Oxaprozin oral caplets (Daypro) - selected label sections
- Product / population
- DAYPRO 600 mg oral caplets. This selected renal summary is for adult osteoarthritis/rheumatoid arthritis use; pediatric weight-based dosing is not supplied here.
- Renal measure
- Qualitative severe renal impairment / dialysis; the selected dose paragraph does not define a numerical CrCl cutoff.
- Source revision
- 11/2024
- Retrieved
- 2026-10-02 (not the revision date)
The official product label and its RX mirror are one underlying evidence family, not two independent clinical validations. Confirm the current exact product label before prescribing.
Renal guidance and important limits
No numerical severe-impairment cutoff is assigned in this summary. Correct hypovolemia and monitor renal function; consider hyperkalemia risk.
Use the lowest effective dose for the shortest necessary duration. Cardiovascular and gastrointestinal boxed warnings remain applicable.
| Renal setting | Source-specific action and limits |
|---|---|
| Advanced renal disease | Avoid unless anticipated benefit outweighs worsening-renal-function risk. This warning still applies to the reduced starting dose. |
| Severe renal impairment or dialysis, when treatment is justified | Start 600 mg orally once daily. Only if symptom relief is inadequate, cautiously increase to 1200 mg with close monitoring. |
Read the retained text before reformatting
| Renal setting | Source-specific action and limits |
|---|---|
| Advanced renal disease | Avoid unless anticipated benefit outweighs worsening-renal-function risk. This warning still applies to the reduced starting dose. |
| Severe renal impairment or dialysis, when treatment is justified | Start 600 mg orally once daily. Only if symptom relief is inadequate, cautiously increase to 1200 mg with close monitoring. |
No numerical severe-impairment cutoff is assigned in this summary. Correct hypovolemia and monitor renal function; consider hyperkalemia risk.
Use the lowest effective dose for the shortest necessary duration. Cardiovascular and gastrointestinal boxed warnings remain applicable.
Source: https://labeling.pfizer.com/ShowLabeling.aspx?id=552