Leg pain symptoms and conditions

My 4y/o son has asthma that was not well under control, so the doctor put him on Singulair and Flovent about 2 months ago. In the first few weeks, he started having severe leg pain. He would be up at night crying. I would massage his legs till he went to sleep. He also started soiling his underwear with small thick amounts of stool multiple times a day; despite the fact that he has large soft bowel movements at least twice a day. His asthma has been well controlled since the start of the medicine. We stopped the Flovent 1month ago to see if the Singulair would continue to control his asthma, which it has. We adjusted his diet, since the doctor attributes his stooling to constipation, which has not helped. He is now frequently peeing his pants and frequently complains of arm and leg pain which comes on suddenly and seems to last for 5 to 15 minutes. I am going to take him back to the doctor for a full check up to rule out anything more serious, such as a spinal tumor, but till then I am going to stop the Singulair and see how things go. I wanted to stop it as soon as the incontinence started, but was afraid of his asthma flaring back up. Is flovent causing anyone's kids any issues. My son also seems to be having trouble getting his words out.

I am so glad I found this site. I'm 42 and the doc put me on these stupid pills because of ovarian cysts. The first few days were fine but by day 4 I had awful stomach and lower back pains and by day 9 I had leg pain. I have had awful insomnia which I NEVER had before. One other thing that I thought was odd I woke up in the middle of the night soaking wet, like I had peed myself but it wasn't urine. I thought I was really sick and then out of curiosity I googled these pills and was shocked at what I found. I will stop taking them tomorrow, it's not worth it. The body and joint aches are awful not to mention the bloating. I look like I'm 5 months pregnant. I wish I had seen this site at the first sign of my symptoms because I would have stopped right away. I was really starting to think I was going crazy.

I am in my 2nd pack of Loestrin 24 FE and was put on them due to my extremely heavy bleeding. I am 39 years old and am not using this for birth control just period control. The first month went great, bled for 3 days and then stopped. My 2nd pack is going horrible. My legs are always cramping and hurting. In general I feel like I have the flu. I started my period after taking the second pack for 1 week and now at week three i am still bleeding and cramping. I am due to start taking the brown pills in three days and do not know if i am going to take them or skip them and go straight into the white pills again or just quit them all together. I do not feel that bleeding like this all the time is of any help. How many of you have experienced bleeding like this and continue the pill to see it quit? Also, I do not always take the pill at the same time, it sometimes varies by an hour or so.

I am a 58 year old female Who has been taking Simvaststin for 16 months .
I have been increasingly bothered with mainly night leg pain ( bilateral) that radites to my hips and back. It's like a tooth ache. I too have had to resort to taking pain medication at night to sleep. During the day when I sit for long periods my legs ( especially the thigh area) aches and standing up , walking etc does not alleviate the ache. It is not constant at this point but very frustrating.
After reading the posted notes I am contemplating going off the Simvastatin for a while to see if my symptoms improve.
Any thought?

Thanks!

I just had mine inserted yesterday. I wish I would have read this before I did it. Today i started having leg pain... I did a search online about leg pain and noticed it could be a sigh of a blood clot.. I called my
Doctor and she said to take some Tylenol and if it does not go away to call her back.. It went away but I am terrified. I cant afford to gain weight or get anymore bacteria or yest infections than i already have.. Thanks for sharing your issues. I will call to have this removed on Monday... I have had a head ache since last night..

I've had my thyroid removed in 2006 and since then I've been on medication, i was ok first and i thought i was ok until now. i had leg pains that woke me up from my sleep and i went to doctor and couldn't figure out why i was having this pain, i thought i had restless leg syndrome or sciatic but doctor said no. now i'm reading all your side effects and I'm in shock, i had no idea that it can cause to leg pain. also I've change my medication to generic (because of insurance issues) since then i guess my itching started. i thought i had allergic reaction to food or bugs or something and i went to allergist of course nothing came out. now I'm reading the side effects of this medication, it can cause hives, rashes, itching and even urticaria which i have right now. i went crazy to find anything in my house to find a bed bug, spider, flea or anything that can make me itch like this. the other side effects that I'm having are hair loss, red/hot face. i can not believe all these symptoms are actually side effects to a medication supposed to make me feel better. whoever says that's they find it weird that this medication has this many side effects, we are not crazy. this effects are real and so many of us has them.

22 years old i have had Coltis for 5 years,flair ups pretty much the whole time, i have been on Prednisone a lot this last time has been the WORSE!!! All i can say is i hate it!! i was put in hospital the 4th time steroid thou the iv for 5 days sent home got worse again back to hospital then to try Cyclosporin thou the iv and also the steroid thou the iv. Ten days later they sent me home on prednisone coming off the iv was hard the pain in my legs was unbelievable!!! finally i was sent home on prednisone,coliform anemas,salfak anemas,and salfak granuls,i thought the worst was over but it was far from it... I turned in to a complete loony,crazy women i don't even know myself anymore my poor partner and kids. Having to deal with the pain and everything eles that comes with having a flair up but then also going though the side effects of the prednisone and the coliform was unbearable, i just wanted to die! My flair up was not getting much better and i hated myself as i felt i did not know myself with the mood swings, the crazy flip outs,crying all the time.My partner has been great having to pick me up off the ground and turn the crying reck into someone half normal. I hate the moon face,weight gain, im hungry ALL the time,night sweats,sleepless nights sore teeth,I have come off it now its been 4 days, so now all i need to stop its the coliform then i will be steroid FREE!!!!! i cannot wait!! For my face to go down and to be normal and back to the good old me! I forget what shes like... Coming off the Prednisone has been hard with the leg pain,muscle aches,head aches,mood swings,nausea. Its just hard as no one around me understands what im going though or what it feels like so i just sound like a sookie cry baby or a raving loony. does anyone know how long it takes for moon face to go away??? I wish everyone luck with there battles with Prednisone, its one of the hardest things i have had to deal with. =) your not alone. stay strong and be positive even throu your lowest times.

I was on NuvaRing for one year and I just stopped. Not only did I get the weight gain, nightmares, back pain, leg pain and sweats but I also had NO sex drive what so ever.
I have also seen on tv that they are recalling the NuvaRing. It has caused epileptic episodes and even death. Horrible horrible thing if you ask me.
I will never take anything again that isn't natural.
I have been off the NuvaRing for one month now and I have been bleeding all month long and having problems sleeping! BE WARNED ABOUT THIS!!

Was on Lipitor 2 years ago and had to come off because of side effects - sever muscle pain.. Prescribed Niaspan instead .. 2 months ago my cholesterol rose to 7.1 and my doc put me straight back on Lipitor - 10mg.. Feeling lousy - neck pain, leg pain, dizziness, fatigue ... head feels fuzzy all the time and get sudden twinges in my chest.. Had stress test done last week and all ok.. Also have severe digestive problems. Going to wait until 2 full months done and going to get bloods done again

my mom has been on simvastatin
40 mg for 3 months & she has had
back pain leg pain & know kidney
failure she is a diabetic but never had any problems before but taking tthis medication it has ruined her life plus she gets lots of night mares & night sweats she
feels & looks like she is drunk
but she has never drank in her life

They think that I have either crohns or ulcerative colitis. I have tried antibiotics, lialda, mesalamine enemas, with no improvement. After another colonoscopy they put me on prednisone at 40mgs, 30, 20, 10, then 5 decreasing weekly. Well the first week was okay. I had some of the side affects, insomnia, extreme hunger, and crazy. I could deal with that. But then when I decreased down to 30mg, my body flipped. I awoke from the middle of the night with burning pain in the knees. So bad I took 4 ibuprofen and threw myself in the tub with epsom salt. I thought okay that was weird because I have never had a joint pain in my life. I saw the gastroenterologist that day bc I was still having abdominal pain. He totally blew off the knee pain and said he had no idea what that was. I thought okay maybe it will go away. A few days went by and nothing. 3 days later and I awoke one morning crying in pain because of my legs. I called the on call doctor who also said he had no idea and go to the er. So I went crying hysterically for 4 hours. Even after 3 rounds of dilaudid I was still in pain. They suggested a Rheumatologist. So I went to one a week later who said I was going through steroid withdrawals. And there is nothing we can do but treat the symptoms of pain. I am now down to 10mgs have been out of work for 2 weeks and am absolutely miserable with severe leg pain, muscle weakness and fatigue. He also adjusted the drop down increments to 5 instead of 10. Anyway I will never take this drug again and I think they rushed to this one. Just wanted to share. I am glad I found this website because I went from a fully functioning physically fit 28 year old to a crippled crying crazy person. I think I was scaring my husband, honestly, until we both read some of your postings which were similar.

Hello to All
I'm 33 yr old female who began taking Topamax 2 years ago, after diagnose with Pseudotumor Cerebri,(elevated intracranial pressure),doctors still don't know why i have PTC, it is common overweight women, certain medications, secondary to disease, which all did not connect with me as I was not overweight, have never taken any medication, other than OTC allergy or pain relievers, and all secondary diseases I was tested, and nothing, with a history of migraines headaches, that suddenly became unstable, with vision disturbance I was put on diamax, it lowers elevated intracranial pressure, finally help for this horrible headaches, , I had a side effect it elevated my glucose levels to dangerous levels, due to elevated intracranial pressure I was hospitalize, undergoing several lumbar punctures and eye surgery for decompression of my optic nerve, doctors still unsure of my diagnosis, but telling me I must have surgery for a spinal fluid shunt, I was terrified, I decided to try and consulted with another neuro ophthalmology who had a totally different opinion, I switch doctors and this is when I was prescribe TOPAMAX 25MG to start, now I'm taking 250mg daily, at first the fact that I was going to be OK, that I can continue my life without shunt, no more lumbar punctures, the fact I was not loosing my eye sight, I can go running, rock climbing, after been told I couldn't, I was convinced TOPAMAX was a miracle. The 1st side effects constipation; decreased sweating, drowsiness, dry mouth, loss of appetite I lost about 20 pounds, family friends were really concern, after a while I gain it back, numbness, tingling, I was ok with it, because I no longer had debilitating headaches, had perfect vision, surgery was out the question. and I was stable, but then I suddenly experience seizure, 3 different occasion, no explanation, severe joint leg pain, trouble with speech, bruising, light sensitivity, severe acne, irregular menstrual cycle, vaginal issues, anxiety, heart palpitations, and the worst one yet, the reason I began to search on line mood swings, I'm in the medical field and the people that I work with tells me I'm just getting older, depression, 1st sings of menopause, I'm very active healthy women, with normal daily stress 2 children and 16 years marriage, I have seen my family doctor, had blood work done, and all normal. I have told my neuro about my experiences, and he says is not topamax, my ob says take birth controls it might help, im just lost any one suggestions?

I'm so glad I found this! I thought I was going mad for a while there. Background: I'm a 34 yr old female. Diagnosed w/ asthma at 12, but they suspect I had it before that. Used only Ventolin for a long time. Five years ago, right around the time I had my second child, my symptoms (and allergies) seemed to get much worse. We moved around that time, to a house with a HUGE Chinese elm in the backyard (which I now know I'm allergic to) and right next to a main freeway. Around this time, Dr. prescribed Advair 250/50 when he realized I was using Ventolin up to 6 & 7 times/ day. The first year, I actually felt so much better (I could BREATHE!!) that I think I wouldn't have noticed any side affects. Year two I had MAJOR hair thinning. Dr said "age and hormones". Following 3 years on it: Almost constant nasal congestion (despite always being on a decongestant), sinus infection, tonsil infections, laryngitis, TWO bouts of pneumonia in 3 years. Around the year mark on it, I did experience the depression and anxiety, however, I had had the "baby blues" with my first child and just thought it was a more severe version of that. Now, I feel CONSTANTLY "run down" and almost always have some low-grade infection (yeast, UTI, sinus, bronchitis...etc.), am always hoarse and am just waiting for another round of pneumonia. I also get dizzy A LOT. I am in the second day of a cold turkey quit and am looking for alternative diet/exercise therapies. Good Luck to everyone!

My son is 8 years old he has been taking Advair for about 3 years and he has leg pain all the time some times he gets up at night wanting something for the pain its so bad we have been to doctors and all kinds of stuff now they are sending us to childrens hospital to see a doctor for joint pain.they sent us to childrens hospital before my son was rolling his eyes and blinking a lot for about 2 and half years the doctors said he has tourettes and he doesn't thats another story (stupid doctors some of them) we
thought he may have a nervous problem or something because his dad works out of state and he misses him and maybe its
anxiety or something.And at night he
would grind his teeth so bad I thought he was going to brake one of them. And when I don't give him the advair at all that day he sleeps so good no teeth grinding , no waking up with leg pain no moving all over. My son is all most 9 and everyone things he is 5 I really think this stuff has did a number on my child I am going today to the Doctors again and telling them I don't want him on ADVAIR no more! MY son and my family has suffered to much over this stuff!

have been taking 20mg for about two weeks. a couple days after i started taking the stuff i started experiencing chest pains at night that would wake me up, coupled with leg pain. it's getting worse; now, after two weeks i am having severe lower back pain that radiates down both legs, similar to sciatica, happens at night but continues throughout the day. also leg spasms at night. i am stopping zocor today. can't face this pain anymore. i have bad knees, and recently had to have a cortisone injection, but this new pain is worse than the knees. owing to the chest pains, i had a stress test today at the heart group, and had such difficulty walking that i could barely make it down the hall with my cane. three of the nurses there said they hear this all the time about the statins, and that the doctors don't want to listen to the complaints but the nurses all agreed that the statins are the culprits. results on stress test were fine.

OMG...I can't stand it anymore!! My legs are killing me!!...I am almost weaned off of it...tomorrow I take one 10 mg pill....and then the next day, I take 5 mg....and I'm done. Thank God!! I pray that I have no bad side effects from weaning off of it. I worry that I won't be able to breath again. Then what??...I will not take prednisone ever again!!...I think I would rather die then live on this horrible drug....If only I knew what it was before I started taking it.

closing throat, sweats, swollen glands, no menstrual period, leg pain, severe headaches, chest pain. I have been taking 100 mg for over a month. I have ulcerative colitis and I am using colocort enemas and canasa, but would like to know by when will I get the befits of imuran?

i just got off of the phon with my ob's office having spo9ken to her nurse about YAZ. i have been on it for a month and for the last week i have been having pain in my calf and behind my knee. i am worried about a DVT or something serious. i wonder if a doctor would do some tests to tell me if i have blood clots or not because i am worried. the pill has greatly reduced my horrible pms symptoms but i don't want to dye of a pulmonary embolism! they may take me off of the pill, don't other pills also have a risk of causing blood clots?

I'm 16 years old, and in November of 2008 i was diagnosed with nephrotic syndrome, or FSGS. i started taking the preds starting at 60mg, and last month i started weaning off. i'm at 20 mg right now. i noticed that i started getting the common moon face right after i started taking the meds. and i hate it so much. also, i've had so much trouble falling asleep at night, but then when i do, i sleep for so long. i've also had the dreadful hair growth, REALLY bad mood swings, headaches, and for sure, increase in appetite. i've gained 30lbs since ive been on the preds and even when i exercise daily, i still cant loose a single pound. normally im a really fit girl, i ran track and i was a dancer. im just really worried that all this "fat" wont go away. i really hope it does. it just feels like prednisone really ruined my sophomore year of high school. and i just don't feel like doing anything anymore. i just wanna wear swearpants, curl up in a ball and lay in my bed and wait until this nightmare is over. But im just glad to know that there are a lot of other people out there that know how i feel.

I am 49 yrs old. Had been on Neurontin from Aug '08-Jan '09. Was taking it for lower back pain & leg pain due to two bulging discs pressing on nerves running down my leg. When I began taking Neurontin, I couldn't walk because the pain was so bad. Long story short, Neurontin greatly helped my pain - it totally went away. HOWEVER, the entire time I was on Neurontin I felt drugged (dizzy, lethargic, depressed, paranoid). I determined it wasn't worth it (for me anyway) to live in this state of mind. So, slowly, I came off Neurontin and found out that my leg/back pain had eased. What I also learned is that I developed Carpal Tunnel Syndrome - Neurontin masked the pain from that as well, so I didn't even feel it coming on! I think it's dangerous to be on a drug that masks all pain. I now go to physical therapy and so far, experience only minor, tolerable pain (I'm lucky so far). But I know one thing, I will go for injections and even surgery before I ever consider this drug again. It was just awful living like that. I hope this posting has helped some of you.

March 3, 2009

I had went to the dr. a few weeks back for sinus problems. My dr. gave me amoxicillin to take. After 1 week, My sinus infection was
not any better at all so he gave me 400mg of avelox to take once a day for 10 days. I immediately experienced dizziness and extreme bouts of tiredness. Since that was the primary warning
on the label I did not pay it any attention and continued to take the meds. After 6 days of taking the meds I have decided to
discontinue using the meds. I have experienced some severe side effects which are dizziness,fatigue, increased headaches,
upset stomach, extremely loose stool, stomach cramps, blurred vision and severe and almost debilitating ankle pain, leg pain, knee
pain, wrist pain, elbow pain, shoulder pain, lower back pain and neck pain.
I have also had a rapid heart rate so bad at times it feels like my heart is
going to beat right out of my chest. I feel anxious and very short
tempered as well. I am snappy with my loved ones for no reason at
all and what is worst is I still have severe sinus pressure and
pain as if the infection hasn't even went away. The only plus is that I can
breathe clearly through my nose for the first time in 3 and a half
weeks. I guess that's not really much of a trade off now is it.

I have been on gabapentin for several months now its suppose to help with my leg pain but only make me tired,i have gained 30 pnds and now trying to loose it but no luck, also the worst is i have dreams that someone is trying to pull me down i can feel there hands on me like its so real that i make myself wake up then cant go back to sleep because im afraid i know this sounds crazy but i feel like its the devil trying to take me to hell i get so scared i make noises in my sleep till i awake im not sure what to do,

been on lisinopril for about 4 years i have had the cough but though is was due to asthma that i have in the last 6 months i have knee and hip feet ankle leg pain i can barely walk can't hardly get off the couch or even out of bed will i am going to see the doctor will try some thing else does anyone have any suggestion b/p around 140-75 some times a little lower

I read with interest several of the posts here. I have been on Lipitor for about 5 years. I have been experiencing leg pain, back pain, neck, and hand pain for likely 4 of the last 5 years. I have arthritis, I thought. Two weeks ago I ran out of Lipitor. I read several other forums where Vitamin C and Omega 3 were suggested as a possibles to replacing the Lipitor along with generous amounts of water. I said, What the hell, I will give that a try. Within days of stopping the Lipitor, most all the pain has subsided to the extent that I have not had to take any other Pain management medications at all. I was prescribed Perocet for the pain I have been experiencing. Two weeks ago, I had a tough time opening a bottle of soda, or even a relish or pickle jar. Today I can! Coincidence, I think not!!

Well ladies let me tell you what... I must be super sensitive to this crap!! I started the ring because I had used it years ago and LOVED it!! I mean LOVED it! It WAS the only bc that didn't give me any issues... they really must have changed it... I'm gonna list my new symptoms and reasons for taking this crazy thing out...

Nausea,
Headaches,
Visual Migraines... spots in eyes
Dry Mouth
Breast Pain
ALL of my hair is FALLING OUT
in 3 days gained 10lbs!!
Mood swings
Think i'm pregnant every day!
Still get cysts (which was my need for the ring)
Horrible constipation/diarrhea... IBS like
Lack of energy
Itchy scalp
Leg pain
Hip pain
All the symptoms of thyroid issues!!
Circulation issues
Took Sudaphed and almost had a stroke!! BP was 180/110 WOW!!
normally is 117/67

My advise... GET OFF THE NEW RING... The old one was great...this new one is DANGEROUS!! I have worked with doctors for years... they prescribe things that the cute sales reps bring...

Contact me if you have felt the same... It's good to know there is someone out there that has been thought it too!!