Bb5a31f81ClaimParallel Bio received approval from the United States Food and Drug Administration to test drug toxicity on human organoids instead of live animal trialsAgreeDisagree
Bb5a31f81ClaimIgnota Labs modifies the molecular structures of shelved drug candidates that failed clinical trials due to organ toxicity to advance them into stage-two trialsAgreeDisagree
Bb5a31f81ClaimCVS Health Corporation owns Caremark, a prescription benefit manager that provides preferential reimbursement to CVS-owned pharmaciesAgreeDisagree
Bb5a31f81ClaimPrescription benefit managers frequently reimburse independent pharmacies at rates lower than the wholesale acquisition costs of medicationsAgreeDisagree
Bb5a31f81ClaimStandard commercial progesterone formulations often contain peanut oil as an inactive ingredientAgreeDisagree
Bb5a31f81ClaimPrescription benefit managers were initially established in 1980 alongside the growth of prescription insurance plansAgreeDisagree
Bb5a31f81ClaimCompounding pharmacies prepare customized medication formulations tailored to individual patient allergies and physiological needsAgreeDisagree
Bb5a31f81ClaimPresident Barack Obama appointed former Monsanto attorney Michael Taylor to lead the food safety division at the Food and Drug AdministrationAgreeDisagree
Bb5a31f81ClaimSierra Leone, Liberia, and Burundi have each functioned with only one psychiatrist for the entire countryAgreeDisagree
Bb5a31f81ClaimA 1970s United States federal law reclassified multiple cognitive and psychedelic compounds overnight under controlled substance schedulesAgreeDisagree
Bb5a31f81ClaimAdderall is composed of a pharmaceutical mixture of four distinct amphetamine saltsAgreeDisagree
Bb5a31f81ClaimMethamphetamine is approved by the United States Food and Drug Administration under the brand name Desoxyn for ADHD and obesityAgreeDisagree
Bb5a31f81ClaimThe United States Food and Drug Administration banned the dietary supplement stimulant DMAA in 2013 due to cardiovascular risksAgreeDisagree
Bb5a31f81ClaimModafinil is classified as a Schedule IV controlled substance under United States federal drug regulationsAgreeDisagree
Bb5a31f81ClaimSelegiline, also known as Deprenyl, is an MAO inhibitor originally approved as a prescription drug for Parkinson's diseaseAgreeDisagree
Bb5a31f81ClaimThe United States Food and Drug Administration removed picamilon from the dietary supplement market in 2015AgreeDisagree
Bb5a31f81ClaimThe United States Food and Drug Administration banned ephedrine from dietary supplements in 2004AgreeDisagree
Bb5a31f81ClaimEphedrine remains legally available behind pharmacy counters in the United States without a prescription for nasal congestion and asthmaAgreeDisagree
Bb5a31f81ClaimTianeptine is an antidepressant in Europe that binds to opioid receptors at elevated dosagesAgreeDisagree
Bb5a31f81ClaimAdderall is classified as a Schedule II controlled substance in the United StatesAgreeDisagree