Remicade and Blood magnesium decreased - from FDA reports
Blood magnesium decreased 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 Nexium, and have Psoriatic arthropathy. This review analyzes which people have Blood magnesium decreased with Remicade. It is created by eHealthMe based on reports of 126,627 people who have side effects when taking Remicade from FDA , and is updated regularly.
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On Nov, 20, 2017
126,627 people reported to have side effects when taking Remicade.
Among them, 61 people (0.05%) have Blood magnesium decreased
Number of reports submitted per year:
Time on Remicade when people have Blood magnesium decreased *:
- < 1 month: 50.0 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 16.67 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 33.33 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
Gender of people who have Blood magnesium decreased when taking Remicade *:
- female: 71.67 %
- male: 28.33 %
Age of people who have Blood magnesium decreased when taking Remicade *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 2.44 %
- 30-39: 12.2 %
- 40-49: 26.83 %
- 50-59: 17.07 %
- 60+: 41.46 %
Top conditions involved for these people *:
- Psoriatic Arthropathy (6 people, 9.84%)
- Primary Pulmonary Hypertension (2 people, 3.28%)
- Pain (2 people, 3.28%)
- Gastroesophageal Reflux Disease (2 people, 3.28%)
- Inflammatory Bowel Disease (1 person, 1.64%)
Top co-used drugs for these people *:
- Nexium (13 people, 21.31%)
- Methotrexate (11 people, 18.03%)
- Pentasa (10 people, 16.39%)
- Prednisone (9 people, 14.75%)
- Lomotil (9 people, 14.75%)
Top other side effects for these people *:
- Blood Potassium Decreased (20 people, 32.79%)
- Dehydration (14 people, 22.95%)
- Hypotension (13 people, 21.31%)
- Nausea And Vomiting (11 people, 18.03%)
- Nausea (11 people, 18.03%)
* Approximation only. Some reports may have incomplete information.
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Questions to the study
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 ...