This is topic Flagyl experiences in forum Medical Questions at LymeNet Flash.


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Posted by AnnaOD20 (Member # 29942) on :
 
About to add in Flagyl (currently on Rifampin and Doxy). I am doing fine w/ the combo of Rif and Doxy but worried about being on all 3 and the little I have read on this site it sounds like a very tough drug.

Any good experiences (as good as it can be on antibiotics) and what kind of side effects did you feel?

Thanks!
 
Posted by lauriemay1 (Member # 24153) on :
 
Well my daughter started taking it two days ago, is bed ridden with 102 fever now. I have to call the LLMD this morning to see if she's allergic to it or not.
 
Posted by AnnaOD20 (Member # 29942) on :
 
Oh no! Sorry to hear that. If you can let me know what the dr. recommends. Hope she feels better soon.
 
Posted by lauriemay1 (Member # 24153) on :
 
Thanks Anna
 
Posted by TF (Member # 14183) on :
 
http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/103056?
 
Posted by Pippi (Member # 21151) on :
 
I finished 4 months on flagyl, minocycline, and biaxin.

On this regime, I had queasiness, skin flushing, overall body aching, lack of physical strength and stamina, head ache, neck ache, cognitive slowing, vision problems, skin flushing, digestive upset.

It was unpleasant for the first 10 weeks. I don't know which were side effects and which was toxic die off reaction to the dying bacteria.

But after 10 weeks, all of them eased considerably and many are completely gone now.

Flagyl has made a significant difference in the pace and degree of my recovery.

I was worried too when I started, but I also knew from the posts that I wanted to persevere if I possibly could, because it seemed to be effective for those who could tolerate it.

N Acetyl cysteine, quercetin and alpha lipoic acid helped me deal with the toxic die off.

Also I had a 2 day break every 5 days, so I could recover somewhat and get ready for the next round.

Each round got easier.

Hope it goes well for you.
 
Posted by SashaC (Member # 18968) on :
 
I didn't have a good experience, but here's my view from the other side of the fence:

Flagyl, even in a tiny dose, gave me splitting daily headaches. I started with a sliver of one tablet. Each time I increased by 1/4 tab, the headache would worsen.

More importantly than that, I noticed that my hands felt like they were falling asleep.

Over the past month, my hands have gotten to the point where they are numb, burning, tingling and stabbing. This sensation lasts for hours at a time.

I've been immersing my hands in the hottest water I could stand, to try to change the pain to anything but what it was.

I called my LLMD today and he said to stop immediately. I would've discontinued it without his blessing, though. I have too many afflictions already to try to deal with something as serious as permanent nerve damage.

I didn't realize that extended use of flagyl could cause permanent neuropathy. I know now, and I'll never take it again.

However, everyone has different experiences with it, and many have found it quite helpful.

So, I would say to just listen to your body, and be aware of what it is telling you!

God bless,
Sasha
 
Posted by AnnaOD20 (Member # 29942) on :
 
Thank you! Picked up the Flagyl tonight and think I will start it on Monday. I am really hoping to see improvement in my blood test results since overall I am feeling pretty good.
 
Posted by canefan17 (Member # 22149) on :
 
Really bad frontal headache for me on day 3 or 4.

I think flagyl hits Bart
 
Posted by bcb1200 (Member # 25745) on :
 
The first time I did a 3 day pulse of 1000mg I had a lot of fatigue and "hit by a truck" feeling. By my 3rd pulse it was like nothing.

I'm currently 1 week in to a 2 week pulse and so far..nothing. Cakewalk for now.

I wonder if this means lyme is not my big problem?
 


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