Alendronate sodium and Vulval disorder - a phase IV clinical study of FDA data

Summary:

Vulval disorder is reported as a side effect among people who take Alendronate sodium (alendronate sodium), especially for people who are 60+ old, have been taking the drug for 1 - 6 months also take Fosamax, and have Sleep disorder.

The phase IV clinical study analyzes which people have Vulval disorder 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 Vulval disorder?

Vulval disorder is found to be associated with 148 drugs and 237 conditions by eHealthMe. Check the latest studies of Vulval disorder.

On Jul, 09, 2026

42,896 people reported to have side effects when taking Alendronate sodium.
Among them, 23 people (0.05%) have Vulval disorder.

Could Alendronate sodium cause Vulval disorder?

Among these 23 people:

How long have people been on Alendronate sodium when they have Vulval disorder? *

What is the age of people who have Vulval disorder when taking Alendronate sodium? *

What are other drugs people take besides Alendronate sodium? *

Fosamax: 21 people, 91.30%
Omega-3 Marine Triglycerides: 12 people, 52.17%
Vitamins: 11 people, 47.83%
Niacin: 11 people, 47.83%
Zocor: 7 people, 30.43%
Elavil: 6 people, 26.09%
Amitriptyline Hydrochloride: 6 people, 26.09%
Vagifem: 6 people, 26.09%
Aspirin: 6 people, 26.09%
Levothyroxine Sodium: 6 people, 26.09%

What are other side effects people have besides Vulval disorder? *

Femur Fracture: 21 people, 91.30%
Fall: 17 people, 73.91%
Osteoarthritis (a joint disease caused by cartilage loss in a joint): 16 people, 69.57%
Pain In Extremity: 13 people, 56.52%
Anaemia (lack of blood): 13 people, 56.52%
Nausea (feeling of having an urge to vomit): 12 people, 52.17%
Joint Pain: 11 people, 47.83%
Headache (pain in head): 11 people, 47.83%
Low Turnover Osteopathy (slow removal of old bone and its replacement by new bone): 11 people, 47.83%
Intervertebral Disc Protrusion (spinal disc protrusion): 9 people, 39.13%

What are the existing conditions these people have? *

Sleep Disorder: 6 people, 26.09%
Multiple Myeloma (cancer of the plasma cells): 1 person, 4.35%
Migraine (headache): 1 person, 4.35%
Itching: 1 person, 4.35%
Essential Hypertension (primary hypertension): 1 person, 4.35%
Asthma: 1 person, 4.35%
Allergic Rhinitis: 1 person, 4.35%

* Approximation only. Some reports may have incomplete information.

Do you take Alendronate sodium and have Vulval disorder?

- Check whether Vulval disorder 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 Vulval disorder:

Vulval disorder (148 drugs)

Browse all the conditions that are associated with Vulval disorder:

Vulval disorder (237 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.