hi guys
have any of you experienced any chest pains and shortness of breath? My GP done an ECG but everything was clear yet I still experience the pain. I no longer take Meloxicam I now use Synaleave and Celebrex for pain.
Any ideas?
hi guys
have any of you experienced any chest pains and shortness of breath? My GP done an ECG but everything was clear yet I still experience the pain. I no longer take Meloxicam I now use Synaleave and Celebrex for pain.
Any ideas?
Yes i feel like i have congestion on my chest all the time.I was at t he drs last week and he sounded my chest and my heart as well. He said that my heart was okay. I am at the rheumy on Wednesday and i am going to speak to her about it. I take Mtx,Sulpha,Naproxan,Cocodamol,Tramadol. Hope you get sorted soon.xxx
Hi Sylvi
thanks, let me know what your rheumy says. I cant use Naproxan, it burns my stomach, and I find that Tramadol doesnt really relieve my pain :-(. I have never tried Cocodamol before. Do you need a script for that?
Yes you do,speak to your dr about getting it. I believe you can get something to protect the stomach when taking these drugs,also speak to your dr. xxxx
I currently use Nozer, which is not too bad. thanks again, will speak to my dr and advise.
What is Nozer Imoches21?
its an anti inflamatory, like altosec
Okay never heard of either to be honest.xxxx
oh okay. its for the burning sensation. i take it twice a day
I have a hiatus hernia and i take Lansoporal for it.xxx
i never heard of that before.
It is used to settle things down. I also have acid reflux as well. xxx
Nozer & Altosec are both brand names for omeprazole Sylvi. I think as both are listed for South Africa I guess that's were imoches21 must be.
lol yes I'm from South Africa
Nozer is a stomach protector, a proton pump inhibitor, probably prescribed to reduce acid & prevent ulcers in your case as you take NSAIDs which can irritate the stomach lining.
Synaleve is co-codamol imoches21. I would think your Rheumy would be the better person to see about your chest pain & shortness of breath. It could be a reaction to one of your specialist meds & it's more likely he could pinpoint which one & reduce or withdraw it to see if your chest problems are relieved.
im currently onn MTX 2.5mg x 7 tablets weekly, folic acid, plasmoquine and BCALD.
Ok, then I would definitely report your chest pains & breathlessness to your Rheumy. Your 2 DMARDs (methotrexate & hydroxychloroquine) are both known to cause chest problems so should really be reported to your Rheumy & he will probably request an x ray or other imaging to determine the cause. I don't know what BCALD is, I'm sorry. Is there another name underneath the brand name? If there is that will be the medication's original (generic) name. Drug names can differ from country to country so sometimes it's easier to use the generic name as that is the same everywhere.
BCALD is calcium combined with Vitamin D. Thanks I will speak to him, and give you guys an update.
That must be like Adcal-D3 (calcium carbonate & Vitamin D3) I would think, chewable tablets. I take those, 1500mg/400iu daily, as defence along with a weekly bisphosphonate to protect bone density. I'm osteopenic/borderline osteoporotic & on long term steroids along with my RD mix.
Do let us know how you get on.
Do you have fibromyalgia with your RA?
Defo see a doctor, lots of causes of chest pain but really should be properly diagnosed, good luck x
Hiya, I asked about the Fibro because it can cause chest pains similar to a heart attack, pains in arm, neck and chest and it can look like a classic heart attack and it can last for one to a few days so becomes worrying, I have been through this for a good few years BUT LIKE WITH ALL CHEST PAINS YOU NEED TO SEEK MEDICAL HELP RIGHT AWAY, I've been in ambulance more times than I would like to remember lol.
Chest pains, arm pain, neck pain shortness of breathe can be caused by fibromyalgia BUT with all chest pains you should seek medical help.
Philip
I hope this is useful.
How are you feeling now, did u get a check up?? Hope all is well xxxA
I do quite often and have been in and out too many times to A,E, It's taken years to find out what it is, Costochondritis.
Apparently this is the answer to the chest pains.
I hope this helps you.