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» LymeNet Flash » Questions and Discussion » Medical Questions » Tindamax Experiences??

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Author Topic: Tindamax Experiences??
lea
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I just started Tindamax today, and I was wondering if anyone had any recent experience with it?

My LLMD warned me to watch for numbness/tingling in hands and feet, but I read a bunch of posts in the past about tindamax and depression.

What can I expect?

Posts: 146 | From California | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
seekhelp
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I'm starting this soon. Should be a fun ride. [Frown]
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baileygirl
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I have been taking it 2x a week since March or April... I used to take it in the morning but it gave me an awful taste in my mouth and I felt VERY tired. Now, I wake up in the middle of the night to take it and I no longer have issues. Good Luck!
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steven
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ill also start it soon. do you take it as a monotherapy or combined with other ab? and how much? 2 x 500?
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lea
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I am also taking rifampin and omnicef, along with cryptolepsis. I am supposed to take 500mg 3x a day.

I have only taken it twice so far, so any experiences would be greatly appreciated.

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JamesNYC
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I started Tindamax about three weeks ago. I have had no major problems yet. For about a week my throat felt a bit constricted, like I needed to cough to clear it but that went away (it's listed as a known side effect) .

I'm on one pill a day. My LLMD wanted me to take 2 a day but insurance wouldn't have it because it was not approved usage.

Good luck,

James

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LittleLymie19
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I'm starting it as well. I'm taking one pill 3x a day too. I'd love to hear more about people's experiences on it.
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