Pleurisy :: Paracetamol And Ibuprofen
Jan 17, 2008
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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Had the symptoms for over a week, went to the doctors to be diagnosed with pleurisy. been given a five day course of antibiotics and ibuprofen. How long does it normally last for before the symptoms ease off. Also can going to work make my condition worse? sorry if this has been asked before , new to this site.
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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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I find these tablets really good for my arthritis. I have arthritis in hips, knees and at the back of my neck.
I do not have any side effects
One day this week I had a toothache and wondered whether I could have taken something for it on top of Naproxen. I wondered about Ibuprofen or co-codamol.
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can I take paracetamol with fluoxetine 20 mg and omeprazole 20mg
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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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Lots of discussion about whether to take ibuprofen or naproxen for periodic pain. Some comment that one should never take these two pain killers because 1) they don't help or 2) they don't interact well. Read earlier today that if either of these drugs (also referred to as NSAIDs) work for you, you don't have PMR. So when some of you "flare" there is a tendency to increase the amount of prednisone as the antidote.
I am interested in your experience here. I have found that both ibuprofen and naproxen help a lot with the pain from periodic flares, and particularly at night. I have not had any adverse reactions in any form. I have resisted increasing the prednisone because I don't want to start tapering all over again.
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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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I have found a UK based online Dr that is willing to prescribe me codeine phosphate tablets. My idea is to taper the dose myself and replace the co codamol 30/500 and Nurofen plus with these instead and come off them gradually. I can't go cold turkey, I've tried and the withdrawals are the most significant problem. My dr did this once before so I am going to follow the same tapering process. When I am down to 0mg I will ask my gp for a non opioid based strong pain killer for my 6 herniated spinal discs. It's going to cost overall far less than I am spending on packets of Nurofen plus. Feeling very determined to do this for good his time.
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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 developed severe blisters, toothaches tightness of the throat and mouth and tongue sores after taking this drug.
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I'm 19 years old and every summer for 4 years i've been working with my brother in law painting houses (for the most I wore a mask while painting) a year ago I graduated from high school and decided to keep working in the painting business also on december I started smoking, I wasn't a heavy smoker maybe 12 cigarettes a week on may I reduced the amount to 6 a week then 3 on may 27 I smoked my last cigarette and 3 days later I went to the ER because I had pressure on my chest ,back pain, and I was coughing,(I also experience night sweats) they took some xrays and everything was clear and I was diagnosed with pleurisy well it's been a month now and I'm still experiencing the same symptoms.
How long does pleurisy last?
Could it be lung cancer? Or is it just the nicotine withdrawals combine with the infection that's causing all this symptoms.
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any idea gave up smoking two months ago been ill two weeks doc said chest infection and pleurisy finished all antibiotics and painkillers still got pain in left shoulder and side doc said its because i gave up smoking and i am prone to infection anybody else been told this also got pain in left calf and down my left arm anybody got the same help me
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I am a carer for my Hubby, who has Pleurisy at the moment. I am his carer & I am meant to be going into Hospital for a hip operation. I am full of acute Anxiety myself as I need to get my Husband better. He is on antibiotics and strong painkillers as well. He also suffers from arthritis and also is deaf & severely sighted.. I am giving him hot fluids as much as possible.
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Just wanted to share my experience, the weekend before Easter I had to go home from work on the Thursday with Flu like symtoms, I returned to work the following Wednesday, still feeling under the whether, coughing but thought to myself that I have a long weekend to come so I would rest and recover. After the Easter break I returned to work still not up to par and still coughing but also had a pain in my lower rib cage as if someone had sharply elbowed me. These symptoms continued onto the weekend and on the Saturday became worse, I had to pick my daughter up and the cold wind hit my lungs and it took my breath away. On returning to the car I couldn't fill my lungs up the pain was so excruciating, after the car warmed up the pain subsided enough to enable me to drive home. On returning home the situation became worse and I waited for my husband to come home and he had to take me to accident and emergency where I was admitted straight away. They had to administer morphine for the pain to enable me to breath more easily, it was as if I were being stabbed with a thousand knives. The doctor, after blood tests and x-ray diagnosed pleurisy and I went home with Ibuprofen, codeine and paracetamol which I took to the maximum daily dosage!
1 week later I was at my own GP who gave me another sick note, I saw him again the following week and after examination he said that the pleurisy had gone but I had had a double whammy as I was also suffering with costochondritis and it could take a while, just to rest and keep taking the tablets.
It is now 28th April and the symptoms on some days have now subsided enough to the enable me to do very light duties and on other days I can't do much at all. The doctor hasn't really given me much indication as to how much I should or shouldn't be doing, feeling very frustrated, the mind is willing but the body isn't. He said that, "many people don't realise that more people die in a year from influenza than meningitis and I had to be patient". Being a full time working Mum who is usually house proud and very busy, is now living with a basket full of ironing and dust that I can write my name in. My employer has been very understanding and great about it all but not sure how long they will be patient and my work will no doubt be building up there too.
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I've felt so frustrated for many years. I too was told muscular/skeletal. While experiencing short breath, extremely tired, pain that shoots like a spear on left side from upper rib cage, center of left breast through to back.
In 2012 after hours of waiting, the blood clot I guess hit me hard, I was out, woke in room with heparin drip. Then told blood clot in upper lobe of lung and pleurisy.
After doctor visit Thursday my pain got so unbearable, and cough, husband drove me to ER this past Sunday. Again sat for hours. Then x-rays, and told had pleurisy. Sent home, told to take tylenol and bed rest.
My pain is off the chart now, I can't take NSAIDS since on coumadin.
I'm feeling very spacey, lightheaded.
I can't drive myself anywhere.
I need to work around husbands very long work hours.
And, if do go, what do they do, say, "more bed rest and stay hydrated"?
I don't have money to burn, for such non-sense.
Is there not any treatment for pleurisy at all?
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I wrote a couple months ago after a Pleurisy diagnosis following chest x-rays. As it turns out, it was a cracked rib that I had, NOT viral Pleurisy as the Dr had suspected. The cracked rib did not show on the chest x-rays, but I was told they don't always show. It took about 5 weeks for the pain to go away. Sometimes I can still feel it slightly when I do certain things. Just wanted to follow up in case anyone else had the same misdiagnosis.
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I had a cough for nearly four weeks, after which it suddenly got more painful. After one cough I collapsed on the floor and after that the pain was so bad I couldn't even push bowel movements (sorry to anyone who thinks that was one detail too many). I hobbled to my GP, who diagnosed pleurisy and gave me antibiotics and painkillers (codeine).
This seemed to help. Things were definitely improving after 3 or 4 days. A week later, I was feeling fine. The cough had stopped too. There was, however, a slight pain on coughing (and not-so-slight pain on sneezing) that did not go away.
That was three weeks ago. For the last 3 or 4 days, discomfort has been returning. It's not nearly as bad as it was, and is now mostly on the lower left side of my chest. I don't think it's bad enough to bother my GP with yet. Has anyone else had a similar experience? What happened next?
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4 weeks ago, I had a lot of pressure in my chest. It eventually worked it's way up and I had a nasty cough. My husband kept urging me to go to the dr. but as I like my body to fight off ailments, I was stubborn. I FINALLY went because I am nursing a 5 month old baby and started fearing pneumonia. I was diagnosed with a mycoplasma bacterial infection - no fluid in the lungs - and like many others, was prescribed clarithromycin and sulfate albuterol with a nebulizer.
On my 5th day of antibiotics, I got an extreme pain in my back, however, I could tell it was internal. I researched it and self-diagnosed as pleurisy. 2 days later I went in, and my GP agreed it was pleurisy w/o effusion and told me to take anti-inflammatories and cough suppressant. The pain has become worse and brings me to my knees when I cough. My cough is almost gone but it is very raspy and trying to come out, but I am hesitant to cough because it hurts so bad!
A few questions - has anyone experienced pleurisy only on the backside? My parents are urging me to get a lung x-ray but I have no reason to think there is a clot, or fluid - any suggestions on that? And last, the million dollar question - is this ever going to go away?????? Will I ever be able to return to a normal gym routine, lifting weights?
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I saw my GP yesterday following sharp stabbing chest pain which had gradually gotten worse. Yesterday morning I coughed up some blood which made me decide to see the doctor. He immediately rang the hospital and I had to get there asap as he suspected a P.E. Fortunately it was not that but I have been diagnosed with pleurisy. I have been given antibiotics but have to go back to the hospital next week for a further x ray to check and also to "rule out blood clots". This has left me a little worried. Does anyone know if blood clots and pleurisy are connected?
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I had pleurisy in December, started with pain in my right shoulder blade and my right rib. Six weeks on I am still suffering with extreme pain, I have had a chest Xray and all is clear but the pain hasn't got any easier. I am constantly out of breath and very tired all the time. The pain is still constant around my right shoulder blade and across my back and also under my armpit. I have been for an MRI Scan today to see if that shows anything but I have to wait another 2 weeks for the results. Its just nice to know I'm not the only one suffering
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