Nurtec odt and Product solubility abnormal - a phase IV clinical study of FDA data

Summary:

Product solubility abnormal is reported as a side effect among people who take Nurtec odt (rimegepant sulfate), especially for people who are female, 50-59 old, have been taking the drug for 1 - 6 months also take Losartan, and have Migraine.

The phase IV clinical study analyzes which people have Product solubility abnormal when taking Nurtec odt. It is created by eHealthMe based on reports of 9,149 people who have side effects when taking Nurtec odt from the FDA, and is updated regularly.

What is Nurtec odt?

Nurtec odt has active ingredients of rimegepant sulfate. eHealthMe is studying from 9,221 Nurtec odt users. Check the latest studies of Nurtec odt.

What is Product solubility abnormal?

Product solubility abnormal is found to be associated with 281 drugs and 327 conditions by eHealthMe. Check the latest studies of Product solubility abnormal.

On Jul, 11, 2026

9,149 people reported to have side effects when taking Nurtec odt.
Among them, 16 people (0.17%) have Product solubility abnormal.

Could Nurtec odt cause Product solubility abnormal?

Among these 16 people:

How long have people been on Nurtec odt when they have Product solubility abnormal? *

What is the gender of people who have Product solubility abnormal when taking Nurtec odt? *

female: 61.54 %
male: 38.46 %

What is the age of people who have Product solubility abnormal when taking Nurtec odt? *

What are other drugs people take besides Nurtec odt? *

What are other side effects people have besides Product solubility abnormal? *

Drug Ineffective: 4 people, 25.00%
Product Taste Abnormal: 3 people, 18.75%
Nausea (feeling of having an urge to vomit): 3 people, 18.75%
Indigestion: 2 people, 12.50%
Paraesthesia Oral (sensation of tingling, tickling, prickling, pricking, or burning of a person's oral with no apparent long-term physical effect): 1 person, 6.25%
Oesophageal Pain: 1 person, 6.25%
Malaise (a feeling of general discomfort or uneasiness): 1 person, 6.25%
Diarrhea: 1 person, 6.25%
Abdominal Pain Upper: 1 person, 6.25%
Abdominal Distension: 1 person, 6.25%

What are the existing conditions these people have? *

Migraine (headache): 9 people, 56.25%
Headache (pain in head): 1 person, 6.25%

* Approximation only. Some reports may have incomplete information.

Do you take Nurtec odt and have Product solubility abnormal?

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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Nurtec odt:

Nurtec odt (9,221 reports)

Browse all side effects of Nurtec odt:

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Browse all the drugs that are associated with Product solubility abnormal:

Product solubility abnormal (281 drugs)

Browse all the conditions that are associated with Product solubility abnormal:

Product solubility abnormal (327 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on rimegepant sulfate (the active ingredients of Nurtec odt) and Nurtec odt (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.