Abilify and Sandostatin lar drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Abilify (aripiprazole) and Sandostatin lar (octreotide acetate). Common drug interactions include paronychia among females and vomiting among males.
The phase IV clinical study analyzes what interactions people have when they take Abilify and Sandostatin lar. It is created by eHealthMe based on reports of 24 people who take the same drugs from the FDA, and is updated regularly.
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.
What is Sandostatin lar?
Sandostatin lar has active ingredients of octreotide acetate. It is often used in acromegaly. eHealthMe is studying from 38,437 Sandostatin lar users. Check the latest studies of Sandostatin lar.
24 people who take Abilify and Sandostatin lar together, and have interactions are studied.

What are the common drug interactions of Abilify and Sandostatin Lar, by gender? *:
female:
- Paronychia (infection in the tissues adjacent to a nail on a finger or toe)
- Periorbital oedema (swelling around the eyes)
- Peripheral swelling
- Pneumonia
- Proctalgia (pain in the rectum)
- Protein urine
- Pruritus (severe itching of the skin)
- Rectal fissure (painful condition in which a cut or tear occurs in the anus)
- Rosacea (a skin condition that causes facial redness)
- Scab (a hard coating on the skin formed during the wound healing)
male:
- Vomiting
- Blood pressure increased
- Eructation (release of gas from the digestive tract)
- Heart rate decreased
- Heart rate increased
- Hyperhidrosis (abnormally increased sweating)
- Nervousness
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Haematochezia (passage of stools containing blood)
- Haemorrhoids (a swollen vein or group of veins in the region of the anus)
What are the common drug interactions of Abilify and Sandostatin Lar, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Blood pressure increased
- Chills (felling of cold)
- Cold sweat
- Diarrhoea
- Diarrhoea haemorrhagic (bloody diarrhoea)
- Dizziness
- Eructation (release of gas from the digestive tract)
- Fatigue (feeling of tiredness)
- Heart rate decreased
- Heart rate increased
40-49:
n/a
50-59:
- Rosacea (a skin condition that causes facial redness)
- Scab (a hard coating on the skin formed during the wound healing)
- Secretion discharge
- Sensitisation (the state of being sensitive)
- Sinusitis (inflammation of sinus)
- Skin irritation
- Skin sensitisation (sensitive skin)
- Sputum discoloured
- Swelling
- Tendonitis (a condition that causes pain and swelling of tendons)
60+:
- Fall
- Blood pressure increased
- Dizziness
- Gastrointestinal disorder (functional problems of gastrointestinal tract)
- Head injury
- Intestinal obstruction
- Mobility decreased (ability to move is reduced)
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Pneumonia
- Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down)
What are the existing conditions these people have? *
- Neuroendocrine Tumor: 11 people, 45.83%
- Schizophrenia (a mental disorder characterized by a breakdown of thought processes): 4 people, 16.67%
- Psychotic Disorder: 3 people, 12.50%
* Approximation only. Some reports may have incomplete information.
Do you take Abilify and Sandostatin lar?
- 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:
- Abilify (101,455 reports)
- Sandostatin lar (38,437 reports)
Browse all drug interactions of Abilify and Sandostatin lar:
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 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 side effects of Sandostatin lar:
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 zBrowse all interactions between Sandostatin lar 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 .
- Saif MW, "Rheumatoid arthritis associated with the use of Sandostatin? LAR? depot in a patient with pancreatic neuroendocrine tumor", An association or a coincidence? The first case report, 2017 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 .
- Azkur D, Yoldas T, Toyran M, Kocabas CN, "A pediatric case of anaphylaxis due to octreotide", Asian Pacific journal of allergy and immunology, 2011 Dec .
- Cetin, M., Celik, M., Cakici, M., Polat, M., & Suner, A, "Aripiprazole-Induced Hoarseness", Turk Psikiyatri Dergisi, 2018 Jan .
- Saif MW, "Rheumatoid arthritis associated with the use of Sandostatin? LAR? depot in a patient with pancreatic neuroendocrine tumor", An association or a coincidence? The first case report, 2017 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 .
- Azkur D, Yoldas T, Toyran M, Kocabas CN, "A pediatric case of anaphylaxis due to octreotide", Asian Pacific journal of allergy and immunology, 2011 Dec .
How the study uses the data?
The study uses data from the FDA. It is based on aripiprazole and octreotide acetate (the active ingredients of Abilify and Sandostatin lar, respectively), and Abilify and Sandostatin lar (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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