Co-codamol :: Bad Reaction
Sep 2, 2010
The week before last I took co-codamol in the evening and went to bed feeling sick which isn't unusual, a few hours later I was woken by severe cramps and knew I had to get to the toilet, I was sat on the toilet and went dizzy and blacked out, I woke up on the floor sweat pouring off me, finally managed to move myself got a drink of water and made it back to bed, a little later I was sick and emptied my bowels, I wonder if it might of been a reaction to co-codamol as i've not really been able to take it since.
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My boyfriend takes 30/500 co codamol and he takes 20-30 a day, you may think this is a lot but that is because my boyfriend has been addicted to them for the past 6 years after being given these tablets following his tonsillectomy.When he wakes in the morning he has bad cramps and my bed is soaking wet this is due to the fact that he's an addict and the codeine has worn off. When he has tried coming off them he has the same symptoms as a heroin addict in cold turkey. He is now gets a daily prescription and is down to fifteen a day but he now takes codeine phosphate as the paracetamol in the co-codamol causes constipation which can't be good on the bowels. He is only 26 and this addiction has made his life sometimes unbearable. I know that if he could turn back time he would never had taken co codamol.
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I was diagnosed with sciatica yesterday morning by my doctor, he prescribed co codamol 30/500.
After taking two, the pain did subside but I felt really dizzy and sick but was just glad that the pain had lessened.
I took another two at bedtime and am still awake at 4.50am! I can't sleep for scratching! I am so itchy. Has anybody else had this terrible itching?
I remember being allergic to morphine following my hysterectomy, I came out in hives. Is it that I can't take these type of drugs, ie codeine based medicines? Tramadol has also caused itching in the past.
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How many dare you take in one day?
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I developed neuralgia on the left side of my face and took co-codamol for pain relief. Within 24 hours this side had swollen drastically. I went to hospital and was given a course of steroids to reduce the swelling. I was diagnosed as being allergic to codeine.
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I can't find ANYTHING that removes the pain! Co Codamol doesn't, the 'so called' pain relieving gels don't (I've tried 3 different types). Can anyone suggest anything else?
Yesterday I twisted my hips somehow as I got out of the chair, the pain was excruciating. Since then I can hardly walk (how does excercise, excercise fit in then?)
I had been doing so well, 20 mins walk per day (and I've always disliked walking!) - physiotherapy, etc.
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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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My Husband has been taking Co Codamol for over 10 years now , he suffers from spondylosis and arthritis. His Doctor has sent him for many x ray.I know that he is in lots of pain and can sometimes be in bad moods because of it but i feel that his addiction to the painkiller has made his moods a lot worse. My husband gets a months prescription of co codamol which is 224 tablets and has taken them all in 5 days, He takes 20 co codamol tablets at once about 3 times a day , so by the end of the day he has taken 60 tablets. When he has run out of his own painkillers he takes his mom's co codamol prescription and then its many trips to different chemists. I have been to the doctors 3 times with him over the last 10 years and at first they stop them and give him other medication for the pain but he ends up going to see the doctor that prescribes the co codamol for him again. He know longer lets me go with to the doctors because he knows i will tell them about his addiction. I now just have to put up with addiction and try and help him when he wants help. The addiction has certainly put a strain on our marriage and family life. The children who are 18 , 21 and 24 have all noticed and commented that they find it hard to chat to there dad and that he has changed.I feel that i am becoming depressed because of the atmospheres his moods create. He has been given appointments for physiotherapy but he does not bother going as he says it does not work
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I am in pain, tired, no appetite, diarrhoea, vague. Are all these symptoms shingles related or are some of them due to Acyclovir, co-codamol or Ibuprofen.
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I have had CS for a number of years but it is worse when I am in bed and when I lie down I go dizzy. I am on Stemetil for the dizziness and
co-codamol for the pain but it stays with me. I don't think there is a cure and I am told to learn to live with it. It drives me mad. I don't socialise any more even with family.
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I was on cocodamol for 7 years and just recently weaned off using a taper plan and good planning.
I didn't realise just how mind and body controlling these drugs were.
Ok to cut a long story short I became ill and was prescribed 30/500 cocodamol the first few weeks I felt great yeah less pain and what a head rush.
I started to get addicted and needed my 2 tablet four times a day fix,was my injury gone I don't know I just needed the fix.
I tried a few times before to go cold turkey and ended up with the worse symptoms possible I sure you have had these.
The restlessness and aches in the legs were the worst I'm sure you will agree.
Through my dependency I became intolerant to any products containing caffeine as I noticed my body would itch and I had pain in my kidneys all the time.I stopped caffeine 6 years ago and cured that issue.
This time around I decided enough is enough and try a taper plan.
week 1
8 tablets a day
2 at 7am
2 at 1pm
2 at 6pm
2 at 8pm
for 7 day only then I started my taper plan and it really works.
week 2
2 at 7am
2 at 1pm
2 at 6pm
1 at 10pm
week 3
2 at 7am
2 at 1pm
1 at 6pm
1 at 10pm
week 4
2 at 7am
1 at 1pm
1 at 6pm
1 at 10pm
week 5
1 at 7am
1 at 1pm
1 at 6pm
1 at 10pm
week 6
1 at 7am
1 at 1pm
1 at 8pm
week 7
1 at 7am
1 at 8pm
week 8
1 at 7am
This worked for me and just remember plenty of water but not mountains of it as too much water can be deadly.
I would say to anyone who has just been prescribed co codamol just be aware that the come down after long term use will really spoil your day.
For the full impact of going cold turkey should only last around 8-10 days from sources I read but I will say this for a easier stage of coming off and less side effects try a taper.
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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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I have suffered with a 'bad back' since i was 21, i'm now 40 in August, and since october 2014 i have been getting worse and worse and went from taking tramadol, naproxen, co-codamol and nortriptyline as and when i needed to. Now i take in a day.... 1800mg of Gabapentin, 20 mg of Zomorph, 180 mg of dihydrocodeine 35 mg of Amitriptyline at bedtime 1000mg of naproxen. I also have an underactive thyroid so take 200mcg thyroxine and for my depression and anxiety i take 150mg of venlafaxine.
With all this i still feel pain, but also a little dopey, i'm currently on the sick from work and am worried about how I'm going to pay my bills - i have been to my psychiatrist and she gave diazepam to take when i feel anxious...... love sweets, me!!!! I needed help and advice.... with all that medication i should be floored, never mind the fact I'm still in pain. I had an X-Ray in Nocv 14 this showed osteoarthritis and then an MRI scan this showed a bulging disc on L5/S1 i think it was. I have been referred to the orthopaedic specialists but its all just a waiting game but all this time i still have all my bills to pay and this leads to horrendous bouts of depression.
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I went in Macmillan hospital for an Iron Infusion, as chronic anemic. I had the iron, and the then administors Cyclizine via IV, i was resting in reclined position on the chair. Suddenly almost not long after maybe 5 mins as if i was either having a heart or stroke, i was struggling to breath serious chest pains,i don't know what my heart rate was since i have Tachycardia, i can say my heart was pounding and chest wall was very fast, i thought i was having a cardiac arrest. Bp from 126 shot up 186/90, i would not speak, my eyes were dialated, my eyes were reported by the nurse as "rolling back in my head", i felt as if paralysed as i could not lift my hands or head, i could not call help. I had tears rolling down my face,it was a few minutes before i could talk. It was the most awful, shocking,distressing,alarming,horrible,frightening experience, to have gone through. To add insult to injury i was sent home, and when i called the Dr acted as if he had never heard of this sort of serious reaction. Not a single note in my after care summary, now covering up. Not a single note about i had no warning about possible side effects, the care has had many failures.
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I was prescribed this drug yesterday for a supposed urine infection. I had suffered with urine infections alot in my teens and into adulthood, however had not had an infection since having my son 8 years ago. I had problems during my pregnancy high blood pressure being one of these problems. As a result I only have one fully functional kidney. I was told that my blood pressure would probably go up again in later life and therefore have had it checked each year since.
On a routine checkup a couple of weeks ago, it appears that the high blood pressure is back and at the checkup I also had my urine dipped. The nurse asked me if I had any problems passing water etc. When I said I hadn't, she said there was something in my water and would send it off to the hospital just in case. I said that I thought I would have noticed if there had been a problem.
Anyway, yesterday I got the results and the surgery informed me that my doctor had left a prescription out for me. I picked it up and took the first tablet at four o'clock. By seven o'clock I had a severe headache, and the most awful chest pain, I thought I was having a heart attack
On reading the side effects we rang the hospital, got an appointment, by which time my back and chest were covered in a rash. My Blood pressure had reached 240/140 extremely high....
The doctor confirmed that it was an allergic reaction to trimethoprim and injected me with an antihistamine. Having checked my urine again, they said I did not have an infection in the first instance and should never have been prescribed this drug and confirmed that it could have been fatal.
I am going to make a formal complaint to my doctor and would like to take this further. Why is this drug being prescribed? I think I am very lucky to be here today and my children could have been left without their mum.
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Was hospitalised for a week 18 months ago with temp over 40 and severe pain in my arms where all the muscles had gone totally solid. Couldn't walk, move or anything. Half way through my week my tongue swelled up and my throat covered in ulcers. Had morphine and antibiotics to treat.No reason ever found as to why -tested for cancer, meningitis and lupus -all clear
Last friday took trimethoprim for urine infection. Within hour all the symptons i had in hospital were back. Doctor told me to take double dose - got worse - went to hospital - got treated - went home. When had enough strength to ring doctor i asked if i was given Trimethoprim before and guess what? I was prescribed it five days before admittance to hospital 18 months ago
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I received a typhoid vaccination as I am going overseas in a month. There was no initial pain, however my arm did feel very numb. A few hours after the vaccination my arm was suddenly severely sore and I felt quite nauseous. The only slight relief I get is when I'm not using my arm or have it resting on my lap. Apart from that, I can't even manage to move it upwards or to the sides or even cough without being in extreme pain. Is this a normal reaction after a typhoid vaccine? What can I do to relieve the pain?
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I have been on quetiapine 25mg tablet 3 times a day for 3 weeks! Within an hour of 1st tablet I started itching but carried on with tablet as I was told it was anxiety! Went to see gp yesterday who told me to stop them as I had a rash! Has this happened to anyone and if so was it down to colour of tablet? I am sensitive to some colours! Do I ask psychiatrist if I can try a higher dose that's a white tablet but cut it up?
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I've had GA for 2 years now but was only diagnosed today, It appeared a short time after a skin reaction- Erythema Nodosum. This was brought on by Rigevidon, the contraceptive pill. Has anyone else experienced GA as a consequence of contraceptives?
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As well as many other side effects, joints, brain fog etc, I was out in my garden for 10 minutes, I had jeans on when I came indoors my legs felt like they were on fire and my tongue has gone tingley, I took my jeans off and I have what looks like severe sunburn all down them, I know this is the cipro has anyone else had this??
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Last night I came up with horrendous lumps, bumps and itchy mosquito type looking rashes all over my body. I have been on Penicillin for about 10 days and only started getting itchy on my scalp maybe a day or so ago, and now these symptoms have seemed to broken out into something very severe!!
The spots keep changing and moving into different spots all over my body, on my face, in my ears, on my knees, arms, hands etc.
The doctor gave me (Prednisone) which is a steroid hormone. This has helped the itching. They say it couldn't have been the penicillin, otherwise I would have reacted far earlier than after 10 days of treatment...
But then I looked at some academic journals, which stated that you can have 'delayed' drug reactions to antibiotics, sometimes a week after first taking them??
I did eat seafood a day or so ago ...but usually am fine eating shellfish etc.
It looks like someone has severely beaten up my legs with a pole! These huge golf ball size hives, very bizarre!
Anyway... my question is...has anyone else had a 'delayed' reaction or unpredictable reaction to antibiotics/penicillin?
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