AB 2418, as amended, Bonilla. Health care coverage: prescription drugs: refills.
Existing law, the Knox-Keene Health Care Service Plan Act of 1975, provides for the licensure and regulation of health care service plans by the Department of Managed Health Care and makes a willful violation of the act a crime. Existing law also provides for the regulation of health insurers by the Department of Insurance. Existing law imposes various requirements on contracts and policies that cover prescription drug benefits. Existing law, the Pharmacy Law, provides for the licensure and regulation of pharmacists by the California State Board of Pharmacy and prohibits the refilling of a prescription without the authorization of the prescriber, except as specified.
This bill would require a health care service plan contract or health insurance policy issued, amended, or renewed on or after January 1, 2016, that provides coverage for
prescription drug benefitsbegin delete and imposes a mandatory mail-order restriction for a drug that has a monthly cost to the health care service plan or health insurer that is less than twice the Medicare minimum specialty tier eligibility threshold to establish a process allowing enrollees and insureds to opt out of the restriction for that drug, as specified. This bill would require a health care
service plan or health insurer to establish and implement a process to authorize emergency refills at a participating specialty or community pharmacy when any drug that is dispensed to an enrollee or an insured through mail order is delivered in a condition that is unsafe to use, not delivered, or delayed for a period of time that would cause the enrollee or insured to not have the drug in time to comply with the prescribed dosage instructions. The bill would require a health care service plan contract or a health insurance policy issued, amended, or renewed on or after January 1, 2016, that provides coverage for prescription drug benefitsend delete to permit and apply a prorated daily cost-sharing rate to refills of prescriptions that are dispensed by a participating pharmacy for less than the standard refill amount if the prescriber or pharmacist indicates that the refill is in the best interest of the enrollee or insured and is for the purpose of synchronizing the refill dates of the enrollee’s or insured’s
medications, provided that certain requirements are satisfied. The bill would also require a health care service plan contract or health insurance policy issued, amended, or renewed on or after January 1, 2016, that provides coverage for prescription drug benefits to allow for the early refill of covered topical ophthalmic products at 70% of the predicted days of use. Because a willful violation of the bill’s requirements by a health care service plan would be a crime, the bill would impose a state-mandated local program.
The California Constitution requires the state to reimburse local agencies and school districts for certain costs mandated by the state. Statutory provisions establish procedures for making that reimbursement.
This bill would provide that no reimbursement is required by this act for a specified reason.
Vote: majority. Appropriation: no. Fiscal committee: yes. State-mandated local program: yes.
The people of the State of California do enact as follows:
The Legislature hereby finds and declares all of
2the following:
3(a) As many as 75 percent of patients do not take their
4medications as prescribed. Poor adherence to prescribed treatments
5poses serious health risks to nonadhering patients, particularly
6those with chronic diseases.
7(b) Poor adherence to prescribed treatments leads to unnecessary
8disease progression, avoidable utilization of inpatient and outpatient
9medical care, higher mortality rates, and increased medical
10spending. According to the New England Healthcare Institute,
11poor adherence to medication results in $100 billion
in excess
12hospital visits and a total of $290 billion in avoidable medical
13spending each year -- 13 percent of all health care expenditures
14in the United States. Adherence to prescription medication prevents
15these unnecessary complications and is a cost-effective and simple
16tool in the treatment of health conditions.
17(c) Given the evidence showing benefits to patients, the federal
18Centers for Medicare and Medicaid Services requires Medicare
19Part D plans tobegin delete permit beneficiaries to choose between mail-order allow for the synchronization of refill dates
20delivery or community pharmacy access to prescription drugs,
21requires Part D plans toend delete
22for patients with multiplebegin delete prescriptions,end deletebegin insert
prescriptionsend insert and
23recommends that Part D plans authorize early refills of topical
24ophthalmic products at 70 percent of the predicted days of use.
25(d) It is the intent of the Legislature to enact legislation that
26promotes policies designed to improve patient medication
27
adherence.
Section 1367.247 is added to the Health and Safety
29Code, to read:
(a) A health care service plan contract issued,
31amended, or renewed on or after January 1, 2016, that provides
32coverage for prescription drug benefits and that imposes a
33mandatory mail-order restriction for some or all covered
34prescription drugs shall establish a process for enrollees to opt out
35of that restriction. The opt out process may require the use of a
P4 1plan’s participating specialty or community pharmacy that is not
2a mail-order-only pharmacy, at the discretion of the plan. The opt
3out process may require 30 days’ written notice before the election
4to opt out is effective. The opt out process shall comply with all
5of the following requirements:
6(1) Not impose conditions or restrictions on an enrollee opting
7out of the mandatory mail-order restriction. For purposes of this
8subparagraph, “conditions or restrictions” include, but are not
9limited to, requiring prescriber approval or submission of
10documentation by the enrollee or prescriber.
11(2) Allow an enrollee to opt out of the mandatory mail-order
12restriction, and revoke his or her prior opt out of the restriction, at
13any time.
14(3) The choice by an enrollee to opt out shall be valid for the
15duration of the plan year or until the enrollee elects to revoke the
16opt out, whichever occurs first, provided that the enrollee remains
17enrolled in the same product with either the same subscriber, with
18respect to individual plan contracts, or the same plan sponsor, with
19respect
to group plan contracts.
20(4) A health care service plan shall provide an enrollee who
21obtains a covered prescription drug that is subject to the mandatory
22mail-order restriction with a separate written notice of the
23restriction and any exceptions upon dispensing of the first fill of
24the drug or no less than 30 days prior to the restriction taking effect
25for the first refill of the drug. This written notice shall be in addition
26to any information contained in the plan’s evidence of coverage
27or evidence of benefits. The notice shall inform the enrollee of the
28right to opt out of the mandatory mail-order restriction and
29instructions on how to do so.
30(b) This section shall not apply to a drug that is not available at
31a participating community pharmacy due to any of the following:
32(1) An industry shortage listed on the Current Drug Shortages
33Index maintained by the federal Food and Drug Administration
34(FDA).
35(2) A manufacturer’s instructions or restrictions.
36(3) Any risk evaluation and management strategy approved by
37the FDA.
38(4) A special shortage affecting the plan’s network of
39participating pharmacies.
P5 1(c) (1) The opt out requirement in subdivision (a) shall
only
2apply to a drug that has a monthly cost to the health care service
3plan of less than twice the Medicare minimum specialty tier
4eligibility threshold.
5(2) For any drug that is dispensed to an enrollee through mail
6order, a health care service plan shall establish and implement a
7process to authorize emergency refills at a plan’s participating
8specialty or community pharmacy when the drug is delivered in a
9condition that is unsafe to use, not delivered, or delayed for a period
10of time that would cause the enrollee to not have the drug in time
11to comply with the prescribed dosage instructions.
12(d) Nothing in this section shall be construed to establish a new
13
mandated benefit or to prevent the application of deductible or
14copayment provisions in a plan contract.
15(e) Nothing in this section shall be construed to limit or prohibit
16differential copayments in the form of financial incentives whereby
17an enrollee’s cost sharing is reduced when he or she uses mail
18order rather than a community pharmacy.
19(f) For purposes of this section, the following definitions shall
20apply:
21(1) For group health care service plan contracts, “plan year” has
22the meaning set forth in Section 144.103 of Title 45 of the Code
23of Federal Regulations.
24(2) For individual health care service plan contracts, “plan year”
25means the calendar
year.
Section 1367.248 is added to the Health and Safety
28Code, to read:
(a) A health care service plan contract issued,
30amended, or renewed on or after January 1, 2016, that provides
31coverage for prescription drug benefits shall permit and apply a
32prorated daily cost-sharing rate to the refills of prescriptions that
33are dispensed by a participating pharmacy for less than the standard
34refill amount if the prescriber or pharmacist indicates that the refill
35for less than the standard amount is in the best interest of the
36enrollee and is for the purpose of synchronizing the refill dates of
37the enrollee’s medications and all of the following apply:
38(1) The prescription drugs being synchronized are covered and
39authorized by the health care
service plan contract.
P6 1(2) The prescription drugs being refilled for less than the
2standard amount are not subject to quantity limits or other
3utilization management controls that are inconsistent with the
4synchronization plan, including, but not limited to, controlled
5substance prescribing and dispensing guidelines intended to prevent
6misuse or abuse.
7(3) The prescription drugs being synchronized are dispensed
8by a single participating pharmacy.
9(4) The patient has completed at least 90 consecutive days on
10the prescription drugs being synchronized.
11(5) The prescription drugs being refilled for less than the
12standard amount are of a formulation that can be
effectively split
13over the required short fill period to achieve synchronization.
14(6) The prescriber has not done either of the following with
15respect to the prescription drugs being refilled for less than the
16standard amount:
17(A) Indicated, either orally or in his or her own handwriting,
18“No change to quantity,” or words of similar meaning.
19(B) Checked a box on the prescription marked “No change to
20quantity,” and personally initialed the box or checkmark.
21(b) This section shall not apply to a drug that is not available at
22a participating community pharmacy due to any of the following:
23(1) An industry
shortage listed on the Current Drug Shortages
24Index maintained by the federal Food and Drug Administration
25(FDA).
26(2) A manufacturer’s instructions or restrictions.
27(3) Any risk evaluation and management strategy approved by
28the FDA.
29(4) A special shortage affecting the plan’s network of
30participating pharmacies.
31(c) Nothing in this section shall be construed to establish a new
32or mandated benefit or to prevent the application of deductible or
33copayment provisions in a plan contract.
Section 1367.249 is added to the Health and Safety
36Code, to read:
(a) A health care service plan contract issued,
38amended, or renewed on or after January 1, 2016, that provides
39coverage for prescription drug benefits shall allow for early refills
P7 1of covered topical ophthalmic products at 70 percent of the
2predicted days of use.
3(b) Nothing in this section shall be construed to establish a new
4mandated benefit or to prevent the application of deductible or
5copayment provisions in a plan contract.
Section 10123.207 is added to the Insurance Code, to
7read:
(a) A health insurance policy issued, amended, or
9renewed on or after January 1, 2016, that provides coverage for
10prescription drug benefits and that imposes a mandatory mail-order
11restriction for some or all covered prescription drugs shall establish
12a process for insureds to opt out of that restriction. The opt out
13process may require the use of a health insurer’s participating
14specialty or community pharmacy that is not a mail-order-only
15pharmacy, at the discretion of the health insurer. The opt out
16process may require 30 days’ written notice before the election to
17opt out is effective. The opt out process shall comply with all of
18the following requirements:
19(1) Not impose conditions or restrictions on an insured opting
20out of the mandatory mail-order restriction. For purposes of this
21subparagraph, “conditions or restrictions” include, but are not
22limited to, requiring prescriber approval or submission of
23documentation by the insured or prescriber.
24(2) Allow an insured to opt out of the mandatory mail-order
25restriction, and revoke his or her prior opt out of the restriction, at
26any time.
27(3) The choice by an insured to opt out shall be valid for the
28duration of the plan year or until the insured elects to revoke the
29opt out, whichever occurs first, provided that the insured remains
30enrolled in the same product with either the same policyholder,
31with respect to individual policies, or the same plan sponsor, with
32respect
to group policies.
33(4) A health insurer shall provide an insured who obtains a
34covered prescription drug that is subject to the mandatory
35mail-order restriction with a separate written notice of the
36restriction and any exceptions upon dispensing of the first fill of
37the drug or no less than 30 days prior to the restriction taking effect
38for the first refill of the drug. This written notice shall be in addition
39to any information contained in the insurer’s evidence of coverage
40or evidence of benefits. The notice shall inform the insured of the
P8 1right to opt out of the mandatory mail-order restriction and
2instructions on how to do so.
3(b) This section shall not apply to a drug that is not available at
4a participating community pharmacy due to any of the following:
5(1) An industry shortage listed on the Current Drug Shortages
6Index maintained by the federal Food and Drug Administration
7(FDA).
8(2) A manufacturer’s instructions or restrictions.
9(3) Any risk evaluation and management strategy approved by
10the FDA.
11(4) A special shortage affecting the insurer’s network of
12participating pharmacies.
13(c) (1) The opt out requirement in subdivision (a) shall only
14
apply to a drug that has a monthly cost to the health insurer of less
15than twice the Medicare minimum specialty tier eligibility
16threshold.
17(2) For any drug that is dispensed to an insured through mail
18order, a health insurer shall establish and implement a process to
19authorize emergency refills at a health insurer’s participating
20specialty or community pharmacy when the drug is delivered in a
21condition that is unsafe to use, not delivered, or delayed for a period
22of time that would cause the insured to not have the drug in time
23to comply with the prescribed dosage instructions.
24(d) Nothing in this section shall be construed to establish a new
25
mandated benefit or to prevent the application of deductible or
26copayment provisions in a policy.
27(e) Nothing in this section shall be construed to limit or prohibit
28differential copayments in the form of financial incentives whereby
29an insured’s cost sharing is reduced when he or she uses mail order
30rather than a community pharmacy.
31(f) For purposes of this section, the following definitions shall
32apply:
33(1) For group health insurance policies, “plan year” has the
34meaning set forth in Section 144.103 of Title 45 of the Code of
35Federal Regulations.
36(2) For individual health insurance policies, “plan year” means
37the calendar
year.
Section 10123.208 is added to the Insurance Code, to
40read:
(a) A health insurance policy issued, amended, or
2renewed on or after January 1, 2016, that provides coverage for
3prescription drug benefits shall permit and apply a prorated daily
4cost-sharing rate to the refills of prescriptions that are dispensed
5by a participating pharmacy for less than the standard refill amount
6if the prescriber or pharmacist indicates that the refill for less than
7the standard amount is in the best interest of the insured and is for
8the purpose of synchronizing the refill dates of the insured’s
9medications and all of the following apply:
10(1) The prescription drugs being synchronized are covered and
11authorized by the health insurance
policy.
12(2) The prescription drugs being refilled for less than the
13standard amount are not subject to quantity limits or other
14utilization management controls that are inconsistent with the
15synchronization plan, including, but not limited to, controlled
16substance prescribing and dispensing guidelines intended to prevent
17misuse or abuse.
18(3) The prescription drugs being synchronized are dispensed
19by a single participating pharmacy.
20(4) The insured has completed at least 90 consecutive days on
21the prescription drugs being synchronized.
22(5) The prescription drugs being refilled for less than the
23standard amount are of a formulation that can be effectively split
24
over the required short fill period to achieve synchronization.
25(6) The prescriber has not done either of the following with
26respect to the prescription drugs being refilled for less than the
27standard amount:
28(A) Indicated, either orally or in his or her own handwriting,
29“No change to quantity,” or words of similar meaning.
30(B) Checked a box on the prescription marked “No change to
31quantity,” and personally initialed the box or checkmark.
32(b) This section shall not apply to a drug that is not available at
33a participating community pharmacy due to any of the following:
34(1) An industry
shortage listed on the Current Drug Shortages
35Index maintained by the federal Food and Drug Administration
36(FDA).
37(2) A manufacturer’s instructions or restrictions.
38(3) Any risk evaluation and management strategy approved by
39the FDA.
P10 1(4) A special shortage affecting the insurer’s network of
2participating pharmacies.
3(c) Nothing in this section shall be construed to establish a new
4or mandated benefit or to prevent the application of deductible or
5copayment provisions in a policy.
Section 10123.209 is added to the Insurance Code, to
8read:
(a) A health insurance policy issued, amended, or
10renewed on or after January 1, 2016, that provides coverage for
11prescription drug benefits shall allow for early refills of covered
12topical opthalmic products at 70 percent of the predicted days of
13use.
14(b) Nothing in this section shall be construed to establish a new
15mandated benefit or to prevent the application of deductible or
16copayment provisions in a policy.
No reimbursement is required by this act pursuant to
19Section 6 of Article XIII B of the California Constitution because
20the only costs that may be incurred by a local agency or school
21district will be incurred because this act creates a new crime or
22infraction, eliminates a crime or infraction, or changes the penalty
23for a crime or infraction, within the meaning of Section 17556 of
24the Government Code, or changes the definition of a crime within
25the meaning of Section 6 of Article XIII B of the California
26Constitution.
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