Claritin and Krystexxa drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Claritin (loratadine) and Krystexxa (pegloticase). Common drug interactions include infusion related reaction among females and infusion related reaction among males.
The phase IV clinical study analyzes what interactions people have when they take Claritin and Krystexxa. It is created by eHealthMe based on reports of 36 people who take the same drugs from the FDA, and is updated regularly.
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.
What is Krystexxa?
Krystexxa has active ingredients of pegloticase. eHealthMe is studying from 2,548 Krystexxa users. Check the latest studies of Krystexxa.
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 >>>.
36 people who take Claritin and Krystexxa together, and have interactions are studied.

What are the common drug interactions of Claritin and Krystexxa, by gender? *:
female:
- Infusion related reaction
- Drug ineffective
- Blood pressure increased
- Hyperhidrosis (abnormally increased sweating)
- Abdominal pain upper
- Therapeutic response decreased (less preventive response)
- Asthenia (weakness)
- Chest pain
- Fatigue (feeling of tiredness)
- Feeling hot
male:
- Infusion related reaction
- Gout (uric acid crystals building up in the body)
- Formication (a sensation that exactly resembles that of small insects crawling on (or under) the skin)
- Type iv hypersensitivity reaction (delayed type hypersensitivity as the reaction takes two to three days to develop)
- Affect lability (emotional incontinence)
- Anaemia (lack of blood)
- Depression
- Haemolysis (breaking open of red blood cells and the release of haemoglobin into the surrounding fluid)
- Infusion site extravasation (flow of (blood or lymph) from infusion site)
- Malaise (a feeling of general discomfort or uneasiness)
What are the common drug interactions of Claritin and Krystexxa, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Infusion related reaction
- Drug ineffective
- Therapeutic response decreased (less preventive response)
- Blood uric acid increased
- Gout (uric acid crystals building up in the body)
40-49:
- Infusion related reaction
- Drug ineffective
- Abdominal pain upper
- Blood pressure increased
- Hyperhidrosis (abnormally increased sweating)
- Blood uric acid increased
- Infusion site extravasation (flow of (blood or lymph) from infusion site)
- Anaphylactic reaction (serious allergic reaction)
- Gout (uric acid crystals building up in the body)
- Therapeutic response decreased (less preventive response)
50-59:
- Therapeutic response decreased (less preventive response)
- Infusion related reaction
- Anaphylactic reaction (serious allergic reaction)
- Blood uric acid increased
- Contusion (a type of hematoma of tissue in which capillaries)
- Fall
- Hypoaesthesia oral (reduced sense of touch or sensation in mouth)
- Pruritus (severe itching of the skin)
- Swollen tongue (swelling of tongue)
60+:
- Gout (uric acid crystals building up in the body)
- Chest pain
- Diarrhoea
- Haemolysis (breaking open of red blood cells and the release of haemoglobin into the surrounding fluid)
- Pruritus (severe itching of the skin)
- Weight decreased
- Weight increased
- Hypersensitivity
- Asthenia (weakness)
- Blood pressure increased
What are the existing conditions these people have? *
- Gout (uric acid crystals building up in the body): 30 people, 83.33%
- Gouty Tophus (a deposit of urates in the skin and tissue around a joint or in the external ear): 5 people, 13.89%
- Urticaria (rash of round, red welts on the skin that itch intensely): 2 people, 5.56%
- Pain: 2 people, 5.56%
- Muscle Spasms (muscle contraction): 2 people, 5.56%
- Back Pain: 2 people, 5.56%
- Asthma: 2 people, 5.56%
- Arrhythmias (irregular heartbeat): 2 people, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Claritin and Krystexxa?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Claritin and Krystexxa:
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 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 side effects of Krystexxa:
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 zBrowse all interactions between Krystexxa 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 loratadine and pegloticase (the active ingredients of Claritin and Krystexxa, respectively), and Claritin and Krystexxa (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.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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