How to Write a Prescription for Lidocaine 5% Patches
Prescribe lidocaine 5% patches with instructions to apply up to 3 patches to the painful area for 12 hours daily, followed by a mandatory 12-hour patch-free interval, with a quantity of 90 patches per month (30-day supply). 1
Prescription Format
Write the prescription as follows:
Medication: Lidocaine 5% topical patch (700 mg per patch, 10 cm × 14 cm)
Quantity: 90 patches (30-day supply)
Directions: Apply up to 3 patches to the painful area once daily. Leave on for 12 hours, then remove for 12 hours. Apply to intact skin only.
Refills: As appropriate for the clinical situation
Key Prescribing Instructions to Include
Application Protocol
- Maximum of 3-4 patches applied simultaneously to cover the painful area 1, 2, 3
- 12 hours on, 12 hours off schedule is mandatory to prevent cumulative toxicity and skin sensitization 1, 2
- Apply to intact skin only over the most painful regions—never on broken or inflamed skin, as this dramatically increases systemic absorption 1, 2, 3
Quantity Calculation
- If using 3 patches daily with the 12-hour on/off schedule, the patient needs 90 patches per 30-day supply 1
- The 5% prescription strength is preferred over the 4% over-the-counter formulation for neuropathic pain 1
Critical Safety Parameters to Communicate
Absolute Contraindications
- Advanced liver failure/hepatic dysfunction—hepatic impairment reduces lidocaine clearance by 60%, creating toxicity risk even with topical application 1, 2
- Known hypersensitivity to amide-type local anesthetics 1, 2
- Application to broken or inflamed skin 1, 2, 3
Important Precautions
- Avoid excessive heat application over patch areas, as this increases systemic absorption 1, 2, 3
- Do not use within 4 hours of other local anesthetic interventions to prevent cumulative toxicity 1, 2
- Remove patches before starting intravenous lidocaine therapy if applicable 2, 3
Signs of Systemic Toxicity to Monitor
Instruct patients to watch for and report:
- Dizziness or confusion 1, 2, 3
- Drowsiness or altered consciousness 1, 2
- Bradycardia 1, 2
- Muscle twitching 1, 2, 3
- Perioral numbness 2
Though these are uncommon with proper topical use, they warrant immediate discontinuation 1, 4
Special Population Considerations
Renal Impairment
- No dose adjustment required for renal impairment with lidocaine patches, unlike gabapentin or pregabalin which require dose adjustment 1, 2
Elderly Patients
- No dose adjustment needed—the patch remains safe in elderly patients due to minimal systemic absorption 2
- Elderly patients are at higher risk with systemic lidocaine but not with topical patches 2
Hepatic Impairment
Expected Efficacy and Trial Duration
Trial Period
- Allow at least 3-4 weeks for an adequate therapeutic trial before determining efficacy 1, 3
- For postherpetic neuralgia specifically, approximately 60% of patients achieve moderate to complete pain relief with proper application 3
When to Add Combination Therapy
- If inadequate relief after 3-4 weeks, consider adding gabapentin (starting 100-300 mg nightly, titrating to 900-3600 mg daily in divided doses) or pregabalin (starting 50 mg three times daily, titrating to 100 mg three times daily) for the neuropathic component 5, 1, 3
- Lidocaine patches may be used as coanalgesic in combination with opioids, antidepressants, and/or anticonvulsants 5, 2
Common Pitfalls to Avoid
- Do not prescribe for widespread pain distribution—lidocaine patches are most effective for well-localized, superficial neuropathic pain rather than deep radicular pain 1, 3
- Do not use for wound care—manufacturers explicitly warn against application to open wounds 2
- Do not exceed 12 hours of continuous application—the patch-free period is essential to minimize skin irritation and prevent toxicity 1, 2, 3
- Do not assume pacemakers are a contraindication—this is only relevant for intravenous lidocaine, not topical patches 2
Pharmacokinetics and Safety Profile
- Minimal systemic absorption occurs even with four patches applied over 24 hours, with highest measured blood levels at only 0.1 micrograms/ml 3, 4
- Adverse events are rare and mild, mostly limited to skin redness or irritation at the application site 6, 7
- No clinically significant drug-drug interactions with anticoagulants (warfarin or DOACs) due to minimal systemic absorption 2