Humira and blood tests

Common Questions and Answers about Humira and blood tests

humira

How often do you have to get blood tests or TB tests and such done? He told me that I should see results within a few weeks. Do you have to avoid contact with people since it suppresses your immune system? I have lots of questions, but anything you can tell me about Humira is helpful.
Has anyone been on Humira and what kind of result did you have? Any side effects? I am on lots of meds which are not decreasing the pain. My doctor wants to put me on Humira and I was wondering if anyone out there has had any success with this drug. I am desperate to NOT be in pain anymore. Help...
I've been on Humira for about 6 months and I have been messing with my injection times a lot over the past couple months. Humira is the only thing that keeps me going, but I have to do it weekly. I noticed when I missed my dose, when I was doing it bimonthly, my symptoms would just keep getting worse. We did a few psychological tests to see if my symptoms were coming back due to an emotional connection. That was quickly proven otherwise as I started to vomit and have bloody stool.
I have monthly blood tests including liver function and everything has been okay until last month when my red cells were enlarged and white cells low. Gastro is keeping an eye on them, but has continued to prescribe it. He did talk some years ago about doing a liver biopsy, but after talking to a heptologist colleague, he said it is a dangerous test, and not warranted at present.
I also have had RA for over 10 years and am recently put on Humira too. My blood tests were TSH of 4;97 Free t4 .064 and the Free T3 was 2.70 both the t4 and the t3 were at the bottom of normal levels. I had an ultrasound on the thryoid and it showed 3 nodules, and then he had me do a radioacitve thryoid uptake that said it was running a littel below normal. Can low thryoid cause such bad night sweats and seomtimes I get them in teh day too.
He has an appointment to learn how to inject and all the paticulars. He hasn't had a blood draw since his liver biopsy in July. They haven't mentioned that he would have another blood draw for his VL. If they don't offer should we ask so we have a more accurate starting point? The nurse said they will teach him with Placebo shots as he will start treatment on a Sunday night. Is there a better place on the body to inject.
I had a similar problem a few months ago, the exception with mine is my period didnt stop, I actually kept my period for two weeks passing the HUGE!!!!
Would the active use of prescriptions used in the treatment of rheumatoid diseases (enbrel, humira, methotrexate, predisone), suppress the creation of anti-bodies and interfere with ability of blood tests to accurately determine a herpes infection?
I also have the same thing. Had it for a few years and went to my doctor who did blood tests and found I had under active thyroid. But I still get the painful bruises in the palm side of my fingers now and again. No one seems to know why. I recently had this happen to two fingers on the same hand in the same day.
I have been treated for rheumatoid arthritis with Humira for 7 months including a combination of Humira and methotrexate for the past 2 months. I also take 5mg of prednisone, and 6 Azulfadine tablets each day. I was taking Humira once every fourteen days and I am on 15mg of methotrexate a week. About a month ago, I started experiencing numbness in my toes and feet. I mentioned it to my rheumatologist but she wasn't concerned and simply told me it wasn't rheumatoid arthritis.
I would consider a colonoscopy to evaluate the lower GI system, as well as sending off the stools for analysis and culture. Blood tests can be done to exclude celiac disease. These options can be discussed with your personal physician. This answer is not intended as and does not substitute for medical advice - the information presented is for patient education only. Please see your personal physician for further evaluation of your individual case. Kevin Pho, M.D. www.kevinmd.com www.
For example-thyroid, parathyroid,) and last but not least did they run a check on your blood gases and electrolytes. Peace and hope you feel better soon.
Saw Gastro last week, prescribed Cipro for 7 days, 3 weeks off, then another course. It has brought the D under control. I had full blood tests last week and a stool test for calprotectin, no results yet. Had this done 3 yrs ago and it was elevated. One of the blood test forms said "Leukaemia?" which worries me as I had FEC chemo and rx for breast cancer. How serious is this, and what does the test mean?
We have a specialist IBD nurse at my hospital whom the gastro said can do them and she can show me how to do them myself so that is an option as it is a 3 hour round trip to the hospital by car, ferry and taxi. I have blood tests once a month locally. As far as I can remember, regarding psoriasis and remicade, the Gastro said he was concerned the injection site could get infected, but I will print your response and discuss with him at next appt in 6-8 weeks.
I would suggest you see a gastroenterologist, pronto, and have a C-reactive protein blood test and calprotectin stool assay test. Both of thest tests will identify if your Crohn's is active if out of the normal range. The pain in your left lower abdomen could be indicative of strictures (narrowing) in either the small or lage intestines. in the right side usually means inflammation in the terminal ileum, the last part of your small bowel. An MRI scan will identify both these problems..
DH has asked me to get some opinions from you gals on here since you've been so wonderful with all of your support and sadly have been through this yourselves. I'm at a crossroads here and considering there isn't much money left or emotions, we could really use an opinion in where to go from here. How many times do you keep doing the same thing hoping for different results but fail time after time?
I have a respiratory infection right now, so I can't start taking the Humira injections yet. I am trying cipro now and so far after two doses I'm doing okay. Cross your fingers. I hope this one works.
If you take immuno-suppressants as detailed above, you need careful monitoring with regular blood tests. I have blood tests every 2 weeks. One thing to watch for, is low B12, as the terminall ileum is the only place in the body where this essential vitamin is metabolised and if your ileum is inflamed, it will not absorb B12, so you will need regular shots. If I can help further in any way, please let me know.
It is used to help many things and has a money back guarantee it also has testimonials of people who have taken it my husband has suffered for many years with chron's and we are fixing to order this item. Humira is so scarry and has so many bad side affects we thought we would give this a try. I hope this helps you. God Bless.
Ive only had it since 2010 but it was severe at the beginning! Flipped my world upside down. I was tried on Humira and Enbrel. They discontinued the Humira because it was not helping. They discontinued the Enbrel because of side effects. Now I am on Plaquenil. I also get Rituxan infusions.I am on 15 mg of Prednisone but being tapered because I have been on it since 2009 and they want me off it because of the problems it is causing me.
I often feel light headed and feel like I could pass out. My blood tests all look fairly normal. Yes, stress is a factor and I have learned that if I don't control it my arthritic symptoms with Reactive Arthritis go down hill rapidly. Thank you again for your information and if you think of anything more I would appreciate it.
the disease activity score for 28 joints, or DAS-28, which assess tenderness and swelling in 28 joints; as well as blood tests that measure inflammation. Seventy of the subjects either dropped out or were lost to follow-up. After six months, the researchers found methotrexate had no significant effect on objective measures of disease activity.
I would not advocate taking any supplement without your gastro's approval. I have 2 weekly comprehensive blood tests, and if I need supplements or dietary supplements they advise me.. I don't believe you can take dietary supplements without your gastro's concurrence, with such a serious incurable disease. Hope this helps...it is a long hard hard with Crohn's...and I do empathasise...I told my gastro I found breast cancer treatment duck soup compared to this foul disease and he concurred.
Linear regression analysis was performed between serum viral titers and liver tests. In addition, for the purpose of comparison, the subjects were divided into two groups: those with low viral titers (50 mEq/mL). Results All subjects were men, with a mean+/-SD age of 47+/-7.8 years. The mean HCV RNA level in the blood was 76.3X10(5)+/-109.1 genome equivalents/mL. There was no correlation between HCV RNA levels and age of the patients (r = 0.
Have seen GP, 2 Neurologists, Orthopedist, Rheumatologist, Chiropractor. Have had blood work, Lumbar and Cervical spine MRI, Brain MRI, urinalysis, nerve conduction study, and most recently Echocardiogram. Without boring you with all the details, I am trying to make a decision about surgery...on my cervical spine. The back will have to wait for now. In regards to my neck pain, my Ortho says that he can only give me about a 50% chance of pain relief since I don't have a lot of pain in my arm.
And of course thats when my blood work continued to show Elevated sed rate. Anyway, The have done all tests possible even cancer tests Blood types vacular types you name it. Thats why I know some of the lingo.... which I'm not proud of. I guess more then anything now that I'm older and have things to care about I need to put my health first so I'm there for them in the end. I'm racing against the clock. Because so many bad things are happening.
but I experienced side effects of high blood pressure(I had no prior history), increased in heart rate, altered my mood severely, and increased my insomnia, decreased my appetite. It was the high blood pressure and heart rate that was deciding factor for me to discontinue the medication. Savella is given in a "starter pack" with instructions to increase doseage pretty rapidly; I increased very slowly and tried continuing on a lower dose.
for the TNF ALpha cytokines, i need to take Humira which is a strong drug that has side effects and can have serious side effects but it is not likely hopefully! Humira is not always accepted my insurance if you don't have Lupus and it is $1600 per shot! For the MTHFR, i will need to take Lovenox. My dr gave me a 70% success rate if i follow the treatment protocol and only a 10% success without it.
I mean that they paced in front of my door and I had a heart monitor and blood pressure every 5 min. I truly believe they messed me up bad and I would like to know just what happened ...I am still numb in both hands and feet. It is only getting worse since now I have pain everywhere in my body. Actually that is when all the back pain started..HMMM? Of course, they cover their hides with the statute of limitations..conveinient..
I am a 38 year old male and have been struggling with health issues for a few years. I have inflammatory arthritis and was previously on Humira for for one year as treatment for this ailment but was discontinued due to reaction to this med. Since being on humira I have had a klebsiella infection, fungal infection and malaise. In addition I now have biliary dyskinesia, enlarged liver and elevated enzymes.
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