Inclusion criteria | |
 Patients 18 years or older diagnosed with cancer | |
 Patients admitted to UC Christus Clinical Hospital | |
 Patients reporting acute pain > or = a 4 in the Verbal Analog Scale | |
 Patients may present with somatic, visceral, or neuropathic pain | |
 Patients with prior opioid use or virgin to opioids were eligible | |
 Patients may be users of NSAIDs or corticosteroids | |
Exclusion criteria | |
 Patients who refuse to enter the study | |
 Patients who are unable to communicate in Spanish | |
 Altered mental status such as delirium | |
 Patients presenting acute liver failure or chronic liver damage Child C | |
 Patients with a history of allergies or hypersensitivity to acetaminophen | |
 Patients imminently dying or with a survival prognosis of less than 72 h | |
Dropout criteria | |
 Patients who are unable to complete assessments due to altered mental status or clinical decline | |
 Patients who died | |
 Patients who withdrew consent throughout the intervention and follow-up period |