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Riluzole

Riluzole is a neuroprotective medication primarily used in the treatment of amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease that affects motor neurons in the brain and spinal cord. It helps to slow the progression of the disease and prolong survival by reducing the release of glutamate, a neurotransmitter that can be toxic to motor neurons in excessive amounts.



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Frequently Asked Questions

How quickly does riluzole start to work?
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Patients may not notice immediate effects, but riluzole is intended to slow the progression of ALS over time. Benefits may be observed after several months of treatment.

Can I stop taking riluzole suddenly?
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It is advisable to consult your healthcare provider before discontinuing riluzole, as stopping the medication may affect disease management.

Are there any specific dietary restrictions while using riluzole?
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There are no specific dietary restrictions associated with riluzole; however, patients should maintain a balanced diet for overall health.

What should I do if I miss a dose of riluzole?
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If you miss a dose, take it as soon as you remember. If it’s close to the time for your next scheduled dose, skip the missed dose and continue with your regular schedule. Do not double up on doses.

Is riluzole safe for long-term use?
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Riluzole is generally considered safe for long-term use in managing ALS, but regular follow-up appointments are essential to monitor liver function and overall health status.

Comprehensive Drug Guide

How Does Riluzole Work?

Riluzole works by inhibiting the release of glutamate in the brain and spinal cord. High levels of glutamate can lead to excitotoxicity, which contributes to the degeneration of motor neurons. By reducing glutamate levels, riluzole helps to protect these neurons from damage and death, thereby slowing disease progression in patients with ALS.



Common Dosages

  • Tablets: Common strength is 50 mg.

Typical Dosing

  • The usual recommended dose for adults is 50 mg taken orally twice daily. The dose may be adjusted based on tolerability and clinical response.


Typical Dosing

FDA Approved Indications

  • Treatment of amyotrophic lateral sclerosis (ALS) to extend survival and/or time to tracheostomy.


Who Shouldn't Take Riluzole?

  • Known hypersensitivity to riluzole or any components of the formulation.
  • Significant liver disease, as it may exacerbate liver function impairment.


Advice From The Pharmacist

  • Instruct patients to take riluzole exactly as prescribed, and emphasize the importance of adhering to the dosing schedule for optimal efficacy.
  • Advise patients about potential side effects, such as nausea or liver function changes, and encourage them to report any unusual symptoms to their healthcare provider.
  • Discuss the need for regular monitoring of liver function, as riluzole can affect liver enzymes.


Side Effects of Riluzole

Common Side Effects

  • Nausea
  • Diarrhea
  • Weakness
  • Fatigue
  • Dizziness


Uncommon/Severe Side Effects

  • Liver enzyme elevations (hepatotoxicity)
  • Severe allergic reactions (such as rash, itching, or difficulty breathing)


Risks and Warnings of Riluzole

  • Liver Function: Patients should be monitored regularly for liver function, particularly those with pre-existing liver conditions or those taking other hepatotoxic medications.
  • Pregnancy and Breastfeeding: Riluzole should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Its safety during breastfeeding has not been established.

Interactions with Riluzole

Common Drug Interactions

  • Other Medications: Patients should inform their healthcare provider of all medications they are taking, as riluzole can interact with drugs that affect liver enzymes, particularly those metabolized by CYP1A2.


Alternatives to Riluzole

  • Other ALS Treatments: Alternatives may include edaravone, another medication indicated for ALS that works as a free radical scavenger. Supportive therapies, such as physical and occupational therapy, are also important components of managing ALS.