Vivelle-dot and Zometa drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Vivelle-dot (estradiol) and Zometa (zoledronic acid). Common drug interactions include pain among females and chest pain among males.
The phase IV clinical study analyzes what interactions people have when they take Vivelle-dot and Zometa. It is created by eHealthMe based on reports of 35 people who take the same drugs from the FDA, and is updated regularly.
What is Vivelle-dot?
Vivelle-dot has active ingredients of estradiol. It is often used in hormone replacement therapy. eHealthMe is studying from 3,545 Vivelle-dot users. Check the latest studies of Vivelle-dot.
What is Zometa?
Zometa has active ingredients of zoledronic acid. It is often used in multiple myeloma. eHealthMe is studying from 71,434 Zometa users. Check the latest studies of Zometa.
35 people who take Vivelle-dot and Zometa together, and have interactions are studied.

What are the common drug interactions of Vivelle-Dot and Zometa, by gender? *:
female:
- Pain
- Abscess (pus)
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Depression
- Faecal incontinence (a lack of control over passing stool)
- Injury
- Lip and/or oral cavity cancer (cancer of lip or mouth)
- Lip discolouration
- Oedema peripheral (superficial swelling)
- Osteopenia (a condition where bone mineral density is lower than normal)
male:
- Chest pain
- Depression
- Cataract (clouding of the lens inside the eye)
- Fatigue (feeling of tiredness)
- Haematuria (presence of blood in urine)
- Hypersomnia (excessive daytime sleepiness (eds))
- Intervertebral disc degeneration (spinal disc degeneration)
- Malaise (a feeling of general discomfort or uneasiness)
- Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
- Metastases to bone (cancer spreads to bone)
What are the common drug interactions of Vivelle-Dot and Zometa, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Accident
- Affective disorder (mental disorder)
- Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection)
- Anaemia (lack of blood)
- Anxiety
- Aortic stenosis (obstruction to the outflow of blood from the left ventricle into the aorta)
- Aortic valve incompetence
- Arteriosclerosis coronary artery (thickening and hardening of arteries- coronary artery)
- Arthralgia (joint pain)
- Arthritis (form of joint disorder that involves inflammation of one or more joints)
40-49:
n/a
50-59:
- Oedema peripheral (superficial swelling)
- Osteoarthritis (a joint disease caused by cartilage loss in a joint)
- Osteoradionecrosis (irradiation of bones causes damage to osteocytes and impairs the blood supply)
- Retching (strong involuntary effort to vomit)
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Gastritis (inflammation of stomach)
- Wound infection staphylococcal
- Atelectasis (partial or complete collapse of the lung)
- Chondromalacia (anterior knee pain due to irritation of the cartilage on the under surface of the kneecap)
- Hydropneumothorax (presence of both air and fluid in the pleural space (lungs))
60+:
- Fatigue (feeling of tiredness)
- Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection)
- Malaise (a feeling of general discomfort or uneasiness)
- Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
- Metastases to bone (cancer spreads to bone)
- Metastases to skin (cancer spreads to skin)
- Osteoporosis (bones weak and more likely to break)
- Pain
- Renal impairment (severely reduced kidney function)
- Sinus arrhythmia (a naturally occurring variation in heart rate that occurs during a breathing cycle)
What are the existing conditions these people have? *
- Bone Density Abnormal: 18 people, 51.43%
- Osteoporosis (bones weak and more likely to break): 6 people, 17.14%
* Approximation only. Some reports may have incomplete information.
Do you take Vivelle-dot and Zometa?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Vivelle-dot (3,545 reports)
- Zometa (71,434 reports)
Browse all drug interactions of Vivelle-dot and Zometa:
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 zSub-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 Vivelle-dot:
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 side effects of Zometa:
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 interactions between Vivelle-dot and drugs from A to Z:
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 interactions between Zometa and drugs from A to Z:
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 zHow the study uses the data?
The study uses data from the FDA. It is based on estradiol and zoledronic acid (the active ingredients of Vivelle-dot and Zometa, respectively), and Vivelle-dot and Zometa (the brand names). 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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