Kidney symptoms and conditions

Are there any meds that are safe? I was taking 10mg norvasc. I started taking 20/25 mg lisinopril. I was doing ok on the norvasc but the added lisinopril has almost killed me. They had cut my norvasc down to 5 mg then to 2.5 mg when I started the lisinopril. 4 days ago I stopped the lisinopril and added back 2.5 mg norvasc. Back to 5 mg. The side effects seem to be letting up. Now im wondering is all of my meds are killing me. I can't live without them. My BP sores. Im so scared of what I should do. Im afraid of all my meds.

Hey Guys,
I'm new to all this but just wanted to share my story with everyone so I feel like i'm not so alone! I'm 23 and was diagnosed with SLE 3 years ago.
It started in my joints and then moved to my kidney's real fast. I now have stage 4 nephritis, finished 6months of cyclophosphamide in Feb and have been on no less than 40-20mg of pred for about 2years. Just when things were starting to look better it has stared in my blood so they are trying to up my dose again. It has thinned my bones so I am on special meds for that now too.
I know taking the pred is something I need to do to live but it comes at a really high price. I don't even look like the same person I used too because of the moon face. I know it's shallow but at 23 it is almost as bad as having to live with this disease. I now have really low self esteem and get anxious all the time, which is affecting my job. As much as I want to come off I also worry that I would have to stop work again as the pred is what keeps me going. All I want to do is get off it though! Anyone know any alternatives? Also, just wondering if you guys are still drinking alcohol while taking pred?
Thanks for listening guys!

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.

After taking remicade for appx. a year, I started having heart problems, A fib, ending up having heart surgery, a kidney has collapsed, and had a lesion appear which was squamous cell carcinoma. All these problems developed have taking remicade; I do blame it for my problems. My Dr. treated me for ankylosing spondylitis, a form of RA. After so many problems, another Dr. told me that I did NOT have AS. And it did not help my pain at all. This is a troubling experience for me, and has been the worst thing that ever happened to me.

hair loss after prednisone?

i took 60 mg of prednisone for 1 month for a kidney inflammation. i tapered down for months and finally have been off it completely for a few weeks. i did lots of natural things and really had no side effects- my face did get puffy when i was tapering, at about 30 mg but that's gone now. and my lip hair came in fuller but it's pale blonde so it wasn't too much of a bother

however, suddenly my hair is falling out like crazy. i took advair for many years (only 1/2 dose) and didn't connect it with my hair thinning until i started reading this site. i weaned myself off advair and noticed soon after that my hair loss in the shower was minimal

then i went on the prednisone and i was still fine. has anyone noticed hair loss after stopping prednisone? will this stop after a while?

I took 1 Levaquin pill 500 mg one evening in September 2007 for a kidney, UTI infection. My left side went numb and started tingling, my left hip hurt, I could not put weight on my left leg, had to limp to walk. I had severe pains shooting through my head, felt dizzy, nauseous, weak, had to stay in bed for 3 days after taking medicine. I could only limp to eat and bathroom. I called doctor, they said KEEP TAKING IT. NOT. They told me that these were normal side effects. I read on the internet that these are NOT NORMAL side effects. I didn't take anymore and read about alternative medicines. I was still in a lot of pain in my kidney and bladder. So I asked for Bactrim, a sulfur based drug. It worked great on the kidney/UTI. But since I took the Levaquin, my joints hurt and pop, my achilles tendon is painful everyday, my shoulders have excruciating intermittent pain and my hip hurts inside when I move it. Also, there is a lot of crackling and strange sounds in my joints now. My wrists have been having a lot of soreness as well. I just read about Levaquin causing these problems for years after you take one pill. I didn't know all of these symptoms might be connected to the Levaquin. Does anyone know how to get the Levaquin out of your body and joints???

Ayurvedic Herbal Treatment for Hypertension

Hello. I have been dealing with my hypertension now for approximately 1-1/2 years now and those of you that have read my findings through my previous posts know that I'm always looking for natural supplements to stay off of the lisinopril. I stumbled onto a new herb for bp. You absolutely have to try this. I went to see my doctor yesterday and I was having a really stressed out day dealing with a family crisis and my bp was 150/100. I left with a prescription, but I received my order of this stuff in the afternoon and I took the recommended two tablets twice a day and woke up this morning with my bp 108/69. This product gets shipped from India and takes approximately two weeks to arrive by registered air mail, but very much worth the wait. I have the link to order it and to read more about the herbal treatment. If you are interested, feel free to e-mail me and I will send it to you. Take care and good luck.

Dear Medications.com:
I cannot thank you enough for this site. Just yesterday I was prescribed Cipro for a nagging UTI which seemed to only partially get better with Doxycycline HYC. After only 3 Cipro pills I am stopping!! And will never take Cipro again. I take responsibility for rushing back to my doctor at the emergency care clinic and asking 'now what' after the Doxycycline was finished--we Americans are so quick to want the next candy pill with more strength! So even though my initial urinalysis showed no dangerous / STD bacteria present, because I was still urinating too frequently my doc suggested Cipro. I trusted him and took the first pill last night--I got a terrible headache, woke up promptly at 3:30 AM and had trouble returning to sleep. Got up this morning, took the 2nd pill and by early afternoon, was so tired and aching I had to lay down for 1.5 hrs..I felt miserable. Then this afternoon, after taking my 3rd pill, that's when I began to feel occasional tingling in my joints, hot pain in my knee capsules, continuing low-grade ache to my head, the feeling that my esophagus was shrinking, etc..... EVERYTHING you guys all have reported.

I got on the internet and thank God I found your site. After 2 hrs of my own research and the testimony of so many people, including tons of once-healthy, athletic persons whose lives have been destroyed irreparably by Cipro, I took my healthcare into my own hands, called my pharmacist and said 'I'm finished touching Cipro...never again will I take it.'.

This drug is more toxic than anything I've ever taken, and the way my body has begun to react in only 24 hrs, it is obvious that the drug co's are playing with fire on this compound. We as people must stand up and take action, and educate our doctors. I am taking some info. into him tomorrow, telling him i will be on a strict cranberry juice and kidney/liver tea detox program for the next few weeks to see if these 'natural' methods might help me rid my system of the bacteria.

In any case, I refuse to use Cipro ever again and hope that many more people will read these pages before ingesting any or too much of this dangerous drug.

d. r.
48-yr old sporty, and very healthy guy who wants to stay that way!

Hi. Im a nurse who was put in Topamax for mood stabilization in January of this year. Tapered up from 25 mg a night and now am on 200 mg a night. I have lost ZERO pounds although I have no appetite and cant stand the taste of a soda. I just wanted to share my nightmare. I have not had any tingling or numbness, which is a main side effect.

I do have a terrible metallic taste in my mouth and my mouth never feels clean. YUCK. Sodas flat. My personality is flat.. I am exhausted. My friends say the person they knew is gone, my appetite is gone.

My back hurts all the time like it's very tight in the kidney region....I cant spell, I cant remember yesterday, I sleep all the time when Im not working...I drop things, I don't remember what I was doing 10 minutes ago, I feel like I am on the outside of my body looking in.

My vision is blurred somewhat at times.

I work for a neuro-psychiatrist. I have decided to taper myself down. I don't think it has done anything but made me so flat I am not here anymore. Who wants that? Looking back, I was not in need of mood stabilization but a vacation.

The only thing it has helped me with is it has stopped the desire for Klonopin which is normal for Topamax. It works on the receptors in your brain that make you crave benzo's. I took my Klonopin as prescribed.

Im thinking I want my old self back. I miss laughter. :(

I'm sitting here in tears reading all of your posts because I've also been on prednisone and have horrible side effects. I was diagnosed with metastatic breast cancer in my lungs in June of 2002 and, after starting at 60 mg/day then, I have been on 20 mg/day for years now. The very first posting that I read mentioned problems with the femur bone. Besides all of the other problems associated with this devastating drug, in December, 2007, I broke a bone in my left foot with no known cause for it. Then I started experiencing pain standing or walking in my left leg and was diagnosed with a fractured femur bone and after several months of trying to get it to heal (including an ultrasonic bone healing system), it just kept getting worse until an orthopedic surgeon recommended that I have a 16 inch rod put into my leg which I did and it ended up to be one of the worst decisions that I have ever made. After experiencing all of the prednisone side effects for almost seven years including depression, severe fatigue, weight gain, moon face, thin skin, cataract surgery on both eyes, hump on my back, mood swings, etc., the pain and suffering that were caused by that operation brought me to seriously consider suicide. I was also diagnosed with chemical neuropathy in both of my legs also which makes my legs so weak that I have to crawl up any steps and have trouble just standing. I actually have an appointment for this evening to have an x-ray done to see what is wrong with my knees and did not realize that this also is yet another side effect. I never make it through the night without waking up in pain and getting a pain pill and then getting up in the morning is almost unbearable with that "burning" pain. I am now on Cymbalta for depression, Xanax for anxiety, Percocet for pain, and of course 20 mg of Prednisone. I was told that I would have to remain on Prednisone for the rest of my life because of the lung scarring and COPD. After reading all of your comments, I have decided that I would rather put up with any breathing problems (and I don't even know how slight they may be at this point) than to remain on the Prednisone. I have tried weaning off several times but get so fatigued that I can't move and that's dropping one mg every week. I'm affected by the decrease but it gets out of hand when I get to 14 mg and I get so frustrated and depressed at not being able to do anything that I just go back up to the 20 mg/day. If you have been able to wean off of it, would you please let me know how you did it and what you had to go through? I'm 65 years old now but I have two wonderful granddaughters (ages 4 and 6) who I can't do any normal "Grammy" things with anymore at this point and I have to change this condition for them and for me. Obviously, the doctors don't recognize the severity of the drug because they just keep prescribing it and out of a regular doctor, an oncologist, an orthopedic surgeon and a neurologist, they can't seem to get together to come up with a solution. I have to say that I haven't considered suicide lately but I do wish that I would just die and be out of this pain. My family and definitely my granddaughters and wanting to see them grow up are the only things that keep me going. There are probably things that I'm forgetting but I'm sure that one of you have covered it in our posting. Although my family is so supportive, no one and I really mean not one of them, realizes knows what we all go through because of this drug. How could they know that something that is supposed to help you could cause these problems? My life is a living hell, all because a pulmonary doctor prescribed prednisone seven years ago and I trusted him to only do what was right without informing me of what was to come. I more than sympathasize with all of you. I sincerely appreciate the time that you took to post to this site and so thankful to know now that this knee pain is not something new that I have but another side effect of the prednisone. I wouldn't have known that if it wasn't for this site because I'd be willing to bet that after I would have had this x-ray done, one of my doctors would have just prescribed another medication to take. Please feel free to contact me directly with any comments or especially any help that you can give me. I know that all of you are going through the same thing so if I can do anything for you, even just listen and understand, please contact me also. Sometimes that's the only thing that people can do is to listen and someone who is in the same situation can always understand. I'm here for anyone who needs a hug for the day.

I was on Yasmin for only a month in November 2008. I quickly got off of it because of the side effects. I wear contact lenses, yet my vision was getting blurry. I was training for a marathon, yet I was gaining weight (and it wasn't the muscle mass I was also gaining from training). I began to have horrible headaches, retaining water and I even got these little red rashes on my arms and breasts. At the time, I didn't know that Yasmin was causing all of this and ruining my life! Now I know it's Yasmin. I went to my doctor, she performed various lab tests (including liver, kidney, thyroid) and I am perfectly healthy. So I did major research on Yasmin and discovered all of my ailments were on there as side effects. My advice for anyone experiencing anything similar is to either change the dosage or just get off of it. It's not worth it. Yasmin is the devil! I mean think about it, we are messing with the natural way our body's hormones function. Oh yeah, and not to mention that I started losing some of my hair as well.

I had a kidney removed at the age of 19. I recently had a UTI and was prescribed sulfameth/trimeth ds for it. With in an hour after taking the first pill my hands turned bright red and were uncontrollably itching and then the rest of my body started to itch, with in about 2 hours it felt like i had been beaten up my entire abdomen hurt (movement like coughing and breathing hurt the most) By the end of the day when it was time for my second dose i was beginning to get really concerned, but i took the second pill thinking i needed to protect the only kidney i have left. The next day i wasn't able to go to work i was in so much pain in the abdominal area. I also feel light headed and short of breath. I DID NOT receive a drug facts paper with the side effects like u would with any other drug ive ever gotten and im starting to wonder why. So I called the doctors office that prescribed it to me to see if it was an allergic reaction or side effect and it took them 2 days to call me in a new prescription! Heres hoping it didn't harm the kidney i have.

I came to this web in hopes to see if the Mirena has ever caused kidney or bladder issues...which I guess it's not fair to say that the Mirena or being pregnant caused my stones since I've had UTI problems most of my life. Yet, reading over your stories I really feel sorry for all the women having problems...I have to admit that since getting my Mirena in about 18mths ago I've had no real problems. Sure at first there was cramping and on and off bleeding for the first month or so, but over-all I love it. I've had no sex-drive problems, weight gain, or abnormal depression...that's saying a lot b/c I'm Bi-polar and haven't taken meds for it in over 7yrs. Now I do have cramps sometimes and never actually start my period, but I'd take that any day over the sever cramps I used to have. Also I was plagued by ovarian cysts, but surprising enough I've had no problems since having it put in...which was a concern for me since it has been known to cause them. I don't know what really to say but just as with any new meds, etc., look into it before you jump in. I had MORE problems with your standard BC pill then with the Mirena.

Dehydration, kidney shutdown, continued urine retention. Almost died from using this drug.

I started taking prednisone when I was only 12 years old and I was on it for about a year and a half. At the age of 10, I was diagnosed with glaucoma, uveitis and cataracts and for about 10 years now I have had all these illnesses. My experience with prednisone had been HORRIBLE. Within two months alone, I gained 50 pounds, my skin started to get really really thin, I started to develop stretch marks ALL over my body with the only exception of my face and hands. I started to get the chipmuk cheeks to the point that my family was afraid that I was going to literally explode. My liver was damaged. My kidney was damaged. The vertebrates in my spine where being chipped away. There was a point in that year and a half where the doctors told me that there was a 70% chance of me going blind. The bottom line was that PREDNISONE WAS BRINGING NOTHING FOR ME EXCEPT RUIN. On top of that, I was constantly depressed. Kids at school would point at laugh hysterically at me. And if people weren't laughing, they were struck by fear and were trying to figure out what exactly I was. I remember this one instance in my school cafeteria where one girl stood up on the lunch table, pointed at me and screamed SHE'S AN ALIEN!!

I was and still am scarred physically and emotionally. My arms and stomach are really saggy because the skin is soo thin. As I said my entire body is scarred with stretch marks. I can't show the slightest bit of my body to anyone because I am so ashamed, embarrassed and afraid of peoples judgments. I am afraid that no one will ever want to be in a relationship with me.

All I can tell you is that though I stopped using it about six and a half years ago, this dreaded drug has truly ruined my life from the very start of my childhood.

On April 21, 2009 I was given Avelox for a sinus infection that I have been fighting since September. I has nausea ,vomiting, hurting all over, headaches, burning pain down my neck, my intestines feel like they want to come out, my kidney s feel like they are trying to rip out my back, i am weak, having crazy dreams, acid reflux, craving salt....i was given a ten day supply ...I took nine. I had no idea that all of this was from Avelox until I found this website I feel like I could just die. When will I get better and how long will the symptoms last I have not taken any since April 29,2009 Can anyone give me answers!!!!!!!!!

I have noticed numerous side effects within the last 2 months. I had mine inserted last year, and it seems the longer I have had this in the more effects I get that stay with me longer also. I would please like to hear replies on any one that has had muscle swelling/fluid in the hip/thigh buttocks area. Like sciatiac pain with swelling.
Mine comes and goes and I would like to know who else has this.
Thank you.

OKAY!!! after reading everyone comments about mirena I decided to tell yall about mine. I'm 19 years old, I recently had my daughter July of 2008. I got my mirena in at my 6 weeks appointment and had it ever since, since then I've had major mood swings, I'm always bitchy and always exhausted like i never get enough sleep. And every month I have the ovarian cyst which my doctor said it normal when your on the mirena and that every month I can feel them rupture which hurts like hell... And also before I had my daughter i weighed 125-127 and when i was pregnant with my daughter i only gained 10 pounds so I weighed around 130-135 NOW get this after having my daughter I weigh 148-150 and im only 5"1' and 19 years old I've never been so big in my life... not only that I have other side effects they are Poor memory, Lethargy Hair loss,
Weight gain around my stomach, Feeling constantly bloated. Agitation, and every time my fiancee touches me or wants to do something I don't want to its like I don't wanna have sex anymore and also get depressed and I get very very irritated with my fiancee to where I just want to pick my things and my daughter and get up and leave him its like his consistly getting on my nerves but after reading everyone input on it im calling my doctor and having it taking out.. thanks everyone for yall input.

Nausea, bloating and pain of the abdomen, stinging around my kidney, I have been taking MOM for 14 days instructed by my doctor, never felt worse, experiencing puffiness in my face and major heart burn, unusual salty taste in my mouth.

Maybe I am having more of an allergic reaction to this product.

Nausea, bloating of the abdomen, stinging around my kidney, I have been taking MOM for 14 days instructed by my doctor, never felt worse, experiencing puffiness in my face and major heart burn, unusual salty taste in my mouth.

Maybe I am having more of an allergic reaction to this product.

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much rennin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued well for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turning straight and my incredibly (can't do nothing with) thick hair started to thin and become style able. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kind of job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... In December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not going to have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA or I would have lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing blood work from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much rennin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much renin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued good for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turing straight and my incredibly (can't do nothing with) thick hair started to thin and become stylable. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kinda job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... in December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not gonna have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA, or I would of lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing bloodwork from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much renin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

I was asked to take Lisinopril by my doctor today, after reading about all of these people bad side effects I want no parts of this drug, and why are doctor's recommending this drug to patient and know that it has so many bad side effects. I really don't know what to do. I'm 58 years old and I'm diabetes. Two weeks go the doctor stated that my kidney was at a 4 and that they found a little protein in my urine. Now to I need more problems add to my health. I looking for answers.

I was prescribed Topamax for prevention of migraines, since they are getting worse, and my usual meds didn't seem to be doing the trick.

I only took it for 9 days at 25mg dose (1X per day) and at day 8 I awoke with the most HORRIFIC back/side pain, I could hardly stand. It worked for my headaches, but now I still have back pain, and I have to call the doctor, as I am showing serious signs of KIDNEY DISTRESS.

To the best of my knowledge, I did NOT have any issues with my kidneys before taking this med, but I may now. I was told about many of the side effects, but NOT this one. I sure hope this drug hasn't pushed me into some kind of renal failure. I would rather deal with the migraines any day. Thanks, Topamax!

had a moderate to severe reaction to levaquin 2 years ago.. we know the symptoms.. Here is what i did to help.
1) Eat only ORGANIC They spray meat that isn't organic with floxins, do NOT eat processed foods, fast foods, start cooking at home and eating RAW You wont believe how much better you will feel when you go organic. Vegetarian and Vegan even better. ALKALIZE get your PH to 7.5. Acidity is the worst when you are sick like this
2) Hulda Clark cleanses...Dental Kidney, Liver , Parasite , Bowel ( *******)
3) Keep moving
4) i used some stuff called waiora its amazing
5) sun, swim in ocean if you can and walk an hour a day 5) be positive 6) JUICES buy a juicer and drink a beet, cucumber, lemon , ( ORGANIC!!!!!) with one tablespoon of organic olive oil, drink every day
7) fish oil, calcium and magnesium , a good pure multivitamin ( crainuls on *****)
8)Don't be obsessed with whats wrong, get into what feels better.