Synagis and Adverse reaction - a phase IV clinical study of FDA data
Summary:
Adverse reaction is reported as a side effect among people who take Synagis (palivizumab), especially for people who are male, 0-1 old, also take Lasix, and have Bronchopulmonary dysplasia.
The phase IV clinical study analyzes which people have Adverse reaction when taking Synagis. It is created by eHealthMe based on reports of 19,108 people who have side effects when taking Synagis from the FDA, and is updated regularly.
What is Synagis?
Synagis has active ingredients of palivizumab. eHealthMe is studying from 19,114 Synagis users. Check the latest studies of Synagis.
What is Adverse reaction?
Adverse reaction is found to be associated with 654 drugs and 658 conditions by eHealthMe. Check the latest studies of Adverse reaction.
19,108 people reported to have side effects when taking Synagis.
Among them, 11 people (0.06%) have Adverse reaction.

Among these 11 people:
What is the gender of people who have Adverse reaction when taking Synagis? *
- female: 11.11 %
- male: 88.89 %
What is the age of people who have Adverse reaction when taking Synagis? *
- 0-1: 100 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 0.0 %
What are other drugs people take besides Synagis? *
- Lasix: 2 people, 18.18%
- Viagra: 1 person, 9.09%
- Levetiracetam: 1 person, 9.09%
- Keppra: 1 person, 9.09%
- Furosemide: 1 person, 9.09%
What are other side effects people have besides Adverse reaction? *
- Wheezing (a high-pitched whistling sound made while you breath): 1 person, 9.09%
- Urticaria (rash of round, red welts on the skin that itch intensely): 1 person, 9.09%
- Rhinorrhea (watery mucus discharge from the nose): 1 person, 9.09%
- Rashes (redness): 1 person, 9.09%
- Nausea And Vomiting: 1 person, 9.09%
- Gastrointestinal Disorder (functional problems of gastrointestinal tract): 1 person, 9.09%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 9.09%
- Crying: 1 person, 9.09%
- Cough: 1 person, 9.09%
- Asthma: 1 person, 9.09%
What are the existing conditions these people have? *
- Bronchopulmonary Dysplasia (chronic lung disorder in infants - enlargement of an organ or tissue by the proliferation of cells of an abnormal type): 2 people, 18.18%
- Pulmonary Hypertension (increase in blood pressure in the lung artery): 1 person, 9.09%
- Premature Baby: 1 person, 9.09%
- Obstructive Sleep Apnea Syndrome (a sleep disorder that involves cessation or significant decrease in airflow in the presence of breathing effort): 1 person, 9.09%
- Low Birth Weight Baby: 1 person, 9.09%
- Aortic Valve Incompetence: 1 person, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Synagis and have Adverse reaction?
- Check whether Adverse reaction 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 Synagis:
- Synagis (19,114 reports)
Adverse reaction treatments and more:
- Adverse reaction (13,279 reports)
How severe was Adverse reaction and when was it recovered:
Expand to all the drugs that have ingredients of palivizumab:
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 Synagis:
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 Adverse reaction:
- Adverse reaction (654 drugs)
Browse all the conditions that are associated with Adverse reaction:
- Adverse reaction (658 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on palivizumab (the active ingredients of Synagis) and Synagis (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.
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