Shins symptoms and conditions

I've been on this for a few days today is my last pill I've had bloody stools & red dots on my shins, I'm scared, & if you read the side effects thoroughly, you will see that it surprisingly mentions fatality as a possibility.

I was prescribed Avelox for a sinus infection that would not go away. After 4 days of taking it I have had severe cramping in my joints around my ankles, knees, shins and calf muscles. I have pain in my fingers too. I feel totally out of it, and dizzy. I have little to no appetite. This is a terrible drug, and should be pulled off the market. I was desperate to get rid of my sinus infection, and now I find myself having bigger problems from the side effects of this drug.
I have had pain now for 4 days. Does anyone know when this pain goes away?

I got the Mirena 1 year ago, at age 46, when my youngest child was 13. My doctor did not do anything to dilate my cervix and the insertion hurt very badly. I almost told them to forget it! I have a high threshold for pain and had both my children without any medical intervention, so it is saying a lot to say the Mirena insertion hurt. I decided to get it because of my heavy periods. My periods are much lighter, but last just as long (6+ days). Since May I've had a weird rash on my legs and tailbone. The one on my tailbone looks like a bruise. My shins are mottled and itchy. I've been to numerous doctors and tried many different medications. They have gotten better, but have not cleared up. It seems that my legs are not getting adequate circulation. Also, my belly and area below my navel are bright pink and itchy. I, too, feel bloated and pregnant all the time. Ugh! I experience heart flutters and once ended up in the emergency room because the school nurse, where I work, thought I was having a heart attack. Does anyone else have a rash like I describe? This darn think was so expensive, I hate to have it removed but, if it is causing this rash, I'll have it removed right away!

I am a 40 year old female and have been on warfarin since september 08 when i developed a blood clot in each lung.Doctor's reckon it was caused by my Crohns disease.I had also given up smoking 9 months before and was feeling good about myself but since starting on the warfarin i feel OLD and FED up with everything,6 weeks after starting warfarin i started getting tired all the time, my head doesn't feel like mine, i feel depressed all the time,i get strange pains in my head,my shins feel weird almost numb,can't concentrate,vision feels weird,excruciating pains in my joints to the point i couldn't walk and WEIGHT GAIN like you wouldn't believe and my whole body generally swollen.I thought i was going mad until i found this website THANK you to everyone xxxxxx

I was given Levaquin for a kidney infection. It seemed to help break my fever but after only one dose, I broke out in rash and later that night had tingling in my legs. My hand felt numb. When I called the oncall doctor she told attributed to anxiety. I told her I was anxious because all of a sudden my hand had gone numb and knowing that was a danger sign I refused to take anymore. Later that night, I could not walk or stand or bear weight on my legs. My shins and Achilles tendons were burning and only because of the internet did I know what was happening to me. Only 1 out of three doctors would agree I was having a drug reaction. For some odd reason, the doctors REFUSE to believe or acknowledge this was caused by Levaquin. No wonder the side effects are "rare" if no doctor will acknowledge the pain their patients are going through....how can the drug companies get any real feedback. Funny thing is only after I sent an email out to my team essentially warning them about this drug did I find out my coworker who had been on medical leave had suffered the same fate of torn achilles tendon and only after 3 months of PT is finally walking without pain. WHAT IS WRONG WITH our world when no one will listen to us. Thank God for the internet. I can walk now and have no pain standing (lasted only 2 and half days) but I am scared about the future as I know the results are lingering. I have been exhausted this whole weekend and wonder if its just me recovering as my PCP had me quit all antibiotics even at the risk of getting my kidney infection back. Well nice to know our stories are the same...and its not in our heads. BTW, my ER doctor told me it was a good drug and very unlikely the cause of my leg pains. They rather believed I had pneumonia or lyme's disease before they would believe it was caused by their beloved drug. All I can think now is I hope one day they are given this drug and it cripples them like it has so many others. Sometimes that is the only way they will acknowledge the truth. It has to happen to them or someone they love.

MY 76 year old mother, on hbp meds for 30 years,METOPROLOL, for quite a few years now ,And she complains of severe pain in her shins, NIGHTMARES, for years now to her Dr. Lately she has been having fainting spells, and at times has short term memmory loss, The Dr did cut her metoprolol in half. dreams aren't as bad, She is going to have a D&C due to uterine polyop, all of this has sent me to the internet researching all the meds she is on, I feel bad I haven't done this research sooner, I just thought the doctors know???? Please we need to do our homework, research and take responsibility, for our health and those we Love.. I have been cooking and shopping for her past month, Lots of RAW fruits and vegetables,garlic and other healthy, herbs and oils, she has lost 10 lbs, bp has dropped 135/70 was 155/90 she is now down to 210 lbs, 5 ft, Im hoping the Dr. will take her off the metoprolol soon

This is the second time i'm writing on here. I posted my Mirena side effects a few months ago and thought i'd update my side effects....

before i had the mirena put in i was doing GREAT losing weight right after my 4th baby. i actually lost 15 lbs and weighed less then when i got preggo. within a 3 week period of getting the Mirena put in, i gained 11 lbs! and my dieting and exercise wasn't doing much good. my doc recommended that i watch was a eat a little more carefully and exercise MORE.... how much more do i have to watch was i eat and exercise?? anyhow, its been almost 6 1/2 months since i had it up it and im just experiencing more and more side effects. now i had what looks like a really bad case of eczema all over my body. especially on my knees, elbows and my knuckles. my scalp is really itchy, i've GAINED 30 lbs, my hair is falling out like crazy, by bones are killing me especially my lower back, ankles and shins, my mood swings are horrible i feel like im PMSing all the time and when i get my period which is still messed up and lasts for 2 weeks i get even moodier! i am always really tired, i feel like my chest is about to explode, whenever i eat i get really nauseous, i feel depressed all the time and have bouts of crying spells.... i've always had migraines but the mirena seemed to make them EVEN WORSE now. IDK, i've just about had it with the IUD. the only good thing about it is...im not pregnant!! and i don't understand why doctors keep brushing all these symptoms off as if we are all crazy when we say we are experiencing something that we know wasn't there before the IUD...

Took 7 days of levaquin to get rid of a persistent, almost bronchitis-like cough & chest condition. Ended on a Monday, and the following SUNDAY (6 days later??!) I broke out in a crazy rash, predominantly on my shins, but literally from head to toe. Most prevalent wherever there's "pressure" of any kind on my skin... waste band, sock lines, watch, and it leaves big nasty red welts when I scratch. Shins surrenty look like I'm a burn victim from scratching, and I'm not really scratching that hard... even light, usually harmless itching/scratching leaves scrape marks. What the heck... I've never had a reaction to a drug before. This is awful -- the worst itch I think I've ever experienced.

I'm 54 and have taken 31 tablets of 5 mg Lisinopril.
I've experienced cramps in both calves.I've had so much pain in my left hip and top of thigh I can barely walk. Had to get my wife to put my socks on!
I'm not overweight I may add (155lbs) . Now started getting niggly aches in shins and fingers. Spoke to my doctor yesterday who said stop taking them and report back to him on Monday.
Seeing these comments make me feel that I'm lucky to have come off this drug so soon - but what the hell is he going to give me instead ????

When I first started taking Alesse I did have nausea for about one week. That was the least of my problems.
I became such a basket case! I cried at everything (both happy and sad movies) and wanted to hurt anyone around me (including myself). I actually felt suicidal at times, even though I'd never ever seriously consider it. This was extreme depression, despite being happier than ever with my boyfriend. It was so confusing. I would burst into tears randomly...and on the last day of taking the pill, (only two days ago!) I burst into tears in public. It was very embarrassing!
I gained ~10lbs during the first month. My appetite had no end to it. I pretty much had all the symptoms of pregnancy, minus breast tenderness. My Dr. scared me and told me I needed a pregnancy test. Luckily, I'm not pregnant.
I developed these painful, red bumps on my shins. At first it looked like bruises, now the Dr. says it's from the pill (but he wouldn't tell me what it was). Now I'm worried about blood clots and the like. I've heard of other women having these symptoms. So, it's not just me.
Finally, I had a lot of trouble sleeping at night. I'd wake up randomly, feeling as though I was high on caffeine, and not be able to relax for ~30mins afterwards. By the time the alarm went off, I was exhausted. I just had mono this past year, and losing sleep weakens me even more now.
Not only is Alesse totally wrong for me, but I'm changing doctors. If you know your symptoms are from the pill, find another one. It's NOT worth ruining your life. Thankfully my boyfriend is understanding!

I started Lupron in April of 2008. The year before this I worked HARD to lose 80 lbs. I finally got down to my goal weight because I was tld my endometriosis symptoms could be relieved if I wasn't overweight. I had a laparoscopy in March of 2008 confirming my diagnosis- Lupron was a last minute decision because of my age and status the doctor didn't want to do the hysterectomy right away. My endometriosis is spread throughout the body- including the lungs. While Lupron helped with the pain I was experiencing, it caused other pain. Pain that I can no longer even deal with. I became lethargic, depressed, and angry. My hair was falling out in large clumps. I didn't gain weight right away.. except a pound the first shot and three pounds hte second shot but I figured that was alright if it was only like 15 lbs total. I oculd deal with that. Here I am almost a year later. my last injection was in August. I gained a total of 47 pounds. I am a fat slob. I couldn't work out because my bones hurt so bad while taking the medication. No one around me knows what I went through physically. They al think that it was just some excuse to be a lazy fat cow but it truly HURT to move. Just simply walking from my bedroom door to my bed killed me. It hurt my ribs, my knees, my shins, my back. There were times when I couldn't even get out of my bed ebcause I just didn't have the energy. Then the depression started shortly after losing a large amount of hair. By now I am thinking about how ugly i've become on top of how fat I am. Nothing went right but my doctor pushed the shot. I figured hes the one with years of experience he couldn't possibly be this wrong. I trusted him. When I would go to him with complaints of my weight gain he would tell me to stop eating. The problem was... I wasn't eating. I was too sick to my stomach to bother. Then when I would get hungry i'd over eat. I bled a lot through the shots and I still had pain here and there but I was too afraid of what he'd put me on next if I complained. I started to forget simple things. My career was going down hill because they were sick of me not being 100% commited to my job any more. I cried all the time. I finally got sick of the weight gain while I was on my shots and I decided to work out regardless of how I felt and three times I passed out in the gym and was transported to the hospital where I had to listen to their advice on being overweight WHICH WASNT THE REASON I WAS PASSING OUT TO BEGIN WITH but no one wnats to hear what I have to say. Every one just assumed that I was this pig who never worked out in her life and over did it this time. What no one understood was that three months before the incident i was my average weight. I was tachycardic all the time- my normal resting heart rate while i was on my shots was 162. During a work out it would get up to 220!

Ive been off them since August and I haven't lost a single pound. I get up at 4am every day and work out. I park as far away as possible. I use the stairs instead of elevators. I eat healthy. I cut out extra sugars and stopped rewarding myself when I deserve it. I started these shots at 155lbs and today I am 215. Ive been on a strict monitored diet, diet pills and work out regimens and I am still 215. My knees kill me nad sound like velcro when I walk- ive even fallen a couple of times because they hurt that bad. My back still hurts and my neck still wont turn to the right completely because of a nerve that pinches or what have you in there that sends the sharp pain through my face when I move. I still have the depression but i think thats more because of my weight now than it is anything else.. and I finally ended up losing my job.

I recently saw my OB for a follow-up where he stuck me on yet another birth control. This one makes me vomit and gives me stomach cramps so Ive decided im done. I won't take another pill because its making me worse. Id rather have my uterus fall on the floor than pop another drug.

hives, redness and severe itching on hands, fingers, and forearms. Pain in shoulder which I can only describe as feeling like I slept on it wrong. Nerve-like pain in lower legs/shins (not muscular) which comes and goes and is not associated with movement or exercise - sort of like if you had a back problem, but intermittent.

I am 23 years old. I was prescribed Levaquin 750mg for a uti. I took my first pill at 3:00pm yesterday. That night, I wasn't able to sleep. I layed in bed, so tired, just wanting to fall asleep but couldn't. Then the cold sweats and trouble breathing started. By 2:00 a.m. I was having what I can only describe as a panic attack. It's 1:00pm the next day, and i've never felt this bad. THIS MEDICINE IS NOT GOOD.

I was prescribed 20mg 3x daily for five days to treat "Reactive Airway Disease/Bronchitis." Yesterday was my 5th and final day of taking the medication and I noticed both of my shins began hurting for no apparent reason when I walked. I didn't think it had anything to do with Prednisone. Then, last night, I suddenly felt weak as if my blood sugar had dropped tremendously and ate a grapefruit while trembling with weakness to stop this feeling. Again, I made no association with this and Prednisone. Last night as well, I noticed that my shoulders suddenly became achey on both sides of my backbone for no apparent reason. This morning, I woke up and the pain from my shoulders had spread to my hips and the entire area between my shoulders and hips is tender to the touch. Today, after not taking any of the medication, I feel mentally blurry, have moments of what feels to be low blood sugar and flu-like symptoms. I'm also still experiencing the muscle pain in my back and hips although my shins seem better. My pharmacist told me to call my Dr. and seemed surprised to learn I was not weaned off this medication. All of the symptoms I have described above are side-effects that should be reported to a Dr. immediately, according to my pharmacist. Another less-serious side-effect that began yesterday is swelling in my feet, hands, stomach and face. I also had diarrhea today.

I am a 67 year old female who has been in good health. I was put on 40 ml of Zocor about three years ago. After taking it for six months I asked to be changed to Lipitor because of stomach pain I felt was caused by Zocor. I didn't have stomach pain with Lipitor.

A year ago I must have had a senior moment because I changed back to Zocor. Generic Zocor was much less expensive than Lipitor.

During the past year I developed most of the side effects that everyone is mentioning: stomach pain, nausea, memory loss, sleep problems. I didn't relate this to Zocor.

Then I woke up one morning and could not stand without severe pain in my left knee. It hurt to touch it. A week later my right knee developed the same symptoms. This didn't happen gradually. It was very fast. I can also identify with those who say that back pain makes them walk bent over. The pain also radiated into my shins and one heel.

I wept when I found this site and read all the posts about similar symptoms. I decided to go off the Zocor for a month and see what happens. I've been off it for three weeks today. The pain is MUCH less but not gone. I'm hoping that it will continue to get better.

55 yo male. I started Vytorin (20mg zocor) in Jan of 2007 until May of 2007. I lowered the dose to 10mg in March but am still suffering side effects (3/29/08) It did lower my cholesterol dramatically but at what price?
I began having tingling/burning in my feet and shins. Also, muscle pains in my calves and something like shin splints. I had been very active but have not fully recovered. B-12, methylcobalimin, has helped the tingling. I was taking as much as 10mg per day. Also, L-carnitine for the muscles, CoQ10, and Ribose. I do feel like I am gradually improving. The tingling is much less but my legs are weaker than before.

I'm a 46 year old guy - I am going on 180 days at 20mg before bed. I am having pain above my knees, weight gain, itchy shins and breasts, daily headaches that go away if I take two aspirin, some short bouts of depression, stomach pain (I feel like I ate rocks), dizziness/loss of balance. I'd rather have high cholesterol and try to do better with what I eat vs having the side effects.

I have been taking Remicade for years. At first it was getting the job done. I started having severe pain that seemed to migrate to different places in my body. Sometimes the bottom of my feet would get so tender I could barely walk. My finger would bend while sleeping and I could not straighten it for days and it would hurt real bad. Knees and ankles would do the same things and then move onto other parts of my body. I thought it was more of a tendon problem, but the pain could also be in any random spots on my body, like shins or maybe a random place on my back. My wrists seem to be a favorite place too. The pain can set in fast and sometimes leave fast. Prednisone is the only thing that seems to help these symptoms. I have been taking 5mg a day for years and when I am having problems that is not enough. I went to a Rheumatologist and he says it is not the Remicade but another antimmune problem. My family doctor thinks it is a side affect of the Remicade and I tend to agree with him. I am going to have my damaged pouch removed in hopes of getting off all medications. I have been living with a colostomy bag for the past three years and it is the least of my problems. Before that I had all my large intestines removed and a pouch which worked well for approx 15 years. I am one of the early people to receive that kind of surgery. I can only pray for all of you that are suffering and lend hopeful advise to your journey.

I have been on synthroid for about 6 months now. Some of the side effects I have been experiencing are numerous.I have hair loss, sometimes I get so ill that no one can stand to be around me, my weight has gone up about 30 pounds, my cholesterol levels went sky high so now I'm taking Crestor, I'm bloated most times, I have episodes where my face flushes and gets so red that it feels like its on fire, and now I've just started experiencing burning and aching of the legs, I'm tired a lot too! My doctor said I would lose the weight but every time I go for check ups and get on the scale it just keeps going up. I would like to know if anyone else out there is experiencing the burning and achy legs because I have been tested for everything and they can't find out what is going on. They of course say it's not the medication.It seems to never be. Does anyone feel me??

I went to my doctor on Monday December 17, 2007, because I was experiencing a fever, chest congestion, with an extremely painful cough. He gave me 7 sample blister packs of Levaquin 500mg, and a sample Pulmicort Flexhaler 180mcg. He also prescribed a cough medicine for night time if I needed it. He said I had bronchitis or a possible pneumonia he couldn’t hear. I also used a nebulizer with Abutrual.

On December 23, 2007 I awoke with the most intense pain I have ever experienced. My wrists, finger, toe, elbows, knees and ankle joints all hurt. My muscles in my legs and back burned. My hands, fingers, feet, toes, and shins felt like they were “asleep” or the worst pins and needles ever.

My husband went online and found out that is was most likely caused by the Levaquin. And thankful I was taking TWO steroids! So when I called the company that makes Levaquin they told me to stay in bed! When I asked them how long this could last they said 1 week to two months.

As of today, the pain in my fingers, toes, wrists, elbows, ankles and knees, which is like tendinitis is mild to moderate. The burning in my muscles in my legs and back is still intense. The “pins and needles” is affecting mostly my hands and feet and my left leg from the knee down. I also still have a deep pain under booth knees. I have also experienced a periodic facial twitch on the left side, below the eye about 1.5 inches.

I am weak, and completely unable to get around do to the pain in my legs and feet. I am furious that my doctor prescribed a medication that could cause these problems without warning me, as samples do not come with warnings. I feel disabled, angry, and would like to know what I am supposed to do now!! Has anyone found anything that helps with the pain?

I am a 34 year old male and was on Lipitor for 3 weeks. I had muscle cramps in my shins and the bottom of my feet. I was light headed, dizzy and suffered from nausea. I didn't have any energy or sex drive. I didn't attribute it to the Lipitor right away. I thought I had MS, ALS, muscular dystrophy, etc. I told my doctor about the symptoms and he told me to stop taking the Lipitor. I've been off of the Lipitor for almost two weeks now and the nausea and dizziness are gone. My energy is getting better each day, but I'm still not 100%. The muscles in the bottom of my feet and shins are also getting better but still not 100%. I take a bath every night just to get relief from the symptoms. My doctor has since told me to take CoQ10 to help battle the side effects of Lipitor. He doesn't know how long these side effects will last. Does anyone know how long I can expect these side effects to last? Are they permanent?

I will praise Lipitor for one thing - The side effects caused by it have scared me in to changing my diet and exercise regimen (when I return to being healthy) so I never have to take a drug of this type again.

You are all completely 100 % right
I have a book here called the high blood pressure hoax
the lady that wrote it is 100 % right in her findings we are all living it !!!!
the list of side effects is overwhelming too many too list
I quit all hypertensive meds yes my blood pressure shot up rebound etc

but I can actually sleep and don't feel depressed and tired anymore

it may not be a good thing but id rather live with no side effects my skin is actually clearing up in 2 days from the itching, the nausea is still coming and going brain fog is clearing up as well as a ton of other horrible side effects for the first time i actually feel good .....in 2 years of taking these horrible drugs ,,,,,yes they are keeping us alive but in the long run they will kill us just as fast as the hypertension !!!!!!!!!! good luck with diet and exercise everyone I am starting it myself this weekend

I was diagnosed with a bacterial infection six days ago and injected with Levauin, followed up by 500mg/day. The morning after the injection, my legs started aching as though I had run a marathon, particularly my shins, calves, ankles. Today, I woke up in more pain than before and am starting to notice knots in my shins. Every step is becoming more painful than the next, and I don't know how to fix this. I stopped taking Levaquin yesterday, but this problem keeps getting worse. Has anyone else had this experience, and when do the knots go away and the pain cease? Thanks for any info.

My daughter has been on prednisone since October, 2006 -today is July 25, 2007. She is a 35 years old with asthma and allergies. Originally the pulmonologist thought she had ABPA (Allergic Bronchio Pulmonary Aspergelosis) and put her on 60 mg daily. This year has been a nightmare for her. That original diagnosis apparently was erronous, but she was kept on the high dose for breathing issues, with instructions to lower it as she could. As of today she is on 30 mg. daily. Side effects? So you know she is no "loser", she is a PhD in Biomechanical Engineering, has two patents to her credit, has spoken at numerous medical conferences (for vascular surgeons and cardiologists), and has had countless articles published in medical journals. Now she can't concentrate much less sit still, has not read a book in months (she used to read at least one book every week), she has two research publications that need to be finished but she can't focus on the work, is totally exhausted and needs to rest after only a couple of hours of mild activity, has a face she has described as looking like a mongoloid. Her beautiful, big, blue eyes are slits in her face. Clothes that fit yesterday wouldn't fit today - and those that fit today won't fit tomorrow. She craves food in the middle of the night and said she usually eats 2 bowls of cereal. She has terrible pain in her torso. Her esophagus has become so eroded she is on 6 different meds for that, and as a result cannot eat salads or raw fruits or anything that might irritate the lining of the esophagus. Her body is covered with huge dark bruises. The latest side effect made evident happened this past Saturday night. She fell striking her shins on a carpeted step. Her skin has become so thin that it actually burst open. She said it reminded her of when we'd blanch tomatoes in boiling water to peel them, and how the tomato skin would just burst open. That's how her leg was. That little fall cost a trip to the ER for stitches, tetanus shot, and antibiotics. Her husband is a career military, so since they married 1 1/2 years ago she's lived in 4 states, there's not much history among doctors. She lives now in Kansas and has started seeing specialists through the university there. We just wish she could go to Mayo Clinic for complete evaluation, but unfortunately military insurance doesn't seem to cover the best.

having night sweats and leg pain