Which antibiotics are safe for patients with myasthenia gravis (MG)?

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Last updated: July 26, 2025View editorial policy

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Safe Antibiotics for Patients with Myasthenia Gravis

Patients with myasthenia gravis should avoid fluoroquinolones, aminoglycosides, and macrolides due to their potential to worsen myasthenic symptoms, and instead use penicillins, cephalosporins, or tetracyclines (except in specific circumstances) as first-line antibiotic choices. 1

Safe Antibiotic Options for MG Patients

First-Line Safe Options:

  • Penicillins (amoxicillin, ampicillin, piperacillin)

    • Generally safe, though rare cases of exacerbation have been reported 2
    • Monitor patients closely after administration
  • Cephalosporins (all generations)

    • No significant neuromuscular junction effects
    • Good alternative when broader coverage needed
  • Tetracyclines (doxycycline, minocycline)

    • Generally safe in patients with normal renal function
    • Dose reduction required when GFR <45 ml/min/1.73 m² 1
    • Can exacerbate uremia in advanced kidney disease

Second-Line/Alternative Options:

  • Tigecycline
    • Has been used successfully in MG patients with community-acquired pneumonia 3
    • Consider when first-line options are contraindicated

Antibiotics to Avoid in MG

High Risk (Absolutely Contraindicated):

  • Fluoroquinolones (ciprofloxacin, levofloxacin, moxifloxacin)

    • Directly block neuromuscular transmission 4
    • Can precipitate myasthenic crisis even at normal doses
  • Aminoglycosides (gentamicin, tobramycin, amikacin)

    • Impair acetylcholine release at neuromuscular junction
    • Can rapidly worsen muscle weakness
  • Macrolides (azithromycin, erythromycin, clarithromycin)

    • Can exacerbate myasthenic symptoms
    • Reduce dose by 50% when GFR <30 ml/min/1.73 m² if absolutely necessary 1

Special Considerations

Infection Management in MG:

  1. Treat infections promptly and aggressively

    • Infections themselves can trigger MG exacerbations
    • Delay in treatment may lead to respiratory compromise
  2. Antibiotic selection algorithm:

    • Identify infection site and likely pathogens
    • Choose from safe antibiotic classes (penicillins, cephalosporins)
    • Consider severity of MG and current immunosuppressive regimen
    • Monitor closely for signs of worsening weakness after antibiotic initiation
  3. Monitoring after antibiotic initiation:

    • Assess for new or worsening muscle weakness
    • Monitor respiratory function (vital capacity, negative inspiratory force)
    • Have rescue medications available (pyridostigmine, corticosteroids)

Risk Factors for Antibiotic-Induced Exacerbation:

  • Previous history of antibiotic-triggered exacerbation
  • Poorly controlled MG symptoms
  • Concurrent use of other medications affecting neuromuscular junction
  • Renal impairment (affects clearance of many antibiotics)

Management of Antibiotic-Induced Exacerbation

If worsening of MG symptoms occurs after antibiotic administration:

  1. Discontinue the offending antibiotic immediately
  2. Switch to a safer alternative from a different class
  3. Consider increasing acetylcholinesterase inhibitor dose (pyridostigmine)
  4. For severe exacerbations, consider IVIG (2 g/kg over 5 days) or plasmapheresis 1
  5. Monitor respiratory function closely and be prepared for possible mechanical ventilation

Conclusion

When treating infections in MG patients, the safest approach is to use penicillins or cephalosporins as first-line agents. Tetracyclines are generally safe but require dose adjustment in renal impairment. Always avoid fluoroquinolones, aminoglycosides, and macrolides unless absolutely necessary, and monitor patients closely after initiating any antibiotic therapy.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Exacerbation of myasthenia gravis after amoxicillin therapy: a case series.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020

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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