Propofol and Procardia drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Propofol (propofol) and Procardia (nifedipine). Common drug interactions include unresponsive to stimuli among females and anxiety among males.
The phase IV clinical study analyzes what interactions people have when they take Propofol and Procardia. It is created by eHealthMe based on reports of 24 people who take the same drugs from the FDA, and is updated regularly.
What is Propofol?
Propofol has active ingredients of propofol. It is often used in colonoscopy abnormal. eHealthMe is studying from 38,224 Propofol users. Check the latest studies of Propofol.
What is Procardia?
Procardia has active ingredients of nifedipine. It is often used in high blood pressure. eHealthMe is studying from 15,151 Procardia users. Check the latest studies of Procardia.
24 people who take Propofol and Procardia together, and have interactions are studied.

What are the common drug interactions of Propofol and Procardia, by gender? *:
female:
- Unresponsive to stimuli
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Gallbladder disorder
- Psychiatric decompensation (worsening of symptoms to the state of a serious mental disorder)
- Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
- Post-operative pain
- Respiratory rate increased (excess breathing rate/min)
- Transfusion reaction (a serious problem that occurs after a patient receives a transfusion of blood)
- Renal failure (kidney dysfunction)
- Anxiety
male:
- Anxiety
- Pain
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Death
- Disability
- Hepatocellular damage (liver damage)
- Hyperkalaemia (damage to or disease of the kidney)
- Nervousness
- Renal impairment (severely reduced kidney function)
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
What are the common drug interactions of Propofol and Procardia, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Gallbladder disorder
- Psychiatric decompensation (worsening of symptoms to the state of a serious mental disorder)
20-29:
n/a
30-39:
- Procedural complication
- Propofol infusion syndrome
- Splenomegaly (enlargement of spleen)
- Vein wall hypertrophy (enlargement of vein wall)
- Ventricular hypertrophy (enlargement of ventricles (lower chambers) in the heart)
- Hyperkalaemia (damage to or disease of the kidney)
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Atrioventricular block complete (heart block complete)
- Blood triglycerides increased
- Bradycardia (abnormally slow heart action)
40-49:
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Blood pressure fluctuation
- Depression
- Disability
- Emotional distress
- Fear
- Injury
- Multi-organ failure (multisystem organ failure)
- Nervousness
50-59:
- Hepatic function abnormal
- Hepatocellular damage (liver damage)
- Hypersensitivity
- Hypotension (abnormally low blood pressure)
- Post-operative pain
- Respiratory rate increased (excess breathing rate/min)
60+:
- Renal failure (kidney dysfunction)
- Anxiety
- Multi-organ failure (multisystem organ failure)
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Asthenia (weakness)
- Drug hypersensitivity
- Hypersensitivity
- Acute respiratory distress syndrome
- Blood potassium increased
- Blood pressure fluctuation
What are the existing conditions these people have? *
- Indigestion: 4 people, 16.67%
- Diabetes: 3 people, 12.50%
- Insomnia (sleeplessness): 2 people, 8.33%
- Hyperlipidaemia (presence of excess lipids in the blood): 2 people, 8.33%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 2 people, 8.33%
- Back Pain: 2 people, 8.33%
- Arrhythmias (irregular heartbeat): 2 people, 8.33%
* Approximation only. Some reports may have incomplete information.
Do you take Propofol and Procardia?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Propofol and Procardia:
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 Propofol:
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 Procardia:
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 Propofol 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 Procardia 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 nifedipine (the active ingredients of Propofol and Procardia, respectively), and Propofol and Procardia (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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