Kidney problem symptoms and conditions

After after a few months on topamax I went on lexapro for my mood change. I lost weight, had the metallic taste, loss of words , stumbling and more. I have weaned off because I could not stand the side effects. I still have migraines frequently. I truly believe the topamax has permanently changed my personality. I cannot get off the lexapro. Also I believe I have some kind of kidney problem left from it. Is all this possible?

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

Hi, I have been reading all the postings and my heart goes out to everyone. I been there, done that. Myself, I have a seizure disorder and been on Lamictal since 2003 (I can't recall/remember) - I had tried 5 other seizure meds that didn't work for me. For quite a while now I take 600mg a day and Keppra 250mg to control my seizures. I lost my driver's license twice so far (I know that is the rule in CA) , and once not long ago (I got my license back) I got totally lost in my town, which I used to know like the back of my hand. I thought I had lost my mind. I asked my doc if I was getting demenia and he said oh no you are too young (53). I have also learned doctor's (for the most part) are idiots too. They don't think outside the box for us. I can't spell anymore, get depressed easily. I really want to work, but I can't. I have tried time and time again, but (yesterday) it just about did me in...people explained to me how to do things on the job many many times but I couldn't retain any thing. People just looked at me as if to say what planet did you come from. I cried on the job so hard I wanted to disappear. I am so sick of my family saying "I know you can't - don't remember this or that..... I can hardly bare that. Now I have a potential kidney problem. Suppose it is from these meds? I am really scared.

I have now tapered to 10mg prednisone every other day and will end 75mg Cytoxan Aug 19th. Just went to the Dr. and she said protein is back in urine (bad) but also rising in blood. (good) I can continue to taper prednisone but will have to have another 24 hr urine speciman to determine wether I have to go on cyclosporine. Was originally diagnosed with Minimal Change Disease, but now she thinks it could be another kidney disease. Has anyone had successful tapering with the addition of cyclosporine? Does the urine protein ever get higher? What about side effects of cyclosporine.

I was diagnosed with Crohn's disease in July. I had my colonoscopy/endoscopy the day before 4th of July. Got sick with what I thought was the flu on June 26th. That's when I first landed in the hospital (dehydrated & sick). After the diagnosis I was first put on Entocort and Pentasa (Pentasa is supposed to be a remission drug - keep you from having flare-ups). Entocort didn't work so they switched me to Prednisone. I've been on Prednisone for about 6 months now. Going from 20 mg to 40 mg and then I'm finally weaned down to 5 mg. I get to go completely off of it Jan. 13th. Scared of what other side effects might occur from coming off the drug. While on it I've had emotional problems, acne(never had a problem with it before), moon face, gained 30 pounds, joint pain (I was in therapy for as long as insurance covered. - I recommend water therapy, it helps for some people as it did me), trouble sleeping (haven't slept a full night since I got sick), certain days I'm really really thirsty, I've had sort of what I'd call restless leg (I had this before I was on this medicine but it has gotten significantly worse - mostly at night or when lying down), and dry skin.I have to say though that the WORST side effect is the FOG. It's horrible. I enjoy learning and using my brain and when I'm on this I can't think, I mix up words, and it feels like my brain is covered in cobwebs.I had to drop a calc 2 class and that got me off the track I'd set with my academics. My inflammation rate is down where it's supposed to be as of the last blood test a couple weeks ago. So I guess the Prednisone and Remicade are doing what they are supposed to - but I still don't feel as if the pain (not associated with Prednisone - caused by the disease) has gone completely away even if the inflammation has gone down. And Prednisone's effects are just horrible. Some nights I feel depressed and just want to cry and cry. The past months have been trying because of several hospital stays, switching to many different doctors (gastrointernologists, nephrologist, urologist (kidney stones), primary doctor - and they think maybe I should see a rheumatologist), and Pentasa (it began shutting my kidneys down). I just hope that when I come off the Prednisone the side effects will fade (hopefully quickly but lets be realistic - ill just be happy if they go away sometime in the next few months) and I won't flare up again. Anyone know the best way to get rid of the weight? I'm already drinking lots of water and I go walking and do exercises everyday.

QUESTION: When tapering Prednisone does anyone have a place(s) on their stomach that are sunken in and feels dry compared to the skin around it?

Anyways, I hope that everyone overcomes their difficulties, whatever they might be or concern. It's hard to have a life when you are constantly fighting your own body to stay healthy.There are plenty of situations in life that are already hard enough to deal with without medical issues of your own. Best of luck to all!

I have been on zocor because of high cholesterol. It was caused by a kidney problem I have. I now can hardley walk across the room because of the hip pain,leg pain, femur, side aches,I even have pain in my back side which makes it hard to sit. I have trouble sitting, standing. and laying down I can not stand to be touched any where below the waist. it sends pain all thought my lower body. My back hurts also. I also have problems with my left arm. I can not even life a cup of coffee with it and at times have to use my right arm to move my left one. We thought I might have fibermyalgia until I came upon this website. I also had my medications changed a month ago and have read on a different web site that if you take zocor with cyclosporine it can increase the chances of muscle damage. I have such sever pain at times I have gone in to the emergency room for relief. Even taking a pain medication and getting pain shots at times has ony relieved it for a few hours. I have not been able to sleep because of the pain. is there any lawsuits against cyclosporine or zocor. No where is there any reference that you can not take both at the same time.

I started Fosomax with D one day -one dose-. I experienced pain in my back so severe I could not walk. I would let out a yell just trying to get dressed or move. It started in my pelvis then worked its way to my back (lower center) it was like a spasm. I thought i would have to go to the emergancy room. Today day two it is a little better. My pysician with be notified.
I will not go on it again.

Hi everyone,

An update for you about my magnesium. I went to a kidney specialist yesterday (my doctor thought I might have kidney issues because my magnesium level was not increasing even with supplements). He was perplexed as to why I was there and basically told me that my magnesium levels were not low enough to be considered for any kidney problem (YAY!!!). He also said that he wasn't convinced that my heart palpitations were caused by my magnesium levels. He asked a little bit about my history and when I told him I was off of Yasmin, he said "GOOD. Find another form of birth control. I won't let my wife take any oral contraceptive". We continued our conversation and I thanked him, expressing how good it was to hear that from a doctor, since most of my friends think I'm paranoid. He repeated the warning to not take oral contraceptives and we ended the visit.

SO, basically I think my heart palpitations have been Yasmin/Orthocyclene related all along. I will wait to see how my body feels in a few months. Also, he said my magnesium levels seemed fine to him and they won't increase with oral supplements because it's very badly obsorbed, and if anything I would get diarrhea instead. (don't want that....)

I'll keep you posted... on the road to better health, I can feel it already! I'm so excited to get that validation from a doctor!

I was diagnosed with a kidney disease when I was 14, and was put on prednisone on and off for a few years. After being free and clear for four years, my kidney problem is back, and I am back on the prednisone, 60 mg a day for the past month. My doctor said I can wean myself off and go to about 40 mg a day for the next two weeks, but this is when I used to have relapses in my condition. I am looking for ward to getting off of the prednisone though, my face is so swolen, and I feel like I look like a bobble-head. My cheeks are so full, and I have the worst double-chin. At first, the prednisone gave me so much energy, which was fine with two kids at home, but now I am just irritable and tired. I am starting to gain weight in my stomach now too. This time of year is the worst too, because the prednisone reall effects my immune system. I have to worst cold, and I had to get a flu and pneumonia shot.

The worst part of the prednisone is the swollen face though. There is no way to hide your face. The weight gain in m stomach can be hidden with a bigger shirt, but I can't seem to hide the ound cheeks. I wish I knew how to apply my make-up to hide it, but I can't It's awful!

My doctor started me on Zocor in December to lower my cholesterol. New Years Eve I developed a fever and a pain in my groin area on my right side. My doctor diagnosed it as kidney stones. I was taking the Zocor, they told me to drink plenty of water. When the stone hadn't passed the next day they gave me Viagra to take and told me to drink beer. I asked about the beer and Zocor because it said not to drink with this drug but the doctor said it was ok. I drank two cans of beer for two days. The third day I drank a can of beer and threw up. The pain in my right side moved and finally stopped. Three days later I had severe lower back pain. The doctor told me that I had a severe kidney infection from passing the kidney stone. He gave me antibiotics and pain killers. After the antiobiotics I was in pain again. It started in my right groin area, I also had pain on my right side, lower back, legs, knees and arms. I was sent to a urilogist to rule out a kidney problem. I told him my symptoms and he said it sounded muscular. At this point I could not walk without help from my husband, I was nausiated, could not sleep at night after taking the Zocor, no sex drive even after the pain got better. For one week I could only lay in bed in pain. There were all kinds of tests done on me and they could not find anything wrong with me. The only relief I got was the shot the urologist gave me and the Viox for the pain. I called my doctor and told them that I thought it was the Zocor. I also experienced numbness in both my hands and arms. Four days since I stopped taking Zocor. Feel better already. I will not take this drug again. I pray symptoms will leave.