Prednisone and Taclonex drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Prednisone (prednisone) and Taclonex (betamethasone dipropionate; calcipotriene hydrate). Common drug interactions include injection site swelling among females and septic shock among males.

The phase IV clinical study analyzes what interactions people have when they take Prednisone and Taclonex. It is created by eHealthMe based on reports of 84 people who take the same drugs from the FDA, and is updated regularly.

What is Prednisone?

Prednisone has active ingredients of prednisone. It is often used in rheumatoid arthritis. eHealthMe is studying from 636,827 Prednisone users. Check the latest studies of Prednisone.

What is Taclonex?

Taclonex has active ingredients of betamethasone dipropionate; calcipotriene hydrate. It is often used in psoriasis. eHealthMe is studying from 1,618 Taclonex users. Check the latest studies of Taclonex.



On Jul, 21, 2026

84 people who take Prednisone and Taclonex together, and have interactions are studied.

Prednisone and Taclonex drug interactions.

What are the common drug interactions of Prednisone and Taclonex, by gender? *:

female:

  1. Injection site swelling
  2. Injection site warmth
  3. Polyp
  4. Post-traumatic neck syndrome
  5. Rash erythematous (redness of the skin)
  6. Road traffic accident
  7. Abdominal discomfort
  8. Abdominal pain
  9. Acne (skin problems that cause pimples)
  10. Anxiety

male:

  1. Septic shock (shock due to blood infection)
  2. Chronic kidney disease
  3. Anxiety
  4. Diarrhoea
  5. Injection site bruising
  6. Pain
  7. Pyrexia (fever)
  8. Anhedonia (inability to experience pleasure from activities usually found enjoyable)
  9. Arthropathy
  10. Bacterial infection

What are the common drug interactions of Prednisone and Taclonex, by age (0-1 to 60+)? *:

0-1:

  1. Premature baby
  2. Arrhythmia (irregular heartbeat)
  3. Foetal exposure during pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect)
  4. Convulsion neonatal (muscle contraction and relaxation rapidly in neonate)
  5. Drug exposure via breast milk
  6. Growth retardation (delayed growth)
  7. Hypercalcaemia (elevated calcium (ca+) level in the blood)
  8. Infantile apnoeic attack (episodes where breathing stops temporarily in infant)
  9. Neonatal disorder (disease of neonates)
  10. Sepsis neonatal (a bacterial infection in the blood. it is found in infants during the first month of life)

2-9:

n/a

10-19:

n/a

20-29:

  1. Hyperthermia (body temperature greatly above normal)
  2. Intestinal obstruction
  3. Pregnancy
  4. Premature delivery
  5. Respiratory tract infection
  6. Pruritus (severe itching of the skin)
  7. Rash

30-39:

  1. Chronic kidney disease
  2. Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
  3. Tubulointerstitial nephritis (a form of nephritis affecting the interstitium of the kidneys surrounding the tubules)

40-49:

  1. Dependence
  2. Depression
  3. Diarrhoea
  4. Dry skin
  5. Dyspnoea (difficult or laboured respiration)
  6. Eosinophil count increased
  7. Erythema (redness of the skin)
  8. Fatigue (feeling of tiredness)
  9. Hypersensitivity
  10. Inflammation

50-59:

  1. Nasopharyngitis (inflammation of the nasopharynx)
  2. Arthralgia (joint pain)
  3. Drug ineffective
  4. Injection site pain
  5. Injection site paraesthesia (abnormal skin sensations at injection site)
  6. Tinnitus (a ringing in the ears)
  7. Headache (pain in head)
  8. Injection site bruising
  9. Injection site pruritus (severe itching at injection site)
  10. Injection site swelling

60+:

  1. Septic shock (shock due to blood infection)
  2. Chronic kidney disease
  3. Depression
  4. Diarrhoea
  5. Hospitalisation
  6. Rash
  7. Vomiting
  8. Bacterial infection
  9. Blood culture positive
  10. Blood sodium decreased

What are the existing conditions these people have? *

  1. Psoriatic Arthropathy (inflammation of the skin and joints with kin condition which typically causes patches (plaques) of red, scaly skin to develop): 23 people, 27.38%
  2. Pain: 16 people, 19.05%
  3. Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 7 people, 8.33%
  4. Insomnia (sleeplessness): 5 people, 5.95%
  5. Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 5 people, 5.95%
  6. High Blood Pressure: 5 people, 5.95%
  7. High Blood Cholesterol: 5 people, 5.95%
  8. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 5 people, 5.95%
  9. Diabetes: 5 people, 5.95%
  10. Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 5 people, 5.95%

* Approximation only. Some reports may have incomplete information.

Do you take Prednisone and Taclonex?

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Prednisone and Taclonex:

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 z

Sub-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 Prednisone:

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 z

Browse all side effects of Taclonex:

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 z

Browse all interactions between Prednisone 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 z

Browse all interactions between Taclonex 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 z

How the study uses the data?

The study uses data from the FDA. It is based on prednisone and betamethasone dipropionate; calcipotriene hydrate (the active ingredients of Prednisone and Taclonex, respectively), and Prednisone and Taclonex (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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