Harvoni and Abilify drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Harvoni (ledipasvir; sofosbuvir) and Abilify (aripiprazole). Common drug interactions include electrolyte imbalance among females and pain among males.
The phase IV clinical study analyzes what interactions people have when they take Harvoni and Abilify. It is created by eHealthMe based on reports of 26 people who take the same drugs from the FDA, and is updated regularly.
What is Harvoni?
Harvoni has active ingredients of ledipasvir; sofosbuvir. eHealthMe is studying from 19,858 Harvoni users. Check the latest studies of Harvoni.
What is Abilify?
Abilify has active ingredients of aripiprazole. It is often used in depression. eHealthMe is studying from 101,455 Abilify users. Check the latest studies of Abilify.
26 people who take Harvoni and Abilify together, and have interactions are studied.

What are the common drug interactions of Harvoni and Abilify, by gender? *:
female:
- Electrolyte imbalance
- Essential hypertension (primary hypertension)
- Hepatic cirrhosis (chronic liver disease characterized by replacement of liver tissue by fibrosis, scar tissue)
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)
- Lymphoedema (localized fluid retention and tissue swelling)
- Magnesium metabolism disorder (disease of magnesium utilization)
- Obesity (having too much body fat)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Septic shock (shock due to blood infection)
male:
- Pain
- Abdominal infection
- Blood cholesterol decreased
- Blood creatinine decreased
- Blood glucose increased
- Blood potassium decreased
- Blood testosterone decreased
- Blood triglycerides increased
- Blood urea increased
- Blood urea nitrogen/creatinine ratio increased
What are the common drug interactions of Harvoni and Abilify, 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:
- Alanine aminotransferase increased
- Arthritis (form of joint disorder that involves inflammation of one or more joints)
- Aspartate aminotransferase increased
- Blood calcium decreased
- Blood cholesterol decreased
- Blood creatinine decreased
- Blood glucose increased
- Blood potassium decreased
- Blood testosterone decreased
- Blood triglycerides increased
50-59:
- Acute respiratory failure
- Adverse drug reaction
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Blood hyposmosis
- Body mass index increased
- Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
- Cardiomyopathy (weakening of the heart muscle)
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
- Electrolyte imbalance
- Essential hypertension (primary hypertension)
60+:
- Arthralgia (joint pain)
- Ascites (accumulation of fluid in the abdominal cavity)
- Atelectasis (partial or complete collapse of the lung)
- Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
- Oedema (fluid collection in tissue)
- Oedema peripheral (superficial swelling)
- Renal failure (kidney dysfunction)
- Transient global amnesia (a temporary short-term memory loss)
What are the existing conditions these people have? *
- Hepatitis C: 11 people, 42.31%
- Hiv Infection: 3 people, 11.54%
- Headache (pain in head): 3 people, 11.54%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 2 people, 7.69%
* Approximation only. Some reports may have incomplete information.
Do you take Harvoni and Abilify?
- 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:
Browse all drug interactions of Harvoni and Abilify:
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 Harvoni:
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 Abilify:
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 Harvoni 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 Abilify 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 zRelated publications that referenced our studies
- Cetin, M., Celik, M., Cakici, M., Polat, M., & Suner, A, "Aripiprazole-Induced Hoarseness", Turk Psikiyatri Dergisi, 2018 Jan .
- Cetin M, Celik M, Cakici M, Polat M, Suner A, "Aripiprazole induced non-cardiogenic pulmonary edema: a case report", Turk Psikiyatri Dergisi, 2014 Dec .
- Cetin, M., Celik, M., Cakici, M., Polat, M., & Suner, A, "Aripiprazole-Induced Hoarseness", Turk Psikiyatri Dergisi, 2018 Jan .
- Cetin M, Celik M, Cakici M, Polat M, Suner A, "Aripiprazole induced non-cardiogenic pulmonary edema: a case report", Turk Psikiyatri Dergisi, 2014 Dec .
How the study uses the data?
The study uses data from the FDA. It is based on ledipasvir; sofosbuvir and aripiprazole (the active ingredients of Harvoni and Abilify, respectively), and Harvoni and Abilify (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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