Cinvanti and Famotidine drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Cinvanti (aprepitant) and Famotidine (famotidine). Common drug interactions include vomiting among females.
The phase IV clinical study analyzes what interactions people have when they take Cinvanti and Famotidine. It is created by eHealthMe based on reports of 14 people who take the same drugs from the FDA, and is updated regularly.
What is Cinvanti?
Cinvanti has active ingredients of aprepitant. eHealthMe is studying from 150 Cinvanti users. Check the latest studies of Cinvanti.
What is Famotidine?
Famotidine has active ingredients of famotidine. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 83,421 Famotidine users. Check the latest studies of Famotidine.
14 people who take Cinvanti and Famotidine together, and have interactions are studied.

What are the common drug interactions of Cinvanti and Famotidine, by gender? *:
female:
- Vomiting
- Nausea (feeling of having an urge to vomit)
- Throat tightness
- Diarrhoea
- Enterocolitis (inflammation of the digestive tract, involving enteritis of the small intestine and colitis of the colon)
- Febrile neutropenia (fever with reduced white blood cells)
- Neutropenia (an abnormally low number of neutrophils)
- Adverse drug reaction
- Drug hypersensitivity
- Obstruction gastric (obstruction in stomach)
male:
n/a
What are the common drug interactions of Cinvanti and Famotidine, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Throat irritation
- Throat tightness
- Vomiting
- Nausea (feeling of having an urge to vomit)
- Obstruction gastric (obstruction in stomach)
50-59:
- Nausea (feeling of having an urge to vomit)
- Vomiting
60+:
- Diarrhoea
- Enterocolitis (inflammation of the digestive tract, involving enteritis of the small intestine and colitis of the colon)
- Febrile neutropenia (fever with reduced white blood cells)
- Neutropenia (an abnormally low number of neutrophils)
- Adverse drug reaction
What are the existing conditions these people have? *
- Pulmonary Embolism (blockage of the main artery of the lung): 2 people, 14.29%
- Multiple Myeloma (cancer of the plasma cells): 2 people, 14.29%
- Hypomagnesaemia (electrolyte disturbance in which there is an abnormally low level of magnesium in the blood): 2 people, 14.29%
- Hypokalemia (low potassium): 2 people, 14.29%
- Febrile Neutropenia (fever with reduced white blood cells): 2 people, 14.29%
- Endometrial Cancer: 2 people, 14.29%
- Dehydration (dryness resulting from the removal of water): 2 people, 14.29%
- Breast Cancer Metastatic: 2 people, 14.29%
- Blood Creatinine Increased: 2 people, 14.29%
- Asthma: 2 people, 14.29%
* Approximation only. Some reports may have incomplete information.
Do you take Cinvanti and Famotidine?
- 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:
- Cinvanti (150 reports)
- Famotidine (83,421 reports)
Browse all drug interactions of Cinvanti and Famotidine:
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 Cinvanti:
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 Famotidine:
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 Cinvanti 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 Famotidine 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 aprepitant and famotidine (the active ingredients of Cinvanti and Famotidine, respectively), and Cinvanti and Famotidine (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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