Trikafta and Kalydeco drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Trikafta (elexacaftor, ivacaftor, tezacaftor; ivacaftor) and Kalydeco (ivacaftor). Common drug interactions include alanine aminotransferase increased among females and acute respiratory failure among males.
The phase IV clinical study analyzes what interactions people have when they take Trikafta and Kalydeco. It is created by eHealthMe based on reports of 23 people who take the same drugs from the FDA, and is updated regularly.
What is Trikafta?
Trikafta has active ingredients of elexacaftor, ivacaftor, tezacaftor; ivacaftor. eHealthMe is studying from 11,852 Trikafta users. Check the latest studies of Trikafta.
What is Kalydeco?
Kalydeco has active ingredients of ivacaftor. eHealthMe is studying from 6,652 Kalydeco users. Check the latest studies of Kalydeco.
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 >>>.
23 people who take Trikafta and Kalydeco together, and have interactions are studied.

What are the common drug interactions of Trikafta and Kalydeco, by gender? *:
female:
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Blood alkaline phosphatase increased
- Blood lactate dehydrogenase increased
- Drug-induced liver injury (diseases of the liver that are caused by physician-prescribed medications)
- Gamma-glutamyltransferase increased
- Maternal exposure during pregnancy (use of substance during pregnancy)
- Premature delivery
- Foetal exposure during pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect)
- Pulmonary haemorrhage (acute bleeding from the lung)
male:
- Acute respiratory failure
- Blood bilirubin increased
- Toxic epidermal necrolysis (a rare, life-threatening skin condition that is usually caused by a reaction to drugs causes wide spread skin destruction)
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Dry eye (lack of adequate tears)
- Gamma-glutamyltransferase increased
- Abdominal discomfort
- Exercise tolerance decreased
- Forced expiratory volume decreased (decreased lung expired air volume)
What are the common drug interactions of Trikafta and Kalydeco, by age (0-1 to 60+)? *:
0-1:
- Foetal exposure during pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect)
- Neonatal respiratory distress syndrome (a serious medical condition where a newborn baby's lungs cannot provide their body with enough oxygen)
- Pulmonary haemorrhage (acute bleeding from the lung)
- Premature baby
2-9:
n/a
10-19:
n/a
20-29:
- Maternal exposure during pregnancy (use of substance during pregnancy)
- Premature delivery
30-39:
- Acute respiratory failure
- Blood bilirubin increased
- Generalised oedema (swelling all over the body)
- Hyperbilirubinaemia (excess of bilirubin in the blood)
- Hypotension (abnormally low blood pressure)
- Lymphopenia (an abnormally low level of lymphocytes in the blood)
- Neutropenia (an abnormally low number of neutrophils)
- Pneumonia
- Rash erythematous (redness of the skin)
- Thrombocytopenia (decrease of platelets in blood)
40-49:
- Abdominal discomfort
- Exercise tolerance decreased
- Forced expiratory volume decreased (decreased lung expired air volume)
- Hepatic necrosis (large portions of liver die off due to severe liver disease)
- Respiratory disorder (respiratory disease)
- Weight decreased
- Hepatitis (inflammation of the liver)
- Death
- Haemoglobin decreased
- Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
50-59:
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Blood alkaline phosphatase increased
- Blood lactate dehydrogenase increased
- Drug-induced liver injury (diseases of the liver that are caused by physician-prescribed medications)
- Gamma-glutamyltransferase increased
60+:
n/a
What are the existing conditions these people have? *
- Cystic Fibrosis (disease of the secretary glands): 20 people, 86.96%
- Infection: 7 people, 30.43%
- Cystic Fibrosis Lung (fibrosis with cyst in the lung): 7 people, 30.43%
- Reflux Gastritis (a condition in which the lining of a person's stomach becomes inflamed as a result of exposure to bile): 6 people, 26.09%
- Cystic Fibrosis Related Diabetes: 6 people, 26.09%
- Bronchial Hyperreactivity: 6 people, 26.09%
- Hepatic Necrosis (large portions of liver die off due to severe liver disease): 4 people, 17.39%
- Respiratory Tract Infection: 3 people, 13.04%
- Gastrointestinal Disorder (functional problems of gastrointestinal tract): 3 people, 13.04%
- Fever: 3 people, 13.04%
* Approximation only. Some reports may have incomplete information.
Do you take Trikafta and Kalydeco?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Trikafta and Kalydeco:
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 Trikafta:
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 Kalydeco:
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 Trikafta 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 Kalydeco 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 elexacaftor, ivacaftor, tezacaftor; ivacaftor and ivacaftor (the active ingredients of Trikafta and Kalydeco, respectively), and Trikafta and Kalydeco (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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