Vyvanse and Fetzima drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Vyvanse (lisdexamfetamine dimesylate) and Fetzima (levomilnacipran hydrochloride). Common drug interactions include abnormal behaviour among females and fatigue among males.
The phase IV clinical study analyzes what interactions people have when they take Vyvanse and Fetzima. It is created by eHealthMe based on reports of 85 people who take the same drugs from the FDA, and is updated regularly.
What is Vyvanse?
Vyvanse has active ingredients of lisdexamfetamine dimesylate. It is often used in attention deficit hyperactivity disorder. eHealthMe is studying from 35,868 Vyvanse users. Check the latest studies of Vyvanse.
What is Fetzima?
Fetzima has active ingredients of levomilnacipran hydrochloride. It is often used in depression. eHealthMe is studying from 2,077 Fetzima users. Check the latest studies of Fetzima.
85 people who take Vyvanse and Fetzima together, and have interactions are studied.

What are the common drug interactions of Vyvanse and Fetzima, by gender? *:
female:
- Abnormal behaviour
- Anger
- Blindness
- Blood potassium decreased
- Blood pressure increased
- Central pain syndrome (neurological condition caused by damage or malfunction in the central nervous system)
- Coeliac disease (simple food intolerance)
- Decreased appetite
- Hospitalisation
- Insomnia (sleeplessness)
male:
- Fatigue (feeling of tiredness)
- Pain
- Psychomotor hyperactivity (feelings of extreme restlessness)
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Therapeutic response unexpected
- Weight decreased
- Malaise (a feeling of general discomfort or uneasiness)
- Cognitive disorder (mental health disorders affects learning, memory, perception, and problem solving)
- Hypnopompic hallucination
- Abdominal discomfort
What are the common drug interactions of Vyvanse and Fetzima, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Panic disorder
- Post concussion syndrome
- Seizure (abnormal excessive or synchronous neuronal activity in the brain)
- Sleep inertia (feeling of grogginess and disorientation that can come with awakening from a deep sleep)
- Sleep paralysis (waking up and unable to move or speak)
- Thirst
- Weight decreased
- Bedridden
- Fibromuscular dysplasia (abnormal cellular growth in the walls of medium and large arteries)
- Headache (pain in head)
30-39:
- Suicidal ideation
- Anxiety
- Blood triglycerides increased
- Disability
- Intertrigo (inflammation (rash) of the body folds (adjacent areas of skin))
- Long qt syndrome (disorder of the heart's electrical system)
- Lumbar radiculopathy (radicular pain in the low back and legs)
- Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
- Obesity (having too much body fat)
- Pain in extremity
40-49:
- Dizziness
- Blindness
- Joint swelling
- Dry mouth
- Dyspnoea (difficult or laboured respiration)
- Glossodynia (a burning or painful sensation in the tongue)
- Palpitations (feelings or sensations that your heart is pounding or racing)
- Pruritus (severe itching of the skin)
- Tongue discolouration (colour change of tongue)
- Weight increased
50-59:
- Inflammation
- Intervertebral disc protrusion (spinal disc protrusion)
- Sleep apnoea syndrome (a sleep-related disorder in which the effort to breathe is diminished or absent)
- Vertigo
- Back pain
- Generalised anxiety disorder (excessive, uncontrollable, unexplained and often irrational worry)
- Headache (pain in head)
- Hypersensitivity
- Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)
- Pain
60+:
- Hallucination, visual (seeing things that aren't there)
- Hyperglycaemia (high blood sugar)
- Hyperlipidaemia (presence of excess lipids in the blood)
- Periodic limb movement disorder
- Pneumonia
- Urinary tract infection
- Weight increased
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 61 people, 71.76%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 37 people, 43.53%
- Drowsiness: 14 people, 16.47%
- Stress And Anxiety: 5 people, 5.88%
- Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 5 people, 5.88%
* Approximation only. Some reports may have incomplete information.
Do you take Vyvanse and Fetzima?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Vyvanse and Fetzima:
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 Vyvanse:
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 Fetzima:
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 Vyvanse 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 Fetzima 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
- Najib J, Wimer D, Zeng J, Lam KW, Romanyak N, Paige Morgan E, Thadavila A, "Review of Lisdexamfetamine Dimesylate in Adults With Attention-Deficit/Hyperactivity Disorder", Journal of central nervous system disease, 2017 Aug .
- Maneeton N, Maneeton B, Suttajit S, Reungyos J, Srisurapanont M, Martin SD, "Exploratory meta-analysis on lisdexamfetamine versus placebo in adult ADHD", Drug design, development and therapy, 2017 Jan .
- Maneeton B, Maneeton N, Likhitsathian S, Suttajit S, Narkpongphun A, Srisurapanont M, Woottiluk P, "Comparative efficacy, acceptability, and tolerability of lisdexamfetamine in child and adolescent ADHD: a meta-analysis of randomized, controlled trials", Drug design, development and therapy, 2013 Jan .
- Najib J, Wimer D, Zeng J, Lam KW, Romanyak N, Paige Morgan E, Thadavila A, "Review of Lisdexamfetamine Dimesylate in Adults With Attention-Deficit/Hyperactivity Disorder", Journal of central nervous system disease, 2017 Aug .
- Maneeton N, Maneeton B, Suttajit S, Reungyos J, Srisurapanont M, Martin SD, "Exploratory meta-analysis on lisdexamfetamine versus placebo in adult ADHD", Drug design, development and therapy, 2017 Jan .
- Maneeton B, Maneeton N, Likhitsathian S, Suttajit S, Narkpongphun A, Srisurapanont M, Woottiluk P, "Comparative efficacy, acceptability, and tolerability of lisdexamfetamine in child and adolescent ADHD: a meta-analysis of randomized, controlled trials", Drug design, development and therapy, 2013 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on lisdexamfetamine dimesylate and levomilnacipran hydrochloride (the active ingredients of Vyvanse and Fetzima, respectively), and Vyvanse and Fetzima (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.
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