Review: could Celebrex cause Dementia alzheimer's type?
Summary: Dementia alzheimer's type is found among people who take Celebrex, especially for people who are female, 60+ old, have been taking the drug for 1 - 2 years, also take medication Ativan, and have Arthritis.
We study 72,911 people who have side effects while taking Celebrex from FDA and social media. Among them, 69 have Dementia alzheimer's type. Find out below who they are, when they have Dementia alzheimer's type and more.
You are not alone: join a support group for people who take Celebrex and have Dementia alzheimer's type >>>
Celebrex has active ingredients of celecoxib. It is often used in arthritis. (latest outcomes from 74,556 Celebrex users)
Dementia alzheimer's type
Dementia alzheimer's type (loss of mental ability with alzheimer's symptom) has been reported by people with high blood pressure, osteoporosis, depression, high blood cholesterol, diabetes. (latest reports from 13,063 Dementia alzheimer's type patients)
On Mar, 5, 2015: 72,903 people reported to have side effects when taking Celebrex. Among them, 69 people (0.09%) have Dementia Alzheimer's Type.
Time on Celebrex when people have Dementia alzheimer's type * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Dementia alzheimer's type||0.00%||22.22%||11.11%||44.44%||22.22%||0.00%||0.00% |
Gender of people who have Dementia alzheimer's type when taking Celebrex * :
|Dementia alzheimer's type||73.24%||26.76% |
Age of people who have Dementia alzheimer's type when taking Celebrex * :
|Dementia alzheimer's type||0.00%||0.00%||0.00%||0.00%||0.00%||12.00%||6.00%||82.00% |
Severity of Dementia alzheimer's type when taking Celebrex ** :
How people recovered from Dementia alzheimer's type ** :
Top conditions involved for these people * :
- Arthritis (12 people, 17.39%)
- Hypertension (10 people, 14.49%)
- Anxiety (9 people, 13.04%)
- Diabetes mellitus (8 people, 11.59%)
- Osteoarthritis (7 people, 10.14%)
Top co-used drugs for these people * :
- Ativan (21 people, 30.43%)
- Aspirin (19 people, 27.54%)
- Norvasc (15 people, 21.74%)
- Vioxx (15 people, 21.74%)
- Prevacid (14 people, 20.29%)
* 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.
Get connected: join our support group of celebrex and dementia alzheimer's type on
Do you have Dementia Alzheimer's Type while taking Celebrex?
You are not alone! Join a mobile support group on :
- support group for people who take Celebrex and have Dementia Alzheimer's Type
- support group for people who take Celebrex
- support group for people who have Dementia Alzheimer's Type
Drugs in real world that are associated with:
Could your condition cause:
- A study of side effects of Celebrex for a 42-year old woman with Degenerative Joint Disease. The patient has Back Pain - Low
- A study of drug interactions between Tramadol, Celebrex for a 65-year old woman with Arthritis - Osteoarthritis. The patient has Palpitations Aggravated, Dizziness Aggravated
- A study of drug interactions between Gabapentin, Celebrex for a 60-year old woman with Fibromyalgia, Spinal Column Stenosis. The patient has Weakness, Muscle Atrophy
- A study of drug interactions between Suboxone, Celebrex, Clonidine for a 32-year old man with Drug Addiction, Carpal Tunnel Syndrome, Adhd. The patient has Constipation Aggravated
- A study of side effects of Celebrex for a 54-year old woman with Arthritis. The patient has Skin - Dry, Eyes - Dry (lack of adequate tears)
Recent Celebrex related drug comparison:
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.