The Morning Journal (Lorain, OH)

Drugs from Canada not answer

- C. Michael White The Conversati­on is an independen­t and nonprofit source of news, analysis and commentary from academic experts.

President Trump has called for ways to allow U.S. residents to buy cheaper prescripti­on drugs from Canada. Many drugs are cheaper in Canada, thanks to government price controls in that country.

I teach a course in medication economics and have written and spoken about drug pricing at the national and state level. My assessment is that buying prescripti­on drugs from our northern neighbor can be risky in terms of quality and safety. And, it isn’t likely to reduce your drug prices.

Canada offers the same drugs at cheaper prices because the Canadian government, which foots the bill for prescripti­on drugs, will not pay for a drug if a government review board believes the cost is excessive. This board, the Patented Medicine Prices Review Board, is a quasi-judicial agency. It was establishe­d by Canadian Parliament in 1987 under the auspices of the minister of health. If the board thinks a price is too high, it won’t pay. Faced with loss of the entire Canadian market if it doesn’t lower prices, manufactur­ers capitulate.

In the U.S., price negotiatio­ns occur between individual insurers and the manufactur­ers. The government is not involved.

Also, drug manufactur­ers in the U.S. can reach consumers and promote drugs directly through advertisin­g, something not allowed in any other country except New Zealand. Thus, they create demand – and incur hundreds of millions of dollars in advertisin­g that they recoup in the prices they charge.

Insurers developed a way to allow consumers choice and save money. In this setup, expensive drugs are still covered, but drugs in tier one have much lower copay costs than drugs in higher tiers.

When consumers find they are paying $100 for a tier two option instead of $20 for a tier one option, they call their doctor and ask for a cheaper alternativ­e. Manufactur­ers with a higher tiered drug have responded by creating prescripti­on coupons instead of lowering the overall cost of the drug. When the consumer goes to the pharmacy, they pay $20 and the manufactur­er pays the other $80 of their copay.

While this pricing system may alleviate the out-of-pocket burden on the consumer, manufactur­ers simply raise the overall price to shift the costs back on the insurers. The additional costs borne by the insurers are then baked into the higher premiums.

Buying drugs from Canada is illegal in the U.S., but the Food and Drug Administra­tion website says it “typically does not object to personal imports of drugs” if there is no commercial­ization or promotion of the drug to U.S. residents; individual­s verify in writing that the drug is for his or her own use; and the drug doesn’t present an unreasonab­le risk.

Safety is also an issue. The FDA stresses that it cannot ensure the safety and effectiven­ess of drugs it has not approved. In fact, four former FDA commission­ers warn that having prescripti­ons filled by foreign pharmacies can put substandar­d, counterfei­t, adulterate­d or contaminat­ed drugs into consumers’ hands.

The Department of Health and Human Services in July announced a drug importatio­n action plan outlining the parameters under which prescripti­on drugs currently routed to Canada could make their way to U.S. consumers.

The agency did this in part because of the need to ensure that the products originate in Canada. In 2005, the FDA seized 1,700 drug products allegedly imported from Canada, and the majority did not originate there.

The plan requires that only manufactur­ing plants certified to manufactur­e drugs for the U.S. market be allowed; that the drugs go to U.S. pharmacies, directly or through a wholesaler; and that the drugs be labeled according to U.S. standards.

Problems would still exist.

The most important would be the loss of an accurate way to track negative drug side effects after drugs reach the market. It would be impossible for the FDA to determine whether adverse events would be due to the U.S. version of the drug, poor quality of the manufactur­er, storage or shipment of the drugs into the U.S.

Second, importatio­n likely would eliminate the pharmacist-patient relationsh­ip. This could possibly increase the risk of medication errors, such as overdoses and the taking of duplicate medication­s. This is because consumers likely would get prescripti­ons from myriad pharmacies. Different drug importatio­n programs would likely focus on certain classes of medication­s.

Simply put, for the next several years, most Americans will be excluded from importing any prescripti­on drugs from Canada, and everyone will be excluded from importing the most expensive ones.

A recent study estimates that the entire Canadian drug supply would be exhausted in 183 days, if only 20% of U.S. prescripti­ons were filled using Canadian prescripti­on drug sources. The U.S. and Canada cannot force the companies to manufactur­e more.

Also, Canadians could end up paying more, and Canadians are not happy about this. U.S. drugmakers could give up on Canada and focus on the more profitable U.S. market.

When profitabil­ity is reduced, there will be consequenc­es. Manufactur­ers will invest fewer dollars in research and developmen­t and will shift their focus from high-cost biological drugs for rare diseases to more reasonably priced drugs for more common diseases. The system will be better for some and worse for others, which is why we haven’t already made these difficult choices in the U.S.

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