Zometa and Full blood count abnormal - a phase IV clinical study of FDA data

Summary:

Full blood count abnormal is reported as a side effect among people who take Zometa (zoledronic acid), especially for people who are female, 60+ old, have been taking the drug for 1 - 2 years also take Ibrance, and have Breast cancer female.

The phase IV clinical study analyzes which people have Full blood count abnormal when taking Zometa. It is created by eHealthMe based on reports of 71,074 people who have side effects when taking Zometa from the FDA, and is updated regularly.

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.

What is Full blood count abnormal?

Full blood count abnormal is found to be associated with 628 drugs and 378 conditions by eHealthMe. Check the latest studies of Full blood count abnormal.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Aug, 31, 2026

71,074 people reported to have side effects when taking Zometa.
Among them, 98 people (0.14%) have Full blood count abnormal.

Could Zometa cause Full blood count abnormal?

Among these 98 people:

How long have people been on Zometa when they have Full blood count abnormal? *

What is the gender of people who have Full blood count abnormal when taking Zometa? *

female: 76.34 %
male: 23.66 %

What is the age of people who have Full blood count abnormal when taking Zometa? *

What are other drugs people take besides Zometa? *

What are other side effects people have besides Full blood count abnormal? *

Fatigue (feeling of tiredness): 42 people, 42.86%
White Blood Cell Count Decreased: 27 people, 27.55%
Impaired Healing: 25 people, 25.51%
Nausea (feeling of having an urge to vomit): 24 people, 24.49%
Pain In Jaw: 21 people, 21.43%
Dyspnea (difficult or laboured breathing): 21 people, 21.43%
Pain: 21 people, 21.43%
Anaemia (lack of blood): 20 people, 20.41%
Diarrhea: 19 people, 19.39%
Swelling: 19 people, 19.39%

What are the existing conditions these people have? *

Breast Cancer Female: 22 people, 22.45%
Pain: 12 people, 12.24%
Neoplasm Malignant (cancer tumour): 11 people, 11.22%
Sleep Disorder: 10 people, 10.20%
Eczema (patches of skin become rough and inflamed, with itching and bleeding blisters): 10 people, 10.20%
Prostate Cancer Metastatic: 10 people, 10.20%
Prostate Cancer: 7 people, 7.14%
Chest Pain: 5 people, 5.10%
Metastases To Bone (cancer spreads to bone): 3 people, 3.06%
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 3 people, 3.06%

* Approximation only. Some reports may have incomplete information.

Do you take Zometa and have Full blood count abnormal?

- Check whether Full blood count abnormal is associated with a drug or a condition
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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Zometa:

Zometa (71,434 reports)

Browse 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 z

Browse all the drugs that are associated with Full blood count abnormal:

Full blood count abnormal (628 drugs)

Browse all the conditions that are associated with Full blood count abnormal:

Full blood count abnormal (378 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on zoledronic acid (the active ingredients of Zometa) and Zometa (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.