Gallbladder disorder is found among people who take Remicade, especially for people who are female, 60+ old , have been taking the drug for < 1 month, also take medication Methotrexate, and have Rheumatoid arthritis . We study 83,070 people who have side effects while taking Remicade from FDA and social media. Among them, 202 have Gallbladder disorder. Find out below who they are, when they have Gallbladder disorder and more.
On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>
Remicade has active ingredients of infliximab. It is often used in rheumatoid arthritis. (latest outcomes from Remicade 83,338 users)
Gallbladder disorder has been reported by people with gastrooesophageal reflux disease, gallstones, weakness, diarrhea, joint pain (latest reports from 14,323 Gallbladder disorder patients).
On Jul, 29, 2016
83,070 people reported to have side effects when taking Remicade.
Among them, 202 people (0.24%) have Gallbladder Disorder
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
I am 71 years old. I have a meninginoma brain tumor & RA. I had brain surgery May 5, 2010. About 2/3 of the meninginoma was removed. The 1/3 that was left shrank to about 3%. In 2013 it started growing back. It had grown back to about original size in 3/2015. Annual check up July 2016 MRI showed that the tumor has doubled in the last 1.5 years. I started remicade infusion at about the same time. COINCIDENCE????
I have started having gallbladder attacks over the past few months and they are debilitating ! Can't believe my Xanax is doing this to me! I kinda felt it but was in Denial for so long. Anybody suing them ?? Can't believe how much I am suffering
Several years ago in 2013 I was"diagnosed" with RA. I went through every medication including, humira, embral, to now IV fusions of remicade which has been almost a year. I am not feeling any better and body aches and joint pains getting worse. I started researching my symptoms and lyme kept ...
Have had Crohnes for 36 years with only one bowel resection and minor flare-ups. Healthy, mostly, but this time on imfliximab cannot sleep. Last time I was on it I had severe attack of pain and sweats, but it was still experimental.
I started having muscle aches after being on Remicade for 4 months. I had a test done to confirm I have Remicade antibodies and it also showed no signs of the Remicade still in my body so the antibidoes have killed it off. My GI has told me to discontinue infusions. I haven;t had an infusion ...
I am 71 years old. I have a meninginoma brain tumor & RA. I had brain surgery May 5, 2010. About 2/3 of the meninginoma was removed. The 1/3 that was left shrank to about 3%. In 2013 it started growing back. It had grown back to about original size in 3/2015. Annual check up July ...
I have just learned I have developed food allergies due to remicade. Unfortunately I have not been seen by allergist yet to determine which allergies. How to deal and cope with unknowingly eating foods I am allergic to?
Hi, My son has Crohns and after his recent flare and non response to intravenous steroids Remicade was offered (he is responding well and is also taking pure gum based turpentine (1 drop on a white sugar cube initially) which produced a white slimy mucous covered stool which we thought might ...
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.