Adriamycin pfs and Syncope aggravated - a phase IV clinical study of FDA data

Summary:

Syncope aggravated is reported as a side effect among people who take Adriamycin pfs (doxorubicin hydrochloride), especially for people who are female, 50-59 old, have been taking the drug for < 1 month also take Cytoxan, and have Multiple myeloma.

The phase IV clinical study analyzes which people have Syncope aggravated when taking Adriamycin pfs. It is created by eHealthMe based on reports of 6,484 people who have side effects when taking Adriamycin pfs from the FDA, and is updated regularly.

What is Adriamycin pfs?

Adriamycin pfs has active ingredients of doxorubicin hydrochloride. eHealthMe is studying from 6,495 Adriamycin pfs users. Check the latest studies of Adriamycin pfs.

What is Syncope aggravated?

Syncope aggravated (a loss of consciousness with an inability to maintain postural tone) is found to be associated with 1,684 drugs and 588 conditions by eHealthMe. Check the latest studies of Syncope aggravated.

On Jul, 09, 2026

6,484 people reported to have side effects when taking Adriamycin pfs.
Among them, 158 people (2.44%) have Syncope aggravated.

Could Adriamycin pfs cause Syncope aggravated?

Among these 158 people:

How long have people been on Adriamycin pfs when they have Syncope aggravated? *

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What is the gender of people who have Syncope aggravated when taking Adriamycin pfs? *

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What is the age of people who have Syncope aggravated when taking Adriamycin pfs? *

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* Approximation only. Some reports may have incomplete information.

Do you take Adriamycin pfs and have Syncope aggravated?

- Check whether Syncope aggravated is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Adriamycin pfs:

Adriamycin pfs (6,495 reports)

Syncope aggravated treatments and more:

Syncope aggravated (17 reports)

How severe was Syncope aggravated and when was it recovered:

Syncope aggravated in Adriamycin pfs

Expand to all the drugs that have ingredients of doxorubicin hydrochloride:

Syncope aggravated and drugs with ingredients of doxorubicin hydrochloride

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 Adriamycin pfs:

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 Syncope aggravated:

Syncope aggravated (1,684 drugs)

Browse all the conditions that are associated with Syncope aggravated:

Syncope aggravated (588 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on doxorubicin hydrochloride (the active ingredients of Adriamycin pfs) and Adriamycin pfs (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.