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IPIR -- For Coaxpone users

View Poll Results: For C users only -- Have you ever had an IPIR (Immediate Post Injection Reaction)?

I have never had an IPIR.

60.00%

I have never had an IPIR.
	12	60.00%

I have had one IPIR. It occurred after I'd been using C for less than a year.

I have had one IPIR. It occurred after I'd been using C for less than a year.
	0	0%

I've had one IPIR. It occurred after I'd been using C for more than a year.

10.00%

I've had one IPIR. It occurred after I'd been using C for more than a year.
	2	10.00%

I've had more than one IPIR.

25.00%

I've had more than one IPIR.
	5	25.00%

Other

5.00%

Other
	1	5.00%

Voters: 20. You may not vote on this poll

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07-27-2009, 01:22 AM

FaithS

Member

Join Date: Jan 2008

Location: Kansas

Posts: 971

FaithS

Member

Join Date: Jan 2008

Location: Kansas

Posts: 971

IPIR -- For Coaxpone users

A friend of mine just posted on another MS board that she had her first IPIR. It occurred after she'd been using Copaxone for about 19 months.

Wondering how many of you have had one, and how long you were on Copaxone before one occurred.

I have never had an IPIR. (If you choose this option, please also post how long you've been on Copaxone.) I've been using Copaxone for about 9 months.

~ Faith

__________________
aka MamaBug
Symptoms since 01/2002; Dx with MS: 10/2003; Back in limbo, then re-dx w/ MS: 07/2008
Betaseron 11/2003-08/2008; Copaxone 09/2008-present
Began receiving SSDI 11/2008

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