Legs feet symptoms and conditions

I posted several months ago on this string and wanted to update. I had bloodwork done for the 1st time since I quit the 20mg of Lipitor in August. LDL went from 123 to 210. Total Chol went from 191 to 285. HOWEVER all shooting pains I had been experiencing in legs, feet, and chst are GONE! Went back to my Dr. today, told her that same result and my serious objection to taking any kind of statin and she prescribed CRESTOR while telling me it was more potent than Lipitor! WTF!!!

I refuse this course, am drinking 30 - 40 ozs. of water each day now like I should have been, doubled my CoQ10 to 200mg/day, finally getting back into the gym to lose weight and get the HDL up from the level of 36 it is now. also started to drink the new yogurt type "shot" of Promise for cholesterol that provides 2 grams of plant sterols per day.

I will not take statins ever. I WILL find a natural way to keep my Chol under control. I've also been convinced that you don't have to be at or under the 200mlg of total chol to be healthy. Look at your C Reactive Protein and Homosiytes (sp?) If they are in range you should be good.

I know Lipitor was the cause of my rupturing each of my Achiller tendons a year apart while playing tennis in my late 40's Muscle pain soon followed.

In people close to me I have seen the following side effects:

All statins have similar side effects. They can come at once or after many years.

Pain in neck, shoulders, elbows, hands, hips, legs, feet

Pains that keep moving to different parts of the body and could be unbearable -like nerve pains.

Head ache

Burning, tingling sensations in the different body parts mentiond above and numbness

Weakness in hands which caused the person to drop things

Hair loss, difficulties to swallow, ringing noise in the ears, loss of taste, memory problems - particularly with short term memory, difficulties to find words and to remember what just had been read, impotens, extreme sensitivity in the skin (abdomen).

Please "educate" yourself.

Read books and look for information in many different places. Remember to find out who is behind a certain webb-adress. Could it be a pharmaceutical company.

Unfortunately I am not allowed to write webb-adresses here - but Google the titles of the books/writers below and you will find some webb-adresses.

The Great Cholesterol Con (Anthony Colpo)

--------------------"--------------- (Malcolm McKendrick) - this is another book

The Cholesterol Myths (Uffe Ravnskov)

Malignant Medical Myths (Joel F. Kauffman)

Overdosed America (John Abramson)

Lipitor - thief of memory (Duane Graveline)
Duane G. has an interesting site

The Truth About The Drug Companies (Marcia Angell)

Google "Stopped our statins" and you will find this webb-site.

Under print articles to the left you will find an interesting article from Weston Price Foundation.

It takes time to look for information and then read it, but often it`s quite essential to do that and to make up your own mind.

It`s your body and you know best how you feel.

Remember it`s a lot of money involved and that`s why news about serious side effects quite often are delayed.

The cholesterol issue - that high cholesterol should cause heart attacks etc - is very controversial. But it`s only the pharmaceutical companies who have the money to "brainwash" by advertisements, ghostwriters etc.

I hope my suggestions can make you more interested in the medications that you are taking.

Finally - a very interesting book about a certain kind of antibiotics - Bitter Pills by Stephen Fried.

English is not my native language but I was forced to read a lot of English books because of the suffering of my relatives, but without the Internet I would not have found them.

Remember new drugs are not necessarily better than old, but always more unsafe. They are also more expensive and that`s why they are so highly promoted.

I was prescribed Bactrim for a staph infection that turned out to be MRSA. I took the pills (2 pill 2x a day for 10 days). It did clear up the infection; but the side effects sent me back to the doctor. After the second dose, I started having a headache and feeling feverish. After the third dose, my muscles started aching and I began having little muscle spasms and numbness in my right arm and a low grade fever, headache and fatigue. The morning after the 5th dose, I woke up with severe muscles cramps in my legs and feet. I took the 6th dose and what a mistake. The muscle cramps and spasms moved to my inner thigh, legs, feet, abdomen and back. I had to use heat packs to quiet the muscles. I stopped taking the meds and notified the doctor. He changed my prescription to doxy and said that I was allergic to sulfer meds. He also gave me flexorial to help with the muscle spasms. It been 3 days since I stopped taking the meds. I still feel severe fatigue, muscle aches, fever, sweating, and anxiety. I will never take this stuff or anything like it again. I have noted it in my pharmacy charts so they will no ahead in case I don't catch it.

Despite having a brush with the big C last year (I finished chemotherapy in January) I have been very fit and healthy during my 61 years! A few weeks ago I started having palpitations, hence a visit to the doctor revealed high blood pressure and cholesterol reading of 9.9!!! Shock, horror. He informed me that it was genetic and prescribed Simvastatin 400mg and Bendroflumethiazide 2.5 mg daily.
Not being satisfied with the enclosed leaflets I have looked up more info. on the net. Should I have done this!!! After reading some of the posting on the site I am feeling a bit apprehensive. Last night I had a terrible night couldn't sleep for the pains in my legs and a bit nausea this morning.
But I need to be sensible, I really don't have any choice but to take these drugs just hoping that I won't have to stay on them for the rest of my life and I don't get any of the side effects that some of you have suffered. I also wonder if the chemotherapy could have caused by raised cholesterol?
Hope to keep you posted and would welcome any comments!

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 taking YAZ for 2 months and just picked my new pack up to start tomorrow but they are going in the trash! I started doing research tonight on YAZ for the first time searching for answers of what could be wrong with me! I have had an MRI checking for MS, blood work checking for Lyme Disease, along with many other tests to try to determine why I am experiencing NUMBNESS is my hands, arms, legs, feet and face, and mostly on the left side. After all the tests have come back negative, I have been left with confusion and sadness wondering what could be wrong. Then I looked at YAZ side effects tonight, and what a realization! I am so sorry for all the women like me that have been going through this. This drug is terrible and should not be on the market. I was just married on July 12th and the happiest time of my life has been covered with the dark cloud called YAZ. No wonder I have felt so sad and so crazy. I started taking YAZ because I wanted to be better for my husband and not make him have to put up with my PMDD. However, I have become someone other than myself, someone who is angry and sad for no reason. Thank goodness I have realized what has been wrong. Now I can get to the marriage I have waited for all my life! Please, if you are taking YAZ, stop, and if you are thinking of starting it, DON"T!

I have been using Advair (250) for many years with no problems. We are remodeling out kitchen which has stirred up a lot of fine dust in the house. That coupled with the smoke caused by the recent forest fires in California I had a severe asthma attack. My doctor increased my Advair to 500. Within a week my voice left me. I have laryngitis of sorts and an accompanying cough that I can not shake. It has been nearly three weeks since it started and two weeks since I quite taking any Advair at all. How long does it take to recover from these symptoms after coming off Advair? I need my voice to function at work.
Secondarily, after reading about cramping being a part of people's symptoms, I have had cramps in my legs feet and toes for several years-mainly at night. Hopefully being off Advair will resolve that as well.

I was put on Prednisone for my COPD. Right after starting a 30 day script (I don't remember the dosage) I started experiencing SEVERE muscle cramps. Legs, feet, hands, abdomen, ribs, back. It was the most terrible experience I have ever had and I refuse to take it again. I also gained 30 lbs in 30 days. Which I have had extreme difficulty taking back off. I am now, two years later, experiencing great difficulty with my knees. I believe that I will always suffer the side effects of this, yet another, wonder drug. The wonder is how many people's lives is it ruining...

Well Hello everyone. I am glad I came across this site, because I thought I was going crazy...I am 35 and just had my first child March 2007. I have had the Mirena for a year now. I went to the Dr. a few weeks ago and told her I was feeling sharp pains once and a while, but other than that I felt fine. She ordered an ultra sound and they found some small cysts...so I go back for a recheck 6 weeks from that date to see if it's gone away?? That did not make sense to me....she said I also had a yeast infection (which I have never had), and pre-cancerous cells which she is biopsying next week. What I thought was completely unrelated was my back pain-sharp siatica pains and my numbness in legs, feet, arms, and hands...my friend told me I should see a neurologist...and I almost started down that road....until now...I think I will have the Mirena out first and see what happens. I also have some twitching in my fingers. I will let you know how I feel after it's out. Oh and Mood Swings....I always have this feeling that I don't know what to do....everything seems like too much!

my husband had never been one to go to G.P.s or have reason to take prescription medication( not even an aspirin ) . Finally had a medical test- Cholesterol was high- was not given a chance to change his eating habits- and was placed on LIPITOR ( this was 18 months ago ) and since- everything has gone downhill from there. He has suffered nausea, blacked out, had headaches/tingling sensation,chest pains, aching/fatigue to legs/feet and arms. - shoulder pain- has problems getting up from bed or from sitting position- has generally lost power in his arms and legs. His doctor was advised over the past several months of his pains- but had no idea what caused them and changed the script to Crestor. ( still a Statin drug ). Have ( on good avice from chemist assistant ) now got him on daily dose of Q10- and he ( 2 weeks ago ) decided to stop taking the Lipitor or any other cholesterol lowering statin drug- of his own choosing. He has had several visits to podiatrist to help alleviate the pain to his feet - which are sore and swollen. His liver levels were also high at on stage. All this has happened to him sine he started the Lipitor statin. Prior to this- He has never had previous medical conditions or medication. Seems to point the finger at one reason- LIPITOR !!!!!- THEY CANT BLAME IT ON ANYTHING ELSE. Just want him to get back some energy. He is 56. One more story to add to the thousands of complaints, Why isn't anyone in the medical field / lawyers commenced a full investigation to all these complaints? thousands of people cant be wrong. Bring on Erin B.

-shooting pain in legs, feet, and toes before i go to sleep causing me to not be able to go to sleep
-shooting pain in lower back, stomach, breasts
-stomach swelling... feel bloated
let me know if any of you get these symptoms if you are on lantus.

I started taking Lisinopril about 10 months ago and now I have had severe redness and heat in my face, neck, and chest. I have constant headaches and my eyes are bloodshot most the time now. I have quick sharp pains throughout my chest arms and legs/feet a lot. I get blurry vision and disorientation every time after taking this stuff.. My heart rate varies from high to low but it feels like my blood is extremely thick no matter if I eat or not, I also get extreme nausea after eating even a salad with no dressing. I hate this stuff so much and it scares me to no end. I have major anxiety disorders anyway but this crap makes it worse. I think I am dying everyday its so nerve wrecking and I am only 25yrs old!!!! I recently stopped taking this junk for about a week but still took my Xanax for my anxiety and my face and neck aren't hot at all most the time anymore only when I move around and work a lot but not bad at all. My heart rate is normal and my blood pressure is staying about the same but maybe bout 8 or 9 notches lower than when i was on this stuff. I think someone is really going to get hurt on this stuff and we are all going to see a commercial on TV saying to call a lawyer for cash rewards because of med induced illness or even deaths... I'm going to the doctor and telling them to give me the most expensive effective and less side effect BP med..

How long will my pain last knees, legs, feet arms all my joints,,,, I feel like I am 100 years old! How long will it take to get better, my doctor took blood Friday to see what was going on but I haven't heard anything yet

I am glad to see I am not crazy!! I started on advair a week and a 1/2 ago. My blood pressure went up and after 6 days of taking advair my bp was 140/99. Heart rate increased from 60's-low 70's up to mid 80's. I have always had really good bp before this and a good heart rate. I also had weird sensation in my arms and legs and a tightness in my chest that would come and go. I had a headache pretty much the whole time I was taking advair. I had horrible cramps in my feet and legs. I also had something strange happen to my face. I got a strange pain in my cheek that went up to my eye feeling like there was severe pressure behind it and then after making my eye water it went back down to my cheek for a minute and then disappeared. I was starting to get really creeped out by all these things happening so I bought a bp machine and monitored my bp. 48 hours after stopping advair my bp was excellent (106/66), heart rate back to the 60's, no more weird sensations, headache is gone, no cramps in my legs/feet, and my crappy mood has improved. All these strange symptoms are gone! I will never take that crap again!! It may work for some but it didn't work for me.

Question: I took celexa 3 times (10 mg) every other day the middle of August. The first night I noticed my legs and feet tingling really bad. Now my legs & feet still tingle and my muscle flutter often. Could this be from taking celexa & birth ctrl pills at the same time? I have had several blood test and all were normal.

Lipitor reduced my Cholesterol from 280 to 140. But... after only 4 months on the drug I developed pain in my legs. After several visits to the doctor I was told to get off the drug. One month later my health had deteriorated to the point that I could hardly walk. After another doctors visit and many tests I was diagnosed with peripheral neuropathy with the symptoms of leg pain, muscle loss and nerve damage in both legs, feet and hands. Also numbness in both hands and feet. Inability to move any of my toes. Liver damage. Of course with the problems with my feet I have poor balance. Additionally I have memory loss. Because of the neuropathy I can not get health insurance without paying a much higher preminum than normal. I am taking Gabapentin 1200 ml 3x day.

My condition has improved gradually but I still have the P. Neuropathy and there is no cure for it. My balance remains poor and the numbness, pain, nerve and muscle damage remain.

This diagnois is from a family doctor as well as a neourologist.

My recommendation is stay away from the statins.

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.

headaches, frequesnt upper resoiratory infections, aggravate allergies, delayed ejaculations with less power, legs feeling tight and jumpy, hit or kick while dreaming. greater than normal libido, especially for minority women.

In late March I went to my Doctor for allergy Meds. He prescribed Singlair. Within two weeks I began feeling as though I had an upper Resp infection (I did have one). My Doctor put me on Levaquin an antibiotic. Then I began feeling as though something was crawling all over my face,& my face began to burn. I went to the ER one week later & was informed that I had Pneumonia. Along with the antibiotics I was still taking Singulair & albuterol inhaler & Allegra D & Histanex cough medicine. I have had Pneumonia 2x before but this time was 2x as bad. It lingered on for over a month. Then I started to smell really bad odors kinda of like a sweaty locker room. I called my Dr's office his nurse thought it was weird & never heard of it before. Then I lost my sense of taste & smell. Finally I went to my Dr on 5/17/07 he informed me that if my sense's doesn't return in 3 weeks to notify him & he would order a CT scan. The scan was ordered & was negative. I still have no sense of smell or taste. Dr's nurse thinks it is psychological. I went to ENT Dr was given a steroid which didn't work. My Dr also asked me to try nasonex nasal spray but that doesn't work for me. Now it is August 1st & my senses have yet to re-surface. Although I can taste sweet, bitter & sour but couldn't tell you what it is I am eating. I also suffered pains in my legs & feet, was really exhausted & had bad dreams.
Please reply if anyone else is or has suffered the way I have & continue to suffer.

wow!
it sounds like everybody hates topamax from all the posts that i read... although i didnt read them all...

anyway, at first i had the memory loss thing but it seems to be ok now. i think i always had memory problems though, but it did get worse for the first couple months on topamax and then a little worse when my doc upped my dose. although now i think that my body may have gotten used to it, bc i feel a bit back to normal with my memory.

i also have the leg tingling. mainly i notice something like a slight throbbing if i put my foot down too suddenly, but it doesnt actually hurt. i notice the actual tingling in my legs/feet when i drink though, but only when i drink.

what else? oh, the hair loss. ALTHOUGH, this could also be from my dying my hair a lot... bc i have always had a hair loss problem, but i think the topamax accelerated it.

however, these side effects arent enough for me to get off the drug until my doc thinks so. i had migraines every week or more. horrible ones where i had to stop what i was doing and lie down. i missed a lot of school , missed a lot of work... sometimes they would last for more than a day. i needed help. now i only get migraines during that time of the month, and several docs have said its bc of the lack of estrogen... even when i get those migraines i only get the symptoms , not the pain. i dont even have to take anything. i have my life back... haha, i sound like a lifetime story or a commercial. anyway, i <3 my topamax and im just going to start taking a biotin supplement to prevent hair loss until i can get off this drug when it is time.

Have been on Lipitor for 3 months and before that, zocor. I have been having such bad muscle cramps in my legs, feet, abdomen and back. I have numbing in my face as well. When I went off zocor, I felt better then doc put me on Lipitor. It took longer for the symptoms but they are back. I take CoQ10 and do all I can. I can't stand it anymore. Doc says the cramping is NOT from Lipitor.

I am an active 63 year old male. I have been on 10mg lipitor for 5 years and have experienced a very gradual muscle degeneration in my legs, feet numbness & tingling and hair loss from my ankles up. I have been to a neurologist, two Chiropactors, and Physical therapy and got some relief, but these symptoms never really disappeared. Recently, my bad cholestrol level increased and my doctor doubled my level to 20mg. After a month, my symptons are now worse and I can hardly get out of bed in the morning with sore muscles in my legs. I have had full skeleton x-rays and MRI's and Bone Bi-op. and have been cleared from other problems such as cancer. I have a strong feeling that my problems are from Lipitor. My doctor is in love with the drug. I am going to stop the Lipitor for a month regardless and see what happens. Joe

I have been on 100 mg of topamax twice a day now for over three years. Most of the early side effects have worn off like soda tasting bad and the memory loss. I never had any hair loss. Also the weight loss has stopped and I did gain it back which really stinks. Anyway, the reason I was looking, was that in the last several weeks, I have been suffering horrible body aches and joint pain. My hands and knees hurt very badly. I am 39 years old and hate to think that arthritis has set in so quickly. And I know that I can't have the flu with no other symptoms and so often. Does anyone else have these symptoms? Also I wonder why these could have started after so many years of taking it.I have tried to wean myself off in the past and the migrains came back full force.

Wow. To all the valid contributors and site owners, top posts and site!

I have SLE and have been found to have Lupus Nephritis (kidney). I was on 60mg, now down to 40mg of Prednisone.

After Pericarditis, I presented with terrible SLE headaches. I'm now also on Cyclophosphamide (Chemo treatment) for my Kidney and other meds for that, as well as the Prednisone, but my side effect I am having which I think is from the Prednisone is SWELLING in the face some, but especially from knees downwards getting worse throughout the day.

After reading a bunch of pages here, I suspect that it could also be not just the Prednisone but because my Kidney functioning poorly. I can't get rid of the water fast enough. I do not have anything diuretic normally because I am also diagnosed with Raynauds Phenomenon.

To balance things out, I've tried to drink the minimum side (2L for 2 days after Cyclophosphamide treatment) and funnily enough, if I have drank too much water in the day time I:
*Sleep with a big pillow under my knees/feet
*Do not drink any at night (if thirst, just have a half mouthful)
*Wee it all out throughout the night

It HAS worked and my weight, the swelling in my legs/feet has come down dramatically... It has also helped my FACE be less swollen and puffy...!

Other symptoms I had when I had prednisone only: EMOTIONAL! Twice I could not stop crying when there was completely nothing wrong with me at all (i.e. bawling my eyes out). At the time I was on 20mg when my SLE was quite much lower in activity level. I was totally "off my head".

Now I'm on 40mg, and I do get emotional more easily - but I brought the husband to my specialist once so he could get side effects explained to him directly. I also get hot flush tingles in my fingers and toes from prednisone.

For all those people worried about WEIGHT - I highly recommend one of those scales (I know I can get one for $40AUD) which can tell you your WATER level as well as weight (you have to input your height). If you are running at 70% instead of 60% water, then you know your weight is 10% overstated, but just due to the water.

meow

I have been taking Levaquin for 12 days...following major stomach surgery--to avoid infection from staple removal. I have the most terrible aches/pains in my arms, legs, feet and neck.....it is almost impossible to move. I was progressing very well from the surgery until this medication was prescribed......now what and how long will this reaction last??