Profen and Tenex drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Profen (ibuprofen) and Tenex (guanfacine hydrochloride). Common drug interactions include metamyelocyte count increased among females and agitation among males.
The phase IV clinical study analyzes what interactions people have when they take Profen and Tenex. It is created by eHealthMe based on reports of 29 people who take the same drugs from the FDA, and is updated regularly.
What is Profen?
Profen has active ingredients of ibuprofen. It is often used in pain. eHealthMe is studying from 245,311 Profen users. Check the latest studies of Profen.
What is Tenex?
Tenex has active ingredients of guanfacine hydrochloride. It is often used in attention deficit hyperactivity disorder. eHealthMe is studying from 1,865 Tenex users. Check the latest studies of Tenex.
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 >>>.
29 people who take Profen and Tenex together, and have interactions are studied.

What are the common drug interactions of Profen and Tenex, by gender? *:
female:
- Metamyelocyte count increased (excess precursor in the granulocytic series)
- Mitral valve incompetence (inefficient heart valve)
- Monocyte count decreased
- Myalgia (muscle pain)
- Myocardial ischaemia (the blood flow through one or more of the blood vessels that lead to heart (coronary arteries) is decreased)
- Nasopharyngitis (inflammation of the nasopharynx)
- Nausea (feeling of having an urge to vomit)
- Neck pain
- Neuralgia (pain in one or more nerves)
- Oedema peripheral (superficial swelling)
male:
- Agitation (state of anxiety or nervous excitement)
- Pneumonia
- Abdominal tenderness
- Ileus (a painful obstruction of the ileum or other part of the intestine)
- Accidental exposure
- Blindness
- Cough
- Decreased appetite
- Dizziness
- Dysphagia (a condition in which swallowing is difficult or painful)
What are the common drug interactions of Profen and Tenex, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Abdominal distension
- Abdominal tenderness
- Ileus (a painful obstruction of the ileum or other part of the intestine)
- Accidental exposure
10-19:
- Aggression
- Agitation (state of anxiety or nervous excitement)
- Anxiety
- Deep vein thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis)
- Emotional distress
- General physical health deterioration (weak health status)
- Injury
- Irritability
- Mania (a state of abnormally elevated or irritable mood)
- Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
20-29:
- Hallucination (an experience involving the perception of something not present)
- Mood altered (changes in mood)
- Myalgia (muscle pain)
- Neuralgia (pain in one or more nerves)
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Suicidal ideation
- Burning sensation
30-39:
n/a
40-49:
- Drug ineffective
- Cough
- Decreased appetite
- Dizziness
- Dysphagia (a condition in which swallowing is difficult or painful)
- Dystonia (abnormal muscle tone)
- Ear pain
- Fall
- Headache (pain in head)
- Hypersensitivity
50-59:
- Renal impairment (severely reduced kidney function)
- Transient ischaemic attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow))
60+:
- Dizziness
- Dyspnoea (difficult or laboured respiration)
- Blindness
- Blindness unilateral
- Blood albumin decreased
- Blood creatinine increased
- Blood glucose increased
- Blood magnesium decreased
- Blood potassium increased
- Blood sodium decreased
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 6 people, 20.69%
- Pneumonia: 5 people, 17.24%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 4 people, 13.79%
- Depression: 3 people, 10.34%
- High Blood Pressure: 2 people, 6.90%
* Approximation only. Some reports may have incomplete information.
Do you take Profen and Tenex?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Profen and Tenex:
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 Profen:
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 Tenex:
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 Profen 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 Tenex 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
- Moslim MA, Sodeman TC, Nawras AT, "A Case of Suggested Ibuprofen-Induced Acute Pancreatitis", American journal of therapeutics, 2016 Nov .
- Moslim MA, Sodeman TC, Nawras AT, "A Case of Suggested Ibuprofen-Induced Acute Pancreatitis", American journal of therapeutics, 2016 Nov .
How the study uses the data?
The study uses data from the FDA. It is based on ibuprofen and guanfacine hydrochloride (the active ingredients of Profen and Tenex, respectively), and Profen and Tenex (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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