Review: could Risperdal cause Death?
Summary: Death could be caused by Risperdal, especially for people who are male, 60+ old, have been taking the drug for < 1 month, also take Risperdal consta, and have Schizophrenia.
We study 41,444 people who have side effects while taking Risperdal from FDA and social media. Among them, 1,847 have Death. Find out below who they are, when they have Death and more.
On Apr, 13, 2014: 41,403 people reported to have side effects when taking Risperdal. Among them, 1,847 people (4.46%) have Death. They amount to 0.35% of all the 532,168 people who have Death on eHealthMe.
Time on Risperdal when people have Death * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Death when taking Risperdal * :
Age of people who have Death when taking Risperdal * :
Top conditions involved for these people * :
- Schizophrenia (339 people, 18.35%)
- Depression (93 people, 5.04%)
- Dementia (69 people, 3.74%)
- Psychotic disorder (68 people, 3.68%)
- Bipolar disorder (66 people, 3.57%)
Top co-used drugs for these people * :
- Risperdal consta (444 people, 24.04%)
- Seroquel (289 people, 15.65%)
- Zyprexa (171 people, 9.26%)
- Abilify (137 people, 7.42%)
- Aspirin (106 people, 5.74%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Related topic: Risperdal, Death
You can also:
On eHealthMe, Risperdal (risperidone) is often used for bipolar disorder. Find out below the conditions Risperdal is used for, how effective it is, and any alternative drugs that you can use to treat those same conditions.
What is Risperdal used for and how effective is it:
Other drugs that are used to treat the same conditions:
Could it be a symptom from a condition:
Drugs in real world that are associated with:
Could your condition cause it?
Comments from related studies:
From this study (11 months ago):
On July 24th 2009 she was given RESPIREDON .O25 MG tablets to control her agitation. Her agitation increased severely. And she began falling therefore, on August 2,2009 her dosage was increased to 1MG. She then completetly lost her ability to walk and she developed severe tremors and she lost her ability to situp. On August 5th, 2009 she was given CEFTRIAXONE, 1GM vial. She died on August 15, 2009.
Jason on May, 31, 2013:
31 year old male. I am taking risperdone and I had bad side effects from it. 2mg before going to sleep. I woke up to go to the bathroom and when I got up I almost dropped to the ground from side effects. I called th Dr. Shantala Umashankar in Norwich, CT and was told to cut pill in half and take 1mg. I took it and I woke up feeling groggy and light sensitive. I have had ADD in the past and I've been misdiagnosed with Bipolar Disorder and take another pill called Lamotrigrine which does nothing. I live with grandparents because I can't get a job because no one is hiring me. I tried to get SSI Benefits but unable to because system is FUBAR. All I hear is get a lawyer to fight to get SSI which is a waste of my time. I rather make my money rather than play the system because someone wants me to be their lab rat. Rather than work resolving a problem these doctors pushing pills like drug dealers to make money rather than provide real assistance to make things better.
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.