Okla. Stat. tit. 63, § 63-1-757.9: Reporting system for certified physicians to report

annually.

A. The State Board of Medical Licensure and Supervision and the

State Board of Osteopathic Examiners shall adopt an electronically

based reporting system for certified physicians to report annually

the following:

1. The number of patients served;

2. Age of patients served;

3. Race of patients served;

4. County and state of residence of patients served;

5. If the patient resides outside the United States, city and

country of residence;

6. County and state of service;

7. A list of staff attending patients including licensing

numbers and evidence of other qualifications;

8. Each medication used or provided per patient, by date;

9. Any known complications or adverse events, and how they were

addressed, by date; and

10. Unresolved cases.

B. This reporting system shall also be used by emergency

department physicians and private physicians who treat post-abortion

complications.

C. Physicians shall protect from disclosure any personally

identifiable information of the patient in accordance with

applicable federal and state law.

D. A certified physician shall also report to their licensing

board, the State Board of Pharmacy and the Medwatch Reporting System

of the Food and Drug Administration (FDA), any complication or

adverse event as defined according to the FDA criteria given in the

Medwatch Reporting System.

E. The State Board of Medical Licensure and Supervision and the

State Board of Osteopathic Examiners shall develop a system of

reporting adverse events from the use of abortion-inducing drugs for

this state. The system shall require reporting of complications and

adverse events including, but not limited to:

1. Death;

2. Blood loss including hemorrhage;

3. Infection including sepsis;

4. Blood transfusions;

5. Administer drug for an ectopic pregnancy; and

6. Other adverse effects requiring hospitalization or

additional medical care.

F. The State Board of Medical Licensure and Supervision and the

State Board of Osteopathic Examiners shall require the following

providers and entities to report complications and adverse events in

writing:

1. Physicians certified to provide abortion-inducing drugs;

2. Emergency room physicians;

3. Any doctor licensed in this state including an

obstetrician/gynecologist who treats women with adverse events;

4. Provision of certification requires that the physician shall

also report adverse events and any patient deaths to the FDA; and

5. Other individuals or entities as determined by the State

Board of Medical Licensure and Supervision or the State Board of

Osteopathic Examiners.