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Gluten Free Medication


MichLab

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MichLab Explorer

I have been using the online website glutenfreedrugs.com as a valuable source for all of my medication since I was diagnosed with Celiac 7 years ago.  Recently, I have been experiencing a lot of stomach discomfort so I turned to GASX which was on the glutenfreedrug list. I believe the GASX made me even sicker.  I then searched the internet and found that it was filled with lots of people getting sick from GASX.  This has me worried on the validity of this list.  I am going to be having an outpatient procedure soon and have a list of medication that I need to be taking.  I don't know where to turn now. It is always so difficult getting answers from drug manufacturers. Does anybody have any ideas or thoughts?


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w8in4dave Community Regular

I don't take gasx but I have a friend that does! I am going to let her know! Thanks for the info! 

Adalaide Mentor

I have always, since diagnosis, used personal contact with every single individual manufacturer, or their website if information is available there as my source. I have never considered second hand information that may be out of date as good enough to stake my health on. I have never had issues getting answers, every manufacturer has provided clear and easy information.

NoGlutenCooties Contributor

Luckily I have had little need to take any medications since going gluten free (its only been 6 months) but I haven't had any issues.  From what I've read, the name-brand prescription drugs are safe if you contact the manufacturer and they verify it to be gluten free.  However, the generics get their filler ingredients from various suppliers and they can't verify that they are gluten-free.  Again - this is just what I've read.  The only prescription drug I've had to take was Vicodin - when I had a root canal.  I just made sure to get the name brand and not a generic.  Other than it making me a bit loopy I didn't have any gluten-related issues with it.  Tylenol and Advil are also ok and most generic versions of these are safe too.  Nyquil is also ok.  If you know ahead of time what you're going to have to take, I would contact each of the manufacturers and/or check their website.

cyclinglady Grand Master

Gas? Any guess regarding the root cause?

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    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
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      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
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      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
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      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
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