Senate
Study
Bill
3115
-
Introduced
SENATE
FILE
_____
BY
(PROPOSED
COMMITTEE
ON
JUDICIARY
BILL
BY
CHAIRPERSON
SCHULTZ)
A
BILL
FOR
An
Act
relating
to
abortions
including
informed
consent,
1
dispensing
abortion-inducing
drugs,
and
reporting
2
abortion-inducing
drug
complications.
3
BE
IT
ENACTED
BY
THE
GENERAL
ASSEMBLY
OF
THE
STATE
OF
IOWA:
4
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_____
DIVISION
I
1
INFORMED
CONSENT
2
Section
1.
Section
146A.1,
Code
2026,
is
amended
by
adding
3
the
following
new
subsection:
4
NEW
SUBSECTION
.
1A.
Prior
to
performing
an
abortion,
5
a
physician
shall
perform
an
in-person
examination
of
the
6
pregnant
woman
including
screening
for
indicia
of
coercion
or
7
abuse.
A
physician
shall,
if
necessary,
refer
the
woman
to
an
8
appropriate
health
care
provider
for
treatment
consistent
with
9
the
examination
results.
10
Sec.
2.
Section
146A.1,
subsection
6,
Code
2026,
is
amended
11
by
adding
the
following
new
paragraphs:
12
NEW
PARAGRAPH
.
0a.
“Abortion”
means
the
same
as
defined
in
13
section
146B.1.
14
NEW
PARAGRAPH
.
00a.
“Health
care
provider”
means
a
15
person
who
is
licensed,
certified,
or
otherwise
authorized
or
16
permitted
by
the
laws
of
this
state
to
administer
health
care
17
in
the
ordinary
course
of
business
or
in
the
practice
of
a
18
profession.
19
NEW
PARAGRAPH
.
0b.
“Physician”
means
the
same
as
defined
20
in
section
146B.1.
21
Sec.
3.
NEW
SECTION
.
146A.2
Dispensing
abortion-inducing
22
drugs
——
licensee
discipline.
23
1.
As
used
in
this
section,
unless
the
context
otherwise
24
requires:
25
a.
“Abortion-inducing
drug”
means
the
same
as
defined
in
26
section
146F.1.
27
b.
“Chemical
abortion”
means
the
same
as
defined
in
section
28
146F.1.
29
c.
“Dispense”
means
the
same
as
defined
in
section
146F.1.
30
d.
“Medical
emergency”
means
the
same
as
defined
in
section
31
146A.1.
32
e.
“Pregnant”
or
“pregnancy”
means
the
human
female
33
reproductive
condition
of
having
a
living
unborn
child
within
34
the
pregnant
woman’s
body
throughout
every
stage
of
the
unborn
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child’s
life
and
development,
from
fertilization
to
full
1
gestation
and
childbirth.
2
2.
A
physician
shall
do
all
of
the
following
prior
to
3
prescribing
or
dispensing
an
abortion-inducing
drug
to
a
4
pregnant
woman:
5
a.
Obtain
the
signature
of
the
woman
on
the
United
States
6
food
and
drug
administration
patient
agreement
form
required
7
for
each
abortion-inducing
drug
authorized
to
be
manufactured
8
or
sold
in
the
United
States.
9
b.
Obtain
written
confirmation
from
the
woman
that
the
woman
10
has
been
informed
of
all
of
the
following
information:
11
(1)
The
gestational
age-specific
risks
of
abortion-inducing
12
drugs.
13
(2)
The
risks
related
to
the
specific
abortion-inducing
14
drug
or
drugs
to
be
used,
including
hemorrhage,
failure
to
15
remove
all
tissue
of
the
unborn
child,
sepsis,
sterility,
and
16
possible
continuation
of
the
pregnancy.
17
(3)
That
the
United
States
federal
food
and
drug
18
administration
recommends
that
the
pregnant
woman
follow
up
19
with
the
woman’s
health
care
provider
approximately
seven
20
to
fourteen
calendar
days
after
the
administration
of
an
21
abortion-inducing
drug
to
confirm
complete
termination
of
22
pregnancy
has
occurred
and
to
evaluate
the
degree
of
bleeding.
23
(4)
That
women
using
abortion-inducing
drugs
have
suffered
24
trauma
from
seeing
the
remains
of
the
unborn
child
in
the
25
process
of
a
chemical
abortion.
26
(5)
That
it
may
be
possible
to
reverse
the
intended
effects
27
of
a
chemical
abortion,
but
time
is
of
the
essence.
28
(6)
That
information
on
reversing
the
effects
of
a
chemical
29
abortion
is
available
on
the
department’s
internet
site.
30
c.
Advise
the
pregnant
woman
how
to
access
emergency
31
surgical
intervention
in
case
of
an
incomplete
abortion,
severe
32
bleeding,
or
other
medical
complications.
33
3.
Subsection
2
shall
not
apply
to
a
chemical
abortion
34
performed
in
a
medical
emergency.
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4.
This
section
shall
not
be
construed
to
impose
civil
or
1
criminal
liability
on
a
woman
upon
whom
a
chemical
abortion
has
2
been
performed.
3
5.
A
physician
who
fails
to
comply
with
this
section
is
4
subject
to
licensee
discipline
under
chapter
148.
5
6.
The
board
of
medicine
shall
adopt
rules
pursuant
to
6
chapter
17A
to
administer
this
section.
7
Sec.
4.
NEW
SECTION
.
146A.3
Informational
materials.
8
1.
As
used
in
this
section,
“chemical
abortion”
means
the
9
same
as
defined
in
section
146F.1.
10
2.
The
department
shall
publish
on
the
department’s
11
internet
site,
in
an
easily
accessible
location
and
format,
all
12
of
the
following:
13
a.
Notice
that
it
may
be
possible
to
reverse
the
effects
of
14
a
chemical
abortion.
15
b.
Information
and
resources
on
reversing
the
effects
of
a
16
chemical
abortion.
17
DIVISION
II
18
DISPENSING
AND
REPORTING
——
ABORTION-INDUCING
DRUGS
19
Sec.
5.
NEW
SECTION
.
146F.1
Definitions.
20
As
used
in
this
chapter,
unless
the
context
otherwise
21
requires:
22
1.
“Abortion-inducing
drug”
means
any
of
the
following:
23
a.
Mifepristone.
24
b.
Misoprostol.
25
c.
Any
other
drug,
measure,
or
chemical
approved
by
the
26
United
States
food
and
drug
administration
when
prescribed
or
27
administered
with
the
intent
to
terminate
the
pregnancy
of
a
28
woman
known
to
be
pregnant.
“Abortion-inducing
drug”
includes
29
off-label
use
of
a
drug
known
to
have
abortion-inducing
30
properties,
which
is
prescribed
with
the
intent
of
causing
an
31
abortion.
“Abortion-inducing
drug”
does
not
include
drugs
that
32
may
be
known
to
cause
an
abortion
but
that
are
prescribed
for
33
other
medical
conditions.
34
2.
“Abortion-inducing
drug
complication”
means
any
physical
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or
psychological
condition
which,
in
the
reasonable
medical
1
judgment
of
a
health
care
provider,
may
occur
as
a
primary
or
2
secondary
result
of
the
patient’s
use
of
abortion-inducing
3
drugs
including
but
not
limited
to:
4
a.
Uterine
perforation.
5
b.
Cervical
laceration.
6
c.
Infection.
7
d.
Bleeding.
8
e.
Vaginal
bleeding
that
qualifies
under
the
common
toxicity
9
criteria
established
by
the
national
cancer
institute
as
a
10
grade
2
or
higher.
11
f.
Pulmonary
embolism.
12
g.
Deep
vein
thrombosis.
13
h.
Failure
to
actually
terminate
the
pregnancy.
14
i.
Incomplete
abortion
or
retained
tissue.
15
j.
Pelvic
inflammatory
disease.
16
k.
Endometritis.
17
l.
Missed
ectopic
pregnancy.
18
m.
Cardiac
arrest.
19
n.
Respiratory
arrest.
20
o.
Renal
failure.
21
p.
Shock.
22
q.
Amniotic
fluid
embolism.
23
r.
Coma.
24
s.
Free
fluid
in
the
abdomen.
25
t.
Allergic
reactions
to
anesthesia
and
abortion-inducing
26
drugs.
27
u.
Mood,
anxiety,
or
trauma-related
disorder
symptoms
as
28
described
in
the
most
recent
diagnostic
and
statistical
manual
29
of
mental
disorders
published
by
the
American
psychiatric
30
association.
31
3.
“Chemical
abortion”
means
an
abortion
performed
by
the
32
administration
or
use
of
an
abortion-inducing
drug.
33
4.
“Department”
means
the
department
of
health
and
human
34
services.
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5.
“Dispense”
means
to
distribute,
administer,
or
send
an
1
abortion-inducing
drug
to
the
ultimate
user.
2
6.
“Health
care
provider”
means
the
same
as
defined
in
3
section
146A.1.
4
7.
“Health
care
setting”
means
a
clinic,
medical
office,
or
5
hospital.
6
8.
“Hospital”
means
the
same
as
defined
in
section
135B.1.
7
9.
“Interested
party”
means
any
of
the
following
persons:
8
a.
A
woman
upon
whom
a
chemical
abortion
was
performed
or
9
attempted.
10
b.
The
biological
father
of
the
unborn
child
who
was
aborted
11
or
was
attempted
to
be
aborted
through
a
chemical
abortion.
12
c.
A
grandparent,
parent,
sibling,
child,
legal
guardian,
13
or
conservator
of
the
woman
upon
whom
a
chemical
abortion
was
14
performed
or
was
attempted.
15
10.
“Medical
emergency”
means
the
same
as
defined
in
section
16
146A.1.
17
11.
“Physician”
means
the
same
as
defined
in
section
146B.1.
18
12.
“Postfertilization
age”
means
the
same
as
defined
in
19
section
146B.1.
20
13.
“Pregnancy”
or
“pregnant”
means
the
same
as
defined
in
21
section
146A.2.
22
14.
“Rural
emergency
hospital”
means
the
same
as
defined
in
23
section
135B.1.
24
Sec.
6.
NEW
SECTION
.
146F.2
Dispensing
of
abortion-inducing
25
drugs
——
restrictions.
26
1.
A
person
shall
not
dispense
an
abortion-inducing
drug
in
27
this
state
unless
all
of
the
following
criteria
are
met:
28
a.
The
drug
is
dispensed
in
a
health
care
setting
directly
29
to
the
woman
prescribed
the
drug.
30
b.
The
person
dispensing
the
drug
is
authorized
to
do
so
31
pursuant
to
section
147.107.
32
2.
Subsection
1
does
not
apply
to
the
dispensing
of
an
33
abortion-inducing
drug
in
response
to
a
medical
emergency.
34
Sec.
7.
NEW
SECTION
.
146F.3
Abortion-inducing
drug
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complication
——
reporting.
1
1.
a.
Within
thirty
calendar
days
of
the
date
of
discharge
2
or
death
of
a
woman
who
presented
with
or
was
treated
for
3
an
abortion-inducing
drug
complication,
a
hospital,
rural
4
emergency
hospital,
or
an
attending
physician
shall
file
a
5
report
with
the
department.
The
report
shall
be
in
a
form
6
prescribed
by
the
department
and
include
a
list
of
the
most
7
common
abortion
complications
and
the
most
recent
international
8
classification
of
diseases
code
as
maintained
by
the
world
9
health
organization
for
each.
The
report
must
be
completed
and
10
signed
by
the
woman’s
attending
physician
and
contain
all
of
11
the
following
information:
12
(1)
The
age
of
the
woman
who
presented
with
or
was
treated
13
for
an
abortion-inducing
drug
complication.
14
(2)
The
state
and
county
of
residence
of
the
woman
who
15
presented
with
or
was
treated
for
an
abortion-inducing
drug
16
complication.
17
(3)
The
date
the
abortion-inducing
drug
was
used
by
the
18
woman.
19
(4)
The
probable
postfertilization
age
of
the
unborn
child
20
on
the
date
of
the
abortion-inducing
drug
complication.
21
(5)
The
identity
of
the
physician
who
performed
the
22
chemical
abortion,
the
facility
where
the
chemical
abortion
was
23
performed,
and
the
referring
physician,
agency,
or
service,
if
24
any.
25
(6)
The
specific
complication
or
complications
that
led
to
26
the
treatment
and
the
most
recent
international
classification
27
of
diseases
code
for
each
complication
as
maintained
by
the
28
world
health
organization,
if
applicable.
29
b.
A
report
shall
not
contain
the
name
of
the
woman
or
30
other
information
or
identifiers
that
would
make
it
possible
to
31
identify
the
woman
who
suffered
the
reported
abortion-inducing
32
drug
complication.
33
2.
A
report
filed
pursuant
to
subsection
1
shall
be
34
confidential
and
not
subject
to
disclosure
under
chapter
22.
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3.
a.
On
or
before
December
31,
2026,
and
every
calendar
1
year
thereafter,
the
department
shall
prepare
a
comprehensive
2
statistical
report
based
upon
the
aggregated
data
gathered
from
3
reports
filed
pursuant
to
subsection
1
for
the
immediately
4
preceding
calendar
year.
The
aggregated
data
shall
be
5
anonymized
to
prevent
public
disclosure
of
either
of
the
6
following:
7
(1)
The
hospital,
rural
emergency
hospital,
or
attending
8
physician
that
filed
a
report.
9
(2)
The
woman
about
whom
a
report
was
filed.
10
b.
The
anonymized
aggregated
data
shall
be
made
available
to
11
the
public
by
the
department
in
a
downloadable
format
on
the
12
department’s
internet
site.
13
Sec.
8.
NEW
SECTION
.
146F.4
Private
cause
of
action
——
14
strict
liability.
15
1.
A
person
who
dispenses
an
abortion-inducing
drug
16
in
violation
of
this
chapter
shall
be
strictly
liable
17
to
any
interested
party
for
all
damages
caused
by
the
18
abortion-inducing
drug.
19
2.
In
addition
to
compensatory
or
punitive
damages,
a
20
prevailing
plaintiff
who
brings
an
action
under
this
section
is
21
entitled
to
all
of
the
following:
22
a.
Statutory
damages
in
the
amount
of
fifty
thousand
23
dollars.
24
b.
Court
costs.
25
c.
Reasonable
attorney
fees.
26
3.
In
an
action
brought
under
this
section,
the
name
and
27
other
identifying
characteristics
of
a
woman
who
sought
or
28
obtained
an
abortion-inducing
drug
shall
be
redacted
without
29
a
court
order
from
all
pleadings
and
documents
filed
in
the
30
action.
The
court
may
make
further
orders
as
necessary
to
31
protect
the
identity
and
privacy
of
the
woman
who
sought
or
32
obtained
an
abortion-inducing
drug.
33
4.
This
section
shall
not
be
construed
to
impose
civil
or
34
criminal
liability
on
a
woman
upon
whom
a
chemical
abortion
is
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performed.
1
Sec.
9.
NEW
SECTION
.
146F.5
Licensee
discipline.
2
A
licensee
who
fails
to
comply
with
this
chapter
is
subject
3
to
licensee
discipline
under
chapter
148.
4
DIVISION
III
5
ABORTION-RELATED
PROVISIONS
6
Sec.
10.
Section
144.29A,
subsection
1,
paragraph
k,
Code
7
2026,
is
amended
to
read
as
follows:
8
k.
The
method
used
for
an
induced
termination,
including
9
whether
mifepristone
or
misoprostol
was
used.
10
Sec.
11.
Section
144.29A,
subsection
1,
Code
2026,
is
11
amended
by
adding
the
following
new
paragraph:
12
NEW
PARAGRAPH
.
l.
If
a
spontaneous
termination
of
13
pregnancy,
whether
the
patient
ingested
mifepristone
or
14
misoprostol
within
fourteen
calendar
days
prior
to
the
date
of
15
the
spontaneous
termination
of
pregnancy.
16
Sec.
12.
Section
144.29A,
subsection
7,
paragraph
c,
Code
17
2026,
is
amended
to
read
as
follows:
18
c.
“Spontaneous
termination
of
pregnancy”
,
commonly
known
19
as
a
miscarriage,
means
the
occurrence
of
an
unintended
20
termination
of
pregnancy
at
any
time
during
the
period
from
21
conception
to
twenty
weeks
gestation
and
which
is
not
a
22
spontaneous
termination
of
pregnancy
at
any
time
during
the
23
period
from
twenty
weeks
or
greater
which
is
reported
to
the
24
department
as
a
fetal
death
under
this
chapter
.
25
Sec.
13.
Section
146B.1,
subsection
1,
Code
2026,
is
amended
26
to
read
as
follows:
27
1.
“Abortion”
means
the
termination
of
a
human
pregnancy
28
with
the
intent
other
than
to
produce
a
live
birth
or
to
29
remove
a
dead
fetus.
“Abortion”
does
not
include
a
spontaneous
30
termination
of
pregnancy,
commonly
known
as
a
miscarriage,
if
31
not
all
the
products
of
conception
are
expelled.
32
EXPLANATION
33
The
inclusion
of
this
explanation
does
not
constitute
agreement
with
34
the
explanation’s
substance
by
the
members
of
the
general
assembly.
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This
bill
relates
to
abortions,
including
informed
1
consent,
dispensing
of
abortion-inducing
drugs,
and
reporting
2
abortion-inducing
drug
complications.
3
DIVISION
I
——
INFORMED
CONSENT.
Under
the
bill,
a
physician,
4
prior
to
performing
or
attempting
to
perform
an
abortion,
is
5
required
to
perform
an
in-person
examination
of
the
woman
6
seeking
an
abortion,
including
screening
for
indicia
of
7
coercion
or
abuse;
if
necessary,
the
physician
shall
make
a
8
referral
to
an
appropriate
health
care
provider
consistent
with
9
the
examination
results.
10
The
bill
requires
a
physician,
prior
to
prescribing
11
or
dispensing
an
abortion-inducing
drug,
to
do
all
of
the
12
following:
have
the
woman
being
prescribed
or
dispensed
the
13
drug
sign
a
patient
agreement
form,
obtain
written
confirmation
14
that
the
physician
has
informed
the
woman
of
specific
health
15
and
safety
information
related
to
abortion-inducing
drugs
16
as
detailed
in
the
bill,
and
advise
the
pregnant
woman
how
17
to
access
emergency
surgical
intervention
in
cases
of
an
18
incomplete
abortion,
severe
bleeding,
or
other
medical
19
complications.
The
bill
specifies
that
these
requirements
20
shall
not
apply
to
a
chemical
abortion
performed
in
response
to
21
a
medical
emergency.
The
bill
provides
that
the
prohibition
on
22
dispensing
of
abortion-inducing
drugs
shall
not
be
construed
23
to
impose
civil
or
criminal
liability
on
a
woman
upon
whom
24
a
chemical
abortion
has
been
performed.
Under
the
bill,
25
a
physician
who
fails
to
comply
with
the
informed
consent
26
requirements
is
subject
to
licensee
discipline.
The
bill
27
requires
the
board
of
medicine
to
adopt
rules
to
administer
28
this
division
of
the
bill.
The
bill
defines
“abortion-inducing
29
drug”,
“chemical
abortion”,
“dispense”,
“medical
emergency”,
30
and
“pregnant”
or
“pregnancy”.
31
The
bill
requires
the
department
of
health
and
human
32
services
(HHS)
to
publish
on
HHS’s
internet
site
notice
that
it
33
may
be
possible
to
reverse
the
effects
of
a
chemical
abortion,
34
and
information
and
resources
on
reversing
the
effects
of
a
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chemical
abortion.
1
DIVISION
II
——
DISPENSING
AND
REPORTING
——
ABORTION-INDUCING
2
DRUGS.
The
bill
defines
“abortion-inducing
drug”,
3
“abortion-inducing
drug
complication”,
“chemical
abortion”,
4
“dispense”,
“interested
party”,
“medical
emergency”,
5
“physician”,
“postfertilization
age”,
and
“rural
emergency
6
hospital”.
7
The
bill
prohibits
a
person
from
dispensing
an
8
abortion-inducing
drug
in
this
state
unless
the
drug
is
9
dispensed
in
a
health
care
setting
directly
to
the
woman
10
prescribed
the
drug,
and
the
person
dispensing
the
drug
is
11
authorized
to
do
so
pursuant
to
Code
section
147.107
(drug
12
dispensing,
supplying,
and
prescribing
——
limitations).
These
13
requirements
do
not
apply
to
a
medical
emergency.
14
The
bill
requires
a
hospital,
rural
emergency
hospital,
15
or
the
attending
physician
to
file
a
report
with
HHS
using
a
16
prescribed
form
within
30
days
of
discharge
or
death
of
a
woman
17
who
presented
with
or
was
treated
for
an
abortion-inducing
18
drug
complication.
The
form
must
be
signed
and
completed
19
by
the
attending
physician
and
contain
the
age
of
the
woman
20
experiencing
the
abortion-inducing
drug
complication,
21
the
woman’s
state
and
county
of
residence,
the
date
the
22
abortion-inducing
drug
was
used
by
the
woman,
and
the
probable
23
postfertilization
age
of
the
unborn
child
at
the
time
of
24
the
abortion-inducing
drug
complication.
The
report
must
25
identify
the
physician
who
performed
the
chemical
abortion,
26
the
facility
where
the
chemical
abortion
was
performed,
27
the
referring
physician,
agency,
or
service,
if
any,
and
28
the
specific
complication
or
complications
that
led
to
the
29
treatment
performed
along
with
the
most
recent
international
30
classification
of
diseases
code
for
each,
if
applicable.
The
31
report
shall
be
confidential
and
not
subject
to
disclosure
32
under
Code
chapter
22
(open
records).
33
The
bill
also
requires
HHS
to
prepare
annually
on
or
34
before
December
31
a
comprehensive
statistical
report
based
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upon
the
aggregated
data
gathered
from
the
reports
filed
on
1
abortion-inducing
drug
complications.
Under
the
bill,
the
data
2
gathered
by
HHS
must
be
anonymized
to
prevent
public
disclosure
3
of
either
the
physician
or
hospital
that
filed
a
report,
or
the
4
woman
about
whom
a
report
is
filed.
HHS
is
required
to
make
the
5
anonymized
data
publicly
available
in
a
downloadable
format
on
6
its
internet
site.
7
This
division
of
the
bill
creates
a
private
cause
of
action
8
against
any
person
who
dispenses
an
abortion-inducing
drug
9
in
violation
of
this
division
of
the
bill
for
all
damages
10
caused
by
the
abortion-inducing
drug
suffered
by
a
woman
upon
11
whom
a
chemical
abortion
was
performed
or
was
attempted;
the
12
biological
father
of
the
unborn
child
who
was
or
was
attempted
13
to
be
aborted
through
a
chemical
abortion;
or
the
grandparent,
14
parent,
sibling,
child,
legal
guardian,
or
conservator
of
15
the
woman
upon
whom
a
chemical
abortion
was
performed
or
was
16
attempted.
A
prevailing
plaintiff
in
an
action
brought
under
17
this
division
of
the
bill,
in
addition
to
compensatory
and
18
punitive
damages,
is
entitled
to
statutory
damages
in
the
19
amount
of
$50,000,
court
costs,
and
reasonable
attorney
fees.
20
In
an
action
brought
under
this
division
of
the
bill,
the
name
21
and
other
identifying
characteristics
of
a
woman
who
sought
or
22
obtained
an
abortion-inducing
drug
shall
be
redacted
from
all
23
pleadings
and
documents
filed
in
the
action
without
a
court
24
order,
and
the
court
may
make
further
orders
as
necessary
to
25
protect
the
identity
and
privacy
of
the
woman
who
sought
or
26
obtained
an
abortion-inducing
drug.
This
division
of
the
bill
27
is
not
to
be
construed
to
impose
civil
or
criminal
liability
28
upon
a
woman
upon
whom
a
chemical
abortion
is
performed.
29
Under
the
bill,
a
licensee
that
fails
to
comply
with
this
30
division
of
the
bill
is
subject
to
licensee
discipline.
31
DIVISION
III
——
ABORTION-RELATED
PROVISIONS.
The
bill
32
amends
Code
section
144.29A
(termination
of
pregnancy
reporting
33
——
legislative
intent)
to
require
a
health
care
provider
that
34
diagnoses
or
induces
a
spontaneous
termination
of
pregnancy
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to
include
in
the
required
report
to
HHS
if
mifepristone
or
1
misoprostol
was
used
to
induce
a
spontaneous
termination
of
2
pregnancy.
Current
law
requires
the
health
care
provider
3
to
only
disclose
if
mifepristone
was
used
to
induce
a
4
spontaneous
termination
of
pregnancy.
The
bill
also
requires
5
the
health
care
provider
to
disclose
whether
mifepristone
6
or
misoprostol
were
ingested
by
the
patient
within
14
days
7
prior
to
the
spontaneous
termination
of
pregnancy.
The
bill
8
excludes
a
spontaneous
termination
from
the
definition
of
9
abortion
for
the
purpose
of
the
reporting
requirements
and
10
penalties
on
abortions
under
Code
chapter
146B
(abortion
——
11
postfertilization
age).
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