Adalat and Alimta drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Adalat (nifedipine) and Alimta (pemetrexed disodium). Common drug interactions include cholestasis among females and platelet count decreased among males.
The phase IV clinical study analyzes what interactions people have when they take Adalat and Alimta. It is created by eHealthMe based on reports of 23 people who take the same drugs from the FDA, and is updated regularly.
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.
What is Alimta?
Alimta has active ingredients of pemetrexed disodium. eHealthMe is studying from 7,702 Alimta users. Check the latest studies of Alimta.
23 people who take Adalat and Alimta together, and have interactions are studied.

What are the common drug interactions of Adalat and Alimta, by gender? *:
female:
- Cholestasis (a condition where bile cannot flow from the liver to the duodenum)
- Liver injury
- Gamma-glutamyltransferase increased
- Transaminases increased
- Pancytopenia (medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets)
- Renal disorder (kidney disease)
- Anaemia (lack of blood)
- C-reactive protein increased
- Diarrhoea
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
male:
- Platelet count decreased
- Blood creatinine increased
- Tendon rupture (tear of tendon)
- Tendonitis (a condition that causes pain and swelling of tendons)
- Asthenia (weakness)
- Gastritis haemorrhagic (inflammation of stomach with bleeding)
- Gastrointestinal perforation (hole in the digestive tract)
- Hypokalaemia (low potassium)
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Peritonitis (inflammation of the peritoneum, the thin tissue that lines the inner wall of the abdomen and covers most of the abdominal organs)
What are the common drug interactions of Adalat and Alimta, 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:
- Blood creatinine increased
- Conjunctival hyperaemia (congestion of conjunctival vessels)
- Constipation
- Erythema (redness of the skin)
- Hyperuricaemia (level of uric acid in the blood that is abnormally high)
- Insomnia (sleeplessness)
- Neutropenic infection (infection with less neutrophil numbers in blood)
- Platelet count decreased
- Pyrexia (fever)
- Tendon rupture (tear of tendon)
50-59:
n/a
60+:
- Interstitial lung disease
- Transaminases increased
- C-reactive protein increased
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
- Gastritis haemorrhagic (inflammation of stomach with bleeding)
- Granulocyte count decreased
- Hypokalaemia (low potassium)
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Infection
- Pyrexia (fever)
What are the existing conditions these people have? *
- Lung Adenocarcinoma Stage Iii (the cancer has spread to nearby tissue or too far away lymph nodes): 6 people, 26.09%
- Constipation: 5 people, 21.74%
- Lung Cancer - Non-Small Cell (lung cancer): 4 people, 17.39%
- Lung Adenocarcinoma Metastatic (a form of non-small cell lung cancer spreads to other part): 4 people, 17.39%
- Insomnia (sleeplessness): 4 people, 17.39%
- Lung Neoplasm Malignant (cancer tumour of lung): 3 people, 13.04%
- Fever: 3 people, 13.04%
- Pain: 2 people, 8.70%
- Dyslipidaemia (abnormal amount of lipids): 2 people, 8.70%
- Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 2 people, 8.70%
* Approximation only. Some reports may have incomplete information.
Do you take Adalat and Alimta?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Adalat and Alimta:
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 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 zBrowse all side effects of Alimta:
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 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 zBrowse all interactions between Alimta 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 nifedipine and pemetrexed disodium (the active ingredients of Adalat and Alimta, respectively), and Adalat and Alimta (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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