Acth and Prolia drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Acth (corticotropin) and Prolia (denosumab). Common drug interactions include infusion site extravasation among females and death among males.

The phase IV clinical study analyzes what interactions people have when they take Acth and Prolia. 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 Acth?

Acth has active ingredients of corticotropin. eHealthMe is studying from 5,402 Acth users. Check the latest studies of Acth.

What is Prolia?

Prolia has active ingredients of denosumab. It is often used in osteoporosis. eHealthMe is studying from 151,389 Prolia users. Check the latest studies of Prolia.

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 >>>.



On Sep, 03, 2026

25 people who take Acth and Prolia together, and have interactions are studied.

Acth and Prolia drug interactions.

What are the common drug interactions of Acth and Prolia, by gender? *:

female:

  1. Infusion site extravasation (flow of (blood or lymph) from infusion site)
  2. Mental impairment (a condition affecting the body, perhaps through sight or hearing loss, a mobility difficulty or a health condition)
  3. Stress
  4. Cystitis (inflammation of the wall of the bladder)
  5. Headache (pain in head)
  6. Urinary tract infection
  7. Adverse event
  8. Blood urine present
  9. Dysphagia (a condition in which swallowing is difficult or painful)
  10. Dysuria (painful or difficult urination)

male:

  1. Death
  2. Pancreatic carcinoma (pancreatic cancer)

What are the common drug interactions of Acth and Prolia, 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:

n/a

50-59:

  1. Death
  2. Bladder neoplasm (bladder tumour)
  3. Blood urine present
  4. Cystitis (inflammation of the wall of the bladder)
  5. Dysuria (painful or difficult urination)
  6. Micturition urgency (urgency to pass the urine)
  7. Nausea (feeling of having an urge to vomit)
  8. Pancreatic carcinoma (pancreatic cancer)
  9. Pollakiuria (abnormally frequent passage of relatively small quantities or urine)
  10. Urinary tract infection

60+:

  1. Asthenia (weakness)
  2. Fatigue (feeling of tiredness)
  3. Adverse event
  4. Dysphagia (a condition in which swallowing is difficult or painful)
  5. Memory impairment
  6. Muscular weakness (muscle weakness)
  7. Oesophageal disorder (disease of oesophagus)
  8. Pain
  9. Panic disorder
  10. Uterine disorder

What are the existing conditions these people have? *

  1. Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 10 people, 40.00%
  2. Gait Disturbance: 8 people, 32.00%
  3. Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 6 people, 24.00%
  4. Dermatomyositis (inflammation of the skin and underlying muscle tissue, typically occurring as an autoimmune condition or associated with internal cancer): 6 people, 24.00%
  5. Polymyositis (inflammatory muscle disease that causes weakness of the skeletal muscles): 2 people, 8.00%
  6. Immunodeficiency Common Variable: 2 people, 8.00%

* Approximation only. Some reports may have incomplete information.

Do you take Acth and Prolia?

- 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:

Browse all drug interactions of Acth and Prolia:

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 Acth:

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 Prolia:

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 Acth 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 Prolia 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 corticotropin and denosumab (the active ingredients of Acth and Prolia, respectively), and Acth and Prolia (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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