Claritin and Xylitol drug interactions - a phase IV clinical study of FDA data
Drug interactions are reported among people who take Claritin and Xylitol. Common interactions include retching among females and anaphylactic reaction among males.
The phase IV clinical study analyzes what interactions people who take Claritin and Xylitol have. It is created by eHealthMe based on reports of 12 people who take Claritin and Xylitol 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.
12 people who take Claritin and Xylitol together, and have interactions are studied.
What is Claritin?
Claritin has active ingredients of loratadine. It is often used in allergies. eHealthMe is studying from 71,087 Claritin users for its effectiveness, alternative drugs and more.
What is Xylitol?
Xylitol has active ingredients of xylitol. eHealthMe is studying from 237 Xylitol users for its effectiveness, alternative drugs and more.
Number of Claritin and Xylitol reports submitted per year:
Common Claritin and Xylitol drug interactions by gender *:
- Seasonal allergy
- Sinus pain
- Swelling face
- Blood pressure increased
- Anaphylactic reaction
- Rash generalised
Common Claritin and Xylitol drug interactions by age *:
- Anaphylactic reaction
- Rash generalised
- Heart rate increased
- Oesophageal spasm
- Sensation of foreign body
- Weight decreased
Common conditions people have *:
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 10 people, 83.33%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 10 people, 83.33%
- Type 2 Diabetes: 1 person, 8.33%
- Constipation: 1 person, 8.33%
- Attention Deficit Hyperactivity Disorder (a chronic condition including attention difficulty, hyperactivity, and impulsiveness): 1 person, 8.33%
* Approximation only. Some reports may have incomplete information.
Do you take Claritin and Xylitol?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.
Alternative drugs to, pros and cons of the 2 drugs:
Browse all drug interactions of Claritin and Xylitol: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 Claritin side effects:
- Drug ineffective: 9,483 reports
- Fatigue (feeling of tiredness): 4,365 reports
- Headache (pain in head): 3,454 reports
- Dizziness: 3,076 reports
- Breathing difficulty: 3,027 reports
- Pain: 2,986 reports
- Rashes (redness): 2,970 reports
Browse 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 z
Common Claritin interactions:
- Claritin and Aspirin: 6,621 reports
- Claritin and Flonase: 4,649 reports
- Claritin and Vitamin d: 4,631 reports
- Claritin and Tylenol: 4,361 reports
- Claritin and Prednisone: 4,315 reports
- Claritin and Singulair: 4,278 reports
- Claritin and Prilosec: 3,836 reports
- Claritin and Synthroid: 3,675 reports
- Claritin and Albuterol: 3,640 reports
- Claritin and Benadryl: 3,318 reports
Browse 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 z
How the study uses the data?
The study uses data from the FDA. It is based on loratadine and xylitol (the active ingredients of Claritin and Xylitol, respectively), and Claritin and Xylitol (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 Claritin and Xylitol.
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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