Ranitidine and Macroglossia - a phase IV clinical study of FDA data
Summary:
Macroglossia is reported as a side effect among people who take Ranitidine (ranitidine), especially for people who are female, 10-19 old, also take Acarbose, and have Epilepsy.
The phase IV clinical study analyzes which people have Macroglossia 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 Macroglossia?
Macroglossia (large tongue) is found to be associated with 114 drugs and 38 conditions by eHealthMe. Check the latest studies of Macroglossia.
233,168 people reported to have side effects when taking Ranitidine.
Among them, 15 people (0.01%) have Macroglossia.

Among these 15 people:
What is the gender of people who have Macroglossia when taking Ranitidine? *
- female: 80 %
- male: 20 %
What is the age of people who have Macroglossia when taking Ranitidine? *
- 0-1: 13.33 %
- 2-9: 0.0 %
- 10-19: 60.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 26.67 %
What are other drugs people take besides Ranitidine? *
- Lasix: 3 people, 20.00%
- Acarbose: 3 people, 20.00%
- Pulmicort Respules: 2 people, 13.33%
- Metoclopramide: 2 people, 13.33%
- Ketamine Hcl: 2 people, 13.33%
- Allopurinol Sodium: 2 people, 13.33%
- Vioxx: 1 person, 6.67%
- Tramadol: 1 person, 6.67%
- Timoptic: 1 person, 6.67%
- Proscar: 1 person, 6.67%
What are other side effects people have besides Macroglossia? *
- Laryngeal Oedema (swelling of larynx): 4 people, 26.67%
- Swelling Face: 3 people, 20.00%
- Dyspnea (difficult or laboured breathing): 3 people, 20.00%
- Drug Ineffective: 3 people, 20.00%
- Tongue Disorder (disease of tongue): 2 people, 13.33%
- Swollen Tongue (swelling of tongue): 1 person, 6.67%
- Infection: 1 person, 6.67%
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 1 person, 6.67%
- Arrhythmia Supraventricular (irregular heartbeat supraventricular origin): 1 person, 6.67%
What are the existing conditions these people have? *
- Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures): 7 people, 46.67%
- Seizures (abnormal excessive or synchronous neuronal activity in the brain): 6 people, 40.00%
* Approximation only. Some reports may have incomplete information.
Do you take Ranitidine and have Macroglossia?
- Check whether Macroglossia 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)
Macroglossia treatments and more:
- Macroglossia (665 reports)
How severe was Macroglossia 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 Macroglossia:
- Macroglossia (115 drugs)
Browse all the conditions that are associated with Macroglossia:
- Macroglossia (38 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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