This is the link to the National CML Society directly to drug and food
interactions:
http://www.nationalcmlsociety.org/living-cml/drug-food-interactions

LOVE YOU ALL!!!!!
Maria

On Sun, Feb 22, 2015 at 6:23 AM, <cmlhope@googlegroups.com> wrote:

>     cmlhope@googlegroups.com
> <https://groups.google.com/forum/?utm_source=digest&utm_medium=email#!forum/cmlhope/topics>
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>
>    -  ponatinib info <#14bb0d02294a4d46_group_thread_0> - 5 Updates
>    -  Food that interacts with TKI's and other meds
>    <#14bb0d02294a4d46_group_thread_1> - 2 Updates
>
>   ponatinib info
> <http://groups.google.com/group/cmlhope/t/5dfb95c0229110ae?utm_source=digest&utm_medium=email>
>   Icandoallttc <icandoall...@aol.com>: Feb 21 10:18AM -0500
>
> Hi John
> Do you you remember how long the eye problem lasted! I have been having
> them a few times daily now thanks.
>
>
> Prayers & Blessings Jeanie [image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ]. 18,s
>
>   John Barrons <jlbca2...@yahoo.ca>: Feb 21 03:55PM
>
> Hi I had them quite a long time go. Each aura lasted about 3 to 5
> minutes. They occurred very intermittingly.  Never found out why. I would
> like to ask what does 18,s mean?
>
> On Saturday, February 21, 2015 10:18 AM, 'Icandoallttc' via CMLHope <
> cmlhope@googlegroups.com> wrote:
>
>
> Hi John Do you you remember how long the eye problem lasted!  I have been
> having them a few times daily now thanks.
>
> Prayers & Blessings Jeanie [image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ]. 18,s
> On Feb 19, 2015, at 3:16 PM, Icandoallttc <icandoall...@aol.com> wrote:
>
>
>
> Thanks John. That's what I having but with pain.  I have suffered with
> migraines most of my adult life but this is different.  I hope it's a side
> effect that will go away.  Looks like the media working --yahoo!
>
> Prayers & Blessings Jeanie [image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ]. 18,s
> On Feb 19, 2015, at 11:47 AM, "'John Barrons' via CMLHope" <
> cmlhope@googlegroups.com> wrote:
>
>
> I have a few auras which I understand they are migraine headaches without
> the pain. I had an MRI to see if there was a problem and there wasn't.
> Haven't them for a long time. No headaches or rashes. John b
>
> On Thursday, February 19, 2015 11:28 AM, 'Icandoallttc' via CMLHope <
> cmlhope@googlegroups.com> wrote:
>
>
> Hi John and thanks for walking me through this new med.   Got a light
> rash.   Did you ever have an eye problem with headache?Thanks again.
> Prayers & Blessings Jeanie [image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ]. 18,s
> On Feb 19, 2015, at 11:01 AM, "'John Barrons' via CMLHope" <
> cmlhope@googlegroups.com> wrote:
>
>
> That's great your down to one pill a day. I am still on two a week. over
> the last to weeks my counts have stayed the same except for wbc up from 5
> to 7. John B
>
> On Thursday, February 19, 2015 10:33 AM, 'Icandoallttc' via CMLHope <
> cmlhope@googlegroups.com> wrote:
>
>
> Thanks Marty. I will get some.  Thank heavens it doesn't itch. My blood
> counts were good today.   Platelets 152.  Doctor put me down to 1 pill
> daily of ponatinib.  Phosphatase is still high.  Going to be a guessing
> game till I get stable.  You are right--still here fighting.  Glad you
> finally got some relief.
>
> Prayers & Blessings Jeanie [image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ]. 18,s
> On Feb 18, 2015, at 7:43 PM, Marty Gartenberg <wa2...@gmail.com> wrote:
>
>
> Hi Jeanie and all of the rest,
> I really feel badly for you having to go through all of this, but on the
> bright side your all stil here to go through this.
> As far as the rash and not being able to put anything on it, well that
> really sucks. When will you be allowed to put something on your rash?
> When I had my total body radiation my skin was burnt, my fingers, toes,
> nose, ears feet, hands and other parts of my body were burned and looked
> like I was in a fire. I was told that while I was having the radiation
> treatments I could not put anything on any of these very severe burns, and
> I really suffered through it.
> As soon as my treatments were over they gave me Keri oil, then lotion.
> Both of them did very little to help me. Then a friend of mine told me
> about Bag Balm and I got it and started using it. Within two days my burns
> were still there because they were from the radiation poisoning but after
> putting that on it didn't hurt anymore. Everything healed up in less then a
> week.
> Then I had to start my immuno-suppression  medication and the rashes were
> severe. So, I remembered that Bag Balm and put that on and there was
> instant relief.
> I don't know if you have heard about Bag Balm but it is used for livestock
> on their utters when all of the milking in cold weather makes their utters
> chapped.
> By the way, I bought the 8 oz tin more then 25 years ago and I still have
> most of it left even though I use it all the time for skin irritations. All
> you need is a very small amount.
> 18's,
> Marty
>
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>
> On Wed, Feb 18, 2015 at 4:10 PM, ICANDOALLTTC via CMLHope <
> cmlhope@googlegroups.com> wrote:
>
> Good evening to all,Below is some info on Ponatinib.  The common side
> effects are listed.The most common side effects reported in the clinical
> trial include hypertension, rash, abdominal pain, fatigue, headache, dry
> skin, constipation, fever, joint pain, and nausea.So far I have the rash,
> headache, abdominal pain, dry skin, and nausea.  Some of these I have had
> before.  The rash is quite bad, but they say don't put anything on
> it.Blessings Jeanie<3Ponatinib
> On December 14, 2012, the U. S. Food and Drug Administration granted
> accelerated approval to ponatinib (Iclusig tablets, ARIAD Pharmaceuticals,
> Inc.) for the treatment of adult patients with chronic phase, accelerated
> phase, or blast phase chronic myeloid leukemia (CML) that is resistant or
> intolerant to prior tyrosine kinase inhibitor therapy or Philadelphia
> chromosome positive acute lymphoblastic leukemia (Ph+ALL) that is resistant
> or intolerant to prior tyrosine kinase inhibitor therapy.  The approval was
> based on the results of the PACE trial, a multicenter, international,
> single-arm clinical trial of 449 patients with disease that was resistant
> or intolerant to prior tyrosine kinase inhibitor therapy. The primary
> endpoints were Major Cytogenetic Response (MCyR) for patients with CP-CML
> and Major Hematologic Response (MaHR) for patients with AP-CML, BP-CML or
> Ph+ALL. FDA required that the sponsor commit to submit 24-month follow-up
> data for all patients as a condition for the accelerated approval. The
> efficacy results demonstrated a 54% MCyR rate in patients with CP-CML.
> Seventy percent of patients with CP-CML with T315I mutation achieved MCyR.
> The median duration of MCyR had not yet been reached at the time of
> analysis. For patients with AP-CML, BP-CML and Ph+ ALL, the MaHR rates were
> 52%, 31% and 41%, respectively. The median duration of MaHR in patients
> with AP-CML, BP-CML and Ph+ ALL was 9.5 months, 4.7 months and 3.2 months
> respectively. Iclusig is being approved with a Boxed Warning alerting
> patients and healthcare professionals that arterial thrombosis and liver
> toxicity have occurred in Iclusig-treated patients. The most common side
> effects reported in the clinical trial include hypertension, rash,
> abdominal pain, fatigue, headache, dry skin, constipation, fever, joint
> pain, and nausea. The recommended dose and schedule for ponatinib is 45 mg
> taken orally once daily with or without food. Full prescribing information
> is available at:
> http://www.accessdata.fda.gov/drugsatfda_docs/label/2012/203469lbl.pdf1 
> Healthcare
> professionals should report all serious adverse events suspected to be
> associated with the use of any medicine and device to FDAโ€™s MedWatch
> Reporting System by completing a form online at
> http://www.fda.gov/medwatch/report.htm2, by faxing (1-800-FDA-0178) or
> mailing the postage-paid address form provided online, or by telephone
> (1-800-FDA-1088).
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>   Icandoallttc <icandoall...@aol.com>: Feb 21 03:37PM -0500
>
> I get real sensitive to light and then the auras and pain start.
>
> Here's what the pamphlet says
> Effects on the eye:
> Serious eye problems that can lead to blindness or blurred vision may
> happen with Inclusig. Perceived flashes of light--light
> sensitive_floaters__dry itchy eyes--
>
> Prayers & Blessings Jeanie [image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image: ๐Ÿ ][image:
> ๐Ÿ ]. 18,s
>
>   John Barrons <jl...@rogers.com>: Feb 21 04:23PM -0500
>
> Hi My eyes are more sensitive to light and I have dry eyes. I put drops of
> Sustane Ultra in my eyes daily. My gp said to disregard the expiry date on
> the bottle and discard the bottle every three after opening it. It is no
> longer sterile. So don't buy a big bottle. John B
>
> Sent from my iPad
>
>   Richard H <rbhuffm...@gmail.com>: Feb 21 08:50PM -0800
>
> John, I'm also using Sustane Ultra for my eyes. I am supposed to be using
> Restasis but was allergic to it. I have secondary Sjorgrins Syndrome from
> a transfusion and Gleevec. The small samples or daily treatment are only
> recommended for three times use. I have my eyes checked every six months
> and am reminded not to touch my eye with the tip of the applicator. I use
> 1 drop 2 times in each eye every day and have had no problems for almost 7
> years. So I guess its depends on the doctor or assistant that gives the
> instructions.
>
> Richard H.
> On Saturday, February 21, 2015 at 3:23:21 PM UTC-6, jb wrote:
>
>   Back to top <#14bb0d02294a4d46_digest_top>
>   Food that interacts with TKI's and other meds
> <http://groups.google.com/group/cmlhope/t/6c581c51d2fd1ef3?utm_source=digest&utm_medium=email>
>   mariacash...@gmail.com: Feb 21 07:52AM -0800
>
> HELLO!!! This is a very important topic and I believe that most of us
> don't
> consider it at all. I have known that there are juices and spices that can
> affect the way different medication interact with your body and even
> between themselves. Medscape is a useful tool for drug interactions.
> However, it is known tha grapefruit juice (which incidentaly I love) is a
> nono with almost all meds. It usually increases the effect of the meds.
> I know, for example, that garlic is a nono for Sprycel, as well as teas of
> any kind....CMLIQ site has some recent information. Also, CML society.
>
> We must keep a watchfull eye on this type of information because it can
> mean a lot in the performance of our medications and our lives!!!!
>
>
> BE HAPPY and DO NOT WORRY!!!! GOD is always with us!!!
>
> Maria
>   Joyce Mesnarich <joy...@htc.net>: Feb 21 12:21PM -0600
>
> Thank you so much for sharing these information sources with us. We are
> all wanting to know as much as possible about this ever-changing disease.
> Joyce in IL
>
>
>   Back to top <#14bb0d02294a4d46_digest_top>
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