Pantoprazole and Zemuron drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Pantoprazole (pantoprazole sodium) and Zemuron (rocuronium bromide). Common drug interactions include cellulitis among females and cerebral ischaemia among males.
The phase IV clinical study analyzes what interactions people have when they take Pantoprazole and Zemuron. It is created by eHealthMe based on reports of 22 people who take the same drugs from the FDA, and is updated regularly.
What is Pantoprazole?
Pantoprazole has active ingredients of pantoprazole sodium. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 285,165 Pantoprazole users. Check the latest studies of Pantoprazole.
What is Zemuron?
Zemuron has active ingredients of rocuronium bromide. eHealthMe is studying from 873 Zemuron users. Check the latest studies of Zemuron.
22 people who take Pantoprazole and Zemuron together, and have interactions are studied.

What are the common drug interactions of Pantoprazole and Zemuron, by gender? *:
female:
- Cellulitis (infection under the skin)
- Abscess limb (limb infection)
- Perirectal abscess
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Necrotising fasciitis (an uncommon life-threatening soft-tissue infection)
- Pain
- Septic shock (shock due to blood infection)
- Subcutaneous abscess
- Drug resistance (reduction in effectiveness of a drug)
- Intestinal ischaemia (decreased supply of oxygenated blood to the intestines)
male:
- Cerebral ischaemia (insufficient blood flow to the brain to meet metabolic demand)
- Heparin-induced thrombocytopenia
- Emotional distress
- Fear
- Injury
- Multi-organ failure (multisystem organ failure)
- Nervousness
- Pain
- Renal failure (kidney dysfunction)
- Renal injury (kidney injury)
What are the common drug interactions of Pantoprazole and Zemuron, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Acinetobacter infection (infection by group of bacteria commonly found in soil and water)
- Diarrhoea
- Diarrhoea haemorrhagic (bloody diarrhoea)
- Graft versus host disease (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the body)
- Haematoma (collection of blood outside the blood vessels)
- Pleural effusion (water on the lungs)
- Pyrexia (fever)
- Septic shock (shock due to blood infection)
- Tooth abscess (pus formation in tooth)
10-19:
n/a
20-29:
n/a
30-39:
- Anaemia (lack of blood)
- Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
- Splenic infarction (tissue damage of spleen)
- Tumour lysis syndrome (a group of metabolic complications that can occur after treatment of cancer, these complications are caused by the breakdown products of dying cancer cells)
40-49:
- Abscess limb (limb infection)
- Necrotising fasciitis (an uncommon life-threatening soft-tissue infection)
- Nerve injury
- Pain
- Perirectal abscess
- Rectal abscess (pus in rectum)
- Scar
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Cellulitis (infection under the skin)
50-59:
- Abscess limb (limb infection)
- Cellulitis (infection under the skin)
- Perirectal abscess
- Subcutaneous abscess
- Hepatotoxicity (chemical-driven liver damage)
- Anal abscess
- Genital abscess (build up of pus in genital)
- Necrotising fasciitis (an uncommon life-threatening soft-tissue infection)
- Panic attack
- Acute respiratory failure
60+:
- Cerebral ischaemia (insufficient blood flow to the brain to meet metabolic demand)
- Drug resistance (reduction in effectiveness of a drug)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Septic shock (shock due to blood infection)
- Hyperthermia malignant (disease passed down through families that causes a fast rise in body temperature (fever) and severe muscle contractions)
- Acute respiratory failure
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Emotional distress
What are the existing conditions these people have? *
- Hypotension (abnormally low blood pressure): 8 people, 36.36%
- Type 2 Diabetes: 6 people, 27.27%
- Weight Decreased: 6 people, 27.27%
- Pain: 4 people, 18.18%
- Nausea (feeling of having an urge to vomit): 4 people, 18.18%
- Sedation: 3 people, 13.64%
- Cardiac Arrest: 3 people, 13.64%
- Fever: 3 people, 13.64%
- High Blood Pressure: 3 people, 13.64%
- White Blood Cell Count Decreased: 2 people, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Pantoprazole and Zemuron?
- 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:
- Pantoprazole (285,165 reports)
- Zemuron (873 reports)
Browse all drug interactions of Pantoprazole and Zemuron:
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 Pantoprazole:
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 Zemuron:
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 Pantoprazole 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 Zemuron 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 pantoprazole sodium and rocuronium bromide (the active ingredients of Pantoprazole and Zemuron, respectively), and Pantoprazole and Zemuron (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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