Adderall and Sandostatin drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Adderall (amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate) and Sandostatin (octreotide acetate). Common drug interactions include blood pressure increased among females and blood calcium decreased among males.
The phase IV clinical study analyzes what interactions people have when they take Adderall and Sandostatin. It is created by eHealthMe based on reports of 17 people who take the same drugs from the FDA, and is updated regularly.
What is Adderall?
Adderall has active ingredients of amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate. It is often used in attention deficit hyperactivity disorder. eHealthMe is studying from 64,224 Adderall users. Check the latest studies of Adderall.
What is Sandostatin?
Sandostatin has active ingredients of octreotide acetate. It is often used in acromegaly. eHealthMe is studying from 46,793 Sandostatin users. Check the latest studies of Sandostatin.
17 people who take Adderall and Sandostatin together, and have interactions are studied.

What are the common drug interactions of Adderall and Sandostatin, by gender? *:
female:
- Blood pressure increased
- Food allergy
- Nephrolithiasis (calculi in the kidneys)
- Fatigue (feeling of tiredness)
- Abdominal pain
- Abdominal pain upper
- Asthenia (weakness)
- Blood pressure decreased
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
- Decreased appetite
male:
- Blood calcium decreased
- Blood chloride increased
- Protein total decreased
- Pruritus (severe itching of the skin)
- Rash
- Red blood cell count decreased
- Red blood cell count increased
- Drug ineffective
- Neuroendocrine carcinoma (cancer tumour that arise from cells of the endocrine (hormonal) and nervous systems)
- Fatigue (feeling of tiredness)
What are the common drug interactions of Adderall and Sandostatin, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Fatigue (feeling of tiredness)
- Abdominal pain
- Abdominal pain upper
- Asthenia (weakness)
- Blood pressure decreased
- Blood pressure increased
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
- Decreased appetite
- Eye haemorrhage (bleeding in the eye)
- General physical health deterioration (weak health status)
40-49:
n/a
50-59:
- Blood pressure increased
- Food allergy
- Nephrolithiasis (calculi in the kidneys)
- Blood calcium decreased
- Blood chloride increased
- Blood glucose increased
- Blood potassium decreased
- Carbon dioxide increased
- Haematocrit decreased
- Haemoglobin decreased
60+:
- Drug hypersensitivity
- Laryngitis (inflammation of the larynx)
- Intestinal obstruction
- Light chain analysis increased
- Nasopharyngitis (inflammation of the nasopharynx)
- Plasma cell myeloma (cancer that begins in plasma cells)
- Rash pruritic (redness with itching)
- Rash generalised (rash on most of body parts)
- Sinusitis (inflammation of sinus)
- Urinary tract infection
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 4 people, 23.53%
- Multiple Myeloma (cancer of the plasma cells): 3 people, 17.65%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 3 people, 17.65%
- Pituitary-Dependent Cushing's Syndrome (pituitary dependent hypercortisolism): 2 people, 11.76%
- Sleep Disorder: 1 person, 5.88%
- Sleep Apnea Syndrome: 1 person, 5.88%
- Neuroendocrine Tumor: 1 person, 5.88%
- Metastatic Carcinoid Tumor: 1 person, 5.88%
- Gigantism (excessive growth and height): 1 person, 5.88%
- Endocrine Neoplasm Malignant (cancerous tumour of endoglands): 1 person, 5.88%
* Approximation only. Some reports may have incomplete information.
Do you take Adderall and Sandostatin?
- 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:
- Adderall (64,224 reports)
- Sandostatin (46,793 reports)
Browse all drug interactions of Adderall and Sandostatin:
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 Adderall:
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:
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 Adderall 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 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
- 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 .
- 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 .
- 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 .
- 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 amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate and octreotide acetate (the active ingredients of Adderall and Sandostatin, respectively), and Adderall and Sandostatin (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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