Review: could Avocado cause Ckd (Chronic Kidney Disease)?
Summary: there is no Ckd reported by people who take Avocado yet.
We study 3 people who have side effects while taking Avocado from FDA and social media. Find out below who they are, when they have Ckd and more.
You are not alone: join a mobile support group for people who take Avocado and have Ckd >>>
Avocado has active ingredients of avocado. (latest outcomes)
Ckd (chronic kidney disease (ckd), also known as chronic renal disease) has been reported by people with depression, high blood cholesterol, hypothyroidism, stress and anxiety, high blood pressure. (latest reports from 42 Ckd patients)
On Jan, 6, 2015: No report is found
Do you have Ckd while taking Avocado?
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- Can saphris cause creatinine levels to rise?
Can Saphris cause Creatinine levels to rise?
- Is lercanedepine causing me to gain weight?
After a very bad road accident in my early twenties I developed giddiness and arthritis. Since then I have had several operations , recently one to remove abdominal adhesion and another to remove a bone from my wrist. I keep active and am the sole carer for my 92 year old husband , who has Alzheimer's .
- Has spireva been proven to cause kidney disease?
I have been diagnosed with ckd about 3yrs. Ago. My gfr has be hovering around 44 except when shingles broke out. I was sick for about 3 months. Then my gfr went down to 30. Now it's at 44 again. I know that some of my other medicines have been connected to kidney problems, but I have been on them for many years, and have no problems. I have been using spireva for 6 yrs. .
Kidney problems started 3 years ago. After searching on the Internet, I stopped using spireva in the hopes that my kidneys may improve. Do you think that could be possible. My GP is a nephrologist, and has said nothing about stopping spireva, even all of the literature states spireva should not be used in the presence of ckd. Any info would be appreciated. Thank you.
- I have a problem with gout, can tolprl contribute to this problem, when i took this drug in the several yrs ago i was on allpurnol for the problem. when i quit the drug the gout stopped.
i RECENTLY HAD A HEART ATTACK AND A STENT HAS BEEN PLACED. MAY 29, 2013 SINCE THEN I HAVE HAD TWO BOUTS OF GOUT. ON PREDNISONE FOR SIX DAYS OFF FOR 7 AND STARTED AGAIN FOR SIX DAYS. i KNOW THAT WITH THE KIDNEY DISEASE MY URIC ACID HAS BEEN HIGHER, HOWEVER THE PROBLEMS i HAVE HAD WITH THE GOUT PRIOR TO STARTING THE TOPROL FOLLOWING THE HEART PROBLEM HAD NOTBEEN NEARLY AS OFTEN
sEVERAL YEARS AGO I WAS ON THE TOPTOL AND HAD A GREAT DEAL OF TROUBLE WITH GOUT AND ON ALLPURINOL. AFTER STOPPING THE TOPROL I STOPPED THE ALLPURINOL AND DID NOT HAVE A PROBLEM UNTIL NOW.
More questions for: Avocado, Ckd
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- I need advise, badly ckd!! (1 response)
The orthostatic BP started in mid April, I was only dizzy upon wakening then it would subside. I have never been a big breakfast eater so I started doing that. We were in Disney later in April and I was extremely fatigued, to the point of not wanting to walk, Disney would be the first time I passed out when getting dizzy. I of course said I had gotten too warm and was exhausted from work the previous week. The dizziness continued in the mornings & I passed out several more times. On May 1st, I passed out while putting my make-up on and hit my eye on the faucet and head on the tile floor, despite that I went to work thinking it would subside, it didn't. I went to the ER directly after work. They ran a B-met on me and my GFR was 11 and creatinine 3.95. They admitted me to a larger hospital for evaluation. While in there, they pumped me with fluids continuously, saying I had severe dehydration. My kidney function improved, my creatinine levels went back down to 1.34. After 5 days I was discharged and told to see a cardiologist and endo. The endo doc cancelled my appointment on the basis it was not his area. I had had a cortisol and ACTH testing which I guess was normal. I saw the cardiologist, who said it wasn't cardio. I had had an echocardiogram in the hospital and EKG monitoring. Cardio sent me to neurology, the PNRN did a basic neurological exam and drew blood for disease markers such as Lupus, sjorgens, hepatitis, ect. All disease markers came back negative, but my GFR was at 11 again and creatinine was 4.25, BUN 50 along with an elevated ACE level. They called me and said I sarcoidosis. I really don't have any of the primary S/S of this autoimmune disease. I don't know where to go from here, they are referring me to another neurologist at a bigger hospital. I can't live my normal life, can't walk on my feet due extreme pain and I pass out at least 2x a week, which is not good for my old body. My BP upon laying and sitting runs like 117/72, upon standing it drops to like 70/50-50/30. I am on 0.1 mg of florinef, I tried increasing it but then my legs swelled up for a gain of 23#. I talked to Mayo Clinic today and all there specialists are booked out thru December. I have to be able to work, I can't stay home any longer than September 8th! Please advise me!
More reviews for: Avocado, Ckd
Comments from related studies:
From this study (6 months ago):
I was prescribed tenofovir since 2006 in many of the combination medications for hIV treatment. doctors did not inform me of the risks. In May of 2014 I was diagnosed with CKD 3. Tis wen un checks all theses years. I was taken off Atripla "to see if my leg pain would go away" and restarted 3 months later on Complera and within days I started suffering from full body pain. The doctors insisted i stay on the medication. Then i was prescribed Stribild in 2013 and my GFR declined to 36. No doctor has yet to warm me of any side effects even when i ask they say there are no side effects. How can someone go to a doctor 6 times a year and have blood drawn 6 times or more a year and they not know you have a kidney problem.? No attorney will take my case.
From this study (1 year ago):
From this study (1 year ago):
before taking these (TC chemo, then tamoxifen 3 years, letrozole 2 years)
my creatinine was 60, GFR 90; now after 5 years my creatinine is 85, eGFR just > 60
will it ever improve?
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