I have noticed that my asacol is not breaking down and is being passed in my stool! Is their a reason for this? What can/should I do?
i have had crohns for 8 years and i have been on just about everything. i have taken 6mp and i actually didnt have any side effects from it. it didnt work for me but no side effects. make sure she is seeing a gastro who specializes in cd. not all gastros are that great at treating cd/uc. tell her that all the meds they give us say they have all these terrible side effects but it doesnt necessarily mean she will get them.
hi there,
i have UC (diagnosed in 2001) and have been on asacol most of the time. however, i had about a year of experience with pentasa... the doctor at the time told me that it was the same thing as asacol, however, i found it to be less effective. another doctor later told me that they have the same active ingredient mesalamine, but pentasa reaches a different part of your track... i think asacol stays intact longer, so it gets released lower down in your system.
I have been on Asacol since my dx in 2005. I haven't had any side effects and it really helps to keep my c.d. under control. Good luck and I sure hope it has helped you.
I tend to notice side effects whenever my dosage is adjusted by my prescribing doctor or when I initially start it or taper off of it. I believe that experiencing side effects are two fold with me. One, there were some side effects, and two I probably tended to 'magnify' or focus in on them more intently and decided that any odd feeling was related to the medication when in reality, it may not have been due to the sertraline.
Hello ,
i have uc and my GP as just prescribed prednisolene 30 mg a day reducing weekly and omeprazole 20mg a day( plus calcium supplements.) Worried about all the side effects i've read about . Anyone had a positive outcome usi
these please????
I do NOT tolerate these tablets as well and have also tried the 10mg capsules with the same effects (less effective more side effects- nausea, dizziness, fat face, racing thoughts, decreased libido, nightmares, sleep disturbances, etc.).. I have called several pharmacies but they all have the blue tablets too -_-... Th side effects persist even after a month on the different pill forms too.. Any options left? Or must I suck it up and take a pill that makes me sick or discontinue usage...
hi any advice much appreciated, i have been previously using Janmut for my diabetics but have run out so i was told Velmetia was the same, while i sent away to CDO for this Velmetia i used Matformin and boy oh boy i got terrible side effects from joint pain to stomach pain to headaches to extreme pain left back shoulder blade pain going from back to my heart, gee that frighten me quite a bit, once i received the Velmetia it worked ok for 1 day then a similar side effect started as previously me
I have been on it for the last year straight and am not totally sure how much it really works. I had some side effects from it such as nausea and hair loss to a certain extent. The nausea was fixed by taking it at night which seemed to really help.
Being on it did not eliminate me from other meds as I am currently back on prednisone 40mg for a month due to a flareup. Pentasa and Asacol never worked for me either.
I guess in short every medication works for different people in different ways.
I just started on Zohydro ER because the idea of not taking acetaminophen with hydrocodone was tempting. (There's a Black Box warning about the acetaminophen in Vicodin).
The first day I started the Z. (about 5 days ago) I got less pain relief and much more pain than I had with 5/375 Vicodin! That's seems totally wrong but it happened. The dose of the Z is the same as I got for the number of 5/375s I took per day.
Anyone else on Z. and how do you like it? Any side effects?
Hi
The abnormal metallic taste sensation or taste perversion is a common side effect seen after Topamax use. These tablets have a bitter taste and lose their effectiveness quickly when broken, so you should swallow them whole. Chewing the tablet may leave a bitter taste. Hence, do not split, chew, or crush them.
There can be side-effects with the use of PPIs - no drug is without side-effects unfortunately. They can include changes to bone density - more ease of fracture - and anemic states due to loss of B12 uptake.
Changes in bowel habits and loose stools can be a result of the use of PPIs. If you cut down on acid, you cut down on the amount of food that's thoroughly digested and able to be absorbed. Those materials will cause changes in the output of the digestive system in a number of ways.
Delayed/missed menstural periods are not listed as one of the side effects of clonipramine. But stress CAN interfer with your cycles. I suggest you speak with the prescribing doctor about your periods as anything unusual when starting a new medication should be reported to your doctor.
In my humble and non-medical opinion, I think when the clonipramine reaches therapeutic levels and you begin to feel better, your periods will return to normal.
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