Alendronate sodium and Oral discharge - a phase IV clinical study of FDA data

Summary:

Oral discharge is reported as a side effect among people who take Alendronate sodium (alendronate sodium), especially for people who are female, 60+ old, have been taking the drug for 2 - 5 years also take Rabeprazole Sodium, and have High blood pressure.

The phase IV clinical study analyzes which people have Oral discharge when taking Alendronate sodium. It is created by eHealthMe based on reports of 42,896 people who have side effects when taking Alendronate sodium from the FDA, and is updated regularly.

What is Alendronate sodium?

Alendronate sodium has active ingredients of alendronate sodium. It is often used in osteoporosis. eHealthMe is studying from 43,608 Alendronate sodium users. Check the latest studies of Alendronate sodium.

What is Oral discharge?

Oral discharge is found to be associated with 172 drugs and 170 conditions by eHealthMe. Check the latest studies of Oral discharge.

On Jul, 17, 2026

42,896 people reported to have side effects when taking Alendronate sodium.
Among them, 12 people (0.03%) have Oral discharge.

Could Alendronate sodium cause Oral discharge?

Among these 12 people:

How long have people been on Alendronate sodium when they have Oral discharge? *

What is the gender of people who have Oral discharge when taking Alendronate sodium? *

female: 72.73 %
male: 27.27 %

What is the age of people who have Oral discharge when taking Alendronate sodium? *

What are other drugs people take besides Alendronate sodium? *

What are other side effects people have besides Oral discharge? *

Osteonecrosis Of Jaw (death of bone of jaw): 12 people, 100.00%
Jaw Fracture: 9 people, 75.00%
Oral Disorder (mouth disease): 6 people, 50.00%
Dry Mouth: 6 people, 50.00%
Tooth Disorder (tooth disease): 6 people, 50.00%
Impaired Healing: 6 people, 50.00%
Osteomyelitis Chronic (long lasting infection of bone marrow): 3 people, 25.00%
Osteomyelitis (infection of bone): 3 people, 25.00%
Osteitis (a general term for inflammation of bone): 3 people, 25.00%
Gums - Swollen: 3 people, 25.00%

What are the existing conditions these people have? *

Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 3 people, 25.00%
High Blood Pressure: 3 people, 25.00%

* Approximation only. Some reports may have incomplete information.

Do you take Alendronate sodium and have Oral discharge?

- Check whether Oral discharge 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 Alendronate sodium:

Alendronate sodium (43,608 reports)

Browse all side effects of Alendronate sodium:

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 Oral discharge:

Oral discharge (172 drugs)

Browse all the conditions that are associated with Oral discharge:

Oral discharge (170 conditions)

Related publications that referenced our studies

Stuckey BG, Sallie R, "Alendronate-induced unmasking or deterioration of coeliac disease: a case series", Osteoporosis International, 2015 Jan .
Lee WY, Sun LM, Lin MC, Liang JA, Chang SN, Sung FC, Muo CH, Kao CH, "A higher dosage of oral alendronate will increase the subsequent cancer risk of osteoporosis patients in Taiwan: a population-based cohort study", PloS one, 2012 Dec .
Stuckey BG, Sallie R, "Alendronate-induced unmasking or deterioration of coeliac disease: a case series", Osteoporosis International, 2015 Jan .
Lee WY, Sun LM, Lin MC, Liang JA, Chang SN, Sung FC, Muo CH, Kao CH, "A higher dosage of oral alendronate will increase the subsequent cancer risk of osteoporosis patients in Taiwan: a population-based cohort study", PloS one, 2012 Dec .

How the study uses the data?

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