Belief symptoms and conditions

Was prescribed HCTZ and started taking it off and on in early August. Pain in the butt cutting the pills in half. Started to feel weird feeling in my left ear and cheek and then numbness spreading up my face, forehead and scalp.(I did have a few beers the weekend before this happened) Took myself to ER. MRI, CT, full blood work, thyroid check, EKG, heart and lung xray. ALL PERFECTLY NORMAL. Of course I was diagnosed with possible MS, Belle's Palsy, and was told I might just be wired weird.

Went to primary the following day for follow up and was told that my blood pressure may have been the cause of the episode. Prescribed Lisinopril and started taking it immediately 10/12.5. Started feeling good pretty quick, but noticed a few crazy dreams and almost like I was falling.

Missed a few doses and and had a few beers over the labor day weekend. Started meds on Monday but started feeling pins and needles coming back in different parts of my body. Continued to take meds and then went camping. Had a few beers around the fire. Woke up next morning with slight case of Vertigo. Continued with meds through the weekend and have felt dizzy, dumb, tired, my eyes don't move correctly, my left arm has felt numb and swollen, my left cheek tingles and I feel so swollen in my gland area under my ears. Knee pain too.

I didn't take a dose today, and I feel 100% better. Still tingly and numb in spots, but better. A little anxious and my heart feels like it's beating really deep and fast. BP is 154/82 after going down quite a bit on the drug.

Anyone else had trouble with the alcohol? Any similar symptoms? This site has calmed me down as I've always been a worrier/hypocondriac type. any response or idea would be really appreciated. Thanks everyone...good luck!

I am so sick of my mirena and I have only had it for about 1 month. First of all cause of my insurance, it cost me, $967 to have this thing and if I have it removed, I am still responsible for this bill... one incentive to keep it but on the other side, I have gained close to 10 pounds in one month and I have not changed diet or exercise, still 5x weekly exercise and healthy eating, the occasional cookie as always. I am crazy irritable and impatient beyond belief and feel more and more guilty that my 6 year old child is witness to my aggravation and mood swings. I have had two yeast infections since and still have a lot of discomfort, very mild down there, not to mention I am still bleeding and feel bloated all the time. I cut the caffeine a little thinking this would help but it didn't, I was more tired.. I swear, Kaiser screwed me over and if I had known, not only the expense of it, but read up prior I would not have had this fitted, now I am going to take it out and be left with a bill for something I don't have.... :( sad face!

My son was on singulair for most of his infancy (11 mos- 22 mos old) we took him off of it when I started staying home with him. He was in daycare and was having breathing issues. We would give him the singulair and Zyrtec every morning. He became a very despondent baby. He would spend the ENTIRE day in the rocking chair at the daycare. After months and months of the teachers telling me this we decided it was best I stay home with him. He came off of the singulair and things got so much better for a while, he began to interact with us and others, not fearful anymore, and slept through the night. However other things have grown to be worse, as he has been developing...every day he seems more difficult to deal with. Now, 5, he is angry, fits of tantrums and rage, can't cope with his emotions, he actually kicked me today during one of these fits. He has been peeing in his room when he is sent there because he has been punished for one of these outbursts. What are the long term after effects of Singlair? Has anyone had this experience? Could the singulair have been given to him too early and now caused some sort of permanent nero or psychiatric condition? PLEASE ADVISE!!!! This Mom is really frightened.

I have been on this for 6 days for a UTI. I personally am not allergic to sulfa drugs and have had absolutely no problem while on it so I can't speak to specific side effects but I do have something to say about it. I'm a little confused as to why so many of you believe that this drug should be taken off the market. Surprise, a lot of people are allergic to sulfa drugs which accounts for the vast majority of adverse events described by nearly everyone on this post. And guess what, every single drug comes with side effects (Tylenol, Advil, Tums, etc. are no exception) and you accept the risk of those side effects when you put it in your body and weigh that risk against the possible benefits. It's not your doctor's or the drug company's fault you're allergic! Antibiotics, including this one, have saved millions upon millions of lives. It seems intuitive but it evidently must be said: if you're allergic to it STOP TAKING IT and call your doctor so he can prescribe a different antibiotic. Seriously people, it's not rocket science. Hives are a pretty straight- forward symptom of an allergy and one that can be diagnosed by the lay person. I am a medical professional, but even if I wasn't, you don't need an MD behind your name to figure that one out. Why would you continue to take it after having an obvious reaction? (a reaction that, by the way, is a well documented, clearly stated possible side effect of this particular medication if you'd taken the time to ask any questions whatsoever regarding your own health, not a surprise adverse event of a bad drug) It's not rocket science, it's common sense people. When I'm prescribed something I'm not familiar with, my first question is, "What do I need to know about this." Even after a satisfactory explanation, I look it up before taking it. In fact, that's how I found this post. Which brings me to my last point, why is it that people blindly put things into their bodies that they know nothing about. If the pharmacist doesn't explain drug information to you in person, that's what the little drug safety pamphlet attached to your Rx is for. Read it, that's why it's there. OR, there's always the option of using this wonderful resource called the internet. Use your brains for god sake and take a more active, responsible, and informed role in your own healthcare process. You are ultimately responsible for your own health, and to be completely honest, you're one of the only people who actually cares about it (guess what, your doctor probably isn't one of them because he has a hundred other pain in the ass patients with no common sense to keep track of). Think people...

I am a 62 year old male who works out and is in good shape. I developed a case of diverticulitis and was prescribed a 10 day course of Avelox, 400 mg. per day. I began taking the pills and they worked on the diverticulitis. However, after 7 pills, I developed pain above and below the knees and down at the ankle. This pain is in the tendons. It feels like a permanent Charlie Horse. I went to the doctor today and his belief is that I do indeed have a side effect, since I am in otherwise good health, the pain is in both legs, and the onset coincides with taking Avelox. Unfortunately, he said they do not really know the mechanism of this reaction; they don't know how long it lasts; don't know if it goes away, etc. Now I must really watch myself for who knows how long because of the danger of popping a tendon. This is incredible to me. Seven pills and perhaps permanent damage? I am wondering if any of the people who have posted tendon issues have improved or gotten worse after time.

Our 19 month old son was diagnosed with RAD (reactive airway disease) and our pediatrician is very hesitant to call what he has "asthma". His two bouts of wheezing were both associated with viral respiratory infections. However, after this infection and the seasonal allergies he seems to have, the dr. prescribed Singulair (4mg granules) to us to help control our son's wheezing and coughing. After being on it three days, he's not the normal laid bad but energetic boy that we know is ours. He's mean...he's aggressive...and he's biting so much at daycare that they have assigned one person to shadow him all day long. We took him off of it yesterday, so we're now 24 hours singulair free. I'll post any differences we see in a few days, but for now it's our firm belief that Singulair is what is making the difference.

I got mine out 9 days ago. I think I'm in the crash phase. Or everything just came down at once yesterday. I was super crabby.
I'm feeling better. my boobs are about half the size (I DO miss those), my stomach isn't bloated beyond belief, I can "feel" a little more. it doesn't hurt to have sex and I'm a little less foggy in my thinking. I hope it keeps getting better. I miss my sex drive.

My husband figured out that it might be Mirena making me nuts (and boy I thought I was going nuts). The only thing I could feel was anger, my sex drive dropped below zero, I put on about a million pounds, stomach looked 5 months pregnant (I've always had a big butt, buy my waist was always small) my boobs got huge and were painful about half the time, and I was absolutely EXHAUSTED almost all the time. I could sleep for days if I could found the time.

My husband has been on remicade since Sept, 2008. He started having what we thought were mini-strokes and had a major one on May 25th, Memorial Day. He was given a clot buster because all along we thought he was having a stroke. After have a specialist examine him, we learned he did not have a stroke but is having seizures and it is medicine related. We are not sure if it is the remicade of some other medicine he is taking for his Crohns. His doctor and another doctor told us they had not heard of Remicade causing seizures but it is listed as one of the side effects - has anyone every had this side effect or know anyone that has - this scared us beyond belief. His doctor is contacting the makers of Remicade but who knows if they will respond. Please let me know!!

Can anyone tell me if you can just stop Lipitor cold turkey or do you have to stop it slowly? I have been taking Lipitor for 5 years now and I have been trying to find out what is causing my leg weakness. I mentioned it to my doctor who said it si just a fact of getting older. The problem is getting worse and I noticed it started about 3 months after taking the Lipitor and has steadily gotten worse. I am 49 years old a little over weight {which I am working on}. I also noticed my asthma which I haven't delt with since a small child has come back. This may or may not have to do with the Lipitor but the pain in my knees and legs I believe do. It really hurts in the joints of my legs and sometimes in my shoulder area.

I had my mirena inserted in July 2007, so we're working on two years. At first, I noticed some sharp pains in my abdomen. When i asked my doctor about it, he told me it could not be related to the mirena and I should try prilosec. I probably had indigestion. I thought...oh, ok. If you say so! But it didn't go away until about 2 months later.

I could list all the same things as everyone else - hair loss, sore breasts, metal taste in mouth, cravings of food just like when I was pregnant, omg, the weight gain and stomach bloating is what kills me the most. I seriously still look pregnant and I didn't even think much about it until I looked at photos of myself post-baby, but pre-mirena. I looked SO much thinner and so much better rested. I seriously don't even look like myself.

I complained to my doctor last May about being super anxious and having trouble sleeping. He prescribed Lexapro for me and told me I probably had some left over baby blues. I took Lexapro until Christmas of this year when I one day just decided not to refill the prescription. I just don't feel like me. The lexapro made me cloudy and I didn't feel anything. I couldn't cry. I'm a TOTAL SAP and I couldn't cry! I couldn't feel anything. So, I took myself off it, which was no picnic in the park. Dizzy beyond belief.

It's been tough because even my husband seems to think this all coincides with becoming a mom and that is what changed me. But, I don't buy it. I love being a mom. I am good at being a mom. I have no anxiety about being a mom and so on. My body is screaming at me to change my hhabits. I've increased exercise, gained weight. I can't stop eating....and I eeat crap.

OK, enough from me. I'm getting this thing out next Monday and I don't intend to tell the doctor why. I am going to suggest I may like to get pregnant again as my reason - because I know he'll honor that reason and take it out. I plan on taking a 6 month rest from inserting any kind of chemicals into my system and seeing what happens. At that point, if my body has changed and gone back to some normalcy, I will probably go back on the pill. (I just didn't want to go back on it after my child because I got pregnant on the pill in the first place!)

A few years back I severely injured my back. As part of my treatment my doctor gave me prednisone. My joints, especially my knees hurt beyond belief. I even had go to my parents house because I couldn't move, it hurt too much. I called my doctor and you know what he told me?!?! it was all in my head.He accused me of trying to get pain pills from him. The joint pain got so bad that I had to be hospitalized. You know what they told me at the hospital. I was having a allergic reaction to prednisone. No S***t!??! anyway, since that time I have not taken prednisone. My concern now is that my doctor wants me to get a cortisone injection. . . I am scared I would get the same reaction. from the research I have done so far, it looks like it is from the same family. Does anybody know?

Thanks
B.

I'm a 38 year old female who took Topamax back in 2003 as a migraine preventative. I don't remember any diminished brain capacity, forgetfulness, etc., but then I also suffer from ADD, so who would know. Anyway, I don't see this particular side affect with anyone, but exactly 72 hours after starting Topamax, then 72 hours after each dosage increase, I would suffer from severe body aches. The worst I've ever felt in my life and I usually get body aches with the flu.......these were much worse. If I remember correctly they would last for several days then gradually fade away. The Topamax didn't seem to help my migraines because six months later the neurologist switched me to something else. I'm seeing a new neurologist now and he wants me to try Topamax again. I'm worried and stressed beyond belief. I don't want to go through the body aches again. Has anyone else experience this? Am I maybe deficient in something that I could beef up on while taking the Topamax to decrease the body aches side affect?

sd

WOW. 1st of all i must say if u r about 2 take budeprion, DON'T!!!! EVER!!!! i read these posts b4 i took it, i read all about the side effects of this drug and didn't take it as seriously as i should have. i figured i would give this drug a chance because my depression was so bad nothing at all helped, ever, and i figured i had nothing 2 lose. well, i lost my f***king mind. i am hundreds of times worse than i was b4, i am insanely irritable, angry, self destructive, depressed, i feel like a monster. i have been taking it 4 2 weeks, and i am very dizzy all the time, i feel like i am losing my vision. everything is really blurry and i swear it feels like i am going blind and i cant see very well at all.

i cant believe i did this 2 myself by taking this awful drug. whoever said it was way better than no drugs was so right... my depression was bad b4 but this is out of control!!! its f***king amazing.... i am whacked out beyond belief and so much worse off... soooooo much worse.... i have the same things running thru my head over and over and over and over all day!! and it is all awful!!!! i was NEVER EVER EVER this bad, nowhere near this bad.... now i am completely psychotic and utterly insane and i feel dizzy, drunk, and i cant see. i feel awful. i am so rattled up... if u want a fair warning from a real person, here is my testimonial, NEVER EVER touch this disgusting stuff. my god... how in the hell do ppl get away with giving ppl this crazy shit???? seriously????? sadly... i know no1 will ever give me an honest answer 2 that question... there isn't one!!!!! =(

I was put into the hospital in March '06 after using a carpet protectant that I purchased at the pet store. The chemicals in the product burned my lungs and I spent about 3 weeks in the hospital and was given prednisone for 10 -12 days. I remained in the hospital after my lung function increased because of the sever pain in my knees. My husband was going nuts trying to tell the doctors that he read on the internet that prednisone causes problems with knees and joints but they didn't believe him and kept running tests. They eventually switched the steroid to solumedrol and the pain decreased. I was sent home with less pain which eventually went away....but not for long. 7 months later, I began to have knee pain, which continued to get worse each day. The 1st Ortho told me that I tore a ligament and that the dead bone on the MRI will grow back. I didn't like that answer and eventually went back to an orthopedic surgeon I saw a few years prior for an injury I had while doing gymnastics. He took one look at my MRI and diagnosed me with AVN in my right knee. I got my 1st total knee replacement in August '07, a manipulation in October '07. While recovering, I noticed that my left knee was hurting and thought it was from using it so much and compensating for the right one......but I was wrong. I got an MRI on my left knee and once again, I have AVN. I got my 2nd knee replacement in January '08, a manipulation in February '08 and a 2nd manipulation in March '08. I'm now 29 years old, with asthma (from the carpet spray) 2 fake knees and have had the worst 3 years ever while going through all of this. I now have pain in my 1st replaced knee......under my knee and toward the inside. I go back to my surgeon tomorrow and am dreading another surgery.

If anyone has any questions, I'll try to help you as much as I can.

J.

After being injected with lidocaine during a root canal procedure, the vision in one of my eyes was beyond distorted (the side they were working on). I had 3 injections prior to prep the tooth which is located upper right near the wisdom tooth. An hour into the procedure, I began to feel the doctor working on the tooth. So I wouldn't experience major pain, he then injected me one more time in the roof of my mouth. Within seconds, I noticed my vision was in that eye was beyond blurry. It was like I was seeing cross eyed, but my eyes were not physically crossed and my vision was distorted beyond belief. This totally freaked me out and lasted for a few hours until the lidocaine wore off. I have had a few root canals and dental work over the course of the years, but they used carbocaine instead, because I get too jittery with regular novacaine. Therefore no epi. What makes matters worse, is that they were unable to finish the root canal procedure, because it freaked me out so bad and my vision was messed up, that I was sent to the ER. I was told that he must have hit an optic nerve during the injection which most likely caused this situation and they were categorizing it as a possible allergic reaction, but again feel as though it was just the optic nerve that the lidocaine traveled to. Now I have to finish the rest of the root canal a week from now and will be having another dentist perform it. I'm so frightened that this will happen again. I honestly thought that my vision wouldn't be restored back to normal. Has anyone ever experienced anything like this?

Thanks.

It seems that this subject has been extensively documented, but just wanted to confirm that I believe this drug is very dangerous. We JUST put our 5-1/2 year old daughter on it one week ago. She has NEVER had any issues sleeping, is most often in a great mood, and has been protected beyond belief by my wife from negative imagery, TV, etc. The last week was unbelievable. Night terrors every night, with the most vivid and negative imagery when asked to describe the content of her dreams. Things that I would have thought she must have gotten from watching a Stephen King movie. Given the lack of fitful sleep could have been a contribute, but her mood all week was very downtrodden. Hard to say a 5 year old can be depressed, but I would have to say she was, very sullen, moody, despondent to affection.

I can positively say this was a blind test. We didn't really read the label on the medicine until yesterday, so we were not looking into things that weren't there, nor were we focusing in on the sleep issues. We took her off yesterday, and hopefully I will be able to report that the night terrors that I am 95% positive must have come from this drug will abate.

I hear because the chewable format is new, this drug is really being pushed. I hope this drug is pulled instead of being promoted. Buyer beware, especially administering to kids. I can't imagine if our daughter had been a little younger and not able to express herself to the level she can at 5.

I was taking Wellbutrin for about 2weeks (i had taken for about 7yrs previously) from Effexor because of sexual side effects. The Welbutrin worked to get rid of that problem and my Dr in the hospital warned me about generic Budeprion, but my regular PA-C said that the 150's were different and made by Glaxo. Huh???? Like an idiot i got the generics and 5 days later I feel like i have no anti-depressant in me. Im having panic like "emotional attacks" where i just cry if I hear or see something that triggers an emotion, sleeplessness (i don't need any more of that), weight loss (what's food and why is my stomach gurgling) and over all lethargy. I hate this drug, its useless beyond belief, I really wonder who got paid at the FDA to pass this one through.

Ok here goes I have posted on here once before when i first saw this site right after i had mine put in back in aug i think it was aug 23rd i got it in and i posted the next week. well i had stabbing and poking pains where it was and you know how its in there pointed side down so they can pull it back out. Well guess what! I went for my follow up visit to check placement and they couldn't find the strings! I freaked out i thought it fell out so and i had been having sex and thought i was going to end up pregnant again which i don't want or need i already have 2 kids and a soon to be step daughter that aggravates me beyond belief. So they did an x-ray and it was still there thats what the girl that did the x ray told me. So i went back to the room thinking that they could just go and get the strings and put them back where they need to be. WRONG! The dr comes in and says well its still there and then he proceeded to tell me the damn thing is UP SIDE DOWN!!! How in the hell does that happen?! I asked him if it would still work and he said yes cause of the hormones. Then i asked him if since the pointed side is up instead of down like it needs to be if it could rupture through my uterus and he said IT SHOULDN'T! Ok now im thinking well it shouldnt have turned up side down, and now your telling me it shouldn't rupture through. So i preceded to ask so when the time comes to get it out how are you going to get it out? He said "I don't Know" "Maybe it will flip back around to how it needs to be by then"

Ok thats not it. I stay up very late like right now its 3:30 in the morning and i haven't slept yet and when i do sleep i can sleep all day long if my boyfriend doesn't make me get up. I am always tired and i have no energy. After i had my daughter i had a lot of energy i had lost 90 pounds on my check up after having her the scale was 90 pounds less than what it was 4 months before i got pregnant with her, so of course i had lots of energy. Then i got this put in and now im dragging ass so to speak. And now im wishing i would have gotten my tube tied instead.
I have hot flashes, i am always hot even when im out side and its like 30 degrees out there now. I don't wear a coat just because i will start to sweat like i have been working out for hours.
Sex is VERY painful, put me into tears painful. I will take it as long as i can before the pain is unbearable and i start to cry and sometime scream because i cant handle it. That is putting a real big strain on our relationship. Also to top this off i am Rapid Cycling Bi Polar. Im 23 years old my kids are 20 months and 4 months then my boyfriend has a 5 year old daughter and i loose my cool with her a lot. My meds are not even able to control this anymore. (and i take a lot of them) My mood swings are not just aimed at her but towards my boyfriend who i have been with for 5 years and that girls mother and grandmother they get a lot of my anger.
I have very rude out burst like i have terets or something i am not myself anymore by no means. I have turned into a mean person. but my kids i can keep my cool with them for the most part except when my son the oldest one starts throwing his fits that last for ever.
I cant concentrate at all and that is hurting my grades a lot in college.
My house is not staying clean because i don't have the energy to get up and clean it and if i do i cant stay focused long enough to do it all (which that could be related to my bi polar syndrome)
I don't want to have sex at all still.
I don't know if all of this has to do with my bi polar or if its the mirena.
I don't want it out because i don't want anymore kids and i don't have insurance to even go see if its still in my uterus. but i get bad stomach pains and i get really hot then very dizzy and start seeing black and purple spots and feel like i will pass out. My psoriasis has broke out even worse.
I have started noticing joint pain.
Im not suicidal or anything but sometimes i go to bed hoping that i don't wake up in the morning and that could be bi polar getting bad but i really honestly don't know what to do. Because if i get it out i cant afford the pill which i wont remember to take, and i will need to get my tubes tied which i cant afford and don't know if i might want more kids when mine get older. But i AHHH!!! I just don't know what to do anymore. I would like to sue the pants off this stupid company cause of how i feel and they might have to do surgery to get it out which can ruin all chances of me having more babies forever.

I don't know what is wrong with you people but its like you can't handle anything. I had the mirena put in November last year and yeah ok i had cramping for the first month or so and yeah i had spotting. But unlike some of you fools i knew what the side effects were i read what came in the package which means i knew what to expect before i got it put in. And yeah there are loads of possible side effects but if you read everything and know what could happen you shouldn't complain if something does happen. Not everyone who has the mirena has these things and for people who are considering it i would recommend trying it and after 3 months if it doesn't feel good then get it removed. That especially goes to people that have just had a baby... i mean really in the first 3 months after having a baby who is really seriously interested in sex right away. The reason i am here was to see if there was more information about them now because UNFORTUNATELY i had to have mine removed for an operation. I had a cyst on my fallopian tube which was not mirena related. In fact almost all women get them when they are menstruating but they go away. Unfortunately with me they don't go away and this is the 2nd cyst to be removed in 3 years. I am planning on getting a second mirena inserted next week. Because frankly i find it ideal. And yeah i may have had mood swings on occasion while i had it but come on think about it what woman doesn't have mood swings. So sure you can blame everything on the Mirena but for the most part besides then for the people where the mirena got stuck or moved during the time you had it... its all in your head. And like i said before i would recommend the mirena and if after 3 or 4 months it doesn't suit you then go for something else... but don't dismiss it because some people have too much time on their hands and like to spend it whining over everything on the net. Remember with the Mirena you have a 50/50 chance of having symptoms or not. Take that risk before taking the risk of going on the pill and forgetting to take it or going on depo provera and putting on 20 pounds.

As many here many recognize, I had tremendous problems after taking Levaquin. This included: distal bicep tendon rupture, a full range of psychological symptoms, extreme and long lasting fatigue, etc. Even after going through this ordeal and still dealing with the fallout almost 2 yrs. later I am once again in disbelief at the medical community. My 18 yr. old daughter just visited a nurse practitioner and came home with a prescription for Levaquin. This alone was enough to make me angry but the fact that it was prescribed for a cold sore (no, I'm not kidding) is just beyond belief! And we wonder why we have the problems we do. Trust no one!

I noticed that everyone has written here the side effects of the Toprol XL but no one has said that they have had success on getting off the drug. I'm 39 years old and I have had some side effects from it too. I'm on Toprol XL 50 mg once a day and everyday my neck gets hot like it's on fire,my face gets flush, my feet sweat and my hands get ice cold. I keep my faith in the Lord that he will help me find a way to get off this poisoning medicine. My blood pressure was 164/110 and I ended up in the hospital back in August of 2008 and after running all the test they chalked it up to anxiety. My belief is that it's the medicine. I'm going to try to find a Doctor who is a Homeopathic and see what he says and I will let you know what I find out.

I have been feeling most of these symptoms for a while but thought it was just in my head or that I was going through early menopause but I am only 38.
Immediately I gained weight in my stomach area which made me mad but I dealt with it. I have have really long periods where I used to have a 3 day period. Now I have anxiety and mood swings where I just feel like being mean. I hate how I am to my husband, mom and kids. I feel like I can't concentrate and I can't remember a conversation that I had 2 days ago. I really feel like I was deceived of all these bad side effects. I just called to have this bitch removed and the nurse said she has never heard of any bad side effects. I guess I am one of the unlucky ones. I also exercise and diet constantly and can't seem to lose the extra weight I put on. It's so frustrating when I try so hard.Now I am a little nervous about getting it taken out. I plan on taking a xanex b.c it hurt so bad when I had it put in! I also am a little nervous about what birth control to use next. I don't want to deal with hormones again. It's not worth it. Also the sex drive is very low for me. I really wish I would have seen this blog ahead of time. I would NEVER of had the mirena inserted and I wouldn't have wasted a year and a half of my life on being miserable!! I'm getting this removed 9am on Friday!!

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.

HI Everyone! I am a 21 year old mother of a 6 month old little boy. I have had the worst experience with the Mirena. I had it inserted in May of 2008. I am trying to have it removed but my ob/gyn won't do it. I have had severe pain everywhere especially in my head. I have been put on migraine meds but nothing has helped. I have had bleeding beyond belief. I have been bleeding almost since it was put it. Pads after pad after tampon after tampon. I have never had bleeding this heavy. I am so frustrated. I rather take a pill everyday than go through these horrible feelings

Besides hair loss, vision problems, pain all the time, dry mouth, diarrhea, sleeplessness, pounding heart, I also had a problem with mucus filling my stomach and my food would get stuck. So I had to vomit to get the mucus up so I can continue eating. The first time I quite taking this poison pill, I got to feeling much better and my stomach got much better too. But never connected Lipitor with my problems. When I started taking this poison pill again, all my problems returned. But only worse, because I was in so much pain that it was hard for me to climb stairs and I had to hold on to everything just to go to the bathroom at night. Than I quit taking this poison pill again and haven't taken anymore since. All my problems disappeared again. I told my new doctor what this poison pill was doing and he told me to stop taking it, which I had already done.

So how many more people is this poison pill going to hurt and kill before Lipitor is taken off the market? I'm once again seeing Lipitor advertised on TV claiming this poison pill is FDA approved. Wasn't Baycol approved by the FDA as well and was taken off the market because it was too dangerous?Scary!

I'm 62