Saphris and Product taste abnormal - a phase IV clinical study of FDA data

Summary:

Product taste abnormal is reported as a side effect among people who take Saphris (asenapine maleate), especially for people who are female, 30-39 old, have been taking the drug for 1 - 6 months also take Levothyroxine Sodium, and have Psychotic disorder.

The phase IV clinical study analyzes which people have Product taste abnormal when taking Saphris. It is created by eHealthMe based on reports of 8,449 people who have side effects when taking Saphris from the FDA, and is updated regularly.

What is Saphris?

Saphris has active ingredients of asenapine maleate. It is often used in bipolar i disorder. eHealthMe is studying from 8,688 Saphris users. Check the latest studies of Saphris.

What is Product taste abnormal?

Product taste abnormal is found to be associated with 556 drugs and 574 conditions by eHealthMe. Check the latest studies of Product taste abnormal.

On Aug, 13, 2026

8,449 people reported to have side effects when taking Saphris.
Among them, 59 people (0.7%) have Product taste abnormal.

Could Saphris cause Product taste abnormal?

Among these 59 people:

How long have people been on Saphris when they have Product taste abnormal? *

What is the gender of people who have Product taste abnormal when taking Saphris? *

female: 73.08 %
male: 26.92 %

What is the age of people who have Product taste abnormal when taking Saphris? *

What are other drugs people take besides Saphris? *

Levothyroxine Sodium: 5 people, 8.47%
Zyprexa: 2 people, 3.39%
Synthroid: 2 people, 3.39%
Depakote: 2 people, 3.39%
Aspirin: 2 people, 3.39%
Metformin: 2 people, 3.39%
Trazodone Hydrochloride: 2 people, 3.39%
Lamictal: 2 people, 3.39%
Lamotrigine: 2 people, 3.39%
Xanax: 2 people, 3.39%

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

Hypoaesthesia Oral (reduced sense of touch or sensation in mouth): 10 people, 16.95%
Taste - Impaired: 10 people, 16.95%
Nausea (feeling of having an urge to vomit): 8 people, 13.56%
Drug Ineffective: 5 people, 8.47%
Agitation (state of anxiety or nervous excitement): 4 people, 6.78%
Dizziness: 4 people, 6.78%
Insomnia (sleeplessness): 4 people, 6.78%
Oral Discomfort (pain or irritation in mouth): 3 people, 5.08%
Drowsiness: 3 people, 5.08%
Pharyngeal Hypoaesthesia (pharyngeal -abnormally decreased sensitivity): 3 people, 5.08%

What are the existing conditions these people have? *

Stress And Anxiety: 2 people, 3.39%
Sleep Disorder: 2 people, 3.39%
Schizophrenia (a mental disorder characterized by a breakdown of thought processes): 2 people, 3.39%
Anger: 2 people, 3.39%
Psychotic Disorder: 2 people, 3.39%
Urinary Retention (the inability to completely or partially empty the bladder): 1 person, 1.69%
Depression: 1 person, 1.69%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 1.69%
Dysmorphism (difference of body structure that is suggestive of a congenital disorder): 1 person, 1.69%
Diarrhea: 1 person, 1.69%

* Approximation only. Some reports may have incomplete information.

Do you take Saphris and have Product taste abnormal?

- Check whether Product taste abnormal is associated with a drug or a condition
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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Saphris:

Saphris (8,688 reports)

Browse all side effects of Saphris:

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

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

Product taste abnormal (556 drugs)

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

Product taste abnormal (574 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on asenapine maleate (the active ingredients of Saphris) and Saphris (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.