Tylenol and Uceris drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Tylenol (acetaminophen) and Uceris (budesonide). Common drug interactions include neoplasm of appendix among females and localised infection among males.
The phase IV clinical study analyzes what interactions people have when they take Tylenol and Uceris. It is created by eHealthMe based on reports of 33 people who take the same drugs from the FDA, and is updated regularly.
What is Tylenol?
Tylenol has active ingredients of acetaminophen. It is often used in pain. eHealthMe is studying from 222,310 Tylenol users. Check the latest studies of Tylenol.
What is Uceris?
Uceris has active ingredients of budesonide. It is often used in ulcerative colitis. eHealthMe is studying from 1,721 Uceris users. Check the latest studies of Uceris.
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 >>>.
33 people who take Tylenol and Uceris together, and have interactions are studied.

What are the common drug interactions of Tylenol and Uceris, by gender? *:
female:
- Neoplasm of appendix (tumour of appendix)
- Alopecia (absence of hair from areas of the body)
- Drug ineffective
- Fatigue (feeling of tiredness)
- Haematochezia (passage of stools containing blood)
- Increased tendency to bruise (increased tendency to injure the underlying soft tissue or bone)
- Osteoarthritis (a joint disease caused by cartilage loss in a joint)
- Thrombosis (formation of a blood clot inside a blood vessel)
- Constipation
- Pregnancy
male:
- Localised infection (infection at the single location)
- Pneumonia
- Device related infection
- Drug ineffective
- Foetal exposure during pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Sepsis (a severe blood infection that can lead to organ failure and death)
What are the common drug interactions of Tylenol and Uceris, by age (0-1 to 60+)? *:
0-1:
- Basal cell carcinoma (a skin cancer, it rarely metastasizes or kills)
- Foetal exposure during pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect)
2-9:
- Low birth weight baby
- Maternal exposure before pregnancy (use of substance before pregnancy)
- Speech disorder
10-19:
- Dehydration (dryness resulting from the removal of water)
- Device related infection
20-29:
- Alopecia (absence of hair from areas of the body)
- Contusion (a type of hematoma of tissue in which capillaries)
- Serum sickness (hypersensitivity reaction that results from the injection of heterologous or foreign protein or serum)
- Skin lesion
- Therapeutic response delayed (late preventive response)
- Type iv hypersensitivity reaction (delayed type hypersensitivity as the reaction takes two to three days to develop)
30-39:
- Constipation
- Pregnancy
- Dry throat
- Fatigue (feeling of tiredness)
- Hypophagia (reduced food intake)
- Influenza
- Irritability
- Malaise (a feeling of general discomfort or uneasiness)
- Middle ear effusion (fluid in middle ear)
- Migraine (headache)
40-49:
- Balance disorder
- Drug ineffective
- Fall
- Foot fracture
- Impaired healing
- Thrombosis (formation of a blood clot inside a blood vessel)
50-59:
- Crohn's disease (a condition that causes inflammation of the gastrointestinal tract)
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Laryngitis (inflammation of the larynx)
- Thrombosis (formation of a blood clot inside a blood vessel)
60+:
- Hypertension (high blood pressure)
- Neoplasm of appendix (tumour of appendix)
- Aspartate aminotransferase increased
- Haematochezia (passage of stools containing blood)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Sleep disorder
- Weight increased
- Drug ineffective
- Impaired healing
What are the existing conditions these people have? *
- Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 8 people, 24.24%
- High Blood Pressure: 6 people, 18.18%
- Fever: 4 people, 12.12%
- Asthma: 3 people, 9.09%
- Oropharyngeal Pain: 3 people, 9.09%
- Nausea (feeling of having an urge to vomit): 3 people, 9.09%
- Diarrhea: 3 people, 9.09%
- Hypersensitivity: 3 people, 9.09%
- Herpes Simplex (herpes simplex is a common viral infection): 3 people, 9.09%
- Herpes Zoster: 2 people, 6.06%
* Approximation only. Some reports may have incomplete information.
Do you take Tylenol and Uceris?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Tylenol and Uceris:
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 Tylenol:
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 Uceris:
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 Tylenol 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 Uceris 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 acetaminophen and budesonide (the active ingredients of Tylenol and Uceris, respectively), and Tylenol and Uceris (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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