Article Contents ::
- 1 Details About Generic Salt :: Chloroqu
- 2 Main Medicine Class:: Anti-infective,antimalarial
- 3 (KLOR-oh-kwin) Chloroquine Phosphate Aralen Phosphate Chloroquine Hydrochloride Aralen HCl Class: Anti-infective/antimalarial
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Chloroqu
Main Medicine Class:: Anti-infective,antimalarial
(KLOR-oh-kwin)
Chloroquine Phosphate
Aralen Phosphate
Chloroquine Hydrochloride
Aralen HCl
Class: Anti-infective/antimalarial
Drugs Class ::
Action Inhibits parasite growth, possibly by concentrating within parasite acid vesicles, raising pH.
Indications for Drugs ::
Indications Prophylaxis and treatment of acute attacks of malaria caused by Plasmodium vivax, P malariae, P ovale and susceptible strains of P falciparum; extraintestinal amebiasis. Unlabeled use(s): Treatment of rheumatoid arthritis, systemic and discoid lupus erythematosus, porphyria cutanea tarda, scleroderma, pemphigus, lichen planus, polymyositis and sarcoidosis.
Drug Dose ::
Route/Dosage
Doses are listed in base equivalents. (Chloroquine phosphate, 500 mg equals 300 mg base; chloroquine hydrochloride, 50 mg equals 40 mg base.)
Acute Malaria
CHLOROQUINE PHOSPHATE: ADULTS: Initial dose: PO 600 mg, then 300 mg 6 hr later and 300 mg qd for 2 days. CHILDREN: Initial dose: PO 10 mg/kg, then 5 mg/kg 6 hr later and 5 mg/kg qd for 2 days. CHLOROQUINE HYDROCHLORIDE: ADULTS: INITIAL DOSE: IM 160–200 mg then repeat dose in 6 hr if needed (maximum 800 mg base total dose in first 24 hr). CHILDREN: 5 mg/kg/dose; repeat dose in 6 hr (maximum 10 mg base/kg/24 hr; do not exceed 5 mg/kg as single parenteral dose).
Malaria Suppression
ADULTS: PO 300 mg base. CHILDREN: 5 mg/kg/dose (maximum 300 mg base) weekly. Begin 1–2 wk prior to exposure and continue for 4 wk after leaving endemic area. If suppressive therapy is not begun prior to exposure, double initial loading dose and give in 2 divided doses 6 hr apart.
Extraintestinal Amebiasis
CHLOROQUINE PHOSPHATE: ADULTS: PO 600 mg base/day for 2 days, then 300 mg base/day for 2–3 wk. CHLOROQUINE HYDROCHLORIDE: ADULTS: IM 4–5 ml (160–200 mg base)/day for 10–12 days.
Contraindication ::
Contraindications Retinal or visual field changes.
Drug Precautions ::
Precautions
Pregnancy: Category D. Lactation: Excreted in breast milk. Children: Especially sensitive to adverse effects; do not exceed recommended dose. G-6-PD deficiency: May induce hemolysis in presence of infection or stressful condition. Muscular weakness: May need to discontinue therapy if muscle weakness occurs. Psoriasis or porphyria: May be exacerbated. Retinopathy: Irreversible retinal damage has occurred. Special risk patients: Monitor patients with hepatic disease or alcoholism or taking other hepatotoxic medications for evidence of worsening liver function such as bleeding.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CV: Hypotension; ECG changes. CNS: Headache; neuropathy; seizures; psychotic episodes. DERM: Pruritus; pigment changes; skin eruptions. EENT: Visual disturbances; retinal damage and deafness with prolonged high-dose use; tinnitus. GI: Anorexia; nausea; vomiting; diarrhea; abdominal cramps. HEMA: Agranulocytosis; blood dyscrasias; aplastic anemia. HEPA: Hepatitis. OTHER: Muscle weakness.
Drug Mode of Action ::
Action Inhibits parasite growth, possibly by concentrating within parasite acid vesicles, raising pH.
Drug Interactions ::
Interactions
Cimetidine: May increase chloroquine serum concentration. Kaolin aluminum or magnesium trisilicate antacids: May decrease GI absorption of chloroquine. Rabies vaccine: Concomitant administration of intradermally administered rabies vaccine and chloroquine may result in diminished antibody response to vaccine. In this situation CDC recommends administering rabies vaccine intramuscularly.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies.
- Review history for blood disorders, eye or vision problems, G-6-PD deficiency, liver disease, alcoholism, porphyria or psoriasis.
- Arrange for a complete eye examination to establish baseline values.
- Perform baseline assessment for signs and symptoms of infection.
- Provide small, frequent meals if GI distress occurs.
- Arrange for and monitor periodic CBCs.
- If sore throat, fever, weakness, fatigue, unusual bleeding or bruising occurs, notify physician.
- Perform periodic neuromuscular examinations, and notify patient if knee and ankle reflexes are weak.
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Drug Storage/Management ::
Administration/Storage
- Administer with food or milk.
- If taken once weekly, take on same day of week.
- Store in airtight, light-resistant container at room temperature.
Drug Notes ::
Patient/Family Education
- Remind patient to take medication with food to minimize GI irritation.
- Stress importance of compliance with full course of therapy. If used for suppression, drug must be taken at least 1 wk before entering and for 4 wk after leaving endemic area.
- Caution patient to drink alcoholic beverages sparingly because of increased GI irritation and higher risk of liver damage.
- Stress importance of eye examinations q 3–6 mon during prolonged daily therapy.
- Inform patient that drug may cause rusty or brown discoloration of urine.
- Advise use of dark glasses in bright light to reduce risk of ocular damage.
- Instruct patient to report these symptoms to physician: blurring or change in vision, buzzing or difficulty hearing, muscle weakness, rash, vomiting or stomach pain, difficulty breathing or swallowing.