85R11971 JSC-D
 
  By: Taylor of Collin S.B. No. 1284
 
 
 
A BILL TO BE ENTITLED
 
AN ACT
  relating to prescriber and dispenser reporting and access to
  patient prescription information under the Texas Controlled
  Substances Act.
         BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:
         SECTION 1.  Sections 481.074(c) and (q), Health and Safety
  Code, are amended to read as follows:
         (c)  Not later than the next business [seventh] day after the
  date a prescribing practitioner authorizes an emergency oral or
  telephonically communicated prescription, the prescribing
  practitioner shall send the information to the board as required by
  Section 481.075 and cause a written or electronic prescription,
  completed in the manner required by that section [Section 481.075],
  to be delivered to the dispensing pharmacist at the pharmacy where
  the prescription was dispensed. A written prescription may be
  delivered in person or by mail. The envelope of a prescription
  delivered by mail must be postmarked not later than the next
  business [seventh] day after the date the prescription was
  authorized. On receipt of a written prescription, the dispensing
  pharmacy shall file the transcription of the telephonically
  communicated prescription and the pharmacy copy and shall send
  information to the board as required by Section 481.075.  On receipt
  of an electronic prescription, the pharmacist shall annotate the
  electronic prescription record with the original authorization and
  date of the emergency oral or telephonically communicated
  prescription.
         (q)  Each dispensing pharmacist shall send all required
  information, including any information required to complete the
  Schedule III through V prescription forms, to the board by
  electronic transfer or another form approved by the board not later
  than the next business [seventh] day after the date the
  prescription is completely filled.
         SECTION 2.  Sections 481.075(g) and (i), Health and Safety
  Code, are amended to read as follows:
         (g)  Except for an oral prescription prescribed under
  Section 481.074(b), the prescribing practitioner shall:
               (1)  legibly fill in, or direct a designated agent to
  legibly fill in, on the official prescription form or in the
  electronic prescription, each item of information required to be
  provided by the prescribing practitioner under Subsection (e)(1),
  unless the practitioner determines that:
                     (A)  under rule adopted by the board for this
  purpose, it is unnecessary for the practitioner or the
  practitioner's agent to provide the patient identification number;
  or
                     (B)  it is not in the best interest of the patient
  for the practitioner or practitioner's agent to provide information
  regarding the intended use of the controlled substance or the
  diagnosis for which it is prescribed; [and]
               (2)  sign the official prescription form and give the
  form to the person authorized to receive the prescription or, in the
  case of an electronic prescription, electronically sign or validate
  the electronic prescription as authorized by federal law and
  transmit the prescription to the dispensing pharmacy; and
               (3)  send all required information, including any
  information required to complete an official prescription form or
  electronic prescription record, to the board by electronic transfer
  or another form approved by the board not later than the next
  business day after the date the prescription is issued.
         (i)  Each dispensing pharmacist shall:
               (1)  fill in on the official prescription form or note
  in the electronic prescription record each item of information
  given orally to the dispensing pharmacy under Subsection (h) and
  the date the prescription is filled, and:
                     (A)  for a written prescription, fill in the
  dispensing pharmacist's signature; or
                     (B)  for an electronic prescription,
  appropriately record the identity of the dispensing pharmacist in
  the electronic prescription record;
               (2)  retain with the records of the pharmacy for at
  least two years:
                     (A)  the official prescription form or the
  electronic prescription record, as applicable; and
                     (B)  the name or other patient identification
  required by Section 481.074(m) or (n); and
               (3)  send all required information, including any
  information required to complete an official prescription form or
  electronic prescription record, to the board by electronic transfer
  or another form approved by the board not later than the next
  business [seventh] day after the date the prescription is
  completely filled.
         SECTION 3.  Section 481.076, Health and Safety Code, is
  amended by adding Subsection (c-1) to read as follows:
         (c-1)  To avoid duplicate entries, the system described by
  Subsection (c) must be capable of associating a report by a
  practitioner issuing a prescription with a report by a pharmacist
  subsequently dispensing the substance under that same
  prescription.
         SECTION 4.  Section 481.0761, Health and Safety Code, is
  amended by adding Subsections (h) and (i) to read as follows:
         (h)  The board, in consultation with the department and the
  regulatory agencies listed in Section 481.076(a)(1) shall identify
  potentially harmful prescribing or dispensing patterns or
  practices that may suggest drug diversion or drug abuse. The board
  shall develop indicators for levels of prescriber or patient
  activity that suggest that a potentially harmful prescribing or
  dispensing pattern or practice may be occurring or that drug
  diversion or drug abuse may be occurring.
         (i)  The board may, based on the indicators developed under
  Subsection (h), send a prescriber or dispenser an electronic
  notification if the information submitted under Sections
  481.074(q) and 481.075 indicates that a potentially harmful
  prescribing or dispensing pattern or practice may be occurring or
  that drug diversion or drug abuse may be occurring.
         SECTION 5.  Subchapter C, Chapter 481, Health and Safety
  Code, is amended by adding Sections 481.0762 and 481.0763 to read as
  follows:
         Sec. 481.0762.  DUTIES OF PRESCRIBERS, PHARMACISTS, AND
  RELATED HEALTH CARE PRACTITIONERS. (a)  A person authorized to
  receive information under Section 481.076(a)(5) shall access that
  information with respect to the patient before prescribing or
  dispensing opioids, benzodiazepines, barbiturates, or
  carisoprodol.
         (b)  A person authorized to receive information under
  Section 481.076(a)(5) may access that information with respect to
  the patient before prescribing or dispensing any controlled
  substance.
         (c)  A violation of Subsection (a) is grounds for
  disciplinary action by the regulatory agency that issued a license,
  certification, or registration to the person who committed the
  violation.
         Sec. 481.0763.  EXCEPTIONS. (a) A prescriber is not subject
  to the requirements of Section 481.0762(a) if:
               (1)  the patient has been diagnosed with cancer or the
  patient is receiving hospice care; and
               (2)  the prescriber clearly notes in the prescription
  record that the patient was diagnosed with cancer or is receiving
  hospice care, as applicable.
         (b)  A dispenser is not subject to the requirements of
  Section 481.0762(a) if it is clearly noted in the prescription
  record that the patient has been diagnosed with cancer or is
  receiving hospice care.
         SECTION 6.  Section 481.0762, Health and Safety Code, as
  added by this Act, applies only to:
               (1)  a prescriber who issues a prescription on or after
  September 1, 2018; or
               (2)  a person authorized by law to dispense a
  controlled substance who dispenses the substance on or after
  September 1, 2018.
         SECTION 7.  This Act takes effect September 1, 2017.