Right foot symptoms and conditions

SIX HOURS POST REMOVAL- I had my mirena removed today after 3 years and nearly 3 months. My side effects included headaches, sore breasts, weight gain, nausea, severe hair loss, depression, severe pitting edema of my right foot, cramping, hip pain, exhaustion, severe mood swings, and acne. During the first six months I had constant bleeding, which I had been told to expect. I took regular pills everyday and the bleeding stopped. Then the hair loss started. My hair came out in clumps and was EVERYWHERE. I lost about 15 inches of my hair in spots. I went to the salon and got a fantastic hair cut, I attributed my hair loss to stress. Now I'm not too sure. I also didn't feel like I was myself with the odor that I developed. No matter how many times I showered I felt not regular. Slowly but surely over the past three years I have gained 30 lbs. I worked out to try to get the weight off, I lost nothing and in fact gained weight! The pitting edema of my left foot started in July of 08. I have been tested for everything including diabetes, heart problems, clotting disorders, pregnancy, high blood pressure, kidney problems, and the list goes on to the tune of $6,000. I went to my OB back in the spring and was told if they could find nothing else then they would remove the IUD. In the interim I lost my job and subsequently my insurance. I luckily was able to get coverage again and immediately set an appointment for the removal. Insertion hurt like nothing I have ever experience, removal was quick and almost painless. I also ended up with BV (bacterial vaginosis). I feel and look as though I am about 6 or 7 months pregnant. My belly is actually the same size as it was when my son was born. I weight about 15 lbs more. My breasts were extremely swollen and sore.

I instantly felt better after removal. My hip immediately stopped tingling. I have no back pain. It felt almost like a lifting if that makes sense. I am curious to see what the next few weeks will bring and I will definitely keep you all posted.

I don't have any new side effects; they're the same as everyone has mentioned. I feel so unhappy almost all of the time. I have experienced the fluttering in my stomach, which looks like I'm 5 months pregnant. Diet and exercise aren't working to take away the 20lbs I've gained. And the acne is annoying. Everyday I get a new pimple. I know that Proactive works because I used it prior to my November 2007 insertion of Mirena. After reading the comments listed on this site, I have decided to have it removed. I'm tired of being tired, sad and popping pimples. I also had a vibrating feeling in my right foot for about a week; Mirena related? Don't know for sure. Good Luck ladies! And thanks so much for your posts.

I am having Mirena removed today at 1:30 pm. I guess i hopped online just now to reassure myself to go through with it and not to wimp out if the doctor suggests (again) that i try to keep it. I got it inserted Dec 15th last year and have bled just about every day it seems since then. It hurt like hell when i got it. I took 3 days off work. I sweat thru a sweater and jeans on my way home from the appointment. I felt like i was going to die curled up at home by myself. Nobody believed me. I have had the worst attitude and mood swings. I am 29 years old, and don't have kids. I have never had acne in my life and have subscribed to ProActive since having Mirena. One time my chest, arms, upper back and shoulders broke out in small red bumps like i was diseased. I was not using any different perfumes or lotions etc. It went away in about a wk but i will bet it had something to do with my Mirena after reading these other posts. Once i was driving and my right foot cramped so bad i had to pull over and relax it to get home. I have not had regular bowel movements since Mirena. I swear to you- its like peristalsis stopped working on me. I always have to have help. Ive been through countless jars of Fleet suppositories and fiber supplements. And i have been on a constant detox type diet full of fiber foods to help move. I recently took my first trip to Europe. I was very worried because i had started to feel hot flashes 2 weeks prior! Hot flashes! Did i tell you im 29? It was a chilly day in October and i wanted to stip down to my undies in the AAA Travel office. I may have had a couple yeast infections in my life (in college) before Mirena. Since Mirena i have had one every couple weeks. Ive had odor out of this world when i never used to. Nothing over the counter ever worked. The doc actually tested me and found nothing abnormal about my swabs. She gave me a handful of the Diflucan pills. (Why give me that if i have nothing abnormal). I read up on vaginal health and flora. I bought the plain yogurt with probiotics etc. I started using tampons dipped in yogurt to calm things down there. Thats the only thing that felt good (but now 100%). My friends started to joke and call me Fruit on the Bottom (like Yoplait- lol). My area down there was sensitive to the touch and in pain at one point. It actually swelled up and looked super crazy one time and went back to the doctor. She again said she found nothing wrong. I asked for removal because that episode actually scared the crap out of me. My underwear even hurt. The blood and discharge burned. It was like my fluids were toxic to me. She didnt seem to believe me! She gave me 2 estrogen patches. Said to use one for the first week, remove and replace with the second one the second week. I did this and the bleeding stopped. I went for a follow up appt and she said ok- the bleeding stopped, you are ok now. The next day- you guessed it! I started bleeding again. I have been a pretty fit chick (even though im curvy/plus sized) and i pay attn to what i eat. At one point i stopped exercising and would eat anything not nailed down! I would be halfway thru a meal and plotting on what to eat next! I consulted a nutritionist and started losing the 23lbs i picked up from my Mirena binge. I have 3 friends who got Mirena and loved it. Its why i got it in the first place- because i was having abnormal periods and wanted to get it regulated. This has been a learning experience for me. I look forward to being myself again. The birth control part of Mirena is that ive been such a damned dragon that no man wants to come within 10 feet of me. LOL! And even if he wanted to I don't know what kinda mood Miss Vagina would be in that day so i don't risk the bad experience. I am going back to Orth Tri Cyclen. I never ever ever had a bad day with it. It wasn't broke so i never should have tried to fix it. I hope some of this stuff helps you. Im definitely going to my appointment to rid my body of this enemy.

Imagine me as King Leonidas on The 300 kicking Mirena into the dark pit of no return. This is Sparta!!!! :) Make your removal appt today. Im changing doctors after this also. Take care of yourself ladies!

D.

About 2 hours after taking my 18th day of generic Wellbutrin XL 150mg. (Sun)the palms of my hands started itching like crazy! No bumps or anything, just intense itching. I immediately applied 1% Hydrocortisone cream to them and after about 10 minutes that pretty much made all the itching go away. I didn't want a replay of that, so I kept applying the HC about every 4 hours all day long, or after washing my hands. That evening everything was okay. Then the next morning, my hands started itching again...so again I applied the HC cream again, and headed off for work...they itched SO bad, and this time it took about half an hour for the HC cream to even begin to work. Then about 20 minutes into the hand itching, the soles of my feet started itching..too wierd! I was driving, so I couldn't apply it to my right foot b/c it was on the gas pedal, but I applied the HC cream to my left foot, ahhhh! Then as soon as I could, I applied it to my right foot. It took about 10 minutes, but it was soon itch free. When it came time to retake my med, I decided not to risk it. I called my prescribing doctor and she was off, and some other doc just said to take Benadryl. Duh, I was at work and #1 didn't have any and #2 it makes me so sleepy, I can't function. Then later on in the day, my wrists got welts on them, then my left elbow got a huge set of welts on it, and itched like crazy...then a few hours later, my left ankle got a huge welt on it and it looked like my ankle was swollen and both my feet and ankles had pin pricking sensations....a few hours after that, my right leg started itching behind my knee...I could feel a welt through my slacks...so again, I went into the ladies room and applied HC cream and it helped. By now I've used 1/2 the new tube of HC cream! When I finally got home, I pulled off my clothes and I had huge welts (hives) all over the back of my right leg. Plus, a big long skinny (horizontal) welt where my bra and wrapped around me. Since I was home, I could take Benadryl...so I took 4 tsp. and jumped into a warm (not hot) bath (they say to use cool water but I couldn't do it) with a cup of baking soda. Felt SOOOO good! By the time I got out they felt much better. I kept taking the Benadryl every 3-4 hours all evening but by the time I went to bed, I had welts on the back of my left leg also and on my buttocks and hips. My head kind of itched here and there in weird places, more like pin pricks but I have really thick hair, so I can't tell if I have any welts there or not. I stayed home from work today to continue on the Benadryl and making sure it doesn't get any worse. It hurts to sit here typing as my panty line is in the middle of a big 3" welt. The Wellbutrin XL seemed to be helping my depression and anger issues, but I assume the MD will put me on something else. I really liked it. It did suppress my appetite during the day but not much at night. Oh well! I'm glad I'm not the only one with these symptoms.

Started taking the Zocor generic Simvistatin just 2 days ago. My legs hurt so bad that I can not sleep. My right knee is swollen to the point I have very limited range of motion and can barely walk up stairs. It is after midnight and I can't sleep. Also having some angina and my little toe on my right foot is somewhat numb. I will be contacting my physician about this tomorrow. My cholesterol was 105 and this doesn't seem to be worth it to me!

One week into taking the meds . I did feel anxiety and nervousness. I have never felt those feeling until I have taken that medicine. i also had diarrhea.I started feeling a sensation above my knee where is would start tingling and it would go numb and then start burning after standing for like 10 mins .I have never had any problems with my legs. Then the second week into in the middle of my thigh started a burning sensation. The third week it just kept getting worse . I went back to my doc and told him he said it was my weight and me walking. So Sept 11,09 I stop taking it. I have been off it for like a 7days . the burning has gone down to a soreness in my right leg but my right foot is very sensitive. It very annoying. I do not what it did to me . It has been the worse 1 month experience in my life. I have lost 25 pounds which is great eating right and walking.If it was not for this website and my mother in law I would of kept taking it. Like a dummy. I am looking for a good doctor in

I was reading your post and had to reply to it!! I have been on toprol xl for about 10 years or a lil longer! Started out at 100mg a day now take 200 mg a day. Am a 37 year old female,feeling like a 90 year old female! For the past 3 years or so experiencing numbness started in my toes, now my left foot to right below my knee is completely numb,right foot and leg getting that way!My hands stay real tingly also! When they are not numb they hurt me so bad. I just couldn't believe your post when I read it! Been to neuro telling me I have severe nerve damage in arms legs and feet? I am like from what? Had all kinds of tests and MRI, nothing.... Thank you for your post,printing it out and taking it to my doc! Maybe we have finally got a diagnosis!!! Sounds like it is the meds to me,Not to mention I am also on 3 other bp meds! Just scared me saying I might have M.S. More like toprol xl huh? How is your numbness now? Was wondering if u experience pain w/ the numbness? Thanx T.

I had this thing placed in April of 2008. I was fine had minor cramping and went back for check up. everything was okay until January 2009 I got a yeast infection. I did an otc med and it went away for about 3 days. It came back with Avengeance not only did I have a yeast infection but it was accompanied with migrated arthralgia. I could hardly walk at one point on my right foot then it moved from my right hand to my left and has settled in to my right foot. I called my PCP and she gave me meds to treat and it went away for a month. I was told that if it came back with the arthralgia she was going to test me for lupus!!!! LUPUS I thought I was in a lot of trouble the next month because it came back. I have had 8 yeast infections in 6 months. Every time my husband and I have sex it feels like a rug burn and I get the infection back. I was told (when I finally thought to call) by my GYN that if you get yeast infection and it doesn't fully go away it can live on the strings and keep coming back. I was treated this last time with a vag cream insert and an oral med. I thought I was free and clear but two months later here I am again. I am going in to see my GYN/PCP to have this removed tomorrow she agrees that the mirena is the issue. I have had all these other symptoms thought mostly the weight issue I can't lose weight not matter how hard I work at it. I have facial swelling and have been very fatigued. Also be warned that you should not have this placed if you have history of endometriosis. I consulted as to why with one of the doc that i am a nurse for and she said that this can cause bleeding to be worse since endometrial tissue can attach anywhere in the body. I have endometriosis removed twice and I am not willing to take the risk of abn bleeding elsewhere I already have enough CRAP to deal with. I am sure that some women have had this and it hasn't been an issue. More power to you!! but for those of you who are suffering form this. You can file a formal complaint with the FDA I think if enough of us file complaints maybe will step back and take a closer look at the TRUE SE of this horrible device!!

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

I am 47 years old and I started these pills 2 months ago to deal with bad headaches,
Since I began taking them: my hands ache, my right foot is swollen, my knees hurt, I have to ice them at night so I can walk in the morning, I'm moody, I have diarrhea, god-forbid I have gas,
I don't want to eat or I'll have to poop almost immediately sometimes before I'm finished with the meal I have to run to the bathroom, my sex drive is up but I'm scared to have sex in case of anything embarrassing in bed.
I have hemorrhoids and because I have to go so often they won't go away.
I HATE these pills.

I've been taking Lyrica for around 8 months for neurapathy in my lower legs and feet. Gez, I gained so much weight I fractured my right foot! It does help with the pain but after reading all this negativity I am going to ask for something else. I HAVE been having strange dreams, not very pleasant and I'm very happy I found out the reason. Thanks so much for all the great info everyone has given me!

A.

I was given Avelox by my Allergist three weeks ago because I had yet another sinus infection, she had me come in and pick up some samples she had with 5 days worth of 400 strength Avelox.
The night of the third dose I was awakened by numbing and tingling and pain in my right arm from the elbow down to my hand, I had never had this before. I called the nurse the next day and she said to stop taking the drug which I did. I figured now that I stopped taking the drug the symptoms would go away.
A few days later I was out shopping and within a few hours of walking around I began to have so much pain in my right foot/ankle/heel that I had to come home, I could not put my foot down.
Then within the next few days my knees began to hurt, behind the knee and in the side. It has been 3 weeks now and the foot pain is better but my hand,elbow and knees are bothering me so much I can't sleep. The other symptom feels like nerve pain in my legs, hands and fingers. I am really troubled by this, I am a very active healthy 62 year old Woman, I have not been able to exercise all of this time.
I went to see my Allergist who prescribed the Avelox and informed her of all of these symptoms. She said that this was a rare side effect and that I was particularly sensitive. I asked her if the symptoms would go away soon and she gently said that it would take time.
Then she said that she had prescribed Avelox to her husband a few months ago, she said he had the same reaction as me (how does this translate to a rare occurrence?) and that he was slowly improving. She thought I should go to a Physical Therapist or a Rheumatologist, I told her I can't afford that.
At this point I am scared I won't get back to how I was before. I have had knee surgery in the past but my knees were doing fine until this.
Have other people slowly recovered as my doc has suggested will happen?
I don;t know what I should be doing at this point. Help!
S.

I have been on 10 MG of Lipitor for almost 3 years. Since I began taking it I have had recurring issues with an anxious feelings, my lower GI is constantly churning and I feel like I am stressed out. I have a low stress job, a stable happy family life and yet I feel nervous all the time. I sleep for 3-4 hours and then wake up and am unable to get back to sleep. I have been forced to take a nap ever day after lunch just to get through the day. Additionally, I developed tremors in my hands and was diagnosed with something called Benign Essential Tremor and put on another medication to control the shaking.

Yesterday I decided I had enough of this and went to see my cardiologist to discuss the symptoms. I stopped taking the Lipitor on my own 2 days before. The doctor told me that none of my symptoms were related to Lipitor! I replied that I was convinced that they were all in fact caused by this drug. He suggested I stop taking the statin for 2 weeks and see if the symptoms stop. I am now on day 4 without lipitor and am already feeling less anxious.

I went to the Nuerologist 2 weeks ago and got her to discontinue the anti-tremor medication. I am going to get all this crap out of my system and hopefully get my life back.

I have been taking Zocor for 6 months. In the past 3 weeks I have developed intense tingling and burning in both legs from my feet to my knees. I also have a feeling of numbness in my right foot that at times is in the whole ball of my foot but will move to the side of the ball of my foot. I have been to the ER twice and all my neuro checks were normal even though my legs felt like they were on fire. I just this past week had a MRI of cervical and lumbar spine. My doctor is thing the symptoms may be related to the significant arthritis I have in my neck and may be due to nerve compression at one of the discs but I don't think so. I was worried about MS and Guillian Barre as these can be symptoms of those diseases as well but I didn't have any other symptoms of those diseases. At my last ER visit the doctor put me on Neurotin for the burning in my legs. I just happened to think to look on line for med interactions and side effects of the meds I am on and would have never expected that Zocor could be the culprit. I was astounded to find that the tingling and burning was more than likely due to the zocor. I stopped taking it about 4 days ago and am showing some improvement but I am still taking the neurotin. Does anyone know how long it takes Zocor to get completely out of your syste.? I also have nerve conduction studies scheduled.

after about a week on my methadone my feet and ankles swell they diagnosed it as cellulitis but cellulitis doesnt go away w/out antibiotic treatment so the next 2x it happened i didnt get antibiotic treatment i just put my feet up and stayed off them and the methadone and the swelling went down! also after about a week i start to do random episodes of passing out once with my face in bowl of cereal and once doing dishes and this was at prescribed dosage!!! be very careful i am on blood thinners and i think the dosage builds up quicker in my system perhaps. i didn't tell doctor because they work for my pain better than anything else he has given me and its hard enough to get something that even takes the edge off my pain i have so many medical problems that three very reputable neurosurgeons refused to operate on me due to my risk of stroke and i am only 49! i have deg disk deg joint rheumatoid arthritis, bilateral neuroforaminal stenosis in lower back l4-5 and s-1 several disks that are dehydrated and dessicated , many bone spurs poking in spinal canal in cervical spine every disk in cervical spin either bulging herniated or previously operated on severe arthritis in feet toes and severe nerve damage in right foot where big toe and baby no longer can lift up neuropathy in right arm radiculopathy in left missing protein s in blood which is the protein that keeps your blood from overclotting so i have been on blood thinners since 29 yrs old and have had several pulmonary embolisms b4 age 29 and proper diagnosis and the list goes on! and yet even though i got my soc sec disability by myself w/out lawyer assistance due to list of medical problems which spoke for itself i still cannot find a doctor who will try to work with me realistically on a pain management program that even manages to take the edge off to enjoy the quality of life enough to be able to spend time with my 4 yr old granddaughter doing things like fishing and playing with her in ways that i would like such as camping amusement park rides (which they have forbidden!!!) can anybody out ther help me find a doctor who will not be afraid to prescribe something that will really work enough to put me back in the game off life ? did i mention that i need right hip replacement it is bone on bone and left isn't far behind and lower back was listed as severe bilateral neuroforaminal stenosis needing surgery also as of 2 yrs ago and also need several cervical surgeries and that i have a benign tumor in thoracic spine that cant be operated on but does still cause pain! so please if you can be of help to me/as winter is upon me now ,which as we all know multiplies most of our pain problems so speed of the essence!!!!xoxoxoxo please e-mail me if you know of any doctor who can be of real help managing pain no surgeon will touch me due to risk of stroke , i stayed awake for last major surgery it had to be done risk outweighed stroke risk if it didn't get done. i am currently on methadone 10mg 4x daily and it barely takes edge off and causes too many side effects which i wont tell dr. because it is the closest thing ive had to pain relief and have been on same dose for 4 yrs ,and my pain has no hope of improving but only the certain knowledge that it is going to get increasingly worse every day and my granddaughter only has me her grand papa and her uncle, my son, that she can depend on being ther in a good role model form as well as being her only consistent source of love ,affection and proper parenting! I love my daughter but her and her boyfriend ,my granddaughters father of course, are 2 of the most self centered people on earth and unfortunately they put their needs b4 thier own daughters on every level and in way to much detail for me to put here i need only say this combine 2 totally self centered individuals with a pretty big cocaine addiction and you will get enough with that to know my dilemma! they buy her many clothes n toys n moviiiies to keep her busy while they play but never enough food or mmeds or real needs such as affection, love ,food, drinks etc!! they both work in a hosp making great money but i have to provide my sweetie(grand baby) with food meds affection love and all the things they should be doing! this is why it is even more urgent i am able to function well w/out as much pain as possible she needs to be here with me and her pa pa in a healthy ,wholesome loving and affectionate home she loves to bake and read and learn with us she never wants to leave and it tears my heart out when i drop her home with her daddy and she cries hysterically because she doesn't want me to go and she wants to stay with me and i cant! so please help me find a good doctor who can help me function at highest level w/out pain but also as coherently and safely as possible!!??? i would be forever indebted to you for your kindness and help! e-mail is ******* please send referrals or recommendations of any and all sorts tysvm, i live in the area of erie county new york tysvm,xxxooo tysvm for all your time ,much love, pained and troubled grandma in n.y who needs your help to be able to help my sweet grandbabyxxxooo

I cannot stand for even a couple of minutes without my feet tingling/burning for the rest of the day. Walking seems to help therefore I thought it was circulation but vein docs say it is not. Symptoms got seriously worse during ivf treatment (3rd ivf, 3rd baby), and now one year later I have a baby but symptoms are worse. I thought drug effects are short term but maybe they are not. I am suspecting lupron but i could not find much info on its long term effects and how to counter those effects, or it could be something else. Saw neurologist who wants to do nerve conduction study but that just sounds very painful and not necessarily helpful.

if you have any feedback, would love to hear. thanks

I have been on Lipitor since 2002 and now I am experiencing numbness in my feet...mostly the right foot. I was thinking I had an autoimmune disease until I read everyone's comments. I am stopping Lipitor today.
Also, I have a lot of wrist pain, leg pain and I bruise easily.

I worry how I will control my cholesterol.

Joyce
8/6/08

I was prescribed Levaquin for a bout of diverticulitis six weeks ago. About a half hour after taking it each morning, I felt completely unwell--dizziness, fatigue, overall weakness, odd sensations of pressure in my head, chest, and bladder, weird bouts of sudden joint pain. The worst side effect was terrible insomnia. I'd go to sleep OK, but wake up after 3 hours and not be able to get back to sleep, sometimes for the rest of the night. Instead of getting the rest I needed to get better, I was getting more and more exhausted. Now, a month after stopping the medication, my sleep hasn't returned to normal. I'm still awake in the middle of the night for two or more hours. Is this a residual side effect from Levaquin? Has anyone else experienced it? When can I expect my sleep to improve? Is there a way to detoxify from this drug?

50 year old male, prescribed Singulair 8 months ago to assist with allergy problems while taken allergy shot treatments. About 2 weeks ago started experiencing numbness/tingling in right foot, then both feet, the spreading up the body to above the waist. The best way to describe the sensation is a combination of the feeling you get when you hit your funny bone and the sensation when you sit or lay in a position that puts one of your limbs to sleep. Had all the blood work tests done at Dr. office to verify no other issues, all blood work is normal, Dr. suggested could be a neuorlogy problem and more tests will be necessary. Receive routine Chiropractic treatments and had him check everything, including new x-rays, nothing there. Read the side effects again for Singulair and realized that this numbness/tingling is just one of the symptoms I have had since starting this drug. The others being unusual weakness, tiredness, which I thought was just part of getting older and severe sinus inflammation, which I had thought was just related to my allergies. Have contacted my allergy doctor that put me on this and he said to stop taking Singulair to see if my side effects go away, since I am near the end of the time that he expected me to take them for anyway.
I will repost after a few weeks or as soon as the side effects go away.

I have been taking 20mg of Lisinopril and 5mg of Felodipine for about a year now, and I am experiencing excruciating joint pain. The back of my knees ache even while sitting and the bottom of my right foot keeps me from walking freely because it hurts so much. My wrists and fingers hurt too. I am overweight, so I just figured it was due to excess weight, but reading these posts made me realize that this is not normal. I am in pain all day long. I feel like I'm going crazy because I can't just get up and go- I struggle to do anything. I did not want to see my doctor because I've switched medicines before- used to take 50mg of atenolol but fatigue was horrible, so doc gave me hydrochlorothiazide and it gave me a terrible rash on my face. I thought I was done switching meds- does anyone know what is a good bp medicine? I'm tired of being tired and in pain.

2 yrs. ago my husband had been on Vancomycin for an infection from a hip operation. He had an allergic reaction and was given Levaquin in the ER. Not long after the dose was given, he was not able to walk at all his fever spiked and he said he was blind at one point. It did not last but since then he had been slowly declining. He has trouble with his inner ear balance and he can hardly lift his right foot to clear the floor. He bearly feels anything from the knee down on both legs. We have been to many specialists/neuros, MRIs, nerve conduction test and there is nothing to show what is the cause. Can anyone tell me how we could find out for sure if Levaquin may be the culprit.

Sue

Hi all, I have had the Mirena since May of 08. I had twins in Feb of this year and was given the little plastic ring for birth control. That gave me TERRIBLE migraines. i hardly ever even have headaches let alone migraines. It was impossible to take care of twin infants along w/migraine pain. I really shouldn't be on estrogen anyway because of a clotting problem in my family. So my doctor recommended the Mirena. I wanted it anyway because I can't remember to take pills now, (I'm a little busy.) Since I had it put in I have been losing my hair in unbelievable amounts which my doctor attributed to my just having twins. My depression and anxiety meds are NOT working anymore. My fourth and fifth toes on my right foot are completely numb and stiff, almost like I have arthritis or something. I have NO interest in having sex w/my husband. But after taking care of twins, who does?? Just kidding. I am not very happy with this IUD, but have decided the alternative (being pregnant) is not a better option at this time. So, for now I will continue to be a bitchy, balding, arthritic, celbate mother of two. Good luck to everyone else

Just started Welchol after trying Lipitor & others. Have now developed severe vertigo & my right upper arm is killing me. I can't drink ANY alcohol because it makes me violently ill, almost to the point of throwing up, My doc says this drug is non-systemic & says I should have a brain scan...I stopped taking it 3 days ago-arm pain is gone but not the vertigo yet...I'll have to weigh my options of going back on it again.
Has anyone else had dizziness & lightheadedness from this?

I started full body internal itching after taking 10 days of Singulair. The physician that prescribed it said it couldn't cause itching. My new doctor tested for Lupus, I have an autoimmune disorder called Churg Strauss. After undergoing several steroid treatments and 3 days of IV Prednisone I got some relief. This has been going on for 6 months now. The itching becomes severe enough to make me want to commit suicide. Luckily it is pretty controlled by taking nightly doses of Atarax along with Periactin. Thank God I found a doctor who cared enough to search out the symptoms and help me get thru day by day.

I am a 34 y/o male who started taking 10mg/day of lisinopril on May 15th. My blood pressure at the time was 140/118, pretty high I guess! I was feeling it too in the form of headaches. The doc wrote the script for me and I filled it that night. I should also mention that this is not the first time I have taken Lisinopril. I stopped taking it back in March because the script ran out. I don't seem to recall any kind of side-effects the first time, but I could be wrong. Anyway, I also take Levoxyl for my hypothyroidism, and it is a pretty hefty dose, 225mcg a day.

So, for the first week, I was doing pretty good on it. No coughing, or any of the listed side effects listed for the med. Then, about a week into it, I started having numbness in the right three toes on my right foot. When I say numb, I don't mean I could not feel anything, it was like touching your skin with a t-shirt over it. I could feel it, just kind of topically numb. I had a 'patch' of this numb skin right behind those same three toes and several other areas up the front and back of my right calve. I delt with this for a few days, thinking it was my shoes I was wearing at work. They were pretty worn out on the outer edges. I got new shoes on Monday, June 2nd. I wore them to work on the next day. At the end of the day, my calves felt kind of tired. The next day, they felt kind of tired still. I found this sort of weird. From that point on, my high anxiety really kicked in. I don't want to mention the thoughts I am having about what it could be that is causing this. I forgot to mention that I have not been sleeping well lately either since I started taking the Lisinppril again. I guess overall, I feel exhausted and weak. More so in my legs. To add to it, my lower back hurts like mad. I have two herniated discs and mild arthritis in it from damage from years ago. Also, for the past week, a pain has been developing in my left shoulder blade in my back. It is worse in the morning, and had gradually been getting worse for about a week. Today, it was awful.

I have ready a lot of the messages about the side effects different people are having. My question is, has anyone ever been on the lisinopril, gone off of it for whatever reason, having had no bad side effects, then gone back on it only to start having these bad side effects that you did not have before?

I have stopped taking the lisinopril on the 5th and have a doctor's appointment on the 9th to find out what is going on. I don't feel good at all. Can anyone relate?