Oklahoma 2025 Regular Session

Oklahoma Senate Bill SB771 Compare Versions

Only one version of the bill is available at this time.
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5353 STATE OF OKLAHOMA
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5555 1st Session of the 60th Legislature (2025)
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5757 SENATE BILL 771 By: Deevers
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6363 AS INTRODUCED
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6565 An Act relating to advertising; stating findings and
6666 declarations; defining terms; prohibiting certain
6767 direct-to-consumer advertising by pharmaceutical
6868 companies; listing prohibited acts; creating felony
6969 offense; providing exceptions; providing for
7070 noncodification; providing for codification;
7171 providing an effective date; and declaring an
7272 emergency.
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7777 BE IT ENACTED BY THE PEOPLE O F THE STATE OF OKLAHOMA:
7878 SECTION 1. NEW LAW A new sect ion of law not to be
7979 codified in the Oklahoma Statutes reads as follows:
8080 The Legislature of the State of Oklahoma finds and declares:
8181 1. Direct-to-consumer (DTC) advertising has the potential to
8282 exploit lay understanding of medical science, exposing the public to
8383 persuasive marketing tactics that may compromise informed decision -
8484 making, mislead consumers by underplaying risks, and cause undue
8585 burden on physicians ’ prescribing practices; and
8686 2. Past instances of misleading DTC pharmaceutical advertising
8787 have resulted in immense harm to public health such as the
8888 aggressive advertising campaigns for OxyContin, Vioxx, and Zyprexa.
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140140 Purdue Pharma’s OxyContin advertising played a huge part in the
141141 opioid addiction crisis and the company settled with the United
142142 States Department of Justice for Eight Billion Three Hundred Million
143143 Dollars ($8,300,000,000.00) for their role in 2020. In 2019, Purdue
144144 settled with Oklahoma for Two Hundred Seventy Million Dollars
145145 ($270,000,000.00);
146146 3. Newly approved medications advertis ed directly to consumers
147147 may present unknown long -term risks, exposing patients to potential
148148 harm, such as with the Vioxx debacle which resulted in Merck paying
149149 Four Billion Eight Hundred Fifty Million Dollars ($4,850,000,000.00)
150150 to end the lawsuits;
151151 4. The United States is one of only two countries globally that
152152 permits DTC pharmaceutical advertising. One hundred ninety-three
153153 out of the world’s one hundred ninety-five countries do not permit
154154 DTC pharmaceutical advertising. Prohibiting this practice woul d
155155 align Oklahoma with the global norm;
156156 5. The costs of advertising are frequently passed on to
157157 consumers in a field where such advertising is not necessary, with
158158 advertising budgets for some drugs in the hundreds of millions of
159159 dollars, resulting in higher drug prices and imposing financial
160160 burdens on patients and health care systems;
161161 6. DTC advertising could compromise the integrity of the
162162 doctor-patient relationship by creatin g improper pressure on doctors
163163 to prescribe certain advertised medications. B anning DTC
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215215 pharmaceutical advertising would encourage better communication and
216216 trust between patients and their health care providers, fostering
217217 informed and responsible medical decision-making;
218218 7. DTC advertising often prioritizes the promotion of lifestyle
219219 medications over essential, life -saving drugs, distorting health
220220 care priorities; and
221221 8. DTC advertising promotes the over -medicalization of common
222222 conditions, often urging consumers to pursue pharmacological
223223 solutions over alternative treatments or l ifestyle modifications.
224224 SECTION 2. NEW LAW A new section of law to be codified
225225 in the Oklahoma Statutes as Section 9000 of Title 63, unless there
226226 is created a duplication in numbering, reads as follows:
227227 As used in this act:
228228 1. “Direct-to-consumer pharmaceutical advertising ” refers to
229229 any promotional communication targeting consumers including, but not
230230 limited to, television, radio, print media, digital pla tforms, and
231231 social media, that markets prescription drugs; and
232232 2. “Pharmaceutical companies” refers to entities involved in
233233 the research, development, production, or distribution of
234234 prescription drugs.
235235 SECTION 3. NEW LAW A new sect ion of law to be codified
236236 in the Oklahoma Statutes as Section 9001 of Title 63, unless there
237237 is created a duplication in numbering, reads as follows:
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289289 A. No pharmaceutical company shall engage in direct -to-consumer
290290 advertising of prescription drugs within this state.
291291 B. Prohibited activities include, but are not limited to:
292292 1. Broadcasting advertisements for prescription drugs via
293293 television, radio, online streaming services, billboards, email,
294294 text messaging, or social media;
295295 2. Publishing advertisement s for prescription drugs in print or
296296 digital publications distributed within Oklahoma; and
297297 3. Targeting Oklahoma residents with prescription drug
298298 advertisements through digital or social media platforms.
299299 SECTION 4. NEW LAW A new se ction of law to be codified
300300 in the Oklahoma Statutes as Section 9002 of Title 63, unless there
301301 is created a duplication in numbering, reads as follows:
302302 A. Any individual or entity violating the provisions of this
303303 act shall, upon conviction, be guilty of a felony.
304304 B. A felony conviction under this act shall be punishable by a
305305 fine not exceeding Five Hundred Thousand Dollars ($500,000.00) or
306306 imprisonment in the custody of the Department of Corrections for a
307307 term not exceeding five (5) years, or by both such fine and
308308 imprisonment.
309309 C. Each instance of prohibited advertising shall cons titute a
310310 separate offense.
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362362 SECTION 5. NEW LAW A new section of law to be codified
363363 in the Oklahoma Statutes as Section 9003 of Title 63, unless there
364364 is created a duplication in numbering, reads as follows:
365365 This act shall not apply to:
366366 1. Educational materials distributed by health care providers
367367 directly to their patients;
368368 2. Internal communications within health care organizations;
369369 3. Communications req uired by federal or state law;
370370 4. Advertisements related to public health cam paigns that
371371 educate the public about medication, treatments, and health
372372 conditions, provided they are not promoting a specific
373373 pharmaceutical product;
374374 5. Advertisements that pro mote clinical trials or other
375375 research opportunities related to prescription drugs, provided that
376376 they comply with ethical and legal standards and are not promoting
377377 the use of the drug outside of a controlled trial setting;
378378 6. Advertisements that inform c onsumers about insurance
379379 coverage for prescription drugs, such as coverage opt ions through
380380 Medicaid, Medicare, or private insurers, provided these
381381 advertisements do not directly promote specific drugs or brands; or
382382 7. Advertisements or communications rela ted to patient
383383 assistance programs that provide financial support or subsidies for
384384 individuals who are unable to afford their medications, provided
385385 these communications are not directly promoting a specific product.
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437437 SECTION 6. This act shall become effective July 1, 2025.
438438 SECTION 7. It being immediately necessary for the preservation
439439 of the public peace, health or safety, an emergency is hereby
440440 declared to exist, by reason whereof this act shall take effect and
441441 be in full force from and after its passage and approval.
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443443 60-1-1438 DC 1/15/2025 3:32:32 PM