Synribo and Compazine drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Synribo (omacetaxine mepesuccinate) and Compazine (prochlorperazine maleate). Common drug interactions include hospitalisation among females and injection site erythema among males.

The phase IV clinical study analyzes what interactions people have when they take Synribo and Compazine. It is created by eHealthMe based on reports of 31 people who take the same drugs from the FDA, and is updated regularly.

What is Synribo?

Synribo has active ingredients of omacetaxine mepesuccinate. eHealthMe is studying from 799 Synribo users. Check the latest studies of Synribo.

What is Compazine?

Compazine has active ingredients of prochlorperazine maleate. It is often used in indigestion. eHealthMe is studying from 13,646 Compazine users. Check the latest studies of Compazine.



On Jul, 26, 2026

31 people who take Synribo and Compazine together, and have interactions are studied.

Synribo and Compazine drug interactions.

What are the common drug interactions of Synribo and Compazine, by gender? *:

female:

  1. Hospitalisation
  2. Platelet count increased
  3. Asthma
  4. Cough
  5. Nasopharyngitis (inflammation of the nasopharynx)
  6. Asthenia (weakness)
  7. Hallucination (an experience involving the perception of something not present)
  8. Urinary tract infection
  9. Wrist fracture
  10. Bacterial infection

male:

  1. Injection site erythema (redness at injection site)
  2. Asthenia (weakness)
  3. Abdominal pain upper
  4. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  5. Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
  6. Intestinal haemorrhage (bleeding from intestine)
  7. Loss of consciousness
  8. Swelling
  9. Drug ineffective
  10. White blood cell count increased

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

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

  1. Drug ineffective
  2. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  3. Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
  4. Injection site erythema (redness at injection site)
  5. Intestinal haemorrhage (bleeding from intestine)
  6. White blood cell count increased

30-39:

  1. Injection site erythema (redness at injection site)
  2. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  3. Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
  4. Intestinal haemorrhage (bleeding from intestine)
  5. Drug ineffective
  6. White blood cell count increased
  7. Haemoglobin decreased

40-49:

  1. Bone pain
  2. Arthralgia (joint pain)
  3. Blood glucose increased
  4. Discomfort
  5. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  6. Irritability
  7. Malaise (a feeling of general discomfort or uneasiness)
  8. Mobility decreased (ability to move is reduced)
  9. Pain
  10. Splenomegaly (enlargement of spleen)

50-59:

  1. White blood cell count decreased
  2. Blood calcium decreased
  3. Blood potassium increased
  4. Haematocrit decreased
  5. Haemoglobin decreased
  6. Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
  7. Hyperkalaemia (damage to or disease of the kidney)
  8. Hypocalcaemia (levels of calcium in blood serum are abnormally low)

60+:

  1. Asthenia (weakness)
  2. Abdominal distension
  3. Back pain
  4. Blood glucose decreased
  5. Blood glucose increased
  6. Burning sensation
  7. Diarrhoea
  8. Dyspnoea (difficult or laboured respiration)
  9. Epistaxis (bleed from the nose)
  10. Feeling cold

What are the existing conditions these people have? *

  1. Chronic Myeloid Leukaemia (long lasting type of cancer that starts in the blood-forming cells of the bone marrow and invades the blood): 29 people, 93.55%
  2. Nausea (feeling of having an urge to vomit): 6 people, 19.35%
  3. Pain: 4 people, 12.90%
  4. Diabetes: 3 people, 9.68%
  5. Stress And Anxiety: 2 people, 6.45%
  6. Dyspnea (difficult or laboured breathing): 2 people, 6.45%

* Approximation only. Some reports may have incomplete information.

Do you take Synribo and Compazine?

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Related studies:

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

Browse all drug interactions of Synribo and Compazine:

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 Synribo:

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 Compazine:

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 Synribo 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 Compazine 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 omacetaxine mepesuccinate and prochlorperazine maleate (the active ingredients of Synribo and Compazine, respectively), and Synribo and Compazine (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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