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1 | | repository, in a form and manner specified by the |
2 | | Department, the following information:
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3 | | (A) The recipient's name.
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4 | | (B) The recipient's address.
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5 | | (C) The national drug code number of the controlled
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6 | | substance
dispensed.
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7 | | (D) The date the controlled substance is |
8 | | dispensed.
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9 | | (E) The quantity of the controlled substance |
10 | | dispensed.
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11 | | (F) The dispenser's United States Drug Enforcement |
12 | | Administration
registration number.
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13 | | (G) The prescriber's United States Drug |
14 | | Enforcement Administration
registration number.
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15 | | (H) The dates the controlled substance |
16 | | prescription is filled. |
17 | | (I) The payment type used to purchase the |
18 | | controlled substance (i.e. Medicaid, cash, third party |
19 | | insurance). |
20 | | (J) The patient location code (i.e. home, nursing |
21 | | home, outpatient, etc.) for the controlled substances |
22 | | other than those filled at a retail pharmacy. |
23 | | (K) Any additional information that may be |
24 | | required by the department by administrative rule, |
25 | | including but not limited to information required for |
26 | | compliance with the criteria for electronic reporting |
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1 | | of the American Society for Automation and Pharmacy or |
2 | | its successor.
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3 | | (2) The information required to be transmitted under |
4 | | this Section must be
transmitted not more than 7 days after |
5 | | the date on which a
controlled substance is dispensed, or |
6 | | at such other time as may be required by the Department by |
7 | | administrative rule.
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8 | | (3) A dispenser must transmit the information required |
9 | | under this Section
by:
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10 | | (A) an electronic device compatible with the |
11 | | receiving device of the
central repository;
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12 | | (B) a computer diskette;
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13 | | (C) a magnetic tape; or
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14 | | (D) a pharmacy universal claim form or Pharmacy |
15 | | Inventory Control form;
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16 | | (4) The Department may impose a civil fine of up to |
17 | | $100 per day for willful failure to report controlled |
18 | | substance dispensing to the Prescription Monitoring |
19 | | Program. The fine shall be calculated on no more than the |
20 | | number of days from the time the report was required to be |
21 | | made until the time the problem was resolved, and shall be |
22 | | payable to the Prescription Monitoring Program.
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23 | | (b) The Department, by rule, may include in the monitoring |
24 | | program certain other select drugs that are not included in |
25 | | Schedule II, III, IV, or V. The prescription monitoring program |
26 | | does not apply to
controlled substance prescriptions as |
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1 | | exempted under Section
313.
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2 | | (c) The collection of data on select drugs and scheduled |
3 | | substances by the Prescription Monitoring Program may be used |
4 | | as a tool for addressing oversight requirements of long-term |
5 | | care institutions as set forth by Public Act 96-1372. Long-term |
6 | | care pharmacies shall transmit patient medication profiles to |
7 | | the Prescription Monitoring Program monthly or more frequently |
8 | | as established by administrative rule. |
9 | | (d) As a means of addressing potential pharmacotherapy |
10 | | needs under emergency conditions, the Prescription Monitoring |
11 | | Program shall be expanded to include every medication for each |
12 | | person within this State by January 1, 2015. |
13 | | (e) By January 1, 2015, each electronic health record |
14 | | system must interface with the Prescription Monitoring System |
15 | | to ensure that each health care provider has access to specific |
16 | | patient records as he or she is treating the patient. |
17 | | (Source: P.A. 97-334, eff. 1-1-12.)".
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