Muscle pain symptoms and conditions

Boy, after reading all the negative testimonials on Lipitor, I will throw mine in the garbage. That is what they are meant for. I have severe headache, and muscle pain, and foggy head, and I have only been on the crap for 2 months. I believe a lot of people's health is being ruined, and a lot of deaths are happening as well because of Lipitor and other statins. Mark my word, one day this drug will be withdrawn from the market, and the poor Pharmacutial companies will be in huge trouble.. They have the world convinced that we all need statins to bring cholesterol down.. The era when my parents lived , and lived long lives, and on farms, with butter, bacon, lots of fats, and never heard the word STATIN. I think every one that is writing to this forum and complaining about LIPITOR, should make a phone call to PYzier and tell them your side effects, that is the only way anything positive will come from this forum.. thank you for listening... I have called Pyzier and told them as well.

MY FATHER WAS DIAGNOSED WITH TEMPORAL ARTHRITIS. HE HAS BEEN ON PREDNISONE FOR ABOUT 5 MONTHS NOW, STARTING FROM 80MG/DAY. HE HAS TAPERED DOWN TO 40 MG/DAY,,BUT TH SIDE EFFECTS ARE STARTING TO BECOME UNBEARABLE.
WATER RETENTION,,SWELLING, MUSCLE PAIN,,WEAKNESS.
HE IS 80 YEARS OLD,,AND IT IS REALLY TAKING A TOLL ON HIM. IF ANYONE CAN GIVE ME ANY HELP OR INFO TO COUNTER SOME OF THE SIDE EFFECTS(MUSCLE PAIN AND WEAKNESS MOST IMPORTANT) IT WOULD BE GREATLY APPRECIATED.
THANK YOU.

I'm a 38 y/o woman. For 7 yrs I knew my cholesterol has been high. I refused to take cholesterol medication and decided to diet and exercise but that didn't work. I've had 2 children in the past 3 yrs. In May of this year I started having chest pains and palpitations. I had blood tests done. I was given Inderal and also prescribed Zocor 20mg for my cholesterol. It was 243 with and LDL of 178. I took Zocor for a week. I felt so awful. I was weak, I lost my appetite. I was constantly tired. I couldn't even carry my 10 month old son, yet alone care for him. I informed my physician and she changed it to Lipitor 20mg. I thought I was doing fine. I checked my levels again after a month. My cholesterol was 113 and LDL 58. I trusted the doctor knew what she was doing. At the same time I also was taking Omega 3's. I asked my doc to lower the dosage to 10mg. From the time I was taking Zocor and the start of Lipitor. I was feeling tingling and numbness in my arms, hands, fingers, toes, feet and legs. I also was having muscle pain. I asked my doctor about that. She mentioned because of my heart palpitations, it could be symptoms of anxiety and panic. I had feeling of pins and needles throughout my body, not knowing when it would occur. I had muscle pain in my arms and legs and neck pain. I went online to see the side effects of Lipitor and came across this website. I decided to do an experiment. I stopped taking Lipitor 9 days ago. I was on statins for almost 4 months. I don't have the feeling of tingling and numbness, but I still have pins and needles and muscle pain. I have to say, I feel so much better. I hope to get better. I 'd really like to know, how long does the medication stay in your system? What are the effects of getting off it so suddenly. I'd love to feel myself again.

I took levaquin for 2 weeks to treat a infection, i am 26 years old and have never had muscle pain for longer than a couple days after working out...now i have moderate pain in my rib area and muscles near the groin area and even upper leg, and have done hardly any physical activity while being treated...i have seen no improvement for a few weeks now, but think my infection is gone... going back to my doctor tomorrow...need help

I have muscle pain, weakness, and chronic lower back pain. Started statin drug, Simvastatin, on 11/21/07. I take no other drugs. Within two weeks, I could not sit without severe lower back pain. Reported problem to family medical doctor on 1/11/08. M.D. sent me to physical therapy for 8 sessions. No relief from physical therapy so I requested an X-ray on 3/20/08. X-ray shows very mild degeneration at one lower vertebrae. M.D. sent me to an orthopaedics doctor who recommended continued physical therapy. Went to a Chiropractor instead. After six chiropractic sessions with little relief, I made an appointment with an Osteopathic doctor. My M.D. sent me to a rheumatologist who prescribed high dose naproxen for two weeks. The rheumatologist ordered and X-ray of my lower back area. The lower back X-ray produced no negatives. The rheumatologist's next step will be to order and MRI of my lower back area. The D.O. suspects statin induced myopathy and because of hyper reflexes he ordered an MRI of my brain and cervical spine. I am now recommended to a neurologist who specializes in the diagnosis of multiple sclerosis. Am I getting the run around? Only one doctor said I might have statin induced myopathy. The rest will not even mention the statin drug theory. I just pray for ache and pain relief. I have some improvement after four months off of the statin which I believe is quite a strong point that it was the statin drug and not some unknown condition. I don't think arthritis or MS conditions improve. All I know is that I had no health issues before taking the simvastatin. Good luck to everyone who has or is taking a statin drug. BEWARE!!!

I am a 54 year old male who started taking Lipitor about 4 years ago. It seemed OK at first, but over the next several years I began to have increasing amounts of joint pain after exercise. Nor muscle pain, joint pain. And it seemed to be a result of exercise. By the time I stopped it, I was hurting after everything, not just exercise. I felt better within the first two weeks, but it took about 4 months for me to be able to exercise vigorously again. Over the years I seemed to have forgotten how much vitality I used to have. I am a physician, and because of the long lag time until I felt better, I wondered whether improvement might have related to other factors, so after about 5 months I decided to restart Lipitor. It surprised me that after just one dose, I got back all of the joint pain and fatigue when I was at my worst on Lipitor. I was really hurting. Needless to say, I didn't take any more.

Coincidentally, a physician friend of mine who had statin induced polyneuropathy had a similar experience. After his symptoms went away he found that after only one dose the entire polyneuropathy came back.

Stopping and restarting the drug is a way to test the correlation between the drug and the side effect. For such a large spectrum of side effects to recur after only a single dose, it argues that the problems that my friend and I had was due to some sort of immune memory response. I have not seen this in the medical literature.

I am off it now for about 8 months and am able to comfortably play singles tennis and jog - much more energy (and I took 200 mg of CoQ10 a day with the Lipitor).

I have been taking Lamictal since October of 2007. I experienced some of the symptoms (muscle pain in the head and neck) before I started the medication. I have experienced panic attacks since July of 2005. I have had mild heart palpations since I was in my mid 20's (I'm 36 now). I have had what I would consider a below normal energy level since my mid 20's also. Ok so like everyone else I am thinking I'm a hypochondriac! However, I was diagnosed August 28th 2007 with having Lyme’s Disease and also Hyper-Thyroid (same time, same lab-work). Two weeks later I was diagnosed with Bi-Polar Disorder (this is one thing I knew I was battling but didn't know how to handle it). My physiatrist started me on Lamictal and I did the standard ramp up to 200mg. I also was started on a 90 day treatment of Dyoxicycline for the Lyme’s and Methimazole for the Hyper-Thyroid. I was very very weak and was only able to stay awake for short periods of time (4 to 5 hours max). Just an fyi, I am not overweight, lazy or unmotivated. I have the physical appearance of perfect health. This, I think works against me as the Dr's seem to think I'm just whining. Mater of fact; my Primary Care Physician never tested me for Lyme’s. I went to an Urgent Care Center which tested me for Lyme’s disease and I came back positive (they also tested my Thyroid levels and found the problem with my THS levels) I told my Dr the results and he insisted I have same test done again. Guess what, new tests, same results.
My symptoms today are very similar to what I have seen posted many times. Muscle pain (entire body, some areas worse than others), heart arrhythmia, racing heartbeat, intense palpitations, nausea, foggy “un-plugged” mind, fatigue, weak muscles, muscle cramping (especially after repetitive motion, such as strumming a guitar), panic attacks (much more severe) and the latest addition to the group, Insomnia. Muscles pain in my head, fore-head, jaw, temple, neck (front and back), shoulders, is terrible to say the least. The pressure in my fore-head (right under my brow) makes me feel like I need to close my eyes or rest (resting does not relieve anything). The front of my neck is so tight at times it feels like my jaw is being pried down. I could go on and on.
On my quest to find out what else is going on with my body I have had 2 Echocardiogram’s on my heart and abdomen, 2Nuclear Stress Tests, blood work out the wa-zoo, MRI of my brain, 2 CT’s of my Head and Neck, Chest X-rays, Endoscopy, Colonoscopy, and all revealing nothing.
Most doctor’s I have encountered seem to want to treat the symptoms, not the problem/disease. I believe I know why; we (the ones who are there for solutions) tell them what the symptoms are (how we feel). We of course are thinking “this will help with a diagnosis of the problem/disease”, when in fact (I feel); the doctor’s thought process stops there. They don't know what’s wrong with you but they do know what your symptoms are so....bingo, let's treat the symptoms. Don’t misunderstand what I am saying. I’m not saying, “Most doctor’s don’t know what they are doing” or “don’t take your meds”. I am saying you and I are one of the 20 to 30 patients most doctor’s see daily (100+ weekly). They may be caring and good people but they are just as human and fallible as you and I. My advice is this; (and I am taking my own advice) don’t always “pop” into your body what the doctor suggests/prescribes, without doing your own research. Heck most of us won’t buy a car or more importantly, send our kids off to a college with out doing your own research (we just don’t trust those shinny brochures). Your body and your health are worth you doing your own research. Just keep in mind, Pharmaceutical Reps are always at your Dr.’s office (sit in the waiting room for 10 minutes and I’m sure you will see one). Reps are paid to do one thing; encourage (push) the Dr.’s to promote use of the Pharmaceutical Companies drugs.
My wife and I have been doing our own research on Lamictal (after a year of taking this stuff) and the side effects associated with this drug. We have searched through many (many,many) web sites for information and we have talked with pharmacists and Dr’s for opinions. Although I’m am not thoroughly convinced that Lamictal is the cause of all of my symptoms, my wife and I have decided to lower my Lamictal slowly from 200mg to 100mg. I am now taking 150mg daily (three days now) and plan on staying at this level for a total of two weeks before lowering to 100mg. I do fear dropping the dosage to quickly (potential side effects) or lapsing into a mania. To help avoid a manic episode my wife and my immediate family are all “up-to-date” with my course of action. They are on “Red Alert” and have promised to keep a close eye on my behavior patterns and moods. (I don't want to put them through another hyper-mania episode, its much too devastating). I do want so badly to feel healthy and alive again and at this point I am rather frustrated with the Dr.'s ability to help me achieve this goal. Remember it is called “Practicing” Medicine. So now I’m going to practice a little, very carefully and cautiously.
As a foot note; I have recently (past two weeks) been re-tested for Lyme's with a negative response. I am keeping in mind Lyme's test are very inaccurate (still hoping this one is accurate). My thyroid is under control and normal, so.... let's see if dropping below 150mg of Lamictal will eliminate some of these other symptoms. I will keep you posted.
Erik

Update on my post of Aug. 11th. I did see a neurologist who was a bit skeptical, but after looking it up did acknowledge that this drug can cause tendon ruptures, etc. Later that week he did a nerve conduction study, both the one with the needles and the one where they shock the muscles. He was happy to report that I did not have any "nerve" damage. I had already told him that I did not think I had neuropathy as the numbness had gone away and was just replaced by the constant pain in my joints, etc. I then went to see my rheumatologist who was also just as skeptical that the drug could be causing all the pain I was describing. She said she had had three patients with tendon ruptures, but nothing else. I really don't care what she believes, and I told her so. I know what happened and what horrible pain I have been in ever since. I hate to report that the pain in my feet, knees, hands, hips, back and now my neck are not any better. My insomnia is some better, but I am taking more Lyrica. I tried a different antibiotic yesterday for the sinus infection called Clindamycin. OMG! I took one pill and within a few minutes had unbelievable heartburn. That lasted for 12 hours, along with reflux, burping, weird stomach noises. Now, I can't take that. Doctor called in a prescription for Augmentin this morning. Afraid to try anything now, but guess I will give it a shot. Is anyone getting any better from their joint or muscle pain? Some encourgement would be good. Thanks.

I've been taking Levaquin for about 3 weeks. Last week, suddenly, every joint in my body started aching. I mean from my neck, hands, hips, knees, ankles, feet, everything. For the past week, when I wake up, I can't even make a fist without experiencing excruciating pain. I've always been very active, running, basketball, soccer, skiing, you name it, so this is scaring the heck out of me. I'm 47 years old, and up until a week ago, I was hiking with my family, running everyday with my dog. Now I feel like I'm 100 years old. It hurts to walk, stand up, etc! I have an appointment with my doctor tomorrow! I'm ticked about this!

I had my Mirena put in about 7 months ago, since then i have been getting sicker and sicker. I was just diagnosed with hypothyroidism in June, but my TSH level is almost back to normal now and I still feeling so ill. I have gained 15 pounds, feel very emotionally unstable, I'm moody, fatigued, have constant joint and muscle pain! I am so depressed and no matter what i do I just can't feel better! I just want to die! My husband had a hunch that it could be the IUD causing this all and started researching it. He found this website and read to me what everyone had said. I was shocked! I'm a nurse so i got off the phone with him and removed it myself, which I do not recommend if you are not a health care professional. I'm sure it's just in my head, but I feel better already! I hope that all of my symptoms resolve now, but either way that is one less thing that could be causing my symptoms. I hope this helps others and let me know if you also had joint and muscle pain! Thanks and GOOD LUCK to you all!

Pam

Hi! I JUST had the Mirena put in Yesterday...Tues. And within one hour I started to feel foggy, light headed and crazy! I started getting a pressure headache. Being the last patient of the day, I knew the office was closed. So I looked online and found you all. I am horrified at this point! I couldn't sleep last night at all! I was so nauseous and had the poops. (sorry, tmi) Today I feel full of anxiety and my heart is racing. I feel like I'm on drugs or drunk! My head is still pounding. I kept calling my OBGYN and didn't talk to him until about 2 hrs ago. He said none of these symptoms are from the Mirena. So I hear that is most of the Docs words around here! He suggested I give it more time and call him in a few days and if I want it out, he will take it out. Well the thing is, I am ready to pull it out myself! I feel like I'm crazy! Seriously! I don't know what to do! I called my PCP and they refuse to take it out b/c they didn't put it in. They suggested going to the ER. Well my insurance for sure won't cover that!! So what do I do? I feel like I'm going crazy and no one will listen! We are moving to Italy in a month nd I need this resolved AWAY before then! Any advice will help! I just know when I call my doc, he will try to make me keep it in! What do I do?? HELP! Thanks for being here! Wish I had found you before. I am really good about researching things and I didn't with this. I trusted my doc! The other thing is I hear a ton of you have gained weight!!! I JUST had a full tummy tuck June 5th and I freaking better not gain weight!! LOL I want this out!! Calling my doc tomorrow and demanding he take it out. Has anyone had a doc refuse taking it out and if so, what is our recourse? It's our body right?? Thanks again for listening to me gripe!!! ;) God Bless!!
Danielle

Oh my I am not alone.. I have tiredness muscle pain and am losing my hair.. has anyone else experienced this side effect.. I am only on this medication and I know it has to be the medication causing the hair loss.. Dr. says none has been reported but yet here I am.. I have a red bumpy like rash on the upper part of my legs that will not go away.. I am so glad for this site.. am calling doctor tomorrow --off this stuff now!

I have been on Welchol since April & have been experiencing several unexplained problems. I have been having "sweats" which I just chalked up to being menopause symptoms.........but now not so sure. I can't sleep & suffer from muscle pain as well as muscle spasms in my face. Is anyone else having any of these issues!

I was prescribed 20mg 3x daily for five days to treat "Reactive Airway Disease/Bronchitis." Yesterday was my 5th and final day of taking the medication and I noticed both of my shins began hurting for no apparent reason when I walked. I didn't think it had anything to do with Prednisone. Then, last night, I suddenly felt weak as if my blood sugar had dropped tremendously and ate a grapefruit while trembling with weakness to stop this feeling. Again, I made no association with this and Prednisone. Last night as well, I noticed that my shoulders suddenly became achey on both sides of my backbone for no apparent reason. This morning, I woke up and the pain from my shoulders had spread to my hips and the entire area between my shoulders and hips is tender to the touch. Today, after not taking any of the medication, I feel mentally blurry, have moments of what feels to be low blood sugar and flu-like symptoms. I'm also still experiencing the muscle pain in my back and hips although my shins seem better. My pharmacist told me to call my Dr. and seemed surprised to learn I was not weaned off this medication. All of the symptoms I have described above are side-effects that should be reported to a Dr. immediately, according to my pharmacist. Another less-serious side-effect that began yesterday is swelling in my feet, hands, stomach and face. I also had diarrhea today.

I am a 72 year old white female who has been on Fosamax over 5 years for osteoporosis which runs in my family. In December, I had severe discomfort in the thigh area of my right leg. X-rays ordered by my GP showed nothing. Sent me to orthopedic surgeon whose x-rays also showed nothing. He ordered bone dye test which showed stress fractures of BOTH femurs. No one, NOT EVEN THE ORTHOPEDIC SURGEON, could figure out how it happened since I had not fallen or had other trauma. When I began to do my own research, I found answers to other problems I had been experiencing, for which no one had answers.....bone and muscle pain, hair loss, depression. I realize doctors are overwhelmed with info but I am especially disappointed in the orth. surgeon who should have known this was a possibility since the study came out in The Orthopedic Journal. As I continued my research, I find that women have been experiencing these side effects for years. I was previously very active and a dedicated walker, but this has robbed me of my confidence since I fear breaking other bones. The femur is the largest and strongest bone in the body and if I broke both of those with no trauma, what else could happen? I want to get the word out to women but am not sure the best vehicle for that. Any suggestions? There are Fosamax lawyers anxious to jump on this but I am more interested in spreading the word, not litigation, however I think there are possibly many unreported cases of the Fosamax side effects just because people don't know where to turn.

I was given 40mg Lipitor for elevated cholesterol. I took it until I started having muscle weakness .I am a retired nurse of twenty five years, and knew this symptom was not correct. So I stopped taking the medication and told my doctor of this.He did not protest in any way.My symptoms now include;two torn ligaments, sob,mental deficits, muscle wasting, night sweats, weakness,h/a's, and more. I have not taken Lipitor for two years now. Damage is done.My doctor said it should be out of my system by now. Is this a cover up?

MY HUSBAND HAD A HORRIBLE REACTION TO AVELOX AFTER TAKING 4 DAYS OUT OF TEN, HE CALLED THE DR. COMPLAINING OF MUSCLE/TENDON STIFFNESS AND PAIN. THE DR. DIDN'T SEEM TO CONCERNED SO HE TOOK IT FOR 3 MORE DAYS AND STOPPED AFTER DOING SOME RESEACH ON-LINE. (THANK YOU MEDICATIONS.COM OR HE MY HAVE TAKING THE FULL TEN DAYS.) NOT ONLY DID HE HAVE THE MUSCLE PAIN, HE ALSO SUFFERED FROM, HALLUCINATIONS, EXTREME MOOD SWINGS, WEAKNESS, TEMPORARY HEARING LOSS, LOSS OF APPETITE,(LOST OVER 20 LBS.), CONFUSION, PARANIOA, EYES WERE DISTANT(ZOMBIE LIKE). I THOUGHT HE WAS GOING TO DIE! I DON'T EVEN KNOW WHY HE WAS PRESCRIBED AVELOX, HE HADN'T EVEN BEEN ON AN ANTIBIOTIC IN OVER 15 YEARS. HE DIDN'T NEED ANYTHING THAT STRONG, AS HE 'S BEEN A HEALTHY 58 YEAR OLD MAN. I TRULY HOPE IT HASN'T CAUSED ANY LONG TERM EFFECTS SUCH AS LIVER DAMAGE. IT'S ONLY BEEN A MONTH AND A HALF SO TIME WILL TELL. BOTTOM LINE NEVER TAKE AVELOX. 08/16/2008

I have been on zocor for over a year, about 8 months ago I began to have pain in my left arm, got and injection and it was better it started again in my left arm , this time there was pain , tingling, numbness, swelling , it got better but it moved to the right arm which is twice as bad, I am often brought to tears from the pain..I sometime describe the pain like shutting your hand in a car door. My Dr keep giving me the same meds.

I have been on lipitor about 4 yrs. I am a runner and keep tract of my times. I have been losing about 4% of my speed each year and have recently had a large amount of muscle fatigue. Today a ran a 940 pace and thought I was not going to make it home. Three years ago my average pace was 805. Could the 20mg dosage be causing this problem?

I am taking lipitor for 3 months and sinds one week i have pain in my left arm and a constant twinkle in my left hand. i stop now for 3 days and wait to see the results

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?

I am a 46 y/o male whom took lipitor 20mg for about 10 days. It was the first medication taken for me aside from occasional antibiotics. Within a week I began to develop severe nausea, weakness, postural dizziness and worst of all, chest pain at rest! I took my last dose last Saturday 8/9/08. Because of the chest pain, I went to the ER on 8/10/08 and discharged the next day after I ruled out for an MI and a negative exercise stress test. My chest pain recurred on 8/12. This AM awoke with nausea, dizziness and chest pain again. I'm going to have an adenosine stress test this PM. I consulted a pharmacologist yesterday about the metabolism of Lipitor and she told me indeed these side effects are not uncommon and in my case, Lipitor will not be eliminated from my body until probably this Sunday or early next week. Anyone experience what I'm feeling?

I have been taking simvastatin since June 28, 2008. I am 44 years old and have always been majorly active with my 17 year old daughter. Recently I have become chronically fatigued so much as to want to go back to bed within 2-3 hours after I get up in the morning, (definitely not me). I have felt spaced out,depressed to the point of wanting to cry all the time, have severe back, hip, knee, leg, and hand pain. I go to pain management for my back and hip problems (past surgery), but the usual pain has been intensified over the last 2 months and I wasn't sure why, until i decided to check out the Simvastatin to see if it has made me put on a few pounds, and boy have my eyes been opened!!!!!!!!! I AM STOPPING THE MEDICATION IMMEDIATELY!!!!!!!!!!!! Thanks to all who have spoken up, I wish I would of checked on this sooner!!!!! I'm calling my Dr. first thing in the morning!!!!!!!!!!!

By exhausted in Canton

I HAVE BEEN ON LIPITOR FOR ABOUT A MONTH NOW AFTER HAVING 3 STENTS PUT IN I AM A 50 YEAR OLD MALE THAT HAS ALWAYS BEEN ACTIVE IN SPORTS, MY LIPITOR SIDE EFFECT ONLY STARTED A FEW DAYS AGO, I HAD SEVERE PAIN IN MY RIGHT SHOULDER SO BAD I COULD HARDLY USE MY ARM THE PAIN GOT SO BAD LAST NIGHT, WE WENT TO THE ER, NO PROB FOUND JUST INFLAMMATION, SO THE DR PRESCRIBED MOTRIN 800 AND A MUSCLE RELAXER, WHICH DID GIVE ME SOME RELIEF IN ABOUT 25 MINUTES .
TODAY WHILE SHOPPING I NOTICED A PAIN NOW IN MY LEFT SHOULDER AND NOW THROUGH THE DAY IT IS JUST ABOUT AS BAD AS THE RIGHT ONE THEN AFTER DOING THIS RESEARCH I WILL AS OF RIGHT NOW STOP TAKING MY LIPITOR I WILL POST MY UPDATE TAKE CARE

I was prescribed Simvastatin four days ago, against my wishes, as I had heard about the side effects of muscle pain and numbness in the joints and feet. However, what I had not expected were the terrible nightmarish dreams that followed. On the fourth night I stopped taking Simvastin as I was literally too afraid to go to sleep.
I then slept fitfully but did not experience the vivid and disturbing dreams of the previous three nights.
I shall ask my doctor for alternative medication. If she cannot offer me anything other than statins, I shall stick to Benecol and research further!

Jacqui M.