Divalproex sodium and Vitamin e drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Divalproex sodium (divalproex sodium) and Vitamin e (tocopherols and tocotrienols). Common drug interactions include drug level increased among females and insomnia among males.
The phase IV clinical study analyzes what interactions people have when they take Divalproex sodium and Vitamin e. It is created by eHealthMe based on reports of 67 people who take the same drugs from the FDA, and is updated regularly.
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.
What is Vitamin e?
Vitamin e has active ingredients of tocopherols and tocotrienols. It is often used in vitamin supplementation. eHealthMe is studying from 42,279 Vitamin e users. Check the latest studies of Vitamin e.
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 >>>.
67 people who take Divalproex sodium and Vitamin e together, and have interactions are studied.

What are the common drug interactions of Divalproex Sodium and Vitamin E, by gender? *:
female:
- Drug level increased
- Dysstasia (difficulty in standing)
- Electrocardiogram qt prolonged
- Limb injury
- Macular degeneration (painless eye condition that leads to the gradual loss of central vision)
- Oxygen saturation decreased
- Pelvic fracture
- Pharyngitis streptococcal (inflammation of the pharynx caused by infection from. streptococcus)
- Streptococcal infection
- Tooth abscess (pus formation in tooth)
male:
- Insomnia (sleeplessness)
- Drug ineffective
- Blood triglycerides increased
- Blood urea increased
- Circadian rhythm sleep disorder (family of sleep disorders affecting, among other things, the timing of sleep)
- Dyskinesia (abnormality or impairment of voluntary movement)
- Gamma-glutamyltransferase increased
- Glomerular filtration rate decreased
- Haematocrit decreased
- Haemoglobin decreased
What are the common drug interactions of Divalproex Sodium and Vitamin E, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Chest pain
- Hallucination, auditory (perceiving sounds without auditory stimulus)
- Suicidal ideation
- Suicide attempt
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Trichomoniasis (a sexually transmitted disease caused by a parasite)
- Angina pectoris (chest pain due to ischemia of the heart muscle)
- Depression
- Family stress
- Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
30-39:
- Cataract (clouding of the lens inside the eye)
40-49:
- Hallucination (an experience involving the perception of something not present)
- Insomnia (sleeplessness)
50-59:
- Weight decreased
- Mental status changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)
- Activated partial thromboplastin time prolonged
- Decreased appetite
- Drug ineffective
- Femur fracture
- Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
- Haematemesis (vomiting of blood)
- Haematochezia (passage of stools containing blood)
- Head injury
60+:
- Urinary tract infection
- Fall
- Asthenia (weakness)
- Cataract (clouding of the lens inside the eye)
- Chronic kidney disease
- Diarrhoea
- Pain in extremity
- Arthralgia (joint pain)
- Blood pressure decreased
- Chronic obstructive pulmonary disease (a progressive disease that makes it hard to breathe)
What are the existing conditions these people have? *
- Immunodeficiency Common Variable: 20 people, 29.85%
- Hypergammaglobulinaemia (elevated levels of gamma globulin): 9 people, 13.43%
- Pain: 8 people, 11.94%
- Neuropathy Peripheral (surface nerve damage): 6 people, 8.96%
- Insomnia (sleeplessness): 6 people, 8.96%
- Rashes (redness): 5 people, 7.46%
- Fever: 5 people, 7.46%
- Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 5 people, 7.46%
- Allergies: 5 people, 7.46%
- Abdominal Discomfort: 5 people, 7.46%
* Approximation only. Some reports may have incomplete information.
Do you take Divalproex sodium and Vitamin e?
- 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:
- Divalproex sodium (9,483 reports)
- Vitamin e (42,279 reports)
Browse all drug interactions of Divalproex sodium and Vitamin e:
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 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 side effects of Vitamin e:
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 zBrowse all interactions between Vitamin e 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 divalproex sodium and tocopherols and tocotrienols (the active ingredients of Divalproex sodium and Vitamin e, respectively), and Divalproex sodium and Vitamin e (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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