Actonel and Rubella - a phase IV clinical study of FDA data

Summary:

Rubella is reported as a side effect among people who take Actonel (risedronate sodium), especially for people who are female, 40-49 old, also take Advair Hfa, and have Pain.

The phase IV clinical study analyzes which people have Rubella when taking Actonel. It is created by eHealthMe based on reports of 28,929 people who have side effects when taking Actonel from the FDA, and is updated regularly.

What is Actonel?

Actonel has active ingredients of risedronate sodium. It is often used in osteoporosis. eHealthMe is studying from 29,369 Actonel users. Check the latest studies of Actonel.

What is Rubella?

Rubella (an infection of the respiratory system caused by a virus) is found to be associated with 102 drugs and 117 conditions by eHealthMe. Check the latest studies of Rubella.

On Jul, 08, 2026

28,929 people reported to have side effects when taking Actonel.
Among them, 20 people (0.07%) have Rubella.

Among these 20 people:

What is the gender of people who have Rubella when taking Actonel? *

female: 100 %
male: 0.0 %

What is the age of people who have Rubella when taking Actonel? *

What are other drugs people take besides Actonel? *

What are other side effects people have besides Rubella? *

Weight Increased: 20 people, 100.00%
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 20 people, 100.00%
Basal Cell Carcinoma (a skin cancer, it rarely metastasizes or kills): 20 people, 100.00%
Blood Pressure Systolic Increased: 20 people, 100.00%
Cough: 20 people, 100.00%
Diarrhea: 20 people, 100.00%
Fever: 20 people, 100.00%
Fungal Infection: 20 people, 100.00%
Gastrointestinal Haemorrhage (bleeding gastrointestinal tract): 20 people, 100.00%
Heart Palpitations (feelings or sensations that your heart is pounding or racing): 20 people, 100.00%

What are the existing conditions these people have? *

Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 19 people, 95.00%
Pain: 19 people, 95.00%

* Approximation only. Some reports may have incomplete information.

Do you take Actonel and have Rubella?

- Check whether Rubella 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 Actonel:

Actonel (29,369 reports)

Rubella treatments and more:

Rubella (194 reports)

Browse all side effects of Actonel:

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 Rubella:

Rubella (102 drugs)

Browse all the conditions that are associated with Rubella:

Rubella (117 conditions)

Related publications that referenced our studies

Hirschmann S, Gibel A, Tsvelikhovsky I, Lisker A, "Late-Onset Psychosis and Risedronate Treatment for Osteoporosis: A Case Report", Clinical schizophrenia & related psychoses, 2013 May .
Ko KD, Cho BL, "Risedronate-related Localized Amnesia in an Elderly Patient with Osteoporosis", Journal of the Korean Geriatrics Society, 2012 Dec .
Hirschmann S, Gibel A, Tsvelikhovsky I, Lisker A, "Late-Onset Psychosis and Risedronate Treatment for Osteoporosis: A Case Report", Clinical schizophrenia & related psychoses, 2013 May .
Ko KD, Cho BL, "Risedronate-related Localized Amnesia in an Elderly Patient with Osteoporosis", Journal of the Korean Geriatrics Society, 2012 Dec .

How the study uses the data?

The study uses data from the FDA. It is based on risedronate sodium (the active ingredients of Actonel) and Actonel (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.