Ranitidine and Vitamin b12 increased - a phase IV clinical study of FDA data
Summary:
Vitamin b12 increased is reported as a side effect among people who take Ranitidine (ranitidine), especially for people who are female, 60+ old, also take Fish Oil, and have Primary myelofibrosis.
The phase IV clinical study analyzes which people have Vitamin b12 increased when taking Ranitidine. It is created by eHealthMe based on reports of 233,168 people who have side effects when taking Ranitidine from the FDA, and is updated regularly.
What is Ranitidine?
Ranitidine has active ingredients of ranitidine. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 234,475 Ranitidine users. Check the latest studies of Ranitidine.
What is Vitamin b12 increased?
Vitamin b12 increased is found to be associated with 217 drugs and 340 conditions by eHealthMe. Check the latest studies of Vitamin b12 increased.
233,168 people reported to have side effects when taking Ranitidine.
Among them, 18 people (0.01%) have Vitamin b12 increased.

Among these 18 people:
What is the gender of people who have Vitamin b12 increased when taking Ranitidine? *
- female: 62.5 %
- male: 37.5 %
What is the age of people who have Vitamin b12 increased when taking Ranitidine? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 14.29 %
- 40-49: 0.0 %
- 50-59: 28.57 %
- 60+: 57.14 %
What are other drugs people take besides Ranitidine? *
- Pamine Forte: 10 people, 55.56%
- Vitamin D3: 10 people, 55.56%
- Jakafi: 10 people, 55.56%
- Fish Oil: 10 people, 55.56%
- Pantoprazole: 5 people, 27.78%
- Aranesp: 3 people, 16.67%
- Fluoxetine: 2 people, 11.11%
- Metoclopramide Hydrochloride: 2 people, 11.11%
- Prochlorperazine: 2 people, 11.11%
- Sinemet: 2 people, 11.11%
What are other side effects people have besides Vitamin b12 increased? *
- Hypoaesthesia (reduced sense of touch or sensation): 10 people, 55.56%
- Nausea (feeling of having an urge to vomit): 10 people, 55.56%
- Nausea And Vomiting: 10 people, 55.56%
- White Blood Cell Count Increased: 9 people, 50.00%
- Peripheral Coldness: 9 people, 50.00%
- Blast Cells Present: 9 people, 50.00%
- Diarrhea: 9 people, 50.00%
- Energy Increased: 9 people, 50.00%
- Fatigue (feeling of tiredness): 9 people, 50.00%
- General Physical Condition Abnormal: 9 people, 50.00%
What are the existing conditions these people have? *
- Primary Myelofibrosis (primary disorder of the bone marrow): 10 people, 55.56%
- Polycythaemia Vera (blood disorder in which the bone marrow makes too many red blood cells): 9 people, 50.00%
- Chronic Renal Failure (kidney failure): 3 people, 16.67%
- High Density Lipoprotein Decreased: 1 person, 5.56%
- High Blood Pressure: 1 person, 5.56%
- Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 1 person, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Ranitidine and have Vitamin b12 increased?
- Check whether Vitamin b12 increased 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 Ranitidine:
- Ranitidine (234,475 reports)
Vitamin b12 increased treatments and more:
- Vitamin b12 increased (990 reports)
How severe was Vitamin b12 increased and when was it recovered:
Expand to all the drugs that have ingredients of ranitidine:
Sub-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 Ranitidine:
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 the drugs that are associated with Vitamin b12 increased:
- Vitamin b12 increased (217 drugs)
Browse all the conditions that are associated with Vitamin b12 increased:
- Vitamin b12 increased (340 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on ranitidine (the active ingredients of Ranitidine) and Ranitidine (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.
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