Lidocaine 15% w/w is a high-potency topical amide local anesthetic, primarily formulated as a patch or medicated plaster. It is indicated for the treatment of post-herpetic neuralgia (PHN) and other localized neuropathic pain conditions. It works by stabilizing neuronal membranes and inhibiting the ionic fluxes required for the initiation and conduction of nerve impulses, specifically by blocking voltage-gated sodium channels.
Adult: Apply up to 3 patches (or the equivalent in plaster size) to the most painful area(s) for up to 12 hours within a 24-hour period. Patches may be cut to size before removal of the release liner. Do not reapply for at least 12 hours after removal.
Note: 1. Apply to intact, dry, non-hairy skin. 2. Clip hair, do not shave. 3. Apply patch to area of maximum pain. 4. Wear for up to 12 hours, then remove. 5. Allow skin to rest for 12 hours before next application. 6. Wash hands after handling. 7. Do not apply with external heat sources.
Lidocaine acts by blocking voltage-gated sodium channels (NaV channels, particularly NaV1.7, NaV1.8) on the neuronal cell membrane. This blockade inhibits the transient influx of sodium ions (Na+) necessary for the depolarization phase of the action potential. By preventing depolarization, it halts the initiation and propagation of nerve impulses, leading to a reversible loss of sensation (analgesia) in the localized area.
Pregnancy: Category B (US FDA). No well-controlled studies in pregnant women. Use only if clearly needed. Systemic absorption is low with proper use.
Driving: May cause dizziness, drowsiness, or blurred vision. Patients should be cautioned about operating machinery or driving until they know how the medication affects them.
| Class I Antiarrhythmics (e.g., Mexiletine, Tocainide) | Additive cardiac toxicity; increased risk of arrhythmia. | Major |
| CYP1A2 & CYP3A4 Inhibitors (e.g., Ciprofloxacin, Fluconazole, Amiodarone) | Increased lidocaine plasma levels, risk of systemic toxicity. | Moderate |
| Other Local Anesthetics | Additive toxic effects. | Major |
| Beta-blockers (e.g., Propranolol) | May reduce hepatic blood flow, increasing lidocaine levels. | Moderate |
Same composition (Lidocaine (15% w/w)), different brands: