Reconstitution of Retatrutide 12mg Powder Vial
Direct Answer
To achieve a 4mg dose from a 12mg vial of retatrutide, reconstitute the powder with 3mL of sterile water, which will yield a concentration of 4mg/mL, allowing you to draw up 1mL for each 4mg weekly injection.
Calculation Method
The reconstitution volume is determined using basic pharmaceutical mathematics to achieve a practical concentration:
- Target concentration: 4mg/mL allows for easy measurement and administration 1
- Calculation: 12mg powder ÷ 4mg/mL = 3mL of sterile water needed 1
- Resulting doses: This provides exactly 3 doses of 4mg (1mL each) from the single 12mg vial 2, 3
Step-by-Step Reconstitution Protocol
Preparation requirements:
- Maintain strict sterile technique throughout the entire process to prevent contamination 1
- Use appropriate sterile syringes for measuring and transferring the sterile water 1
- Ensure all materials are at room temperature before beginning 1
Reconstitution procedure:
- Draw up exactly 3mL of sterile water for injection using a sterile syringe 1
- Inject the 3mL slowly into the 12mg powder vial, directing the stream against the vial wall rather than directly onto the powder 1
- Gently swirl (do not shake vigorously) until the powder is completely dissolved 1
- Inspect the reconstituted solution visually for particulate matter and discoloration before use - the solution should be clear 1
Storage and Stability
Critical storage guidelines:
- Label the reconstituted vial immediately with medication name, concentration (4mg/mL), date and time of reconstitution, and expiration 1
- Store at 4°C (refrigerated) to extend stability compared to room temperature 1
- Discard after 24 hours if manufacturer-specific stability data is not available 1
- Never freeze the reconstituted solution 1
Administration Details
For each weekly 4mg dose:
- Draw up exactly 1mL from the reconstituted vial (1mL = 4mg at 4mg/mL concentration) 2, 3
- Administer subcutaneously as studied in clinical trials 2, 3
- The clinical trials used weekly subcutaneous administration with dose escalation protocols starting at 2mg for higher doses 3
Critical Safety Warnings
Important considerations:
- Reconstituting without manufacturer-specific instructions poses significant patient safety risks including incorrect concentration leading to dosing errors 1
- Incompatibility with certain diluents can cause drug degradation - only use sterile water for injection unless otherwise specified 1
- This calculation assumes the powder volume is negligible; actual final volume may be slightly greater than 3mL 1
- In clinical trials, retatrutide demonstrated dose-dependent gastrointestinal adverse events (nausea, diarrhea, vomiting) that were mostly mild to moderate 2, 3
- Dose-dependent increases in heart rate were observed in trials, peaking at 24 weeks 2
Alternative Concentration Option
If you prefer smaller injection volumes or different dosing flexibility: