“…Notwithstanding all the benefits of small molecule drugs, it remains the case that they are also widely associated with various morbidities and mortalities, often referred to as “adverse drug reactions” (ADRs) (e.g., [ 326 , 327 , 328 , 329 , 330 , 331 , 332 , 333 , 334 , 335 , 336 , 337 , 338 , 339 , 340 , 341 , 342 , 343 , 344 , 345 , 346 ]). Despite the lengthy and complex regulatory hurdles that drugs must overcome before being marketed (and toxicity remains a major cause of so-called “attrition” where drug candidates are pulled before they even get to market [ 347 , 348 , 349 , 350 , 351 , 352 , 353 ]), ADRs are extremely common (and hard to anticipate, given the huge genetic and phenotypic variation in human populations [ 354 ]).…”