Folate and Premarin drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Folate (folic acid) and Premarin (estrogens, conjugated). Common drug interactions include tooth disorder among females and dysphagia among males.
The phase IV clinical study analyzes what interactions people have when they take Folate and Premarin. It is created by eHealthMe based on reports of 39 people who take the same drugs from the FDA, and is updated regularly.
What is Folate?
Folate has active ingredients of folic acid. It is often used in rheumatoid arthritis. eHealthMe is studying from 6,546 Folate users. Check the latest studies of Folate.
What is Premarin?
Premarin has active ingredients of estrogens, conjugated. It is often used in hormone replacement therapy. eHealthMe is studying from 99,630 Premarin users. Check the latest studies of Premarin.
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 >>>.
39 people who take Folate and Premarin together, and have interactions are studied.

What are the common drug interactions of Folate and Premarin, by gender? *:
female:
- Tooth disorder (tooth disease)
- Visual impairment
- Anaemia (lack of blood)
- Cognitive disorder (mental health disorders affects learning, memory, perception, and problem solving)
- Pain
- Skin papilloma (a general medical term for a tumour of the skin or mucous membrane with finger-like projections)
- Bone disorder
- Colonic polyp (extra part of colon tissue grow in intestine)
- Decreased interest
- Dysgeusia (disorder of the sense of taste)
male:
- Dysphagia (a condition in which swallowing is difficult or painful)
- Insomnia (sleeplessness)
- Bone density increased
- Bone disorder
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Calcinosis (calcium deposits in any soft tissue)
- Cardiac arrest
- Carotid artery stenosis (narrowing of carotid artery)
- Cellulitis (infection under the skin)
- Cerebral atrophy (decrement in size of brain)
What are the common drug interactions of Folate and Premarin, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Pain
- Actinic keratosis (skin disease due to sun exposure)
- Adenomyosis (presence of ectopic glandular tissue found in muscle)
- Anaemia (lack of blood)
- Anxiety
- Arteriosclerosis coronary artery (thickening and hardening of arteries- coronary artery)
- Balance disorder
- Bone density increased
- Bone disorder
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
20-29:
n/a
30-39:
n/a
40-49:
- Supraventricular extrasystoles (premature electrical impulse in the heart, generated above the level of the ventricle)
- Adverse event
- Dysphagia (a condition in which swallowing is difficult or painful)
- Dysphonia (speech disorder attributable to a disorder of phonation)
- Fatigue (feeling of tiredness)
- Gait disturbance
- Insomnia (sleeplessness)
- Movement disorder (neurological syndromes where they may be excess of movement or a paucity of movement that is not connected to weakness)
- Muscular weakness (muscle weakness)
- Pain in extremity
50-59:
- Anaemia (lack of blood)
- Arthralgia (joint pain)
- Aspartate aminotransferase increased
- Atelectasis (partial or complete collapse of the lung)
- Atrophic vulvovaginitis (inflammation of the vulva)
- Bilirubin conjugated increased
- Blood alkaline phosphatase increased
- Blood bilirubin increased
- Blood cholesterol increased
- Blood pressure increased
60+:
- Anxiety
- Fall
- Dysgeusia (disorder of the sense of taste)
- Endometrial hyperplasia (enlargement of uterus wall)
- Femur fracture
- Foot deformity (functional disability of foot)
- General physical health deterioration (weak health status)
- Haematoma (collection of blood outside the blood vessels)
- Haematuria (presence of blood in urine)
- Hyperkeratosis (thickening of the outer layer of the skin)
What are the existing conditions these people have? *
- High Blood Pressure: 5 people, 12.82%
- Pain: 4 people, 10.26%
- Depression: 4 people, 10.26%
- Sleep Disorder: 4 people, 10.26%
- Stress And Anxiety: 3 people, 7.69%
- Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 3 people, 7.69%
- Chest Pain: 3 people, 7.69%
- Constipation: 3 people, 7.69%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 3 people, 7.69%
- Muscle Aches (muscle pain): 3 people, 7.69%
* Approximation only. Some reports may have incomplete information.
Do you take Folate and Premarin?
- 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 Folate and Premarin:
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 Folate:
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 Premarin:
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 Folate 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 Premarin 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 folic acid and estrogens, conjugated (the active ingredients of Folate and Premarin, respectively), and Folate and Premarin (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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