Metronidazole and kidney disease
Common Questions and Answers about Metronidazole and kidney disease
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I went to the obgyn last week they ran urine samples and std tests and everything was okay, I told them I’m spotting still for two weeks now three and cramping the test came back for BV so they prescribed me Metronidazole I felt way too anxious about taking it , Friday I went in for a ultrasound and pelvic ultrasound I believe and got the results today that it was fine. They now prescribed me clindamycin gel which I will pick up tomorrow due to pharmacy out of stock.
Many tests and procedures later and her vet diagnosed her with inflammatory bowel disease and put her on Metronidazole and prescribed cat foods with duck, rabbit and deer. Well, both of my cats reaction to the new food was to try to bury it. The Metronidazole made Pixel sick and she stopped eating and her weight fell to under six pounds and the vet then put her on steroids. During this time I bought brand after brand of cat food, hoping to get her to eat anything.
During this exam I was diagnosed with pelvic inflammatory disease and prescribed Metronidazole 500 mg 3X daily along with a dose that they gave me in the hospital because it was of bad. There was no mention of herpes during his exam. The following day of taking the medication the swelling and discomfort had improved significantly, the sores began clearing up by day two. I stopped taking the Acyclovir because after 3 - 4 days there was no change and the Metronidazole was the only thing helping.
I am 22 and have just found out I have kidney disease. I do not want to tell my family, because I know they wouldn't deal with it very well. Is it likely to be easy keeping this from them (I live with them)? I am considering not receiving any treament for now to make extra certain family don't find out.
i have kidney disease my creantine 2.12 my gfr 33.5 my normal is 1.
Hi there, about a month and a half ago I started feeling like something was always under both my ribs and it has been persistently like this and it's really uncomfortable, I'm also always itchy at night and have been feeling really dizzy and lightheaded constantly. I've went to my doctors and they took my bloods and all that came up was that my potassium levels were slightly high.
Hi there, about a month and a half ago I started feeling like something was always under both my ribs and it has been persistently like this and it's really uncomfortable, I'm also always itchy at night and have been feeling really dizzy and lightheaded constantly. I've went to my doctors and they took my bloods and all that came up was that my potassium levels were slightly high.
Hi recently I had pain on my adominal, usually the pain is on the right upper abdomen and the pain seem to move to lower left and right. I haven't did my kidney function test yet but I already did liver function test and my ALT is 9 U/L does this low ALT indicate that I have kidney issues?
Im very sick and cant get anyone to help. Ive even had a dr tell me he wont diagnose me with kidney disease until I get insurance so I got insurance and they denied coverage before he even diagnosed me. I then had to quit working due to illness. Now Ive got no job and no insurance and no help. What do all these results mean? Whats the next step? Who will help me?
Hello,
The symptoms are definitely suggestive of kidney disease. You should get an ultrasound kidneys and kidney function tests done to confirm the diagnosis.
It is very difficult to precisely confirm a diagnosis without examination and investigations and the answer is based on the medical information provided. For exact diagnosis, you are requested to consult your doctor. I sincerely hope that helps. Take care and please do keep me posted on how you are doing.
Obviously, he has severe anemia and no amount of iron will fix this kind. I have never heard of chemotherapy for kidney disease or kidney damage. I have kidney damage (kidney disease) due to an autoimmune disease. Kidney function is at 26% now, up from 20%. Autoimmune disease is in remission since I had all the mercury fillings removed from my teeth.
I would encourage both of you to talk with his endocrinologist about looking into possible changes that can bring his a1c levels well down below 7. That truly is his best protection not only against kidney disease, but against other complications. If sugar levels are maintained at near normal levels, damage cannot happen.
I have a 14 year old cocker spaniel who was recently diagnosed with kidney disease. She originally got sick a few weeks ago with pacreatitis, and when she recovered her lab work showed the kidney problems. We have been giving her fluids every other night as well as the epakitin powder with her food. Her blood report was better this last time. However she seems pretty good, has a good appetite ect and I'm wondering if there is anything else that could be causing this disease?
We took her to the vet and they ran all the tests and prescribed metronidazole (250mg taken twice a day). All tests and blood work came up negative. She refuses to eat and drinks very little water. Sunday we took her into the vet after one day of force feeding and hydrating her. They performed an x-ray of her abdomen and gave her lactate ringers for dehydration. The x-ray was negative for any type of blockage and it appeared all normal. We took her back in to the vet today for more fluids.
Your digestive issues could be caused by thyroid disease, and can be treated. Any muscle or joint pain, depression and anxiety issues are also symptoms of thyroid disease. Post the results if you have them, if you have not been tested, request your MD do the following tests, TPO and Tgab for Hypothyroid (Hashimoto's Disease) thyroid autoimmune antibody, and for Thyroid Hormone Levels Free T3 and Free T4, and a new TSH, Then post the results with ranges.
Right now im on metronidazole and doxycycline. And its giving me now 3 days diarrhea. Its making me feel sick. I really wnna stop the medication but im afraid it might get worse on the future, i think the meds (antibiotics) making me feel weak.
Later this week I have an appointment with a doctor who treats Hep C and who is part of a group that has been running various clinical trials on HepC drugs. I'm getting my questions together as I want to be prepared for the office visit and I have concerns with regards to HepC TX and kidney disease.
I am Genotype 1a and had TX (pegalyated interferon and ribavirin) ten years ago but relapsed after a viral breakthrough at 6 months.
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