DYNEXAN OINTMENT
AMETHOCAINE HYDROCHLORIDE
What it does
Amethocaine is a local anesthetic used to numb specific areas of the body to relieve pain during medical procedures.
Commonly used for: pain relief during minor procedures, anesthesia for skin and mucous membranes
Read more in plain English ↓Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.
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Source: South African Health Products Regulatory Authority · fetched 2026-04-15 21:25:43 · updated 2026-10-21 04:01:57
About this medicine
Amethocaine is a local anesthetic used to numb specific areas of the body to relieve pain during medical procedures.
What it treats
- pain relief during minor procedures
- anesthesia for skin and mucous membranes
How it works
Amethocaine works by blocking the nerves in the area where it is applied, preventing pain signals from reaching the brain.
Who it's for
Amethocaine is suitable for adults and children needing local pain relief.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
Clinical monograph: amethocaine
BNF-referencedAmethocaine, also known as tetracaine, is a local anesthetic of the ester type, commonly used for its rapid onset and prolonged duration of action. It is primarily employed in procedures requiring localized numbing, such as minor surgical interventions and dental procedures. Its effectiveness is due to its ability to block nerve impulse transmission.
Indications
- Local anesthesia for minor surgical procedures
- Dental procedures requiring local anesthesia
- Topical anesthesia for mucous membranes
Dosage
Children: Refer to BNF for Children for appropriate dosing guidelines in pediatric populations.
Adults: Refer to the BNF for recommended dosages, which may vary based on the specific procedure and formulation used.
Mechanism of action
Amethocaine produces local anesthesia by blocking sodium ion channels involved in the initiation and conduction of neuronal impulses, preventing the propagation of action potentials in nerve fibers.
Pharmacodynamics
The local anesthetic effects of amethocaine occur through the reversible inhibition of sodium channels in neuronal membranes. By preventing sodium influx during depolarization, amethocaine effectively stabilizes the neuronal membrane, leading to a decrease in nerve excitability and conduction. This results in a loss of sensation in the targeted area.
Pharmacokinetics
Amethocaine is well-absorbed at the site of administration. It has a relatively slow systemic absorption rate compared to other local anesthetics due to its higher lipid solubility. The onset of action is rapid, typically within minutes, and the duration of effect can last from 1 to 3 hours, depending on the concentration used. Metabolism occurs primarily in the plasma by hydrolysis through esterases, and it is excreted in the urine as metabolites.
Adverse effects
- Allergic reactions
- Local irritation
- Nausea
- Dizziness
- Hypotension
Precautions
- Use with caution in patients with a history of hypersensitivity to local anesthetics
- Monitor for signs of systemic toxicity, especially in large doses or when used in sensitive areas
Pregnancy
Amethocaine should only be used if the potential benefit justifies the potential risk to the fetus. Consult with a healthcare professional.
Breast-feeding
Use with caution, as it is not known whether amethocaine is excreted in breast milk.
Storage
Store at room temperature, away from moisture and heat. Keep out of reach of children.
Formulations
- Topical solution
- Ointment
- Gel
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Molecular reference: amethocaine
PubChem CID 5411Molecular formula: C15H24N2O2
Mechanism of action
Tetracaine is an ester-type anesthetic and produces local anesthesia by blocking the sodium ion channels involved in the initiation and conduction of neuronal impulses.
Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.