Legs feet symptoms and conditions

I am taking omeprezole & blood pressure medication & am having muscle cramps in my legs & feet mostly, but even in my chest (Thought I was having a heart attack).I am experiencing severe fatigue & like one of the previous posts, I'm having difficulty even holding the steering wheel of my truck.It's difficult for me to stay awake ,especially if I relax for more than 5 minutes.I assumed it was the blood pressure meds, & stopped taking them recently to see if that would help.(It didn't) I'm going to stop all synthetic meds ASAP & hope for recovery.I've been taking these for 3 years & am experiencing many of the same symptoms as other posts,including swollen breasts (I'm a male)...THANK GOD FOR THIS SITE!!! I'll keep you posted on my progress. Best to all fellow sufferers.P.S: My doctor thinks I have more symptoms than "a 90 year old lady" (I'm 54)God Bless, & I'm praying for you all.

I am a 70 year old woman, I have been on 20mg Lipitor for high cholesterol, 200 total and 25mg of Spironolactone for a not so high blood pressure, for 3 1/2 yrs. Oh, my God, the Spironolactone is a potassium sparing diuretic that is very dangerous and has many uses I didn't know about or the terrible side effects, it causes breast cancer. It's also used to treat women who have an over growth of hairiness, or on a higher dose to treat hair loss and I've gone bald on the top of my head! Plus all of the good foods we're supposed to eat for high cholesterol, fruit & veggies one isn't to eat on this drug, because of lot's of potassium, what a huge contradiction. And muscle pains, and rashes, (eczema, atopic dermatitis) that I've suffered from both.
Anyway, Lipitor, had know idea about the side effects until I looked it up on the internet and read these posts on here.
I stopped taking Lipitor last week and Spironolactone 2 days ago.
I had cholesterol test last week too and saw my dr. Wednesday. He said it was okay that I stopped the Lipitor, but not the other one, why not the other one worse then Lipitor and why am I on this strong drug, geez.
The pain and burning started in my hip for no reason, then my ankles with eczema which started soon after Lipitor, then my fingers, numbness, can't pick things up, tingling, burning. Then my feet, yes, just like all of you I have these same problems. This is not just coincidental, this is from the drug Lipitor. I get severe joint cramps in my legs, feet and fingers.
For now on before I take any drug I've prescribed I will thoroughly check for side effects and not take it if they're seriously impairing like Lipitor. I feel like a cripple and older then I should feel, I almost just felt like why live anymore if this is how it's going to be.
Since I've stopped Lipitor I feel a little better, I read that it causes permanent muscle and nerve damage though, oh I hope not, I can barely walk anymore or get up out of my chair. This is all drug induced toxicity of my system. Thanks so much everyone who posted for sharing and enlightening all of us who are suffering from this drug and others.
It should be banned along with Baycol, (a statin) which was banned a few months ago because of these same side effects. With the studies that it only helps maybe to prevent heart attack, well I'd rather be able to walk again and hopefully all this will go away, the rash, etc.

wow- glad I found you guys! I'm female, 54, thin, healthy, have always exercised and watched my diet. cholesterol went up to 280 a couple of yrs ago- tried more diet/exercise but it only came down to 250, so since then have tried 4 low-dose (40 mg) statins (crestor, lipitor, zocor, and now pravastatin), all of which after 2-6 months made me feel like I was jumping out of my skin and caused chest pain and palpitations that stopped almost immediately when I discontinued them. Also, I've always fallen asleep quickly and now take an hour or more, and recently my fingers have started falling asleep/tingling. I'm stopping the pravastatin today! Maybe 250 isn't so bad, if this is the alternative. Does anyone have any remedies to suggest besides low fat/low sugar diet? I just read that we should avoid reduced-fat milks (I drink 1%) because they contain oxydized cholesterol, which irritates the artery wall.

My name is Katie, I am 31 years old. I have been suffering with what doctors call Chronic Idiopathic urticaria for 16 years now. I was prescribed Zyrtec 14 years ago and remained hive free until I had my first son. After a complicated pregnancy and emergency delivery the hives returned full force. The doctor prescribed Singulair in addition to the Zyrtec.

The hives went away; however, I have so many other problems now. I have been seeing a specialist thinking I have lupus or some other disorder, but all my tests are normal. It wasn't until I had my singulair refilled yesterday that I realized instead of symptoms, what I am experiencing may be side effects.

-- I have gained 60 lbs.
-- I have horrible headaches almost daily
-- I am so tired that when I am not working it is impossible to even make myself leave the house
-- I have taken myself to the hospital 3 times thinking I was having a heart attack and told I suffer from acid reflux
-- I have so much pain in my legs/feet/back that I can hardly walk
-- My hands and feet like to go numb for no apparent reason
-- I am always anxious & moody.
-- Can't sleep
-- Clearly I am not myself. Lately, I have felt the quality of life I am leading is horrible.

Wouldn't it be something that I have spent all this time & money trying to figure out what else is wrong with me when it is the medicine I thought was keeping me well really making me sick. Why do the finest doctors not realize when your symptoms are actually side effects?

I am pretty out raged at this point. I would take myself off this medication today if only I knew how to control the edema.

I was placed on Topamax, off label, for suspected bipolar illness (now disproven). My cognition, word finding abilities, memory has been so adversely affected that I am now on disability. I had 5 kidney stones due to the development of Renal Tubular Acidosis, nearing renal failure (a side effect doctors don't warn patients about). This in turn led to osteomalacia, softening of the bones, only discovered after I broke all three major bones in my leg and snapped off my foot stepping off the lowest seat of a bleecher. I've suffered tingling in arms, hands, legs & feet (nerve damage), lesions in the brain, muscle spasms, heat & cold intolerance, insomnia etc... Although I lost weight, I gained it back (then some) as soon as I reduced the dosage of 800 mgs. Upon stopping the drug to save my kidneys, thus my life, my kidney function returned to almost normal within a few months, although there is residual damage. All other side affects remain two years later. Losing weight is not worth dying! Beware of this drug being used off label! I would never trust this drug!

I want to know if anyone has experienced severe joint pain while on Doxy. I was prescribed this med on a Monday. I (like an idiot) doubled up on my first dose Monday evening because I know you can do that with other antibiotics to jump start the process. What can I say? I don't like being sick. Well....Tuesday morning, I took my 2nd dose and went to work. Very soon after taking the second dose, I broke out into a very itchy rash all over my back that soon spread to other parts of my body. I called my doctor and was immediately taken off the Doxy and prescribed Augmentin. Later that night, I began aching all over. I woke up in severe pain throughout all of my joints, and was in a terrible mood.....obviously. As the day progressed, the pain continued, but seemed to be moving randomly about my joints. My ankles would hurt for a while, then my arms, the my shoulders, etc. That night, I took a Benadryl (still itching from the rash a little), some ibuprofen, and went to bed. I woke up feeling a lot better. A lot less pain in most of my joints. It was a good day. However, today, Friday, I am still in some pretty bad pain in my hands. Anyone else have a similar experience??????

I have been on NuvaRing for over 3 years now. When I first went on birth control I was using the ortho evra patch however, I was suffering from side effects such as nausea, always feeling sick and tired. I eat a lot and everything but while using the patch I felt TERRIBLE eating the blandest toast. I am not a heavy drinker but even one cocktail would cause me to be extremely sick. I switched to NuvaRing and since then I was back to my normal self. Not only that but while on the NuvaRing my period is like CLOCKWORK, I know exactly when I am getting my period. I did not experience any breakthrough bleeding and my periods are extremely light. Overall the switch to NuvaRing was so worth it.

I am a male, 61. and have a history of switching around cholesterol meds, most recently because of cost due to my high number of medical conditions and large number of medications for, but not limited to: CAD. CHF, diabetes, hypertension, renal impairment, and herniated disks. I have barely been on zocor a month and have experienced extreme weakness, pain in neck, shoulder, hands, legs & feet. Because I have both cervical & lumbar herniations, I was somewhat uncertain until I began reading these posts. I took myself off zocor yesterday and emailed my doctor's nurse. It also occurred to me that after any length of sitting, my legs hurt upon standing while i was on Lipitor, but don't really recall other symptoms. Sometimes, when you have a number of health issues, you come to believe this is "as good as it gets," but now I believe differently, otherwise why bother with the meds at all.

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.

I had Mirena inserted in May 04 and have been miserable ever since!
I had my 2nd child and did not want any more, I was scared to get my tubes tied because I had a newborn & a 4 year old to take care of.
Since I had Mirena, I have had severe back pain, weight that won't budge no matter what, severe constipation, swollen legs & feet, panic and anxiety attacks, moodiness, hot flashes, miscarriages, severe stomach cramps, depression, bloated stomach, almost constant nausea, headaches, you name it I have it.
My husband got a vasectomy 4 weeks ago and I can't wait until I can get this horrible evil thing out of me.
I didn't think it was the IUD until recently. My doctor played it up like it was a miracle contraceptive-even told me it was better than tubal ligation and vasectomy. ha!

c.

Hi to all,
I have read all comments in complete shock. I am a 53 year old female.
I was prescribed Simvastatin just over 6 months ago (40mg). I am hypothyrod and also have very high blood pressure. About 6 weeks ago I started to have severe (and I mean severe), night sweats. The sheets are absolutely wringing wet as if someone has thrown a bowl of water over me,
The headaches that start within about 30 minutes of getting up every morning radiate from the middle of my forehead right across my right eye and it throbs all day. My throat is sore, my skin very dry, my vision seems very blurred (especially first thing in the morning), and I don't seem to be able to focus very well. My appetite is almost non existent and my shoulder, legs & feet hurt dreadfully and although I hate to admit this I am quite depressed at how I feel.
Three nights ago I decided to stop taking Simvastin and guess what...hay-ho, no night sweats, no cramp and the headache today was much less severe.
I am glad I found this site and for sure I will be visiting my doctor next week to advise my findings.
I think I would rather live on a diet of bread & water rather than go through this again.
Good Luck to all fellow sufferers.

My husband had been taking lotrel 10/20 for approx. 1 month. He has developed an annoying uncontrollable cough, insomnia, tingling sensation in his fingers, swollen hand, legs, feet and ankles, he has to use crutches in order to get around. He now has an uncontrollable appetite which has caused him to gain weight. The scary ones are the anxious feeling & depression. He is complaining of headaches throughout the day, constantly urinating multiple times during the night. He owns his own business so he uses to be able to work 12-16 hrs a day or longer. But, since he has been on "THE LOTREL" that is longer true, because he is tired most of the time. My husband was on Hazar but the cost was outrageous. After all of this we are willing to pay the cost of the Hazar…

I had the Mirena put in a year ago. Experienced bleeding for approx 3 weeks.Not really seen my period since(Wooohoooo),except for some light spotting round "that time of the month". I recently have been experiencing very bad acne breakouts.Have always felt that my tummy is bloated and have a very low sex drive. But my BIG QUESTION is Has anybody experienced a burning sensation in either of their bum cheeks,(especially when sitting,feels like it's on fire)which is unexplainable by numerous doctors and endless tests I have had done. Not sure if it's related,but so desperate for this burning to stop.

I must be living in a vacuum without knowing it. I have been on Lipitor for a few years now. I do slur words on occasion... the cramps are occasionally unbearable. I get cramps in my rib cage, legs, feet and have to watch myself making move like reaching for something that requires anything other than a normal move or twist.. or I get a cramp. I also get cramps in my hands, muscles knotting up with horrible pain... I have to watch how grasp things my fingers.... occasional just cutting a steak holding the knife or fork and applying pressure... I had a discussion with a complete stranger today who said he had similar side effects with Lipitor... I thought it was old age (I'm 62).... and not very physically active. I looked it up on the internet and found this very informative site.

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.

I had been suffering from bronchitis for over a week; my doctor believed that it may have been developing into pneumonia so he prescribed a seven day supply of Avelox along with an inhaler (for my congested airways). About an hour after taking the second pill (day two) and a couple puffs from the inhaler, it felt as if my throat was spasming (possibly closing), my chest hurt, and I felt incredibly anxious. I actually called 911 (which I have never done before) and the EMS suggested I stop using the inhaler. So I did. I stupidly finished off the week's worth of Avelox (yesterday 11/9) and am still struggling with moderate to severe anxiety. My stomach has hurt almost all day today, and it still feels at times as if my throat is spasming. Has anyone else experienced this?? I thought it may be anxiety-related, but now I'm not so sure.

I'm seeing my doc again tomorrow and plan on telling him that I never want to use Avelox (or any fluoroquinolone) again!!

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!