Provera and Vytorin drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Provera (medroxyprogesterone acetate) and Vytorin (ezetimibe; simvastatin). Common drug interactions include breast cancer female among females and anxiety among males.
The phase IV clinical study analyzes what interactions people have when they take Provera and Vytorin. It is created by eHealthMe based on reports of 46 people who take the same drugs from the FDA, and is updated regularly.
What is Provera?
Provera has active ingredients of medroxyprogesterone acetate. It is often used in birth control. eHealthMe is studying from 54,943 Provera users. Check the latest studies of Provera.
What is Vytorin?
Vytorin has active ingredients of ezetimibe; simvastatin. It is often used in high blood cholesterol. eHealthMe is studying from 20,084 Vytorin users. Check the latest studies of Vytorin.
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 >>>.
46 people who take Provera and Vytorin together, and have interactions are studied.

What are the common drug interactions of Provera and Vytorin, by gender? *:
female:
- Breast cancer female
- Weight fluctuation
- Breast cancer
- Diarrhoea
- Rash
- Dyspnoea (difficult or laboured respiration)
- Flushing (the warm, red condition of human skin)
- Gingivitis (inflammation of gums)
- Stomatitis (inflammation of mucous membrane of mouth)
- Depression suicidal (suicide depressive disorder)
male:
- Anxiety
- Blood glucose increased
- Breast cancer female
- Depression
- Asthma
- Facial pain
- Headache (pain in head)
- Hyperhidrosis (abnormally increased sweating)
- Nasal congestion (blockage of the nasal passages usually due to membranes lining the nose becoming swollen from inflamed blood vessels)
- Sinusitis (inflammation of sinus)
What are the common drug interactions of Provera and Vytorin, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Activated partial thromboplastin time prolonged
- Chest pain
- Weight decreased
30-39:
- Drug hypersensitivity
- Eye pain
- Facial pain
- Headache (pain in head)
- Myalgia (muscle pain)
- Nasal congestion (blockage of the nasal passages usually due to membranes lining the nose becoming swollen from inflamed blood vessels)
- Rhinalgia (pain in the nose)
- Sinusitis (inflammation of sinus)
- Teething (process by which an infant's first teeth grows)
- Throat irritation
40-49:
- Depression suicidal (suicide depressive disorder)
- Diarrhoea
- Rash
- Vomiting
- Abdominal pain upper
- Dyspnoea (difficult or laboured respiration)
- Feeling hot
- Pruritus (severe itching of the skin)
- Swelling
- Tachycardia (a heart rate that exceeds the range of 100 beats/min)
50-59:
- Breast cancer
- Breast cancer stage i
- Breast cancer female
- Dental care
- Gingivitis (inflammation of gums)
- Glossodynia (a burning or painful sensation in the tongue)
- Stomatitis (inflammation of mucous membrane of mouth)
- Weight increased
60+:
- Breast cancer female
- Diarrhoea
- Anaemia postoperative
- Atrophic vulvovaginitis (inflammation of the vulva)
- Breast cyst
- Cervical polyp (tumour on the surface of the cervical canal)
- Concussion (short loss of normal brain function in response to a head injury)
- Cyst (a closed sac)
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Fall
What are the existing conditions these people have? *
- Quit Smoking: 7 people, 15.22%
- Depression: 7 people, 15.22%
- Insomnia (sleeplessness): 5 people, 10.87%
- Diabetes: 5 people, 10.87%
- Menopause (end of monthly cycles in women): 4 people, 8.70%
- Menopausal Symptoms: 4 people, 8.70%
- Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 4 people, 8.70%
- High Blood Pressure: 4 people, 8.70%
- Weight Loss: 3 people, 6.52%
- Type 2 Diabetes: 3 people, 6.52%
* Approximation only. Some reports may have incomplete information.
Do you take Provera and Vytorin?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Provera and Vytorin:
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 Provera:
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 Vytorin:
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 Provera 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 Vytorin 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
- Bahall M, Reyes AJ, Ramcharan K, Hosein N, Seegobin K, Bahall K, Sharma H, Dhansingh S, Mahabir A, "Neuro-ophthalmological manifestations after intramuscular medroxyprogesterone: a forme fruste of idiopathic intracranial hypertension?", Neurology international, 2016 Sep .
- Bahall M, Reyes AJ, Ramcharan K, Hosein N, Seegobin K, Bahall K, Sharma H, Dhansingh S, Mahabir A, "Neuro-ophthalmological manifestations after intramuscular medroxyprogesterone: a forme fruste of idiopathic intracranial hypertension?", Neurology international, 2016 Sep .
How the study uses the data?
The study uses data from the FDA. It is based on medroxyprogesterone acetate and ezetimibe; simvastatin (the active ingredients of Provera and Vytorin, respectively), and Provera and Vytorin (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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