Lab tests symptoms and conditions

Prednisone has messed up my head. I had Bells Palsy (which is paralysis of one half of the face) and can be very scary. I have had some depression before but this stuff made me fall off the face of the earth. I went from someone in control and quite happy to the absolute pits. The depression was quite severe and sudden and I had no ability to stop the downward spiral. It has played havoc with my life. In its defense, it cleared the Bell's Palsy up very quickly but the grief it has caused me through my altered mind state wasn't worth it. Insomnia (eg - no sleep for 6 nights straight) was a trigger and then the mood swings took over and then bang....full blown depression and an inability to focus, work properly or function. I am now on the road to recovery but it has been a pretty turbulent 2 months. Be very careful with this drug....very, very careful.

I was prescribed levaquin 750mg for 5 days. I took my first dosage and within 2 hours I was feeling itchy, tired, anxious and felt as if my skin was burning. On the first night I had a panic attack and felt my heart rush and couldn't breathe normally. The very next day I felt as if I was exhausted and believed it was the medication, so I called my doctor to ask if I should discontinue. Fifteen minutes too late she called me back and old me to discontinue, sadly I had just taken the second dosage. Within fifteen minutes of the second dosage my body started to undergo an extreme amount of itching, burning and pinching sensation. I was disoriented and depressed. I suffered sharp pains all day and night and just tried to focus on the next day. I figured after 24 hrs I wouldn't feel the pain and the medicine would be out of my system. I waited a day and a half. When I woke up on the second day after being off the medicine I was feeling extreme pains and nothing had gotten better my husband had enough and took me to the ER. I was admitted and stayed three days. Three horrible days of lab tests, xrays and lots of pain. The doctors could not manage my low blood pressure and had mo idea how the levaquin was attacking my body. I've been out for 2 days now and am still in pain and at time I still feel disoriented.

I was on Yasmin for only a month in November 2008. I quickly got off of it because of the side effects. I wear contact lenses, yet my vision was getting blurry. I was training for a marathon, yet I was gaining weight (and it wasn't the muscle mass I was also gaining from training). I began to have horrible headaches, retaining water and I even got these little red rashes on my arms and breasts. At the time, I didn't know that Yasmin was causing all of this and ruining my life! Now I know it's Yasmin. I went to my doctor, she performed various lab tests (including liver, kidney, thyroid) and I am perfectly healthy. So I did major research on Yasmin and discovered all of my ailments were on there as side effects. My advice for anyone experiencing anything similar is to either change the dosage or just get off of it. It's not worth it. Yasmin is the devil! I mean think about it, we are messing with the natural way our body's hormones function. Oh yeah, and not to mention that I started losing some of my hair as well.

I made an appointment today to see whats going on.I have been on yaz for about 3 weeks..yes i too have all the same symptoms however i also have a horrible pain right in between my breast..it feels like someone is standing on me.i wake in the night in tears cause i cant roll over i cant pick my 3 kids up cause the pain is always there.... maybe its something else but at the same time im thinking it might be this pill.. as of today im off it.. and when i find out what my doctor says i will let everyone know.. i personally think out of the blue im seeing all these commercials on this pill and doctors are pushing it like crazy so im feeling a little like a ginny puig and no one will tell us this pill is causing all this crap in our lives! so im off to
the docs to see whats hes going to say not too hopeful...

33 year old, 125lb female with cholesterol of 234. I was put on Simvastatin 40mg, which I took fot 3 night only. All hell broke loose, insomnia, hands are numb, severe joint/back pain, extreme weakness... The thing is, I took it for 3 nights & realized it wasn't for me. I've been off of it for 3 weeks, but the symptoms still persist, rendering me pretty much dead.... I was told by a few that putting me on 40 mg to start off probably did the job... Three week of living hell & my primary physician don't have answers for me!

I had the mirena inserted about a year and a half ago. Since then I have gained 20 pounds. I have never had to fight weight gain. I'v been a stable 130 for probably 10 years. Never had to worry about what I ate or when I ate. Now, I'm eating salad, low fat stuff, fat free stuff and exercising. Of course that's all good for me, but, if I hadn't gained the 20 pounds, I would never have to eat this stuff. I've been meeting with a dietician and everything. It's been 4 1/2 weeks and I haven't lost a pound. My GYN is going to do lab tests tomorrow to see if it's my hormones, or maybe perimenopausal. I'm 46 years old with 3 kids. If the tests come back negative, I'm going to have it taken out. Hopefully I'll be able to loose this 20 pounds. I feel huge. Other than that, I have had no problems with it. The insert process was a little painful, spotting for a few months, but nothing else. Good luck with the rest of you.

i had my mirena for 4 months and gained almost 70 lbs. I have gone through so much with the doctors i have had the same responses as all the other posts. it has been out 1 yr and i am still not normal. I haven't had a period since it was removed,they have checked every inch of my body with lab tests and basically they said i am crazy.i am very distraught about this whole thing its horrible and no one will listen. I have started seeing an alternative med doctor who says it is an adrenal prob caused by mirena.has anyone had any positive effects with any treatment please help

17/2/09 I was prescribed Keflex 500mg 3 times a day (every 8 hours) last week after being told that the symptoms I had were possibly due to a kidney infection and to take this over the weekend & ring for the results of the lab test on the urine sample given early Monday morning - I experienced loss of appetite, lower back pain, tingling in my lips & the side of my face(by Sunday night that occurred) severe foot cramps, pains in my leg & stomach pain - my husband advised me Sunday night to stop taking the drug until I had spoken to the surgery. (incidentally the Doctor had been wrong the lab tests showed no kidney infection!!) following cessation I woke up this morning with my whole body drenched in sweat!! My appetite though has returned. I will never take it again!! & all because of a wrong diagnosis!!

I was prescribed Zocor for high cholesterol. Almost immediately I began to experience body aches -- some days more severe than others. I would take ibuprofen and it would help. Then, I started getting a pretty strong pain on my hip which radiated down my leg onto my foot. The pain was so severe, even the Motrin 800 mg. pills didn't help it. I am 53 years old, but I felt like a 90 year old. I had problems walking, especially after sitting for an hour or so. I had problems with stairs. Even laying down was painful. I tried heating pads, ointments, etc. When I told my doctor about it, she said that this was a typical side effect of statins, and that because I am diabetic, I need to continue taking Zocor to keep my cholesterol down. Just the other day, I stopped taking Zocor for 3 glorious days and guess what? NO pain!!! I resumed it because my doctor insists that I stay on it, but I wish there was something else I could take that wouldn't cause pain.

I do not know if my symptoms are related to the Zometa treatment I received 11 mos. ago or not but am desperate to come up with some explanation for my symptoms. Over the past yr. I have had the occasional bend over wrong and experience upper back muscle pain, once about 7 mos. ago for no reason I had right groin muscle pain, couldn't lift my leg or cross it, eventually it went away. Then on 8/22 I had what the Dr. called acute tendinitis in my right hand, a week later my right groin, 2 days later my left groin,2 days later my left hand and now my right jaw. Each time the tendinitis pain is crippling but lasts usually only a few days and never more than one area at a time. So far my lab tests are coming up negative for most everything. Anyone else ever experience this transient tendinitis pain and so long after receiving the treatment?

How interesting to find this site! I, too, was diagnosed with temporal arteritis on February 29 (no more leap years for me!). Because I was already blind in one eye (had no idea) and losing sight in the other eye, I was put on 100 mg daily of prednisone. I had no idea of what I was in for. Since that time I have been able to taper down to 42.5 mg daily, but I don't think I've missed a single side effect. Horrific headaches. A 25-pound weight gain so rapidly it was unbelievable, moon face like I've never seen, was thrown into diabetes right away. My blood pressure went haywire, my cholesterol went haywire (had never had problems with either of them). I think I agree that the most debilitating has been the muscle weakness and leg cramps. I have no balance, have had 3 serious falls. The latest is my skin is breaking down and I'm losing my hair. What hair I have is like somebody held a match to it and frizzed it. I'm short of breath, keep trying to exercise and it's like climbing a high-altitude mountain. Swelling of my feet to where I can wear NO shoes except for Crocs in about three sizes bigger than I ever wore in my life. Now I have a liver problem, am being sent to an "ultra-specialist" for this. The good news is that my remaining eyesight has been stable, and I am very thankful for that. I have been assured by multiple specialists that I would have been blind by now if not for the prednisone. Although it is very difficult for me to read by the time night arrives, and that was my chief "hobby." The other part of this whole sad saga (ha) is how much money my husband and I have been out this year -- unbelievable. Lab tests or doctors every single week and sometimes every single day. I am now under the care of 5 different specialists (ophthalmology, rheumatology, cardiology, hepatology and internal medicine), and it has been so incredibly expensive. This is even with fairly decent insurance. I have been told that I have at least six more months to go on this treatment, and then possibly another year on methotrexate. Thank God I have NOT experienced the depression that seems to be a common thread here. I am trusting in Him to get me through this itme and to come out on the other side completely cured. But it does get difficult in the meantime.

I am a retired Psychologist and former nurse. In April 2008 I went for a post -op check-up following ankle reconstruction surgery in July 2007 ( nine months after the surgery). I was still having a little pain and a lot of swelling in my ankle. The Orthopedic MD gave me a 1 c.c Injection of Kelalog and 3 C.C. of Lidocaine. He knew I am diabetic and didn't take this into consideration.He didn't tell me what he was injecting just got the shot and put it into my ankle with no information or explanation, telling me about risk factors or getting my consent .Three days later my lower legs became very heavy, weak and numb. The next day these feelings moved 12 more inches up my legs, and continued to move up my both legs anf then up body until it got to the middle of my chest and I was having a hard time breathing. I went to the local University hospital and was admitted to the neurology unit. After three days they couldn't figure out what the problem was and discharged me falsifying the discharge diagnosis saying that I was getting better. The neurology residents and their attending MD's emphatically refused to even consider that the injection of Kenalog was the problem.And so it was with another three neurologists I was referred to see. From then until now six months later my life has been hell. My diabetes has been out-of -control ( I had it under good control before the shot). My electrolytes are crazy, calcium high, potassium low, I have had three MRI's, 2 CKat scans, 2 EMG tests, nuclear scans of my para thyroid glands, at least 100 lab tests, dimpling in both my ankles and lower legs, and the heaviness, weakness and numbness coming and going in my legs so bad that I can hardly walk at times. I contacted Bristol-Myers to ask if there is any treatment. Their response was to get records form my doctor--I thought to help me--- but a phone call to their office made me realize it was to cover their own ass's and they don't give a S--- about me or how this drug had messed up my life.I had to cancel two consulting jobs to do Professional presentations costing me over $5000.00. I am 75 years old and now six months later all I can do is wait until this crap gets out of my system and hope I can get my diabetes back under control. I have been put on at least 6 more medications to control my symptoms including insulin shots. What a nightmare!

I was prescribed a 10 day course of Doxycycline Hyclate for a strep infection six days ago. On the third day of my medication treatment, I experienced a feeling of exhaustion. On Day 5, the exhaustion became more severe with a little difficulty breathing and some "pin" like pain near my heart, while at work. I called my hospital and was advised to take an aspirin and to come into urgent care, as long as I deemed that it wasn't an emergency. After arriving at my hospital, I took an Xray, had blood drawn for multiple lab tests, hooked up to an EKG machine, and provided a urine sample. All of the test results thus far were negative. All of the specialists who I encountered while at the hospital conveyed to me that exhaustion isn't a side effect of this medication. After reading everyone else's postings about extreme fatigue being a side effect, I am convinced that it is indeed a side effect. I have got another four days to go on my medication therapy. I guess using my sick leave for the side effect isn't such a negative, as long as this medication cures my strep.

I had cough for almost a month when I started to feel a light localized pain in the lower rib area, between the breast and the upper abdomen. ( when taking a deep breath or coughing).Then I was prescribed levofloxacin (levaquin) 500 for 10 days for a “supposed” pneumonia and sinusitis, no RX or lab tests done, by one pneumologist. Well, I felt others side effects but what really matters is that after 2 days taking the medication the pain worsen a lot, felt like a stab. I could not move in bed, was difficult to move, seat, get up, drive, work, whatever… In the fifth day I complained to the doctor who said I had muscular pain and the pneumonia was gone, but I should continue the 10 days treatment. So I did. After 7 days I felt when coughing that something was stretching and unsticking in the pain area. After the total disconnection the pain diminished a lot. Second week, back stabbing pain, third week front pain again, same type and disconnection, then diminished. Fourth week I felt something was loose , crackling in the area while driving or doing some movements. I also felt painful, loose knees and painful elbows. After many doctors, many exams and RXs done, now I know I had chronic bronchitis and costochondritis and I ended up with two ruptures of the costal cartilage, ( costochondral junctions ) 6ª and 7ª ribs, caused by levofloxacin. The RXs now show calcifications , body repairing the ruptures. I can not exercises now for 3 months. Ah…The sinusitis was back 2 weeks after stopping the medication. What I say now is: God protect us from some stupid doctors and these dangerous medicines !!!

I found this web site in February, and posted my side effects at this time, and stopped taking lipitor. I have been getting better every day and most of my muscle weakness has gone away. I started including Co Q-10 100mg daily and 2000 of vitamin C if i don't take the Co Q-10 for a few days my burning pain seems to be back especially in my arms and calfs I have no health insurance so I have been unanable to have any blood work done. or even seen a doctor for any of my concerns regarding the Lipitor. I just know that when I did go to the doctor with complaints about weakness and pain they would give me more medications for the symptoms.

concerned citizen,i enjoy reading your posts and research you have been so helpful,but i do have to say,i do expect the doctors that write prescriptions to do their homework and research on these drugs,i do feel that they should be extremely knowledgeable about what they are giving our children,that is why i pay them the big bucks.I told them of my concerns and they poo pooed me,when as it turns out now i was quite possibly right,i will asked them to do another blood test now he is not on meds,and if as i suspect it has gone down i will loudly shout i told you so and demand answers from them.I so often questioned the meds and was always made to feel dumb,Ignorance is not a defense and someone was very ignorant

I am Cody Millers mom ,the boy who died from Suicide while on Singulair for 17 days, I just wanted to say one thing to all of you that take the time to post.GO ONE STEP FURTHER CONTACT THE FDA and report to medwatch .The investigation needs evidence like your stories to help make informed decisions about this drug.The poorly orchestrated disclosing campaign that Merck had supposedly set out to accomplish in 2007, has obviously not reached the mass majority of people using this drug .Seeing now how many people did not make the connection to these HIDDEN AND DANGEROUS SIDE EFFECTS.Our child's pharmacy sheet that came with the medicine ,showed none of the updated side effects.They were added in April 2007,I filled the prescription in July 2007.Nothing had been disclosed until we put forth this effort to get the FDA's attention ,by asking the Senate and Congress to look into this matter.Go to your doctor and insist that they report YOUR SIDE EFFECTS to the company and the FDA.It is of the utmost importance.,Kate and Dave M.

No serious side effects. I want to add my experience as I see everyone
here has a side effect. I am always wary about medication, and I have taken
statins mainly Zocor and Lipitor off and on for 10 years or so. I have familial
hypercholesterolemia, so diet hasn't helped much, and I have tried all kinds
of food supplements etc. I do take CoQ10 based on reports I have read, not from any side effect. If there are any side effects its not significant that I can
notice it. Sometimes I am forgetful, hard to say if its caused by the drug, as
the times I have been off it, has been much different.

I wonder if high cholesterol is a real problem, I wonder if high triglycerides are worse? Lately I found what seems like an improvement by eliminating high glycemic foods like rice and replacing with barley and oats. Barley also has some fiber and other things that are apparently helpful. Grapefruit is also helpful, but there is a warning not to take it, if you are already taking statins. Based on all this side effects reported here, I feel I might need to try once again, to try an alternative. I am maintaining my 10mg Lipitor, though I had been planning to move back to Zocor as its cheaper for me. I will take a test
in 2 months to test my current barley diet, and recent exercise routine to see
what improvements can happen. Then if successful, I might get off statins,
maintain the non-glycemic diet, exercise and in addition take a lot of grapefruit and a reasonable dose of niacin.

In the past I have tried ginger, garlic, Chinese herbs, and more then I can list here without much help. Occasionally I had been surprised by low readings,
once when I had come back from a 10 day meditation retreat. I have read that cholesterol can change due to stress, and this is a very variable thing. I have
taken lab tests within 2 days from the same lab and seen almost 20% difference (with fasting). I think each body is different and one needs to take a very long term, positive attitude of experimenting and not feeling discouraged too much, but always reading and trying different things and being careful of how you interpret the results.

I would rather ignore the high cholesterol, except my brother died at 65 from cardiac issues, but he also had diabetes. I am now 51.

openlotus

I've been taking medication for hypothyroid since 1987 with some changes of dosages and brands based on lab tests and, I suppose, doctor preferences. Until 2 days ago I was taking 112mcg Levoxyl, with no side effects, I thought. Recently, my pharmacy ran out of the usual brand and substituted another brand with 7 pills until their shipment came in. No problem. Without medication my throat and tongue starts to swell within 3 days and in 10 days I'm sitting around trying to see how little I can breath. Even that wasn't so bad but the heart beat slowing and then quickening gives an unsettling adrenaline type feeling. OK back to the switch. I retrieve my usual brand when it came in and was 5 days into that when BAM!. intense chest pain woke me up 2:30 in the morning. I took aspirin and TUMS, thinking I covered everything. The pain radiated from the center of my chest to my back, continued tingle sensation down the undersides of my arms, and achy ears. It even hurt to breathe. 30 Minutes later, and after unsuccessfully trying to minimize symptoms using WebMD, I decided to go to the ER. Lots of test later that rule out heart they said I was taking way too much Levoxyl and wrote a prescript for .75mcg. Since researching I've notice other symptoms I attributed to age (am 52) painful joints especially hands, wrist, feet, ankles, and knees that I've been popping Tylenol for 2 years. Stiffness. I'd like to blame the 20 pound weight gain in 8 months on it too but seems like I should have lost weight.
Since I can't go without medication it seems like I'm but to the hunt and peck method of finding the right dosage and brand. Any recommendations on which direction to take?

Hello fellow sufferers,
Several years ago I had a CT of my face and head due to frequent migraines...They had thought maybe there was a tumor or blocked blood vessels, but to my complete surprise all of that was normal, but I had all the sinuses on the right side of my face completely blocked...The doctor @ that time asked me some questions about my breathing and pain...Of course my breathing through the nose wasn't that great, but I had always taken that as a bonus since I work in the hospital...NO pain really either...Due to the fact that sinus infections have a direct pathway to the brain they decided that I needed Levaquin...On the second day of taking the medication I was in complete tears...The bottom half of my body ached like someone had kicked the %^&* out of me...First off I thought that maybe it was because I had my leg in a full cast and that had just been adjusted so stupidly I continued with the med another 2 days and the symptoms got to the point that I couldn't walk...I called the pharmacy right away and told them of my symptoms and they said they had no documentation of such side effects so I continued thinking it was something else ( they always tell you to complete the full course of an antibiotic so you don't kill off half the "bug" and the other half goes resistant)....Stupid....I finally made an appointment and had my husband literally carry me cast and all down there...The doctor had no explanation for the symptoms I had but did lab work to kinda shut me up and low and behold it reviled that I had full blown arthritis so off to a rheumatoid specialist...We went through my health history and other that the sinus infection, migraines and a broken leg I was fine except for the constant pain from the waist down........It took 7 months to return to "normal" blood test went back to normal too...I had made a second trip to the pharmacy and insisted on filling out a form for side effects and had proof of it with the weird lab tests that had since gone back to normal...This form was supposed to be sent to the drug company (not sure if it ever was).....Thought I would just share my experience with you and hope it helps others...I am an RN with 15 yrs surgical experience and thought I was going nuts when on this stuff...Since then I have always included this as an ALLERGY since it is one of the best and most common drugs used for things like sinus infections and I don't ever want to take this again.
Sincerely,
Debbie

I have been on synthroid for about 6 months now. Some of the side effects I have been experiencing are numerous.I have hair loss, sometimes I get so ill that no one can stand to be around me, my weight has gone up about 30 pounds, my cholesterol levels went sky high so now I'm taking Crestor, I'm bloated most times, I have episodes where my face flushes and gets so red that it feels like its on fire, and now I've just started experiencing burning and aching of the legs, I'm tired a lot too! My doctor said I would lose the weight but every time I go for check ups and get on the scale it just keeps going up. I would like to know if anyone else out there is experiencing the burning and achy legs because I have been tested for everything and they can't find out what is going on. They of course say it's not the medication.It seems to never be. Does anyone feel me??

I've had my Mirena for about 15 and a half months and I am having it removed today at 2 o'clock. At first I had sharp pains when I would sit down and I felt like the cords were poking me and irritating me. My OB/GYN requires patients to come back one month after having it put in so he can check it and make sure it is still in place. At this visit he also trimmed the cords although he acted like he didn't believe me when I told him that I could feel them poking me when I sat down and that it hurt. At first I didn't notice any bad side effects, but I did have one good one: my periods stopped, but I still had occasional and sporadic spotting. I didn't think to look for any bad side effects because I got the device under the impression that it had no bad side effects. I thought it only had a rare complication of perforating the uterus, but since mine was in place at the one month check, I didn't think about anymore until I started thinking about having another baby recently. I went online to see if I had to have a doctor remove the Mirena or if I could do it myself, and I found out that it's best done by a professional because bad things can happen and then you'd have to go to the doctor anyway. Plus, I didn't want to hurt my chances of having another baby. While online I discovered this whole world of message boards where women were having a lot of the same problems I'd been having in recent months and they all blamed their Mirenas. Some claimed that their problems had gone away since having it removed. I never thought to link my circumstances to the Mirena, but when I saw how many women are having the exact same problems as me I knew that I needed to go ahead and get mine out ASAP. Here is a list of my side effects, and I've found other women have had them as well with Mirena: weight gain, bloated stomach, depression, short temper with husband and daughter, acne, low sex drive, spotting, cramps, constipation, and back pain. There may be more, but I can't remember them all right now. Some of them may not even be related to the device, but I've read of so many women with Mirena who are having or have had the same issues, so I suspect a link between my problems and Mirena. I hope this helps someone out there looking for answers. God Bless!

I AM SOOOO RELIEVED THAT I' M NOT ALONE!!!

I thought I was going crazy or something. I started taking Lipitor 10mg in Oct '06, then in January 2007 my "a.r.n.p" not an MD, increased my dosage to 40mg.....(the lab tests indicated that my cholesterol had not gone down any), which she didn't bother to check up on after prescribing such a huge dose. You know, like within 2-3 mos. Now comes my appointment with her Dec 4 2007, they do labs and low and behold I have inflammation of my liver!!! She called me in a panic and told me to immediately stop taking the Lipitor. Now my body feels like it's going to break. (a couple of weeks before I went to the doctor I started feeling like crap.....lethargic, can't raise my arms above my head without crying, knees aching to the point of not being able to walk,etc) It's even worse now.....now I can't hardly go to sleep at night, my arms just below my shoulders ache to the point of agony, I had arthritis in my knees - but now I can hardly walk without holding onto something - which is very hard to do when your arms won't function properly. I HATE THIS !!!

There was absolutely nothing wrong with my liver prior to this medicine. Now I'm worried that I'll have irreparable damage to my liver, not to mention all this pain in my arms, wrists, thumbs, knees and hips. (Last night I just couldn't take it anymore and I took some Tylenol - I was instructed by my physician not to take anything at all for pain.....RIGHT) I've been wishing this misery on her since it started - just for her prescribing this mess to me!!!!

I am 50 yrs old and feeling older as time goes by.
Thanks so much for listening and letting me share with you all; someone who really understands my pain!! I'm so glad to know I'm not alone in this. I have contacted an attorney - this is ridiculous that humans could do this to other humans. I'll look for another means to get my cholesterol down (right now it's only 129!! - But I feel like I just crawled out of my grave. I'd rather have high cholesterol....

I dread the night coming (pain is almost intolerable then)

Good luck you guys - I'll include you all in my prayers!! B. Carpenter

I too was taking LIPITOR. After 3 months I became short of breath. At first I put it down to the weight that I had regained.I had lost 18kg.the year before. I had muscle pain, nausea, headaches.The Lipitor reduced the LDL alright,but the shortness of breath became worse and worse. If I was sitting on a chair and dropped a piece of paper on the floor I would be completely out of breath from bending over and picking it up! If I was walking for more than a few minutes I would be out of breath and had to stop. I quickly regained my breath; but the moment I started to walk again I would become breathless again!! My heart specialist decide to do an angiogram, that was o.k. He told me it was my weight that made me short of breath, I disagreed with him. My G.P. did not know what caused it either. I had had problems with Pravachol, severe muscles stiffness and pain. I could not straighten a bend leg or bend a straight leg.It was only after I studied the enclosed leaflet in the box of Lipitor that I noticed the RARE BUT SERIOUS SIDE EFFECT: Shortness of breath, if you suffer from this stop straight away and see your Dr. it said. It turned out that the ALVEOLI are affected. I had a lung function test done which showed my lung capacity was down by 20%.After cortisone treatment it has improved a bit but it is still 10% down and it effects me every day. I tire quickly and get out of breath walking uphill or against the wind.If there is a class action going let me know please! I am so fed up . I am only 63 but feel like an old woman.I will not take anymore cholesterol lowering medication; I rather live 5 years less, if that is the consequence.

I started taking 20mg 6 weeks ago for High Blood Pressure ...im experiencing extreme muscle and stomach cramps...excruciating low back pain....joint pain...i spent this weekend curled in a ball unable to move with elevated pulse and heaviness on my chest. I feel like im slowly poisioning myself. I am med sensitive anyway and cannot force myself to take anymore....the dr says its not the lisinopril...but all these side effects started right after beginning the med. I have no health insurance and cant afford more lab tests and dr appts. Im going to try to survive by using strict DASH diet. I hope it works.