Could Remicade cause Mastocytosis - from FDA reports
Mastocytosis is reported only by a few people who take Remicade. We study 119,153 people who have side effects while taking Remicade from FDA and social media. Among them, 5 have Mastocytosis. Find out below who they are, when they have Mastocytosis and more.
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Remicade has active ingredients of infliximab. It is often used in crohn's disease. (latest outcomes from Remicade 120,151 users)
Mastocytosis (an excessive number of apparently normal mast cells in the skin and, occasionally, in other organs) has been reported by people with multiple myeloma, urticaria pigmentosa, osteoporosis, high blood pressure, bipolar disorder (latest reports from 404 Mastocytosis patients).
On Dec, 08, 2016
119,153 people reported to have side effects when taking Remicade.
Among them, 5 people (0.0%) have Mastocytosis
Number of reports submitted per year:
Gender of people who have Mastocytosis when taking Remicade *:
- female: 40 %
- male: 60 %
Age of people who have Mastocytosis when taking Remicade *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 40 %
- 40-49: 20 %
- 50-59: 0.0 %
- 60+: 40 %
Top co-used drugs for these people *:
- Tylenol (2 people, 40.00%)
- Isoniazid (2 people, 40.00%)
- Imuran (2 people, 40.00%)
- Benadryl (1 person, 20.00%)
- Albuterol (1 person, 20.00%)
Forecasts by ePatient.care (We will alert you to new symptoms or undetected conditions when you take Remicade, learn more )
* 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.
Do you have Mastocytosis when taking Remicade?
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Can you answer these questions?
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 ...
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