ZYPREXA RELPREVV


What it isEvery-two-to-four-week intramuscular olanzapine pamoate for schizophrenia — the only long-acting olanzapine.
Why this oneIt brings olanzapine’s efficacy to patients who respond to the molecule but cannot sustain oral adherence.
What limits itPost-injection delirium/sedation syndrome is the defining hazard: a REMS program requires administration at a registered facility with three hours of observation after every dose.
Read the full label on DailyMed ↗
| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Schizophrenia | Adults | First 8 weeks (per target oral olanzapine dose): 210 mg/2 wk or 300 mg/2 wk or 405 mg/4 wk | Maintenance after 8 wk: 150 mg/2 wk, 210 mg/2 wk, 300 mg/2 wk, or 300 mg/4 wk | 405 mg/4 wk or 300 mg/2 wk (higher doses not evaluated) |
Renal Undefined
Hepatic Undefined
Administered every 2 to 4 weeks
Available strengths
Pregnancy Third-trimester exposure risks neonatal extrapyramidal and/or withdrawal symptoms; epidemiologic data have not established a drug-associated risk of major birth defects
Lactation Present in human milk; reports of excess sedation, irritability, poor feeding, and extrapyramidal symptoms in exposed infants
| Strength | #/mo | generic $/unit | CostPlus | |
|---|---|---|---|---|
| 210 mg | inj | per unit | not offered | |
| 300 mg | inj | per unit | not offered | |
| 405 mg | inj | per unit | not offered |
⚠ BOXED WARNING
Legacy pregnancy categoryC
Defining liabilityPost-injection delirium/sedation syndrome requires monitored administration; metabolic toxicity is substantial.