Kadcyla and Ranitidine drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Kadcyla (ado-trastuzumab emtansine) and Ranitidine (ranitidine). Common drug interactions include cardiac failure among females and bacteraemia among males.
The phase IV clinical study analyzes what interactions people have when they take Kadcyla and Ranitidine. It is created by eHealthMe based on reports of 38 people who take the same drugs from the FDA, and is updated regularly.
What is Kadcyla?
Kadcyla has active ingredients of ado-trastuzumab emtansine. eHealthMe is studying from 5,813 Kadcyla users. Check the latest studies of Kadcyla.
What is Ranitidine?
Ranitidine has active ingredients of ranitidine. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 234,475 Ranitidine users. Check the latest studies of Ranitidine.
38 people who take Kadcyla and Ranitidine together, and have interactions are studied.

What are the common drug interactions of Kadcyla and Ranitidine, by gender? *:
female:
- Cardiac failure
- Hypertrophic cardiomyopathy (a condition in which the heart muscle becomes abnormally thick)
- Epistaxis (bleed from the nose)
- Vitamin d deficiency
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Diarrhoea
- Blood bilirubin increased
- Performance status decreased
- Nausea (feeling of having an urge to vomit)
male:
- Bacteraemia (presence of bacteria in the blood)
- Dizziness
- Febrile neutropenia (fever with reduced white blood cells)
- Headache (pain in head)
- Malignant neoplasm progression (cancer tumour came back)
- Muscular weakness (muscle weakness)
- Skin cancer
What are the common drug interactions of Kadcyla and Ranitidine, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Bacteraemia (presence of bacteria in the blood)
- Dizziness
- Febrile neutropenia (fever with reduced white blood cells)
- Headache (pain in head)
- Malignant neoplasm progression (cancer tumour came back)
- Muscular weakness (muscle weakness)
- Pulmonary embolism (blockage of the main artery of the lung)
- Skin cancer
40-49:
- Mean cell volume increased (more than normal average red blood cell volume)
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Neutrophil count increased (excess than normal number of neutrophil a type of blood cell)
- Platelet count decreased
- Protein total decreased
- Red blood cell count decreased
- White blood cell count decreased
- Hypertransaminasaemia
- Metastases to central nervous system (cancer spreads to central nervous system)
- Alanine aminotransferase increased
50-59:
- Cough
- Weight decreased
- Pulmonary oedema (fluid accumulation in the lungs)
- Blood cholesterol increased
- Disease progression
- Drug intolerance (drug sensitivity)
- Haemorrhage (bleeding)
- Hepatitis (inflammation of the liver)
- Hepatotoxicity (chemical-driven liver damage)
- Inflammation
60+:
- Thrombocytopenia (decrease of platelets in blood)
- Palmar-plantar erythrodysaesthesia syndrome (hand-foot syndrome)
- Diarrhoea
- Performance status decreased
- Hypocalcaemia (levels of calcium in blood serum are abnormally low)
- Nausea (feeling of having an urge to vomit)
- Dysaesthesia (abnormal sensation)
- Dysgeusia (disorder of the sense of taste)
- Dysphagia (a condition in which swallowing is difficult or painful)
- Skin toxicity (skin damage due to toxin/poison)
What are the existing conditions these people have? *
- Breast Cancer: 15 people, 39.47%
- Breast Cancer Metastatic: 10 people, 26.32%
- Hypertensive Crisis: 7 people, 18.42%
- Thrombosis (formation of a blood clot inside a blood vessel): 6 people, 15.79%
- Rickets (softening of bones): 6 people, 15.79%
- High Blood Pressure: 6 people, 15.79%
- Skin Toxicity (skin damage due to toxin/poison): 4 people, 10.53%
- Nausea (feeling of having an urge to vomit): 3 people, 7.89%
- Taste - Impaired: 2 people, 5.26%
- Swallowing Difficulty: 2 people, 5.26%
* Approximation only. Some reports may have incomplete information.
Do you take Kadcyla and Ranitidine?
- 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:
- Kadcyla (5,813 reports)
- Ranitidine (234,475 reports)
Browse all drug interactions of Kadcyla and Ranitidine:
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 Kadcyla:
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 Ranitidine:
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 Kadcyla 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 Ranitidine 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 ado-trastuzumab emtansine and ranitidine (the active ingredients of Kadcyla and Ranitidine, respectively), and Kadcyla and Ranitidine (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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