Travoprost and Ureaplasma infection - from FDA reports
Ureaplasma infection is reported only by a few people who take Travoprost. We study 811 people who have side effects while taking Travoprost from FDA. Among them, 1 have Ureaplasma infection. Find out below who they are, when they have Ureaplasma infection and more.
How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.
Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our original studies have been referenced on 500+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO. On eHealthMe, you can research drugs and monitor them (see testimonials).
811 people reported to have side effects when taking Travoprost.
Among them, 1 person (0.12%) has Ureaplasma infection
Number of reports submitted per year:
Gender of people who have Ureaplasma infection when taking Travoprost *:
- female: 100 %
- male: 0.0 %
Age of people who have Ureaplasma infection when taking Travoprost *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
Top conditions involved for these people *:
- Glaucoma (increased fluid pressure in the eye with vision loss): 1 person, 100.00%
- Depression: 1 person, 100.00%
- Crohn's Disease (condition that causes inflammation of the gastrointestinal tract): 1 person, 100.00%
Top co-used drugs for these people *:
- Valdoxan: 1 person, 100.00%
- Humira: 1 person, 100.00%
- Desloratadine: 1 person, 100.00%
Top other side effects for these people *:
- Urinary Tract Infection: 1 person, 100.00%
- Pneumonia Klebsiella (pneumonia caused by bacteria klebsiella): 1 person, 100.00%
- Pneumonia Bacterial (pneumonia associated with bacterial infection): 1 person, 100.00%
- Intraocular Pressure Increased: 1 person, 100.00%
- Infection Susceptibility Increased: 1 person, 100.00%
* Approximation only. Some reports may have incomplete information.
FDA reports used in this study
- Want to find out more about the FDA reports used in the study? You can request them from FDA.
Do you have Ureaplasma infection while taking Travoprost?
- Check whether a drug or a condition causes Ureaplasma infection
- Subscribe to monitor Ureaplasma infection in Travoprost
You are not alone:
Travoprost has active ingredients of travoprost. (latest outcomes from Travoprost 820 users)
Ureaplasma infection has been reported by people with hiv infection, immunodeficiency disorders, staphylococcal infection, crohn's disease, lung transplant (latest reports from 87 Ureaplasma infection patients).
Drugs that are associated with Ureaplasma infectionUreaplasma infection (42 drugs)
Could your condition cause Ureaplasma infectionUreaplasma infection (35 conditions)
Travoprost side effects
- Travoprost side effects (814 reports)
Browse all side effects of Travoprosta 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
What would happen?
Recent general studies
- Will you have Suppressed Lactation with Unisom? - 5 seconds ago
- Will you have B-Lymphocyte Count Decreased with Tamsulosin? - 8 seconds ago
- Will you have Radiation Injury with Sudafed? - 11 seconds ago
- Hydroxyzine Pamoate and D-Alanine drug interaction - 12 seconds ago
- Soma and Advil drug interaction - 13 seconds ago
Recent personal studies
- A study for a 55 year old woman who takes Cosentyx - 17 minutes ago
- A study for a 19 year old girl who takes Humira - an hour ago
- A study for a 29 year old man who takes Sertraline, Prilosec - 2 hours ago
- A study for a 21 year old woman who takes Nexplanon, Cotempla Xr-odt - 2 hours ago
- A study for a 54 year old woman who takes Maxalt, Wellbutrin - 3 hours ago
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
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, and has not been supported by scientific studies or clinical trials unless otherwise stated. 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.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.