Scopolamine and Divalproex sodium drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Scopolamine (scopolamine) and Divalproex sodium (divalproex sodium). Common drug interactions include death among females and weight increased among males.
The phase IV clinical study analyzes what interactions people have when they take Scopolamine and Divalproex sodium. It is created by eHealthMe based on reports of 15 people who take the same drugs from the FDA, and is updated regularly.
What is Scopolamine?
Scopolamine has active ingredients of scopolamine. eHealthMe is studying from 4,945 Scopolamine users. Check the latest studies of Scopolamine.
What is Divalproex sodium?
Divalproex sodium has active ingredients of divalproex sodium. It is often used in epilepsy. eHealthMe is studying from 9,483 Divalproex sodium users. Check the latest studies of Divalproex sodium.
15 people who take Scopolamine and Divalproex sodium together, and have interactions are studied.

What are the common drug interactions of Scopolamine and Divalproex Sodium, by gender? *:
female:
- Death
male:
- Weight increased
- Blood triglycerides increased
- Disease progression
- Extrapyramidal disorder (involuntary muscle spasms in the face and neck)
- Neutropenia (an abnormally low number of neutrophils)
- Pancreatic enzymes increased
- Parkinson's disease
- Pneumonia
- Seizure (abnormal excessive or synchronous neuronal activity in the brain)
- Weight decreased
What are the common drug interactions of Scopolamine and Divalproex Sodium, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Disease progression
- Blood triglycerides increased
- High density lipoprotein decreased
- Weight increased
40-49:
n/a
50-59:
- Death
- Neutropenia (an abnormally low number of neutrophils)
60+:
- Confusional state
- Death
- Fall
- Hallucination (an experience involving the perception of something not present)
- Hospitalisation
What are the existing conditions these people have? *
- Schizophrenia (a mental disorder characterized by a breakdown of thought processes): 8 people, 53.33%
- High Blood Pressure: 4 people, 26.67%
- Wheezing (a high-pitched whistling sound made while you breath): 1 person, 6.67%
- Stress And Anxiety: 1 person, 6.67%
- Secretion Discharge: 1 person, 6.67%
- Parkinson's Disease: 1 person, 6.67%
- Motion Sickness (travel sickness): 1 person, 6.67%
- Lung Neoplasm Malignant (cancer tumour of lung): 1 person, 6.67%
- Lennox-Gastaut Syndrome (epilepsy characterized by frequent seizures and different seizure types): 1 person, 6.67%
- Increased Upper Airway Secretion: 1 person, 6.67%
* Approximation only. Some reports may have incomplete information.
Do you take Scopolamine and Divalproex sodium?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Scopolamine (4,945 reports)
- Divalproex sodium (9,483 reports)
Browse all drug interactions of Scopolamine and Divalproex sodium:
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 Scopolamine:
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 Divalproex sodium:
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 Scopolamine 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 Divalproex sodium 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 scopolamine and divalproex sodium (the active ingredients of Scopolamine and Divalproex sodium, respectively), and Scopolamine and Divalproex sodium (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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