Experiences with

Co-danthrusate

Hello you lovely well informed people. Does anyone have any experience of Co-trimoxazole? I've been prescribed it to treat a mycobacterium called nocardia. I have Brochiectasis and this blighter has taken lodgings in my lungs. I'm due a conversation with my consultant soon as he wants / needs to discus

I live I. The UK and have suffered RLS for at least 40 years. I was recently sent sor by a GP at my surgery who I have never met before. She wanted to discuss my medication. I was previously on Pramipexole (not sure of dose) , but approximately 3 years ago my prescription was changed to 50gms of Pregabalin

I am trying to come off Ropinirole. I have gradually reduced my dosage from 2.5mg to a half mg. I’m not getting much sleep and am unable to sit from midday onwards without the rls being a problem. My GP is not very helpful and is unlikely to prescribe an opioid to help this final stage. She has prescribed

Six days I hurt my back. I took co codamol and ibrufen every 4 hours and then amitriptyline 20mg for two nights. From Wednesday night to Thursday night. I then stopped. I have been reading about ototoxicity in meds and the potential damage to the ear. Apparently al these meds are ototoxicite. I already

I’ve been bobbing around between 10 mg and 8 mg for the past six months. I manage to get the dosage down and then my hips/legs start playing up and feel very uncomfortable, so I'd up the dosage. On the advice of my rheumatologist I’m slowly reducing my dosage and am now down to 8.5 mg and I’ve now

I have moderate RLS treated by co codamol and PanadolI take a good multivit,magnesium and turmeric.A pro and prebiotic and avoid processed food. Yet my Ferratin levels remain very low not near 100 advised How can I increase them and any other advise please?

My GP referred me to rheumatology in December for an 'official' fibromyalgia diagnosis and POTS investigation. I was on Patient Access yesterday to check the date of the referral and chase it up, when I spotted a document I hadn't seen before and clicked on it to see what it was. It was a letter from

Following a heart attack & stent (Jan 2024) I was mostly fine for almost a year but since last December I am getting chest pains with nausea on a regular basis. I have been given a spray & told it is stable angina (I was sent to A&E twice when it started). I think it is unstable angina as it usually

I have had to pick out this very hard stone like pebbles for at least 8/9 months if not longer I had colonoscopy 19th Oct 2024 ( polyp history) none that time thanks it is March and still doing it now up to 2/4 times a day that leaves me shredded to bits up my bum I feel I have "NO CHOICE" but to carry

Last year was awful. Pneumonia 4 times and respiratory infections every 6 ish weeks. My daily antibiotic was stopped,Doxycycline, because of ? Arthralgia. So much joint pain some days I just cried. Had a routine call from the ILD nurses a fortnight ago. Come in for a repeat blood test they suggested

Last Saturday night (it’s Thursday now) I turned over in bed and felt excruciating pain in my lower back. I was very uncomfortable all Sunday and went to GP on Monday am. She asked all the relevant questions and like me thought I may have had my first fracture. She arranged for me to have an X-ray which

RA has thrown everything at me over the years awful pain etc,methotrexate made me sick had to leave lefluminide off even tho it worked well due to clots in lungs,now on sulfasalazine 2000 mg a day,I had 2 infections in hand and foot last year ,I can't seem to get better now my body is like slow motion

At night I take pregabalin and co codamol now to relieve my RLS symptoms. Could one of these be the cause of my infernal back scratching? I know itching is a side effect of codeine but I've been taking co codamol for years without the itching. It is increased no though. Has anyone experienced itching

Hello Everybody Hard to keep this short.....I think I had a bit of a virus last Friday, as well as total sleep deprivation the night before due to husband being ill and us staying in a place where the wind howled through the double glazing all night! Only ate a poached egg at lunchtime and some protein

I've found that when i get rls and find the trigger point with my tsubo then rub the painful area with a roll on antiperspirant up and down my leg the sensation stops 🤔,with having peripheral N, I can get shocks from my feet to my ribs ect, so I googled electric skin and it mentions static electric

I understand that ibuprofen can interactwith anticoalgulates and should be avoided. Normally paracetamol does the job for me . I have a painful back strain, is it ok to take co-codamol.

I've only just found this site and already learning. May I outline my journey so far and hope helpful as opposed to waffle. Early April 2024 I slipped on a slimy wet paving stone and fell very heavily on my left thigh. After a couple of weeks then top of opposite arm started to be painful and achy.

If anyone can help with these symptoms what to do. ? Please. Chest pain and back pain at the level of the heart and fatigue feeling very exhausted. Little coughing. Blood test showing infection but nothing on the X-ray. Dr prescribed only co-codamol and codeine. Please tell me what to do with this exhaustion

Hi, I have an appointment tomorrow with a new GP who I think might be more open to discussing any help I can get. I'm hoping for some good questions to ask, please. I'm on amitriptyline & sertraline, which aren't helping. I've had co codamol, which bagged me up & I didn't like. They diagnosed me with

I take co-codamol 8/500 over the counter. Otherwise stronger co-codamol from the doctor.