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Charlotte Lozier Institute

Phone: 202-223-8073
Fax: 571-312-0544

2776 S. Arlington Mill Dr.
#803
Arlington, VA 22206

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Charlotte Lozier Institute

Phone: 202-223-8073
Fax: 571-312-0544

2776 S. Arlington Mill Dr.
#803
Arlington, VA 22206

abortion complication

abortion complication

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February 12, 2025 Are Pro-life Laws Harming Women and Children? An Examination of Claims Against Texas Are Pro-life Laws Harming Women and Children? An Examination of Claims Against Texas February 7, 2025 Abortion Reporting: Iowa (2023) Abortion Reporting: Iowa (2023) February 7, 2025 Abortion Reporting: Nevada (2023) Abortion Reporting: Nevada (2023)
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abortion complication

New Study Reveals Increasing Severity and Frequency of Emergency Department Visits Following Use of Abortion Drugs

A new study published in the International Journal of Epidemiology and Public Health Research by Dr. James Studnicki, Dr. Ingrid Skop, Tessa Cox, and other CLI scholars, reveals the increasing severity and frequency of emergency department visits among Medicaid-eligible women from 17 states where Medicaid pays for abortion following different pregnancy outcomes.

charlotte-lozier-institute Charlotte Lozier Institute
September 10, 2024
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abortion complication

Study finds 75% of women treated at ERs after taking abortion pills rated ‘severe or critical’

Women who visit emergency rooms after taking abortion pills are more likely to be seen for serious medical problems than their cohorts whose pregnancies end with surgical abortions or live births, according to newly released research.

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abortion complication

First Pregnancy Abortion or Natural Pregnancy Loss: A Cohort Study of Mental Health Services Utilization

While both induced abortion and natural pregnancy loss have been associated with subsequent mental health problems, population-based studies directly comparing these two pregnancy outcomes are rare. This study compared mental health morbidity after an induced abortion to natural loss. Only the abortion cohort experienced significant increases in mental health services use following the first pregnancy outcome.

abortion complication

The State of Abortion Reporting in 2024 America: Still Striving Toward a Better National Standard

This paper evaluates each state’s abortion reporting requirements and publicly accessible abortion reports (or lack thereof). It is an update to CLI’s 2016 survey of abortion reporting across the country, and analyzes state-wide, regional, and national trends that could inform public health officials and policymakers.

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abortion complication

United Kingdom Data Deficiencies Influencing U.S. FDA Decisions

CLI's VP of Medical Affairs Ingrid Skop, together with Calum Miller, MD, and Kevin Duffy, MPH, recently published an article in Issues in Law & Medicine arguing that decisions by the FDA to pull back regulations on the abortion drug mifepristone in part relied on "flawed studies with significantly undercounted complications" from the U.K.

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New Study Reveals FDA Relied on Cherrypicked Data to Approve Dangerous Mail-Order Abortion Drugs

A new peer-reviewed article highlights major flaws in the data used by the U.S. Food and Drug Administration (FDA) to remove medical safeguards and in-person administering of abortion drugs. These flaws illustrate the ongoing problem of lack of quality abortion reporting data in the U.S. as well as in the United Kingdom.

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abortion complication

New Study: Abortion Increases Risk of Cardiovascular Diseases

A new longitudinal peer-reviewed study by the Charlotte Lozier Institute has shown that abortions are an independent risk factor for increased risk of cardiovascular diseases (CVD), the leading cause of death among women.

abortion complication

Fact Sheet: Three Problems with the FDA’s Abortion Drugs Complications Data

The FDA’s abortion drugs complications data is woefully incomplete. From 2020-2022, the six states that report complications by type of procedure reported 1,004 total complications from drug-induced abortions. Meanwhile, the FDA Adverse Event Reporting System data reflects just 17 unduplicated abortion-related adverse events over this same period.

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