Remifentanil hydrochloride and Magnesium sulfate drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Remifentanil hydrochloride (remifentanil hydrochloride) and Magnesium sulfate (magnesium sulfate). Common drug interactions include neutrophil count decreased among females and pneumonia among males.
The phase IV clinical study analyzes what interactions people have when they take Remifentanil hydrochloride and Magnesium sulfate. It is created by eHealthMe based on reports of 27 people who take the same drugs from the FDA, and is updated regularly.
What is Remifentanil hydrochloride?
Remifentanil hydrochloride has active ingredients of remifentanil hydrochloride. eHealthMe is studying from 1,327 Remifentanil hydrochloride users. Check the latest studies of Remifentanil hydrochloride.
What is Magnesium sulfate?
Magnesium sulfate has active ingredients of magnesium sulfate. It is often used in migraine. eHealthMe is studying from 18,024 Magnesium sulfate users. Check the latest studies of Magnesium sulfate.
27 people who take Remifentanil hydrochloride and Magnesium sulfate together, and have interactions are studied.

What are the common drug interactions of Remifentanil Hydrochloride and Magnesium Sulfate, by gender? *:
female:
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Cardiac failure acute
- Drug ineffective
- Maternal exposure during delivery (use of substance during pregnancy)
- Overdose
- Premature baby
- Septic shock (shock due to blood infection)
- Acidosis (build-up of carbon dioxide in the blood)
- Anaesthetic complication
- Anaphylactic reaction (serious allergic reaction)
male:
- Pneumonia
- Pneumonitis (inflammation of the walls of the alveoli in the lungs)
- Tachyarrhythmia (disturbance of the heart rhythm in which the heart rate is abnormally increased)
- Abdominal pain
- Clostridial infection (infectious conditions by clostridium bacteria)
- Conjunctivitis (pink eye)
- Depressed level of consciousness
- Diarrhoea
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
- Febrile neutropenia (fever with reduced white blood cells)
What are the common drug interactions of Remifentanil Hydrochloride and Magnesium Sulfate, by age (0-1 to 60+)? *:
0-1:
- Abdominal pain
- Clostridial infection (infectious conditions by clostridium bacteria)
- Conjunctivitis (pink eye)
- Diarrhoea
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
- Febrile neutropenia (fever with reduced white blood cells)
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Pain
- Penile ulceration
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Acidosis (build-up of carbon dioxide in the blood)
- Anaphylactic reaction (serious allergic reaction)
- Blood ph decreased
- Bronchospasm (spasm of bronchial smooth muscle producing narrowing of the bronchi)
- Dermatitis allergic (inflammation of the skin due allergic reaction)
- Drug ineffective
- Hypercapnia (too much smoke)
- Hypertensive crisis
- Hypoventilation (too shallow or too slow breathing, which does not meet the needs of the body)
- Maternal exposure during delivery (use of substance during pregnancy)
40-49:
- Anaesthetic complication
- Drug exposure during pregnancy
- Neuromuscular block prolonged
- Placenta praevia (a condition that occurs during pregnancy when the placenta is abnormally placed, and partially or totally covers the cervix)
- Premature baby
- Threatened labour (premature labour is the onset of labour between 24 and 37 weeks of pregnancy)
50-59:
n/a
60+:
- Pneumonia
- Pneumonitis (inflammation of the walls of the alveoli in the lungs)
- Pulmonary alveolar haemorrhage (acute bleeding)
- Pyrexia (fever)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Septic shock (shock due to blood infection)
- Tachyarrhythmia (disturbance of the heart rhythm in which the heart rate is abnormally increased)
- Depressed level of consciousness
- Drug ineffective
- Glossoptosis
What are the existing conditions these people have? *
- Sedation: 12 people, 44.44%
- Haemostasis (stopping of bleeding): 8 people, 29.63%
- Urination - Excessive Volume: 8 people, 29.63%
- Asthma: 6 people, 22.22%
- Blood Potassium Decreased: 5 people, 18.52%
- Oesophageal Squamous Cell Carcinoma (cancer that begins in flat cells lining the oesophagus): 5 people, 18.52%
- High Blood Pressure: 5 people, 18.52%
- Productive Cough: 4 people, 14.81%
- Cardiac Disorder: 4 people, 14.81%
- Arrhythmias (irregular heartbeat): 4 people, 14.81%
* Approximation only. Some reports may have incomplete information.
Do you take Remifentanil hydrochloride and Magnesium sulfate?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Remifentanil hydrochloride (1,327 reports)
- Magnesium sulfate (18,024 reports)
Browse all drug interactions of Remifentanil hydrochloride and Magnesium sulfate:
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 Remifentanil hydrochloride:
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 Magnesium sulfate:
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 Remifentanil hydrochloride 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 Magnesium sulfate 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 remifentanil hydrochloride and magnesium sulfate (the active ingredients of Remifentanil hydrochloride and Magnesium sulfate, respectively), and Remifentanil hydrochloride and Magnesium sulfate (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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