Bethkis and Claritin drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Bethkis (tobramycin) and Claritin (loratadine). Common drug interactions include bronchiectasis among females and death among males.
The phase IV clinical study analyzes what interactions people have when they take Bethkis and Claritin. It is created by eHealthMe based on reports of 22 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 Claritin?
Claritin has active ingredients of loratadine. It is often used in allergies. eHealthMe is studying from 77,316 Claritin users. Check the latest studies of Claritin.
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 >>>.
22 people who take Bethkis and Claritin together, and have interactions are studied.

What are the common drug interactions of Bethkis and Claritin, by gender? *:
female:
- Bronchiectasis (abnormal widening of the bronchi or their branches, causing a risk of infection)
- Infective pulmonary exacerbation of cystic fibrosis (severe infective lung disease with production of abnormally thick mucus)
- Pyrexia (fever)
- Fatigue (feeling of tiredness)
- Acne (skin problems that cause pimples)
- Alanine aminotransferase increased
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Cough
- Device dislocation
- Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
male:
- Death
- Dyspnoea (difficult or laboured respiration)
- Upper respiratory tract infection
- Wheezing (a high-pitched whistling sound made while you breath)
- Adverse reaction
- Rash papular (redness with papule)
- Abdominal pain
- Gastric disorder (disease of stomach)
- Pneumonia
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
What are the common drug interactions of Bethkis and Claritin, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Asthma
- Bronchiectasis (abnormal widening of the bronchi or their branches, causing a risk of infection)
- Cystic fibrosis (disease of the secretary glands)
- Infective pulmonary exacerbation of cystic fibrosis (severe infective lung disease with production of abnormally thick mucus)
- Pyrexia (fever)
- Rash papular (redness with papule)
- Pneumonia
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
- Procedural complication
- Upper respiratory tract infection
10-19:
- Death
20-29:
- Cough
- Device dislocation
- Fatigue (feeling of tiredness)
- Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
- Infective pulmonary exacerbation of cystic fibrosis (severe infective lung disease with production of abnormally thick mucus)
- Pancreatitis (inflammation of pancreas)
- Pyrexia (fever)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Adverse reaction
- Abdominal pain
30-39:
n/a
40-49:
- Dyspnoea (difficult or laboured respiration)
- Gastric disorder (disease of stomach)
- Weight fluctuation
50-59:
- Dyspnoea (difficult or laboured respiration)
- Respiratory disorder (respiratory disease)
- Wheezing (a high-pitched whistling sound made while you breath)
60+:
n/a
What are the existing conditions these people have? *
- Cystic Fibrosis (disease of the secretary glands): 14 people, 63.64%
- Pseudomonas Infection (pseudomonas infection is caused by a bacterium, pseudomonas aeruginosa): 5 people, 22.73%
- Chronic Respiratory Failure: 4 people, 18.18%
- Infective Pulmonary Exacerbation Of Cystic Fibrosis (severe infective lung disease with production of abnormally thick mucus): 3 people, 13.64%
- Cystic Fibrosis Lung (fibrosis with cyst in the lung): 3 people, 13.64%
- Constipation: 3 people, 13.64%
- Asthma: 3 people, 13.64%
- Nausea (feeling of having an urge to vomit): 2 people, 9.09%
- Hypersensitivity: 2 people, 9.09%
- Fungal Infection: 2 people, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Bethkis and Claritin?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Bethkis and Claritin:
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 Claritin:
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 Claritin 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 zHow the study uses the data?
The study uses data from the FDA. It is based on tobramycin and loratadine (the active ingredients of Bethkis and Claritin, respectively), and Bethkis and Claritin (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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