Mirtazapine and Cabergoline drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Mirtazapine (mirtazapine) and Cabergoline (cabergoline). Common drug interactions include neutropenia among females and death among males.
The phase IV clinical study analyzes what interactions people have when they take Mirtazapine and Cabergoline. It is created by eHealthMe based on reports of 39 people who take the same drugs from the FDA, and is updated regularly.
What is Mirtazapine?
Mirtazapine has active ingredients of mirtazapine. It is often used in depression. eHealthMe is studying from 82,120 Mirtazapine users. Check the latest studies of Mirtazapine.
What is Cabergoline?
Cabergoline has active ingredients of cabergoline. It is often used in prolactinoma. eHealthMe is studying from 6,257 Cabergoline users. Check the latest studies of Cabergoline.
39 people who take Mirtazapine and Cabergoline together, and have interactions are studied.

What are the common drug interactions of Mirtazapine and Cabergoline, by gender? *:
female:
- Neutropenia (an abnormally low number of neutrophils)
- Back pain
- Diarrhoea
- Dyslipidaemia (abnormal amount of lipids)
- Leukopenia (less number of white blood cells in blood)
- Type 2 diabetes mellitus
- Urinary tract infection
- Vulvovaginal candidiasis (vulvovaginal infection by fungi)
- Abdominal pain
- Chronic kidney disease
male:
- Death
- Drug ineffective
- Emotional distress
- Multiple fractures
- Osteoporosis (bones weak and more likely to break)
- Pain
- Renal failure (kidney dysfunction)
- Spinal fracture (fracture in one of vertebrae)
- Tooth loss
- Abnormal behaviour
What are the common drug interactions of Mirtazapine and Cabergoline, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Breast cancer female
- Chronic kidney disease
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Renal failure (kidney dysfunction)
- Renal tubular necrosis (death of kidney tubules)
- Breast cancer
- Heart valve incompetence (heart's valves do not work correctly)
40-49:
- Basophil count increased
- Blood prolactin decreased
- Blood thyroid stimulating hormone increased
- Conjunctival haemorrhage (bleeding underneath the conjunctiva)
- Corneal bleeding
- Eosinophil count increased
- Headache (pain in head)
- Petechiae (a small red or purple spot caused by bleeding into the skin)
- Pitting oedema (skin discoloration)
- Thrombocytopenia (decrease of platelets in blood)
50-59:
- Back pain
- Diarrhoea
- Dyslipidaemia (abnormal amount of lipids)
- Leukopenia (less number of white blood cells in blood)
- Neutropenia (an abnormally low number of neutrophils)
- Type 2 diabetes mellitus
- Urinary tract infection
- Vulvovaginal candidiasis (vulvovaginal infection by fungi)
- Abdominal pain
- Chronic kidney disease
60+:
- Death
- Blood prolactin increased
- Renal failure (kidney dysfunction)
- Spinal fracture (fracture in one of vertebrae)
- Tooth loss
- Agitation (state of anxiety or nervous excitement)
- Arthralgia (joint pain)
- Blood creatinine increased
- Chest discomfort
- Chest pain
What are the existing conditions these people have? *
- High Blood Pressure: 12 people, 30.77%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 8 people, 20.51%
- Hyperprolactinaemia (abnormally high levels of prolactin in the blood): 7 people, 17.95%
- Type 2 Diabetes: 5 people, 12.82%
- Prolactin-Producing Pituitary Tumor: 4 people, 10.26%
- Parkinson's Disease: 4 people, 10.26%
- Acromegaly (body produces too much growth hormone, leading to excess growth of body tissues): 4 people, 10.26%
- Psychotic Disorder: 4 people, 10.26%
- Secondary Hypothyroidism (pituitary gland and its failure to secrete tsh): 4 people, 10.26%
- Pituitary Tumor Benign: 3 people, 7.69%
* Approximation only. Some reports may have incomplete information.
Do you take Mirtazapine and Cabergoline?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Mirtazapine (82,120 reports)
- Cabergoline (6,257 reports)
Browse all drug interactions of Mirtazapine and Cabergoline:
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 Mirtazapine:
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 Cabergoline:
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 Mirtazapine 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 Cabergoline 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
- Gürbüz F, Ya?c?-Küpeli B, K?r Y, Yüksel B, Zorludemir S, Gürbüz BB, Küpeli S, "The first report of cabergoline-induced immune hemolytic anemia in an adolescent with prolactinoma", Journal of Pediatric Endocrinology and Metabolism, 2014 Jan .
- Harris YT, Harris AZ, "Cabergoline associated with first episode mania", Psychosomatics, 2012 Jan .
- Gürbüz F, Ya?c?-Küpeli B, K?r Y, Yüksel B, Zorludemir S, Gürbüz BB, Küpeli S, "The first report of cabergoline-induced immune hemolytic anemia in an adolescent with prolactinoma", Journal of Pediatric Endocrinology and Metabolism, 2014 Jan .
- Harris YT, Harris AZ, "Cabergoline associated with first episode mania", Psychosomatics, 2012 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on mirtazapine and cabergoline (the active ingredients of Mirtazapine and Cabergoline, respectively), and Mirtazapine and Cabergoline (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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