# Not sure whether to start  Pirfenidone nextweek

**URL:** <https://community.patient.info/t/not-sure-whether-to-start-pirfenidone-nextweek/674423>\
**Category:** Chest and lungs\
**Tags:** Pulmonary fibrosis\
**Created:** [19 August 2018 22:38 UTC](https://community.patient.info/t/not-sure-whether-to-start-pirfenidone-nextweek/674423 "2018-08-19T22:38:48Z")\
**Posts on this page:** 5\
**Page:** 1

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**Author:** ![nh\_user\_1196618](https://community.patient.info/letter_avatar_proxy/v4/letter/n/97f17d/32.png) [@nh\_user\_1196618](https://community.patient.info/u/nh_user_1196618)\
**Post date:** [19 August 2018 22:38 UTC](https://community.patient.info/t/not-sure-whether-to-start-pirfenidone-nextweek/674423/1 "2018-08-19T22:38:48Z")

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Been diagnosed now with CPFE and every thing I have read seems to show that this treatment has not had enough trials for this combination of lung diseases, at the moment I feel better than I have done in ages and am loathe to go on to something that may make me sick again, I am allergic to many medications.&nbsp; Any one any experience of the two diseases combined ?&nbsp; (emphysema and Pulmonary Fibrosis, non idiopathic) plus treatment

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**Author:** ![nh\_user\_976860](https://community.patient.info/letter_avatar_proxy/v4/letter/n/8baadc/32.png) [@nh\_user\_976860](https://community.patient.info/u/nh_user_976860)\
**Post date:** [20 August 2018 19:32 UTC](https://community.patient.info/t/not-sure-whether-to-start-pirfenidone-nextweek/674423/2 "2018-08-20T19:32:31Z")

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Hi Reglois:

I have both IPF and Emphysema&nbsp; and I am on the medication but bear in mind that the medication is only to treat my IPF, it has nothing to do with the treatment of my Emphysema.

Also i'm a little surprised.&nbsp; I am not a physician but Pirfenidone (or OFEV as it is marketed here in North America) is a drug developed SPECIFICALLY for the treatment of IFP and not for the treatment of PF.&nbsp; &nbsp;This medication has been widely tested and is in active use with IPF patients here is North America and I believe in Europe also.&nbsp; In regard to treating PF I can only suggest your double check with your physician or with the drug's manufacturer.

Good luck.

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**Author:** ![nh\_user\_1196618](https://community.patient.info/letter_avatar_proxy/v4/letter/n/97f17d/32.png) [@nh\_user\_1196618](https://community.patient.info/u/nh_user_1196618)\
**Post date:** [21 August 2018 17:29 UTC](https://community.patient.info/t/not-sure-whether-to-start-pirfenidone-nextweek/674423/3 "2018-08-21T17:29:01Z")

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Thanks Bob, that is what I have read, not used to treat CPFE could in fact be harmful, I have industrial relatedCPFE and can find absolutely nothing on it.&nbsp; Bearing in mind I live abroad so everything for me is in a foreign language, I am fairly fluent in French but this is medical and technical French, not the same thing at all.&nbsp; So maybe I will have to get in touch with the manufacturer.&nbsp; I am quite at ease with the fact that CPFE is dire and life shortening, just want to feel well for as long as I can.&nbsp; By the way I also have asthma, just to top it all off&nbsp; lol. I do not need to worry about finances as I have been put on 100% free care but also don't want to&nbsp;burden the system as it will cost the state 2,000 odd&nbsp; Euros per week I have read.&nbsp; If I do take the meds Brexit is&nbsp; a real worry, as part of my treatment will be paid for by Great Britain or will it when they withdraw from Europe.?

Thanks once again&nbsp; Hope you continue to stay as well as you can&nbsp;&nbsp; Sue

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**Author:** ![nh\_user\_976860](https://community.patient.info/letter_avatar_proxy/v4/letter/n/8baadc/32.png) [@nh\_user\_976860](https://community.patient.info/u/nh_user_976860)\
**Post date:** [21 August 2018 21:31 UTC](https://community.patient.info/t/not-sure-whether-to-start-pirfenidone-nextweek/674423/4 "2018-08-21T21:31:07Z")

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Sue:

Please do not refuse the medication until you double check either with your physician or the manufacturer.&nbsp; There may well be facts I am not aware of and the last thing I want to do is lead you in the wrong direction.&nbsp; Also don't worry about burdening the state....you have made your contribution through taxes and deserve whatever treatment at whatever cost.

If you are able to confirm the drug is appropriate I can tell you that I have had no side effects and I am halfway through my second month.&nbsp; Just make sure you take with food and sufficient food to give your stomach a good base.

I'm in Canada and when you go on the drug here, you are assigned a nurse by the manufacturer who checks with you frequently and is available to you also.&nbsp; Plus you will be monitored by your doctor.

Good luck and stay in touch.

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**Author:** ![nh\_user\_1196618](https://community.patient.info/letter_avatar_proxy/v4/letter/n/97f17d/32.png) [@nh\_user\_1196618](https://community.patient.info/u/nh_user_1196618)\
**Post date:** [21 August 2018 22:08 UTC](https://community.patient.info/t/not-sure-whether-to-start-pirfenidone-nextweek/674423/5 "2018-08-21T22:08:11Z")

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Thank you Bob, I know I won't have the luxury of a nurse or anything like that, of course I know I will be monitored. I&nbsp;live very out in the sticks. Don't get me wrong I have been very fortunate to be diagnosed so quickly, my own fault it has taken 5 years as I really don't like going to the doctors, was VERY sick 5 years ago and hospitalized three times in a three month period, I now know these were what they call exacerbations, refused to stay in hospital as I am widowed and have dogs. Until recently could breathe fairly well, live in the mountains and could walk the dogs with no more than a bit of breathlessness on steep climbs,&nbsp;caught a virus at Christmas, ignored it&nbsp;and have had yet another exacerbation and now struggle to breathe&nbsp;at all normally. Long uphill walks are very much a thing of the past.&nbsp;My thinking now is I would rather have quality over quantity and as I am nearly always so allergic to meds I am loathe to try, and as an old un think money could be better spent on some one younger.&nbsp;Also as an \*immigrant\* even though I have been here 28 years, I have not paid into the health system to any great extent and still rely on GB in a \*reciprocal agreement\*&nbsp; GB may well refuse to pay.

Wish you the very best and hope that the drug works for you and slows things down&nbsp;I really do please keep in touch.&nbsp;
