Active life symptoms and conditions

I am a 25 year old female who at 24 had never had any experience with birth control other than a quick prescription to a generic hormone to take care of a long period at 16 (due to stress.) Only a few pills were taken and I was fine. Now, at 25 I have been on YAZ for a year. I began taking it because I became sexually active at 24. Why? Well, I was mature both mentally and physically. I have had friends who became sexually active at a young age and who started birth control young. The side effects were pretty dramatic. I had seen a slim friend gain a whole lot of water weight. She even said it was the patch and later monthly injection causing the problem but the side effect was well worth the pregnancy prevention. I was against the use of birth control due to my preconceived notion of horrible side effects. However, once the monogamous sexual activity began I knew that I needed to take something. I had heard about YAZ and knew that it was something new and different. A different hormone used for prevention. I researched the pill and looked into any side effects. The posts I found seemed a little too ridiculous. I decided to find actual accounts and spoke to a co-worker who had been using YAZ for awhile. In fact, the majority of females I know use the product with no problem. Thus, after my yearly checkup I requested YAZ. My gyno welcomed the suggestion and even gave me several packs for free. It’s been a year without a problem. However, this morning I was hounded by my mother because there is a warning and lawsuit against YAZ and YASMIN (seen by a commercial-lawsuit.) This is due to severe side effects and death associated with blood-clots (when presented with heart disease, diabetes, etc.) I am a healthy 25 year old that frequents the gym weekly. I do not smoke. I drink every now and then. NO SIDE EFFECTS. My period starts after the 3rd pill is taken. It is quick and simple. I enjoy being able to plan things around my period. Cramps are light compared to what I use to go through. I can take one Ibuprofen the day of the third non-active pill and not feel a thing. I use to have horrible leg cramps and now I have no problem. My pre-menstrual mood has improved and I think it is because my period is no longer a strong factor in my life. I use to dread it and now I welcome it. I do not have any skin issues, no bloating, and no weight gain. Heartburn occurrence which is slim to none is similar to what I would have had before YAZ. I was appalled to find this site and to discover that people are having problems. I do not understand why people are so quick to blame this pill on everything. It seems like a lot of users who are posting on this site are extremely young. The body is still growing and maturing at 18 and even into the early 20’s. In my late teens, I was extremely moody and stressed due to college, etc. Any hormonal regulation then would have probably put me overboard! I am going for my yearly check up next month and will discuss this lawsuit with my gyno. I am concerned about this lawsuit. More importantly, I am concerned that this pill will be taken off the market. Call me a statistic but I like YAZ and would recommend it.

Wow! I must be the latest in a long line of Lipitor users and apparently pain sufferers. I have been on Lipitor for over a year. I am 56 years old, active and healthy (thank God). Around November 2008, I noticed a "twinge" in my left hip while sleeping. This has gotten progressively worse over the months and I thought it was due to arthritis (which runs in my family). But after reading these blogs, I am not so sure. If anyone has anything definitive regarding this, ie: tests, studies, etc., I would really appreciate a point in the right direction for more information. I was thinking (until today) that I was headed for hip surgery or something equally drastic. Now that I have a clue that it may be the Lipitor, I want to investigate further and then, if necessary, change to another medication that won't break me down like this. My heart goes out to anyone that has suffered through hip pain. It is a miserable, painful condition that saps your energy and your desire to even move sometimes. I appreciate any help you can offer. God bless all of you. - L. B. ******

I started taking Lipitor in 2004 and by 2008 was taking 40mg daily. I'm not sure exactly when certain symptoms manifested themselves, as looking back they now seem insidious, but I do know they became bad enough in 2008 I went off the drug myself, especially after reading postings like those at this website. After being off the drug for a month, it was clear to me the most of the symptoms dissipated, but it did have a residual affect. I realized I had suffered a loss of range of motion (ROM) in my left arm (frozen shoulder) and have been in physical therapy for over a month to restored 80% of it. I could not have done this while staying on Lipitor as I was experiencing “deep” muscle pain and weakness. I still have some weakness and pain in my left arm and shoulder and don’t know if it is permanent.

I am Hypothyroid and take Synthroid and am currently going through menopause and am on partial HRT. I took no other meds other than the Lipitor. At one point, I thought my symptoms were stress related, but realized my symptoms were causing the stress. Aside from the muscle pain, spasms, tingling and numbness experienced in my left extremities, I experienced gastro intestinal disturbances, occasional vertigo, some lower back problems and other aching in other extremities (like that of flu symptoms). I also suffered recurrent mental fogs, which I initially attributed to some lack of regular exercise (although I lead a relatively an active life), but that was not the case, as even after aerobic activity the tingling and pain would resume.

When I told my physician I had stopped taking the Lipitor (at that time for nearly a month), he didn't blink an eye. I agree with previous blog; the idea of statins are to lengthen your life, but what kind of life is it when you are in misery and nothing short of ceasing the medication brings relief?

I'm not advocating everyone "doctor themselves. Listen to your physician, but most importantly listen to your body and trust your instincts when it comes to these types of medications. Symptoms listed about scripts described as "rare" are usually not that rare at all. You are not crazy.

We have a 5 year old daughter who has been on singulair for about 2 - 3 years. She went on singulair due to coughing asthma. We were soo happy about how well the medication worked, it took about three months, but wow, she finally got over her coughing and was living a more active life. I actually was soo impressed with it, I remember mentioning it and promoting it to some of our daughters friends' parents with children in similar situations....wow do I ever feel awful. Anyway, our daughter came down with a terrible flu a few weeks ago and although she didn't seem feverish, had not one, but 2 night terrors, something that we have been worried about and comforting her with for a couple of years. These 2 threw the 2 of us over the edge this time....we thought we had to get her to a psychologist.....she was terrified, and although we were holding her and comforting her, she was still screaming for us, and there was NOTHING we could do this time....we were doubting ourselves and the environments she was exposed to......what could have happened in her life to make her have such awful dreams??? It was about a 1/2 hour later when my husband asked about the possible side effects of the singulair.....I ran and grabbed the pamphlet, of course this is the first time that I actually sat down and read it, which I should have done some time ago....anyway it was then that I discovered how many issues weren't normal that everyone just kept ensuring us was fine. We had been questioning ADHD for some time, and had actually had it on our list to discuss with her teacher as she was sooo hyper on a regular basis...at the age of 5 she still couldn't sit through a movie at a movie theater, as much as she loved going, she couldn't sit through it....anyway, the only thing that made it difficult to think she could have ADHD was she was such a great learner. She was very eager to learn and loved learning and teaching things. But when giving her instructions or asking her to listen, she'd be so jumpy. She complained of severe leg pains which we chalked up to growing pains...poor thing! Her temper tantrums were out of this world.....she is a child that is soo full of love, but when she was in tantrum mode, she was soo destructive and she would feel soooooo awful for her actions, it was like she couldn't control herself. We just feel awful that we couldn't help her and we didn't realize that what she was experiencing was not so much disobedience, but an imbalance due to the medication. We have since taken her off the singulair, we took her off of it immediately following reading the pamphlet. We found that she was VERY emotional for about 3 days, then she pretty well recovered. She has since become a normally active 5 year old, she is soo good, and has not experienced any night terrors, complained of leg pains, and absolutely no tantrums. Oooh how we love her so much.

I've been on Paxil for almost 9 years. I suppose it's a success for me because it has kept the depression away most of these past years. I'm on the maximum dose - 40 mg a day.

I've always been an over-achiever, a type A personality, friendly...with the Paxil I am lazy, no longer care about details, VERY friendly.
My home used to be pristine and comfortable....now I rarely put things away, there are stacks of books, magazines, and 'stuff' everywhere. Because of the mess, we haven't had visitors in our home for YEARS! I used to host parties on a regular basis in our home but these days I would die of embarrassment if anyone saw my home!

My memory is shot...I can't remember names, faces, details...seriously, I can watch a movie over and over again because I NEVER remember the ending!

My sleep cycle is shot as well. In years past, I only required about 5 hours of sleep. On Paxil, I don't fall asleep so I take lots of over-the-counter sleep aids to fall asleep and they knock me out...I can't wake up until almost noon!

I MUST take the Paxil at the same time each day otherwise the "zapping" starts. It isn't painful...just very annoying.

On the positive side, I have achieved many great things because I'm no longer apprehensive about public speaking. I've chaired several successful fundraisers for charities. But because the memory loss has become so profound, I'm no longer capable of chairing these types of events.

I've gained weight but it may be due to having thyroid cancer & having the entire gland removed...metabolism is shot.

I've only tried to go off the Paxil once but the depression resurfaced immediately and I cried for days on end...it was frightening! Of course I went back on it.

Speaking of crying, when on Paxil, it's almost impossible to cry! The tears just won't come.

Now for the really scary part...the effect of the Paxil on my depression is not what it used to be....but I'm on the maximum dose! I've tried several other meds but they just don't work as well. So what in the world will happen when it doesn't work for me anymore? That black hole called depression is the last place I want to be.

I'm 58 years old and I've been on 10 mg Simvastatin for 14 months since I was diagnosed with Diabetes 2. Also Metformin and Glipiside as my bs got up to 499 at diagnosis with high cholesterol.

I had NO IDEA that my suffering the past year could possibly be tied to one of the drugs I've been prescribed. In the first three months after diagnosis, my Diabetes was controlled and I've even backed off some of the meds. My cholesterol also came down beautifully. However, the debilitating weakness and muscle aches (which has increased over the 14 mos.) has become so bad (especially this last week) that I came to the Internet looking for possible reasons for 'body ache'.

And get this: I take a packet of vitamins every day which includes a daily dose of Q10... BUT I haven't been able to take them for about a week and this last week I felt like I was ready for a wheel chair~!!! Worse than it's ever been, knees and feet in horrible condition, hands and wrists unable to open a water bottle. Total body aches so severe it made me want to research something, anything to see what might be the problem.... before seeing the doctor about it!

My shock at seeing my medication here listed with the horrible side effects I'm experiencing has been a revelation~!! I am going to stop the Simvastatinn and see what happens. BTW, I've been an active person all my life, was a 2nd Degree Black Belt and taught Tang Soo Do and know what muscle aches and pains are, know my body (at least I did) and pretty much thought my active life was over.....

Not now~!!! I'm FURIOUS!!

My wife is experiencing severe muscle pain in the back and rib area after taking this drug. Has anyone gotten better after they stopped taking the medication or is everyone still suffering?

Levaquin is a wonderful drug and one of a very few that help men with prostatitis. If you have ever suffered with a prostatitis infection you know what i mean. No problems here with Leviquin.

Hi all, I was amazed to find this site. I too have had a rough life for the past eight years! I am going to be 39 in a few days but this story starts back in August 21, 2000. The day that put me in HELL for the next eight years and still going through it. Prior to this day, I had a lot of UTI's and Pneumonia and several times prescribed both Levaquin and Cipro. I did develop Achillies tendinitis but I thought this was due to my active life style, see I was an LPN and a firefighter. So I went for treatment to fix the Achillies tendinitis. This was a foot Dr that of course gave me a cortizone shot in it. I cant remember how much earlier this was that this took place and I am still not sure if this is what did it but as I am thinking back these are the things that come to mind. On August 21, 2000 I was on a fire call and my right Achillies tendon popped off the bone! They took me away by ambulance. The Dr in the ER said to go home with an air cast on, eat or drink nothing and come back in at 10:00am and they would possibly do surgery. Well, I did just that. The orthopedic Doc said oh yeah it is achillies rupture will have to go in and tie back all the little fibers. So away to the operating room I went. They gave me a spinal and just knocked me out. I was awakened suddenly by my Dr. voice loudly saying " Holy shit it peeled off the bone!" And another nurse saying let me see! I came up on my hands and they grabbed me put me back down and knocked me back out! (I still have night mares over that!) Anyway, I spent the next 3 months in a cast. During this time, I was told from over usuage of my left foot, I now was developing tendinitis in my achillies tendon in the left foot! Which this sent me to a wheel chair. They took the cast off in 3 months then I was still no weight bearing for another month. Then i had physical therapy for about 6-8 months with little improvement. I complained to the Dr about the left achillies tendon and he said he would not do anything about it unless it too popped! So now many Dr later, and many many medications tried and many surgeries later, and now diagnosed with Lupus, Sjogrens, and Fibromyalgia, the most my rheumatoligist says is I have a connective tissue disorder, and taking cancer medication (Methotrexate) I am now disabled at 39! My life taken from me. I have situational depression, panic attacks, sleep trouble, Suffer from post traumatic stress, nightmares, basically my life is a mess and it is over. On July 1, 2008 I had to go to the ER cause I was sick. I had been run down and feeling bad and sleeping a lot, disoriented, couldn't stay awake. They found I had another UTI and a sinus infection. The Dr Says we will put you on Levaquin and that should take care of both problems. So he left, it took me a while for it to sink in that I should stay away from that drug, so I caught him and told him, he said to me that this was only found to be in kids while they are young and developing that it causes tendon rupture, and besides he said, one dose will not hurt you. I took 5 pills, one a day. Since then I have been in so much pain all over my body it is unreal! It still took me days to figure out that it was the Levaquin doing this to me! I feel like at random someone is sticking a knife in different muscles in my body! I felt like I had done Tie bo for 24 hours straight! Even my butt muscles hurt so bad to sit here and write this email! I have days when I cant even use my hands! Write my name with a pen. I am not sure if this is all due to these drugs, but I am most miserable and not a bit better. I may have just made it worse by taking this last round of them. Has anyone else had this kinf of symptoms?

Do NOT take Avelox! As a result of taking it for a sinus infection, I now have acute hepatitis. On Feb. 14, 2008, Bayer Corp., which makes Avelox, notified its doctors in Europe that dangerous liver damage and/or skin rashes can occur in "rare cases." U.S. docs weren't notified. My doc prescribed it to me along with prednisone. Gastric problems began almost immediately, but I didn't make the connection. I thought I just felt so bad because of the sinus infection. My urine turned orange and I became deathly ill. Tests revealed non-viral hepatitis (not contagious, in other words). My liver counts were in the thousands! They are slowly going down, but I have lost two months of my formerly active life so far. I lost 15 lbs. in a week. I am weak and still have problems eating. I was healthy as a horse before. My life was hell for the first month--sweating, itching, dry eyes, dry mouth, couldn't sleep, diarrhea. I still have no energy can can't eat enough to gain weight. You don't want to mess with your liver. I feel lucky that a GI doc has been watching my counts and guiding my care. All you can do is rest and try to eat and stay hydrated. I have a long way to go, but at least I'm not on the liver transplant list--it was that bad before. I am angry that U.S. doctors weren't warned. The side effects listed for Avelox don't mention what happened to me. I am trying to get info on a possible class action suit against Bayer for knowing this drug causes liver failure and not telling U.S. doctors.

My chronic pain has really increased since being on Lamictal for 15 months for bipolar. I have had fibromyalgia for years. The bipolar developed after that. Since starting Lamictal, I have developed headaches so severe that I have been off work 3 times in the past 7 months, inc. 5 weeks recently. I've always had headaches, but these new, more severe headaches are non-stop. I have to take 3 time-release 100 mg codeine tablets every day, plus Gravol to keep the headaches bearable. Even then, many days I end up bed-ridden. I've also developed chronic, very bad plantar facsiitis in my left foot since starting Lamictal. I did weeks of intensive physio, plus swimming therapy to no avail. Finally had to get a cortisone injection in my foot.

I hate being like this; I like my job and was used to leading a very active life, despite the fibromyalgia, before I went on Lamictal. I briefly tried Lithium recently, but it had a whole other set of side effects, so I am really frustrated.

Has anybody else had increased or new pain since being on Lamictal?

Rosslyn

I started taking Levaquin last Friday ( the 11th) for a severe sinus infection. I was prescribed 750 mg for 5 days. I finished that but my sinus infection didn't improve so I was prescribed another 5 days of 750 mg. I took the pill yesterday and today ( totally 7 pills) I noticed on about day 2 or 3 that my legs felt tight, but thought it was a normal side effect. Then my lower back. I wasn't in serious pain at all so I ignored it. Today my knees, knuckles, shoulders, elbows, are extremely sore and i get sharp pains every now and then. It also hurts to sit for too long. I started researching the drug and now am so terrified after reading all these horror stories. Has anyone had this only last while taking it and not for months afterwards? Or am I pretty much in this for the long haul. And to the people who say that it lasts for months or years is it pain that disables you from working and doing daily things? I'm only 23 and I live a very active life and I'm totally freaked out now. PLEASE HELP

I have been on Lisinopril since the first of November. I had a dry cough at first but nothing really bad. After about three weeks I got a fever and sick for about a day and 1/2. The fever went away but I had shoulder and back pain (between my shoulder blades) The doctor listened to my lungs and told me I had pleurisy!!!! Treated me with antibiotics - got a little better. The soreness still there in my lungs up into my neck - some chest pain. Went to the ER - took chest x-rays.. found everything normal. Still coughing - congested all the time - I am 41 years old and I WAS on 5mg of this drug 1time a day. Not a lot at all but the ER doctor took me off the drug. He said after about three days the drug should be out of my system and then I can evaluate whether it was the lisinopril causing my lung problems. Also I have noticed that I have been having anxiety and worrying about things to excess lately, which is not like me. The anxiety started about a month after starting the drug. Maybe it is from the physical problems that I have been having. I was very healthy before all of this - I am very active and a non-smoker. Since these things starting happening I feel like I have aged 10 years!!! I also have some troubling getting air sometimes - like I feel as if I have to take a deep breath. Anyway - this is the only drug I am on so it only makes sense that it is causing all of this. The first night I stopped taking it I had terrible dreams - anyone else had this after stopping the drug?

I had a sore throat. The first doctor said mono. The 2nd doc. said no mono or strep --must be viral. Third doc says viral and puts me on predinsone, levaquin and darvocet because my uvula was swelling from infection. White count was elevated and had low grade fever. That was Friday..............................The Monday after that I had severe pains in my left side. After teaching went to ER they said gas after 2 minutes. Next day level 8 pain same side went back to ER. They said skeletal prescribed me 4 more drugs and told me it was viral too. Went to internist on Wednesday had to miss teaching he scheduled CT on Thursday morn. Level10 pain almost passed out on Thursday eve missed school/teaching. Friday admitted to ER at different hospital beyond any level of pain I have ever had, blood pressure through the roof, heart palp, they gave me morphine and phenagrin and muscle relaxer for spasms.

Here I am a perfect state of health get a sore throat and the next week I am in the hospital because of the 2nd ct saying that I am full of poo. 4 weeks later I am still in pain, missed 12 days of teaching and now they say i have ibs. I miss my active life before. I believe the combination of these drugs caused this. I am young no children and very healthy. Ultrasound,s blood works, 2 ct scans with dye, colonscopy, xrays show no probs. Which is great but still in pain. Anyone PLEASE HELP the doctors are taking their sweet time while I have lost weight and stay in bed which helps the pain. Bending over, lifting, eating, pooing, sneezing, coughing, hiccuping can make it worse. It is intense SHARP pain. I have cut out everything med wise except for Miralax and now I have diarrhea and joint pain.

They want me to take Dicyclomine and IMIPRAMINE, MIRALAX and Levisin sublingual and Diflucan.

I am a physician and have prescribed levaquin to many people. I have had some of them complain of what they thought were serious and variable side effects but mostly I attributed their problems to anxiety and hypochondiasis. I now know differently. I took levaquin, and for over a year I have had serious CNS anxiety, insomnia, joint and tendon pain, and widespread peripheral neuropathy. It has been an awful time and since realizing that the effects are often long term I have been able to identify many other patients who have developed serious long term problems with anxiety, depression, arthropathy and tendonopathy, neuropathy and possibly endocrine effects like gonadal failure and worsening of diabetes. There are no long term studies done post marketing to identify these effects and to unify all of these problems into one syndrom of fluoroquinolone toxicity. This is a big problem and I believe thousands of patients have been adversely affected by the use and misuse of levaquin and probably the other fluoroquinolone antibiotics. I have other colleagues who are beginning to recognize the long term consequences of levaquin and the fluoroquinolones. More research and study needs to be done. In the mean time I am sure that Johnson and Johnson, Ortho- Mcneil, will continue to refute that the incidence of serious adverse reactions is much higher than they report.

This is a great site for learning more on this subject where we can get the real facts from real experiences.( Vs. the deception from drug companies who are in the business for profit.)

Lipitor is pure poison, and Dr.'s hand it out like candy. All cholesterol reducing drugs that contain statins can trigger dangerous side effects. Not many of us are informed about the real danger of statins when we are handed the perscription. Inappropriate prescribing of medications will continue to be one of the leading causes of death. And we, the patients,do not always receive enough info. from our Dr.'s about the dangers and side effects from prescription drugs.

I'm 48 yrs. young. Female, small build, (was) healthy and active, happy, and an empty nester! My husband and I had moved to another province and hence had to find a new Dr.

I was prescribed lipitor 10 mg. daily after a routine check up by my Dr. because my cholesterol was a little high.

I started taking it in the winter 2005. I stopped taking it in mid June 2007... My side effects were progressive , drug induced, and it escalated to near disabling.

I knew something was terribly wrong. Was it A.L.S., M.S., West Nile, Lupis, Alzhiemers Disease, or a new designer disease? I did not suspect that the drug lipitor was the cause until much later.

At first, my Dr. said it was menopause. I should mention; since I've quit taking the drug 3 months ago, I have no symptoms of menopause !
At least my Dr. has acknowledged and diagnosed the cause of these profound symptoms." Myopathy as a result of statins."

Signs & symptoms I experienced are as follows;

Severe stomach pain.
Muscle pain, aching , weakness, stiffness, tenderness esp.to the lower extremities. Eventually, I could only shuffle to walk.
Pain in the palms of hands.
Stiff neck, shoulders, arms and lower back.
Trouble getting up from a seated position, and climbing stairs.
Extreme fatigue.
Hot and cold sweats
Night sweats
Fevers. High and low grade fevers.
Ringing in the ears.
Difficulty swallowing, and fear of choking.
Pain in the esophagus.
Memory loss, difficulty concentrating, forgetfulness.
NO appetite, yet a lot of weight gained around the abdomen area.Bloated.
NO taste buds.
Speech affected, slurring words and mispronouncing. Tongue felt swollen.
Trouble breathing at night, would wake up coughing ( and I was not smoking then).
Trouble sleeping.
Loss of balance and coordination.
Blurred vision esp. in the morning.
Sharp shooting pains in the Rt. thigh.

Most of the symptoms have now subsided. I still have some foot pain and leg cramps and muscle stiffness... and poor concentration. Putting this together has been done with great difficulty, as I seem to pause a great deal and forget what I was trying to say. The recovery process is slow but at least it's progress. My Dr. has not prescribed any more medication. I've done my own research, after the fact, and started taking coQ10. and I've noticed a big difference!

Quality of life? Well, I'd rather have high cholesterol and die from that, than be poisoned again by statins. What quality is there, to live an extremely painful, useless and unfulfilling life? We were all guinea pigs, and we paid a terrible price for this! I hope we all can recover from this with no long term side effects.
If you are considering taking cholesterol lowering drugs do some careful research on statin drugs before you take them, and read the testimonies from those effected by them.
sj.

I am 27 year old female I lived a very active life went to the gym 5 times a week for 2hrs.I been on coumadin Since Feb. I gained so much weight. almost 50lbs.I had a disection of my right artery (one of the main veins in your head). I have no idea what caused it the doctors in Houston have no idea. I had 2 strokes.I take 15 Mg of coumadin my INR is never stable I range from 13-15 Mg of coumadin. If any one can help please let me know Im tired of being fat.

It was comforting to read the stories from patients whom have the same issues with the prednisone as myself to assure me I AM NOT CRAZY. I am 43 years old and have severe asthma. Just this past April I was hospitalized for a week with asthma and was given so much steriods via shots, pills and IV drip that I have gained 25 lbs since April 16. Have swelling of the face, facial hair, swollen legs and a bloated belly. I cannot take it any more. I do not feel attractive and am in constant pain from the carpal tunnel I have developed in my hands, wrist and arms. I wish there was some way to return back to my normal active life and my normal body.

Took leviquin 500 for 8 days before I realized what was happening to me. Side effects included: severe panic, altered mental state, constant sleep, loss of appetite, pounding heart rate. After 2 trips to the ER no help was provided. I stoped the Leviquin early (was supposed to take it for 3 wks) and immediately started feeling better. The anxiety is much less but still present and I still sleep all the time.

Has anyone had similar experiences and, more importantly, how long does this last?

Please help!

I had mild heart attack 6 weeks ago. I had a 90% blockage in one artery and minimal or none in the others. I Left the Hospital with a mdicated stent and on Topral XL and Lisinopril, and Lipitor. Since then, no energy, depression, insomnia, generally bad feeling. I stopped topral and lisinopril 4 days ago. My BP and heart rate are still very low 40 to 60 beats per minutes, BP 110 to 120 over 60 to 80. How long do these drugs stay in your system? 52 year old male with no other health issues and previously active life.

Took Simvastin for two years,took off it by GP when I experienced severe pain in both legs, after over another year I am left with severe pain in the whole of my left leg and upper right thigh.After many visits to hospital both my GP and hospital are hoping I will stay away, both have refused to supply written evidence that the statin was the cause.My active life is in ruins. Is there any legal body in UK that are interested. If all the people on this site got together there would be a powerful body to get compensation, come on!! it has been done in USA. Brian Walder.

the doctor just increased toporal from one 50 mg to another 25mg. I feel very tired which lasts about 3-4 hours. I take a total of 10 pills as result of all my previous operations I do lead a very active life and like to work out at the fitness center. I am all of 77 years old