Ankles symptoms and conditions

I was given a Rx for Levaquin on Dec 17th (5 day dose). I started it on the 17th. By Saturday the 20th, I wasn't feeling good at all, my ankles, knees, hips, elbows, wrists and finger joints hurt. I only had one dose left so stupid me, I took it.

I have had pain ever since. I had read the sheet you get from the drugstore when I had the Rx filled. I remembered something about possible joint pain but didn't think much about it until the pain didn't go away after I stopped taking the drug.

Wednesday the 24th, I looked Levaquin up on an internet drug site and looked at the side effect list again. That is when I realized that the pain I was having was under the "notify your doctor" category. Their office was closed until the 29th. I tried to call the 29th but the phone was always busy. I finally got through today and told them my symptoms and told them to put in my chart to not give me that drug again. The nurse called back to say that they put it in my chart and to take otc stuff for the pain.
I have been taking Advil and a combination pill of glucosamine and condroitin (those are probably not spelled correctly - sorry). I am better but still not 100%.

Today is the 31st and my last dose of Levaquin was Dec 21. I am down to knee pain and a puffy feeling (not really swollen externally but feels swollen internally), left shoulder pain (worse in the morning when I wake up), my hips hurt off and on and my ankles hurt off and on. I am concerned about one of my ankles because I already have a haglund deformaty there so there is already damage to the area.

When I try to get out of a chair, I feel like I am 90 (I am only 49). I really hope this gets better soon. I haven't heard anything about a law suit or anyone who has a way to speed the recovery. Please, let me know if anyone knows how to help this get better faster.

Have stopped taking Zocor today after finally accepting that my life has changed since taking this medication....am too weak to open a soda bottle, keep twisting words, memory is shot, Hips, knees and ankles scream whenever I have been sitting for more than 15 minutes....light headed, dizzy and constant headache...want to just curl up in a ball and cover my head for loss of ambition. I am exhausted all of the time.

Today is Christmas day 2008. And a Merry Christmas to me ha!!!!!!!! I was given a prescription for the drug Levaquin on the 19th of December for a suspicion of pneumonia. The x rays done at the hospital found no evidence of pneumonia but my doctor wanted me to take it anyway because since I have asthma and my lungs sounded so bad I was told that I was at risk for developing any secondary infection that was out there. My husband filled the prescription on the 20th which was Saturday, took the first one of a seven day supply 500 mg tablets. About 4 hours after taking just one pill was awakened by severe and agonizing pain in both of my feet and my knees that I was writhing in pain. Since I have nerve damage in my feet anyhow I know what the pain that I normally experience feels like and instantly knew that this was not normal for me. When I thought that I finally might be able to walk I hobbled into the kitchen and dug the list of side affects out of the garbage (stupid me had not read them first.) I discovered that it was one of the side affects. Called the on call doctor in the morning since it was on the weekend and he stopped it immediately and put me on something else. I only took that one pill and since Saturday night every night I wake up in agonizing knee pain and I have never had pains in my knees before. The pain is so bad that I feel like I am ready to go on a morphine drip, or cut my legs off above the knees. Six days now from one pill, how much longer can this go on? I really feel bad for the people that contined to trust their doctors and continued with the full course of the medication and I realize that what I am experiencing is minor compared to what others are going through. This drug should come with a handout that says: Take this drug at a risk to your health!!!!!! Last night the pain lasted all night and I cried all night. Have to get through this day am entertaining for the holiday and have had no sleep. Actually getting afraid to go to sleep at this point.............D.

Extreme fatigue, inability to eat, terror attacks, and a tendon rupture. These were just some of my side effects. It has been 2 yrs and although I am recovering (ever so slowly) I have some PERMANENT damage that I am living with. The tendon was repaired surgically but my arms are in daily pain and it's not the "take an aspirin and sit with a heating pad" kind of pain. It pretty much makes my arms useless. I also have problems with knees and ankles too. I never imagined this would happen given how fit I was at 46. Now at 48 I like to remember how I used to be.

Why in the world would anyone suggest "just take it with lots of water" or "be sure to take it on a full stomach" or "after it's out of your system you will be ok"??? How condescending and inconsiderate. It is NOT worth the risk. Please don't take the chance. I only hope my suffering can help someone else.

This stuff is poison. It's not "like a poison", it is a poison. I'm sure it does kil lots of bad things..... along with way too many good things. I am not left to suffer the long term effects and it is not fun.

I have been having difficulty with my legs from the knees down since taking Remeron for over a year. Normal walking is a chore, but let me get in a department or grocery store and I am in such agony with leg pain from the knee to my ankles. It is a heavy, throbbing ache. Pain pills, heat and sleep is the only cure. Never had this problem before this. If I ween myself off them, my migraines come back with a vengence.

I've been on NuvaRing for 3-4 months now. Before using the ring I'd tried the pill, which made me horribly sick, and the patch, which gave me rashes and clots. My doctor recommended the ring and raved about it (as they all do) so I figured I'd give it a shot. The first month was fine. But since the second month I've experienced the following: dizziness, nausea, migraines, increased discharge (so much so I have to wear pantiliners EVERY day) swelling in my ankles, weight gain, and decreased sex drive...wait, let me correct that-no sex drive.
Im so jumpy and irritable my boyfriend is scared to try to touch me or say the wrong thing. I'm not sure what to do. I need to use some type of birth control and I don't trust just condoms alone but I'm scared this damn thing is going to kill me.

I am a 64 yr. old female that just started using Meloxicam on 10-24-08. I am having swelling in my legs, ankles, and feet. Also, I'm tired and fatigued all the time. Called my druggist and he said to stop using it. I will call my doctor on Monday and see what he says.

Since having a Lupron shot three weeks ago,my ankles and feet are swollen,has anyone else experienced this?

On 7-15-08 I had a total abdominal hysterectomy and was given Levaquin thru IV while I was in the hospital.3 weeks to the day later I had a abscess next to my bowel that had to be removed and again was given Levaquin thru IV while I was in the hospital,both times I got very sick right after I was given Levaquin and when I was discharged on the 2nd.trip I was sent home with Levaquin 500mg pills.After taking 2 of the Levaquin pills I again was so sick and could not keep anything down so I called my DR.and explained to him what was going on and I was told I had to keep taking the Levaquin.After a few more days had passed I went into the office to see the DR.and again told him how sick I was and that I was unable to go to sleep,again I was told to continue the Levaquin and that my hormones were out of balance and that was why I was unable to go to sleep.On 9-2-08 I finally went back to work after being off for 7 weeks. I still was suffering from insomnia and was only getting 2-3 hours of sleep a night but was feeling better.On 9-30-08 I had a follow up with my primary care DR.my blood pressure was 211/160 and my pulse was 177 and also had a bad cough with wheezing and was sent straight to the ER.I was admitted and for the next 6 days was given Levaquin thru IV and the more I got the sicker I was to a point I thought I was dying.I ended up with a rash all over my face and finally on day 7 a Lung DR.came into the room and took one look at me and said "oh my god,we have to take you off of that antibiotic")
I was sent home on day 8 and after being home for 3 days all of the Tendons in both legs,ankles,arms,hands and right shoulder were inflamed to a point where the DR.was afraid that they were going to rapture so I was on complete bed rest for 3 weeks.I am now suffering from both ankles swelled and ache all the time along with all of the minerals in my body have completely bottomed out along with the calcium and potassium and also now I have several inflammatory markers in my blood and have to go see a Rheumatology & Arthritis DR.My lungs have also been damaged from Levaquin and I am now using 3 different inhalers and I have never had a breathing problem previous to this.Now for those who have commented that we should have researched the drug before taking the meds in my case I was unable to do so being as though I was given it in the hospital ! I still have no idea how much damage I will be left with and what will be permanent.I will post again when I find out more on the damage that this drug has done to my 44 year old body.

I had a CT with Isoview in Sept 08, experienced flu-like symptoms that same day and for the following week. Developed pain in both legs about 2 inches above my ankles, had a urinalysis was told I have a UTI. Currently taking Nitrofurantoin. The leg pain went away for a couple of days, but is now back.

Ok here's my story with Prednisone. Let me first give you a little back ground info on me. Born with a VSD, that was repaired at 8 months of age, only after developing severe pneumonia. Was fine as a child growing up until at 18 i developed asthma. i am 29 now and have been on and off prednisone during that time. During that time however I have always been on a metered dosage pack that has always tapered usually within 5 days with no side effects.

Now lets talk present day with me. First off I went in back in early Sept. for what I thought was just a sinus infection, turns out my lungs were so tight, i was immediately put on 80 mg for 5 days straight, and you guessed it no tapering. Those 5 days were the worst five days of my life. I have SVT- taychcardia and the med made it worst, I was running around like I was on Speed or something. Also, I had started to urinate like crazy. Headaches, nausea, muscle pain as well as joint pain. i can not walk without feeling as though my knees, and ankles are going to break. Also, i am not as foccused as I usually am. Ever since that faithfully day in September I have been on this stuff. it has already been 2 months and im on 40mg now. And I cannot sleep at all at night and during the day now i crash once it seems like the prednisone starts wearing off. its horrible. I am going to go see the Pulmanologist Monday hopefully he will have some answers, and Im dreading him telling me i may have COPD, from a protien defiency(sorry for spelling, this med is messing with my thought process). Any who, i cant just stop taking it, i have been warned about that. something has to give or my body may give up.

hope this helps.

this med is good if used correctly but i agree Doctors need to fully warn patients before hand of all possible side effects.

I have been on Synthroid and Levothyroxine for 12 years (I am 34 years old). All of a sudden, I had very achy fingers which got much worse over the course of two weeks until I could barely move them. Then my ankles hurt. I mentioned it to a coworker who told me the same thing happened to her but when she switched to armour it went away. So I drove an hour across town to the only doctor who prescribes it, and now just a few days have passed, and my pain has nearly ceased. I thought I had rheumatoid arthritis. I'm so glad I my coworker shared her experience with me. That is why I am posting now.

What exactly do we need for a class action suit, guys?

Side effects: Severe disorientation as if very drunk (vertigo, dizziness, feeling "out-of-body" or high), hallucinations (including feeling things crawling on me), overwhelming fatigue (as if I hadn't slept for days), muscle soreness (as if I'd exercised for hours), joint and tendon pain (especially in hands, wrists and ankles), insomnia, nausea (lost 8lbs in a few days), racing heartbeat, dehydration, ringing in ears, stomach cramps, yeast infection and spotting.

The drug immediately made me sick but I thought it was just the sinus infection, and unfortunately kept on taking it. The side effects were actually worse AFTER I stopped taking it (I got much worse before I got better).

If you're on this stuff, STOP IMMEDIATELY. If you're scared and experiencing side effects as I did, PLEASE KNOW that they are real (you're not imagining things) but they WILL go away. Listen to your body, rest as much as you can, and drink plenty (and I mean PLENTY) of fluids. Despite the nausea, eat SOMETHING (toast, bananas, applesauce).

This is a 24-hour drug, so (verified by my pharmacist) due to its half life, it takes a MINIMUM of four days to leave your system. I only started feeling non-drugged a full 7 days after I stopped taking it. The fatigue lingered (kind of like getting over the worst bout of flu EVER) but now it's slowly going away, too. This stuff was an overwhelming blow to my physical health (I've NEVER been this sick), but I'm getting better. YOU WILL, TOO!

I had an injection into a Bursae about a week and a half ago. My face was hot and bright red for about three days, if i went out in the sun it made it worst almost like i was allergic to the sun. I have had headaches daily, since. Vicodin will not help these headaches, my heartburn was so bad i stopped taking all medicines, birth control, antibiotic, pain meds. My stomach hurt so bad the second night that i could not make a sudden movement. and i couldn't stand straight up. i have been so nauseated, ive thrown up twice, once i was taking a sip of milk to get rid of the side effects and as soon as i swallowed i puked, the second time i just smelled something. i have been bouncing around in the bed all night. and so depressed i need to be committed. my head has hurt so bad many days i don't want to hear my one and a half yr old speak. but i am stay at home mom and i have to do what i have to do. i had told my doctor that i had these effects, but another physician treated me. i told him and he assured me it would be a very small amount. also a my ankles hurt especially, feel like they are gonna snap, as well as all my other joints when i come off of these. someone email me plz *******

I have Autoimmune Hemolytic Anemia (AIHA), was diagnosed in Feb. 2008. Have been ill for several years and finally it came to a head in Feb. I had a blood transfusion and then in the hospital 6 days later with a hgb of 4.0. I was so toxic and my blood so screwed up I nearly died. I was given another transfusion then (total of 5 pints of packed red blood cells) and started on Prednisone. For 3 days given liquid Pred injections, starting at 1000mg, tapering down to 250mg., then on the pill form at 100mg. Sweat poured off of me dosing down. I was off work for 2 months. I am still tapering but am now at 1mg. DR. added another drug, Danazol, after getting to about 10mg because my blood started going crazy again. My side affects with Prednisone have been, Euphoria, no depression, LOTS of hyper brain activity, thoughts running a 100 miles an hour but body at slow speed.Visual problems and a feeling of being highly drugged. 2 to 3 hours of sleep each night, compulsive behaviors and a lot of pacing back and forth. Couldn't hold my concentration because my mind wandered so much. Extreme Tremors in my back, hands and head. Wanted to talk constantly, if no one was around I talked to my Chihuahua or the TV. My cheeks puffed up and became hard and had a fat pocket puffed up on left side of my neck. My dog thought I was crazy, she was tired of the lights being on at 3 or 4 in the morning. Legs looked skinny but didn't gain weight until I got to about 60mg. Gained 25 lbs total. Tapering caused bad spasms in my calves, feet and hands. Thigh muscles would get extremely weak each time I went down a dose. At 50mg I started getting sleepy and could hardly stay awake. Went back to work at 35mg and couldn't remember how to sign on to my computer. Some memory problems since I was in the hospital, couldn't remember how to spell words I knew as a young girl. Started having hip pain about 3 months into the Pred, that hasn't stopped. At 10mg feet, knees, shoulders hurt deep in the sockets, muscles below my neck knot up, may take a while to totally get off this. Read on a couple of blogs where people cut a 1mg tab into 4 pieces to taper off the Pred. because of side effects. Had thrush in the beginning and break outs of shingles. I hope to God I never have to get back on this drug again, it is so HARD on the body but it did do what it was given for, to repress my immune systems. My next step is Spleen surgery, hope this is a cure for me, am sick and tired of being sick and tired. Wouldn't advise anyone to take Pred unless it's a life or death situation. It's prescribed too liberally and people have multiple problems, worse than I have experienced. I've probably forgotten some things, but there's enough I've mentioned to give you an Idea it's not good, but if Pred is all you have then you do what you gotta do!! My puffy cheeks have went down though, now my hair has become curly but at least I have hair and my chihuahua stills loves me!!!

Can Fosamx D 70 mg be the cause of Ecchymosis Petechiae, I have developed what looks like an "under the skin" rash, on the ankles and upward on the leg, sometimes dark and also gets lighter, Doctor is doing blood work now, concerned about my platelets, it is possible there is no relation to Fosamax, but I am curious if anyone else has had this symptom. Thank you, dalecjim

i have been taking lotrel for a year and i have swollen hand,feet and ankles, terrible ringing in the ears, as most of the side-effects i have that anxious feeling but i just couldn't put my finger on what that was. i have so many headaches throughout the day. and my doctor really has no answer, but to give another medicine,and i end up with several more side-effects!

I have a 4yr old boy who has been on singulair for 5 months. Before he began singulair he was the most happy, kind, gentle, loving boy. We had an awesome close relationship. I enjoyed just sitting there watching him play. I could not wait for him to learn something new, but EVERYTHING has changed now. I took him off of singulair on Sept 19, 2008 after accidentally running into this site while looking up children and OCD. Thank God I did. It has been 12 days since I found this and took him off. I couldn't type then because I was to upset. My son who never had ANY mental problems or anxiety is now completely riddled with it. Instead of playing all day care free like 4yr old are supposed to do, my son spends his days now clinging to me in fear that I may leave or go into a room without him and he will not be there to open the door. He obsessively has to open every door now. He spends his days getting upset at the smallest things. He now gets mad at everything I say, or I don't say it right. Our relationship is not the same now, and I am devastated. Before Singulair he slept through the night every night. Now he wakes up every couple of hours to go to the bathroom and say "are you still there mom?" ok "I love you" "Don't let the bed bugs bite" I have to answer "I love you to" and "you either" If anything different is said he will go nuts, and he will obsessively say this over and over and over again. This is not my son. He is a totally different person. I am so very scared that this poison has permanently ruined him. I mean he is so young and his brain is developing. It has been developing with this poison in it, that has ruined him. It has been 12 days and he is still doing the same ocd stuff. He still seems really agitated. His muscles hurt, his tummy hurts, his eyes hurt, his ankles hurt, and he has diarrhea. My beautiful boy is now mentally and physically SICK because of singulair. I feel really bad to, because I did not know at first that the singulair was causing this and I was always getting on to him for his behavior and putting him in his room. At pre-school a couple of days after first giving singulair to him he started crying ALL DAY at school, and I made him stay there because I thought it was just because he had gotten a new teacher and he needed to get used to her. I feel terrible!! Does anyone know if the ocd will go away or has he now learned the behavior?

I had bronchitis (being an asthma sufferer, during a bad cold this is expected). I went to my doctor, who handed me 5 days worth od samples of Avelox (400mg). Approximately 1 hour after my first dose I started shaking, feeling dizzy and nervous, had an upset stomach and abdominal pain and was itching on my knees, wrists, ankles, legs, elbows, arms and neck. I called my doctor who told me it was a mild side effect and to continue taking it. So, I did. Considering that I had been out of work with bronchitis and lacked the time to start a new antibiotic, I decided to listen to my doctor. The side effects intensified. I have now been off of Avelox (which I will NEVER take again) for 4 days and I am still not side effect free. They have definitely lessened, but not completely gone away.

This is a HORRIBLE antibiotic. I implore all who read this...do not take Avelox. Get amoxicillin, Ceclor,, Erythromycin... anything else will do just as good a job without side effects.

I am a healthy female with little to no history of adverse reactions to medications. I was prescribed a 10 day dose of Levequin (500 mg) for a minor but stubborn skin abscess. After the third day, I woke up with significant joint soreness in my fingers. Progressively the soreness spread daily to my wrists, elbows, ankles, knees, hips, etc. I did not suspect the antibiotic at first, but I know my body, and I know something was WRONG.
After my 8th dose I decided to look online...it is at least good to know that what I'm experiencing is definitely from Levequin. Thank you all for sharing your stories.

I especially found MERCEDESLANE posting on April 15th interesting. I guess this person works in the health care system. Considering this uncompassionate individual, who apparently wants everythone to know he has a Mercedes, can't spell (whine), and does not have basic grammar skills. Wow...my faith in the our health care system is stronger than ever. But what do I know, I'm just an "IDIOT" with shingles that needs to have a couple of glasses of whine while I pop my remaining Levequin.

My daughter, 21yo, took prednisone off/on for 4 months, both oral and IV form, with the highest dose of 90mg over a two week period. The risk of bone death (Osteonecrosis, aka Avascular Necrosis) is not disclosed as a risk and 7,000 people a year get this from steroids! They gloss it over under the guise of "bone pain" or "bone fracture" near the osteoporosis risk so you think that by taking calcium and vit D supplements you're protected. What's really going on here is that the steroids cause the bone to die so if you have pain, PLEASE INSIST on an MRI because a regular x-ray will not show ON until it's in the advanced stages..and then you'll most certainly need joint replacement.
I'm not making light of the weight gain, or loss of hair or any of the myriad of other side effects that come with this drug, but when you're told that the joints in your body are dead...and that they'll eventually become brittle and break and cause so much pain it is often compared to bone cancer, then you'll really want to sue someone. But, I've tried that...it doesn't work. Because the drug is FDA approved...the manufacturer can't be held liable.

My daughter has ON in her right shoulder, both elbows, both wrists, both knees, and both ankles. She's considered "collateral damage" by the medical/legal communities because Prednisone is the "gold standard." This disease is a slow progressing disease which is often found as late as 10 years after stopping the steroid treatment. If you find it early enough, some surgical options exist to prevent the collapse of your bones, so if you have joint pain...PLEASE investigate with an MRI

I was on topamax for about 2 years. I took it for frequent migraines caused by my sinus's. I had all the normal side affects but got used to it after awhile. The only one i didn't get used to was the hair loss. During this time I started allergy injections and now i'm up to my maintenance level. So i decided to ween myself slowly off the topamax. I have been off for about 2 months now and I have been fine on the headache side, but i have started to get other symptoms (i think withdrawal symptoms). They have progressively gotten higher in number as the days go by. First my hair loss has not stopped. I gained about 10-15lbs, I am edgy and climbing the walls all day. I have a really hard time relaxing. I recently developed horrible insomnia, and about a week ago i started having digestive problems including water retention, bloating, gas, irregular bowl movements, and acid reflux. And I've recently had bouts of tightness in my chest and throat which make it difficult to breath (lasts about an hour). I didn't have any of these symptoms while i was on the topamax (except the hair loss), nor did I have them before it.
I am seeing an endocrinologist in a few weeks to make sure nothing on that front is causing any of this, but i really feel it's from taking and going off the topamax. If you can find other ways to deal with your migraines, DO!

I have Crohns and had a flare up so I'm back on 40mg of Prednisone. I've been on 40mg now for 3 weeks and I start to tapper off in another 3 weeks. Well every time I start the prednisone again I get new side effects. This time, my gum are bleeding all the time and the pain in my knees are horrible! I still get the regular side effects, ie: Mood swings, joint pain, sleeplessness, sweating, swelling of my legs and hands, wanting to eat everything under the sun, moon face and my hair falls out! I wish the drug manufactures could develop a drug that would not be so hard on our bodies. I have to struggle with the pros and cons with every flare up. Do I want the weight gain, mood swings and hair loss or do I want to look good and be very sick! I'm 37 and was 16 when I found out I had Crohns.

I was prescribed 7 days 750mg of Levaquin on 9/10 and finished 9/16. I was originally diagnosed with bronchitis but went back to the Dr. yesterday cause I was not doing any better and he now says it's viral. I've gone to the hospital because I passed out on 9/13 and continue to faint at least once a day. I have tingling/numbness in my hands, ankles, toes, my knees hurt, my lower back is in a lot of pain, almost to where it is not tolerable, I'm dehydrated (I'm drinking and eating, just not as much) it is extremely painful to eat, my tongue and my gums hurt terribly. Last night I had a horrible dream (I don't dream usually, not nightmares) and today I started to hallucinate (mildly) A week ago I was functioning normally, a mother of 3, playing with my kids and now I can hardly walk without assistance, I can't go to work, I'm in constant pain. Someone please give me some kind of guidance. Will these feelings ever go away? What should I do? Thank you!!!!

I was on Lisinopril for about 3 1/2 months. I coughed the entire time-day & night. I coughed until I vomited almost daily. I had diarrhea, severe muscle cramps in my sides and toes. The coughing was HORRIBLE and I really thougth it was going to kill me. I saw a new doctor who told me Lisinopril is notorious for causing coughs. My first doctor told me to take Mucinex. He is a moron. Thank God I changed doctors. It took an additional 16-17 days for the cough to subside once I stopped taking Lisinopril. Now I am taking Norvasc 10MG. It makes my ankles swell. Not thrilled with it but I could not cough another day.