Aldactone and Erbitux drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Aldactone (spironolactone) and Erbitux (cetuximab). Common drug interactions include lethargy among females and mucosal inflammation among males.
The phase IV clinical study analyzes what interactions people have when they take Aldactone and Erbitux. It is created by eHealthMe based on reports of 70 people who take the same drugs from the FDA, and is updated regularly.
What is Aldactone?
Aldactone has active ingredients of spironolactone. It is often used in acne. eHealthMe is studying from 46,063 Aldactone users. Check the latest studies of Aldactone.
What is Erbitux?
Erbitux has active ingredients of cetuximab. It is often used in cancer. eHealthMe is studying from 19,276 Erbitux users. Check the latest studies of Erbitux.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
70 people who take Aldactone and Erbitux together, and have interactions are studied.

What are the common drug interactions of Aldactone and Erbitux, by gender? *:
female:
- Lethargy (tiredness)
- Malaise (a feeling of general discomfort or uneasiness)
- Melaena (the passage of black, tarry stools)
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Platelet count decreased
- Anorexia (eating disorder characterized by immoderate food restriction and irrational fear of gaining weight)
- Blood alkaline phosphatase increased
- Cyanosis (lack of oxygen in body leads to blue appearance of skin ,mucous membrane nails)
- Death
- Dysphagia (a condition in which swallowing is difficult or painful)
male:
- Mucosal inflammation (infection of mucous membrane)
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
- Pulmonary oedema (fluid accumulation in the lungs)
- Dermatitis acneiform (dermatoses including acne vulgaris, rosacea, folliculitis, and perioral dermatitis)
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
- Dysphagia (a condition in which swallowing is difficult or painful)
- General physical health deterioration (weak health status)
- Pain
- Stevens-johnson syndrome (an immune-complex-mediated hypersensitivity disorder. it ranges from mild skin and mucous membrane lesions to a severe)
- Acute respiratory distress syndrome
What are the common drug interactions of Aldactone and Erbitux, 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:
- Hyperbilirubinaemia (excess of bilirubin in the blood)
- Anaemia (lack of blood)
- Hepatic failure (liver failure)
- Platelet count decreased
- Malignant neoplasm progression (cancer tumour came back)
- Metastases to liver (cancer spreads to liver)
- Pyrexia (fever)
50-59:
- Febrile bone marrow aplasia (bone marrow greatly decreases or stops production of blood cells)
- Herpes zoster
- Infusion related reaction
- Neuropathy peripheral (surface nerve damage)
- Pruritus (severe itching of the skin)
- Stomatitis (inflammation of mucous membrane of mouth)
- Asthma
- Cyanosis (lack of oxygen in body leads to blue appearance of skin ,mucous membrane nails)
- Oedema peripheral (superficial swelling)
- Pain in extremity
60+:
- Mucosal inflammation (infection of mucous membrane)
- Diarrhoea
- Cardiac failure
- Pneumonia
- Pulmonary oedema (fluid accumulation in the lungs)
- Dehydration (dryness resulting from the removal of water)
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
- Hepatic cirrhosis (chronic liver disease characterized by replacement of liver tissue by fibrosis, scar tissue)
- Radiation skin injury
- Septic shock (shock due to blood infection)
What are the existing conditions these people have? *
- Colon Cancer: 32 people, 45.71%
- Oedema (fluid collection in tissue): 10 people, 14.29%
- Insomnia (sleeplessness): 7 people, 10.00%
- Hypopharyngeal Cancer: 7 people, 10.00%
- Cancer Pain: 6 people, 8.57%
- Cancer - Throat Or Larynx: 6 people, 8.57%
* Approximation only. Some reports may have incomplete information.
Do you take Aldactone and Erbitux?
- Personalize this study to your gender, age, symptoms and drugs
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Aldactone and Erbitux:
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 Aldactone:
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 Erbitux:
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 Aldactone 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 Erbitux 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 zRelated publications that referenced our studies
- Gupta D, Shukla P, Bisht SS, Bhatt ML, Pant MC, Srivastava K, "Deep vein and artery thrombosis associated with cetuximab-based chemoradiotherapy", Indian journal of pharmacology, 2011 Jan .
- Gupta D, Shukla P, Bisht SS, Bhatt ML, Pant MC, Srivastava K, "Deep vein and artery thrombosis associated with cetuximab-based chemoradiotherapy", Indian journal of pharmacology, 2011 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on spironolactone and cetuximab (the active ingredients of Aldactone and Erbitux, respectively), and Aldactone and Erbitux (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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