Kidney problems symptoms and conditions

SIX HOURS POST REMOVAL- I had my mirena removed today after 3 years and nearly 3 months. My side effects included headaches, sore breasts, weight gain, nausea, severe hair loss, depression, severe pitting edema of my right foot, cramping, hip pain, exhaustion, severe mood swings, and acne. During the first six months I had constant bleeding, which I had been told to expect. I took regular pills everyday and the bleeding stopped. Then the hair loss started. My hair came out in clumps and was EVERYWHERE. I lost about 15 inches of my hair in spots. I went to the salon and got a fantastic hair cut, I attributed my hair loss to stress. Now I'm not too sure. I also didn't feel like I was myself with the odor that I developed. No matter how many times I showered I felt not regular. Slowly but surely over the past three years I have gained 30 lbs. I worked out to try to get the weight off, I lost nothing and in fact gained weight! The pitting edema of my left foot started in July of 08. I have been tested for everything including diabetes, heart problems, clotting disorders, pregnancy, high blood pressure, kidney problems, and the list goes on to the tune of $6,000. I went to my OB back in the spring and was told if they could find nothing else then they would remove the IUD. In the interim I lost my job and subsequently my insurance. I luckily was able to get coverage again and immediately set an appointment for the removal. Insertion hurt like nothing I have ever experience, removal was quick and almost painless. I also ended up with BV (bacterial vaginosis). I feel and look as though I am about 6 or 7 months pregnant. My belly is actually the same size as it was when my son was born. I weight about 15 lbs more. My breasts were extremely swollen and sore.

I instantly felt better after removal. My hip immediately stopped tingling. I have no back pain. It felt almost like a lifting if that makes sense. I am curious to see what the next few weeks will bring and I will definitely keep you all posted.

I am a few days away from my 19th birthday and i've been taking Yasmin since the age of 11. I was diagnosed with PCOS when i was 11 and Yasmin has been what's keeping my period regular and more or less pain free since then. In May of 2008 i was switched to the generic version of Yasmin called, Ocella and started to notice more and more symptoms and side effects. My stomach pain in the mornings grew greater by the day and when i was on my sugar pill i would gain an unbearable migraine. Thinking it was just part of being a woman i ignored it and went about my life. It wasn't until December of 2008 while out with a group of friends i came into some serious stomach pain. thinking it was just a typical stomach ache that i normally got i ignored it. when i came to be about 4 am and the pain hadn't stopped i started to worry. first thing in the morning i went to the doctor who referred me to get an ultrasound. The ultrasound showed that i had gall stones and that i should have my gall bladder removed before more complications were to occur. Being a college student only a week away from returning to my second semester i opted to wait until spring break to have the surgery. During the 3 month wait i experience extreme diarrhea whenever something was put in my mouth, extreme stomach pain, heartburn, nausea, headaches, sore muscles, the list goes on and on i felt like i had been hit by a truck every day and i still had to go to class. in March of 2009 i had my gall bladder removed thinking that the symptoms would finally stop i returned to school only to find that nothing got better. It's been 7 months since my gall bladder has been removed and i'm still having the same symptoms as before and now i've added depression, stress, lack of energy and interest and many other things to the list. I'm still taking Ocella because i've never been advised otherwise but the symptoms are taking over my life. I am a sophomore majoring in electrical engineering at college and it's just become harder and harder to focus on my work or to enjoy the aspects of college that i should be with the frequent trips to the bathroom or having to opt out of a fun activity because of stomach pain. I was wondering if anyone can help me, maybe point me in a direction where i can get better and get back to enjoying what a 19 should be. Thanks.

I took levaquin for an ear and sinus infection in 2007. On my last 500mg pill, I had such a cramp I could not walk. Since then I have had severe food allergies, severe muscle and joint pains,kidney problems and rheumatoid factor is real high. Before taking this drug I have never any joint pains, or kidney problems. I was recently diagnosed with aggressive Rheumatoid Arthritis. It has been 2 years since I took Levaquin, but the side effects weakened my body and did a number on me.

I'm a 65 year old type 2 diabetic with low-functioning thyroid. I was put on lisinopril over a year ago to prevent kidney problems. I have been on 10 mg tablets. Even before I was diagnosed with diabetes I had low blood pressure so that was not a problem.

My main side effects are hair loss, coughing, insomnia and leg cramps, joint pain. I think the lisinopril is pulling nutrients from my body. I told my family doctor about the side effects I had found but he seemed more concerned about the possibility of kidney problems than any of the side effects. I know my hair loss is not age related as both of my parents had full heads of hair when they died and my mother was also a type 2 diabetic.

My blood sugar is under control, tests usually 85-90 twice a day, last A1c was 5.5 which is quite good. I take Byetta and metformin twice a day, levothyroxine, enablex. I recently started taking magnesium as it was besides calcium plus D, a multivitamin all ordered by the doctor. I also take crestor. Feels like all I do is take pills!

My weight is 166 but I'm short, 4' 10", so still heavier than I should be for my height. I try to get exercise but have degenerative arthritis in lower spine. Funny that I developed bursitis in my right hip recently, I just thought the arthritis was spreading. Now I'm not so sure it might not be due to the lisinopril also. I stopped using it yesterday so we'll see how long it takes my body to recover from this drug.

Does anyone have any experience with how long it takes to stop coughing or for the hair to regrow after quitting lisinopril?

I took Benadryl for over a year with my topamax (for migraines). The doctor said it was ok so I continued and got a good nights sleep. A few weeks ago I got up and went to the bathroom. My urine was cloudy and smelled terrible. I started drinking water and even drank a full glass before I went to bed. I woke up with the same problem. I quit taking the topamax and benadryl.My urine cleared up the next day. About a week later I took a benadryl before bed (no topamax) and woke up with the same terrible smell in my urine. I know think that long term use is going to cause kidney problems.

I recently began using the Nuvaring (about a week and a half ago). I've suffered from Migraines for 14 years and take regular medication that allows me to control the symptoms. Since beginning this BC method, I have been unable to manage the headaches. Taking my normal medication will work for a few hours, but then the headache will come back. My only options are to take more medication (and risk over medicating, thus causing other problems; liver problems, kidney problems, etc.) or deal with the pain. The migraines interfere with my vision and cause serious nausea, making it nearly impossible to continue with school, work, or anything else for that matter.
Additionally, I have been experiencing a dramatic increase in vaginal discharge, serious mood swings ranging from anger to depression with really no triggers, anxiety about my safety in strange situations such as driving or walking through campus, abdominal cramping in the region of my ovaries, what I can only assume is vaginal tenderness due to the rings presence, and I have been waking up at the same time in the middle of the night since I started the NR. I usually sleep an average of 9 hours each night, without interruption. Now I'm sleeping about 4 hours, waking up, and then sleeping another 4. I wake up feeling tired and with the feelings of an onsetting migraine.
The only benefit I have experienced is an increase in sex drive. I have gone from wanting sex an average of once or twice a month to wanting it several times throughout each day. I do have low levels of "free" testosterone according to my Gyno, so she recommended the NR.
Finally this morning I had enough of the symptoms. I took out the ring and within just one hour, my headache dulled, my abdominal pain lessened, and I feel slightly happier.
My question is, has anyone experienced symptoms like mine, that only lasted a few weeks when starting NR? I really love the convenience of the NR, but if I had to choose, I would not take the symptoms for the one benefit.

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....

lactaid milk for a NON lactose intolerant person! eating regular dairy all day long, lots of normal cheese and ice cream daily... bought the lactaid for my cat..but ended up making COFFEE with it..latte style.. a full 8-10 ounces...
for a month now... and ended up with an ammonia smell to my urine and underarms..skin in general.. afraid of kidney problems as I also developed TERRY's NAILS..or "half and half nails" WHITE nails!!! the ammonia smell and the white nails indicate kidney troubles... my tests came back normal for kidney and liver... I attribute this to the lactaid so I hope this helps someone who may read this!!! these symptoms 100% coincide with the lactaid, NOTHING else is different in my diet..maybe my body got confused having lactase enzyme..AND normal dairy at same time.? maybe its not for people who are NOT lactose intolerant or for people who will ALSO include some regular dairy in their day... (without use of tablets) from what ive read here, you people are mistakenly believing you are intolerant... when all you need is probably PROBIOTICS after a course of antibiotics..which killed your healthy bacterias..and rendered you ineffective at digestion. That happened to me. takes months to re-establish the bacterias..and can even be a YEAR or two even, AFTER you took antibiotics that your digestion finally gave up..your antibiotic use didn't have to be "recent"
Thank you

My 10 year old daughter was given Bactrim at an ER for infected bites. Within a couple days she was running a 104.8 temp that would not go away and from her knees up she had a rash with whelps that was driving her crazy. She was pale under the rash and every bone in her body hurt. We rushed her to the hospital and she was admitted. They said her blood palates were low and her white blood count was low...then her potassium also dropped. We spent 3 days and 4 nights there. Today we go back for a check up with her doctor...and I will express my concerns about the kidney problems I have read about today. I am now warning everyone I talk to about this drug. Seems the more I share her story the more people I found out this has happened to ..I feel like I should of been warned of the side effects of the medication

All that I can say is anyone taking this medication, be prepared. I am 24 years old and was diagnosed with Crohn's disease. I was in a severe flare up and was prescribe Prednisone. I looked like a balloon in the Macy's parade. Along with looking like I was 500 lbs in the face I was a woman on a rampage. I would blow up at the drop of a hat. I could not sleep, I was not the person to be around. Even after I was taken off of it, it took some serious time for me to be back to my normal self. This is an absolutely HORRIFIC drug and whomever invented it should be jailed for what it does to the people taking it.

I have been on Levoxyl for about 9 years and have felt awful. I have had weight loss, dry hair, thinning hair,dry skin, muscle aches, migraines and the list goes on. I just got out of the hospital Monday after 4 days of testing of my heart and lungs. I was admitted for racing heart. The doctor's conclusion was anxiety! They said that Levoxyl has nothing to do with my rapid heart rate. The endocrinologist prescribed taking levoxyl .050 on day and .075 the next also a beta blocker, Xanax and Zoloft. I can not take any of these meds b/c they make it almost worse. I KNOW it is not Anxiety and it from the Levoxyl but what do I do?? I am a mess right now can not be in this condition with four young kids and a husband. None of the doctors would say it was the Levoxyl and instead prescribed more and told me to check up with blood work in 6 weeks. I took the .050 yesterday around noon and by 7:30pm my heart rate picked up again and continued until 4:30 this morning. I can not sleep more then 2 hours at a time and wakeup feeling like I am crawling out of my skin. PLEASE let me know of any solutions.

I am a 49 years old Hispanic who was given 10 Milligrams of Lisinopril a day for what i understood was to prevent some potential kidney problems I may be having. "Just to make sure the doctor said". After about a month of taking it and feeling tired and irritable, I decided that I needed to look this medicine's symptoms to see if that was the source of my being so tired, anxious and feeling like doing nothing but sleeping, when I am usually a very energetic person who likes to stay busy all the time. I am very surprised to know that this medicine is for treatment of HBP which I have none. My BP has always been normal so I don't understand what was the purpose of this medicine. I am taking myself out of this drug and calling my doctor tomorrow because he has some explaining to do.

the truth of the matter is that this medicine did make me very tired, irritable and depressed

I am 43 yr old woman and have been on simvastatin on and off for the past 3yrs, it's only since coming across this website that I have actually managed to find a connection between this awful drug and a whole heap of medical problems. The most recent course made me so ill that I thought I had an incurable illness that no one could diagnose, at times I have been in so much pain I thought I was going to die. It started with severe knee pain, I have a little arthritis in the knee but doctors were baffled at why it would hurt so much as x-rays on knees and hips were ok. I ended up having an operation to cut a ligament, that was over a year ago and had been in crippling pain ever-since. Also; foggy head, headaches everyday lasting all day, pain in jaw, shoulders, neck, swollen throat, incredible limb swelling, numbness all down right side, kidney problems, weakness in muscles, aching hips and legs, itching, insomnia, to name a few. I complained to my doctor when I was prescribed 50mg of this poison because as soon as I took it, I immediately felt ill and collapsed from terrible weakness, couldn't even lift a feather. They reduced it to 20mg, and I blindly kept taking it, in the meantime, my leg function was worsening, my back was killing me, I couldn't sleep because of the unbelievable burning in my shoulders, hip, neck and legs, everything hurt so much. I have been in tears from the pain and frustration of not knowing what was happening to me, painkillers, even high potency prescriptions just didn't work. I was a healthy gym-going person with a slightly high cholesterol reading, and suddenly, I was almost crippled, unable to function or look after my family, couldn't even handle simple chores that I had done a thousand times before, couldn't think, speak well, do crosswords, it was unbelievable. I have had ECG's, heart stress tests, been to and fro to doctors, hospitals, specialists, even seen an osteopath with these pains, they must have thought I was a hypochondriac! Finally, I insisted on an MRI on my thigh as it had changed shape as there was a lot of muscle wasting in both my right arm and thigh, and so much pain. A lump had also appeared and was really worrying me. The doctor tried to fob me off and said it was a fat lump, I argued that if it was fat it wouldn't hurt so damn much, so the result of the MRI is that I have a tumor which is getting bigger. If I find out that this is a result of the medication, the gates of hell will open.
I took myself off this lethal stuff immediately as soon as I realized there was a connection between it and my debilitating condition, though it's too late to save my 12 yr relationship, that went down the tubes because I just couldn't function well, oh, and my job. and any chance of working after being ill for so long.
I have been off it just a few days but already I feel almost human again. I know it'll be a while before I can see a marked difference and do some of the things I used to be able to do like walk the dog!! but I am furious with my doctor's and have written a letter of complaint, and have told them that I would rather take my chances with god and be a happy person than ever trust them again. I am in no doubt whatsoever that this drug has ruined the last 3 years of my life and probably caused irreversible damage to my leg muscles. Why take a pill because the doctor said so??NEVER AGAIN from now on everything will be checked via websites like this, I am so disgusted that instead of helping me, my own doctor just prescribed other medications I need not have had because of this pill when all he had to do was take me off it. I find it hard to believe that they don't know of these side effects, or pretend not to, how can they not make the connection?? Absolutely furious. I am in worse health now than I ever was, there should be a serious health warning before this is given to anyone, and the first port of call for any complaints should be the doctors who prescribe them instead of offering alternative solutions. This is a time bomb waiting to explode.

I was diagnoed back in november with Hashimoto Disease and had a complete thyroidectomy in December. I have been switched three times since Dec. 07 (only April 6 '08) to different doses of Synthroid. I still experienced weight gain and cannot lose weight, irritability, depression, hair loss, exhaustion... I decided last month to stop taking it all together and was wondering what effects this may have on me. Any clues as to the effects of NOT taking the medication after having a my thyroid completly removed?? I feel the same (depressed, irritable, still losing hair, exhausted...) but am sure this is probably not a good thing to not take any medication when I don't have a thyroid anymore.

I have been on Yasmin for about 3 years. In that time I have had many different problems but never thought it could be my BC. I have been told that I have IBS, often have UTI's, chronic pelvic pain, and now kidney problems that cannot be traced through blood tests. I have been to MANY different specialist about each thing they all told me they could find nothing, and each time I was told that it could possibly be something different. In this process I have been given test after test after test including a colonoscopy, exploratory surgery and ultrasounds. It was not until today that I was talking with a co-worker about the pain that she mentioned that it could be Yasmin. My medical coverage sent me a letter stating that they would no longer pay for the bc but never told me why. I found this site and am grateful that other people are having symptoms and it is not my body falling apart. Thank you to everybody who shared.

In my opinion, Lisinopril is a silent and deadly killer. I was on the original drug Zestoretic for a long time without any problems. Within the first 24 hours of tasking Lisinopril I became very ill. I was on a trip and did not immediately realize it was caused because they switched me to the generic version called lisinopril. I have not had any other side effects from any other generic, nor do I have a problem with generics...only generics that posion the user!!!

I have had blurred vision, confusion, eye problems, heart palpitations, weight gain, sweating, rashes, and blood pressure that either falls to dramatic lows or rises to dramatic highs. I have lost feeling in my right foot and now am starting to experience numbness in my hands and other extremities. I have complained to doctors, pharmacists and to my medical provider. I am now in the process of fighting the state I live in to carry and cover the real product, Zestoretic, for me in my insurance. I have made at least twenty or more attempts to get this straightened out but all of my warnings are falling on deaf ears. Five of my other friends were put on Lisinopril in the last year. Most thought I was just being too radical about the effects of the drug. They used it and got by for about three to six months.

Guess what? They are all having serious side effects now too. Three have ended up in the hospital. One with a heart attack. One with a mild stroke. And a couple with kidney problems. My liver began to fail me and now my doctor wants to send me to a neurologist.... I know what the problem is. Believe me. I will switch back to Zestoretic this Monday. but here's the killer punchline America. Prinzide no longer makes their safe version. It is discontinued and from what I understand, Zestoretic has stopped producing all but one strength...their 20/25. My guess is with Walmart selling the generic for $4 bucks for a month's supply...it won't be long until Astra Zeneca pulls the 20/25's off the market... Got the picture!!!!!!!! Posion or nothing. P/S I will wriotge back aftger I have been on the Zestoretic for a week.

Hi Guest 39434

My doctor thought I was having kidney problems because she believed I was having trouble with my magnesium levels, but it turns out my magnesium levels are fine and my kidneys are great.
No urinary or bladder "problems", but I did have an increased need to urinate when on Yasmin. Now that I'm off it has gone away.

IPJ

Has anyone had any urinary, bladder or kidney problems on Yaz??

I have been taking Maxide for about one year. Lots of anxiety, depressive feelings and fatigue despite the use of additional antidepressant. I cut the Maxide in half because of fears of kidney problems and noticed immediate improvement in mental symptoms. So I stopped it altogether and feel wonderful. Now using diet, exercise and relaxation to control edema and hypertension.

I started Zocor the night I had a heart attack and the leg aches and muscle problems started that next day. I was even taken to ulta sound lab looking for blood clots the pain was so bad. I continued taking 40mg twice a day for six months before the Dr. listened and then he tried other statin products. I am female and 57. This yo-yo affair with statin drugs continued for another 18 months before I refused to take them again. I am still having problems, muscle aches and etc. I have been sent to other specialists from gastric, arthritis, neurologist, and now I am seeing an orthopaedic Dr. I have had physical therapy to try to get my muscles working correctly, but no Dr. will even give the slightest acknowledgement it just might be statin drug side effects. The arthritis Dr. said I did not have any form of arthritis and did not fit the profile of any patient he'd ever had and sent me to the neurologist. My muscles respond to electric shock and are coming back according to the neurologist and as a bit of advice he said that even Dr.'s have had problems like mine and have had no problems until one morning the wake up weak, unable to exercise, and general muscle weakness. There is no way to prove our problems are because of the statins. My last blood work now show I may have liver problems and kidney problems. This slow death is not over for me, even though I am off the statin drugs. My last drug was red yeast rice used under Dr.'s care and it too is a statin. They all caused problems. I have tried them all. My advice is to listen to your body and your gut feelings about these products. I have had 3 heart attacks even on the statin drugs so they did not prevent future problems for me. I now have nine stents and am thankful to be alive, but my quality of life is deteriorating. I teach school and continue to do so, but I am having difficulties with extreme fatigue. I am looking at early retirement from something I have always enjoyed doing.

hi guest 32977,
hi, a couple of things jumped out at me there from your post. The no sex drive is really common on many brands of birth control but one of the quite often mentioned side effects of contraceptive pills (especially yasmin) is the vaginal pain.This could be because the hormone levels are not right for you and cause the vagina to atrophy (ie become tight and dry) as happens during and after menapause.that is why some ladies have problems inserting tampons etc. the other thing that jumped out at me was that you said you had kidney surgery. have you checked that it is ok to take yasmin,did you have your pottasium levels checked? yasmin is a pottasium sparing diuretic and is not recommended for people with kidney problems. also you mentioned anxiety????? has this just begun whilst you have been on yasmin? you may find that once you stop taking it (if you choose to) that the anxiety will vanish on it's own. so many ladies have ended up taking meds for the anxiety when all they needed to do was stop taking the pill.
good luck to you whatever you decide.

sarah

I have taken toprolxl 300mg. daily for 6 years, can this cause kidney problems

rjrcows,
it sounds like you may be dehydrated,yasmin has a strong diuretic effect,up your water intake to at least 2 litres of water daily to avoid any worsening of side effect or kidney problems. hope that helps.

sarah

I have used Benadryl long term to help with insomnia.I am having kidney problems. has anyone else had this?

I have been on Yasmin for 2 1/2 years and off of it for 5 months. The only side effects I experienced when going on the pill were thinning hair, severe depression (and I do mean SEVERE) mood swings, panic attacks and bad anxiety attacks. I've always been a very social person and never had problems like this before. I felt as if i was living my whole life in a cloud. My husband and I decided that I should get off of them. However the side effects of discontinuing Yasmin have been worse. I have been sick for the past 1 1/2 months with what I thought was bad food poisoning and gastroenteritis. But now that I have read your other posts I realize that it's all side effects. I went to ER twice, the first time told me that my potassium levels were extremely low (and no I don't have kidney problems) and I was dehydrated. I had severe diarhea, severe nausea, depression, I felt like my whole body was shaking, and I felt like I was going crazy. I hadn't had much of an appetite which is very unusual for me. I got my period on time the first month after stopping, but then my 4th and 5th month I was 2 weeks late both times. I've never had irregular periods since I started at age 12. I'm still dealing with dizziness, motion sickness, anxiety depression. I occasionally have nausea in the mornings and afternoons. When they tell you that your body returns to normal about 3 months after you stop taking it, is not true. I'm into my 6th month and I still do not feel like myself. I'm so glad I found this website because it's literally like I'm reading my own testimonial because all of our symptoms are so much alike. I will never take the pill again. Thank you for all of your posts regarding this and hopefully everyone is on the road to recovery from taking this pill.
Tiffany