Hips symptoms and conditions

I was given Levaquin for a UTI about 2 years ago and ended up in the ER, the side effects were so bad. Thought I was having a allergic reaction,
heart poundings, felt like a just drank 3 cups of coffee, also muscles reacting slowly, like I couldn't move my arms and legs how I wanted to.
Unfortunately I have take Cipro a couple times in the last year, and the last dosage of that did it for me. On the 5th day I all of a sudden had extreme pain in my left knee, could hardly walk. I took a couple Advil and rubbed some icee stuff on it and it went away but that night my lower back and hips became also extremely painful. Severe pain. That was the last dose for me. (The pain was much less the next day and almost completely gone after about 4 days.) I called the Dr. and they told me to stop taking Cipro- which I had already done. What really bothers me though is I mentioned this to my orthopedic Dr. and he said he never heard of Cipro causing joint pain!
I am going to send him some literature, but wow!! couldn't believe that.

I was prescribed Pravachol after experiencing a reaction to Zocor. In hind sight, this was probably the worst thing my doctor could have done to me. Only weeks on the Pravachol I began to experience lower back and hip pain. I blamed it on my mattress! Then one morning I went to roll over in the bed and pain shot through me up to my head. My hips were frozen the pain was unbearable. I cried and my husband got some old crutches from the garage. I needed help getting to and from the bathroom. He left for work and left me with the heating pad and Ibuprofen. I realized that this was extremely similar to the knee and leg pain I'd experienced on Zocor only to a much more significant degree and much more painful. I immediately stopped the Pravachol and a week later began to see improvement. Within two to three weeks I recovered to a degree of functionality. My doctor actually pushed me to try the Pravocol again! I got a new doctor instead. Turns out my cholesterol isn't even that bad!! I'm furious for the long term damage done to me and furious at a system that would put people through this knowing what it does!

hi there i have been on simvastatin about a year now and have felt so ill since taking them i am now due to have several blood test to see what they can find " as i suffer with nausea, pains in my legs and body /and terrible depression and i cant remember me feeling like this before i started taking these tablets i really don't feel like me no more / and i can easily sit down and cry because off feeling like i do / now i have been told to take double dose because my cholesterol is higher / i have spoke to others of these tablets and they have had same reaction so i have decided on my own thoughts to stop i will tell my doctor.and i am hoping i will get back to my old self i will try and keep my cholesterol in control and i think its well worth a try than to have all these side affects B.

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'm 18 years old and live in Florida, while at the gynecologist for a routine visit my doctor strongly suggested that I start the Gardasil 3 shot cycle. After checking with my mom (who was unfortunately given biased information from my doctor without first doing research on the product) agreed since we both figured that my doctor would be knowledgeable enough on the subject (or you would think since she was the one administering the drug.) The first two shots went fine and I had no reaction at all. After the third shot (in October of 2007) I woke up the next morning with swollen hands and extreme swelling at the injection spot. I immediately returned to my gynecologist where I was told “there is no possible way you can be allergic to this medication” by my doctor, and that those reactions would go away in a few days. A few days following this I developed sores in the back of my throat and under my tongue, however my gynecologist still insisted there was no possible way it was an effect of the Gardasil (EVEN THOUGH IT WAS THE VERY NEXT DAY) & I had no previous illnesses. Within the week following I developed body-wide hives so severe that I cannot sleep and they affect my breathing. I’ve seen several doctors (allergist, dermatologist, primary physicians, and immunologists) none of which can determine why exactly I have these hives, besides that it is a “drug reaction” (it took 11 vials of blood to determine that). However when one of my dermatologists questioned Merck about it they simply said that there is no evidence and I cannot sew!!! That’s all they cared about! A law suit! WHAT EVER YOU DO, DO NOT GET THIS SHOT, TELL EVERYONE YOU KNOW! It has ruined my life. As an 18 year old girl living in Florida I love to go to the beach however because of these hives they get so severe when I’m exposed to sunlight I can no longer go. It’s also extremely embarrassing when people stare at them since they cover most of my body on a daily basis.

I was given a prescription for Trazodone four days ago beginning with a 150mg dose. I have a very long history of getting by on three to four hours of sleep and was constantly tired. That first dose really knocked me for a loop the next morning. When I first stood up after the alarm went off I was spacey, groggy, unsteady on my feet, joint pain in my knees and hips, and slight pain in the muscles of my legs. It was a full three hours before I felt somewhat better although I felt unsteady on my feet and when I walked, I walked as though I had a hangover. I decided to only take 75mg tab the second night. I slept twelve hours. When I awoke the above mentioned symptoms were still there but were much, much lest in intensity. The third night I took 50 mg. I slept nine hours and when I awoke the symptom were really minimal and felt quite normal after an hour or so.

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.

I'm 42 and have 2 children. I had Mirena fitted end April 08 after a recommendation from a friend. A month later I noticed joint pain in my left thumb which over the weeks and months spread to all my fingers, then my hips and finally general stiffness all over. I was training for a 5K at the time and just put this down to post running achiness. I didn't initially connect this to Mirena, I just worried that I was showing signs of arthritis and went to see my GP. No mention of Mirena from her but she just did some tests to see if it could be viral or some form of rheumatism. All results came back negative which was a relief but nothing more was suggested as to why I was having these problems. (which for someone who rarely visits a doctor made me feel as if I was going mad and imagining things) It didn't improve - I was also getting palpitations from time to time so after googling mirena and joint pain I was surprised (and a bit relieved) to find many blogs about this problem, mainly in the US (I live in the UK). Went back to doctor at local family planning clinic who told me yes mirena could cause some arthritic symptoms but she was noticeably reluctant to concede that this was causing my problems. I was urged to keep the Mirena and see a rheumatologist first.

I got the distinct impression that the professionals I spoke to are going to extreme lengths not to say for certain that this device can cause serious and debilitating arthritic pain in many cases.

I have an appointment to see a rheumatologist and I decided to have the mirena removed 5 days ago. I'm hoping the joint pain will go. But am worried this IUS may have triggered something in my system that may not go away.

I've had Mirena for almost 2 years. I am bloated and fatigued. My joints hurt, especially my hips. I've gained 5 pounds and cannot lose it, even working out 7 days a week. I workout regularly but not with the stamina I used to have. I am 39 and in great shape. I can't make it through my classes the way I used. I struggle and it's very depressing. For the past few months my sex drive is zero. I am considering having it removed. Was it extremely painful?

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 am was diagnosed with Hyperthyroidism about 2 years ago. I took the radiation treatment and was placed on Synthroid. Every 4 weeks the dosage was adjusted until my Dr doc determined 0.125mcg worked best for me. Well, at the time I was diagnosed I weighted about 150 pounds. Two years later I am at 180. I'm 5'8 so my doctor(s) tell me my weight is in portion to my height. Well, the extra weight is centered around my stomach and hips, I am extremely fatigued and lethargic, I have brain fog and would like to exercise but I'm just too tired. I heard about Armour but from reading some of the other experiences, it doesn't appear to be the 'cure all' solution either.

I have had my kenalog shot last April '08 for allergy relief. After a few months, I have noticed an indention and discoloration where the needle was injected; it is an ugly sight. After reading this article, I could assume that my menstrual irregularity, my period would come twice a month, was also another side affect of Kenalog.
Just like a lot of you, I would be interested in a class action against Kenalog, pls contact me.

Have been taking Diovan HCT for 2 1/2 years increasing dosage to 320 mg. Good control of blood pressure, but have developed severe pain in low back and hips, with pain, numbness of feet and legs when walking. In fact unable to walk more than 3 blocks without legs and feet going completely numb, sore and stiff to the point of stumbling and falling. Told Doctor about it 3 months ago and he suspected PAD, for which I was tested. The good news is that those test results came back negative. Doctor doesn't think Diovan can be the cause of my symptoms, so I made an executive decision and stopped Diovan 2 days ago and after "withdrawal" headache first day, have noticed marked improvement in hip and low back pain. Feet no longer go numb, but am still having some discomfort in calves.

I am a 43 year old male in good health that decided to get off lipitor about 3 days ago due to the advice of my physician. I have been on it for 3 years at 20 mg daily. I am an avid runner completing 3 marathons in the last 4years, but lately haven't been able to run more than a mile or so without feeling tightness in my abs, legs, hips, and most recently my hands and elbows have mild to moderate pain. I've been noticing this over the past few months or so. I always thought it was due to over training, but I am convinced these are not normal muscle soreness/strain and I am eager to share my results as to how I feel in a few weeks/months. Today, which is day 3 without the drug, I have INCREASED pain in my hand, and an overall fatigue feeling. Has anyone else noticed this upon stopping the drug? God help all of us. This can't be doing mankind any good other than making the drug companies rich, and unfortunately, most physicians believe that these statins are wonder drugs, and prescribe them like candy.

I am a 51 y/o white female that has been on Lipitor for 2 years. I am 5' 1" and when I had to go on it my cholesterol was 267 I weighed 112 lbs. I was shocked.... my doctor told me weight had nothing to do with cholesterol. She kept a close watch on me and my cholesterol came down...... and then my ex-husband of 17 years and I re-connected and got back together and I moved so I had to get another primary care physician. I took all my meds to her, she also kept a close watch on everything. At this time my cholesterol is down to 109 and I asked if I could stop taking it, as I take quite a lot of meds, due to different things and if I could stop anything it would be great, but she said it I stopped it, my cholesterol would go right back up. So since I am not experiencing any side effects I'm okay with continuing it.

I surely hate to hear what you all are experiencing with your Lipitor..... could your doc try another cholesterol medication?

The only one of my meds that is giving me any problem is TOPAMAX........ that we are using as a Migraine preventative! HORRORS!!! Today is pretty good day. But my cognitive abilities are in the trash... I say the wrong word when I mean something else...... I search my mind looking for a memory...... I am also on disability since 2002 because of the Migraines....... I have has them since 1978, but they got progressively worse over the years until I was sick more days per week, sometimes more than 7-10 days at the time, having to be in the hospital being rehydrated and on IV pain meds.......... and as awful as the TOPAMAX is.....it has been reduced the migraines to approx 2 per month and they do not last nearly as long.

So sorry, I got waaay off topic, but I know that it is not the Lipitor that is giving me the side effects as it the last med I had to go on and I had no new side effects....... but that TOPAMAX is kicking my behind.

Was previously on Micardis HCT; dr. switched to generic Lisinopril HCTZ 12.5 in 11/07 when I went on Medicare & was concerned about cost of Micardis. Since that time I've put on 10 lbs. and had increased pain/muscle fatigue and general lethargy. Unusual, as I've exercised 4-5 days per wk. (incl. aerobics/strength trng/flexibility.) for 20+ yrs. Also, frequently, have problems swallowing pills due to feeling of obstruction in esaphogus tube. In July '08 I awakened to slight numbness/tingling in lips and my lips then proceeded to the swell to the point of pain and my lips (in profile) protruded further than my nose. I received steroid injection and prescription for steroid pack. Diagnosis was possible allergic reaction to new cosmetic product. Today (9/3/08) I woke up with the same symptoms and again had to go to the dr.for a steroid injection & meds. Diagnosis this time (different dr.) was possible side effects of "blood pressure meds." Has anyone else experienced edema of the lips, wt. gain, and problems swallowing?

I've been taking Fosamax once a week for about 4 months. During that time what began-before taking Fosamax-as mild pain in my lower back-has gotten progressively worse. This is the only negative possible symptom I’ve experienced, but of late it has increased and spread to my hips. I decided to stop taking it today, and see if it makes any difference. If it does, I will post another reply here with details.

I think all reading these personal accounts should consider this: obviously many medical professionals see far more benefit than loss in the majority of users. My osteoporosis was only diagnosed via a bone scan 6 months ago. -2.5 The increased pain and worsening conditions in my back might in fact be much worse if I hadn’t started taking the Fosamax. One must beware of apophenia setting in with self diagnosis.

Most posting here already had serious medical needs to have Fosamax prescribed in the first place, given a small percentage of diagnostic errors. Most of the conditions I’ve seen described vary greatly, and without a serious study are purely antidotal. I suspect there are legitimate adverse reactions, but for now the percentage and severity remains a big unknown. There seem to be some activists here, so get a campaign going for publicly funded analysis of the now considerable amount of data on file.

If my back gets better, I’ll still be unsure as it might have been a delayed benefit from the drug. Likely I will take Fosamax again either way. If it doesn’t improve in several months I’ll assume F-max wasn’t the cause and begin taking it again. If it gets better, I will take F-max again to see if the problems return when I do. If they don’t I’ll keep taking it. If they do, that will red-line my ‘coincidence meter’ and I’ll never touch the stuff again.

I hope some will find my approach to our common dilemma helpful. We all have to be our own advocates within the modern health care cabal. I worry about the old adage that when we do so, we have a fool for a client. Feel free to criticize my reasoning, and thanks to all the others that took the time to share your experience. It helped me make my decision, and I’ll share the results in about 6 months.

Hi, I am a 57 year old female who was just recently put on Fosamax to counteract the bone loss caused by Femera that I am taking to keep my breast cancer from coming back. The first two weeks I felt okay albeit I did have stomach ache for two days and loose bowels. Then the bone pain began and I mean pain, not light, not moderate as the labels say, and it was especially severe at night. I found myself also feeling dizzy, depressed, no energy, kinda weird. I couldn't have relations with my husband because my hips and pelvis were so painful, also my neck, lower back and legs. Not fun. I took myself off it....Bone pain subsiding..also gastric upsets were getting worse. I tend toward gastritis and have IBS so this drug did not agree with me. I hate it! Will not go on any of these again, as I have also had lots of jaw problems in the past, and dental problems and DO NOT WANT that horrible jaw thing to happen. Yike... Love Pam

I have had trouble with eczema/psoriasis for several years and it has spread to most of my body. Hands, arms, elbows, back, chest and stomach, hips, back-side of my thighs, knees, bottoms of my feet, scalp, inside my ears, forehead, what haven't I mentioned? So far, Prednisone is the only medication I can take that clears it up. Trouble is, the doc won't let me take it long enough to completely clear the rash before I'm tapered off. After reading some of the other posts, I've got to say that I've never noticed any adverse reaction. My appetite is up a little, but my energy level is also up and I burn off any extra calories. I sleep better (no itching) and for longer periods, wake feeling better, have a better outlook for the day and am ready to go. I'm a salesman, so my mental attitude is important, and my wife and family all agree that I'm less moody and in a generally better frame of mind while taking Prednisone. I've noticed no stomach or bowel distress except for being a little less regular than normal. But no constipation and no diarrhea. I'm 61 so a few muscular aches and pains and joint stiffness are to be expected, but I've noticed no unusual incidents. While I don't advocate taking large doses (define large doses???) for long periods, I've read that taking Prednisone on an every-other-day basis can be effective while greatly reducing the risk of side-effects. I think Prednisone has been a real "miracle drug" for me and just wish there was something as effective without the side-effects.

Update on my post of Aug. 11th. I did see a neurologist who was a bit skeptical, but after looking it up did acknowledge that this drug can cause tendon ruptures, etc. Later that week he did a nerve conduction study, both the one with the needles and the one where they shock the muscles. He was happy to report that I did not have any "nerve" damage. I had already told him that I did not think I had neuropathy as the numbness had gone away and was just replaced by the constant pain in my joints, etc. I then went to see my rheumatologist who was also just as skeptical that the drug could be causing all the pain I was describing. She said she had had three patients with tendon ruptures, but nothing else. I really don't care what she believes, and I told her so. I know what happened and what horrible pain I have been in ever since. I hate to report that the pain in my feet, knees, hands, hips, back and now my neck are not any better. My insomnia is some better, but I am taking more Lyrica. I tried a different antibiotic yesterday for the sinus infection called Clindamycin. OMG! I took one pill and within a few minutes had unbelievable heartburn. That lasted for 12 hours, along with reflux, burping, weird stomach noises. Now, I can't take that. Doctor called in a prescription for Augmentin this morning. Afraid to try anything now, but guess I will give it a shot. Is anyone getting any better from their joint or muscle pain? Some encourgement would be good. Thanks.

I've been taking Levaquin for about 3 weeks. Last week, suddenly, every joint in my body started aching. I mean from my neck, hands, hips, knees, ankles, feet, everything. For the past week, when I wake up, I can't even make a fist without experiencing excruciating pain. I've always been very active, running, basketball, soccer, skiing, you name it, so this is scaring the heck out of me. I'm 47 years old, and up until a week ago, I was hiking with my family, running everyday with my dog. Now I feel like I'm 100 years old. It hurts to walk, stand up, etc! I have an appointment with my doctor tomorrow! I'm ticked about this!

Ok my doctor Gave this to me 1 cause its cheap and 2 cause I pulled some muscles in my back. well today is day 2 of taking the pills and I cant hardly sit. my hips hurt so bad its insane. im not sleeping cause of the pain and its not helping my back at all. Im very disappointed. cheaper isn't always better is it!
Ive had a headache ever since i started taking it! Im exhausted. and my back pain is getting worse, Im going to call my doctor tomorrow and hope that she will give me something better.

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.

Im only 16 years old and ive been on levaquin for about 3 days now. My doctor told me off the bat that the only thing wrong with the drug were some "theories" on cartilidge damage, how ever, now i see for myself, and for many other people that is not the only side effect. He told me that no one under 18 is supposed to have it but i caught a severe case of sinutitus, and a uti which ive had for 2 months and nothing was working, so he put me on levaquin, once a day for 7 days. Ive now been having the following symptoms and im extremely scared!!
1. Constant fatigue
2. Extreme Migraines
3. Nausea, vomiting
4. Rapid heart beat (and chest pain)
5. Stiffness in joints and horrible pain...
6. Constant anxiousness, to where i cant get to sleep
7. Dizziness

Is there anyone i can talk to who's had these same problems? please email me or something im scared and i don't know what to do my mother doesn't believe me and she says its just a head cold....

******

Please help me!!

I am so glad that I found this website, because I thought all of this was just me! Nine days ago, I was prescribed 750mg of Levaquin/once a day for 14 days. I was just about to take today's dose but after reading only page 1 on this site, will NOT be taking the 9th dose, nor will I be taking any more of this stuff at all! Mine all started with a toothache a few weeks ago, and ended up in the ENT's office with the above prescription with a CT-Sinus scan after 14 days of being on Levaquin. I always read the side effects of any prescription that I'm given, and I was aware that Levaquin could cause ruptured tendons so I've been very methodical with every move that I make...my husband had a ruptured achilles tendon a couple of years ago and that's the LAST thing I want to go through. However, after reading this site, I now understand that all of the other symptoms that I've been experiencing over the last several days are most definitely side effects of Levaquin that they aren't admitting to. Plus, it doesn't seem to appear that being cautious about how you move makes much of a difference when you're taking this stuff. Metallic taste in my mouth; Thrush and a lack of having full taste; swollen knees, extremely sore and aching legs, hips, and back/neck area; nausea; jittery spells very shortly after taking the medicine; hot, then cold spells...everything listed here! Why are doctor's continuing to prescribe this stuff left and right?? I'd rather just have a sinus infection!