Parenteral Manual

Propafenone (SPECIAL ACCESS PROGRAM)

Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.

Classification: 
Antiarrhythmic
Original Date: 
August 2005
Revised Date: 
September 2011
Indications: 
  • Treatment of ventricular arrhythmias
Reconstitution and Stability: 
  • Available as a 3.5 mg/mL injection
  • Propafenone 1 mg/mL  is stable for 48 hours at 21-23°C in D5W when stored in polypropylene syringes or PVC bags.
Compatibility: 

- Solutions Compatible: D5W ONLY

- Additive/buretrol Compatible: amiodarone, dopamine, lidocaine

- Y-site Compatible: no information

- Incompatible: heparin, nitroprusside, NS

Administration: 

(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)

SC NO
IM NO
IV Direct

NO

IV Intermittent Infusion

Yes

Usual dilution: 1 mg/mL

Infusion time: 2 hours

IV Continuous Infusion

Yes

Usual dilution: 1 mg/mL

Click here to access SDC Drug Infusion Sheet

Dosage: 

(For neonatal dosages, refer to Neonatal IV Drug Manual.)

Pediatric:    

  • IV load: 2 mg/kg over 2 hours
  • IV infusion: 4-7 mcg/kg/minute
  • Decrease dose if QRS complex > 0.12 seconds or PR interval >0.24 seconds

Adult:
- Ventricular Tachycardia:

  • 2 mg/kg IV push, followed by 2 mg/minute by IV infusion

- Ventricular Arrhythmias:

  • 1-2.5 mg/kg IV
Potential hazards of parenteral administration: 
  • Hypotension with rapid administration
  • Tremor
  • Bradycardia, hypotension, arrhythmia
  • Anemia, thrombocytopenia, agranulocytosis
  • Bitter taste, vomiting, abdominal pain
Notes: 
  • May increase serum digoxin levels
  • Monitor blood pressure and heart rate

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