Micardis and Diclofenac sodium drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Micardis (telmisartan) and Diclofenac sodium (diclofenac sodium). Common drug interactions include malaise among females and pneumonia among males.
The phase IV clinical study analyzes what interactions people have when they take Micardis and Diclofenac sodium. It is created by eHealthMe based on reports of 44 people who take the same drugs from the FDA, and is updated regularly.
What is Micardis?
Micardis has active ingredients of telmisartan. It is often used in high blood pressure. eHealthMe is studying from 27,605 Micardis users. Check the latest studies of Micardis.
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.
44 people who take Micardis and Diclofenac sodium together, and have interactions are studied.

What are the common drug interactions of Micardis and Diclofenac Sodium, by gender? *:
female:
- Malaise (a feeling of general discomfort or uneasiness)
- Nausea (feeling of having an urge to vomit)
- Dry mouth
- Hypoxia (low oxygen in tissues)
- Interstitial lung disease
- Cardiac disorder
- Chest pain
- Drug ineffective
- Heart rate increased
- Oedema peripheral (superficial swelling)
male:
- Pneumonia
- Anaphylactic reaction (serious allergic reaction)
- Local swelling (swelling at the site of some application of substance or injury)
- Localised oedema (fluid retention in a particular part of the body)
- Pyrexia (fever)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Swelling face
- Vomiting
- Wheezing (a high-pitched whistling sound made while you breath)
- Colon cancer
What are the common drug interactions of Micardis and Diclofenac Sodium, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Cardiac disorder
- Chest pain
- Drug ineffective
- Heart rate increased
- Oedema peripheral (superficial swelling)
- Suicide attempt
- Supraventricular tachycardia (rapid heart rhythm originating at or above the atrioventricular node)
- Eating disorder
- Malaise (a feeling of general discomfort or uneasiness)
- Nausea (feeling of having an urge to vomit)
50-59:
- Tinnitus (a ringing in the ears)
- Depression
- General physical health deterioration (weak health status)
- Haemoglobin decreased
- Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)
- Surgery
60+:
- Dyspnoea (difficult or laboured respiration)
- Hypersensitivity
- Face oedema (swelling of face)
- Hypoxia (low oxygen in tissues)
- Interstitial lung disease
- Laryngospasm (an uncontrolled/involuntary muscular contraction of larynx)
- Local swelling (swelling at the site of some application of substance or injury)
- Localised oedema (fluid retention in a particular part of the body)
- Pneumonia
- Respiratory failure (inadequate gas exchange by the respiratory system)
What are the existing conditions these people have? *
- Pain: 5 people, 11.36%
- Diabetes: 4 people, 9.09%
- Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 3 people, 6.82%
- Enlarged Prostate: 3 people, 6.82%
- Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 3 people, 6.82%
- Bladder Cancer: 3 people, 6.82%
* Approximation only. Some reports may have incomplete information.
Do you take Micardis and Diclofenac sodium?
- 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:
- Micardis (27,605 reports)
- Diclofenac sodium (43,018 reports)
Browse all drug interactions of Micardis 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 Micardis:
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 Micardis 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 zRelated publications that referenced our studies
- Kato Y, Mukai Y, Rane A, Inotsume N, Toda T, "The inhibitory effect of telmisartan on the metabolism of arachidonic acid by CYP2C9 and CYP2C8: an in vitro study", Biological and Pharmaceutical Bulletin, 2017 Sep .
- Kim HK, Youm JB, Lee SR, Lim SE, Lee SY, Ko TH, Nilius B, Noh JH, Ko KS, Rhee BD, Kim N, "The angiotensin receptor blocker and PPAR-γ agonist, telmisartan, delays inactivation of voltage-gated sodium channel in rat heart: novel mechanism of drug action", Pflügers Archiv-European Journal of Physiology, 2012 Dec .
- Kato Y, Mukai Y, Rane A, Inotsume N, Toda T, "The inhibitory effect of telmisartan on the metabolism of arachidonic acid by CYP2C9 and CYP2C8: an in vitro study", Biological and Pharmaceutical Bulletin, 2017 Sep .
- Kim HK, Youm JB, Lee SR, Lim SE, Lee SY, Ko TH, Nilius B, Noh JH, Ko KS, Rhee BD, Kim N, "The angiotensin receptor blocker and PPAR-γ agonist, telmisartan, delays inactivation of voltage-gated sodium channel in rat heart: novel mechanism of drug action", Pflügers Archiv-European Journal of Physiology, 2012 Dec .
How the study uses the data?
The study uses data from the FDA. It is based on telmisartan and diclofenac sodium (the active ingredients of Micardis and Diclofenac sodium, respectively), and Micardis 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.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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