On Monday, the discussion of Canada’s Schedule I substances was brought up and it got me thinking about how drugs are
classified in the U.S. A Schedule I drug in the U.S. is any drug that has a
high potential for abuse and has no accepted medical use. Marijuana is listed
as a Schedule I drug, however it is legal medicinally in 23 states and in
Washington D.C. This disparity has always confused me – it poses several
problems for health care professionals, patients, and health care in
general. How can the best form of health care be delivered if everyone
from the state to federal level is not on the same team?
To get around the federal legal restrictions,
physicians can only recommend medical cannabis, not prescribe it. Without
doctors’ prescribing power, patients are typically left to decide what to take,
which can be harmful if they are not educated on the safest forms of
treatment. Some physicians feel
uncomfortable recommending medical marijuana because they do not trust the
unregulated and uncontrolled safety of the supply chain.
The states that have legalized medicinal
marijuana all have different requirements pertaining to dosage forms offered
and what qualifies a patient for treatment. They also have different
requirements for how much cannabis or cannabis-containing product a person can
own. For instance, Texas only legalizes medicinal cannabis oil for epilepsy (no
other condition) if they have not responded to any other treatments. However,
in California, there is a completely opposite law. Under the Compassionate Use
Act (Proposition 215), patients are legally protected if they are diagnosed
with an illness where use of marijuana is “deemed appropriate and has been
recommended by a physician.”
Two states (Connecticut and Minnesota) have made
it legal for pharmacists to dispense medical marijuana. Dispensing centers in
these states are pharmacist-led and pharmacists work with patients to determine
dosing regimens based on their condition. I got to wondering – how comfortable
would you feel preparing a dosing regimen for a substance that has very minimal
clinical data and is also classified as illegal by the federal government? Perhaps
rescheduling medical marijuana to a Schedule II drug would allow for more
clinical studies approved by the FDA. Uncertainties about risks, benefits, and quality control could be answered. But until then, it seems like a gray area will remain.
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