off what I was going through saying that it was anxiety and asked if I still wanted the thing removed!!! of course I did. Having that thing removed was very empowering. I was feeling so helpless and it was the one thing that I could do to possibly help my situation. The feeling of relief was amazing.
I did see my family physician again who agrees that what I am going though is related to the Mirena. She did ordered a CAT scan (came back negative) just in case.
Post removal (It has been 17 days) I have been slowly getting better. My "episodes" are getting more and more diminished and further apart. I have noticed that I am flooded with exhaustion after each of these "episodes". I also never know when there going to strike making it hard to make plans. My husband has been very supportive through out and was convinced before I was that it was the IUD. He has volunteered to get a vasectomy.
GOOD LUCK TO ALL YOU LADIES.
If you have stumbled across this because you are desperately searching for answers, all I can tell you is that I believe that the Mirena IUD has had devastating effects on many, many women, but hang in there you are not alone and you are not insane. What you are experiencing is very real. Have it removed ASAP!!!!!!!!!!

i am so happy i have found this site! ive had the mirena coil removed just the other day (Thursday 16th oct) im now hoping that all the symptoms ive been suffering will fade away. i had my coil inserted a year ago last October. since having it inserted i have experienced headache, light periods that last around ten days which seem like forever every two weeks, with spotting in between which i was was told seven months after insertion by the doctor it would calm down and be less frequent but did that happen? NO! slowly but surely around two and a half month ago i started experiencing achey back pains where no matter how hard you try and get comfortable its impossible till it subsides, mild abdominal pain, pain in my neck and shoulder blades, chest pains, breast pain, shortness of breath, tearful, and paranoia thinking that theres something terribly wrong and im going to die and constant moaning about my ailments which im sure my poor boyfriend is secretly tired of! i just thought to myself hopefully putting two add two together that it may be the mirena coil thats making me feel so unwell. i have bled since having it taken out but i think thats the norm. so two days on im looking at this site that i found and its given me hope to know im mot the only one thats suffered with these awful side effect. im still going to get a check up to rule anything els out but im quite sure that its the coil that has done this to me. my advice to anyone would be don't have it fitted or get it taken out! good luck.

I am just starting (hopefully) to come off the Medication Ride From Hell. I I am 61 and take estrogen, diovan, vytorin, boniva, and just started back taking Prozac (1/2 dose) after this fiasco. Two weeks ago today I started having pain in my face like I got hit by a MACK truck for 5 days, especially one tooth hurt if I touched it. Then on Tues, I went to dentist, took x-ray, no abscess. So figured sinus infection. Wed I go to have epidural shots in my back for 3 bulging discs. But I had a slight fever and suspected sinus infection, so they would not do an epidural, for fear of introducing bacteria into my spine which could result in paralysis. OH BOY So this doc gives me tramedol 50 mg for pain in 3 of my discs. Eventhough 2 ibuprophens work great, I can't take advil because of stomache issues. I am sensitive to meds, so a little goes a long way. So then back to my reg doc who gives me AVELOX . And now the nightmare begins......At 7:30 pm I took Avelox and 1/2 half of a tramadol (never took either one before). Around 9:00 pm took another 1/2 tramadol. Figured I was tolerating well. At 1:30 a.m. took a whole one. (RX is 1-2 3 times a day) A few hours later I wake up itching all over. By 5:30 a.m. the slightest move I make I am spinning and nauseous. Fall back to sleep, get up and am having vertigo and nausea. I think maybe a little sprite will settle my stomach. I immediately throw it up. My body feels paralyzed with muscle spasms, pain and extreme weakness. Also pain between my shoulder blades, heart palpitations, sense of panic, extreme heaviness in my limbs, headache and continued dizziness and nausea. Felt as if I had a slab of concrete on top of my chest, as if the muscles would not move to let me breath. Call my hubby home. He takes me to urgent care, they started an IV ad then because of "possible heart symptoms" they ambulance me to the hospital. At hospital, they gave me anti nausea meds in IV. The ride in ambulance was a big blurr. My first time in 61 years ever in an ambulance. They confirmed my sinus infection with a CAT scan which probably ruled out some other things too. I leave hospital around 5 pm and am feeling somewhat better, as all meds are now out of my body for about 15 hours. Fri, no Avelox...took a break. Sat, Sun took it and all the symptoms came back except for the vertigo and nausea which was caused by the tramedol. Skipped Monday, to test theory that it is the drug. Take it Tues, within 2 hours symptoms back with a vengeance and major panic attack out of no where, hearting pounding. I am at work so I manage to get through and when I get home I collapse in chair and can't move. Finally Wed I said thats it NO MORE AVELOX. Thurs, back to doc. She gave me Bactrim DS. I am still having some muscle weakness and fatigue. Woke up at 11:30 a.m. and took pill around 2:00, fell back to sleep around 4:30 pm with spasms in upper back and shoulders, causing weakness in my arms. I hope I can tolerate the Bactrim for the next 9 days and my side effects let up. The doctors and pharmacist look at you like your crazy when you tell them what happened. When I found this site I was so relieved when other people described the same symptoms as mine down to the smallest details. Thanks for being here.

I was on Minocycline (a cousin to Doxycycline Hyclate) for years. I’m not sure how long exactly as I didn’t write down the date that I started, but I believe I have been on it around 3-4+ years. Well I went to a dermatologist and he instantly looked at the outer area of my arms (just above the elbow) and recognized I am suffering from skin discoloration, and prescribed Doxycycline, and told me to stop taking Minocycline right away. I also have this blue-gray skin discoloration on my back near my shoulder blades. I took my Minocycline for the next two weeks till the Doxycycline came in then stopped the minocycline, and started Doxycycline on Sunday. I take a 100mg pill twice daily with a meal, and thus far have had no issues. Keep in mind that I have been on Minocycline for the past 4 years or so and maybe I’ve been suffering similar side effects on that drug, thus I would be unable to see the difference with Minocycline’s cousin Doxycycline. I am pretty sure the first year or two that I was on Minocycline I was depressed (other things in life may have contributed to this depression, but now that I see all of these people saying they have had mood swings, I must state that I have had many more mood swings in recent years then I ever remember before being on these meds). I have also been extremely sleepy the past few years. I used to NEVER be able to fall asleep in public, but (I believe about the same time I started Minocycline) I gained the ability to sleep anywhere. Now I mean, anywhere. I can sleep even after I get anywhere between 6 and 14 hours of sleep. I have had approx 7-9 hours of sleep on average for the past 6 months, yet am always tired. I can’t remember the last time I haven’t been sleepy, and have had many doctor visits to attempt to discover the reason for this, but hadn’t read the side effects of Minocycline. I’ve still been pretty sleepy since Sunday, but I’ll hope that this Doxycycline isn’t as bad. Anyone else have a similar issue, where you used to be awake, but now you are always sleepy (wake up in the mornings a bit dizzy and confused), and have a hard time concentrating on one thing at a time?

Hi I have severe lower-back cramps and ache going all he way up to my shoulder blades.
I guess its from the Euthyrox 25micro grams(Livothyroxine sodium) which I am taking now for over a week.
I was diagnosed for hypothyroidism and my T3, T4 levels were marginally high so my practitioner started me on the lowest dose.

But this side effect is quite disturbing and need to get rid of this to handle the work pressure in the office.

thanks
Abhishek

I've been on Simvastatin for about 4 years but have been suffering pains in my arms as well as very tender soles of my feet.

Hi! I was diagnosed with wegener's in Dec. 2007. I was hospitalized for 6 days. When I left the hospital I was taking 80mgs of pred's. After 8 weeks I am now down to 60mgs.{per day} I found it amazing how the doctors didn't inform me on the very well on the side effects of pred's. Plus bactrim,actonel,protonix,vitamin-d and cytoxin chemo once a month for six months or more.{i have had 2 four hour infusions,getting ready for my 3rd one in a few days}.
I have severe moon face,buffalo hump. My neck and throat feel full. Almost as if I was drowning.I've gained 25 lbs.,I have severe pain in my legs and knees,my back between my shoulder blades from the massive hump that I have,which by the way makes it hard to sleep. I am puffy all over,I feel like a huge sponge in the ocean!!!!! I only hope that when the med's are over I will return to normal. I cry a lot because of all the changes to my body! I don't feel like getting out, afraid people are laughing at me, my clothes look horrible,and my memory has been fading! I sometimes feel like I'm in the "o" zone.
I am grateful for the wonderful care my doctors have given me,I just wish that they would of prepared me a little better for what I was facing for possibly a year!
For every one out there that are facing all types of effects,just remember not to forget who you are and things will get better.

61 year old female, on Lipitor 2002-2005 10 mgs a day. Doc increased dose 2006-current to 20 mgs a day. No muscle problems BUT hair has thinned out dramatically! Doc called today and reduced dose back to 10 mgs for 6 weeks as liver enzymes up with tests last week. Also have tingling in feet. Haven't read all the posts here yet as just found site today but anyone else losing hair and taking drug? If you had hair loss and quit the drug, did your hair come back? If your liver tests were higher and you cut back on the dose, did your numbers go down?

I was on Prilosec for 3 days, then switched to Aciphex for one day. Within hours after starting the medication, I was extremely drowsy, dizzy, and just "out of it." I also have dry mouth and facial numbness. The side effects are pretty incapacitating, and the most distressing thing is that I stopped the meds 5 days ago, yet the symptoms persist. My doctor has run a series of tests to rule out other problems, and agrees this may be a bad reaction to Prilosec. Has anyone ever experienced anything like this, and if so, how long until the side effects went away?

Dear Users,
At first I thought it was just my imagination seeing that I have recently undergone angioplasty with stenting I should be feeling on top of the world but then I started developing breathlessness and muscle aches with the occasional sleepless nights which my specialist could not explained and attributed it to my genes as my elder sister had the same experience. However, now it has gotten worse with sudden piercing pan to both my shoulder blades right to my finger tips. I am in a way glad to have found this site and know that others have the same problems as myself. It would be a good thing if all patients are warned of these side effects.