posted
I am told that even though factive is in the quinolone family there are far fewer reported cases of nerve / tendon damage as compared to Cipro
I have read most everything posted on the cipro and experienced many of the issues listed but need something to get the Bart under control.
Could it be that factive works somewhat differently hence the reduced incidents?
Opinions please.
-------------------- If you play at the beach, expect to get some sand in your shorts Posts: 223 | From central pa | Registered: May 2010
| IP: Logged |
-------------------- If you play at the beach, expect to get some sand in your shorts Posts: 223 | From central pa | Registered: May 2010
| IP: Logged |
BoxerMom
Frequent Contributor (1K+ posts)
Member # 25251
posted
I did fine on Cipro then ruptured my Achilles' tendon on day 5 of Factive.
Now I get tendon issues with all the Flouroquinolones.
The fewer reported cases could be because it's prescribed less frequently than the others.
posted
Thank you for the reply BoxerMom. I appreciate the input. I think I will just stay away from everything in that family.
You are probably right about the lower incidents being due to lower usage. I hadn't thought of it that way.
I have taken rifampin in the past and did ok with it. My concern with that is there are warnings about developing kidney issues when restarting after it has been stopped.
I don't know what time frame they are alluding to with those warnings. Is it a week, a month?
It has been a few years since I took the rifampin so I would imagine it would be alright. The last thing I need though is kidney issues so I would be apprehensive about taking it again.
-------------------- If you play at the beach, expect to get some sand in your shorts Posts: 223 | From central pa | Registered: May 2010
| IP: Logged |
BoxerMom
Frequent Contributor (1K+ posts)
Member # 25251
posted
If you've been off Rifampin for a few years, your risk is minimal. The biggest danger is with stopping and starting (week on/week off or month on/month off).
You can ask for monthly CBC and Chem panel if you're concerned. I went to a hospital lab for blood draws, with results sent to my LLMD. I never had any problems with Rifampin.
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
![[Smile]](smile.gif)
Printer-friendly view of this topic