Arches symptoms and conditions

What a rotten drug. The past seven months have been hell for me. I am 42 years of age and put on this crap last November. I have suffered from bad headaches, leg cramps, Insomnia, Plantar Fasciitis, mood swings and the list goes on. After seeing this site and all your responses I believe the best thing to do is get of the crap. I will write in 2 weeks to give an update.
cheers from Down Under

I had my kenalog injection over a week ago. The winds here in the desert have been horrible this year and i was experiencing a daily sinus headache and my allergies were beyond what a claritin, allegra and a sudafed combined could combat. Within a day of getting an injection in right butt cheek area all of my sinus problems have ceased. Day three i stopped taking all of my medications for my allergies. I was also able to stop taking an anti inflammatory for my knee and the arches of my feet. They have never felt so good. My excema and asthma symptoms although mild have also cleared up. On the down side. I seem to be eating like a horse, insomnia and wild dreams seem to be plaguing me. But this is also the case when i take prednisone. I had this shot a few years back for the knee and foot arch pain and back then before my hysterectomy i did experience break through bleeding on my birth control pills a week early and very heavy. i decided that was the worse of my side effects back then. now that i wasn't able to have that problem i figured lets go for it again since i recall my sinuses clearing last time too, which was a bonus side effect for me then. overall i have found the positive effects definitely outweigh the negative effects for me.

I have been on Diovan HCT 160 for several years. The other day I woke up with joint pain in my hands. The next day it was in both ankles and arches of my feet, also both elbows and my right knee felt swollen and painful. I am a physical therapist and am
In tune with my body. I know this is atypical joint pain and not from physical activity. I was afraid of rheumatoid arthritis so I am shocked and a bit relieved to read others with same effects. I am going to my MD for full blood work and a new BP med for sure. I will post any new info if it might help others.......

I have posted before with all the pains I am experiencing but just began with a new one! I am now getting charlie horses in the arches of both my feet. When will this runaway train ride end? How much can a person take and be told the FDA does not recognize that something criminal is being done to the public!

I am 43 (female) and have been on Singulair for a couple of months now and the benefits have been AMAZING! I have chronic generalized eczema and pronounced facial flushing which led to swelling and Rosacea. Since starting Singulair (with a Zantac and Reactine) my skin is almost always cool (it's been YEARS). The benefits for me have been as great as what the steroids do for my skin. I can tolerate more triggers and the freedom and self-esteem boost is unquestionably life changing.

But recently I started to bruise, over every-little-thing -- even a blood pressure cup created a ring of broken blood vessels. Then about 3 - 4 weeks ago I started getting deep lower leg pain, and cramping in my calves and arches. This grew more regular, and my hips joined in and I am now rarely without the pain and deep aches. Then the weakness started, it was most pronounced in my dominant hand, I can hardly write or hold a pen now. Typing is difficult now as my hands and forearms are so weak. Yesterday I couldn't pinch my fingers to pick up a potatoe chip! My arches are curled with aches, I am weak all over and getting really uncoordinated. Going up the stairs is a chore, going down is just wacky -- it's harder than going up I am so wobbly and my knees want to give out. It's getting so pronounced that I realized that this must due to something I'm taking and the only thing I'm taking new is Singulair so I decided to Google "Singulair Side Effects" and the first link I clicked was Carrie's post, which I replied too. Then I realized there was more and have been reading all the other posts.

I am grateful that it is just side effects and nothing more sinister. This weekend the accumulated symptoms had me a bit frightened. I was washing my hands and it felt like I sprained my fingers doing it. The ligaments just sort of let go and things began bending the wrong way. It happened when I bent over to put something in the dishwasher, it was like the rib cage lost it's shape for a moment (I don't know how else to describe it). THAT felt bizarre and got my attention. Not being able to pinch my fingers to pick up a chip was the final clue that something is going wrong here. I will stop taking the Singulair now. It's a shame this happened, it was really doing it's job for me. The price of the side effects is too high though.

I am 40-years-old and took Singulair for about two months. I first took it for about two weeks and got horrible symptoms and then stopped for a week and then tried it again for about a month. Never again will I put Singulair into my body. My symptoms were chronic and severe muscle cramps and twitching, restless legs, body aches, numbness, tingling, hair loss, weight gain, and skin changes (urticaria and angioedema). I also used to suffer from menorrhagia to where now I barely get a cycle. I cannot blame Singulair for the headaches/migraines because I have been a headache/migraine suffering for many years.

When I first stopped taking Singulair the symptoms calm down. But since then they have come back with a vengence. I have been to several specialty doctors (family doctor first, endocrinologist, neurologist, allergist and rheumatologist). Now please let me defend myself by saying I see my family doctor and gynecologist yearly for a physical and also when I am sick and I have always been basically a very healthy, and slender woman with thick hair. I was on no other medications other than ibuprofen and acetaminophen for the headaches/migraines. What they have found so far is that I have secondary autoimmune hypothyroidism (only my TPO antibody and thryoglobulin are extremely elevated, but my TSH, T3 and T4 are completely normal), and allergies to everything outside (no food or pet allergies) and idiopathic lupus (because my skin has developed urticaria and angioedema).

I am going for an EMG and MRI of the brain in one week because they are trying to rule out MS. They have been saying that my symptoms look like MS or lupus. They have ruled out lupus because my blood tests do not show lupus only my skin is acting like lupus. My allergist put me on doxepin for my skin and twitching symptoms. This medication has helped my skin and slowed down the twitching.

I am not trying to blame Singulair, but it is very strange that I was a basically healthy person with some outdoor allergies and mild asthma. I would get pneumonia once a year also (always around the holidays). Now, I feel like crap since taking Singulair. My legs are the worst of all the symptoms along with the constant twitch under my right eye. This can drive a person insane, especially when you are trying to relax and your body cannot.

Thanks for listening,
Carrie

It seemed to begin with a 2 day headache. As I had a severe UTI, I was not sure if the symptoms I was having were because of the Levaquin or the infection. The headache was the first "unusual" symptom I had within 1 hour of taking the Levaquin. Then the muscle aches, tendon pain, arches of feet hurt, arthritis in hands became more painful than I had ever experienced, very fatiqued, skin sensitive to touch, tingling sensation on arms, racing heartbeat (may have been due to anxiety of other symptoms). These symptoms continued for 6 days until 24 hours after stopping medication. I discontinued it after researching side effects on internet as Patient Information sheet that came with medication was vague. I still have tendon pain in left elbow, and arches of feet. Amazingly, I have had knee surgery and back surgery, but neither of these areas seemed to have been affected. Still don't feel "right", but hopeful will continue to improve.

I started taking Lipitor Sept, 2006. Soon after I thought I had the flu and was really sick for about 3 weeks. I assumed the muscle pain was due to the flu. I've felt really tired, aches all over, muscle pain, horrible lower back pain (I also have 2 bulging discs but the pain is worse than it's ever been) and I can't sleep a whole night through. I wake up in the middle of the night due to pain in my hands (the joints in my fingers almost feel like there's fluid around them and it's hard to move them), or back and leg pains. For the last month the pain in the arches of my feet and heels have been getting worse, to the point that I can't walk without pain. I have to have good suppory tennis shoes on at all times to be able to walk. The aches and pains started slowly and kept adding up so I just didn't pin point any one thing as the source of my problems. When my husband watched me hobble into the kitchen tonight he told me that everything started after my physical in Sept. The only medication that was added to my daily meds was Lipitor. (the only other med I take is 1/2 of a .25 HCTZ for slight elevated bp) I am schedule an appt with my doctor ASAP but I think I will stop taking Lipitor as of tomorrow. If the pain is reduced then I will be able to report that I believe Lipitor to be the culprit.

Within 2 days of beginning Lisinopril for an "elevated blood pressure event", I bagan to experience labored breathing, like I had just walked up 10 flights of stairs. And that was at rest! I had some anxiety and was generally lethargic. I also began experiencing severe cramps in my legs, feet, and toes. My arches would cramp so bad I coulld hardly stand it. I thought this might be related to the diuretic in the medication. I also experienced muscle weakness. I called my doctor who told me to take half a pill each day. The effects were basically the same at half the dosage! The breathing still labored, less cramping, but same feeling of tiredness and lethargy. I quit taking it, made some lifestyle changes (less sodium laced foods, more exercise) to bring down the pressure.

In June I was prescribed Levaquin for a urinary tract infection. Didn't have any problems at that time, but two weeks later my UTI was back, so they prescribed me Levaquin again. The day after I started taking it, I was experiencing sharp pains in the palms of my hands and the arches and heels of my feet. Since I've been on Levaquin many times before, it didn't even occur to me. By the third day my feet hurt so bad it was painful to walk, and I started breaking out in hives ALL over my body, and I experience some nausea. I obviously had developed an allergic reaction to Levaquin. I was able to look online at my pharmacy's website and track all the times I've been on levaquin. Six times in eight months for ear infections, UTIs and sinus infections. Wow-do you think maybe the doctors rely a little too much on this drug? I'm thinking my body had had so much of it that it finally rejected it. And now I just want to crawl out of my skin-four days of prednizone plus a shot and the hives will NOT go away. It's been a week since I've been off the Levaquin. How long does it take to get it out of my system already????

took my first dose and last dose of levaquin yesterday up all night sweating and cramps in the arches of my feet today i have sore knees and hips when i walk my skin fills itchy and the chest heat is really bad. was in the hospital 2 months ago for chest infection and was on levaquin then had some of the same side affects but had no clue that was the problem but after one day of levaquin again it all started again and there will be no more of that drug for me

I have been taking 20mg of Lipitor for several years and could only get my cholesterol down to about 230. Now I have a new doctor and she has doubled the dose of Lipitor. I have several of the symptoms that are mentioned in the other postings. My hands and feet are affected more than anything. I have some ringing in my ears. I have also had two readings of increased pressure in my eyes. I tried going off of the drug for about 6 weeks and nothing much changed. I am about ready to go off of the drug for at least 3 months to see if anything changes. I hope this muscle damage I have been reading about is not permanent. One other symptom I have is an increased popping in my thumb joints along with increasing pain in the arches of my feet and palms of my hands. They seem to coincide. Please e-mail me if you are having any of the same symptoms! I am going to quit taking the drug as of today and see if I can re-gain my old self!