Parenteral Manual

QuiNINE Dihydrochloride (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: 
Antimalarial Agent
Original Date: 
August 2005
Revised Date: 
February 2017
Indications: 
  • Treatment of severe Plasmodium falciparum infection or unable to tolerate oral medications

*See  "Pediatric Management Guidelines for Malaria Treatment "  on CHEOnet

Reconstitution and Stability: 
  • Available as 300 mg/mL injection
  • Protect from light
  • Must be diluted just prior to use
  • Stable for 24 hours at room temperature in D5W, 0.9% NaCl, and D5W-NS
Compatibility: 
  • Solutions Compatible: D5W, 0.9% NaCl, D5W-NS    ** D5W-NS is preferred as quinine dihydrochloride and malaria can cause hypoglycemia
  • Do not mix with other medications; run in dedicated line
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: in D5W/0.9% NaCl

- if weight less than or equal to 5 kg - 50 mL minibag
              greater than 5 kg to 10 kg - 100 mL minibag
            greater than 10 kg to 25 kg - 250 mL minibag
                         greater than 25 kg - 500 mL minibag

 - fluid restricted patients or if unable to tolerate large volumes - dilute in 5 mL/kg
Infusion time: over 4 hours

IV Continuous Infusion NO
Dosage: 

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

LOADING DOSE:

  • quiNINE dihydrochloride [salt] 20 mg/kg by IV infusion over 4 hours
  • Maximum: 600 mg quiNINE dihydrochloride 
  • Omit loading dose if patient received quiNINE, quiniDINE, or mefloquine in previous 24 hours                     

MAINTENANCE DOSE:

  • quiNINE dihydrochloride  [salt] 10 mg/kg IV Q8H over 4 hours
  • Maximum: 600 mg quiNINE dihydrochloride 
  • Start 8 hours after loading dose
  • If IV therapy is required for greater than 48 hours, reduce maintenance dose by 1/3 to avoid accumulation
  • A minimum of 24 hours of parenteral therapy (3 maintenance doses) should be administered before switching to oral therapy

 

DOSING ADJUSTMENT IN RENAL FAILURE:

  • Decrease maintenance interval to Q 12 hours
Potential hazards of parenteral administration: 
  • Cinchonism: tinnitus, nausea, headache, blurred vision
  • Hypoglycemia
  • Occasional cardiac conduction disturbances
  • Hypersensitivity, hemolysis (rare)
  • Hepatotoxicity, skin rash
  • Restlessness, confusion, vertigo, apprehension
Notes: 
  • Monitor CBC, liver function tests, blood glucose
  • To be prescribed in combination with IV clindamycin
  • Switch to oral quinine as soon as possible
  • 300 mg quiNINE dihydrochloride = 245 mg quiNINE base
  • Contraindicated in G6PD deficiency
  • Use with caution in patients with myasthenia gravis, impaired liver function
  • Quinine can increase plasma concentrations of digoxin and oral anticoagulants
  • Amiodarone, verapamil and cimetidine increase serum quinine concentrations
  • Barbiturates, phenytoin and rifampin decrease serum quinine concentrations

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.