Combivir and Abortion - a phase IV clinical study of FDA data
Summary:
Abortion is reported as a side effect among people who take Combivir (lamivudine; zidovudine), especially for people who are 30-39 old, also take Sustiva, and have Malaria.
The phase IV clinical study analyzes which people have Abortion when taking Combivir. It is created by eHealthMe based on reports of 15,371 people who have side effects when taking Combivir from the FDA, and is updated regularly.
What is Combivir?
Combivir has active ingredients of lamivudine; zidovudine. It is often used in hiv infection. eHealthMe is studying from 15,450 Combivir users. Check the latest studies of Combivir.
What is Abortion?
Abortion (termination of pregnancy) is found to be associated with 211 drugs and 544 conditions by eHealthMe. Check the latest studies of Abortion.
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 >>>.
15,371 people reported to have side effects when taking Combivir.
Among them, 15 people (0.1%) have Abortion.

Among these 15 people:
What is the age of people who have Abortion when taking Combivir? *
- 0-1: 20 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 70 %
- 40-49: 10 %
- 50-59: 0.0 %
- 60+: 0.0 %
What are other drugs people take besides Combivir? *
- Viramune: 6 people, 40.00%
- Sustiva: 6 people, 40.00%
- Kaletra: 3 people, 20.00%
- Tenofovir Disoproxil Fumarate: 2 people, 13.33%
- Reyataz: 2 people, 13.33%
- Isentress: 2 people, 13.33%
- Folic Acid: 2 people, 13.33%
- Truvada: 1 person, 6.67%
- Septra: 1 person, 6.67%
- Isoniazid: 1 person, 6.67%
What are other side effects people have besides Abortion? *
- Intra-Uterine Death: 3 people, 20.00%
- Drug Exposure During Pregnancy: 3 people, 20.00%
- Foetal Exposure During Pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect): 2 people, 13.33%
- Vaginal Bleeding Between Periods: 1 person, 6.67%
- Oligohydramnios (a condition in pregnancy characterized by a deficiency of amniotic fluid): 1 person, 6.67%
- Foetal Maturation Impaired (impaired foetus development): 1 person, 6.67%
- Complications Of Maternal Exposure To Therapeutic Drugs: 1 person, 6.67%
- Birth Control: 1 person, 6.67%
What are the existing conditions these people have? *
- Malaria (a parasitic disease due to mosquito bite): 1 person, 6.67%
* Approximation only. Some reports may have incomplete information.
Do you take Combivir and have Abortion?
- Check whether Abortion 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 Combivir:
- Combivir (15,450 reports)
Abortion treatments and more:
- Abortion (3,880 reports)
How severe was Abortion and when was it recovered:
Expand to all the drugs that have ingredients of lamivudine; zidovudine:
Sub-studies by age:
0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Combivir:
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 Abortion:
- Abortion (211 drugs)
Browse all the conditions that are associated with Abortion:
- Abortion (544 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on lamivudine; zidovudine (the active ingredients of Combivir) and Combivir (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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