Gout And Pseudogout :: Allopurinol - No Results
Nov 27, 2010
I was on diclofenac 25mg tablets for a number of years for gout - however when I had a double heart bypass I was taken of this medication and put on allopurinol 200mg tablets - I have suffered the last 8 weeks with gout on my left ankle which has now also gone to my left ankle in that time I have been to the doctors 4 times and had 1 x ray. I do not think that allopurinol is the medication for me but my doctor will not take me off it. I have had another blood test and waiting for results, in the meantime I suffer with this. I do not think that the doctor is acting on my best interest
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Why do all sites differ on what food you can and cannot eat !! I'm new to this and looking for a few tips on how to lower Uric acid levels pls
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To stop forming Calcium Oxalate stones one needs to take Allopurinol 300 mg daily along with potassium citrate 10 meq 2 pills daily along with hydration and diet.
Allopurinol is used for gout
I am a physician and had my 4th lithotripsy over a year ago
I was miserable
I spoke with many stone sufferers along with medical research. This treatment has been around forever but you will never be prescribed it by a kidney doctor. Lithotripsy is big business
I had recent small stone that passed. My new CT scan showed that the multiple stones seen on my CT scan a year prior were gone.
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I am a 29yr old male, in good shape and not obese. I had my first gout attack 2 years ago, most certainly due to high blood pressure (on meds now). About 6 months ago I had a bad fall and injured the same toe that had previously gotten a gout attack, so I had a resulting 2nd gout attack. I had uric acid of 7.5 and started taking Uloric.
I read alcohol (especially beer) is very bad for gout. I can't say that I've ever noticed alcohol to cause an attack, maybe a few times my big toe has been a little tender the day after drinking a little too much, but never an attack.
So my question is how would you know if alcohol affects your gout or not? I'm a social 29yr old and drink pretty regularly, so I'm worried that it's hurting my gout without me knowing it, if that makes any sense.
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I took the drug for High BP for many years at max dose 5mg/day.
Can cause awkward need to pass water at inconvenient times- but effective against high BP - in my case used in conjunction with ACE inhibitor Trandolapril with some success.
However, if you have a familial tendency to Gout (ie Arthritis in family- as a precursor) then this drug type will make Gout pretty likely.
You will not want to experience the pain of Gout, believe me!
At the first sign of joint reddening (esp. with alcohol usage) then review use of this drug. Certainly reduce alcohol intake.
It took me 6 weeks to adjust to cessation of this diuretic -with some fluid retention problems and BP surging up again.
I've talked to many people over the years about this -and the link between any diuretic and Gout seems very common.
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i have just been prescribed lansoprazole for gout, how will this help?
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Doctor diagnosed gout as my uric acid level is high. I went to see the doctor because my ankles were swollen, he prescribed allopurinol, but so far after 3 weeks my ankles are still swollen and painful, but what's weird is that my right ankle is more swollen than the other. Any explanation?
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Have taken several forms of ppis over the past year on and off and for the past six months cimetidine. Now have gout lower back. You tell the doctor this and he doesn't want to accept it. I do not eat much in the way of acidic - bad diet - and this can be the only cause of it. Yet doctor tries to fob me off with how it is just some temporary thing - a month later it is still there. I have insisted on blood tests for kidney and liver as I know it is not some muscle strain and that would not last a month or have fatigue and
dizziness with it either. He had also told me that people do not get a lot of coughing from ppis. WellI go it and nothing else could have caused it. I only ever had the bad coughing when taking the ppis, it would stop when I came off and start again when I started again. I then found about 50 people online with the same problem.
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My wife got gout in her foot yesterday after eating mushrooms, I believe there is a connection.?
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I have suffered from gout for many years often in big toe on either foot, eventually in most joints to the point of swelling and deformity of joints.
Now it has been named as TOFI which is uric crystals forming as lumps on joints on my fingers, toes , knuckles of hand
I have as many as seven lumps formed on one toe all around toe joint, now it has formed an abscess oozing a thick white mucus now with a gaping oozing hole,this is also happening on another toe.
Went to my doc told me it is tofi I know that, then I saw another locum doc to ask for referral to consultant told NO
take antibiotics finished course to no difference at all in desperation went to a podiatrist she is so shocked to see the state my toes are in and put a dressing on them with a urgent referral to my own doc my condition is so bad now that it has been mentioned I will need amputation.
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I've just been told my Uric acid levels are dangerously high (7.5) has anyone else had or heard of this during menopause? I'm worrying now what with everything else going on during peri.
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My uric acid level when checked yesterday is 13.0 mg/dl... ,how can i reduce uric acid level? also i read in internet that drinking lemon juice,eating tomato will reduce uric acid..is it true?
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I am a 32 year old man and i had my first gout attack 5 months ago (right knee), my gp put me on allopurinol 300 mg daily . the medication brought my uric acid levels down to around 5 and my gp says this is the target , it took several weeks for the first attack to clear and left me in pain when i walk for months . my uric acid levels are still 5 ish and i have been getting really bad flares in my right foot quite regular 3 times in 4 weeks now , is it meant to be possible to have attacks when on medication . i feel like a oap with this , i don't drink alcohol anymore (since first attack) and eat a low purine diet , if anyone has any advise on this it would be good.
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I've had this nasty gout episode for four days now and I am reading conflicting information, perhaps a few of you with some experience can help. First, is it better to apply heat, cold or both? Second, will walking around and staying active even through the pain make it worse, better or stay the same? Third, is there any prescription out there that works without any nasty side effects? And lastly, knowing that I have gout, is it really necessary to see a doctor?
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Is it OK to start colchicine after taking naproxen?
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I am aware that us folks with a gout flare-up are taking many different types of medications but I wanted to know if any of the folks in this forum are also taking Lipitor or the generic Atorvastatin for high cholesterol?
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I’ve been dizzy for almost 6 months now. Vestibular dysfunction, tried VRT with no real improvement and my neurologist put me on Nortriptyline. He said it would take about a month to really start working and he’d see me back in two months.
About two weeks into it, I found my limbs were feeling weak and shaky, making walking even more difficult and anything requiring a lot of standing or balancing on one leg very hard. I called to let him know, and he said to keep going since I wouldn’t know yet, I was still adjusting and he’d see me at the end of two months.
Well, it’s over a month (this is my 32nd day) and things keep getting worse. The dizziness is stronger and more persistent, the shaking hasn’t gone away, my eyesight is worse, I sometimes feel like I’m plain going to pass out and all this has given me chronic headaches for the past two weeks straight – I feel like I live on pain relievers. But I’m scared to call the doctor – he’s made it clear, two months.
So… has anyone else taken Nortriptyline for the dizzies? Is one month just when getting better might start and you need to leave it longer to see real effects?
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I had a Prostatic Arterial Embolization (PAE) procedure done at the University of Miami on June 2, 2015 by Dr. Shivank Bhatia. Prior to the procedure I had completely lost my urinary function and was wearing an in dwelling Foley Catheter. I had been told by a prominent Urologist at UM that I would never urinate on my own again, I needed to learn how to self catheterize and that if I chose to have the PAE procedure I should expect it would not be successful. My prostate was over 100 grams, I was not a candidate for the TURP and I should go home and have a nice weekend.
My attitude was I had nothing to lose. If the PAE did not work I was no worse off than if I did not try. Dr. Bhatia was an expert in this procedure so I took a shot. My results have been nothing short of miraculous. The procedure was done on 6/2/15. I never had one ounce of pain, either during or after the PAE. I continued to wear the Foley, but it was horrible. I went for my first follow-up 10 days after the PAE. I still could not pee on my own. Dr. Bhatia wanted me to continue wearing the Foley for another week, but I just could not. He was understanding of my discomfort and I was shown how to self catheterize and went home without the Foley, thank God!
I used the catheters approx. every 6 hours or 4 times per day. Each time I used them, I would try to urinate on my own. On June 25th at around midnight I attempted to pee on my own and 6 drops came out. It was a revelation. I then used the catheter and went to bed, arising at 6 am. This time when I went to use the catheter 12 drops came out. Each time I went to use the catheter things would improve. From a weak stream to ultimately a regular pee. I reduced using the catheter from 4 times per day to 3, then 2, then I was comfortable knowing I did not need them at all. On July 1, 2015 I stopped using catheters. I never have looked back.
Three months post procedure I had an MRI. My prostate had shrunk from 0ver 100 grams to 72 grams. My PSA had gone from 8.7 to 2.5. I no longer had any symptoms that would indicate prostate or urinary issues. I sleep through the night. I pee when I have to go, but can go 6-8 hours in between bathroom breaks. I have no discomfort, no pain, my sex life is outstanding and I am 66 years old! Dr. Bhatia has given me my life back.
My suggestion to anyone who is having symptoms: Explore ALL OF YOUR OPTIONS!! I am certain the PAE will become Standard of Care in the future. Try and understand what the potential side effects are of the "traditional" surgical procedures. They may be acceptable for some, but they were not acceptable for me. I take no drugs or medications. The PAE had no side effects. There was no possibility of becoming incontinent or impotent or having an orgasm without an external ejaculation. Find a facility that is doing clinical trials with the PAE and a Dr. who is experienced. Peeing through a straw for the rest of my life was a real possibility. Now I function like I was 40 years old, not 66 years old. I highly recommend Dr. Shivank Bhatia of the University of Miami. He learned this procedure from the man who invented it and he trained with him in South America to perfect it. You have very little, if anything to lose, and you have getting the rest of your life back to normal to gain. Happy to answer any questions or inquiries. Good Luck to all.
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I have recently had blood tests again and have a low esr. I have symptoms of pmr and discussed these with my gp. I begged her for prednisolone and she reluctantly agreed but only one week. I felt great! I was walking normally, getting out of bed for the whole day where I was bed bound a lot before, just felt so wonderful having so little pain in my hips and shoulders. My blood tests came back normal and she said she cant give me any more and is referring me to rheumatology again. The pain has come back, my hips are crippling me my shoulders are so so painful again and nothing else has worked, just the prednisolone. My orthopaedic specialist may give me one more injection in ten days, vpbut that will be the third and he said 3 is the max so I should have relief for 3 weeks, if previous injections are to go by but after that.
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I have been on roaccutane for while now, about a year or so. My skin has healed significantly, but I still get some small pimples from time to time but my face has become red on the parts that . Recently, I got a small pimple, it bursts by itself while I was asleep. 2 days later, the pimple healed by itself, the hole by the pimple has totally sealed, but there is this Small patch of redness where the pimple used to be. My questions are:
1) will the patch of redness go away on its own?
Recently, i have also taken up water polo, but with my condition, can I still play?
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Has anyone had gestational diabetes? I was diagnosed with it and everyone says I'm gonna have a big baby. Is this always true? I've only gained in my belly. I'm all belly pretty much. I think my size is normal for 35 weeks. I'm close to what I was with my first and I was all belly with him.
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