Adult
Oxytetracycline
Warning
General Information
Tetracycline
Formulary antimicrobial: Use in accordance with Trust guidelines
AWaRe antibiotic classification: 'Watch'. Use as per guidelines. All other indications to be discussed with Micro/ID.
For all information regarding interactions, contraception, pregnancy and breastfeeding and additional information, see BNF and Summary of Product Characteristics (SPC).
Dosing
| Oral dose | |
| Susceptible infections | 250mg-500mg QDS |
| Acne or rosacea | 500mg BD |
Renal and hepatic impairment
Renal impairment
- Avoid if possible in renal impairment, due to potential nephrotoxicity and increased risk of azotaemia, hyperphosphataemia and acidosis. Use only after consideration of risk v benefit.
|
eGFR (mL/min/1.73m2) |
Oral dose |
|
51 or more |
Dose as in normal renal function |
|
20-50 |
250mg-500mg OD-BD |
|
Less than 20 |
250mg-500mg OD |
|
HDF/High Flux |
Unknown dialysability Dose as in eGFR less than 20mL/min/1.73m2 |
|
PD |
Not dialysed Dose as in eGFR less than 20mL/min/1.73m2 |
Note: Doses are based on Renal Drug Database
Hepatic impairment
- Contraindicated in hepatic dysfunction.
- Use with caution in patients with hepatic impairment or those receiving potentially hepatotoxic drugs; avoid high doses in these patients.
References
- Crescent Pharma Limited. Oxytetracycline 250 mg Tablets summary of product characteristics. Last revision of the text 02/12/24. Accessed via https://products.mhra.gov.uk Accessed 5/4/26
- The Renal Drug Database. Oxytetracycline. Last updated 13/11/24. Accessed via https://renaldrugdatabase.com Accessed 5/4/26.
- British National Formulary. Oxytetracycline. BNF online accessed via www.medicinescomplete.com Accessed 5/4/26.