Mechanism of action: Hydrocodone ER (q12h) balliculeVisual mnemonic: Hydrocodone ER (q12h) mascot “Viking Hydrant code” Viking for Vicodin (combo with acetaminophen)
What it isFirst single-agent hydrocodone (ZOHYDRO ER, 2013) — q12h ER capsule with no acetaminophen, freeing dosing from APAP hepatotoxicity limits.
Why this oneSame molecule and receptor pharmacology as the parent card — the formulation (and its label) is the difference.
What limits itClass warnings of the parent molecule apply unchanged.
Molecular structure: Hydrocodone ER (q12h)
Hydrocodone ER (q12h) prescription history
Animated chart of estimated U.S. prescriptions per year, Opioid analgesics (1900–2026). Hydrocodone ER (q12h) enters in 2013 (estimated).
Severe and persistent pain requiring an opioid analgesic, not adequately treated with alternatives (incl. IR opioids); not for prn use
Adults (opioid non-tolerant)
10 mg q12h
Individualized
Undefined (single dose >40 mg or total daily dose >80 mg only in opioid-tolerant patients)
Severe and persistent pain (conversion from other opioids)
Adults (opioid-tolerant / converting)
Oral hydrocodone: half the total daily dose q12h; other oral opioids: Table 1 conversion, reduce by 25%, round down, divide q12h; fentanyl patch: start 18 h after removal, ~10 mg q12h per 25 mcg/hr
Individualized
Undefined
Titration Increase by 10 mg q12h (20 mg/day) every 3 to 7 days
Renal Use a low initial dose; regularly evaluate for respiratory depression, sedation, and hypotension
Hepatic Mild–moderate: no starting-dose adjustment; severe: initiate 10 mg q12h and titrate carefully
Every 12 hours dosing; single dose >40 mg or total daily dose >80 mg only for opioid-tolerant patients (≥ one week of ≥60 mg oral morphine/day or equivalent)
Instructions
Swallow capsules whole; do not cut, break, chew, crush, or dissolve
Administer orally every 12 hours; not for as-needed (prn) use
Do not consume alcohol or alcohol-containing products
Discuss/prescribe an opioid overdose reversal agent (naloxone, nalmefene)
To discontinue in physically dependent patients: patient-specific taper, initial reduction no greater than 10% to 25% of total daily dose, then reduce every 2 to 4 weeks; briefer-use patients may tolerate a faster taper; pause or slow if withdrawal; do not stop abruptly
Available strengths
ER cap 10, 15, 20, 30, 40, 50 mg
Contraindications
Significant respiratory depression
Acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment
Known or suspected gastrointestinal obstruction, including paralytic ileus