Propofol and Adalat drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Propofol (propofol) and Adalat (nifedipine). Common drug interactions include abdominal pain upper among females and hypokalaemia among males.

The phase IV clinical study analyzes what interactions people have when they take Propofol and Adalat. It is created by eHealthMe based on reports of 63 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 Adalat?

Adalat has active ingredients of nifedipine. It is often used in high blood pressure. eHealthMe is studying from 20,940 Adalat users. Check the latest studies of Adalat.



On Jul, 16, 2026

63 people who take Propofol and Adalat together, and have interactions are studied.

Propofol and Adalat drug interactions.

What are the common drug interactions of Propofol and Adalat, by gender? *:

female:

  1. Abdominal pain upper
  2. Acute respiratory failure
  3. Anaemia (lack of blood)
  4. Asthenia (weakness)
  5. Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
  6. Blood pressure decreased
  7. Cardiac arrest
  8. Cardiac failure congestive
  9. Cardiac valve disease (heart valve disease)
  10. Coronary artery occlusion (complete obstruction of blood flow in a coronary artery)

male:

  1. Hypokalaemia (low potassium)
  2. Liver carcinoma ruptured (ruptured liver cancer tumour)
  3. Drug eruption (adverse drug reaction of the skin)
  4. Hepatitis b
  5. Anaphylactic reaction (serious allergic reaction)
  6. Hepatocellular damage (liver damage)
  7. Hepatomegaly (abnormal enlargement of the liver)
  8. Hyperkalaemia (damage to or disease of the kidney)
  9. Kidney transplant rejection
  10. Loss of consciousness

What are the common drug interactions of Propofol and Adalat, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

  1. Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
  2. Atrioventricular block complete (heart block complete)
  3. Blood triglycerides increased
  4. Bradycardia (abnormally slow heart action)
  5. Cardiac arrest
  6. Cardiogenic shock (inadequate circulation of blood)
  7. Electrocardiogram qt prolonged
  8. Hepatic steatosis (fatty liver disease)
  9. Hepatitis (inflammation of the liver)
  10. Hepatocellular damage (liver damage)

40-49:

  1. Hypokalaemia (low potassium)
  2. Liver carcinoma ruptured (ruptured liver cancer tumour)
  3. Aspartate aminotransferase increased
  4. Abdominal pain
  5. Diarrhoea
  6. Hepatic failure (liver failure)
  7. Kidney transplant rejection
  8. Loss of consciousness
  9. Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
  10. Anaphylactic reaction (serious allergic reaction)

50-59:

  1. Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
  2. Nausea (feeling of having an urge to vomit)
  3. Organ failure
  4. Pancreatitis (inflammation of pancreas)
  5. Pharyngeal oedema (abnormal accumulation of fluid in the cavities and intercellular spaces of the pharyngeal)
  6. Pneumonia
  7. Pyrexia (fever)
  8. Renal failure acute (rapid kidney dysfunction)
  9. Sepsis (a severe blood infection that can lead to organ failure and death)
  10. Septic shock (shock due to blood infection)

60+:

  1. Oxygen saturation decreased
  2. Stevens-johnson syndrome (an immune-complex-mediated hypersensitivity disorder. it ranges from mild skin and mucous membrane lesions to a severe)
  3. Fear
  4. Injury
  5. Renal failure (kidney dysfunction)
  6. Blister (small pocket of fluid within the upper layers of the skin caused by forceful rubbing (friction), burning, freezing, chemical exposure)
  7. Death
  8. Emotional distress
  9. Multi-organ failure (multisystem organ failure)
  10. Renal impairment (severely reduced kidney function)

What are the existing conditions these people have? *

  1. Nausea (feeling of having an urge to vomit): 11 people, 17.46%
  2. Pain: 10 people, 15.87%
  3. Hypoalbuminaemia (levels of albumin in blood serum are abnormally low): 9 people, 14.29%
  4. Oesophagitis (inflammation of oesophagus): 9 people, 14.29%
  5. Headache (pain in head): 9 people, 14.29%
  6. Hepatic Neoplasm Malignant (liver cancer): 9 people, 14.29%
  7. Hepatitis B: 9 people, 14.29%
  8. Abdominal Pain: 9 people, 14.29%
  9. Palmar-Plantar Erythrodysaesthesia Syndrome (hand-foot syndrome): 9 people, 14.29%
  10. Weakness: 8 people, 12.70%

* Approximation only. Some reports may have incomplete information.

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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 Adalat:

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 z

Sub-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 z

Browse all side effects of Adalat:

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 z

Browse 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 z

Browse all interactions between Adalat 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 z

How 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 Adalat, respectively), and Propofol and Adalat (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.

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