Kidney pain symptoms and conditions

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?

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.

Light Rash, dizziness, BAD blurred vision making it hard to drive, BAD heavy bleeding(changes in menstrual cycle lasting three weeks with spotting then heavy bleeding) easy bruising sometimes black and blue ...headache,cant think, kidney pain I have (VUR) and am not sure if i should have been givin Lamictal.... I just stopped taking it went from 200mg to 100mg for a week now not taking any its been two days. and im hoping I start to feel better soon.

I am 45, male on lipitor for about 2 months now. I am experiencing kidney pains that wake me up at night. I have been noticing dark urination prior to the kidney pain coincidently. After doing a quick search for information on it I find that the statin medication Lipitor is the culprit - OBVIOUSLY. Not waiting for advice from a doctor to tell me what to do about it. Bye Bye Lipitor and hello more excercise with an increase in fresh friuts and vegetables in my diet. Good luck to all taking this drug.

I have been taking Lisinopril for nearly a year and have experienced nearly all the bad side effects I have read about. I have had severe cough that does not respond to cough medications, copious amounts of clear slimy mucous that chokes me frequently. I even choke frequently when I am trying to speak because of the secretions. I have had severe bronchitis 4 times in 6 months. I am tired all the time and my anxiety is much worse. I now have insomnia which I've never had before. During one of the bronchitis rounds I had to take a very strong anitbiotic because it was trying to turn to pneumonia. The antibiotic made me very nauseated so I couldn't take my other meds. After two weeks without the Lisinopril, my symptoms cleared up completely. I resumed the lisinopril when I finished the antibiotic and all of my symptoms returned.

My second run in with a blood clot resulted in passing out on my way to pick up my 8 yr old daughter and being rushed to the ER because of a PE (near death), I'm thankful to be alive however (no reason for PE and being on coumadin for the rest of my life) I feel so tired now, I don't want to go to work, I can't concentrate, I suffer from dizzy spells, I'm always hungry (weight gain), nausea sometimes. before passing out I was working out, doing Taebo, the balance ball thing, walking. Now I feel like I'm and old woman. I'm 32 yrs old and taking #5 coumadin and I feel so bad the majority of the time and yes the doctors say "it's shouldn't be the coumadin" but I think it is my whole world has changed and I'm just trying to get back to being the fun, outgoing, active me. I miss myself so much, its like I'm depressed. I MISS MYSELF.

Hello- I was Dx with Sarcoidosis in February, 2007. My lung specialist put me on 20mg Prednisone, increasing to 40mg within two weeks. My Sarcoid symptoms were from enlarged lymph- extreme trouble breathing, middle and lower back pain, kidney pain. Within a week of being at the 40mg level my heart rate and BP became so erratic that he had to start weaning me down. Initially I had extreme energy which felt good after suffering from fatigue but was short lived due to the cardiac problems.

The Prednisone has resolved much of my inflammation for the Sarcoid but I will not go on this again. I have been weaning now for over three weeks. Down under 5mg of Prednisone and it is almost unbearable. Each time I took a drop my mental symptoms became intolerable. Anxiety, extreme fatigue with extreme weakness, irrational thoughts, blurred vision. Within the last couple of days I could hardly get myself out of bed. My weight has increased steadily, bloating stomach, stiff joints, skin rash.

My biggest complaint is that doctors are not giving us enough information as to how this will affect from a negative side. Yes, it takes care of the inflammation but no one prepared me for these awful side effects and withdrawal symptoms. I feel like a nut case most of the time with no coping skills.

My daughter is 19 and has been on yasmin since 16 for heavy periods and pain in the last year she has experienced severe kidney pain and horrible mood swings all blood work, ultrasound and catscans show nothing...neddless to say we are at our wits end the only thing i can keep going back to is this yasmin with dsrp. is any one else out their having kidney or liver problems or unexplained renal back pain? Help!!! anything at this point would benefit my research.

Concerned Mom in the south

kidney pain, itching
nausea

Started Zocor in May 2005, took for approx. three weeks. Had been given samples by GP. Stopped June 10, 2005 due to problems. Following is a list of symptoms as they occurred. Head shake, thinking and speaking problems, difficulty swallowing, weakness, low back pain, muscle spasms, pain in legs (especially left leg) Kidney pain, dark urine for one day only, and especially extreme fatigue. GP said was Myopathy. didnt seem to know cause. Continued to get worse untill approx. July 15, 2005. Started phy therapy. This helped to build back the muscles lost but would only build to a certain point. Presently, april 2006, Most of the symptoms have abated but I still have difficulty walking and standing very long. Had to quit working, could not handle. I will keep updating as I progress. This has been some nightmare.