Pain medicine symptoms and conditions

I am 56 years old and I was put on Lisinopril about three months ago.

We had just moved to a different town with a new doctor. The reason I went to the doctors was that I had a bicycle accident where I went over the handle bars (front brakes locked up on me). I was also due for a periodic check up. I was sore from my bike accident (jammed my LH wrist, RH elbow, both shoulders and knees). The doctor had no x-ray machines so he sent me to the urgent care, nothing was broken. My doctor said that I would be sore for awhile and gave me some Vicodin pain medicine.

Due my periodic exam the doctor suggested that I go on Lisinopril because I am a diabetic, even though my blood pressure is OK. He said that he actually takes it because of the preventive nature of the drug.

Well, as the weeks went on I continued to have aches and pains in my joints (wrist, elbow, shoulders and shoulders), which I thought was from my bike accident. I also play seniors softball which is not a very aggressive sport. Well I've had a pulled hamstring and achilles tendon pull during playing. Thought this was normal but these injuries continued to plague me.

At nights sleeping my shoulders & neck would ach. My knees would shoot pains. My ankles constantly ache, day & night.

A friend of mine told me about taking black cherry juice for joint pains, maybe from gout. After taking this black cherry juice it seemed to help, but still not normal.

Today I stopped at our local taven to have a berr and talk softball with the guys. I broke out in a heavy cold sweat and almost pasted out, lightheaded. I thought I was having a heart attack or something. Being very concerned I told my wife who is an RN. She read the side effects of Lisinopril and it clicked. This web site helped me figure it out also.

I am taking myself off Lisinopril today and expect improvement and my life back. I thought all this was from my accident and getting older. I am excited to see the results, which I feel very positive about.

I will be on prednisone for the rest of my life so my Pulmonologist says. I have an auto-immune disorder called allergic broncho pulmonary aspergillosis. I thought I was alone until I read all your messages when it comes to leg, and joint pain. My doctor acts as if I am crazy, and that it is not a side effect of the medication I am taking. It has gotten worse the longer I have been on the drug. I rarely sleep, and I have an appointment with him tomorrow. If anyone can suggest something that helped them I would love to hear it. I have tried everything, and the only relief is when I take pain medicine which I do not want to be on forever.

My 12 year old daughter completed the 3rd round of the Gardasil shot in late August of 2008. School started the next week. A couple of weeks later, she became ill and I rushed her several times to the doctor and to the emergency room only to have the doctor say she had a virus. After 2 weeks of horrible pain, nausea, and headaches, I took her to the emergency room at Wake Forest Baptist Medical Center. She was referred to a Gastroenterologist where she has been going ever since. The doctor has had her on pain medicine since December to help her cope. I analyzed all of her information and compared it to the 12,000 cases in the VAERS database and I am convinced that the shot made her sick. NO DOUBT! The database is located at http://www.medalerts.org/ and you can run the lot # of the dose given to you through the database to determine if their has been any adverse effects noted. The first dose that Lauren had was listed 78 times. Her second dose was listed 70 times. Her third dose was listed 74. I researched the ingredients contained in the shot and the one that I am concerned with is Aluminum. After researching the effects of aluminum poisoning, I believe that she has all of the signs. I begin treating my daughter at home with sublingual (dissolves under the tongue) Vitamin B12 and Vitamin C tablets available at the local drug store over the counter. My daughter has been sick for 7 months and has missed almost her entire Eighth Grade year. As you can see, since starting the vitamins, she has gone from being sick 97% to only being sick 28% of the time. This is a BIG improvement and this may help other young ladies who are affected. I don’t think it will help all, but as sick as these girls are, I don’t see how it could hurt. Her doctors at Wake Forest are aware of what I am doing and agree.

Month Sick Well
SEPT 93% 7%
OCT 97% 3%
NOV 83% 17%
DEC 87% 13%
JAN 71% 29%
FEB 43% 57%
MAR (WK 1-3) 28% 72%

My daughter has been referred to Duke Medical Center now and will go for her first appointment in about 1 month. The FDA and CDC need to pay attention to what is going on and pull this drug off the market. If you have been affected, please ensure that you report your reaction to the VAERS Database. Your doctor is required to report adverse effects, so demand that they do so.

I hope this helps, and if anyone tries the vitamins and it does help or if you would just like to ask me some questions about my daughters experience, email me at ****** and let me know. I will update the doctors at Wake Forest and Duke. Hopefully, if we band together, we can get to the bottom of this and figure out what to do help these vaccine injured girls.

Like many of the other stories my daughter was a happy healthy 14 year old high school freshman prior to receiving the Gardasil vaccine. Now she is chronically ill suffering from pancreatitis, gastrointestinal disorders including extreme nausea,vomiting,and diarrhea,headaches,blurred vision,pain,fatigue,hypersensitivity to light and sound,and has had pneumonia twice.We have recently spent 8 weeks in two different hospitals to return home with still no answers as to how to end this nightmare. She has a central line so that we can give her IV nutrition TPN and Lipids, is on 5 nausea medicines and 1 pain medicine every 6 hours round the clock just to keep her comfortable. We are going to take her to Mayo's with the hope they can help us, I refuse to accept the fact that this is what her life has become and that our only option is to treat the symptoms. The doctors so far are completely clueless without it being in black and white on a piece of paper from a test result they seem to dismiss you with out any compassion at all, I wonder if they would have that same additude if this was their daughter. If anyone out there has found any kind of help please let me know. I can't believe Merck is still being allowed to poison our young girls while the FDA looks the other way!

I'm 25 and diagnosed with IC when I was 23. I'm taking elmiron 100mg/3 times daily. I have to down ibuprofen quite often for side effects from IC. It doesn't seem to go away. I'm taking amitriptyline(using for muscle relaxer) 25mg/twice daily for spasms. That seems to help quite a bit but just for spasms. My doc told me I was having issues because the acid(from food or drinks) in the bladder was bringing the IC back. So, I started taking Prelief which is suppose to remove the acid from whatever eating or drinking. But, unfortunately it seems to work with everyone else but me. So, I'm completely lost and my doctors don't seem to think I have enough issues to worry about. I've tried going to other doctors and they either don't deal w/ IC at all or they still aren't accepting new patients. Or my doctor wants me to keep coming in twice a month to give more money when absolutely nothing has changed. What to do?

I had a Prostate Infection that Bactrim and Doxycyline would not cure. So the doctor said the only thing that would cure i is Cipro or Levaquin. I was on it for a month. I tuffed it out and I had to take Tramadol to kill the leg pain. One day I accidentally took an extra Cipro pill and within a half hour, I had a hard time walking. I actually could feel my achilles heel pulling when I walked like it had shrunk. I've been off it two months now and I don't feel any better. I am tired and aching all the time. I have no strength. My back and knees hurt everyday to where I can't function without taking some kind of pain medicine. How long does this last? I talked to a lawyer who is doing the Cipro lawsuits and he said unless I had a ruptured tendon or can get a doctor to say I have chronic tendinitis, I have no case. I have never felt so bad in my life.

In 2003 at the age of 31. I had been taking singulair for over 2yrs. I started experiencing muscle weakness and I got to the point I could not sit or lay down. I was extremely in a lot of pain and taking large amounts of pain medicine. It went on for several weeks. I went to the doctor because I was having muscle spams or what I thought was a ruptured disk. I had a MRI done and it didn't show anything. I was sent to a back surgeon and he checked me out and wanted me to list all my medications. I began to tell him about zyrtec and singulair. He asked me how long I had been on singulair? I told him almost 2 years. He told me to get off of it right now because it would kill me. He said the singulair was deteorating my muscles
and causing me to have muscle spasm. I had no muscle tone. He sent me to a massage therapist 3days a week for 6 weeks and I came off of the meds. The doctor told me he had at least 10 patients that had happen to them.That was a wake up call. The doctor also told me his wife was on it 6 months and started throwing up blood and took her to the ER. All because of singulair and my kids have been on it for 3 years and have not had one problem. They are 10 and 7.
My husband is a pharmacist and he had not heard anything bad about it. He filled out a card about the side effect. It only happens in 2% of people taking it.

I just got mine inserted Thursday and am having cramps on my right side with a light brown discharge, anxiety, depression, tiredness, mood swings, dizziness with a lack of concentration and all this has taken place since Thursday. The first night I had an anxiety attack and I could feel the Mirena inside me when I would move around. 600mg of ibuprofen and other pain medicine would not even stop the cramping. I could feel it in my sleep and am having problems sleeping because of it. To believe all this was within 24 hours of insertion. Based on my symptoms and other peoples side effects and problems, I am making an emergency appt for tomorrow to have it removed. This product is very expensive and sounds really good on paper, but my current and longterm health is priceless. I just wish I had found this website before mine was inserted. Please don't take anymore chances with your health if you are having problems with Mirena.

Recently, I had an experience very similar to pocoloco's experience with Lactaid. The main difference is that pocoloco experience seems to have wained within hours, mine were much more severe and lasted for days.

On a Monday, I took some Lactaid before eating a salad, that had perhaps 2 tablespoons of Ranch dressing. The next morning I awoke with very painful stomach pains. Like pocoloco, I feel I have a high threshold for pain, but throughout the day, I was unable to concentrate on my work because the pain was so severe. I went to my doctor the following day as I had not made a connection between my pains and Lactaid. The doctor had bloodwork done and a sonogram performed. She thought that my pain may have been the result od some gallbladder trouble or a viral infection. She prescribed a strong antibiotic, pain medicine and ulcer medicine to attack it from multiple angles as I am a healthy 32 yr old.

Over the next several days, I was feeling better, but still in discomfort. On that Friday, I took a Lactaid pill with a bowl of cereal for dinner around 7-8 pm. By 11 pm I was vomiting violently and had extreme abdominal pain. Again, because I had feeling better, I thought that perhaps I had a bad reaction to the combination of antibiotics and pain medicine. I vomited over a period of 4 hours, and like pocoloco, was expelling yellow/green liquid (bile?) near the end of the experience (3-4 am).

Between Saturday and Tuesday, I was still in discomfort, but was 90% better by Tuesday. I decided on Mexican food for dinner. I took a Lactaid pill and had some Queso with chips for an appetizer. By 11 pm, I was vomiting more violently than the first time and had a strong bitter taste associated. I finished vomiting around 5 am this time and the following day was still nauseated and in very strong discomfort from stomach pains. This was all it took to finally connect the dots and realize that the effects were the result of Lactaid, not a viral infection or stomach flu.

I would say my experience was very similar to pocoloco's, except that my stomach pains lasted over several days and my vomiting was over 4-5 hours as opposed to his 1-2 hour experiences.

Like most of you state in your posts.........I cannot begin to describe how relieved I am to have found this site. I honestly thought I was losing my mind. I had Mirena placed in December '06. It was uncomfortable during the actual procedure, but not too bad. Then within a day or two I was in severe pain and bleeding like crazy with severe lower back pain. I was told to take ibuprofen and allow my body to "adjust". I went for my follow-up ultrasound and the placement looked fine although I was still bleeding like crazy and very uncomfortable. After several more calls they brought be back in for another ultrasound, told me that my uterus must have gotten bacteria in it during placement and that I had an infection. They sent me home on antibiotics and pain medicine. I bled pretty regularly for 6 months straight accompanied by lower back pain, fatigue, and headaches. Finally the bleeding let up only to be followed by a multitude of other nasty side effects. Depression, anxiety, fogginess, forgetfulness (severe), waking up with headaches every morning, nausea (to the point that I can't tell you how many pregnancy tests I've taken), weight change (redistribution, thicker waist, tummy, and hips even though actual number only changed by about 5 pounds), feeling swollen and bloated when I wake up in the morning, NO libido whatsoever and feel like crying during sex because it's nearly impossible to reach orgasm (this has never been a problem previously), hair loss (becoming more noticeable over time), dandruff, boil-like acne on my face and back, dry eyes and blurred/double vision, chronic yeast infections and dryness in that area too. The list goes on and on. I went to three different doctors and had tons of bloodwork done, all came back normal (thyroid, hormones etc....) I was told over and over that it couldn't be the Mirena. HA! How can this many women be delusional? I called last week and got an appointment for May 20 to get it removed. After reading this forum my husband called the doctor himself and I don't know what he said, or how he managed to do it.........but I'm going in tomorrow morning at 10:20 am to get it removed and you better believe I'm going in armed with this website and others I've found. Physicians need to be more aware of this! Even if it's not common, it's miserable for the 1 in 1,000 woman who gets the worst of the side effects. It's literally ruining my life and my marriage. It's impossible to be a good wife and mother when you feel terrible everyday.

-Amanda

About 3 years ago my doctor precribed Libitor for mr to help reduce my high cholesterol. After about 3 months I started having these sharp pains in my legs. So another trip to the doctor and he prescribed a pain medicine. The pain medicine didn't help. So, I read about the side affects of Lipitor and there it was. I stopped talking the Lipitor, the sharp pains are gone but my legs muscles are weak and ache. I've tried pain medicine, theropy, walking and riding bicycles trying to build up my muscle tissue. Nothing works. Now I'm getting to the point of not wanting to do anything because weak and painful leg muscles. Has anyone found something that workd?

I am going to be 42 in April. I had the Mirena inserted in 2005. Initially I was aware of the side effects. I did not linked all of the side effects together until coming to this site and searching for reasons for having extensive hair loss. I have experienced the back pain, the skin itching, horrible acne that looked like mountains forming on my face, night sweats, headaches, depression and nausea. I used pain medicine like crazy......Out of all of these the hair loss drove my search for answers. I made an appointment to see a dermatologists who proceeded to shoot my head with approximately 30 cortisone shots and subsequently provide me with cortisone cream to trigger hair growth. I could pull on my hair and end up with a hand full of strands. It was unreal! It has been two weeks since I have had the Mirena removed. It was not painful at all and I had very little bleeding. Just spotting. My body is now suffering from Hormone Naive. My stomach is bloated and I am craving food. I feel like I am pregnant. The good is: I am no longer suffering from the headaches, back pain, the acne is gone, hair breakage has slowed down a great deal, and my mind is clear. I can put words together that make sense. I recommend to all women to have the Mirena removed and want to thank you all for this site. I would have never put all the pieces together. It is not worth the damage to our bodies. Because of my age, being divorces and not wanting more children (I have two) I will be getting my tubes tied in the near future.

I was taking Levaquin for a sinus infection. After taking the first dose of 750 mg, I noticed that I started having tingling and numbness in my hands and arms. After the second dose, I started feeling the same tingling and numbness in my arms, hands, and legs. Because I had been having severe headaches anyway, I started wondering if I had some kind of neurological problem and my headaches were linked to the strange sensations. However, I noticed that I didn't have any problems with my arms and legs until after I started taking Levaquin. Some of my other symptoms were: tightness in my neck muscles and sore muscles. I also remember seeing a flashing light from the corner of my left eye and floaters. I stopped taking Levaquin after just 2 doses because it began scaring me and I feared what might happen after my third dose. I can't afford to take any chances with my health. That's why I appreciate this post, and I see that I wasn't just imagining these side effects. Since I've stopped taking this medication I still have problems with my arms. They feel heavy like I've been lifting weights and the ache. A couple of times, I've had to take pain medicine for the pain in my arms because they've hurt so bad, it feels kind of like when you hit your funny bone and you try to figure out why they call it a "funny bone" because it's definitely not funny! My arms hurt so bad I couldn't lift them, and I could type or write so I just took some medicine (tremadol) and laid down. It's been weeks since I've taken levaquin, but I still I have sensations and aching and heaviness in my arms. Has anybody been off of Levaquin for a considerable amount of time and found that the symptoms go away? Please give me some hope! :) Thanks.

I saw a news headline last week that linked Lipitor and forgetfulness and immediately thought "uh-oh'. Three years ago I was in a bad car wreck and started taking a lot of ibuprofen to counteract inflammation and pain. Somewhere within three to six months of this accident my doctor did routine blood work and said I needed to lower my cholesterol. She did talk about diet changes, but because there is a history of heart disease in my family she thought it would help to put me on a Statin. She talked a little about the acknowledged side effects and I went ahead with the drug (Lovastatin at that time). My focus at the time was on the amount of ibuprofen I was taking; as I went through p.t. for the accident I expected I would be able to reduce the amount I was taking. Ten months later I was still using 800 - 2400 mg. ibuprofen a day to combat muscle aches and joint pain - from the accident I thought. Then my doctor decided I need to raise my Lovastatin level from 20 mg. to 40. mg. I immediately began to have such pain that it overwhelmed the pain medicine. I immediately stopped the Lovastatin. Within a week my pain reduced dramatically - in 2 weeks I could go days without pain med. Within the 10 months after the accident I also had dizziness and vertigo and some trouble remembering things, but I attributed all that to effects of the accident. Didn't know the Statin might be contributing to those symptoms... When I finally went back to my doctor and told her I had stopped the Statin and why, she rechecked my lipid levels and said I really needed to be on something. A few months later I warily agreed to try 10 mg. of Lipitor every other day. Doesn't sound like much and it has been enough to keep cholesterol level down - though the good stuff had dropped some, too. At first it seemed okay, I didn't feel symptoms like I had before. After about a year I told my doctor. I thought I was going into menopause because I was having mood swings and being forgetful and my libido had died. Estrogen level denied this. So I thought well maybe I'm getting depressed - depression also runs in my family. So I went to a psychiatrist and told him how I was feeling. Now I am on Wellbutrin, which seemed to help at first, but isn't helping much now - even at a higher dose. My shoulders and arms have been hurting a lot the last couple of months and I've had to up the ibuprofen again to cope. This is nuts! The Lipitor goes - now! All these posts I have read make me believe that I am not a hypochondriac and complaining about the inevitable symptoms of aging (I'm 49). I expect to feel a lot better real soon!

I was prescribed Sulfamethoxazole-TMP tablets for a severe UTI that I developed. I was given 10 tablets total--and instructed to take two per day. Within an hour of taking the first tablet, my UTI felt much better, however, the rest of me felt horrible! I got nausea, dizziness, extreme confusion and depression, and stiffness and pain in my neck and shoulders. I continued the medication anyway, b/c I never had sulfur or ANY medicinal allergies. I had difficulty sleeping the next few nights, I would wake up in the middle of the night for no reason. The soreness of my neck and shoulders then extended to my butt and thighs. I can't describe how uncomfortable this was. I was sitting at work literally writhing in pain from what I felt in my legs. (and I blamed it on my poor desk chair!!) This happened on day three of five. Also, while at work I had an "episode" if you will, where I became extremely confused and disoriented, and nearly had a panic attack. It felt like the world was crashing down on me!! It only lasted for 15 minutes or so, but I will not forget the way I felt. All the while, my UTI symptoms were getting better and better. I was completely unable to have a bowel movement...sorry for this information...but it will start to make you worry if you can't poo for 5 days!! Day four of five is what I like to call "The Enlightenment". I was getting in the shower, still dizzy as hell, and noticed that I was very itchy. I looked at my lower back and I was covered in red, itchy bumps. I was say they looked like small mosquito bites, all in a cluster of about 8 on either side of my lower back. I realized then and there that this medication really was ravaging my body like I had feared. I found this site and others online which confirmed that I wasn't crazy...just poisoned. Later that day I was resting on my couch and looked in the mirror and saw that my entire face was covered in a red rash. (and I got a horrific headache) The worst part is you don't really look outwardly sick or anything...you just feel terrible. Everyone I told was very nonchalant about it..."Oh just take some Benadryl". I've lost my faith in the FDA. I stopped this medication one pill shy of my last dose. I am terrified of the possible lasting effects and will never take this drug again!! PLEASE!! NEVER TAKE THIS MEDICATION!! YOU WILL REGRET IT!!

I have had a bad reaction with Femcon FE I have had my period two weeks into the first pack and my period is still here for almost 4 weeks now I called my dr and they said just to take 2 pills everyday. My period is worse and cramps are bad about a half hour I started taking the pills even just one I get nausea I do not recomend this pill sorry if my spelling is wrong I am on pain medicine. Percocet 10-650 for the pain. Bad choice and if I stop now then I will have my period longer don't know what to do anymore.

Has anyone taking Lantus had a ringing in the ears and a slowing down of their bowel movements because I have since taking it.

Within a month of starting to take Vytorin began to have trouble breathing especially at night and in the morning, and neck began to ache so bad that purchased a neck brace---it's like my head was too heavy for my neck. This continued and apparently progressed to my upper back leading to extreme, constant pain. Ended up with an MRI, going to a pain specialist and physical therapy. I have had 5 surgeries and have never needed to use pain medicine nor get OT nor PT. This pain was ruining my life in all aspects. Quit vytorin about a month ago. Back is getting better, still have other issues.

I don't remember when I started taking Zocor - I think it was late 1990's. Recently I've been having pins and needles in my legs, arms and other parts of my body. Doctor did an EMG and it came back normal. Blood tests were also normal. He's now sending me to a neurologist. I researched Zocor and found that it can cause nerve damage which is what my doctor said I probably have. The research said that it starts in the feet then travels to the rest of the body. In 1999 I went to the doctor with pins and needles in the feet and he diagnosed it as arthritis and gave me quinine. I was in a car accident in 2001 and have been on pain medicine since then which was covering up the pain. The pain sometimes has me using a cane.

Originally prescribed Ultracet(actually generic Tramado/apap) for arthritis pain. As instructed, I took two pills at night and one in the morning. By mid-morning I was ill--vomiting, dizziness, extreme fatigue, some itchiness. The arthritis pain was diminished though.
It also gave me weird dreams --black and white television stories super-imposed on colorful dreams. Those were actually kind of interesting, not scary.
I don't think this is the right pain medicine for me.

Started taking Fosamax 2 weeks ago. First week I noticed some leg stiffness. This week My knees are so sore and weak I can barely get up from a chair. Having to take pain medicine to walk through the day. No more Fosamax for me. The side effects are to painful!

I am taking methylprednisolone on the 6 day course, am on day two. I am also taking Panlor pain medicine. The combination of these two has produced a very interesting and for me a very pleasing side effect. When I am layed down to sleep, but not quite asleep, I get a somewhat mild euphoria. Then followed by hypnogogic pre-dreamstate imagery that is sexual in nature. Then when actually asleep and dreaming the dreams have been incredibly vivid and intense, in one case a nightmare that resulted in my physically yelling and waking up, which is highly uncommon for me. For me nightmares or intense dreams are a good thing, I am a sometimes lucid dreamer and I enjoy such experiences. I am hoping that these side effects continue. Other than that I get a mildly upset stomach because I do not follow the directions and drink a full glass of water. I should note that this side effect is not present on the Panlor alone, only in combination with the corticosteroid. I was given the steroid to reduce inflamation of my sciatic nerve, and so far it does not seem to have helped, but its only day 2. I might also add that I have been happier, more likely to laugh, although I am not typically depressed or anything, I assume this is a more latent form of the euphoria some people experience.

I took meprozine after having my wisdom teeth removed and after about a day a started vomiting. I was prescribed a different pain medicine and the vomiting stopped. This stuff sucks!!! if you enjoy seeing you food after you eat it, take this... if you want to minimise your pain and suffering take something else!!!

I have been taking ambien on and off for two years on the advise of my doctor (neuroligist) Ever since I had lower back surgery I have developed this irritable and shaky leg syndrome, which causes me not to sleep. I have been taking all kinds of pain medicine, which i seem to have alergic reactions to most (Hives, upset stomach etc.)
The only thing that has helped me sleep is Ambien. However, I have noticed that after I eat, my stomach really hurts and i get heavy palputations (In the stomach area).
About 6 weeks ago I was rushed to emergency beacause of stomach pain, bowel movement was black ( thought I had a bleeding ulcer) But they found nothing.
Could this be the side affects of Ambien?

I started taking Levaquin and after a few days I started having severe pain in my knees. I kept telling my husband that it was excruitiating pains in my knees and pain medicine was not making it better. I finished 10 days of Levaquin not knowing that it was the cause of my severe pain. I took my last one yesterday and looked up the side effects today. I am still in extreme pain in my knees, the bottoms of my feet are hurting and my hip. KNEES ARE THE MAIN CONCERN. Does anyone know if this is a lasting side effect or will this go away. I can't function like this and we have sold our house & I am suppose to be packing to move and I walk around like I'm 90. I am 58 but never had anything like this. Any info would be greatly appreciated.