Lovastatin and Emla drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Lovastatin (lovastatin) and Emla (lidocaine; prilocaine). Common drug interactions include haemoglobin decreased among females and lentigo maligna stage unspecified among males.
The phase IV clinical study analyzes what interactions people have when they take Lovastatin and Emla. It is created by eHealthMe based on reports of 18 people who take the same drugs from the FDA, and is updated regularly.
What is Lovastatin?
Lovastatin has active ingredients of lovastatin. It is often used in high blood cholesterol. eHealthMe is studying from 33,048 Lovastatin users. Check the latest studies of Lovastatin.
What is Emla?
Emla has active ingredients of lidocaine; prilocaine. eHealthMe is studying from 5,276 Emla users. Check the latest studies of Emla.
18 people who take Lovastatin and Emla together, and have interactions are studied.

What are the common drug interactions of Lovastatin and Emla, by gender? *:
female:
- Haemoglobin decreased
- Platelet count decreased
- Headache (pain in head)
- Hypoaesthesia (reduced sense of touch or sensation)
- Abdominal hernia
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Constipation
- Diarrhoea
- Drug ineffective
- Full blood count decreased
male:
- Lentigo maligna stage unspecified (colour forming cells cancer of in situ on skin unspecified)
- Anaemia (lack of blood)
- Aortic stenosis (obstruction to the outflow of blood from the left ventricle into the aorta)
- Cardiac failure congestive
- Disease progression
- Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
- Malignant neoplasm progression (cancer tumour came back)
- Myelodysplastic syndrome (a group of conditions that occur when the blood-forming cells in the bone marrow are damaged)
- Rectal haemorrhage (bleeding from anus)
What are the common drug interactions of Lovastatin and Emla, 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:
- Arthralgia (joint pain)
- Arthritis (form of joint disorder that involves inflammation of one or more joints)
- Back pain
- Bone lesion (bone with abnormalities. bone lesions can result from growth formations, infections, or injuries)
- Bone marrow disorder
- Contusion (a type of hematoma of tissue in which capillaries)
- Disease progression
- Drug ineffective
- Fall
- Fatigue (feeling of tiredness)
60+:
- Lentigo maligna stage unspecified (colour forming cells cancer of in situ on skin unspecified)
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Dry mouth
- Fatigue (feeling of tiredness)
- Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
- Malignant neoplasm progression (cancer tumour came back)
- Muscle spasms (muscle contraction)
- Rectal haemorrhage (bleeding from anus)
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Visual impairment
What are the existing conditions these people have? *
- Nausea (feeling of having an urge to vomit): 9 people, 50.00%
- Multiple Myeloma (cancer of the plasma cells): 5 people, 27.78%
- Renal Cell Carcinoma (a kidney cancer): 3 people, 16.67%
- Nausea And Vomiting: 3 people, 16.67%
- Urinary Tract Infection: 2 people, 11.11%
- Herpes Simplex (herpes simplex is a common viral infection): 2 people, 11.11%
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 2 people, 11.11%
- Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 2 people, 11.11%
- Constipation: 2 people, 11.11%
- Cough: 2 people, 11.11%
* Approximation only. Some reports may have incomplete information.
Do you take Lovastatin and Emla?
- 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:
- Lovastatin (33,048 reports)
- Emla (5,276 reports)
Browse all drug interactions of Lovastatin and Emla:
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 Lovastatin:
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 Emla:
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 Lovastatin 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 Emla 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 lovastatin and lidocaine; prilocaine (the active ingredients of Lovastatin and Emla, respectively), and Lovastatin and Emla (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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