Carbimazole And Propranolol - How Long To Take Effect?
Jan 2, 2016
I was diagnosed with overactive thyroid and have been taking 10mg of Carbimazole for approximately 4 weeks, however nothing seems to have changed i still have all symptoms! Do you think i need a higher dose or am i being impatient and eventually symptoms will subside i know it takes a few weeks for meds to work? I also take 40mg of propranolol so that has stopped racing heart palpitations etc! The tiredness is overwhelming i have slept most of Christmas.
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I've only recently been put on the medication, can you tell me if any of you have had any of the side effects? and how long before I start to look and feel normal again?
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Have just been given carbimazole 5mg x 2 a day until I see my endocrinologist in December. I am on propranolol x 10mg x 3 a day. Just a query- when do you stop propranolol?
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I have just started carbimazole and to be honest I feel worse. I have aches and pains everywhere. This has come as a bit of a shock. Within two
Years I have been diagnosed with PA and coeliacs and now this.
Can anyone tell me how long it will take for shakes to go and the general
of being unwell. I am now on 5mg twice a day, I was on 20mg, but my body shakes and tremors got lot worse. I am also on 10mg of Propranolol.
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My wife has had migraines every day since January 2014. The last 9 months have been very difficult. We have tried many types of medication/treatments.
Currently she is trying Gabapentin (600mg per day).
Does anybody know how long it can take for Gabapentin to have an effect?
Is it possible for Gabapentin to make migraines worse?
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I have been in depression for quite a few years now with one adversity following other. Have been on Mirtazapine 15 mg for 5 days now. How long does it take to show benefits?
Resorted to meditation for healing self and keep myself going personally and financially. Now felt unable to carry on and felt like doing something drastic.
Went to the doctor last week to tryy out medication and was prescribed Mirtazapine 15 mg.
Slept well the 1st day but was restless the next. Hit the treadmill in the evenings from 3rd day for the fear of staying awake and the mind wandering. This helped me tire out and sleep, but feel totally down, frustrated, hopeless and angry during the day.
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I have been on a gluten free diet for about 4 weeks now. I had originally went on this diet because I am having the same symptoms and someone that may have a gluten sensitivity bad headaches, feeling very fatigued, joint pain, depression, numbness and foggy brain I was to a point where I couldn't get the word out of my mouth that I was trying to say and that's the point where I really started to research some things. I went to a neurologist and had an M.R.I. done all came back negative the Dr. said there is nothing wrong with me. Quite frankly I can't believe this so I started doing my own research since I wasn't going to get help from that Dr. I do plan on getting a second opinion done here soon, But none the less frustrating. So I found that pretty much all the symptoms that describe a gluten sensitive individual is everything I felt as well, so I thought I might as well give this a shot. I started this diet 2 weeks in I noticed that the numbness went away for the most part the pain still lingered the foggy brain hasn't shown its ugly face still fatigued and still had the headaches. So now 4 weeks in the numbness and the pain has been coming back more frequently and the headaches are still around foggy brain is still gone for now. But as the numbness and pain intensify and start showing up more often now it kind of makes me think am I really having to do this diet, and for the record I am not one of those people that cheat diets nor thinks its okay to cheat a diet especially with this kind of health dependency. I have been very strict with this hence why the frustration with it seeming like its not helping so high. I have done my research on the hidden gluten what to look for etc I actually try to buy only certified gluten free foods that say on the packages. I mean if all I have to do is change my diet to a gluten free one and it changes my life for the better because of this i'm all on board not just half way. Some places I read 6 weeks others say 6 months before you start to add wheat back into your diet to see if it affects you in a negative way, of course only if you feel like its not working for you. I definitely don't want to do this to soon because any chance that this is helping me I would hate to ruin that. At first I thought it was helping me, But not so sure anymore.
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I'm b12 deficiency. I was diagnosed with vitamin b12 deficiency in December 12th 2014. I've had 4 weekly injections so far.i get 1 more on Monday. Then every 3 months. I know it gets stored in the liver but how long will the 5 injections last. Before the 3 month injection. I'm on neo-cytamen 1000 micrograms. I'm scared confused I don't understand this.. my stomach won't produce b12.. I'm taking centrum for all the other vitamins because I don't know what else to do. My tongue is sore and the roof of my mouth.
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I have been using a lotion called dalacin t topical lotion from about october 2007, it really improved the big spots i used to get on my back, and it helped my face a little, but not much.So i went back to the doctors and she prescribed me with Oxytetracycline, which i take 2 tablets 2 times a day, so in total 4 a day. I have been on them for a month on this monday coming up (18th), that will then be a month, i think the doctor told me they would take about 3 weeks to a month to have a visual effect, im just hoping they do work! how has everyone's experience been with this medication? how long did it take for it to start working?
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Can anyone please tell me how long it takes for these blocks to take effect,had them done a week ago and still in bad pain,MRI report said severe deep space narrowing at L4-5,have had 3 microdiscectomy and 12 epidurals over the past 9 years.
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Just started taking the tablets and wondering how long the side effects last for, Particularly the nausea.
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I have been on Carbimazole for only about a month and have started to gain weight. I was diagnosed with hyperthyroidism at Easter and am seeing the endocrinologist tomorrow. I am coming off the stuff as I'd rather be dead than fat and will tell him that. I'm 51 and work in the media. Weight gain could cause me to lose my job and it's just out of the question to be overweight. People in my industry are being made redundant everyday and my job is really at risk.
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Off to Endo tomorrow to see what they say, I was wondering if anybody is taking Carbimazole with HRT. Had complete hysterectomy last year so taking HRT and just wondering if this has anything to do with my over active thyroid, a few people spoke to know of women who have had hysterectomy and gone on to have OA thyroid.
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I started on carbimazole about 3 weeks ago after being diagnosed with an overactive thyroid. I was ok at first, but have now developed a bad throat (not sore as such, but dry and tickly - very irritating). The meds say that you should see your doctor immediately if you get these symptoms, so I am now also on antibiotics which don't seem to be helping. I'm also quite achy, and even climbing a flight of stairs seems to take a lot of effort. Should I be worried?
It's all very annoying as I have taken such good care of myself recently, losing 2 and 1/2 stone and eating really well. All in preparation for trying to get pregnant, and I'm now unsure how well that is going to go. I know overactive can affect your fertility, but I don't know how all the drugs will have an effect (or be harmful if I do get pregnant). Unfortunately, the doctor appears to be completely disregarding this aspect of my life and is not offering any advice. Still waiting to see the specialist - maybe he/she will be more helpful.
I'm also concerned I spend 18 months on this drug and it doesn't help. Wouldn't I be better getting the radioiodine and putting off trying to get pregnant for 6 months to a year since at least I will have some certainty over the outcome of the radio?
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I've had mild acne for a few years now but it never used to bother me as using dermalogica would clear up outbreaks. Since I started taking Levothyroxine and Carbimazole my spots just don't seem to go away. They're just small red bumps with no pus and it's driving me crazy.
It's killing my confidence. I have a noticeable goitre and now these constant spots on my face. Has anyone else had this problem with thyroid medication?
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Only been diagnosed for a few weeks now and sorry if this question has been asked before but my hair's falling out in clumps now and wondered if this is 'normal' on this drug it is completely heartbreaking for me also I am due to get my hair dyed next weekend worried this will cause more loss ...
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I been taking this tablets for 6 weeks now (3 5 mg 3 times a day). I read in the leaflet that came with it if you got sore throat STOP taking the tablets and see your doctor, what I would like to know is how bad must the sore throat be to stop taking the tablets? Can anyone tell me before I rang my GP.
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Can anyone please help I was diagnosed with over active thyroid last August I only started taking one 5mg tablet that did nothing I'm now on three and having regular blood tests as I've been told I need to have the thyroid taken out but I see a lot of people are on a much higher dose and I can't have the op in till my bloods are normal but nothing seems to be happening and the tablets I take makes me fell worse
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I have today been diagnosed for the 2nd time with an overactive thyroid.
The first was about 6 years ago and I was put on 25mg of Carbimazole a day. Unfortunately my weight went from a 12 1/2S to 16st once I started the tablets. I took the decision to stop them as I suffered from some of the side effects and my white blood cells were being affected. Since stopping the tablets my weight has gone down (from 16st to 9st) and people say I look great.
I have been told today that I should restart the tablets as my T4 is now instead of the norm of 10 to 25 gone up to 70. I am worried that if I start the tablets my weight will go up very quickly. I have all the symptoms, shaking hands, lump in the throat, can't stand heat etc.
Having been in this situation before I am very worried and not sure what to do even thought I have told my doc my concerns re weight gain.
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My Neo Mercazole has been changed by my pharmacist to a generic form of Carbimazole and I have been having more palpitations on this new medication.Has anyone else had this problem.I know that they are supposed to have the same quality but I certainly don't feel that they work as well.
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This is my second time on carbimazole, my first was about four months after the birth of my son, i had the racing heart and heat intolerance and other symptoms but mostly of underactive thyroid and i too gain two, three stone. My doctor did more bloods and my levels had returned to normal so my doctor took me off them. Recently I've been feeling quite unwell so decided to go docs for bloods and was quite shocked to find my thyroid had gone overactive again but all my symptoms point to underactive thyroid, feeling exhausted, aching muscles, one and a half stone weight gain, my doctor has never known anyone put weight on, which i thinks is the worst problem after losing three stone I'm almost back to square one again, an really fed up with it an feeling so shattered aren't we meant to be full of life. My doctors not the best and not very helpful just told me i would stay on them a lot longer as I'd had it before, do people stay on them for life or can the carbimazole correct it for good, don't have much info on overactive thyroid.
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