Kenalog-40 and Ibu drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Kenalog-40 (triamcinolone acetonide) and Ibu (ibuprofen). Common drug interactions include erythema among females and gingival disorder among males.
The phase IV clinical study analyzes what interactions people have when they take Kenalog-40 and Ibu. It is created by eHealthMe based on reports of 25 people who take the same drugs from the FDA, and is updated regularly.
What is Kenalog-40?
Kenalog-40 has active ingredients of triamcinolone acetonide. It is often used in back pain. eHealthMe is studying from 2,099 Kenalog-40 users. Check the latest studies of Kenalog-40.
What is Ibu?
Ibu has active ingredients of ibuprofen. It is often used in pain. eHealthMe is studying from 246,531 Ibu users. Check the latest studies of Ibu.
25 people who take Kenalog-40 and Ibu together, and have interactions are studied.

What are the common drug interactions of Kenalog-40 and Ibu, by gender? *:
female:
- Erythema (redness of the skin)
- Swelling face
- Anaphylactic reaction (serious allergic reaction)
- Alopecia (absence of hair from areas of the body)
- Blood potassium decreased
- Dizziness
- Hyperhidrosis (abnormally increased sweating)
- Hypoaesthesia (reduced sense of touch or sensation)
- Insomnia (sleeplessness)
- Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect)
male:
- Gingival disorder (gum disease)
- Intervertebral disc protrusion (spinal disc protrusion)
- Anaphylactic reaction (serious allergic reaction)
- Blindness unilateral
- Optic neuritis (optic nerve inflammation)
- Vision blurred
- Multiple fractures
- Muscle atrophy (a decrease in the mass of the muscle)
- Muscle strain (an injury to a muscle in which the muscle fibres tear)
- Musculoskeletal pain (pain affects the bones, muscles, ligaments, tendons, and nerves)
What are the common drug interactions of Kenalog-40 and Ibu, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Cushingoid (obesity and weakening of the muscles)
- Weight increased
10-19:
n/a
20-29:
- Alopecia (absence of hair from areas of the body)
- Acne (skin problems that cause pimples)
- Amenorrhoea (absence of a menstrual period in a woman of reproductive age)
- Anxiety
- Depression
- Dyspnoea exertional (breathlessness or shortness of breath)
- Fatigue (feeling of tiredness)
- Formication (a sensation that exactly resembles that of small insects crawling on (or under) the skin)
- Hyperhidrosis (abnormally increased sweating)
- Hypertension (high blood pressure)
30-39:
- Injection site pigmentation changes
- Vision blurred
40-49:
- Anaphylactic reaction (serious allergic reaction)
- Injection site abscess
- Respiratory disorder (respiratory disease)
50-59:
- Swelling face
- Anaphylactic reaction (serious allergic reaction)
- Gingival disorder (gum disease)
- Intervertebral disc protrusion (spinal disc protrusion)
- Multiple fractures
- Muscle atrophy (a decrease in the mass of the muscle)
- Muscle strain (an injury to a muscle in which the muscle fibres tear)
- Musculoskeletal pain (pain affects the bones, muscles, ligaments, tendons, and nerves)
- Pain in extremity
- Renal pain (kidney pain)
60+:
- Blindness unilateral
- Blood potassium decreased
- Hyperhidrosis (abnormally increased sweating)
- Insomnia (sleeplessness)
- Muscle spasms (muscle contraction)
- Night sweats (sweating in night)
- Optic neuritis (optic nerve inflammation)
- Pyrexia (fever)
- Vaginal haemorrhage (vaginal bleeding)
What are the existing conditions these people have? *
- Intervertebral Disc Degeneration (spinal disc degeneration): 4 people, 16.00%
- Hyperlipidaemia (presence of excess lipids in the blood): 3 people, 12.00%
- High Blood Cholesterol: 3 people, 12.00%
- Urticaria (rash of round, red welts on the skin that itch intensely): 2 people, 8.00%
- Radicular Pain (pain ""radiated"" along the dermatome (sensory distribution) of a nerve due to inflammation): 2 people, 8.00%
- Osteoarthritis (a joint disease caused by cartilage loss in a joint): 2 people, 8.00%
- Joint Pain: 2 people, 8.00%
- Back Pain: 2 people, 8.00%
- Arthritis (form of joint disorder that involves inflammation of one or more joints): 2 people, 8.00%
* Approximation only. Some reports may have incomplete information.
Do you take Kenalog-40 and Ibu?
- 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:
- Kenalog-40 (2,099 reports)
- Ibu (246,531 reports)
Browse all drug interactions of Kenalog-40 and Ibu:
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-40:
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 Ibu:
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-40 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 Ibu 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 triamcinolone acetonide and ibuprofen (the active ingredients of Kenalog-40 and Ibu, respectively), and Kenalog-40 and Ibu (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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