Rilutek (riluzole) vs Nuedexta (dextromethorphan HBr and quinidine sulfate)

Rilutek (riluzole) vs Nuedexta (dextromethorphan HBr and quinidine sulfate)

Rilutek (riluzole) is primarily used to treat amyotrophic lateral sclerosis (ALS) by slowing the progression of the disease and extending survival, whereas Nuedexta (a combination of dextromethorphan HBr and quinidine sulfate) is approved for the treatment of pseudobulbar affect (PBA), a condition characterized by sudden and uncontrollable episodes of crying and/or laughing. Rilutek works by modulating glutamate signaling, which is thought to be involved in the nerve damage associated with ALS, while Nuedexta works by affecting the signaling pathways in the brain that control the expression of emotions, with quinidine serving to increase the effectiveness of dextromethorphan. The choice between these medications would depend on the specific condition being treated: Rilutek is for ALS management, and Nuedexta is for PBA, and they are not interchangeable.

Difference between Rilutek and Nuedexta

Metric Rilutek (riluzole) Nuedexta (dextromethorphan HBr and quinidine sulfate)
Generic name Riluzole Dextromethorphan hydrobromide and quinidine sulfate
Indications Amyotrophic lateral sclerosis (ALS) Treatment of pseudobulbar affect (PBA)
Mechanism of action Glutamate antagonist Dextromethorphan acts on the central nervous system to reduce the excitability of the neuron and quinidine increases the bioavailability of dextromethorphan
Brand names Rilutek, Tiglutik Nuedexta
Administrative route Oral Oral
Side effects Dizziness, gastrointestinal disturbances, elevated liver enzymes, decreased lung function Diarrhea, dizziness, cough, vomiting, weakness, swelling of extremities, urinary tract infections, flu symptoms
Contraindications Liver impairment, caution in patients with renal impairment Patients taking MAOIs or with a history of heart rhythm abnormalities
Drug class Riluzole is a member of the benzothiazole class Dextromethorphan is a morphinan and quinidine is an antiarrhythmic agent
Manufacturer Sanofi Avanir Pharmaceuticals

Efficacy

Efficacy of Rilutek (Riluzole) in ALS

Rilutek, with the active ingredient riluzole, is a medication specifically approved for the treatment of amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. Clinical trials have demonstrated that Rilutek can extend survival and/or the time to tracheostomy in individuals with ALS. The exact mechanism by which riluzole exerts its therapeutic effects in ALS is not fully understood, but it is believed to involve the inhibition of glutamate release, which can be toxic to nerve cells. While Rilutek does not cure ALS or reverse the damage already done, it can slow the progression of the disease in some patients.

The efficacy of Rilutek was established in several clinical trials, where patients treated with the drug showed a modest increase in survival. In a pivotal clinical trial, patients receiving riluzole experienced a median survival time that was approximately two to three months longer than those receiving a placebo. It is important to note that the response to Rilutek can be variable, and not all patients with ALS may experience the same level of benefit from the medication.

Efficacy of Nuedexta in ALS

Nuedexta, a combination of dextromethorphan HBr and quinidine sulfate, is not primarily indicated for the treatment of ALS itself, but rather for the management of pseudobulbar affect (PBA), a condition associated with various neurological diseases, including ALS. PBA is characterized by uncontrollable episodes of laughing and/or crying that are disproportionate or incongruent to the patient's emotional state. The efficacy of Nuedexta in the treatment of PBA in ALS patients has been supported by clinical trials.

In a key clinical study, patients with ALS who were treated with Nuedexta experienced a significant reduction in the frequency and severity of PBA episodes compared to those receiving placebo. The improvement in PBA symptoms can contribute to better quality of life for ALS patients, who often struggle with this socially debilitating condition. While Nuedexta does not have a direct effect on the progression of ALS, its role in managing PBA symptoms is considered beneficial in the overall care of patients with ALS.

Regulatory Agency Approvals

Rilutek
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medicines & Healthcare products Regulatory Agency (MHRA), United Kingdom
  • Medsafe (NZ)
Nuedexta
  • Food and Drug Administration (FDA), USA

Access Rilutek or Nuedexta today

If Rilutek or Nuedexta are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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