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RYANODEX®

Clinical Comparison

RYANODEX® vs Traditional Dantrolene Sodium (Dantrium®)

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Comparison FactorRYANODEX®Traditional Dantrolene
Formulation & Technology
Technology
Advanced nanosuspension technology with lyophilized formulation
Traditional lyophilized powder
Reconstitution Time
10 seconds per vial
60+ seconds per vial
Administration & Dosing
Vials Needed (100kg patient)
1 vial (250mg)
12.5 vials (20mg each)
Sterile Water Required
5 mL per vial
60 mL per vial
Total Administration Time (100kg patient)
<1 minute
>22 minutes
Healthcare Providers Needed
1 provider
Multiple providers typically required
Clinical Benefits
Onset of Action
Rapid - within minutes
Within minutes (once administered)
Bioavailability
Enhanced due to nanosuspension
Standard
Safety Profile
Indication
Treatment and prevention of malignant hyperthermia
Treatment and prevention of malignant hyperthermia
Common Adverse Events
Muscle weakness, drowsiness, dizziness (similar to traditional dantrolene)
Muscle weakness, drowsiness, dizziness, nausea

Key Clinical Benefits of RYANODEX®

Rapid Response

Critical time savings in malignant hyperthermia emergencies

Resource Efficiency

Requires fewer healthcare providers and less preparation time

Reduced Complications Risk

Earlier treatment reduces risk of serious complications

Enhanced Workflow

Simplified preparation reduces procedural complexity

Clinical Evidence

Pharmacokinetic Study

RYANODEX® demonstrated bioequivalence to traditional dantrolene with enhanced dissolution profile due to nanosuspension technology.

Time-Motion Studies

Preparation time reduced from >22 minutes to <1 minute for a 100kg patient, representing a 95% reduction in preparation time.

Healthcare Provider Satisfaction

Significant improvement in healthcare provider satisfaction scores due to simplified preparation process and reduced workflow burden.