Proleukin and Sedation aggravated - a phase IV clinical study of FDA data
Summary:
Sedation aggravated is reported as a side effect among people who take Proleukin (aldesleukin), especially for people who are female, 60+ old, also take Habitrol,.
The phase IV clinical study analyzes which people have Sedation aggravated when taking Proleukin. It is created by eHealthMe based on reports of 1,862 people who have side effects when taking Proleukin from the FDA, and is updated regularly.
What is Proleukin?
Proleukin has active ingredients of aldesleukin. eHealthMe is studying from 1,865 Proleukin users. Check the latest studies of Proleukin.
What is Sedation aggravated?
Sedation aggravated is found to be associated with 1,153 drugs and 493 conditions by eHealthMe. Check the latest studies of Sedation aggravated.
1,862 people reported to have side effects when taking Proleukin.
Among them, 11 people (0.59%) have Sedation aggravated.

Among these 11 people:
What is the gender of people who have Sedation aggravated when taking Proleukin? *
- female: 54.55 %
- male: 45.45 %
What is the age of people who have Sedation aggravated when taking Proleukin? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 9.09 %
- 40-49: 27.27 %
- 50-59: 18.18 %
- 60+: 45.45 %
What are other drugs people take besides Proleukin? *
- Tylenol: 2 people, 18.18%
- Habitrol: 2 people, 18.18%
- Zantac: 1 person, 9.09%
- Thalomid: 1 person, 9.09%
- Rituxan: 1 person, 9.09%
- Restoril: 1 person, 9.09%
- Paxil: 1 person, 9.09%
- Metoclopramide: 1 person, 9.09%
- Lanoxin: 1 person, 9.09%
- Intron A: 1 person, 9.09%
What are other side effects people have besides Sedation aggravated? *
- Confusion: 5 people, 45.45%
- Blood Creatinine Increased: 4 people, 36.36%
- Hypotension (abnormally low blood pressure): 4 people, 36.36%
- Hemiplegia (paralysis of one side of the body): 2 people, 18.18%
- Weight Decreased: 2 people, 18.18%
- Cerebral Ischaemia (insufficient blood flow to the brain to meet metabolic demand): 2 people, 18.18%
- Thrombocytopenia (decrease of platelets in blood): 2 people, 18.18%
- Anorexia (eating disorder characterized by immoderate food restriction and irrational fear of gaining weight): 2 people, 18.18%
- Nuclear Magnetic Resonance Imaging Abnormal: 2 people, 18.18%
- Chills (felling of cold): 1 person, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Proleukin and have Sedation aggravated?
- Check whether Sedation aggravated 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 Proleukin:
- Proleukin (1,865 reports)
Sedation aggravated treatments and more:
- Sedation aggravated (20 reports)
How severe was Sedation aggravated and when was it recovered:
Expand to all the drugs that have ingredients of aldesleukin:
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 Proleukin:
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 the drugs that are associated with Sedation aggravated:
- Sedation aggravated (1,154 drugs)
Browse all the conditions that are associated with Sedation aggravated:
- Sedation aggravated (493 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on aldesleukin (the active ingredients of Proleukin) and Proleukin (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.
Recent studies on eHealthMe:
- Drug interactions of Amoxicillin and Halflytely - 2 seconds ago
- Could Citicoline cause Cardiac Arrest? - 14 seconds ago
- Drug interactions of Remodulin and Avapro - 33 seconds ago
- Could Sudafed cause Broken Bone? - 34 seconds ago
- Drug interactions of Heparin Sodium and Milrinone Lactate - 42 seconds ago
- Parkinsonism Aggravated and Enteritis Infectious - 45 seconds ago
- Asthma and Gilles De La Tourette Syndrome - a minute ago
- Could Vyvanse cause Facial Pain? - a minute ago
- Drug interactions of Capsaicin and Metformin - a minute ago
- Could Vyvanse cause Faeces Discolored? - 2 minutes ago