tetracaine: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
tetracaine: clinical details
Prescribing considerations
- Limit application to intact, normal skin and ensure the planned procedure does not risk middle-ear exposure.
- Use cautiously in epilepsy despite low systemic availability through intact skin.
- Repeated exposure may increase contact sensitisation; minimise contact and wash hands after handling.
- Parahydroxybenzoate preservatives may cause allergic reactions, including delayed reactions.
Contraindications and cautions
- Hypersensitivity to tetracaine, another ester-type local anaesthetic or a formulation excipient.
- Premature babies until one month after the expected delivery date, and full-term infants younger than one month.
- Application to broken skin, mucous membranes, eyes or ears.
Monitoring
- Inspect the site for excessive redness, oedema, itching or blistering.
- Remain alert to neurological toxicity if ingestion, excessive exposure or inappropriate application is suspected.
Clinical pharmacology
Tetracaine blocks voltage-dependent sodium conductance in peripheral nerves and is rapidly hydrolysed in blood, mainly by plasma pseudocholinesterase. Percutaneous systemic availability from intact skin is low but variable.
Formulation and product differences
- The selected product is a white, opalescent cutaneous gel supplied in single-use aluminium tubes.
- It contains sodium methyl and propyl parahydroxybenzoates, which can cause allergic reactions.
- It requires refrigerated storage, must not be frozen and should be protected from heat.
tetracaine interactions
No medicine interactions are listed as known for the selected gel. Tell the healthcare professional about other medicines and local anaesthetics being used.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.