Experiences with

Colchicine

I’ve recently been put on daily colchicine after years of treating my behcets-symptoms with prednisone. Its only been about 4 days on colchicine and i still have my mouth ulcers. My question is just this; does anyone have any experience of a potential overdose/allergic reaction by colchicine??

I’ve had a lot of bleeding from my gums, not sure if it’s from colchicine, flecainide, bisoprolol or tablets to protect stomach. Does anyone suffer with this and any tips to stop bleeding or protect gums . Plus has anyone experienced weight loss with colchicine. Thank you.

Anyone had experience of Naproxen, as its the same drug group as Colchicine

I am taking azathioprine, colchicine and prednisolone at present, with minimal effect. Has anyone else suffered with nose issues?

I'm 6 weeks into treatment with Colchicine and am worried it will be a long road to recovery, so reassurance would be great! :)

I wonder how many were given Colchicine after their ablation and for how long? Were you able to stay on it or did side effects cause you to discontinue it? Reading medical journals it appears to reduce early AFib reoccurrences by up to 40% in some trials.

Does colchicine make you cold by any chance.

I'm now worried that the drug may have elevated my Tinnitus permanently as it doesn't seem to be receding and its very concerning Any experiences of Colchicine causing T?

Not sure if it’s the colchicine helping with that , I can’t remember last time I took it how it made me feel.

Now on colchicine. Anyone else had this issue after vaccine or Covid

Do you think Colchicine will increase energy levels if I can tolerate it? The Rhuematologist has given me a prescription to cash in if I feel it necessary. Thanks in advance for any advice.

I’m taking ibuprofen and colchicine. The pain is easing, but only very slowly. At first I couldn’t move much, eat, sleep or even speak for long due to the pain. Now I am getting up and moving a little but I am exhausted just with a few steps and get the achy pain back in the chest.

My 10 year old son has been diagnosed with FMF and prescribed with Colchicine for long term use. I am devastated and would like some help on others that have gone through this experience. Any help would be greatly appreciated

Been getting chest tightness for the last week when I was walking to my daughters school , this changed to chest pain so thought I should get checked over , I was seen in cardiac assessment and I have raised infection markers they have started me on colchicine again as in December 2020 I was very unwell

Prescribed steroids and colchicine. It was effective. But when she stopped they started to pop up again whenever I stand and sit longer for a period of time. These past few days I am worried since I have kids. Is there any natural remedy for this?

Does anyone know if it’s ok to take colchicine before or after the Covid vaccine? Are there any contraindications? Thanks.

Hello, sorry this in three parts but I keep remembering things after I have done other posts, the consultant has put me on colchicine anti inflammatory which he said will make me sick and have loose bowel movements, I looked it up and it sounds very toxic , has any one had experience of being on this

since having a bad allergic reaction to the fabulous jab I'm still in solitary confinement grrrrr.i wanted to ask if anybody has any ideas of how I can get a bit of peace as last week I had to go into hospital as I had a major acute attack of gout and still in quite alot of pain I've had a course of colchicine

I’m currently on Aspirin, Cholesterol tablets, Colchicine, Bisoprolol &something they inject in my stomach. It seems they’re using a lot of blood thinning.

My Gp has given me 12 Colchicine 500 ug. Ive taken 3 spaced out in 19 hrs, first one at 3pm yesterday. As they can be toxic i'll take another this evening but i dont appear to have any side effects! Very painful and ive hardly slept for 2 nights.