Zetia and Quadriparesis - from FDA reports
Quadriparesis is found among people who take Zetia, especially for people who are female, 50-59 old also take medication Prozac, and have Psoriatic arthropathy. This study is created by eHealthMe based on reports of 37,374 people who have side effects when taking Zetia from FDA, and is updated regularly.
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).
37,374 people reported to have side effects when taking Zetia.
Among them, 7 people (0.02%) have Quadriparesis
Number of reports submitted per year:
Gender of people who have Quadriparesis when taking Zetia *:
- female: 100 %
- male: 0.0 %
Age of people who have Quadriparesis when taking Zetia *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
Top conditions involved for these people *:
- Psoriatic Arthropathy (inflammation of the skin and joints with kin condition which typically causes patches (plaques) of red, scaly skin to develop): 5 people, 71.43%
- Multiple Allergies (allergy to multiple agents): 2 people, 28.57%
- Fungal Infection: 2 people, 28.57%
Top co-used drugs for these people *:
- Actos: 5 people, 71.43%
- Synthroid: 5 people, 71.43%
- Simvastatin: 5 people, 71.43%
- Amaryl: 5 people, 71.43%
- Prozac: 5 people, 71.43%
Top other side effects for these people *:
- Urinary Tract Infection: 7 people, 100.00%
- Weakness: 5 people, 71.43%
- Muscle Tightness: 5 people, 71.43%
- Conjunctivitis (pink eye): 5 people, 71.43%
- Demyelination (loss of the myelin covering of some nerve fibres resulting in their impaired function): 5 people, 71.43%
* 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 Quadriparesis while taking Zetia?
- Check whether a drug or a condition causes Quadriparesis
- Subscribe to monitor Quadriparesis in Zetia
You are not alone:
Zetia has active ingredients of ezetimibe. It is often used in high blood cholesterol. (latest outcomes from Zetia 38,321 users)
Quadriparesis (muscle weakness affecting all four limbs) has been reported by people with multiple sclerosis, high blood pressure, depression, rheumatoid arthritis, high blood cholesterol (latest reports from 1,095 Quadriparesis patients).
Drugs that are associated with QuadriparesisQuadriparesis (640 drugs)
Could your condition cause QuadriparesisQuadriparesis (507 conditions)
Zetia side effects
- Zetia side effects (37,386 reports)
Browse all side effects of Zetiaa 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
- Seroquel and Unisom drug interaction - a second ago
- Focalin Xr and Tysabri drug interaction - 2 seconds ago
- Will you have Seasonal Allergy with Propecia? - 3 seconds ago
- Will you have Gout with Creon? - 3 seconds ago
- Will you have Weight Increased with Zingiber Officinale? - 4 seconds ago
Recent personal studies
- A study for a 14 year old girl who takes Trazodone Hydrochloride, Singulair, Guanfacine Hydrochloride, Lamictal, Flovent, Latuda - 27 minutes ago
- A study for a 21 year old woman who takes Adderall 10, Adderall 30, Kariva - 43 minutes ago
- A study for a 19 year old girl who takes Prozac, Enskyce - 43 minutes ago
- A study for a 61 year old woman who takes Mobic, Meloxicam - an hour ago
- A study for a 61 year old woman who takes Melatonin, Mobic - an hour 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.