Votrient and Vitamin d3 drug interactions - a phase IV clinical study of FDA data
Drug interactions are reported among people who take Votrient and Vitamin d3. Common interactions include pain among females and diarrhoea among males.
The phase IV clinical study analyzes what interactions people who take Votrient and Vitamin d3 have. It is created by eHealthMe based on reports of 103 people who take Votrient and Vitamin d3 from the FDA, and is updated regularly. You can use the study as a second opinion to make health care decisions.
Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 600+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.
103 people who take Votrient and Vitamin d3 together, and have interactions are studied.
What is Votrient?
Votrient has active ingredients of pazopanib hydrochloride. It is often used in metastatic renal cell carcinoma. eHealthMe is studying from 24,021 Votrient users for its effectiveness, alternative drugs and more.
What is Vitamin d3?
Vitamin d3 has active ingredients of ergocalciferol. It is often used in mineral supplementation. eHealthMe is studying from 91,432 Vitamin d3 users for its effectiveness, alternative drugs and more.
Number of Votrient and Vitamin d3 reports submitted per year:
Votrient and Vitamin d3 drug interactions by gender *:
Votrient and Vitamin d3 drug interactions by age *:
Common conditions people have *:
* Approximation only. Some reports may have incomplete information.
Do you take Votrient and Vitamin d3?Personalize this study to your gender and age
How to use the study?
You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.
Related publications that referenced our studies
- Kapoor S, "Influence of Vitamin D Consumption and Levels on the Development of Psychiatric Disorders", Lee, Y. J., & Park, K. (2018). Secondary Raynaud’s Phenomenon and Skin Necrosis of Toes in the Paraplegic Patient with Hypertension.?Drug safety-case reports,?5(1), 7., 2014 Aug .
- Costa DA, de Almeida SB, Barata PC, Quintela A, Cabral P, Afonso A, Silva JM, "Pazopanib-Induced Cutaneous Leukocytoclastic Vasculitis: An Exclusion Diagnosis of a Multidisciplinary Approach", Case Reports in Oncology, 2013 Jan .
Alternative drugs to, pros and cons of the 2 drugs:
Browse all drug interactions of Votrient and Vitamin d3: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
Common Votrient interactions:
Browse all interactions between Votrient 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 z
Common Vitamin d3 interactions:
Browse all interactions between Vitamin d3 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 z
How the study uses the data?
The study uses data from the FDA. It is based on pazopanib hydrochloride and ergocalciferol (the active ingredients of Votrient and Vitamin d3, respectively), and Votrient and Vitamin d3 (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. Patients in the study may take other drugs besides Votrient and Vitamin d3.
Who is eHealthMe?
With medical big data and proven AI 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 600+ 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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