Parenteral Manual

Phenytoin

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.

Alternate Name(s): 
Dilantin
Classification: 
Anticonvulsant
Original Date: 
July 2025
Indications: 

Treatment of Status Epilepticus

Reconstitution and Stability: 
  • Available as 50 mg/mL colourless injection 
  • Store vials at 15 – 30°C, avoid freezing. Protect from light. 
  • Diluted solution stable for 4 hours at room temperature (do not refrigerate). Observe solution for particulate matter prior to administration and discard if particulate is present. 
Compatibility: 
  • Solutions Compatible: ONLY in NS or RL  
  • Y-Site Compatible: Do NOT mix with other IV medications  
  • Incompatible: Incompatible with KCl, dextrose containing solutions 
Administration: 

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

SC NO
IM

YES. Due to slow and erratic absorption, the IM route is NOT recommended for the emergency treatment of status epilepticus. 

IV Direct NO

IV Intermittent Infusion 

YES cardiac monitoring (BP, HR) recommended 

Usual dilution: 1 – 6 mg/mL 

 

Doses ≤ 300 mg: dilute in syringe up to 50 mL

Doses 301 mg – 600 mg: dilute in 100 mL 0.9% NaCl bag 

Doses > 600 mg: dilute in 250 mL 0.9% NaCl bag 

 

Infusion rate: 1 mg/kg/min to a maximum of 50 mg/min. For patients with cardiovascular disease, do not exceed 25 mg/min. 

Administer via large peripheral vein or centrally (preferred) using a large gauge needle or IV catheter.  

 

Use a 0.22 micron in-line filter. Flush line with 0.9% NaCl before and after dose. 

IV Continuous Infusion NO

 

Dosage: 

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

Status Epilepticus  

  • Loading Dose: 20 mg/kg/dose IV x1 
  • Dose Limit 
    • < 50 kg: 1000 mg/dose 
    • ≥ 50 kg: 1500 mg/dose 

Anti-Epileptic

  • < 3 years: 8 to 10 mg/kg/day divided q12h
  • 3 to 6 years: 7.5 to 9 mg/kg/day divided q12h
  • 7 to 9 years: 7 to 8 mg/kg/day divided q12h
  • 10 to 16: 6 to 7 mg/kg/day divided q12h
  • > 16 years: 4 to 6 mg/kg/day divided q12h

 

Potential hazards of parenteral administration: 
  • The infusion site must be inspected every 30-60 minutes and documented when in use and if extravasation or infiltration is suspected
  • Severe hypotension and cardiac arrhythmias are associated with rates of infusion above 50 mg/minute or above 25 mg/minute in patients with cardiovascular disease 
  • IM Phenytoin may cause pain, necrosis, abscess formation at the injection site 
  • IV formulation may cause soft tissue irritation and inflammation, and skin necrosis at IV site 
  • Avoid IV administration in small veins. 
  • Purple glove syndrome (i.e., discoloration with edema and pain of distal limb) may occur following peripheral IV administration of phenytoin. This syndrome may or may not be associated with drug extravasation. Symptoms may resolve spontaneously; however, skin necrosis and limb ischemia may occur; interventions such as fasciotomies, skin grafts, and amputation (rare) may be required. To decrease the risk of this syndrome, inject phenytoin slowly and directly into a large vein through a large gauge needle or IV catheter; follow with NS flushes through the same needle or IV catheter
Drug Category Management Supportive Measures
Phenytoin Irritant with vesicant properties

Treatment not usually required 

 

Hyaluronidase: May consider for refractory cases in addition to supportive management (Stefanos 2023) 

Apply dry warm compresses

 

Notes: 
  • Oral Phenytoin is approximately 90% bioavailable. Plasma phenytoin concentrations may increase when IV phenytoin is substituted for oral phenytoin
  • Continuous cardiac monitoring is recommended during administration: Monitor blood pressure, pulse every 15 minutes during infusion for up to 1 hour after infusion is complete 
  • Monitor for infusion site reactions 
  • Monitor serum phenytoin concentrations 
  • Slight yellow color discolouration does not indicate potency loss 
  • Slowing infusion rate/decreasing solution concentration can alleviate pain at injection site 
  • Therapeutic Drug Monitoring
    • Therapeutic Serum concentration: 40 – 80 micromol/L 
    • Usual sampling time: Pre-Dose (0-60 minutes prior to next dose) 
    • When to order levels 
      • Post-Loading Dose: At least 60 minutes post IV load 
      • Maintenance (Steady State): 3 days after dosing change 
References: 

Phenytoin Sodium Injection USP monograph, Omega Laboratories  

Phenytoin, Lexicomp  

The information contained on this website is provided for informational purposes only, as a guide to assist physicians, nurses and other healthcare providers in deciding on the appropriate care required for a particular patient. At all times, physicians, nurses and other healthcare providers must exercise their independent clinical judgment, based on their knowledge, training and experience, taking into account the specific facts and circumstances of each patient, when deciding on the appropriate course of investigation and/or treatment to recommend in a particular clinical situation.

CHEO has made every effort to ensure that the information contained on this website is as current and accurate as possible. However, changes can occur due to ongoing research and the constant influx of new information. Where possible, hospitals and healthcare practitioners should verify the information before acting on it.

Reliance on any information in this website is at the user's own risk. CHEO is not responsible or liable for any harm, loss or other consequences from the use or misuse of the information on this website.