Will you have Sudden death with Albenza - from FDA reports
Sudden death is found among people who take Albenza, especially for people who are male, 30-39 old , have been taking the drug for 1 - 6 months, also take medication Klonopin, and have Neurocysticercosis. This study is created by eHealthMe based on reports of 328 people who have side effects when taking Albenza from FDA, and is updated regularly.
eHealthMe is a health data analysis company based in Mountain View, California. eHealthMe monitors and analyzes the outcomes of drugs and supplements that are currently on the market. The results are readily available to health care professionals and consumers.
eHealthMe has released original studies on market drugs and worked with leading universities and institutions such as IBM, London Health Science Centre, Mayo Clinic, Northwestern University and VA. eHealthMe studies have now been referenced in over 500 peer-reviewed medical publications.
How we gather our data?
Healthcare data is obtained from a number of sources including the Food and Drug Administration (FDA). This information is aggregated and used to produce personalized reports that patients can reference.
The information that eHealthMe collects includes:
- Side effects (including severity and how people recover from them)
- Associated conditions or symptoms
- Drug effectiveness
- Demographic data regarding drug use
How the study uses the data?
The study is based on albendazole (the active ingredients of Albenza) and Albenza (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Synonyms of Sudden death are also considered in the study.
What is Albenza?
Albenza has active ingredients of albendazole. (latest outcomes from Albenza 340 users)
What is Sudden death?
Sudden death has been reported by people with multiple myeloma, primary pulmonary hypertension, pain, chronic myeloid leukaemia, diabetes (latest reports from 484,550 Sudden death patients).
How to use the study?
Patients can bring a copy of the report to their healthcare provider to ensure that all drug risks and benefits are fully discussed and understood. It is recommended that patients use the information presented as a part of a broader decision-making process.
328 people reported to have side effects when taking Albenza.
Among them, 6 people (1.83%) have Sudden death
Number of reports submitted per year:
Time on Albenza when people have Sudden death *:
- < 1 month: 0.0 %
- 1 - 6 months: 100 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
Gender of people who have Sudden death when taking Albenza *:
- female: 50 %
- male: 50 %
Age of people who have Sudden death when taking Albenza *:
- 0-1: 0.0 %
- 2-9: 50 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 50 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 0.0 %
Top conditions involved for these people *:
- Neurocysticercosis (cysts in the functional part of the brain): 2 people, 33.33%
- Pinworms: 1 person, 16.67%
Top co-used drugs for these people *:
- Klonopin: 2 people, 33.33%
Top other side effects for these people *:
- Nausea And Vomiting: 2 people, 33.33%
* Approximation only. Some reports may have incomplete information.
Do you have Sudden death while taking Albenza?
- Check whether a drug or a condition causes Sudden death
- Subscribe to monitor Sudden death in Albenza
- Subscribe to monitor Albenza
You are not alone, use our "Ginger Health" app to:
- connect with people like you who take Albenza and have Sudden death
- use your healthcare experience to help people like you, and be rewarded
Drugs that are associated with Sudden deathSudden death (3,551 drugs)
Could your condition cause Sudden deathSudden death (3,584 conditions)
Albenza side effects
- Albenza side effects (328 reports)
Browse side effects by gender and age
Browse all side effects of Albenzaa 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?
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.
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