Kidney pain symptoms and conditions

I used NuvaRing for 1 year and 5 months before I threw in the towel. At first it was great. No weight gain, no change in my cycles, no problem during intercourse, everything was perfect... a great alternative to a pill. Until I started taking NuvaRing in 2008 I had not been on any birth control. The last time I was on anything was in 2000 after the birth of my only daughter. In 2000 I used Depo Provera (spelling?) and had horrible side effects from that. I had extreme hair loss & the worst mood swings you could imagine. I knew that his time around I didn't want the Depo shot & I can't remember to take a pill everyday. I struggle to take a full round of antibiotics without accidentally forgetting a dose. After talking to my Gyno in 08 I decided to try NuvaR. After getting my 6 mo. checkup with my doctor we decided to keep me on it since I was pleased with the results. So months went by, still no problem. Then one afternoon I started getting a pain in my left side that was the worst achey/uncomfortable nagging pain I had ever felt. I started to keep a log of when my pain would come & how long it lasted before it finally subsided. After a few weeks I began looking through the internet to find out more of my anatomy & try to come up with an idea of what was causing my strange pain. As it turns out the pain was in the same area as my spleen & a little piece of the liver comes across to the left side as well. I knew that this was not a kidney issue since I am prone to kidney infections at least 3 times a year. I know kidney pain & this was not it. My boyfriend started complaining about how I was always complaining about not feeling well. When we started dating in July of 08 I was somewhat outgoing, always going here or there for any get together-friends from work, daughters cheer stuff, jazz shows, beach etc. He was tired of me being tired. That is when we started wondering if I had anemia. The spleen pain could have been explained by that. Or maybe it was my gall blader we thought. I started looking for signs & symptoms but nothing was obvious. I just dealt with the pain in my side and wondered too if I was developing a stomach ulcer. Then one day my shins started hurting for no apparent reason. Then it was the forearm bones. I literally hurt inside my bones. The shins were the most painful of all. It hurt to walk, I couldn't get comfortable sitting, lying, standing, sleeping & I was at my whitts end. After talking about it with my boyfriend he said that I needed to go ahead & make an appointment because my quality of life has been reduced to zilch. I was always uncomfortable with pain or aches or moody. I went to see my doctor. Of course when I went I had a UTI, as usual-nothing abnormal about that. I told him about all my pain so we ran some tests. He did some blood work & saw that my white blood cells were through the roof. We decided to culture my urine specimen & a few days later we found I had a MRSA staff UTI. Typically you get these if you are catheterized but I fell into the unlucky 5% that just get it w/o any reason. (In the back of my mind I still wonder if NuvaRing had anything to do with it.) So, I took all the antibiotics making sure not to miss a dose. 14 days later at a check up I still had a little bit of bacteria in my urine & we ran more blood tests. My white count was even higher. Now my doctor takes my bone pain & side pain more seriously. The infection was getting better but my body was fighting something else or was it? He decided to check my kidneys by ultrasound to make sure there were no cycts. They also did a full abdominal ultrasound to look at the spleen & liver for enlargement. No enlargement but possibly a little kidney stone. Then I had an appointment with an infectious disease/internal medicine Dr. He made sure my infection was gone. I told him about all my weird pain & he ran a lot of blood work. White count still high, did a lap stain to look for leukosytes for leukemia, all was clear. So, after a week, off for a CT I went to check on the stone. Of course no stone on CT. Finally my boyfriend said hey, don't put a ring in this month & see if that's the problem. Sure enough after spending soooo much on all the tests after I took it out I was back to my old self in about a months time. I still had a pain in my side once in a while for the first 2-3 months but I have been completely symptom free now for 4 mos! The only worry I have now is that I started gaining weight after I stopped taking it. I have gained 20 lbs (some of that is because I got lazy & lethargic for so long) and my hair is beginning to come out more often in clumps again. I have an area thinning in my eyebrow & my nails are breaking more easily. I think I need to go get my thyroid checked. Yet again, I can't help but wonder- was it caused by the NuvaRing? Have I damaged myself thanks to what was supposed to be a great easy alternative to a pill? I guess we'll see how it goes. Never again will I use it, nor will I recommend it to anyone. Oh, and my love life is great again, I go places & do things again now. It's amazing how far I spiraled down before we realized it was preventable. DON'T USE THE RING!

Works well.
Retrograde ejaculation not a problem (semen backs up into the bladder - so what, it comes out later)
This forum taught me that Flomax is the cause of
- ringing in my ears (now I'm relieved because I know what it is)
- sinuses plugging up

My urologist asked me to stop the Flomax and "see how it goes" - I've tried 2 times...each time I get kidney pain on the 3rd day. Taking Flomax again cures the pain. Now I take one every other day.

I'd like to stop it, but dribble pee and kidney pain are no fun either - what to do? what to do?

I had Mirena put in on July 2nd. I had it removed today (August 4th). I gained 10lbs in 3 weeks, my hair is falling out like crazy, my face is breaking out, I was having kidney pain and the most recent was on Sunday when I couldn't get out of bed due to severe back pain and I couldn't lift my right leg. My husband had to pull me out of bed so I could use the bathroom. Any time I sat down, he had to pull me up. As the day went on, I could slowly start moving more. Yesterday and today my back was still very tender. I had it removed @ 3:30 this afternoon and my back pain and tenderness is completely gone (it's now 8:15 p.m.) My doctor told me that Progesterone is what causes all of those symptoms so he recommended I wait 2-3 months before trying any kind of birth control to get all of the hormones out of my body and make sure it's not a thyroid issue. Two people I know have Mirena and they have no symptoms and they love it. I on the other hand, can't say the same. I think people sensitive to progesterone need to find a different route.

I was prescribed Bactrim for UTI and took two pills. Yesterday morning I woke up with a rash on my upper back and forearms, and had headaches off and on all day. I also had some slight kidney pain, especially on my right side. I took that day's dose anyway, even though I was sure it was the Bactrim causing it. I woke up this morning and the rash had spread all down my torso and arms, front and back, and I am still having headaches. I also had a hard time sleeping last night, not because I was itching, but was restless. I have stopped taking the Bactrim and the doctor wants to prescribe a different antibiotic. I don't think I will take them unless the UTI comes back later.

I first started Lisinopril hctz about 3 years ago. Within the first day I had hives, a rash, itchy skin and RED RED face. Dr says it will go away. So I keep taking it. Fast forward a month and I start coughing, coughing at night so bad my husband can't sleep. It's so bad I feel like I'm choking and cough so much I am almost throwing up from the dryness and my throat being so constricted. During that time, I also start having some big whopping sinus pain and pressure. Felt like there was a tennis ball in my sinuses. Big time pain, headache. Dr says nothing wrong, just some allergies. I start taking Benadryl at night to sleep, to help with the itching, wheezing, coughing. It seems to help a bit. So I deal with all this. ALong with the coughing at times I am having trouble getting in air. Almost like I have to force it in. Not sure if it's my throat, sinuses or my chest. Next comes, some bass drum booming of my heart. I think it's so loud in my chest and my ears that others can hear it. This still happens on occasion. At times my legs feel like tree trunks or cement and I just don't have the energy to do anything. My hair started falling out in GOBS. I go to derm doctor, they say it's stress. It'll go away. Next I have kidney pain.... this goes on for a few months... come to find out I have a stone. But I never had any kidney problems before. Doctor's say it could be from the hctz and my kidneys having to work harder, but they were speculating. GP says keep taking Lisinopril hctz the benefits outweigh the side effects. I asked him if he has ever had a kidney stone he says no. I keep taking it. Leg cramps come next, bad cramps. I go to dr and he says it's my potassium, the hctz has depleted the potassium in my body and need to start on some big styrofoam potassium pills. All this goes on for almost two years. Fast forward to now. I'm still beat red in the face (and cannot handle the sun), coughing, sinuses full, itchy and bass drum beating (on occasion), heart flutters (on occasion).... four days ago I almost fainted because I was so dizzy within two hours of taking my pills in the morning. I am by no means able to sit on my butt and do nothing because of all these side effects. I have a farm to run, horses to feed and ride, hay to bale and put up, and I'm ready to get my body safe enough to start trying to get pregnant. I start doing research and find Lisinopril to be UNSAFE for a fetus. I start to think, well if it is unsafe for a fetus why is it safe for me? So then I googled side effects of Lisinopril and it brought me here. Thank God, I have a GP appointment tomorrow. I'm taking control back of my own body. I've had enough....

I had been on simvastatin a couple months when the debilitating fatigue started. Since I have hypothyroidism I blamed it on that. The fatigue got worse along with severe depression, brain fog. Numbness in my hands and feet and kidney pain kept me up at night. And then the shoulder pain started. It was excruciating. While pulling a dress over my head, my shoulder literally blew up. Turns out my biceps tendon rupture and filled my shoulder joint with chunks of cartilage. After looking at my MRI the orthopedic surgeon said if I didn't have surgery, the excruciating pain would only get worse and I'd lose the use of my arm.
Now, after stopping simvastatin my LDL has gone up to 300. Dr. wants me to start Welchol. After reading the side effects on this site....um...I don't know.

I began having right hip pain a month after the mirena was inserted. I assumed it was from running. All the doctors I have seen for the past year stated I strained a muscle. They ordered MRI's and physical therapy. I have completed all, but still have the same hip pain-over a year now. Has anyone had hip pain due to the mirena? And did your hip pain stop completely after your mirena was removed? I am considering getting it removed. Although the doctors tell me they are not connected, I can't help but think there is a coincidence.

this is my story... I am 41 and wombless. Was prescribed Yasmin for a cyst which they say is an ovarian cyst, but I have no ovaries. May i say I have never taken contraceptives in my life. began taking prescription 28 days ago today. from the very first day it brought on kidney pain that was dormant for months and a feeling of nausea and headaches. That checked with antibiotics in a week, with the exception of headaches which i still have on and off, it has been smooth sailing. problem is yesterday i woke up bleeding. I haven't had a period in almost 3 years so i am in a dilemma. Its weekend and i don't see my gyn until Monday. The only thing i can put this to is the tabs and i am not gonna take any more. I quit.

Had a heart attack in July and had a stent put in blocked artery. Prior to that I was taking Cartia for blood pressure. Cardiologist switched me to Lisinopril.
I've been having severe pain in my lower back on both sides and also around my rib cage. I'm in cardiac rehab and today my nurse/therapist told me they are increasing Lisinopril from 10 mg to 20 mg. After reading posts on this site, I'm a bit concerned.

I have used the NuvaRing for about 3.5 years, starting after my 6 week check up when my daughter was born in 2004. In the beginning I felt like it decreased my sex drive but also that maybe post baby body that caused that too. For three years I had no problems. I had noticed breast tenderness throughout but other than that no side effects. About 8 months ago it began with a missed period, then two periods in one month. My OBGYN recommended 'resetting' my body by taking out the ring until my next cycle and starting it up again. I followed his directions but the next cycle came along with a bladder infection followed by a yeast infection. Over the next 4 months I either had one or the other, continually visiting my doctor I didn't make any connection to the two. Stomach pain, chronic fatigue and kidney pain also added to the list. My doctor prescribed a series of medications followed by blood tests and a referral to a specialist. Over the summer my husband asked that I stop using the ring because my sex drive had hit rock bottom. After a few weeks of taking out the ring, the burning sensation during urination has gone away. Stomach cramps and back pain has ceased and no infection to date. I am in my early thirties and after a week off the ring I realized what they mean by 30's sex drive. My husband and I are both happy with the changes. I visit my OBGYN again in a few weeks to revisit non-hormone options for BC

Husband taking 10mg. He is having dizziness, confusion, memory lapse, depression, short-temper, severe leg cramps, chills, loss of appetite, constipation and severe stomach cramps. We are discontinuing this medication. He thinks it's literally killing him like being poisoned.

I took Levaquin for a kidney infection 500 mg. I was inchy all over. stomach pain. sever neck pain, and pain all over I feel like I was hit by a truck. no energy. my eyes get all heavy like I haven't slept in weeks. Alls I do is sleep and when I do I wake up very confused. I've been taking naps in the day time which I've never been able to do even if I was sick. I don't feel normal like I'm drunk and I don't even drink my sister says I even sound drunk. I get headaches. I have bruises all over in the places that I had itched. I still have kidney pain it feels like it's flopping around in there. Sweat a lot at night time. My heart sometimes beats really fast then thunks hard and then slows down. anxiety attacks. I cry for no reason. I called my doctor and he said he don't think it's from the levaquin that people only get a couple side effects not this many and put me back on antibiotics.

I was given a shot of Rocephin and oral penicillin about 2 months ago. I have been allergic to Penicillin all my life, but my Dr decided to give it to me because I had strep throat so bad and it kept coming back. We had hoped that my allergy had miraculously gone away! With in a day, I got the worst heartburn I've ever had (and I have a hiatal hernia and esophogitis, so I'm pretty familiar with heartburn) and my shoulders were killing me. I got hives on my chest and face (no doubt from the penicillin) and my urine was bright orange. I called my Dr and told him of the symptoms and he said, must be the penicillin and put me on a z-pack. Now, another separate episode...Last week, I developed urinary tract infection symptoms and called my Dr. He gave me Bactrum and I got worse, running fever, blood in my urine, kidney pain, disorientation... etc. So I went to see the doctor and he gave me a shot of Rocephin, and oral Cipro. My urinary symptoms seemed to get better that evening and the next morning. Around 9 am I started getting a slight cramping feeling in my abdomen near my belly button. It quickly spread to my upper abdominal area and into my shoulders and upper back and the pain was so severe I was doubled over screaming like a woman giving birth to a 10 lb baby with no drugs! This pain intensified and lasted for 2 hours. My brother took me to the ER but by the time the Dr saw me, the pain had subsided. They ran blood work, and did an ultra sound and found nothing. Go figure! I even told the nurse I had been given a shot of Rocephin and that last time I had it, I had the above mentioned symptoms (orange pee...etc) While I was in the hospital, my lower back... close to my tailbone started hurting, so I figured I might have pulled something when I was having that 2 hour spaz attack. Well by that evening, I can't walk and I have pains radiating down my butt and leg. The location of where I received the shot is pretty much on fire, and sensitive to the touch. I don't know what's going on here, but I'm 100% blaming the shot of Rocephin and it makes me mad that my doctor, nor the ER doctor can put 2 and 2 together, but I have to figure it out on my own. What am I paying them for?

Lisinopril is poison, literally!!!! I have had high blood pressure in the past and recently it became a bit too high. My doctor placed me on Lisinopril. I am 41 years old and have NEVER had any problems with my heart rate. After just 5 days of taking this poison I had to be rushed to the hospital with a heart rate of 178 bpm!!!! 2 days later I have intense kidney pain. I am glad I found this site to answer my questions. My cardiologist's nurse's response when I asked her if the Lisinopril caused my kidney pain "Oh no, it couldn't be the medicine". The ER doctor's response when I asked him if Lisionpril could have caused the rapid heart rate "Oh no, it couldn't be the medicine". What are these people on????????? It's like the work for the medicine companies! I can't wait to show the nurse all of the stuff I have printed out about Lisinopril.....No one should ever take this poison, ever!!!!!!!! Stop before you take it and don't take it. It has even killed people before from kidney failures. Read up about it first, I wish I had..........now I am stuck with it in my system and don't know how long before it comes out completely.

I was diagnosed with carpal tunnel after starting 40 mg simvastatin, my wrist had never bothered me before, was one step away from surgery. Other joints started giving me problems. As joint problems grew I also was getting weaker. I felt so weak I couldn't get out of bed. Headache, neck stiffness, nausea, and kidney pain. Doctor just told me blood test does not show anything is wrong. I stopped the pills 4 days ago and my wrist no longer hurts. I'm still weak. I think they haven't found the test that proves the way this drug is the cause. How can I be is such bad shape but the tests look normal?

hello all,
I had my Mirena put in on October of 07. due to heavy bleeding which caused severe Enemia. I have since had problems with very Low potassium, re-occurring yeast and bacterial infections and some heart palpitations. The latest symptom I have been experiencing is numbness in my left leg and foot. sometimes totally numb. My dr. told me that it could be a pinched nerve in my back but I have not done anything to strain or stress it. after reading this website i am convinced that these symptoms are caused by my IUD.
I am going to call my OBGYN tomorrow and have this IUD removed!!!!!

kidney pain, light headedness

I am not sure if the Lisinopril is my problem. I have been on it for 3 yrs now. I do not have HBP -never had it. I developed Type II diabetes and am on Metformin. In the last two months, I have developed dizziness and light headedness. Also, last two months, heart palpations - and the itching is driving me crazy. Skin has developed tender sites - like the skin feels like very thin paper. I think I am going to stop it - even reading what's on this page - it may be what's causing these strange things. I did not know it was from viper venom. I also have dry mouth, but no consistent cough. Every now and then.

I am 56 year old New Zealander, had stent inserted 1 year ago.
Was first put on Lipex, after 6 months on that would have welcomed departure. Came off it voluntarily and problems went away.
NZ is too mean to provide Lipitor with out a fight, so after much cajoling my doctor finally got permission to provide me with it.

At first it was fine, but slowly the same symptoms as with Lipex returned.
I have every single symptom I have read about here.
Joint pain, short term memory loss, nausea, swollen ankles and by association I am getting pretty depressed.

I had to come off beta blockers for similar reasons.

Finally this week I have developed kidney pain and have decided that that is it.
Lipids are out for the duration, I am told that half an onion a day will reduce your cholesterol naturally, so that is where I am going.

Thank you all for providing me with proof that these drugs do not work for all of us.

I came across this site purely by entering "swollen red foot and kidney pain" into my search engine, imagine my shock when up came a site listing kidney pain and lisinopril!! I have been taking lisinopril for about 7 months now and as I had no adverse side effects in the first week carried on popping my "little lifesaver" no questions asked. Over the last 3 months I have experienced kidney pain to the extent that I was beginning to think I would pass a kidney stone! dry persistent cough, sleeplessness which means I am up at all hours throughout the night and catnapping (when I can) during the day, nausea ,stomach pain and headache!! The swollen foot I don't think I can attribute to the lisinopril....but who knows? I appreciate that in medicine we use various "poisons" as cures and remedies for illness, but when I read of the side effects that so many people are experiencing and am able to see a definite link to the ones I am experiencing then I start to wonder ....the good thing is that this drug and I take 10mg daily has reduced my B.P to a rather good level.....but I have decided to stop taking it for a few days to see whether my symptoms stop and have made an appointment to discuss this treatment with my G.P as a matter of urgency!! Thanks...Jill xx Oh almost forgot to add the incessant itching as well!!

I agree, for me this is a horrible drug! This is the 2nd time my allergist prescribed it to me (last time was this past summer and I had severe panic attacks and thought I was losing my mind) this resulted in me returning back to my GP and him putting me back on Paxil (which I had been off of for a year). I was extremely reluctant to use this again but thought i might be able to manage it this time (with the help of Paxil).

My allergist prescribed Prednisone to me 2 weeks ago (5mg 3x's day for 3 days then, 2 2x's day then 1 for 5 days) I made up until the last 3 pills. I had severe brain fog and felt like I was floating through space. I couldn't even remember driving to work and parking my car! Extremely fatigued (I have diabetes (which is under control, but I had to keep checking my bg because I thought my sugar was dropping to low). Now, within the last week of taking the Prednisone I have experienced aching in my kidneys and I think I have a kidney infection.

Can Prednisone do this to you??

I am calling the doctor tomorrow. Today is the first day without Prednisone and I feel like I am totally out of it - really spaced out, dizzy, panicky and a bit nausea.

How long does it take for you to get Prednisone out of your system?

Roughly 8-9 hours after taking Imitrex, I often get excruciating kidney pain that can last up to 8 hours. It feels like broken glass passing through my kidneys. I always try to drink LOTS of water when I take Imitrex, to minimize the kidney pain. Is the Imitrex and ensuing kidney pain worth it? I ask myself that question every time I have a migraine.

been on simvastan for about 3 years, started getting left side kidney pain mounths ago and it's not going away. very tender at times, take ibprofen and it helps somewhat. gona stop taking the statin tonight.

I had my Mirena put in Sept '06. My sister talked me into getting it, she said she bled for 5 months afters. I was expecting the same.. I only bled for about 2 months. But it's like living every day the day before my period starts. Extreme heavy discharge, constant cramps and severe dry skin on my head forcing me to get medical attention for that. I have other health issues, so I'm not sure if my back and kidney pain can also be attributed to the Mirena. I am finding an OB in my new state to have it removed. I can't take this anymore.. My sister had hers removed last week because of severe pain in her Pelvis. I've also had mood swings and headaches, more than normal.

I have been on NR for 5 months. I have experience all of the symptoms metioned in these postings. I have to tell you its a relief to hear I'm not the only one. I feel like I'm falling apart. My periods are about 2 days of brown spotting, the nightsweats are terrible. I know its summer but for no reason I just break out into a sweat and not only at night. Also I have been having kidney pain and what are described as "ice pick headaches". I didnt see these mentioned here. Anyone else feel it? It also feels like I have something in my stomache but it turns out its all the bloating. I also read one poster how she would drink and drink and not go to the bathroom. That happens to me too. I will be making an appt to see my OBGYN to discuss other options.