Diprivan and Bextra drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Diprivan (propofol) and Bextra (valdecoxib). Common drug interactions include aptyalism among females and anxiety among males.
The phase IV clinical study analyzes what interactions people have when they take Diprivan and Bextra. It is created by eHealthMe based on reports of 28 people who take the same drugs from the FDA, and is updated regularly.
What is Diprivan?
Diprivan has active ingredients of propofol. eHealthMe is studying from 6,496 Diprivan users. Check the latest studies of Diprivan.
What is Bextra?
Bextra has active ingredients of valdecoxib. It is often used in pain. eHealthMe is studying from 20,994 Bextra users. Check the latest studies of Bextra.
28 people who take Diprivan and Bextra together, and have interactions are studied.

What are the common drug interactions of Diprivan and Bextra, by gender? *:
female:
- Aptyalism (deficiency or absence of saliva)
- Cardiac failure congestive
- Asthma
- Bone disorder
- Bone erosion
- Bone fragmentation
- Bone pain
- Bronchopneumonia (inflammation of the lungs, arising in the bronchi or bronchioles)
- Cellulitis (infection under the skin)
- Colitis ulcerative (inflammation of colon with ulcer)
male:
- Anxiety
- Emotional disorder
- Fear
- Injury
- Multi-organ failure (multisystem organ failure)
- Renal failure (kidney dysfunction)
- Renal impairment (severely reduced kidney function)
- Renal injury (kidney injury)
- Stress
What are the common drug interactions of Diprivan and Bextra, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
n/a
50-59:
- Aptyalism (deficiency or absence of saliva)
- Cardiac failure congestive
- Asthma
- Bone disorder
- Bone erosion
- Bone fragmentation
- Bone pain
- Bronchopneumonia (inflammation of the lungs, arising in the bronchi or bronchioles)
- Cellulitis (infection under the skin)
- Colitis ulcerative (inflammation of colon with ulcer)
60+:
- Anxiety
- Emotional disorder
- Fear
- Injury
- Multi-organ failure (multisystem organ failure)
- Renal failure (kidney dysfunction)
- Renal impairment (severely reduced kidney function)
- Renal injury (kidney injury)
- Stress
What are the existing conditions these people have? *
- Systemic Lupus Erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue): 27 people, 96.43%
- Osteoporosis (bones weak and more likely to break): 27 people, 96.43%
- Thrombocytopenia (decrease of platelets in blood): 11 people, 39.29%
* Approximation only. Some reports may have incomplete information.
Do you take Diprivan and Bextra?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Diprivan and Bextra:
a b c d e f g h i j k l m n o p q r s t u v w x y zSub-studies by gender and age:
Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Diprivan:
a b c d e f g h i j k l m n o p q r s t u v w x y zBrowse all side effects of Bextra:
a b c d e f g h i j k l m n o p q r s t u v w x y zBrowse all interactions between Diprivan and drugs from A to Z:
a b c d e f g h i j k l m n o p q r s t u v w x y zBrowse all interactions between Bextra and drugs from A to Z:
a b c d e f g h i j k l m n o p q r s t u v w x y zHow the study uses the data?
The study uses data from the FDA. It is based on propofol and valdecoxib (the active ingredients of Diprivan and Bextra, respectively), and Diprivan and Bextra (the brand names). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.
How to use the study?
DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.
Who is eHealthMe?
With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).
WARNING, DISCLAIMER, USE FOR PUBLICATION
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. Our phase IV clinical studies alone cannot establish cause-effect relationship. 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.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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