What are the side effects of terbinafine (Lamisil)?

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Side Effects of Terbinafine (Lamisil)

Terbinafine commonly causes gastrointestinal side effects (49% of cases) such as nausea, diarrhea, dyspepsia, abdominal pain, and flatulence, as well as dermatological reactions (23%) including rash, pruritus, and urticaria. 1, 2

Common Side Effects

  • Gastrointestinal effects:

    • Nausea
    • Diarrhea
    • Dyspepsia (indigestion)
    • Abdominal pain
    • Flatulence
  • Dermatological effects:

    • Rash
    • Pruritus (itching)
    • Urticaria (hives)
    • Eczema
  • Sensory disturbances:

    • Taste disturbance or loss of taste (may be prolonged or permanent)
    • Smell disturbance or loss of smell (may be prolonged or permanent)

Serious Side Effects

Hepatotoxicity

  • Liver enzyme abnormalities are common
  • Rare cases of serious hepatic toxicity have been reported 1
  • Not recommended in patients with active or chronic liver disease
  • Liver failure requiring transplantation or resulting in death has occurred 2
  • Pretreatment serum transaminase testing is recommended

Severe Cutaneous Adverse Reactions

  • Stevens-Johnson syndrome
  • Toxic epidermal necrolysis
  • Erythema multiforme
  • Exfoliative dermatitis
  • Bullous dermatitis
  • Drug reaction with eosinophilia and systemic symptoms (DRESS) 2

Neuropsychiatric Effects

  • Depressive symptoms 2
  • Changes in mood
  • Loss of energy or interest in daily activities

Rare but Serious Adverse Events

  • Severe neutropenia (discontinue if neutrophil count ≤1,000 cells/mm³) 2
  • Hypersensitivity syndrome reaction (cutaneous eruption, fever, lymphadenopathy, hepatic dysfunction) 3
  • Rhabdomyolysis with acute kidney injury (characterized by muscle pain, weakness, dark urine) 4

Drug Interactions

Terbinafine inhibits CYP450 2D6 isozyme and may interact with:

  • Antidepressants (particularly tricyclics)
  • Antipsychotics
  • Cardiovascular medications
  • Desipramine
  • Caffeine
  • Cyclosporine
  • Fluconazole
  • Rifampin
  • Cimetidine 2, 5

The combination of terbinafine with tamoxifen should be avoided as it can reduce tamoxifen's efficacy 5.

Special Populations

Pregnancy and Breastfeeding

  • Contraindicated in pregnancy 1
  • Manufacturers caution against men fathering a child for 6 months after therapy 1
  • Passes into breast milk and may harm babies 2

Patients with Comorbidities

  • Not recommended in patients with active or chronic liver disease 1
  • Terbinafine clearance is decreased in severe liver or kidney disease 1
  • Generally well-tolerated in older and multimorbid patients due to fewer drug interactions compared to azole antifungals 5

Monitoring Recommendations

  • Obtain pretreatment serum transaminases 2
  • Discontinue terbinafine if:
    • Signs of liver injury develop
    • Taste or smell disturbance occurs
    • Depressive symptoms emerge
    • Severe skin reactions appear
    • Neutropenia develops

The overall incidence of serious adverse events with terbinafine is low (0.04% in postmarketing surveillance) 1, making it generally well-tolerated for most patients when proper monitoring is implemented.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Hypersensitivity syndrome reaction to oral terbinafine.

The Australasian journal of dermatology, 1998

Research

Rhabdomyolysis and Acute Kidney Injury Associated With Terbinafine Use: A Case Report.

Canadian journal of kidney health and disease, 2020

Research

[Terbinafine : Relevant drug interactions and their management].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2016

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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