Micronor and Poor venous access - a phase IV clinical study of FDA data
Summary:
Poor venous access is reported as a side effect among people who take Micronor (norethindrone), especially for people who are also take Inflectra, and have Crohn's disease.
The phase IV clinical study analyzes which people have Poor venous access when taking Micronor. It is created by eHealthMe based on reports of 1,220 people who have side effects when taking Micronor from the FDA, and is updated regularly.
What is Micronor?
Micronor has active ingredients of norethindrone. It is often used in birth control. eHealthMe is studying from 1,344 Micronor users. Check the latest studies of Micronor.
What is Poor venous access?
Poor venous access is found to be associated with 677 drugs and 480 conditions by eHealthMe. Check the latest studies of Poor venous access.
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 >>>.
1,220 people reported to have side effects when taking Micronor.
Among them, 13 people (1.07%) have Poor venous access.

Among these 13 people:
What are other drugs people take besides Micronor? *
- Inflectra: 13 people, 100.00%
- Zopiclone: 4 people, 30.77%
- Prednisone: 4 people, 30.77%
- Pentasa: 4 people, 30.77%
- Mesalamine: 4 people, 30.77%
- Dilaudid: 4 people, 30.77%
- Ativan: 4 people, 30.77%
- Adderall: 4 people, 30.77%
What are other side effects people have besides Poor venous access? *
- Maternal Exposure During Pregnancy (use of substance during pregnancy): 12 people, 92.31%
- Anal Fissure: 9 people, 69.23%
- Migraine (headache): 9 people, 69.23%
- Asthma: 9 people, 69.23%
- Hair Loss: 9 people, 69.23%
- Soft Tissue Infection: 8 people, 61.54%
- Weight Decreased: 7 people, 53.85%
- Heart Rate Increased: 5 people, 38.46%
- Nasopharyngitis (inflammation of the nasopharynx): 4 people, 30.77%
- Dyspnea (difficult or laboured breathing): 4 people, 30.77%
What are the existing conditions these people have? *
- Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 9 people, 69.23%
- Ulcerative Colitis (inflammatory bowel disease (ibd). it causes swelling, ulcerations, and loss of function of the large intestine): 4 people, 30.77%
- Stress And Anxiety: 4 people, 30.77%
- Pain: 4 people, 30.77%
- Osteoporosis (bones weak and more likely to break): 4 people, 30.77%
- Insomnia (sleeplessness): 4 people, 30.77%
- Abdominal Pain Upper: 4 people, 30.77%
* Approximation only. Some reports may have incomplete information.
Do you take Micronor and have Poor venous access?
- Check whether Poor venous access is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, long term effects of, and alternative drugs to Micronor:
- Micronor (1,344 reports)
Poor venous access treatments and more:
- Poor venous access (14,290 reports)
How severe was Poor venous access and when was it recovered:
Expand to all the drugs that have ingredients of norethindrone:
Sub-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 Micronor:
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 the drugs that are associated with Poor venous access:
- Poor venous access (677 drugs)
Browse all the conditions that are associated with Poor venous access:
- Poor venous access (480 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on norethindrone (the active ingredients of Micronor) and Micronor (the brand name). 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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