Fenofibrate and Sirolimus drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Fenofibrate (fenofibrate) and Sirolimus (sirolimus). Common drug interactions include bell's palsy among females and blood urea increased among males.
The phase IV clinical study analyzes what interactions people have when they take Fenofibrate and Sirolimus. It is created by eHealthMe based on reports of 72 people who take the same drugs from the FDA, and is updated regularly.
What is Fenofibrate?
Fenofibrate has active ingredients of fenofibrate. It is often used in high blood cholesterol. eHealthMe is studying from 40,456 Fenofibrate users. Check the latest studies of Fenofibrate.
What is Sirolimus?
Sirolimus has active ingredients of sirolimus. eHealthMe is studying from 11,823 Sirolimus users. Check the latest studies of Sirolimus.
72 people who take Fenofibrate and Sirolimus together, and have interactions are studied.

What are the common drug interactions of Fenofibrate and Sirolimus, by gender? *:
female:
- Bell's palsy (facial paralysis)
- Bladder disorder
- Blood pressure decreased
- Blood pressure increased
- Bruxism (habitual grinding of the teeth, typically during sleep)
- Candidiasis (candidiasis or thrush is a fungal infection)
- Decreased appetite
- Dehydration (dryness resulting from the removal of water)
- Dizziness
- Dyspnoea exertional (breathlessness or shortness of breath)
male:
- Blood urea increased
- Glomerular filtration rate decreased
- Proteinuria (presence of protein in the urine)
- Pulmonary cavitation (cavity in the lung)
- Rash
- Acidosis (build-up of carbon dioxide in the blood)
- Blood creatine phosphokinase increased
- Chills (felling of cold)
- Diarrhoea
- Dysgeusia (disorder of the sense of taste)
What are the common drug interactions of Fenofibrate and Sirolimus, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Blood potassium increased
30-39:
- Blood urea increased
- Glomerular filtration rate decreased
- Haemoglobin decreased
- Urinary tract infection
- Protein urine present
- Proteinuria (presence of protein in the urine)
- Renal failure (kidney dysfunction)
- Erythema (redness of the skin)
- Injection site erythema (redness at injection site)
- Injection site pain
40-49:
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Immunosuppressant drug level increased
- Pruritus (severe itching of the skin)
- Pyrexia (fever)
- Rash
- Renal failure (kidney dysfunction)
- Blood creatine phosphokinase increased
- Low density lipoprotein increased (cholesterol increased in blood)
- Pneumothorax (the presence of air or gas in the cavity between the lungs and the chest wall, causing collapse of the lung)
- Pulmonary cavitation (cavity in the lung)
50-59:
- Headache (pain in head)
- Tremor (trembling or shaking movements in one or more parts of your body)
- Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
- Abdominal pain upper
- Acidosis (build-up of carbon dioxide in the blood)
- Adverse drug reaction
- Aggression
- Agitation (state of anxiety or nervous excitement)
- Back pain
- Bell's palsy (facial paralysis)
60+:
- Diarrhoea
- Vomiting
- Blood creatinine increased
- Blood glucose increased
- Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
- Chills (felling of cold)
- Cough
- Feeling cold
- Glomerular filtration rate decreased
- Heart rate increased
What are the existing conditions these people have? *
- High Blood Pressure: 12 people, 16.67%
- Chronic Graft Versus Host Disease (immune cells attack the host's body cells after transplant): 9 people, 12.50%
- Anaemia (lack of blood): 6 people, 8.33%
- Pain: 5 people, 6.94%
- Lipids Increased (excess lipid in body): 5 people, 6.94%
- Vasospasm (sudden constriction of a blood vessel, reducing its diameter and flow rate): 4 people, 5.56%
- Urination - Excessive Volume: 4 people, 5.56%
- Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 4 people, 5.56%
- Red Blood Cell Count Decreased: 4 people, 5.56%
- Heart Disease: 4 people, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Fenofibrate and Sirolimus?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Fenofibrate (40,456 reports)
- Sirolimus (11,823 reports)
Browse all drug interactions of Fenofibrate and Sirolimus:
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 Fenofibrate:
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 Sirolimus:
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 Fenofibrate 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 Sirolimus 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 fenofibrate and sirolimus (the active ingredients of Fenofibrate and Sirolimus, respectively), and Fenofibrate and Sirolimus (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.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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