Ariz. Admin. Code § R9-10-1511 - Medications and Controlled Substances
A medical director shall ensure that:
1. The abortion clinic complies with the
requirements for medications and controlled substances in A.R.S. Title 32,
Chapter 18, and A.R.S. Title 36, Chapter 27;
2. A medication is administered in compliance
with an order from a physician, physician assistant, registered nurse
practitioner, or as otherwise provided by law;
3. A medication is administered to a patient
or to a viable fetus by a physician or as otherwise provided by law;
4. Medications and controlled substances are
maintained in a locked area on the premises;
5. Only personnel designated by policies and
procedures have access to the locked area containing medications and controlled
substances;
6. Expired, mislabeled,
or unusable medications and controlled substances are disposed of according to
policies and procedures;
7. A
medication error or an adverse reaction, including any actions taken in
response to the medication error or adverse reaction, is immediately reported
to the medical director and licensee, and recorded in the patient's medical
record;
8. Medication information
for a patient is maintained in the patient's medical record and contains:
9.
d. If medication is administered to the patient:
a.
i. The
date and time of administration;
b.
ii. The name, strength,
dosage form, amount of medication, and route of administration; and
c.
iii.
The identification and signature of the individual administering the
medication; and
a. The patient's name, age, and
weight;
b. The medications the
patient is currently taking;
c.
Allergies or sensitivities to medications, antiseptic solutions, or latex;
and
9. If administered to a fetus delivered
alive, the following are documented in the fetus's medical record:
a. The date and time of oxygen
administration;
b. The amount and
flow rate of the oxygen;
c. The
identification and signature of the individual administering the oxygen;
and
d. For a viable fetus:
i. The date and time of medication
administration;
ii. The name,
strength, dosage form, amount of medication, and route of administration;
and
iii. The identification and
signature of the individual administering the medication.
Notes
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.