Ultane and Post procedural complication - a phase IV clinical study of FDA data

Summary:

Post procedural complication is reported as a side effect among people who take Ultane (sevoflurane), especially for people who are male, 10-19 old, have been taking the drug for < 1 month also take Fentanyl, and have Anaesthesia.

The phase IV clinical study analyzes which people have Post procedural complication when taking Ultane. It is created by eHealthMe based on reports of 676 people who have side effects when taking Ultane from the FDA, and is updated regularly.

What is Ultane?

Ultane has active ingredients of sevoflurane. eHealthMe is studying from 677 Ultane users. Check the latest studies of Ultane.

What is Post procedural complication?

Post procedural complication is found to be associated with 1,088 drugs and 1,362 conditions by eHealthMe. Check the latest studies of Post procedural complication.

On Jul, 09, 2026

676 people reported to have side effects when taking Ultane.
Among them, 14 people (2.07%) have Post procedural complication.

Could Ultane cause Post procedural complication?

Among these 14 people:

How long have people been on Ultane when they have Post procedural complication? *

What is the gender of people who have Post procedural complication when taking Ultane? *

female: 35.71 %
male: 64.29 %

What is the age of people who have Post procedural complication when taking Ultane? *

What are other drugs people take besides Ultane? *

Fentanyl: 4 people, 28.57%
Propofol: 3 people, 21.43%
Bupivacaine: 2 people, 14.29%
Midazolam Hydrochloride: 2 people, 14.29%
Halothane: 2 people, 14.29%
Atropine Sulfate: 2 people, 14.29%
Cefazolin: 2 people, 14.29%
Fenofibrate: 1 person, 7.14%
Famotidine: 1 person, 7.14%
Extraneal: 1 person, 7.14%

What are other side effects people have besides Post procedural complication? *

Pulmonary Haemorrhage (acute bleeding from the lung): 3 people, 21.43%
Anaesthetic Complication: 2 people, 14.29%
Apnea (temporary absence or cessation of breathing): 2 people, 14.29%
Aspartate Aminotransferase Increased: 2 people, 14.29%
Platelet Count Increased: 2 people, 14.29%
Gamma-Glutamyltransferase Increased: 2 people, 14.29%
Ventricular Fibrillation (abnormally irregular heart rhythm): 1 person, 7.14%
Delayed Recovery From Anaesthesia: 1 person, 7.14%
Hepatocellular Damage (liver damage): 1 person, 7.14%
Haemorrhagic Diathesis (bleeding tendency): 1 person, 7.14%

What are the existing conditions these people have? *

Anaesthesia: 9 people, 64.29%
Pain: 2 people, 14.29%
Post Procedural Oedema (excessive build-up of fluid in the body's tissues after procedure): 1 person, 7.14%
Neuromuscular Blockade Reversal: 1 person, 7.14%
Lip And/or Oral Cavity Cancer (cancer of lip or mouth): 1 person, 7.14%
Hypotonia (low muscle tone): 1 person, 7.14%
High Blood Pressure: 1 person, 7.14%
Dyslipidaemia (abnormal amount of lipids): 1 person, 7.14%
Analgesic Effect: 1 person, 7.14%

* Approximation only. Some reports may have incomplete information.

Do you take Ultane and have Post procedural complication?

- Check whether Post procedural complication is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

Effectiveness of, long term effects of, and alternative drugs to Ultane:

Ultane (677 reports)

Browse all side effects of Ultane:

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 the drugs that are associated with Post procedural complication:

Post procedural complication (1,088 drugs)

Browse all the conditions that are associated with Post procedural complication:

Post procedural complication (1,362 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on sevoflurane (the active ingredients of Ultane) and Ultane (the brand name). 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.