Doxazosin :: Horrible Mouth Pain, Muscle Pain, Anxiety
Feb 9, 2015
I was put on doxazosin after a period of great stress (xmas), and although it's lowered my BP, I've had horrible side effects.
I've had the racing heart, swollen ankles, breast pain, chest pain (muscular), sore throat, sore jaw, headaches, anxiety, etc.
I was on 4mg for one day and my right leg gave out from under me, so I went down to 1mg.
Since then, I haven't had that the leg caving thing (thank God!), but I feel very unwell.
I feel heady, like I have a very bad cold. My nose hurts, my throat hurts, my teeth hurt, my ears hurt, and the roof of my mouth hurts.
The anxiety the drug induces is magnified because of the side effects, and the side effects increase the anxiety. The anxiety raises my blood pressure, and the cycle goes on, ad infinitum.
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I am French. I’m 28, it’s being 2 years and a half that I have blood in the urine with horrible pain.
I had 3 ureteroscopies who have given nothing and now the professor who follows me told me I have the loin pain hematuria syndrome, and there was nothing to do. The only thing I can do is to wait till it’s going better. He refuses to make a biopsy and told me to take aspirin.
I wanted to know if you know doctors who offer other drugs. I've heard of self transplantation and kidney innervation;
I've been in different hospitals and doctors tell me that the pain is bearable and advised me to consult a shrink. I do not think my pain is psychic. I wanted to know if U.S. medical research is more advanced than the French one.
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I came across this syndrome when searching the Internet about extreme pain I have when I take the first bite EVERY time I eat and sometimes drink. That this could be a symptom of this syndrome but I don't know. I do have some of the other symptoms, i.e. neuropathy, blurry vision, muscle pain, fatigue but these can also be associated with Type 1 Diabetes which I have. Also, came across parotid/salivary glands are affected which also can cause the jaw to ear pain I'm having. Has anyone heard that the Coxsackie virus can have anything to do with it? How do you know for sure if it is Sjogren's and what type of doctor do you see about it - a primary?
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I am on my 5th week post-op TAH (removed uterus, cervix and Fallopian tubes). I was recovering well in the past few weeks with reducing pains.
Of all sudden, I had a painful swelling abdominal and soreness/pulling pain around waist yesterday coupled with giddiness and headache. Is it normal having a regression during recovery period? Any remedy members could share esp. now I still can't exercise. I put on an abdominal binder now to ease the pain slightly.
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Couple days ago I stepped out of bed and almost hit the floor as the excruciating pain shot through my calves. I have not exercised or done anything extreme. I have tried stretching and over-the-counter pain meds ..
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After my mistake (HIV scare) I have all these symptoms heart wall pain, chest wall pain, radiating pain to the whole body, and headache, and cough and sputum. X-ray 6 times in 6 months and doctors can not see what is wrong with me. Do I have a virus going inside my body? A viral infection?
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I have horrible muscle spasms in my back, sometimes they seem like cramps though. I turned 18 about a month ago, will a doctor prescribe me a muscle relaxer for this? Is there a different class of medication to look into that might be more effective? My dad recommended baclofen. I have read about some health complications using this though. Not asking how to get a RX. WILL they write me one or blow me off as an 18 year old drug seeker, and WILL it help (possibly). I've done trigger point injections, deep tissue PT for years and nothing helps. The problem comes back like a week after stopping and my insurance only covers x appointments. My therapist noticed my ribs keep elevating up and need popped back in place. This may be due to muscle spasms? I'm just tired. Tired of pain, doctors not doing anything, and nothing changing.
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I have been experiencing horrible head pain for the past 6 months. I've been to a neurologist and had multiple tests (MRI's/CT scans) performed and everything has come back normal. The only thing that has come up has been "lordosis" in my neck and "slight changes in C5 and C6" in my neck. My headaches started back in May when I was moving out of my apartment and seemed to have strained myself. I have been going to a PT and that has not helped. Additionally, I have had 2 nerve blocks, trigger point injections, and dry needling, none of which have helped. I am scheduled to get botox injections in my neck and lower head to hopefully help. Additionally, I am going to a neck/spine specialist. Both happening next week. Can anyone relate to the pain that I have been having? My pain seems to start in my neck and travel all over my head, on one side of head to the other, behind eyes, behind ears, etc. It feels like a stinging, uncomfortable pain. Someone please help, give suggestions, relate to me!! Feeling desperate and feeling like my head will never get better.
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I have already read a lot of good information about fatty liver and other people's symptoms. I am not sure what is going on with me but thought I would see if anyone can relate or help. I was actively working out my abs doing core exercises for a couple of weeks and noticed maybe (trying to remember) a day later, horrible pain on my right side under my rib cage. I was also diagnosed with a fatty liver about a year or so ago. When I was first diagnosed, I had a mild pain (more annoying than painful) and thus underwent an ultrasound. My triglycerides are pretty high and HDL and LDL are a little off but not too bad. Everything else seems pretty good. I haven't really changed my diet since I was diagnosed and do have my starbucks fraps almost daily, but did start a strict exercise with cardio and walking almost everyday.
Getting back to the pain, it started about 5 days ago and yesterday I thought it was going away. It is still there today. I don't know if I strained it, it is my gallbladder, or my fatty liver. I am so afraid of doctors and don't want to go. The pain is more intense when I move my torso to the left and to the right.
Can anyone help or give your opinions as to what could be going on or if they have the same symptoms.
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I know that it's known that lipitor has the side-effect of muscle tiredness and aches. Has anyone else have to deal with this? Man it's off the hook. I almost am paralyzed fro, lipitor. This horrible and I would like to talk to someone who's been through it. This is a very under-rated affliction IMO. I've been tested and it doesn't look like I have the Rabadolosis<sp? That spelling isn't even close. I was very scared before I realized what was causing this severe problem.. Now I know that lipitor has helped a lot of people, it brought my cholesterol down a bunch very quickly. Frankly i would rather have high cholesterol. I did have a stroke at the end of November, small, deep in the cerebellum. Hence the lipitor.
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took a 2nd dose of oxycodone 3 hrs ago and my pain is only gotten worse i'm crying and shaking - called my doc at 630am -1 hour ago before i was crying and shaking he told me to take 2 aleve and the 2 oxy every 4... is this normal or should i call back?
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for the past week I had severe joint pain and weakness, muscle weakness, bone pain in extremities ( had a blood test for lupus and RA[ no family history of either] Starting to get a bit better as long as I rest. recently sexually active with one person, now I just noticed feeling swollen like I was getting a UTI ( hurt when I urinate), but noticed it hurt in my vagina not urethra, checked and there are 4 small red bumps in my right labia minora and 1 in my left labia minora-odorless, feels inflamed and hurts now. Is this related to possible lupus or separate problem? I feel exhausted and run down.
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Before I start I'll just state that I'm 19 years old, slim and generally healthy. I've been suffering with a cough for 3 weeks now, and it only seems to be getting worse. It is a constant violent cough, dry, but wet if that makes sense? I cough up clear mucus. It seems worse at night, I can't lie down without having a coughing fit and the pain in my throat and my ribs is unbearable I also have awful pains in my upper back, and weird shooting nerve pains in my arms. I've been to the doctors twice, first time he listened to my heart and lungs said they were clear and said I had Costochondritis which is causing my pain. Didn't say anything about my cough. So I went back to see a different doctor, by now I was also having pains in my left leg and googling this and as always it comes up with the worst case scenario... Blood clots which got me really worked up. She told me I didn't have blood clots, just by feeling my leg and saying it was soft, and said I have acid reflux which is causing my cough and all the other symptoms. I still can't stop worrying that my cough is something much worse and I have been misdiagnosed and there is something wrong with my lungs I also keep worrying about the pain in my leg, which is getting worse... I feel as if it was just brushed off but when I read online about others who ended up having blood clots their symptoms were just like mine and I'm so scared of this happening to me
I realise I have really bad health anxiety, but it makes it worse that I haven't even had proper tests or anything done to rule out the worst things!
I'm finding it so hard to deal with this, I feel like this anxiety is taking over my life Thanks to anyone who reads this essay of a post, I feel I just needed it off my chest.
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Hi I'm female 60 years old recently put on meds for high BP. I also have Fibromyalgia I mention that because it seems whatever tablets I'm given for BP (,Losartan being the 4th tablet) my joint and muscle pain become some bad I struggle to even do the housework and where I used to walk the dog's for at least an hour I can only manage 15 mins also I could walk round the shops for hour's now can't wait to get my weekly food shop done and get back home . My BP when I take it at home is anything from 116/71 ,to 133/77 on the meds , I have stopped taking Losartan for 2 week's now and BP is 136/76 to 149/74 when I go to the docs the readings are always high 162/84 for example. I really can't cope with the pain when taking these tablet's especially in my knees has anyone else experienced this , is there even a tablet for BP that doesn't make you feel ill .I have stopped these but not told the doc yet as can't face being put on another tablet I am feeling so well at the moment I take my BP daily it's usually 140 something over 82 is that really too high for my age.
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I was on simvastatin for 4 years and developed bad pain in both legs when standing up. I have to steady myself before I can start walking. I have CK in my blood tests. I was told by my doctor to stop taking the statins. I have got worse in my legs after 6 months. Doctor put me on another statin. When I read the same side effects as simvastatin I didn't take any. I couldn't believe that doctor would put me on a tablet that caused the same bad side effects. I will be going to have my blood tests done soon but would like to know whether anyone has asked about sueing the statin drug company and would the doctor be helpful about it?
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Hi my name is Michele and i am wondering if there is anyone out there who has suffered as much as my grandmother...she has been in really bad shape here is what happened..My grandma was prescribed omeprazole back in July of 2008 for acid reflux...She seemed to be doing fine until the first part of december when she was getting muscle spasms so bad she could hardly walk and is still dealing with the muscle pain, pain in the middle of her chest and her right shoulder so bad that she has to stop what she is doing to catch her breath, this chest pain also came with a rash that was very itchy and dry between the breasts, she couldn't figure out what to do until it dawned on her that it must be these pills...she stopped taking them the beginning of december and is slowly getting better but is getting frustrated with the pain that she is still enduring...is there anyone who has hope for her who has taken this medication who had the same symptoms as her..we do not know what to do to make it easier!!
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About 10 days ago, I began to feel little prickly feelings, like a light needle poke, in random places on my body. I was a little concerned but figured it would go away. After a day or 2, I began experiencing a little muscle cramp in my left and right legs but my cholesterol and blood had just been checked so I called my doctor's office to find out if it might be a blood clot. They told me there were no blockages (they had just done a routine cholesterol test on me about a week before). Another day went by then my muscles began to get sore and my joints were popping sometimes. My muscles in my legs, arms (mildly), around my ribs (sometimes) and my under arms (sometimes) felt sore. I used a heated massaging pillow to make them feel better but was perplexed as to why I was having these aches. Sometimes I felt an arthritic ache also like the pain might have been in my bones. I was also having mild dull headaches. Then came a day when I felt extremely fatigued and so after a couple of days I went to the doctor. She said she was thinking I might have anemia so she had me go to the hospital and get a CBC test, a CPK test and to have my thyroid tested (I have hypothyroidism which I take medication for). The day I had my blood work done (yesterday) I felt very fatigued and was asleep by 9:00 pm, which is very unusual for me. I didn't feel muscle pain just weakness sort of. Today I feel a little muscle pain but not much, but I do feel a little weak. Also I had been having panic attacks a few times during all of this. I called the doctor's office today and the nursing staff told me the results of the blood tests from yesterday morning were all normal. I had thought it could be anemia which at least then I would have a diagnosis and could be treated but now I am even more scared because I don't know. What could this be?
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I had a heart attack in June 2012 and was put on many medications one of them being Atorvastatin (Lipitor) 40mg per day. After a couple of months I was in absolute agony with muscle pain which started in my left arm and shoulder, even had some numbness in fingers. The pain over the last 18 months or so has worsened going into my left shoulder and left side of my neck and now is in the whole of both my shoulders and all the back of my neck. The doctor has constantly denied it is any of the meds that I am taking and has sent me to physiotherapy many times, needless to say none of the various therapists have helped. I have been to see an osteopath, this didn't help either. I have had steroid injections into one of my shoulders, no help from that.
My pain gets worse by the week and is seriously affecting my daily life from work (I am a secretary) to driving to doing any of my enjoyed sports of fishing and golf.
I have spoken to many friends on this statin and they all complain of similar muscle pain. Why won't the doctors listen to me when I tell them this.
I have today stopped taking the Lipitor as I cannot take this pain any more. I have previously stopped this on two separate occasions and found the pain almost went away until the Doctors got quite stroppy with me and told me I was going against medical advice doing what I was doing in stopping the medication.
Is there others out there that have suffered this and have found what to do to get GP's to listen to their patient?
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For 11 years I have suffered with this condition. The 1st diagnosis was claudication, 2nd arthritis, 3rd peripheral artery disease, 4th nerve interference from protruding spinal disc , 5 6 7 8 9 10 etc. I have taken every known treatment . Where would you suggest I try next ?
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I have always had the same symptoms with my right sided sciatica being buttock and calf pain worse on sitting but for the last few months intermittently and permanently for the last couple of weeks I have also been getting knee pain in both knees and leg / thigh muscle weakness worse on walking.
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My condition, hypophosphatemia and oncogenic osteomalacia started about 3 years ago, however, was not diagnosed until six months ago. It started very gradually with body stiffness that over time worsened to bone and muscle pain and weakness. Was examined by all kinds of specialists who really didn't know why I had so much pain just walking, sitting and getting in and out of bed. My Rheumatologist had been very puzzled by some of my blood test results concerning alkaline phosphates being 3 times as high as they should be. Vitamin D testing showed I was severely deficient. Subsequent examination, blood tests and bone biopsy by an Endocrinologist indicated oncogenic osteomalacia and hypophosphatemia being caused by a tumour somewhere in my body. The tumour gives off something that causes my Vitamin D and phosphates to become deficient in turn causing the bone pain and muscle weakness. Subsequent CT scans and PET scan have not located the tumour. Am taking medications that are helping somewhat. Want to communicate with someone who has this condition or recovered from it. Have questions about medications, rehabilitation and generally knowing about their experience.
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