Symbicort and Shock - a phase IV clinical study of FDA data
Summary:
Shock is reported as a side effect among people who take Symbicort (budesonide; formoterol fumarate dihydrate), especially for people who are female, 60+ old, also take Spiriva, and have Pain.
The phase IV clinical study analyzes which people have Shock when taking Symbicort. It is created by eHealthMe based on reports of 112,650 people who have side effects when taking Symbicort from the FDA, and is updated regularly.
What is Symbicort?
Symbicort has active ingredients of budesonide; formoterol fumarate dihydrate. It is often used in asthma. eHealthMe is studying from 114,792 Symbicort users. Check the latest studies of Symbicort.
What is Shock?
Shock (a life-threatening condition with symptoms like low blood pressure, weakness, shallow breathing, cold, clammy skin) is found to be associated with 1,212 drugs and 1,755 conditions by eHealthMe. Check the latest studies of Shock.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
112,650 people reported to have side effects when taking Symbicort.
Among them, 76 people (0.07%) have Shock.

Among these 76 people:
What is the gender of people who have Shock when taking Symbicort? *
- female: 67.61 %
- male: 32.39 %
What is the age of people who have Shock when taking Symbicort? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 11.94 %
- 20-29: 0.0 %
- 30-39: 2.99 %
- 40-49: 5.97 %
- 50-59: 10.45 %
- 60+: 68.66 %
What are other drugs people take besides Symbicort? *
- Spiriva: 15 people, 19.74%
- Xolair: 12 people, 15.79%
- Lyrica: 11 people, 14.47%
- Zyrtec: 10 people, 13.16%
- Calcium: 10 people, 13.16%
- Nasonex: 10 people, 13.16%
- Proair Hfa: 9 people, 11.84%
- Zantac: 8 people, 10.53%
- Advair Hfa: 8 people, 10.53%
- Claritin: 8 people, 10.53%
What are other side effects people have besides Shock? *
- Dyspnea (difficult or laboured breathing): 19 people, 25.00%
- Hypoaesthesia (reduced sense of touch or sensation): 17 people, 22.37%
- Malaise (a feeling of general discomfort or uneasiness): 16 people, 21.05%
- Acute Kidney Failure: 15 people, 19.74%
- Cardiac Arrest: 15 people, 19.74%
- Pneumonia: 15 people, 19.74%
- Respiratory Acidosis (respiratory failure or ventilatory failure, causes the ph of blood and other bodily fluids to decrease): 13 people, 17.11%
- Fatigue (feeling of tiredness): 13 people, 17.11%
- Anaphylaxis (serious allergic reaction that is rapid in onset and may cause death): 12 people, 15.79%
- Nausea (feeling of having an urge to vomit): 12 people, 15.79%
What are the existing conditions these people have? *
- Pain: 13 people, 17.11%
- Hypersensitivity: 10 people, 13.16%
- Osteoporosis (bones weak and more likely to break): 10 people, 13.16%
- Migraine (headache): 9 people, 11.84%
- Osteopenia (a condition where bone mineral density is lower than normal): 9 people, 11.84%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 8 people, 10.53%
- High Blood Pressure: 7 people, 9.21%
- Hiatal Hernia (hernia resulting from the protrusion of part of the stomach through the diaphragm): 6 people, 7.89%
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 6 people, 7.89%
- Fibromyalgia (a long-term condition which causes pain all over the body): 6 people, 7.89%
* Approximation only. Some reports may have incomplete information.
Do you take Symbicort and have Shock?
- Check whether Shock 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 Symbicort:
- Symbicort (114,792 reports)
Shock treatments and more:
- Shock (28,534 reports)
How severe was Shock and when was it recovered:
Expand to all the drugs that have ingredients of budesonide; formoterol fumarate dihydrate:
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 Symbicort:
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 Shock:
- Shock (1,212 drugs)
Browse all the conditions that are associated with Shock:
- Shock (1,755 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on budesonide; formoterol fumarate dihydrate (the active ingredients of Symbicort) and Symbicort (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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