Morphine symptoms and conditions

I took Zocor for 25 days when I suddenly had such pain at night in my upper arms that I couldn't raise my arms up at all. It's been 2 full weeks since I stopped taking Zocor, and every single night around 7 I develop severe pain somewhere in my body, usually in my hands, knees or feet. It's in a different place almost every night. Tonight it's in my left hand across the whole top of my hand, below the wrist. Can Zocor cause this kind of pain so long after stopping taking it? And I only took it for 25 days! Please help - this really hurts and I hope it will improve.

I am a 52 year old female and my bad cholesterol is fine but my good cholesterol is low. I have been taking Lipitor now for a few years and have numb hands and feet to the elbows and knees. My feet are extremely sensitive, worse at night and now I'm getting sharp pains that feel like a bug just bit me. My tongue is also always numb and I do get migraines.I have insane stomach issues and food intolerance. I also take medication for high blood pressure, acid reflux, & thyroid. I have now been diagnosed with type 2 Diabetes but control that with diet so far. Until four years ago I had nothing wrong with me. I am slim and healthy. I had a lump in my thyroid which was removed and there was a trace of cancer. Then like dominos all the other conditions lined up. I have had MRIs and all the tests and doctors insist that I am not a severe enough diabetic to have neuropathy. I can hardly wear shoes now and it hurts when I wear runners while I walk and exercise. Does any of this sound familiar to anyone? I hate that my health has become so much a part of my daily life. Does anyone have neuropathy as a result of Lipitor and am I even taking the the right medication since I don't have high cholesterol?

I just got my Mirena removed today. I am SO excited. I have had it in for 1 year and it has been the worst year of my life. My symptoms were :MIGRAINES!- for which I was admitted to the hospital, they did all kinds of tests, and found nothing-( they even gave me an IV of morphine, and the migraine was so intense, i still felt it with the morphine.), arthritis- (or EXTREME ACHING in all of my joints, especially my hips, knees and lower back area., pain in my chest- like unable to breath, pain in my neck, I was sleeping 9 hrs a day and still exhausted and lately its been severe insomnia, cramping in my lower stomach and bloating really bad. I am 5"3, 21 yrs old, originally 107 pounds, and have two kids. After my daughter I was on Seasonique and although it made me have mood swings it was NOTHING in comparison to this. After my daughter I lost all the baby weight and then some. Even after I had my son in the 6 weeks before I got the Mirena, I lost all of the baby weight and was back down to 107 pounds. Now I weigh 130 pounds- and thats doing the same exercises and eating the same that I have always done. I have also never had ANY UTI's and I have had consistent UTI's since I have had it in, that have NOT gone away with various medications. I have had NO sex drive. Absolutely NONE, and I am 21years old! I felt very fatigued every day and it took all my strength and energy and mostly motivation that I HAVE TO provide for my family, to get up and go to work everyday. I read the brochure for Mirena when I got it inserted, and there were NONE of these side effects. I found some of these side effects on the Canadian website, and found people's horror stories of having Mirena in. I am SO happy to have finally gotten it out and am looking forward to being a normal healthy person again.

I was diagnosed with pneumonia on July 6 and prescribed Levaquin 500 mg for 10 days. I took my last pill tonight and could not understand the pain in my right hip, red eyes which I suspect comes from the insomnia I have been experiencing since July 10. I am still having difficulty sleeping and tonight I feel extremely tire with discomfort in the back and shoulders. I wish I had read these comments earlier, I would have discontinue using this drug. I have not experience any depression, but lack of appetite, stomach pain and upset stomach. I have had intermittent diarrhea. How long will it take for this drug to get out of my system.

My healthy, active 55 yr old husband of 30 yrs was prescribed SIMVASTATIN in Aug. of last year. He started having pains in his legs & back and had an appointment in Oct. with the dr. to check on how he was doing with the new drug. When he went in to the office, he was having terrible pains in his chest, legs & back. The dr. immediately called 911 thinking he was having a heart attack. He was in the hospital for a week while they ran a multitude of tests. All came back clear for his heart. He kept telling the dr. that the back & leg pains were still there. They didn't seem to be concerned about anything except his heart. He was dismissed continuing to have pain. The pain steadly increased over his whole body, then in Feb. of this year, he suffered a major seizure and spent another week in the hospital. This time they wrote it off as epilepsy and put him on anti-seziure pills. After he was released, the symptoms increased, his memory, vision & balance are all effected, he has chest pains, depression, and is in constant pain. He's been sent for numerous MRI's, bone scans, blood tests,etc. He has been to neurologists, neurosurgeons, chiropractors, physical therapists, etc. The entire time, his health has declined because he was being poisoned by Simvastatin. Finally, after doing our own research, we found a neurologist that recognized the problem. He told us that this drug distroys muscle tissue and that the damage may be irreversible. My husband can no longer work, drive, or enjoy life. He walks without a cane or walker, and depends on pain pills because the pain is so severe. He stays in bed most of the time due to the pain and lack of energy. He has been off Simvastatin for a week now with no change. We are hoping & praying for improvement over time. PLEASE, if you are your loved one are taking this drug-STOP IMMEDIATELY. The results can be devastating. I can't imagine why the FDA would approve a drug like this that destroys quality of life.

I am happy to find this site. I was given Levaquin for UTI. A few weeks prior to getting this prescription I was given a sulfa based drug (generic for Bactrim) and started feeling some pain in right wrist and hand. Dr. prescribed Levaquin since this sulfa based drug didn't clear up infection. Took 2 doses of 250mg and the reactions hit - both hands swelled, joints ached, both knees swelled and both feet and ankles swelled. Went to ER and admitted and spent 3 days in hospital on morphine and started prednisone treatment of 20mg a day with Aleve to also help with pain. This Levaquin is NASTY stuff. I can't believe doctors prescribe this medication. I am still not well. How long does it take to recover? I still am stiff and ache. I too am very active runner and finding myself frustrated in the slow recovery.

This is the 3rd time I am taking levaquin in about 3 years. I had a MRSA type infection in my eye 2 years ago that I got in the hospital visiting my dying mother. She by the way died of a mysterious"infection" in her spine but frankly reading all of this I suppose it could have been caused by levaquin because they never found an infection but she complained of so much pain in her spinal collumn that they had to put her of morphine. No cause was ever determined but she was a dialysis patient and was given Levaquin on a regular basis for the infections that are common with having a stint in her arm. Her circulatory system collapsed and they could not do dialysis on her and she died after a week.
Getting back to my situation. I got the infection when rubbing the tears out of my eyes and woke up the morning of her funeral with a bad infection in the eye. Was going to eye doctor every week for 3 months thought I was going blind. Took 3 months of 750 mg dose. And multiple eye ointments. My eye sight took a hit and I now need to wear glasses for driving always. Used to have near perfect vision before this. This past year I took it again for Lyme's disease and after about a month after I developed and nerve or tendon pull in my neck that they could not explain how I got it. But I went to the emergency room and they gave me a neck support to wear.
Just was on Levaquin again for upper respiratory infection. Woke up in the middle of the night second day I was taking it. My head was pounding and it felt like it was going to explode (literally). At the same time my chest felt like it was collapsing. I thought I was really going to die and I was entirely coming undone in my mind. I called a friend at 2:30 AM and asked him (who is religious) if he knew any prayers for those who are about to die. I truly felt this was it - the end. No one told me about Levaquin's side effects until the other day when I was reading on the internet. I now have a pulsating sound in my ears that sounds like it is linked to my heartbeat. Never heard this sound before. Its been there for almost a week and it started a few days after I stopped taking the levaquin. I also have been noticing I have a shortness of breath and I am trying to move in a week. I keep getting very fatigued and have to lay down. Find myself falling asleep quite frequently.

When taking morphine sulfate SR for lower back pain, taking urine tests will show traces of methadone. Try explaining you don't to your doctor!

I have taken Avelox before with only minimal side effects nausea and diarrhea were the only ones I got but they were enough. I have been suffering from chronic sinus and ear infections for going on two years now. My doctor gave me samples again of avelox on Monday. Last night I had to be rushed to the hospital. After throwing up all day I got a severe headache. I felt dizzy and out of sorts all day but when I couldn't take the headache anymore I tried laying down. With this medicine you can't take any pain relievers so I thought if I just went to lay down maybe it would ease up some. Well it didn't, and before I knew it I was shaking uncontrollably with tremors and could no longer put sentences together. My head hurt so bad I just wanted to stab myself to make the pain go away. At the er they gave me an IV with something to help with the headache.Anyway after taking a Ct scan and not seeing anything on there the er doc gave me the ok to go home and gave me a script for pain meds. I was having hallucinations, anxieties, and could not speak correctly. I am still having trouble making sentences, I am stuttering, which I have never done before. And I can't get words to go together to make a sentence. The Er doctor wants me to follow up with a neurologist. My tremors still haven't stopped and now I sound like the guy from rain man when I am trying to make a sentence. This is pure torture and I feel like I am in someone else's body.

Lumps under the skin all over my body and severe pain that feels like it is under my skin--like I've been skinned and the skin just laid back down raw and bruised feeling. I have to take time-released morphine for this pain and no doctor can explain the lumps other than to say it might be a side effect of the prednisone. I have never heard of anyone else having these lumps and skin pain, though. One post I read said their tongue was sore, which mine also gets when I take it.

One thing I want to emphasize is that the last time I read the printout that comes with an unopened new bottle of prednisone and that the pharmacists don't give you unless you ask, it said that the newest research suggests that you take the prednisone only EVERY OTHER DAY. Some symptoms may become a bit worse on the day off, but unless you are dealing with a potentially lethal disease, this keeps your body on its regular rhythm of making its own form of prednisone and thus prevents many of the side effects. I have been back on prednisone for 3 months now with the new one day on, one day off schedule, prescribed by my pulmonologist, and have much less of the side effects--no ravenous appetite and thus no weight gain, no swelling, no "moon face" and my lungs are still functioning much much better.
Please ask your doc about this or get the info sheet from the pharmacist (it is the very long one on tissue paper, not the one-page info sheet they are now giving us with each Rx.)

I started taking prednisone along with Cytoxan, a chemotherapy drug 15 years ago when I was diagnosed with an undifferentiated connective tissue disorder that led to symptoms like idiopathic pulmonary fibrosis. After a couple of years, the inflammation cooled off and I no longer had increasing scar tissue in my lungs (IPF is almost always terminal) so I was glad of that. However, sometime in that first year or so I developed hardish lumps under my skin and severe pain that felt like it was "under my skin" but not my muscles, as in fibromyalgia. The lumps are even more painful, and the skin feels as if someone tried to "skin" me and then just llay the skin back down.
I have had to be on timed-release morphine for years in order to function with this pain, as it is especially painful if I brush up against something or sitting or lying down pressure is intense. Also the skin on my tongue gets so tender I have to use kids' toothpaste or it burns terribly.
After 15 years some of the lumps have gone away, but I've recently had to go back on the prednisone for my lung inflammation.
The last time I got a new prescription for prednisone I read the tissue-paper printout (not the short one you get with every Rx, the one written for professionals which includes all the new data, tests, side effects, etc.) What I want to point out, as I've not read one person saying this, is that to avoid a lot of the side effects and the harm to the glands which produce our own natural steroids, is that they are now recommending that it is taken only EVERY OTHER DAY. They say there may be some slight increase in symptoms on the "off" day, but that this keeps the natural cycle in place in bodies subjected to this drug and therefore reduces symptoms.
This is what my last pulmonologist prescribed for me and so far I have had minimal side effects--no ravenous appetite and weight gain, no "moon face" and it has still helped my symptoms.
Please ask your pharmacist for the flyer that comes with the new package and read this for yourself and then take it to your doctor. It may not work for those in dire need of the prednisone but could perhaps be tapered to this once the first lethal symptoms die down. ASK YOUR DOC--I cannot believe I have not heard more about this as it's right on the flyer--but docs are so busy, it's understandable. I'm grateful my doctor is up on the new research because I don't mind taking the prednisone this time, and I used to HATE it!
Good living to all and I wish you all the healthiest life possible.

Reading all this horrifies me since I have been on Remicade for almost 4 years for Crohn's and a still unidentified Inflammatory arthritis of some kind. I will pray for you all. But, on another note and by no means an attempt to diminish the severity of each account in this blog, I have had no such side effects and for the most part have had great success until recently. My Crohn's is and has been in complete remission since the beginning of the infusions. However, I have had increasing inflammatory issues in joints between infusions. I get 5 vials and they give me Solumedrol in the IV. I ended up in the ER last night because my joints were all frozen up and it was just unbearable. They gave me Solumedrol and Morphine, and I am 75% better today. The frequency and severity of the arthritis issues has gotten increasingly worse over the last 6-8 months. I get infusions every 8 weeks, and start to have severe joint pain after about 4 weeks. All that being said, it is appearing like Remicade is still working brilliantly for Crohn's but is having little to no effect on the inflammatory arthritis. The steroid they give during the infusion is what I think is doing the job for the joint pain since I was a 10 last night in the ER, and I am 3 this morning pain wise after getting the steroid. My case is unique and frustrating to the Rheumy b/c my sed rates and RA factures and C-Reactives are all relatively normal when I am in tremendous pain. So, they just ran alternate tests the other day to look into things like Myeloma and so on. I don't believe that Remicade has done any of this. I believe that Remicade's benefits for MOST people greatly outweigh the risks, especially when you are incapacitated with Crohn's etc. But in my case, it just does not seem to be working for my joint inflammation.

I've been on Wafarin since September of 2008 because of a massive DVT stretching from my jugular vein to my right arm. Since the initial injection of Heparin and oral consumption of Wafarin I have experienced daily migraines. They seem almost like 'pressure-headaches' pushing on the sides of my head, temples, forehead and the bridge of my nose. My thrombosis doctors have sent me for Ophthalmology tests, MRIs, and plan to send me for Neurology tests as well to discover the cause of my headaches. They've put me on codeine, Tylenol 3's, Gabapentin, Naproxen, and Co Sumatriptan because of the fact that I'm so immune to painkillers in general (For the blood clot pains themselves, I was on Hydromorphone, Morphine and Codeine). Although the Co Sumatriptan along with the Tylenol 3's give me some relief, I can't help but wonder if the cause of my daily migraines are from the Warfarin itself.
My doctors are reluctant to agree with me, saying that they plan to take me of Warfarin within the next few months, but aren't certain of exactly when.

First off I will begin by saying I was diagnosed with Fibromyalgia in 2006.
I just finished 10 days worth of Levaquin 500 mg.,(for a sinus infection) that seemed to be reoccurring after 2weeks of Augmentin generic), the whole time while on it I've been experiencing horrible side effects. I'd say the worst one is joint pain..(.especially knees & hips), Left shoulder, neck,upper back burning-miserable pain, unable to sleep (from what I remember of the last 6 days only 21 hrs. of sleep!!) dizziness, nausea,bad muscle pain, lower back pain, weird stomach pain, bloating, urinary retention, (was tested for an UTI-negative! )
6 days into it returned to Dr. because I'd been up all night itching like CRAZY, along w/the lower bk.pain,urinary problems, and a rash on face, chest, &upper back. (she attributed the rash to sun-photo sensitivity....had not even been outside!!) I also developed a yeast infection.( Expected I guess after 24 days total of antibiotics.)
debilitating headache, Very irritable, weepy,anxious, sore throat, very VIVID nightmares twice.
On the last day of taking it 3/3/09...had to run a couple of errands...felt dangerous behind the wheel..just plain weird & ILL!!!!!
Had taken this twice before since 2006 (also for sinus inf's.) thinking back...I felt like hell then too...but attributed to a Fibro. Flare. Now I believe that it was BAD REACTIONS to the Levaquin. I will NEVER take this med. again, have been so miserable would have rather been dead. (and I KNOW that's terrible to say!!) I take Morphine Sulf SR on a daily basis for the fibro, but it WOULDN'T even begin to touch the pain I've been experiencing while on Levaquin. ( Had mentioned that at the Drs. appointment, she didn't EVEN put 2+2 together....well I have!!) I'm VERY upset about it!! I reported it to the FDA.GOV/medwatch. This drug should be taken off the market in my opinion. I will be returning to see her if these pains,ETC. do not stop by tomorrow.....I'd had my fibro fairly under control before the Levaquin. Just to mention I was drinking plenty of water..due to dry mouth. I'm happy I found this site, I was looking for info as to how long this med. stays in your system. After reading many other postings here, I KNOW that what I've been feeling is NOT just a FMS flare, but caused by this Levaquin.

All these stories touch home. I recently lost my metal strings. My mate said he hasn't felt them for a while now. Men I sware wouldn't it be nice if they told us these things. I have extreme pain in my ovaries for the last two weeks, the pain is so bad it makes me ill. My mood has been fine however I do tend to cry easily. So I guess I am emotional. I like a dumb arz threw away all the papers the doctor gave me after he inserted the iud. I just wanted to forget about it because it hurt so bad. I am tired a lot more, I started taking diet pills to boost my energy and even they don't work. I am breast feeding only at night now because it drains me so much. After reading all of your comments I want this thing out of me. I am totally freaking out about the iud being lost in my uterus. I hope i'm not pregnant and miscarrying. The pain I fel resembles a miscarriage. I was have symptoms of pregnancy early on when I first got it put in. I'm so tired of bleeding and the embarrassing odor. I thought it was an infection but was to embarrassed to see the doctor about it. I guess it's another side effect. So we are the gunie pigs for this New IUD. Great.....

I'm calling kaiser Monday to have it taken out hopefully it doesn't hurt to much. Over the counter meds won't help that area of the body if they do have to dig around to find it. I am positive it is not in my cervix because I checked.

Ugh.....

I got sick on 1/21 I went to the doctor, I was starting to see yellow phlegm every morning for the past 3 days. The next day I was really messed up. My chest started to hurt and I was all congested, accompanied by lots of phlegm and loss of appetite. I called the doctor and she ordered amoxicillin because it works better for me. She wanted to order zpack, but I was reluctant because in the past I have gotten yeast infections from taking it. I felt worst with the asthma, chest congestion that I just wanted immediate relief. By the 3rd day, my throat irritation began, so I went to the emergency room. They order zpack and prednisone and as a precaution gave me a pill for a yeast infection. I started both meds and by the 4th day, the chest congestion was clearing and it was the first day I started feeling a bit better. I went back to the doctor, but I went back and still needed a treatment in the office. I was making a turn for the best. I finished the zpack on Friday and by Saturday, I was noticing a tinge of pain in my left side on Saturday. By Sunday, this pain was constant and stabbing accompanied by a yeast infection. The pill did not clear it up completely yet. Monday, the pain on my left side was unbearable, so I took a Tylenol which had no effect. So I went to the Emergency Room again and now they did an exam, touched my side and ran a ct scan, chest xray and blood test.

Get this, the results showed that I have gallstones on the right which were not causing my pain, a UTI and possibly passed a kidney stone. They gave me morphine and a nausea pill. Ultimately, they said they do not know what was causing my pain, so they gave me levaquin for the UTI and hydrocodine for the pain. I know the UTI came from not drinking enough fluids, but I would like to know where this pain is coming from. For Tuesday and Wednesday after leaving the ER, I could not use the bathroom with a bowel movement. I took a laxative today and used it fine this afternoon, Now my right ear feels like I have to swallow to open it. but the pain is still there and without the hydrocodine, it is unbearable. I have never had gallstone, kidney stones or pain like this. I called the doctor today and will see the doctor on Friday. This pain is unbearable, but the chest congestion, throat irritation are all gone. Why are the side effects so severe for a medication that seems to heal immediately.

exactly two weeks to the day after receiving the gardasil shot, i was awaken in the middle of the night with severe stomach pains, vomiting, and uncontrollable diarrhea. after two hours of this my hands and feet went numb, i became extremely dizzy, and passed out. my husband took me to the emergency room right away. i was in the hospital for 3 days receiving morphine for pain and several several bags of fluid. i ran a 101.4 fever and was so weak i was unable to get out of the hospital bed. i have had stomach viruses plenty, this was not a stomach virus. i feel like i got severe poisoning from the gardasil shot. i will not be going back for the 2nd or 3rd shots.

I experienced a lot of pain while I was on YAZ . I was taking it as a treatment for PCOS. I took it for 3 weeks. I was instructed be my GYN to take it on the first day of my period. The first week, I had no complaints. The second week, instead of it ending - my period became a lot heavier. I started experiencing constant headaches, and sever bloating. My wedding band is usually loose around my finger. One morning I woke up and my finger was red and I could not get it off my finger. The third week, I started experiencing a lot of pain. The pain first started in my lower back, it felt a lot like back cramps. Then it started to intensify. By this time I also had cramps in my abdomen and groin area, and my ovaries felt like they were going to burst. The pain I was in , was equivalent to being in labor. I was rushed to the ER where they gave me morphine. I was in so much pain that the first two batches of morphine did not work. On top of all that, I was so sick. I was not able to hold anything down the whole last two weeks prior to there ER visit. I had no idea that YAZ was causing the pain, until the ER Dr. explained that I was not reacting well with the Yaz , and that I should stop taking it immediately. Oh and let me mention - I experienced sever mood swings, sometimes accompanied with rage like feelings. I went back to my GYN and she put me on Femcon Fe. I will never recommend the birth control YAZ to anybody. It is a horrible birth control pill in my opinion. It did not help me in any way it just made it worse. I give YAZ a big fat zero.

I am 34 years old and was prescribed Advair about two years ago. I have had minor asthma issues over the years but nothing major. So the doctor gave me an inhaler. Then one winter I get sick and started going through the inhaler in about a month, so he prescribed Advair.
To back up I had lower back surgery for a bulged disc. So I had a lot of pain and was taking vicodin. Six months after surgery my back started feeling better than it had for a long time. I was able to exercise and get by with one vicodin in the morning. This went on for about a year. The pain was stable for the most part, but would increase every now and then.
Now enters the Advair. When I first started taking it I felt a little weird but it made my breathing a lot better. After a little while I would forget to take it or just feel like I didn't need it. But I could not stop taking it because my breathing got to bad without it. Over time my pain was getting worse and worse. I ended up being put on time release morphine because we thought the back pain was increasing. Then after being on morphine it seemed like I was always sick. I have been to the hospital twice for breathing and lung infections. I thought my back pain was turning into sciatica!!!! All along it is this F@#$ ADVAIR!!!! I have had a super short temper,daily head ache's,depression, HORRIBLE PAIN in my legs and back. I am so glad I found this site. ADVAIR IS EVIL!!!!! I have stopped taking it for two days now. I really need help from anyone who has info about quitting it. PLEASE CONTACT ME. Thanks : )

Very high tolerance for medications incl 60mg morphine, 20mg oxycontin 4x day, however, I just cannot seem to tolerate Fentanyl. Have tried it two times in past, both the 25mcg and 50mcg. The first week or so is great, after that the side effects are more than I can tolerate. All of these side effects were extreme and unbearable not just mild. They affected my ability to function and sent me to bed on more than one occasion. Extreme fatigue, nausea, sweating, anxiety and weakness. I felt as though I had a very bad case of the stomach flu. Both occasions I stuck it out for 2-4 weeks till I finally had to quit using it. Any suggestions as to why would appreciated. Some of my side effects aren't even listed in brochure.

Today is Christmas day 2008. And a Merry Christmas to me ha!!!!!!!! I was given a prescription for the drug Levaquin on the 19th of December for a suspicion of pneumonia. The x rays done at the hospital found no evidence of pneumonia but my doctor wanted me to take it anyway because since I have asthma and my lungs sounded so bad I was told that I was at risk for developing any secondary infection that was out there. My husband filled the prescription on the 20th which was Saturday, took the first one of a seven day supply 500 mg tablets. About 4 hours after taking just one pill was awakened by severe and agonizing pain in both of my feet and my knees that I was writhing in pain. Since I have nerve damage in my feet anyhow I know what the pain that I normally experience feels like and instantly knew that this was not normal for me. When I thought that I finally might be able to walk I hobbled into the kitchen and dug the list of side affects out of the garbage (stupid me had not read them first.) I discovered that it was one of the side affects. Called the on call doctor in the morning since it was on the weekend and he stopped it immediately and put me on something else. I only took that one pill and since Saturday night every night I wake up in agonizing knee pain and I have never had pains in my knees before. The pain is so bad that I feel like I am ready to go on a morphine drip, or cut my legs off above the knees. Six days now from one pill, how much longer can this go on? I really feel bad for the people that contined to trust their doctors and continued with the full course of the medication and I realize that what I am experiencing is minor compared to what others are going through. This drug should come with a handout that says: Take this drug at a risk to your health!!!!!! Last night the pain lasted all night and I cried all night. Have to get through this day am entertaining for the holiday and have had no sleep. Actually getting afraid to go to sleep at this point.............D.

I am so glad that I found this website, I just left my OB/GYN only to be told I have a UTI. I haven't had a UTI for 2 years, and even then I was pregnant. Since the Mirena which I had inserted in Jun 08 I have have been placed on Zoloft. I have been rushed to the ER for SEVERE abdominal pains that felt worst than childbearing. The pain was so bad, I had to have morphine to help me relax, and even then, the doctor stated she could not find anything wrong with me. I have gained 10 lbs., up out the blue, and I cannot get my stomach down for anything. Acne, on face and back, yuck. Hunger to the point that I eat as if I am pregnant, I never had cravings like this before. Finally, headaches. I am unclear if I want to get it removed or not. I am saddened that there isn't more info available to women regarding this.

I have been on BP medication about 4 years now. I was on Avalide and recently switched to Lisinopril HCTZ. About 3 years ago I had hip surgery. The evening of the surgery my back was hot and beet red, the next morning the rest of my body looked like I lay in the hot sun and was very burned. The docs and I felt it was pain killer. Last year I had another surgery, indicating I was allergic to pain meds, codiene, morphine, percocet, all of which I had with the firat surgery. Again, the same reaction. Last week I had another surgery, no pain meds as indicated, again, same burn reaction. I peel horribly, my face swells, around my eyes swell, I was a mess. I wonder if the BP meds caused it. No one said to d/c them as they did the supplements of multi-vit, omega 3 fish oil, aspirin. Prior to being on BP meds, have had several other surgeries with no reactions. I feel it is the BP med. causing this. Anyone have any such reactions? HELP.

I am taking Adalat XL 60 mg. once a day.. as far as BP went was working fine.. They found I needed a stent in my heart... specialist put me on metropol 12.5... after the operation i went back to him.. BP was 80/53.. wow, no wonder I was feeling tired.. he advised me to stay on it.. NO WAY.. just my Adalat XL is working fine.. BTW.. and for the Gladys1948.. a few days after i started the metropol (lisiopril) I noticed a floater in my right eye... was disconcerting.. but is slowly leaving since stopping the drug.

Despite having a brush with the big C last year (I finished chemotherapy in January) I have been very fit and healthy during my 61 years! A few weeks ago I started having palpitations, hence a visit to the doctor revealed high blood pressure and cholesterol reading of 9.9!!! Shock, horror. He informed me that it was genetic and prescribed Simvastatin 400mg and Bendroflumethiazide 2.5 mg daily.
Not being satisfied with the enclosed leaflets I have looked up more info. on the net. Should I have done this!!! After reading some of the posting on the site I am feeling a bit apprehensive. Last night I had a terrible night couldn't sleep for the pains in my legs and a bit nausea this morning.
But I need to be sensible, I really don't have any choice but to take these drugs just hoping that I won't have to stay on them for the rest of my life and I don't get any of the side effects that some of you have suffered. I also wonder if the chemotherapy could have caused by raised cholesterol?
Hope to keep you posted and would welcome any comments!