Muscle pain symptoms and conditions

First off, I want to thank everyone who has posted on this site. My heart goes out to all of the mothers/fathers who feel lied to by their physician, and to all of the young ladies, like myself, who chose to take this shot in order to protect myself and my partners. I have had two shots and WILL NOT receive my third.

I am a healthy 24-year-old woman who started my GARDASIL shots February 08'. The first shot, no problem. Second shot, wow. I felt like I was literally going to break. All of my joints, muscles hurt and felt very, very weak. I went to bed with a 102 fever, huge swollen glands, sore throat and cold sweats. I called my doctor and she said I "probably had the flu before I got the shot and I was just feeling my illness now.." she dubbed my issue an "coincidence". Well, I believed her because I wanted to. I didn't want to think I put myself in harms way, so I went on.

Well it's been 7 months and I can tell you my memory loss, muscle pain and bouts of depression have been a big issue. These are all things I have never dealt with in the past. Could it be GARDASIL, I'm not 100% sold that it is, but I am not throwing that idea out either.

I am really starting to struggle with the idea that we don't know the long term side effects yet.

Looks like we are all Lab Rats.

In seek of the truth,
L.

I experienced severe muscle pain in my shoulder and upper arms after using Tobradex for several days. I stopped the medication and the pain subsided. After two weeks I started using Tobradex again and two days later the pain began again. It was relieved quickly with Ibuprofen. Apparently severe muscle pain--like having sprained a muscle-- is a side effect of Tobradex.

Eight years ago I started with 10 mg. Lipitor and took it without problems for about five years. Doctor wanted me to change to Crestor and within four months I could hardly walk, shuffled my feet and had pain in muscles. Switched back to Lipitor two years ago and this week began to experience muscle pain so I stopped taking it three days ago. Any time I am in a prone position, or sitting, the leg pain is incredible. Walking there is minimal discomfort. Tried a massage today to no avail. Any way to alleviate this withdrawal reaction, if not, when might it dissipate?
J. in Pain

I have been off this pill for 6 days...was taking it for 11 months and I feel horrible today. My side effects while on this pill where:hair loss, complete loss of libido, vaginal dryness, headaches, muscle pain and twitching in my legs, rash on my breasts that was very itchy, nervousness, bladder problems: constant need to urinate and feeling pressure in my kidneys. The list goes on and on. I am scared coming off these pills, I have had dizzy spells all day and feel very nauseated, I have bad cramps. I stopped the pack mid-cycle and I have been bleeding fully since yesterday. I am so scared of whats going to happen next.

Ive been taking berocca for almost a year now. but not really taking it straight like once in a day for a year, but there was also a time that i skip for a month.

Im a recreational biker and there was a month that i took berocca 2 week straight and i take it during night time before i sleep so ill be pump up for the ride in the morning.

After the two week straight this is where the symptoms took place i am having a manageable pain on my lower right rib (the part where my last rib ends), my wife told me its the liver part on that area of the body. I was thinking its just a muscle pain on one of my bike rides.

but i stopped taking it not because of the pain but its because i run out of stock. I already forgot about the pain but after a month i bought the vitamins again i drank one tablet and hit the road, while on my bike i felt the pain on my lower right rib again. but this time it made me think its not a muscle pain at all because its been 3 weeks i stopped biking. Just today when i want to just bike around the city.

I haven't gone to the doctor yet/

Hi so glad to read this im calling my dr as i read!! i got my mirena in apr of 2005, i was one of the 1st pts my dr did one on. I have no children and am married, we wanted to wait to have kids and i have frequent migraines so the pill is a no-no. the day i had it put in i passed out while leaving the office. they said "oh wow that never happens"...hmmm wonder how many others passed out after i did!

i cant really report any bad side effects until about 1 yr after insertion. i started having terrible cramping where i couldn't even stand up. this would come and go every few months. then i noticed i couldn't urinate as well anymore...the stream was weak and it seemed like my muscles were tense or something. i now have constant pain and pressure of the pelvic floor, my abdomen is always bloated, i have gained 20lbs and i do weight watchers and cant lose a pound, i retain tons of water, i have fatigue and joint/muscle pain. I attributed the joint pain and fatigue to fibromyalgia which i have been dx'd w/ in 2007 but now i wonder if its this mirena!

i have been to different doctors and specialists because i don't feel well, i haven't for a few years now...now i wonder if its because of this mirena. im going to have mine removed and see how i feel. the urination problem is the worst! i always feel like i have to pee but nothing comes out...the urologist said all my tests were normal.

im so glad i read all these posts...i hope every woman reads this before deciding on the mirena.

recently was prescribed simvastatin. Pharmacist advised that 50% of people will experience severe muscle & joint pain and burning in the muscles. I can see by reading the site that this is true. Must try since cholesteral and bp are high and dr thinks at 51 I had two mini strokes (tia's). If I experience the severe pain that is discussed i will stop taking. Thank you for all the info! This site is awesome.

I am taking Levaquin one time a day, 500 mg. for diverticultis. I have fibromyalgia so attributed symptoms of EXTREME FATIGUE to that but this is fatigue like I've never known. I can't do much of anything. I don't work outside the home so will just deal with it if it cures my infection. I'm using sleep meds too...but that could be fibromyalgia kicking in too. But fatigue is much worse. I hope it kills those bad bacteria!

I am a 52Yr old male and was diagnosed with T2 Diabetes 2 1/2 yrs ago ....The doctor prescribed me simvastin a few month later 20mg once a day all had been fine till about 6 months ago when I developed tinnitus and started feeling very tired...My concentration started to lapse especially when driving as i found i couldn't remember driving down a stretches of the road etc ie passing speed cameras etc ...my memory also seems to have slowed down and i have problems recalling recent conversations or things i have done etc...just recently i have been getting severe itching on the soles of my feet almost becoming painful i have pains /aches all over and now especially have pain in my left arm right knee and fingers...when i get up in the mornings i feel like i have run a marathon the day before as i ache especially my neck and shoulders...needless to say i have now stopped taking the tablets after reading this forum and i am seeing my doctor next week initially i put all this down to getting older ...
Steve

I was prescribed 7 days 750mg of Levaquin on 9/10 and finished 9/16. I was originally diagnosed with bronchitis but went back to the Dr. yesterday cause I was not doing any better and he now says it's viral. I've gone to the hospital because I passed out on 9/13 and continue to faint at least once a day. I have tingling/numbness in my hands, ankles, toes, my knees hurt, my lower back is in a lot of pain, almost to where it is not tolerable, I'm dehydrated (I'm drinking and eating, just not as much) it is extremely painful to eat, my tongue and my gums hurt terribly. Last night I had a horrible dream (I don't dream usually, not nightmares) and today I started to hallucinate (mildly) A week ago I was functioning normally, a mother of 3, playing with my kids and now I can hardly walk without assistance, I can't go to work, I'm in constant pain. Someone please give me some kind of guidance. Will these feelings ever go away? What should I do? Thank you!!!!

I am 45 and have been taking statins for 5 years since having 3 heart attacks in a 4 day period.At first I was on Atorvastatin 10mg and didn't suffer any side affects,I was put on Simvastatin 40mg 2 years ago due to cost.Since then I suffer with very sore muscle pain down the length of my right arm.My GP keeps on prescribing painkillers and doesn't mention the fact it may be side affects of the Simvastatin.I find it sad that costs of drugs are the reason I am in pain.

Iv been on 40mg for a year now i could be feeling perfectly fine then suddenly an intense tiredness comes over me and i feel very sick and start heaving quite violently and desperately need to lie down until it passes, sometimes i fall asleep and sometimes not. This is a day occurrence, sometimes even 2 to 3 times a day. This only started when i started taking these tablets. The doctor says is not anything to do with the medication but im convinced it is. Has anyone else got these side effects?

I've been on simvastatins for about 2 years after TIAs. I'm 56. I had two small Strokes about year ago despite being on simvastatins. Had brain scan which showed two small areas of scarring and carotid artery scan- arteries fine. Started experiencing dizziness last year and GP diagnosed vertigo and gave me seasickness pills which didn't do much good. Since then I've experienced headaches which last for weeks, increasing fatigue (now struggle to get out of bed in morning) muscle pain which is getting really bad and sore feet (?). Increasing memory loss, confusion, lack of concentration, eye problems (when I first wake in morning my vision is blurred for ab out 30 minutes or so. I've been worried i mmay be developing Alzheimers. I've also piled on weight and the texture of my hair has changed - it has become very soft and silky and become thinner - normally my hair is very thick. Also I've had two perms in last 6 months which won't hold curl - been having perms for years and never had this problem. I've had several blood tests including for under-active thyroid and they have all been clear. I've been really worried about all these problems and did some research and came up with this site. I am beginning to think my problems stemm from taking 40mg Simvastatins so am going to stop them and book appointment with GP. Any comments/advice would be appreciated.

I have been on Diovan 160 for two years. Have put on 10 - 12 lbs. Have developed low sodium levels, muscle pain and slightly elevated blood sugar levels. Is low sodium level a possible side effect of taking Diovan?

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