Myasthenia Gravis: Safe and Unsafe Medications

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Understanding Medications Management
Myasthenia Gravis (MG) is an antibody-mediated autoimmune condition that affects the communication between nerves and muscles, leading to muscle weakness and fatigue. Proper management of MG often involves a combination of drugs and lifestyle adjustments. However, certain medications can exacerbate MG symptoms or interfere with treatment, making it essential to know which drugs are safe and which are not. Understanding medications to avoid is crucial for effective disease management.
Contraindicated Drugs & Antibiotics
Contraindicated drugs are medications that should be completely avoided by individuals with Myasthenia Gravis due to their potential to worsen symptoms or cause severe complications. These drugs can interfere with neuromuscular transmission and significantly impact muscle function, potentially leading to MG exacerbation.
Aminoglycoside Antibiotics
Aminoglycoside antibiotics, such as gentamicin, streptomycin, and neomycin, are known to exacerbate muscle weakness in MG patients. These antibiotics can impair neuromuscular transmission, leading to increased neuromuscular weakness and respiratory difficulties.
Fluoroquinolone Antibiotics
Fluoroquinolones, including ciprofloxacin and levofloxacin, are another class of antibiotics that can negatively affect individuals with MG. These drugs can induce muscle weakness and even trigger severe exacerbations of MG symptoms.
Beta-Blockers
Beta-blockers, commonly used to treat hypertension and heart conditions, can worsen muscle weakness in MG patients. Medications like propranolol, metoprolol, and atenolol should be included in the myasthenia gravis medications to avoid list as they can interfere with neuromuscular function.
Other Drugs to Avoid
In addition to contraindicated drugs, there are other medications that should generally be avoided by those with Myasthenia Gravis. These drugs may not be as harmful as contraindicated drugs, but they can still exacerbate symptoms or complicate treatment. It's important to be aware of these cautionary drugs to prevent worsening MG symptoms.
Magnesium-Containing Medications
Magnesium can interfere with neuromuscular transmission and should be avoided in high doses. Medications and supplements containing magnesium, such as certain laxatives and antacids, can increase muscle weakness and should be used cautiously.
Certain Anesthetics
Some anesthetics can pose risks to individuals with MG. For example, neuromuscular blocking agents used during surgery can cause prolonged muscle weakness. It is essential to inform healthcare providers of an MG diagnosis before undergoing any surgical procedures, especially when iodinated radiologic contrast agents may be used.
Calcium Channel Blockers
Calcium channel blockers, used to treat high blood pressure and heart conditions, can also affect muscle function in MG patients. Drugs like verapamil and diltiazem should be used with caution and under close medical supervision.
Other Medications to Watch
Several other medications require careful consideration for MG patients:
- Hydroxychloroquine and chloroquine: These drugs may exacerbate MG symptoms in some patients.
- Statins: While often prescribed for cholesterol management, statins can sometimes worsen muscle weakness.
- Quinine and related compounds: These can interfere with neuromuscular transmission.
- Macrolide antibiotics: Some macrolides, like telithromycin, carry a black box warning for MG patients.
- Botulinum toxin: This should be used with extreme caution in MG patients.
- Penicillamine and D-penicillamine: These drugs can induce MG-like symptoms.
- Immune checkpoint inhibitors: A newer class of cancer drugs that may trigger or worsen MG.
Permissible Medications for Myasthenia Gravis
While many drugs should be avoided, there are also several medications that are considered safe and beneficial for managing Myasthenia Gravis. These permissible medications can help control symptoms and improve the quality of life for MG patients.
Anticholinesterase Agents
Anticholinesterase agents, such as pyridostigmine (Mestinon), are commonly prescribed to treat MG. These medications improve neuromuscular transmission by preventing the breakdown of acetylcholine, thereby enhancing muscle strength and reducing fatigue.
Immunosuppressants
Immunosuppressants, including azathioprine and mycophenolate mofetil, are often used to manage MG by suppressing the immune system's attack on neuromuscular junctions. These medications can help reduce the severity of symptoms and prevent exacerbations. However, patients should be aware of the potential drug side effects associated with immunosuppression.
Corticosteroids
Corticosteroids, like prednisone, are another class of drugs used to treat Myasthenia Gravis. These medications reduce inflammation and immune system activity, helping to manage symptoms effectively. Long-term use requires careful monitoring due to potential drug interactions and side effects.
IVIG and Plasmapheresis
Intravenous immunoglobulin (IVIG) and plasmapheresis are treatments used during severe MG exacerbations. IVIG involves infusing antibodies to modulate the immune system, while plasmapheresis involves filtering the blood to remove harmful antibodies. Both treatments can provide temporary relief from symptoms.
Conclusion
Managing Myasthenia Gravis requires careful consideration of drugs to avoid exacerbating symptoms or causing complications. Being aware of contraindicated drugs, understanding which drugs to avoid, and knowing permissible medications is essential for effective management of the condition.
Always consult with healthcare providers before starting or stopping any medication, and stay informed about the latest updates in MG treatment to ensure the best possible care. Regularly review resources on things to avoid and safe antibiotics to maintain optimal health management.
Discover a new level of personalized health support for Myasthenia
• Learn more about your disease
• Be more confident in dealing with symptoms
• Access the knowledge of other patients

Sources
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This resource provides a comprehensive overview of Myasthenia Gravis, including its etiology, clinical manifestations, and management strategies.
Link to article - Myasthenia gravis: subgroup classification and therapeutic strategies
This review discusses the classification of Myasthenia Gravis subgroups and outlines various therapeutic strategies.
Gilhus, N. E., & Verschuuren, J. J. (2015). Lancet Neurology, 14(10), 1023-1036. DOI: 10.1016/S1474-4422(15)00145-3 - Myasthenia Gravis: New Drugs and a Road to Individualized Treatment
An article discussing recent advancements in treatment options for Myasthenia Gravis, including FDA-approved medications.
Link to article - A Practical Approach to Managing Patients With Myasthenia Gravis
This review outlines practical management approaches for adults with ocular and generalized Myasthenia Gravis.
Gilhus, N. E., & Tzartos, S. (2020). Frontiers in Neurology, 11, Article 604. DOI: 10.3389/fneur.2020.00604 - Myasthenia Gravis | New England Journal of Medicine
A detailed article on the pathophysiology and management of Myasthenia Gravis, emphasizing individualized immunosuppressive therapy.
Gilhus, N.E., & Verschuuren, J.J.G.M. (2016). N Engl J Med, 375:2570–81. DOI: 10.1056/NEJMra1602678