Nucynta and Fluoxetine drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Nucynta (tapentadol hydrochloride) and Fluoxetine (fluoxetine hydrochloride). Common drug interactions include increased tendency to bruise among females and loss of consciousness among males.
The phase IV clinical study analyzes what interactions people have when they take Nucynta and Fluoxetine. It is created by eHealthMe based on reports of 81 people who take the same drugs from the FDA, and is updated regularly.
What is Nucynta?
Nucynta has active ingredients of tapentadol hydrochloride. It is often used in pain. eHealthMe is studying from 31,818 Nucynta users. Check the latest studies of Nucynta.
What is Fluoxetine?
Fluoxetine has active ingredients of fluoxetine hydrochloride. It is often used in depression. eHealthMe is studying from 98,824 Fluoxetine users. Check the latest studies of Fluoxetine.
81 people who take Nucynta and Fluoxetine together, and have interactions are studied.

What are the common drug interactions of Nucynta and Fluoxetine, by gender? *:
female:
- Increased tendency to bruise (increased tendency to injure the underlying soft tissue or bone)
- Loss of consciousness
- Osteoarthritis (a joint disease caused by cartilage loss in a joint)
- Pregnancy on oral contraceptive
- Sinusitis (inflammation of sinus)
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Tachycardia (a heart rate that exceeds the range of 100 beats/min)
- Therapeutic response unexpected
- Tibia fracture (fracture of lower leg bone)
- Abasia (inability to walk)
male:
- Loss of consciousness
- Serotonin syndrome (occurs when two drugs that affect the body's level of serotonin are taken together at the same time)
- Renal impairment (severely reduced kidney function)
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Sudden onset of sleep
- Weight decreased
- Renal failure (kidney dysfunction)
- Abasia (inability to walk)
- Injury
- Haemoglobin decreased
What are the common drug interactions of Nucynta and Fluoxetine, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Arthropathy
- Bone disorder
- Bone pain
- Cataract (clouding of the lens inside the eye)
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
- Fracture delayed union (delayed cure of broken bone)
- Humerus fracture (injury to the upper arm bone)
- Osteoporosis (bones weak and more likely to break)
- Squamous cell carcinoma (a cancer of a kind of epithelial cell)
- Upper limb fracture
20-29:
- Agitation (state of anxiety or nervous excitement)
- Coma (state of unconsciousness lasting more than six hours)
- Drug withdrawal syndrome (interfere with normal social, occupational, or other functioning. are not due to another medical condition, drug use, or discontinuation)
- Hyporeflexia (a condition of below normal or absent reflexes)
- Loss of consciousness
- Pyrexia (fever)
- Rash
- Respiratory rate decreased (less breathing rate/min)
- Restlessness (not able to rest)
- Somnolence (a state of near-sleep, a strong desire for sleep)
30-39:
- Abnormal behaviour
- Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
- Deafness bilateral
- Hallucinations, mixed (sensations that appear real but are created by your mind -mixed)
- Abdominal pain upper
- Drug ineffective
- Chronic kidney disease
- Nephrogenic anaemia (anaemia due to kidney disease)
- Renal failure (kidney dysfunction)
- Endometriosis (appearance of endometrial tissue outside the uterus and causing pelvic pain)
40-49:
- Dermatitis allergic (inflammation of the skin due allergic reaction)
- Dizziness
- Drug ineffective
- Ear infection
- Fall
- Fungal infection
- Gastroenteritis viral (inflammation of stomach and intestine caused by virus infection)
- Hepatic enzyme increased
- Immune system disorder
- Infusion site pain
50-59:
- Haemochromatosis (body to absorb more iron than usual from food)
- Hypersensitivity
- Sleep apnoea syndrome (a sleep-related disorder in which the effort to breathe is diminished or absent)
- Adrenal adenoma (benign tumour of the glandular type (adenoma) in the adrenal gland)
- Alopecia (absence of hair from areas of the body)
- Anaemia (lack of blood)
- Angiopathy (generic term for a disease of the blood vessels)
- Ankylosing spondylitis (type of arthritis affecting the spine)
- Aortic disorder
- Arthralgia (joint pain)
60+:
- Loss of consciousness
- Serotonin syndrome (occurs when two drugs that affect the body's level of serotonin are taken together at the same time)
- Pollakiuria (abnormally frequent passage of relatively small quantities or urine)
- Renal impairment (severely reduced kidney function)
- Sudden onset of sleep
- Weight decreased
- Abasia (inability to walk)
- Renal failure (kidney dysfunction)
- Haemoglobin decreased
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 19 people, 23.46%
- Back Pain: 16 people, 19.75%
- High Blood Pressure: 14 people, 17.28%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 11 people, 13.58%
- High Blood Cholesterol: 11 people, 13.58%
- Indigestion: 10 people, 12.35%
- Migraine (headache): 8 people, 9.88%
- Joint Pain: 8 people, 9.88%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 7 people, 8.64%
- Neuropathy Peripheral (surface nerve damage): 7 people, 8.64%
* Approximation only. Some reports may have incomplete information.
Do you take Nucynta and Fluoxetine?
- 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:
- Nucynta (31,818 reports)
- Fluoxetine (98,824 reports)
Browse all drug interactions of Nucynta and 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 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 Nucynta:
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 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 interactions between Nucynta 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 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 zHow the study uses the data?
The study uses data from the FDA. It is based on tapentadol hydrochloride and fluoxetine hydrochloride (the active ingredients of Nucynta and Fluoxetine, respectively), and Nucynta and Fluoxetine (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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