Quinine Sulfate

A to Z Drug Facts

Quinine Sulfate

  Action
  Indications
  Contraindications
  Route/Dosage
  Interactions
  Lab Test Interferences
  Adverse Reactions
  Precautions
Patient Care Considerations
  Administration/Storage
  Assessment/Interventions
  Patient/Family Education


(KWIE-nine SULL-fate)
Class: Anti-infective/antimalarial

 Action Causes pH elevation in intracellular organelles of parasites; also has skeletal muscle relaxant effects and cardiovascular effects similar to those of quinidine.

 Indications Treatment of chloroquine-resistant falciparum malaria; alternative treatment for chloroquine-sensitive strains of P. falciparum, P. malariae, P. ovale, and P. uivae. Unlabeled use(s): Prevention and treatment of nocturnal recumbency leg cramps.

 Contraindications G-6-PD deficiency; optic neuritis; tinnitus; history of blackwater fever and thrombocytopenic purpura associated with previous quinine ingestion; pregnancy.

 Route/Dosage

Chloroquine-Resistant P. Falciparum Malaria

ADULTS: PO 650 mg q 8 hr for 5 to 7 days. CHILDREN: PO 25 mg/kg/day in divided doses q 8 hr for 5 to 7 days.

Chloroquine-Sensitive Malaria

ADULTS: PO 600 mg q 8 hr for 5 to 7 days. CHILDREN: PO 10 mg/kg q 8 hr for 5 to 7 days.

Nocturnal Leg Cramps

ADULTS: PO 260 to 300 mg at bedtime.

 Interactions

Aluminum-containing antacids: Causes delayed or decreased quinine absorption. Anticoagulants, oral: May cause depression of hepatic enzyme system that synthesizes vitamin K-dependent clotting factors and may enhance action of oral anticoagulants. Cimetidine: May reduce quinine's clearance and prolong its half-life in body. Digoxin: May cause increased digoxin serum concentration. Mefloquine: May cause ECG abnormalities or cardiac arrest and may increase risk of convulsions. Do not use concurrently. Delay administration 12 hr after last dose of quinine. Neuromuscular blocking agents: May potentiate neuromuscular blockade and may result in respiratory difficulties. Urinary alkalinizers: May increase quinine serum concentrations and potentiate toxicity.

 Lab Test Interferences Urinary 17-ketogenic steroids may have elevated values with Zimmerman method.

 Adverse Reactions

CV: Anginal symptoms. CNS: Vertigo; dizziness; headache; fever; apprehension; restlessness; confusion; syncope; excitement; delirium; hypothermia; seizures. EENT: Visual disturbances (eg, photophobia, blurred vision with scotomata, night blindness, amblyopia, diplopia, diminished visual fields, mydriasis, optic atrophy) tinnitus; deafness. GI: Nausea; vomiting; diarrhea; epigastric pain. GU: Renal tubular damage; anuria. HEPA: Hepatitis. HEMA: Acute hemolysis; hemolytic anemia; thrombocytopenic purpura; agranulocytosis; hypoprothrombinemia. OTHER: Cinchonism (headache, tinnitus, nausea, diarrhea, disturbed vision, skin, CV and CNS symptoms at very high doses); hypersensitivity (rash, pruritus, flushing, sweating, facial edema, asthmatic symptoms).

 Precautions

Pregnancy: Category X. Lactation: Excreted in breast milk. Cardiac disease: Patients with cardiac arrhythmias may have exacerbation of symptoms with quinine, which acts similarly to quinidine. May cause cardiotoxicity. In patients with atrial fibrillation, quinine requires same precautions as for quinidine. Hemolysis: Has been associated with G-6-PD deficiency. Discontinue immediately if hemolysis appears.


PATIENT CARE CONSIDERATIONS


 Administration/Storage

 Assessment/Interventions

OVERDOSAGE: SIGNS & SYMPTOMS
  Tinnitus, dizziness, skin rash, GI disturbance, diarrhea, arrhythmias, convulsions, blurred vision, headache, nausea/vomiting, fever, confusion

 Patient/Family Education

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Copyright
© 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts