Kenalog and Lovaza drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Kenalog (triamcinolone acetonide) and Lovaza (omega-3-acid ethyl esters). Common drug interactions include hyperlipidaemia among females and dry mouth among males.
The phase IV clinical study analyzes what interactions people have when they take Kenalog and Lovaza. It is created by eHealthMe based on reports of 52 people who take the same drugs from the FDA, and is updated regularly.
What is Kenalog?
Kenalog has active ingredients of triamcinolone acetonide. It is often used in pain. eHealthMe is studying from 10,692 Kenalog users. Check the latest studies of Kenalog.
What is Lovaza?
Lovaza has active ingredients of omega-3-acid ethyl esters. It is often used in high blood cholesterol. eHealthMe is studying from 17,340 Lovaza users. Check the latest studies of Lovaza.
52 people who take Kenalog and Lovaza together, and have interactions are studied.

What are the common drug interactions of Kenalog and Lovaza, by gender? *:
female:
- Hyperlipidaemia (presence of excess lipids in the blood)
- Hypersensitivity
- Hypertension (high blood pressure)
- Hypoalbuminaemia (levels of albumin in blood serum are abnormally low)
- Hypokalaemia (low potassium)
- Hypotension (abnormally low blood pressure)
- Injection site mass
- Malaise (a feeling of general discomfort or uneasiness)
- Mental status changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)
- Nausea (feeling of having an urge to vomit)
male:
- Dry mouth
- Diverticulitis (digestive disease which involves the formation of pouches (diverticula) within the bowel wall)
- Abdominal pain upper
- Blindness
- Blood testosterone decreased
- Diverticulum (out pouching of a hollow (or a fluid-filled) structure in the body)
- Headache (pain in head)
- Hepatic enzyme increased
- Influenza
- Insomnia (sleeplessness)
What are the common drug interactions of Kenalog and Lovaza, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Cellulitis (infection under the skin)
20-29:
- Tooth infection
30-39:
n/a
40-49:
- Arthralgia (joint pain)
- Arthropathy
- Asthma
- Biliary dilatation
- Cardiac failure chronic
- Depression
- Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
- Hyperhidrosis (abnormally increased sweating)
- Hyperlipidaemia (presence of excess lipids in the blood)
- Hypersensitivity
50-59:
- Carbon dioxide increased
- Fluid retention (an abnormal accumulation of fluid in the blood)
- Urinary tract infection
- Abdominal discomfort
- Ageusia (loss of taste functions of the tongue)
- Agitation (state of anxiety or nervous excitement)
- Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
- Anosmia (partial or complete loss of the sense of smell)
- Arthritis (form of joint disorder that involves inflammation of one or more joints)
- Cancer in remission (a decrease in or disappearance of signs and symptoms of cancer)
60+:
- Dry mouth
- Dizziness
- Chronic kidney disease
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Disease recurrence
- Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
- Gout (uric acid crystals building up in the body)
- Headache (pain in head)
- Injection site mass
- Overdose
What are the existing conditions these people have? *
- Stress And Anxiety: 10 people, 19.23%
- Constipation: 9 people, 17.31%
- Hypersensitivity: 6 people, 11.54%
- Insomnia (sleeplessness): 6 people, 11.54%
- Nausea (feeling of having an urge to vomit): 5 people, 9.62%
- Anaemia (lack of blood): 5 people, 9.62%
- Dry Skin: 5 people, 9.62%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 5 people, 9.62%
- Vitamin D Decreased: 5 people, 9.62%
- Abdominal Pain: 5 people, 9.62%
* Approximation only. Some reports may have incomplete information.
Do you take Kenalog and Lovaza?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Kenalog and Lovaza:
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 Kenalog:
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 Lovaza:
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 Kenalog 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 Lovaza 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 triamcinolone acetonide and omega-3-acid ethyl esters (the active ingredients of Kenalog and Lovaza, respectively), and Kenalog and Lovaza (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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