Paracetamol With Alcohol - Light Headed And Anxious
Sep 20, 2013
Last week I was under the weather so started taking Paracetamol. The problem is that I was a) A bit loose with the guidelines (i.e. 4-6 hours, more like every 2-3) and b) I was taking Lemsip and Sudafed when obviously you are not supposed to take different types of paracetamol.
On Friday I went out for a few drinks (lager & vodka). Since Saturday I have been feeling incredibly anxious (not a normal character trait) and on Sunday had what I can only describe as my first ever panic attack. Since then I have been feeling anxious, sometimes light-headed and heart racing.
Sunday was the lowpoint and it was starting to improve and by Thursday I felt back to normal…so I went to the gym. 30 mins into what was not an overly strenuous routine, I was back to feeling light headed, anxious etc – just sometimes coming over me in waves.
Could this be linked to the over-use of paracetamol combined with the booze or have I maybe something more serious to worry about?
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So I just ended my period a week ago and had a little bit of bleeding when I wiped for the past few days then today my bleeding was really heavy and I've had cramps and horrible headaches for the past few days. I've also felt a little light headed and my cramps have been pretty bad but different than period cramps. What is wrong with me?
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I have damage to my heart from chemotherapy I had as a child and it is progressing and I have now been put on Lisinopril to try to help keep it from worsening any further or as quickly. I do not have high BP (my BP tends to run normal to a little low if anything). I started on Lisinopril Wed. night and Saturday morning I went grocery shopping & while pushing the cart and walking I got extremely light headed, a little dizzy, & my vision went a little blurry, I thought I was going to pass out. I ended up having to stop and sit down for a few minutes. I was able to complete my shopping but had to stop several times throughout due to the sudden light headed feeling coming back. I have never had this happen before and I don't know if my body just needs to adjust to the Lisinopril or if it is lowering my BP too much and causing these issues. Do I just need to let my body adjust or do I need to call doc & get back off of it.
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I was having frequent headaches and occasionally feeling lightheaded with floaters. I went to the opticians and they referred me to the ophthalmologist who put eye drops in and said that at the back of my left eye the optic nerve was sheeted. (I don't understand what this term means and cannot see anything on the internet to explain either) He just said that I didn't have any other symptoms for Optic Neuritis and wasn't sure but didn't think it was anything sinister. I am now waiting for a scan of the eye to see what that shows.
However, the last couple of weeks I have been getting pins and needles all over my body, mainly in arms and legs. I've also had general aching pains.
I have read online about symptoms and they point to all kinds of things, Fibromyalgia, Anxiety and possibly MS. As you can imagine this has really scared me as I have read that problems with the optic nerve can also be related.
Has anyone else had these symptoms or are they too few for me to be making assumptions?
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Hello my name is Brandon, I started off with a common cold about a month ago and been too many doctors all saying this way part of a virus. The cold symtoms went away but what stayed was my constant headaches, dizziness, fatigue, light headed and just unable to do any physical activity without getting dizzy or light headed. Doctors have put me on meds that have not worked and im still like this, I havnt been able to go to work or go to the gym in over a month, does anybody have any cases like this?
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Hi, for the past 2 weeks I have been getting these symptoms, dizziness, nausea, lightheaded, weak, headaches, neck pains, and tired. It is getting severe and im worried. I have had urines tests and blood test, they are all negative. Its constant and all day, it never goes away although some hours are worse then others. I have been on a medication called pristiq which is an antidepressant for almost 2 years, I tried increasing the dose in case that was causing it but it didn't work, can anyone help me please? Thank you
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I am debating if I should go to the Emergency Room, as it's a Sunday. My story - 26 year old male, healthy. Since age 10, I have had an intermittent feeling of my breath being stuck in my upper abdomen (solar plexus area) and a little in my chest but not much. Sometimes when going for a deep breath, I feel pain in the chest, but very rare. It almost feels like there is a wall in between my stomach and my lungs that prevents air coming out. I know it's weird because you breath out of your lungs not your stomach. The only way it comes out is when I finally catch my breath, which means I need to wait for it to be able to escape and then I finally get the deep breath I need. Also yawning often allows the breath to occur. When this is happening, I can still breath but it's like only 10% of my lungs fill up with air, like someone is standing on the other 90% of my lungs, preventing them from filling up.
My BASELINE/ usual status is having the breath being stuck symptom maybe 10 times a day, usually while eating. This has become normal for me and I don't even think about it until people who I am eating with say, "what is wrong with you?"
When it is GOOD, it happens even less, maybe once a day and I will barely realize it happened.
When it is BAD, it happens often, maybe 20 times an hour.
The last week it has been EXTREME to the point where I will be struggling for a full breath once a minute. It is so bad that I have been feeling light headed (main reason for the alarm here). I have class on weekends and I was walking to the train for class, and my body was telling me to stay home (i am the type of person who doesn't make a big deal out of anything and never skips stuff).
Background- I sleep very well, usually 7-8 hours a night, am very healthy, 6 feet tall, 180 pounds, run 6 miles 3 times a week (it happens the same when I run but it doesn't prevent me from running), played sports my whole life, doctors always tell me my blood work and everything is off the charts good. The reasons I just listed, combined with my Mom (nurse) always telling me I am fine have made me stop seeking cures for this. I had every test under the sun done when I was 15 (EKG, Barium Swallow, Blood work, etc) and everything came back clear. I have a concave chest (my chest caves in) and the doctor told me that my chest bone is interfering with my breathing (eyes rolling). But now that I am feeling light headed, I think it's time to go to the emergency room. I am going to go to a heart center in my town (Brooklyn, NY). Also, I LOVE doing research about stuff and have been reading about this a lot and tons of people have similar symptoms which has comforted me. But now it's time for me to get tested again I think. Maybe this just talked me into going to the ER.
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2 Days waking up tired, feeling miserable,slight headache and light cramps above my bladder. little bit of nausea in the mornings.
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I Had been feeling a bit tried for a week and had to go home from work last thursday as had really bad headache,(something i don't really get)
last friday i was out of breath going up the stairs so went to the doctors (i've had pneumonia before so was worried it was back)i had a temp of 38 and was told it wa a viral infection,i was told to take paracetamol and ibuprofen and if not better to go back on Monday.Come monday the breathing was better but i was getting a stabbing pain in my chest which was shooting up my left shoulder and down my arm. i thought something was wrong with my heart.I saw the doctor in the morning he asked what i was doing when i left the doctors and i said i wa going to work, he just started laughing and said you're not you have pleurisy,you have to rest for at least a week.He gave me a prescription for codeine for the pain and said if it got worse go back asap.
Monday night i though i was having a heart attack and tues wasnt any better.wednesday i started to feel very sick aswell so called the docs, they told me to go there asap so i did and was sent for blood tests and also told the sickness was due to the codeine.I was given Naprosyn for the pain and told to go back again on friday if i wasnt better.today is Thursday and im no better so looks like im going back tomo.
I tried to fold a small amount of washing this morning and had to stop as it hurt too much,i'm so fed up now as want to go back to work and get better. i feel that i can't take anymore time off work as i don't feel they give much sympathy. but i can hardly move without feeling like i'm having a heart attack.I'm only 25 and fit and healthy normally i can't understand why i get all the illnesses that older people are meant to get.
I'm so glad there are other people feeling the same and to know that this pain is normal for pleurisy.
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I have been taking paracetamol with codeine for sinus pain and toothache-more the form. I'm very worried about addiction so will take a single dose of an evening 2-3 days a week. Then I can have weeks and 2-3 months of none. I don't experience withdrawal or addictions when I do not take. Is it ok to use paracetamol & codeine sparingly like this and avoid addiction. Can I have balanced feedbacks please-well weighed up good and not so good experiences.
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can I take paracetamol with fluoxetine 20 mg and omeprazole 20mg
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I am new to this, but at the moment I'm wishing I had never had this done. I had a TKR done on Friday, the epidural and sedation didn't work so had to have a general. The pain relief I got whilst in hospital was good, came home yesterday and all I've got is paracetamol and codeine, which has no effect at all, slept in 20 minute intervals all night. Our dog had her crucial element ligament done about 17 months ago and she was on better pain relief. I am honestly regretting what I have done, sorry for sounding so negative.
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In 2007 I had true frozen shoulder in my left (non-dominant shoulder). After freezing and while waiting for arthroscopic release I spent five months on dihydrocodeine and tramadol and didn't sleep. Nosleep. None. I don't really remember much about 2007, I was 42. I continued working, but like a zombie.
I had the arthroscopic release and was off all pain meds within 2 days – was magic.
Surgery performed by Mr Cameron Hatrick in Sussex on the NHS.
However I had severe muscle wastage and was very unfit, so months and months of physio followed before I regained full movement and fitness.
Exercises I found particularly useful was being able to windmill my arm – simulating swimming movements in addition to the other recommended exercises.
In October 2014 I suspected the onset of frozen shoulder in my right arm. I completed as many of the exercises I did post op last time, as possible and went to gp and physiotherapist.
I maintained mobility much longer but had pain when sleeping and lying down, so disrupted sleep.
In late January I lost all mobility within 2 weeks, much more rapidly than last time, but I assumed it was because I had been keeping the strength and mobility exercises up. Up till this point I was coping with just paracetamol.
I was referred to Mr Hatrick again. In the meantime, while waiting, I was back on the dihydrocodeine, then back on the tramadol too. I also used heat patches – the kind that last 12 hours and you wear on clothing, not skin. Still managing sleep in 2 and 3 hour spells to add up to 6-8 hours a night.
However I felt my whole health was deteriorating with the use of the dihydrocodeine and tramadol, as they made me an idiot and I was in a new job and trying to impress. (Well at least look professional).
When they recruited me in February I explained about my condition and that I was waiting for keyhole surgery and would expect to be back at work in a few days. The new job was great because I could go by train as I had given up driving as could open and close the driver's door or use reverse gear.
Before seeing the consultant, I returned to my GP and he wrote a letter to point out how this was adversely affecting my mental health, recommending the procedure be done quickly. I saw Mr Hatrick on March 30th and had the op on April 1st in Brighton.
However, this time the discharge included notes and graphic images and explained the complications encountered. I did not only have arthroscopic release and manipulation under anaesthetic. As I had inflammation ++, impingement ++ and a thickened bursa, I was given a nerve block and had bone shaved.
I went home, tried the dihydrocodeine and tramadol and suffered. Went to the gp twice, spoke to the gp twice, saw the nurse to have my stitches removed and returned to the hospital for examination by a duty registrar. I saw the physiotherapist for an assessment who looked at my discharge notes and said I had had two real extremes of experiences of easy and complicated. I then had a follow up with Mr Hatrick on day 17, who said in 14 years he had never recommended a steroid injection any sooner than 4-6 months post op as there was a risk of infection. However, he recommended it as urgent and on day 20 I had a steroid injection under x-ray.
Now it is day 22 and I am still suffering and am still off work.
Since day 5 I have been on Morphine, Naproxen and Paracetamol. Since day 17 I have also been on Gabapentin. This cocktail will sometimes mean I get 3 or 4 hours sleep. I certainly have better mobility since the release, but pain is still awful, despite the meds and plenty of ice.
Given up taking one day at a time, I now take every 4-6 hours at a time.
No idea when I will be able to return to work.
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I have recently been put onto Losartan, after developing a Ramipril cough. After some adjustment, it has been agreed with my GP to put my dosage to 50mg taken at night.
However, the last few days I have been feeling very woolly-headed when moving around. I have now taken a few readings at various times and I think I may be getting a drop in pressure when standing. Sitting pressure is showing 130/78. Standing straight after the sitting reading is give my 118/70. Should I go back to GO?
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I'm 20 years old.
Right now im lightheaded, dizzy, anxious for one one week. I think it maybe had something to do with my fall, but im not sure. I was drunk that night, was walking and lost balance, falled on right side of head, no vomiting, no memory loss. Just the next day i felt like crap, not only hangover, but my head was hurting so bad on the left side. It was in July btw.. Then after that i felt weirder, had episodes of lightheadedness and i knew something was not right, i never had these things before. Then about 8 days ago it all started, i was working and just felt like i have weakness in body and lightheadedness, i felt terrible, my ears kinda "closed" for some 15 seconds, horrible feeling. That they i went home and slept all that day and from that day i feel like crap, my left side of head feels like pressure in there and behind eye. I was sleeping for 2 days and felt worse and worse. It was so bad i couldn't walk out off bed few steps, that was last drop, my mom called paramedics, I was taken to hospital, they did blood test, ct scan to my head, I had to wait like 6 hours until they told me results, and there was moment when i was sitting and felt worse condition in life, i was about to pass out, they then put me in bed, and i felt better within hour... After waiting for 6 hours they told me everything is okey, ct scan good, blood test good. Then some ear doctor came to see me, she said it could be bppv, so they sent me home with some medications. I had to take Medrol for 6 days, the first day of it was just horrible, my heart was pounding, couldn't sleep, i felt worse then before. So i consulted my family doctor and she told to stop taking them, so i took them for 3 days after that i felt terrible side effects, my headache was so bad, the worst ever, i felt my whole body was weak.No Onee told what I have, i dont think its BPPV maybe im wrong. I kept reading online about my symptoms and possible things that i could have, i was just getting more and more anxious, scared, just feel soo bad. I gotta say, before that i did 3 x rays to head, neck, all good, and i did ultrasonography to head, all good.
On 21 october i went to neurologist, she told me that everything seems okay, that i need to relax and only think positive, she asked me questions what I wanna do in future and things like that, that helped with my anxiety, but not with my dizziness, vertigo. Right now I'm waiting for 29 october, i got visit otolaryngologist, for consultation and audiogramm. It seems so far away, and i can just guess whats wrong with me... Right now symptoms are: vertigo, dizziness, when i move my head side to side its much worse and start to feel pressure in head, if i hold my head straight, almost no dizziness, im sensitive to light, i cant sit long time to computer or smartphone, max 1 hour, if i sit longer i get weird feeling and dizziness, i hate going to sleep now, when i lay in bed i feel like falling, everything is spinning, if i lay on any side it gets even worse, like my head is spinning, but others thing stay in position, plus if i lay on sides i get more head pressure. What helps me walking and making myself something to eat is medical head holder, its used for neck injuries, but it helps me!! Well the dizziness is less with it and im taking betahistine 24mg 3 times a day and it makes dizziness less. And i got some pain around heart, but that could be from anxiety and all time that i sleep on my back. I just wanna get back to normal life, its so hard with dizziness, can't do basic things, im listening to motivational speeches and videos that is what helps me everyday. I was thinking maybe its like message from higher powers, that i need to change, because i really need to had some bad habits, drinking, smoking and things like that. Right now im making something like diary, i write down how i feel everyday and i wrote things that i need to accomplish, when i will feel good I will start doing them one by one!
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I've been on Citalopram for 10 weeks now. 2 weeks 10 mg, 5 weeks on 20mg, 3 weeks on 30mg. In my second week on 30mg I was back to my normal happy, confident self. Finally relief! Then last Saturday I felt the anxiety creeping back in & now I feel anxious & depressed again. My hand shakes & body jerks are back too. I don't know if I'm just having a blip but I seem to be going back to square one after that week of relief. Although I have only been on 30mg for 3 weeks. I'm just starting to feel like Citalopram isn't going to work. I also have a really fuzzy head. Has anyone else experienced a week of feeling great then back to square one? Should blips last as long as this?
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My partner has been on Lisinopril for the last 2 weeks, he has been suffering with feeling anxious and his Tinnitus has been a lot worse than usual also not sleeping like he normally does, we have our own BP machine and taking it at home it's fine often 120/73, but at the Doctors it can be 150/100 is this just white coat, my BP is almost the same at home and at the doctors as his, he has not taken one today and is going to see how he is over the weekend and try to get an earlier appointment, when speaking to a nurse recently she thought that he didn't have high BP, so why is he on them then?
Sorry I forgot to mention when on Lisinopril my partners BP is as low as 97/66, is this too low?
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For the past three years, every time I smoke weed, I become extremely anxious and depressed. I always feel worthless, anxious, and extremely sad after I smoke - my mind produces really negative thoughts about my life, beliefs, self- image, as if all that I am and say is worthless. I feel this way even when I smoke around people who I am comfortable with. When I was in high school, I used to smoke weed on a frequent basis and feel so happy, calm and relaxed. All I want is that feeling again.
Does anyone know how I can feel good again when smoking?
It's strange - even when I THINK about smoking I get that anxious feeling!
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I went to see my GP only five days ago for clinical depression and I was taken off mirtazapine 30mg that I had been on for roughly six months and put onto sertraline 50mg. I was advised by my GP to reduce the mirtazapine down to 15mg immediately. My question is this.... Is it just me or has Sertraline made anyone else feel worse? As of day one I've felt like what I can only describe as a 'zombie'.
It feels like I'm constantly wading through thick mud, I now feel constantly anxious, I have no appetite whatsoever, I wake up at 3-4am and can't get back to sleep because all these thoughts keep whizzing around in my head, when it is time to get up I feel utterly shattered. I don't want to go out and everything I used to find enjoyable I cannot now face. I have a 7 y/o son whom I love and adore but feel like I can't even look after myself at the moment let alone him, the guilt of this is now exacerbating my feelings.
The thought of facing another day feeling like this is terrifying me, let alone moving forward with life. I've restarted with my private councillor and am avoiding alcohol etc as my GP advised, but just feel terrible.
I'm not expecting miracles overnight or anything but I think I'm just searching for some reassurance I guess?
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I have been on these steroids for 1 week following pneumonia.
They have cleared chest but have left me exhausted through lack of sleep and feeling constantly anxious. Has anyone else suffered the same side effects. Finished last dose today.
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I was prescribed gabapentin by my ent specialist for sinus headaches which i still suffer from after three operations. I have been taking 300mg six times a day for about 18 months and have found that i have become moody, anxious, and find it very difficult to unwind or hold a decent conversation with anyone as my concentration level seems to be next to nothing. Does anyone think this could be the tablets?
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