Bisoprolol :: Coming Off And Extremely Tired, Have Headaches
May 14, 2013
I am new to this forum and really would welcome some advice..
In February following a period of sudden very high blood pressure I was put on Amlopidine 5mg and Bisoprolol 2.5mg. I had a few headaches, felt tired but my blood pressure and pulse reduced and was consistently at 128/72 and 66.
My gp suggested me reduce my bisoprolol to 1.25mg and as my blood pressure and pulse stayed pretty much the same has now suggested I stop taking the bisoprolol. I am now on day 3 of this and do not feel great. I am extremely tired, have headaches and although my blood pressure is slightly increased 132/80 pulse 76 I am concerned how I feel. I have also read that side effects can be serious.
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Was prescribed 5mg bisoprolol 5 days ago after admission to hospital with atrial fibrillation. It seems to be working in terms of getting the pulse under control, but I have been suffering really debilitating tiredness, to the point where I sometimes barely have the energy to walk from one room to another. The medics at the hospital told me that if I got "short of breath" then I should go back into hospital, but it isn't so much shortness of breath as feeling completely leaden, especially walking up stairs.
Something I don't understand is whether this is the effect of the drug, or the result of the underlying condition, ie that my heart has been working very inefficiently. (Why doesn't anybody tell us these things?). Degree of tiredness also seems to be influenced by things such as whether I have just slept or eaten, time of day, and anxiety/stress levels!
Does anyone else have any experiences they can share about this?
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I take Bisoprolol as part of a cocktail to reduce my blood pressure. I also take 40 mg Adalat and 10 mg Ramipril each day. I have been taking this medication for around two years now and whilst my blood pressure has been reduced I feel so so tired. I have always been healthy and energetic, I've never experienced this feeling of tiredness. I have gained weight, my hands and ankles swell up. I'm going back to my doctor to have my medication re-evaluated...
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I have been on this drug (5 mg/day) since having an M.I. on Jan 2nd 2007.
I have developed a tickly cough that stops me getting to sleep at nights, my metabolism is in my boots and I have put on over 56lbs in weight.
I feel slow and lethargic all the time.
I spoke to my GP at my yearly review this week and told him I don't want to take this drug anymore. He said he can't recommend i stop taking it as it is "protecting" my heart.
I never had a BP problem before my Angina attack and the M.I. always being 128/78 all my life.
So, I have decided to stop taking both the bisoprolol and the ramipril and monitor my BP 3 times a day.
I think doctors are too scared about getting it wrong to try any alternatives.
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After comments I read on here I went to my Doctor (I live in Spain) and asked why I was actually taking Bisoprolol, i have been taking 2.5 mg a day since Dec 2012, I had a stroke in November 2011, I take statins and sintrome *spanish warfrin* The only reason he gave me bisoprolol is because I told him I was slightly breathless walking up hills, I do not have high blood pressure but I do have a slight irregular heart beat........which may have caused my stroke.........they are not sure........I used to smoke and drink however which also did not help!
If I needed the Bisoprolol, why did the consultant not give it to me in 2011? when I asked the Dr he said it is to prevent another stroke, not to cure anything but I should continue taking.it.......I have not felt any advantage taking the drug and like many people on here feel more tired and have gained weight as I have little energy to do anything. Not sure what to do really, I am frightened to stop taking it, so going to try taking in the evenings and see if less tired.
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Is anyone else 7 weeks pregnant? I'm 24 and this is my first pregnancy. I'm concerned because I haven't had any morning sickness. I have been extremely tired and have breast tenderness. I have already gone up a cup size and my lower tummy is already poking out a bit but it's firm not fat. I really don't have anyone to compare notes with :)
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I'm sick all the time, flu like symptoms, achy joints, headaches, tired all the time, fatigue.
lab results
Ana titer 1:640 speckled
anti-dna titer 1:20
ra- neg
everything else is neg and normal. What can be wrong with me?
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I cant find current discussion on suboxone and headaches. I was on suboxone, by prescription for 3.5 years for back pain and to assist with getting off of the prescribed opiates for the surgery for the back pain. I detoxed from suboxone with methadone at our local hospitals detox unit for one week. That in itself was fine. No issues. Except on day two I woke with a terrible headache and it has been 8 months and I still have the migraine type headaches almost 24/7. I have been on a medical leave from work as they are so bad. Been to neurologists, they keep saying they are bounce back headaches due to the length of time on suboxone and will eventually pass. Have tried numerous drugs, most recently depakote and now nortriptyline without much success. I have read the posts about folks with migraines from this, but when will these ever end?? I do admit that the pain level as gone down a notch or two, but they still are there and driving me and my life crazy. Very frustrated that my neurologist and family doctor must think that I am some kind of hypochondriac. I have not seen posts about this length of time with the migraines due to the suboxone.
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12 Jan I had a riding accident, hurt my shoulder. It was previously injured (dislocation/fracture of humerus) and it's been weak ever since. Doc put me on cocodamol as of 14th, and then on the 17th I was back at docs because they were making me sick. He put me on tramadol. 2x 50mg tablets three times a day.
I wasn't warned about any possible side effects, other than they may cause drowsiness.
11 weeks later, I can't kick it. I no longer require the tramadol for pain. They tried a weaning programme. I was given Tramadol SR tablets. I cut from 300mg a day to 200 mg. One tablet morning, one tablet evening for a week. The week after I was cut down to 100mg tablet in the morning, then nothing.
I lasted a day before I used some left over regular tramadol.
The effects were horrific when I initially changed the dosage, but I thought it would be okay with cutting down and then coming off completely. I was ready for some side effects, but not what happened in reality.
Headaches, nosebleeds, sickness, sweats, freezing cold, aggressiveness, exhaustion, tearful, restless, insomnia.
I had some very very dark thoughts that I haven't had in years. I took the tramadol and felt ten times better.
I have a doctor's appointment today, but they tend to be as much use as a chocolate teapot.
A nurse over the phone expressed she thought that the time frame for coming off them was too short, and the leap from 100mg to none was too much.
I know I have a problem, but I'm scared to come off them and become the horrid, nasty person I was at the weekend. My rational thoughts tell me once I stop for good I'll be back to normal, but I don't have those rational thoughts when I try and come off them. I need them to cope with the most simple of tasks.
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I'm only 17 years old. I have felt the way i feel now for months. I am not pregnant before anyone suggests that!
I suffered from a disease/illness where my glands swelled up til they were huge and you could clearly see them. I had a fever all day, i would go cold and the hot, i had no energy at all and was generally sick! The doctor gave me some antibiotics and it cleared up.
Ever since then i have not been myself. I feel sick at some point during the day, i constantly have a weird feeling in my head, its not pain as such, but like a numbing feeling and irritation. I feel like im going to faint all the time, im weak and very tired, i also get chest pains from time to time & my breathing is rubbish, its hard to breath at times, i generally feel like im dying
I have had countless blood tests and all of them showed nothing!
This totally upset me because im frustrated, i just want it to be over!!
The doctor told me just to have lots of water and exercise.
My family were convinced that i suffer from anxiety and panic attacks!
As i had a panic attack due to the fact i felt so ill i thought i was dying!
It wasn't just happening to me for no reason the attack.
so they took me to the doctor where he told me my symptoms were that of anxiety and panic attacks so he gave me some tablets to take.
But i still feel the same!!
I do not believe that i have anxiety
I am sick if people believing that is what it is!!
.......
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I have been having joint pain, general body pain, fatigue, depression and anxiety for years. I was dx with fibro about 3 years ago. It was first suspected almost 20 years ago. My mouth and eyes are painfully dry. My lips constantly crack. I recently had a PAP done and the GYN remarked how dry my vagina was (I'm not sexually active so I never noticed).
I recently saw a rheumatologist here in the State (I had previously seen one in Korea). She did a bunch of blood work. My Vit D was 28 (reference range was 30-70). RF, ANA were negative. CRP not done, but has been elevated in the past (multiple draws over a two year period, but none in the last year). ESR was 58 and has been elevated for 20 years (I went through a lot of blood work in high school and nothing was ever found, but it was with ID, not Rheum).
Rheum was next to useless. She said the sed rate wasn't relevant and that there was no need to worry about the Vit D (which was lower in the past) even though I was taking 2000 IU a day.
After talking to my GP, he had me increase the D supplement to 4000 IU/day. He also wrote me a new referral to a different rheum. This one specializes in seronegative arthritis.
I try to be an informed consumer. Current rheum just wants to throw more pills at the issue without getting to the root of it. It seems like if I go in with a fibro dx, everything must be fibro. How do I approach this new appointment (in September!!) to finally figure things out? This new doctor will be in the UH system as are all my other docs. I think she'll have access to previous lab results, if not I can pull them up in my EMR.
I could use words of wisdom, advice, a kick in the butt (if necessary), etc.
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I can't wait to be able to sleep any position I want especially on my tummy. 10 days till due date.. I know I'll be able to sleep better whe. Babe is here eve with having the nightly feeding.
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i am new to these discussions but I do know how many of you feel. I have mentioned that I was diagnosed with mixed connective disease, lupus, fibromyalgia and who the hell knows what else. I can't work becuause if I sit to long, my legs start falling asleep. If I stand to long, my legs start aching. I feel exhausted all the time like when I wake up in the morning, I could just as easily go back to bed and sleep my entire life away. I wish there was something in a bottle that gave you energy. I miss my old life when I used to work out all the time and had enough energy for 10 people and then one morning I woke up and couldn't bend my leg back, it just wouldn't work so my family doctor sent me to a rheumatoidologist and he is the one that took all my blood from my body, that's what it feels like sometimes, and gave me the great news of having all these diseases but no medication seemed to work. I went to another rheumatoidologist and he put me on Lyrica which helps my upper joints but my legs were in such pain I felt like it was to much to even walk down the hall. Now along with my family doctor, my rheumatologist and my pain doctor, I take Lyrica for joint pain and oxycodone and fentenal patches for pain, especially when my mixed connective disease starts up, it just brings my systemic lupus to life and I get the butterfly rashes mostly on my upper arms which adds to my stress which makes my fibro flare up and gives me pain in my legs and then it just starts over. It seems to be a cycle especially when it's hot. I also start sweating like I was in a sauna all day just on my head and face. People look at me like did you know your sweating like a pig. It's embarrassing but I don't know what to do about that so I put ice on my head at night to keep my head cool so I won't start swearing. I've never had that problem before but only since these diseases came and decided to stop on my little doorstep. I am a true believer that stress can cause all sorts of bad things including diseases. I am just going to try to start yoga but I have to absolutely force myself to do this. I start next week. The worse thing I could have done 12 years ago when I was diagnosed with all this crap was to stop exercising.
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Here's a brief background and symptoms I've been having. I've been a migraine sufferer since my preteens. Mainly migraines with aura but also morning headaches etc. about 7 yrs ago I gained 40 lbs very quickly over a 1-2 yr period and was exhausted all the time. I went to pcp office and saw a dr other than my own. She commented on my weight gain like she was appalled and asked if I was depressed. I did not feel depressed just frustrated mostly. She did a tsh test and said it was normal. I was also having what I was told was possibly ibs (mostly d but also c) and have dealt with this for the past 7 yrs as well. Skip ahead a couple years I noticed a correlation between the ibs and eating gluten products. I visited with my dr and he had me get a celiac panel. The results came up negative. I should also mention I was eating gf before the test so wonder how that may have effected the results. Fall/winter 2011 I was extremely fatigued, sore joints, muscle aches, hard time falling and staying asleep, noticed cold bothering me more ( I live in New England) so in January I found a new dr near where I lived. He basically said that it may be seasonal affective disorder even tho I told him I really didn't feel depressed just exhausted. After basic bloodwork as well as tsh and the wrong vitamin d test he said all was normal, get some rest. All I could think was gee thanks. So I saw another dr shortly after who was great but he tested me for Lyme and lupus which were both neg and also the correct vit d test which showed I was at a 6 and severely deficient. After a few months 50000 iu and then continued 1000 iu daily with some results of less fatigue. A couple months ago I started to feel the extreme leg cramps again, joint pain especially in knees and wrist, extreme fatigue as well as new symptoms of ringing in ears, dry scaly skin that I can literally rub off. I have always lost a lot of hair with showering and brushing but it seems like more lately. I called my pcp and asked for another vit d test thinking it may be related. come to find out it was a 17 so not as low as before but still low. I've done a little research and I feel like it could be hypothyroidism but I am unsure exactly what I should request for tests from my dr. I don't want to waste money on something if it doesn't seem needed. Any advice would be greatly welcome. I am just tired of being tired and frustrated.
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I've been having migraine headaches, pressure headaches, dizziness and nausea. I kept chalking it all up to menopause. Because as most of you know, so many of these symptoms are menopause.
Last Friday, Jan 2nd at around 7:30PM my boyfriend and I were leaving a restaurant, suddenly I started getting shocks in my right leg like my leg was falling asleep, while I was walking to the car. This shocking feeling quickly radiated up my arm and into my head, all on the right side. My boyfriend quickly started toward the hospital. On the way I lost the ability to formulate sentences and words. I would say one sentence and a totally different sentence would come out. I would try to say one word and a totally different word came out. Being a former medic the only word I wanted to relay was "stroke". It felt like someone had tasted my right side. It was the most frightening thing I'd ever experienced and I was awake for the entire ride. After getting to the hospital I was in the ER for about 3 hours. Then sent to Neurology/Stroke ward. For the next few days I had a battery of MRI's, EEG, EKG's, CT Scans, Blood Work, Ultrasounds and a Spinal (Lumbar Punch). Within 6 or so hours I was able to formulate sentences and say words again. I forced myself the entire time. My right side started getting feeling back within a few days. I still have some numbness in my right hand and am experiencing peripheral neuropathy symptoms in my right leg and foot.
The neurologist found a mass in my brain. Thanks be to God that it is benign. I just found out yesterday that I am cancer free. However, they still don't know what the mass is. It could be a tumor or a jelly bean I stuffed in my nose as a child. (joking) But we won't know for a while.Also it might be inoperable too. I will be seeing the Dr on the 13th for an MRI Rx. In a month we'll do the MRI and see what has happened with this mass. Is the edema gone, has it shrunk or grown? Things like that.
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9 years after 2 cardiac stents angina pain has returned. Doctor doubled my dose of Bisoprolol from 2.5 to 5 now I find my libido has gone from 50% to zero, no erection anymore, is this common, any way around it ?
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After a mild episode of unstable angina I had a single stent inserted in 2010. Since then I take the usual quartet of ramipril (2.5 mg), bisoprolol (2.5 mg), aspirin and simvastatin. I started Phase 4 rehab in January 2011 and now go to the Gym 2/3 times a week. The man aerobic component is a 20 minute row. I was advised not to allow my heart rate to exceed 75% of [220 -73 (my age) -30 = ] 97 but as I became fitter the average HR during rowing is 105 and the peak 111-113.
I feel fine, have never experienced any cardiac symptoms and the HR drops below 80 within 60 secs of stopping.
Am I taking a big risk? If not are there guidelines on HR during exercise for people like me?
I also have Parkinson's (no tremor) and exercise is very helpful in maintaining lung function and muscular tone so I have two reasons for exercising!
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I've been taking bisoprolol 2.5mg for about 2 years for my S V T. I'm 30
it's been a lifesaver for me. has all but stopped my palpitations. I'm now 17 weeks pregnant and have just been transferred from midwife led to consultant led at maternity .
she has told me she wants me to stop taking it because their is a small chance i could have a small baby.
i am so worried that my quality of life is going to go back to heart racing and feeling faint.. and feeling awful again...my doctor told me I could continue it. has anyone other ladies took this when pregnant. I get regular scans and baby is big for dates.
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I was prescribed a 3 day course of Trimethoprim, for cystitis, which I have suffered from many times before in the past. However, this time the medication made me extremely nauseous. Within about 10 minutes of taking the tablet I began retching violently and about an hour later developed a very itchy red rash on the inside of my lower arms. The rash gradually disappeared over about an hour but every time I took another tablet (two per day) I started to retch violently. I have taken the last tablet this evening but have now woken at 3.30am feeling sick again. I wish I had read your website sooner as I now realise I am far from alone in my reaction to this drug. I find it strange that I have taken it many times in the past without any obvious side effects.
[i:f8ec489ea7]This message was automatically imported from the original Patient Experience[/i:f8ec489ea7]
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I've started to become extremely thirsty lately. I've also had an issue with having to pee a lot, which has been happening for a much longer time than the thirst. The troubling thing is that I had a fasting blood test about 1-2 months ago, and also did a bunch of self-tests, and they were all normal.
Not sure how exactly I should approach this - My doctor wants another fasting blood test, and that's a whole other issue. It's hard to fast, as I feel extremely bad if I have to go without sugar, especially with the driving/waiting to take the test/etc...But like I said, that's another issue.
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I didn't know where to put this, because I don't really know why I have been feeling so thirsty, just that I am and have been. Kind of hard to put a time frame on it, but I think it's been a couple of months, more or less. As far as diabetes, that's an easy answer, but I had blood tests a month ago, and I was normal (had a large range of tests in many areas and was pretty much normal). I also had been checking my sugar manually a month ago just because I wanted to see if I had it.
I notice that if I have a savory meal (i.e. with salt, obviously), I am more thirsty, but I pretty much never eat anything that salty ever, and I also have been eating the same types of food that I've always eaten my entire life, and haven't had this issue.
I already emailed my doctor, and will eventually set up an appointment with her.
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