Fluoxetine and Norepinephrine bitartrate drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Fluoxetine (fluoxetine hydrochloride) and Norepinephrine bitartrate (norepinephrine bitartrate). Common drug interactions include atrioventricular block first degree among females and renal failure among males.
The phase IV clinical study analyzes what interactions people have when they take Fluoxetine and Norepinephrine bitartrate. It is created by eHealthMe based on reports of 12 people who take the same drugs from the FDA, and is updated regularly.
What is Fluoxetine?
Fluoxetine has active ingredients of fluoxetine hydrochloride. It is often used in depression. eHealthMe is studying from 98,826 Fluoxetine users. Check the latest studies of Fluoxetine.
What is Norepinephrine bitartrate?
Norepinephrine bitartrate has active ingredients of norepinephrine bitartrate. eHealthMe is studying from 2,370 Norepinephrine bitartrate users. Check the latest studies of Norepinephrine bitartrate.
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 >>>.
12 people who take Fluoxetine and Norepinephrine bitartrate together, and have interactions are studied.

What are the common drug interactions of Fluoxetine and Norepinephrine Bitartrate, by gender? *:
female:
- Atrioventricular block first degree (heart block first degree)
- Atrioventricular block second degree (heart block second degree)
- Bezoar (mass found trapped in the gastrointestinal system)
- Drug ineffective
- Hypotension (abnormally low blood pressure)
- Pulseless electrical activity
- Renal impairment (severely reduced kidney function)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Vomiting
male:
- Renal failure (kidney dysfunction)
- Anaemia (lack of blood)
- Klebsiella sepsis (klebsiella causes a potentially fatal whole-body inflammation)
- Acute respiratory distress syndrome
- Acute respiratory failure
- Bradycardia (abnormally slow heart action)
- Cardiac arrest
- Chronic kidney disease
- Drug ineffective
- Dyspnoea (difficult or laboured respiration)
What are the common drug interactions of Fluoxetine and Norepinephrine Bitartrate, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Hypotension (abnormally low blood pressure)
- Renal impairment (severely reduced kidney function)
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
n/a
50-59:
- Fear
- Injury
- Pain
- Renal impairment (severely reduced kidney function)
- Renal injury (kidney injury)
- Hypotension (abnormally low blood pressure)
- Acute respiratory distress syndrome
- Acute respiratory failure
- Bradycardia (abnormally slow heart action)
- Cardiac arrest
60+:
- Atrioventricular block first degree (heart block first degree)
- Atrioventricular block second degree (heart block second degree)
- Bezoar (mass found trapped in the gastrointestinal system)
- Drug ineffective
- Pulseless electrical activity
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Vomiting
What are the existing conditions these people have? *
- Retinopathy Proliferative (a condition in which very small blood vessels grow from the surface of the retina and damages retina): 3 people, 25.00%
- Thrombocytopenia (decrease of platelets in blood): 2 people, 16.67%
- High Blood Pressure: 2 people, 16.67%
- Urination - Painful: 1 person, 8.33%
- Hypotension (abnormally low blood pressure): 1 person, 8.33%
- Anaemia (lack of blood): 1 person, 8.33%
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 1 person, 8.33%
- Dyslipidaemia (abnormal amount of lipids): 1 person, 8.33%
- Febrile Neutropenia (fever with reduced white blood cells): 1 person, 8.33%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 8.33%
* Approximation only. Some reports may have incomplete information.
Do you take Fluoxetine and Norepinephrine bitartrate?
- Personalize this study to your gender, age, symptoms and drugs
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Fluoxetine (98,826 reports)
- Norepinephrine bitartrate (2,370 reports)
Browse all drug interactions of Fluoxetine and Norepinephrine bitartrate:
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 Fluoxetine:
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 Norepinephrine bitartrate:
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 Fluoxetine 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 Norepinephrine bitartrate 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 fluoxetine hydrochloride and norepinephrine bitartrate (the active ingredients of Fluoxetine and Norepinephrine bitartrate, respectively), and Fluoxetine and Norepinephrine bitartrate (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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