Strattera and Diclofenac sodium drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Strattera (atomoxetine hydrochloride) and Diclofenac sodium (diclofenac sodium). Common drug interactions include sleep talking among females and anxiety among males.
The phase IV clinical study analyzes what interactions people have when they take Strattera and Diclofenac sodium. It is created by eHealthMe based on reports of 56 people who take the same drugs from the FDA, and is updated regularly.
What is Strattera?
Strattera has active ingredients of atomoxetine hydrochloride. It is often used in attention deficit hyperactivity disorder. eHealthMe is studying from 29,323 Strattera users. Check the latest studies of Strattera.
What is Diclofenac sodium?
Diclofenac sodium has active ingredients of diclofenac sodium. It is often used in arthritis. eHealthMe is studying from 43,018 Diclofenac sodium users. Check the latest studies of Diclofenac sodium.
56 people who take Strattera and Diclofenac sodium together, and have interactions are studied.

What are the common drug interactions of Strattera and Diclofenac Sodium, by gender? *:
female:
- Sleep talking (talking during sleeping)
- Tachycardia (a heart rate that exceeds the range of 100 beats/min)
- Thyroid cyst
- Tonsillar hypertrophy (enlargement of the tonsils)
- Toothache (tooth pain)
- Chronic kidney disease
- Hypertension (high blood pressure)
- Nausea (feeling of having an urge to vomit)
- Weight decreased
- Anxiety
male:
- Anxiety
- Emotional distress
- Asthenia (weakness)
- Coronary artery disease (plaque building up along the inner walls of the arteries of the heart, which narrows the arteries and restricts blood flow to the heart)
- Dehydration (dryness resulting from the removal of water)
- Hyperhidrosis (abnormally increased sweating)
- Hyperphosphaturia (excess of phosphates in the urine)
- Influenza
- Mobility decreased (ability to move is reduced)
- Multiple fractures
What are the common drug interactions of Strattera and Diclofenac Sodium, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Anxiety
- Cardiomyopathy (weakening of the heart muscle)
- Confusional state
- Constipation
- Delirium (wild excitement)
- Disturbance in attention
- Drug withdrawal syndrome (interfere with normal social, occupational, or other functioning. are not due to another medical condition, drug use, or discontinuation)
- Fall
- Hallucination (an experience involving the perception of something not present)
- Hallucinations, mixed (sensations that appear real but are created by your mind -mixed)
30-39:
- Renal failure (kidney dysfunction)
- Chronic kidney disease
- Back pain
- Cholecystitis chronic (long lasting infection of gallbladder)
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Dyspepsia (indigestion)
- Nausea (feeling of having an urge to vomit)
- Scleroderma renal crisis (malignant hypertension develops and causes acute renal failure was once a common cause of death)
- Suicidal ideation
40-49:
- Blood cholesterol increased
- Blood triglycerides increased
- Chronic kidney disease
- Obesity (having too much body fat)
- Type 2 diabetes mellitus
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Bone atrophy (decrease in bone mass)
- Bone density decreased
- Bone pain
50-59:
- Muscle mass
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Drug ineffective
- Headache (pain in head)
- Hearing impaired
- Hypersomnia (excessive daytime sleepiness (eds))
- Hypoacusis (loss of hearing)
- Nausea (feeling of having an urge to vomit)
- Sleep talking (talking during sleeping)
60+:
- Gastric ulcer (stomach ulcer)
- Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
- Nausea (feeling of having an urge to vomit)
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 35 people, 62.50%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 21 people, 37.50%
- Stress And Anxiety: 9 people, 16.07%
- Pain: 8 people, 14.29%
- Depression: 6 people, 10.71%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 5 people, 8.93%
- Drowsiness: 4 people, 7.14%
- Insomnia (sleeplessness): 4 people, 7.14%
- Infection: 4 people, 7.14%
- Panic Disorder: 4 people, 7.14%
* Approximation only. Some reports may have incomplete information.
Do you take Strattera and Diclofenac sodium?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Strattera (29,323 reports)
- Diclofenac sodium (43,018 reports)
Browse all drug interactions of Strattera and Diclofenac 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 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 Strattera:
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 Diclofenac 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 interactions between Strattera 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 Diclofenac 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 zHow the study uses the data?
The study uses data from the FDA. It is based on atomoxetine hydrochloride and diclofenac sodium (the active ingredients of Strattera and Diclofenac sodium, respectively), and Strattera and Diclofenac sodium (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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