Daytrana and Remicade drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Daytrana (methylphenidate) and Remicade (infliximab). Common drug interactions include hypersensitivity among females and irritability among males.
The phase IV clinical study analyzes what interactions people have when they take Daytrana and Remicade. It is created by eHealthMe based on reports of 18 people who take the same drugs from the FDA, and is updated regularly.
What is Daytrana?
Daytrana has active ingredients of methylphenidate. It is often used in attention deficit hyperactivity disorder. eHealthMe is studying from 16,561 Daytrana users. Check the latest studies of Daytrana.
What is Remicade?
Remicade has active ingredients of infliximab. It is often used in crohn's disease. eHealthMe is studying from 224,011 Remicade users. Check the latest studies of Remicade.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
18 people who take Daytrana and Remicade together, and have interactions are studied.

What are the common drug interactions of Daytrana and Remicade, by gender? *:
female:
- Hypersensitivity
- Infusion related reaction
- Loss of consciousness
- Malaise (a feeling of general discomfort or uneasiness)
- Raynaud's phenomenon (discoloration of the fingers, toes, and occasionally other areas)
- Small intestinal stenosis (abnormal narrowing of small intestine)
- Therapeutic response unexpected
male:
- Irritability
- Pruritus (severe itching of the skin)
- Drug ineffective
- Fall
- Gait disturbance
- Movement disorder (neurological syndromes where they may be excess of movement or a paucity of movement that is not connected to weakness)
- Muscle spasms (muscle contraction)
- Muscular weakness (muscle weakness)
- Musculoskeletal stiffness (stiffness of the body's muscles, joints, tendons, ligaments and nerves)
- Rash
What are the common drug interactions of Daytrana and Remicade, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Movement disorder (neurological syndromes where they may be excess of movement or a paucity of movement that is not connected to weakness)
- Muscle spasms (muscle contraction)
- Muscular weakness (muscle weakness)
- Musculoskeletal stiffness (stiffness of the body's muscles, joints, tendons, ligaments and nerves)
- Rash
- Stiff person syndrome
- Upper respiratory tract infection
- Anaemia (lack of blood)
- Anti-gad antibody positive
- Back pain
10-19:
- Irritability
- Pruritus (severe itching of the skin)
- Hypersensitivity
- Infusion related reaction
- Loss of consciousness
- Malaise (a feeling of general discomfort or uneasiness)
- Small intestinal stenosis (abnormal narrowing of small intestine)
20-29:
n/a
30-39:
- Drug effect decreased
- Overdose
40-49:
n/a
50-59:
n/a
60+:
n/a
What are the existing conditions these people have? *
- Migraine (headache): 4 people, 22.22%
- Hypersensitivity: 4 people, 22.22%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 4 people, 22.22%
- Depression: 4 people, 22.22%
- Mental Disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability): 3 people, 16.67%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 2 people, 11.11%
- Inflammatory Bowel Disease: 2 people, 11.11%
- Disturbance In Attention: 2 people, 11.11%
- Thyroid Diseases: 1 person, 5.56%
- Therapeutic Response Decreased (less preventive response): 1 person, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Daytrana and Remicade?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Daytrana and Remicade:
a b c d e f g h i j k l m n o p q r s t u v w x y zSub-studies by gender and age:
Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Daytrana:
a b c d e f g h i j k l m n o p q r s t u v w x y zBrowse all side effects of Remicade:
a b c d e f g h i j k l m n o p q r s t u v w x y zBrowse all interactions between Daytrana and drugs from A to Z:
a b c d e f g h i j k l m n o p q r s t u v w x y zBrowse all interactions between Remicade and drugs from A to Z:
a b c d e f g h i j k l m n o p q r s t u v w x y zHow the study uses the data?
The study uses data from the FDA. It is based on methylphenidate and infliximab (the active ingredients of Daytrana and Remicade, respectively), and Daytrana and Remicade (the brand names). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.
How to use the study?
DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.
Who is eHealthMe?
With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).
WARNING, DISCLAIMER, USE FOR PUBLICATION
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. Our phase IV clinical studies alone cannot establish cause-effect relationship. 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.
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