Bethkis and Ceftazidime drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Bethkis (tobramycin) and Ceftazidime (ceftazidime). Common drug interactions include weight decreased among females and infective pulmonary exacerbation of cystic fibrosis among males.
The phase IV clinical study analyzes what interactions people have when they take Bethkis and Ceftazidime. It is created by eHealthMe based on reports of 20 people who take the same drugs from the FDA, and is updated regularly.
What is Bethkis?
Bethkis has active ingredients of tobramycin. eHealthMe is studying from 2,409 Bethkis users. Check the latest studies of Bethkis.
What is Ceftazidime?
Ceftazidime has active ingredients of ceftazidime. eHealthMe is studying from 10,327 Ceftazidime users. Check the latest studies of Ceftazidime.
20 people who take Bethkis and Ceftazidime together, and have interactions are studied.

What are the common drug interactions of Bethkis and Ceftazidime, by gender? *:
female:
- Weight decreased
- Cystic fibrosis (disease of the secretary glands)
- Hospitalisation
- Infective pulmonary exacerbation of cystic fibrosis (severe infective lung disease with production of abnormally thick mucus)
- Inflammation
male:
- Infective pulmonary exacerbation of cystic fibrosis (severe infective lung disease with production of abnormally thick mucus)
- Acidosis (build-up of carbon dioxide in the blood)
- Constipation
- Cough
- Cystic fibrosis (disease of the secretary glands)
- Diarrhoea
- Dysphagia (a condition in which swallowing is difficult or painful)
- Dyspnoea (difficult or laboured respiration)
- Gastroenteritis norovirus (inflammation of stomach and intestine caused by norovirus infection)
- Gastrointestinal disorder (functional problems of gastrointestinal tract)
What are the common drug interactions of Bethkis and Ceftazidime, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Cystic fibrosis (disease of the secretary glands)
- Hospitalisation
- Infective pulmonary exacerbation of cystic fibrosis (severe infective lung disease with production of abnormally thick mucus)
- Inflammation
30-39:
- Infective pulmonary exacerbation of cystic fibrosis (severe infective lung disease with production of abnormally thick mucus)
- Acidosis (build-up of carbon dioxide in the blood)
- Constipation
- Cough
- Cystic fibrosis (disease of the secretary glands)
- Diarrhoea
- Dysphagia (a condition in which swallowing is difficult or painful)
- Dyspnoea (difficult or laboured respiration)
- Gastroenteritis norovirus (inflammation of stomach and intestine caused by norovirus infection)
- Gastrointestinal disorder (functional problems of gastrointestinal tract)
40-49:
n/a
50-59:
n/a
60+:
n/a
What are the existing conditions these people have? *
- Cystic Fibrosis (disease of the secretary glands): 19 people, 95.00%
- Wheezing (a high-pitched whistling sound made while you breath): 9 people, 45.00%
- High Blood Pressure: 9 people, 45.00%
- Asthma: 9 people, 45.00%
- Attention Deficit Hyperactivity Disorder (a chronic condition including attention difficulty, hyperactivity, and impulsiveness): 9 people, 45.00%
- Blood Glucose Decreased: 9 people, 45.00%
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes): 9 people, 45.00%
- Cough: 9 people, 45.00%
- Sedation: 9 people, 45.00%
- Fungal Infection: 9 people, 45.00%
* Approximation only. Some reports may have incomplete information.
Do you take Bethkis and Ceftazidime?
- 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:
- Bethkis (2,409 reports)
- Ceftazidime (10,327 reports)
Browse all drug interactions of Bethkis and Ceftazidime:
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 Bethkis:
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 Ceftazidime:
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 Bethkis 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 Ceftazidime 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 zRelated publications that referenced our studies
- Chen F, Zhan Z, "Severe drug-induced immune haemolytic anaemia due to ceftazidime", Blood Transfusion, 2014 Jan .
- Chen F, Zhan Z, "Severe drug-induced immune haemolytic anaemia due to ceftazidime", Blood Transfusion, 2014 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on tobramycin and ceftazidime (the active ingredients of Bethkis and Ceftazidime, respectively), and Bethkis and Ceftazidime (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.
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