Indications |
Oral Acute bacterial sinusitis Adult: 400 mg once daily for 10 days. Oral Acute bacterial exacerbation of chronic bronchitis Adult: 400 mg once daily for 5-10 days. Oral Community-acquired pneumonia Adult: 400 mg once daily for 7-14 days. Oral Skin and skin structure infections Adult: Complicated: 400 mg once daily for 7-21 days; uncomplicated: 400 mg once daily for 7 days. Intravenous Acute bacterial sinusitis Adult: 400 mg by IV infusion over 60 minutes every 24 hr for 10 days. Intravenous Acute bacterial exacerbation of chronic bronchitis Adult: 400 mg by IV infusion over 60 minutes every 24 hr for 5-10 days. Intravenous Community-acquired pneumonia Adult: 400 mg by IV infusion over 60 minutes every 24 hr for 7-14 days. Intravenous Skin and skin structure infections Adult: Complicated: 400 mg once daily for 7-21 days; uncomplicated: 400 mg once daily for 7 days. Dose to be infused over 60 minutes. Intravenous Intra-abdominal infections Adult: 400 mg for 5-14 days. May change to oral therapy when clinically appropriate. Dose to be infused over 60 minutes. Ophthalmic Bacterial conjunctivitis Adult: As 0.5% ophthalmic solution: instil 1 drop in the affected eye tid for 7 days. Child: >1 yr as 0.5% ophthalmic solution: instil 1 drop in the affected eye tid for 7 days. |
Contraindications |
Hypersensitivity; child, adolescent; pregnancy, lactation. |
Warnings / Precautions |
Maintain adequate fluid intake; exposure to strong sunlight/sunlamp. Epilepsy, history of CNS disorders, DM. Not recommended in severe hepatic impairment. May worsen myasthenia gravis. Discontinue in case of tendon pain, inflammation or rupture. High level of resistance with S. aureus infections. Increased risk of tendon inflammation/rupture especially in elderly taking corticosteroids. Caution in patients with proarrhythmic conditions e.g. clinically significant bradycardia or acute MI. Existing QT prolongation, bradycardia, heart failure with reduced left ventricular ejection fraction; uncorrected hypokalaemia. Avoid concomitant usage with drugs that are known to prolong QT interval. Prolonged use may increase risk of fungal or bacterial superinfection. |
Adverse Reactions |
GI disturbances, CNS effects, hypersensitivity-type reactions, reversible arthralgia, abnormal liver function tests, hepatitis, haematological disturbances, tachycardia, superinfection, pain and irritation at the Inj site, tendon damage, phloebitis and thrombophloebitis, peripheral neuropathy, photosensitivity, abdominal pain, headache, vaginitis. |
Overdose Reactions |
Stomach should be emptied and hydration maintained. Activated charcoal may be useful soon after oral overdosage. Treatment should be supportive, dialysis may be of some limited use. |
Drug Interactions |
Moxifloxacin should be taken 4 hr before or 8 hr after admin of magnesium or aluminium containing antacids or iron and zinc containing products. Increased risk of CNS stimulation and convulsions with NSAIDs. May increase adverse effects of corticosteroids when used together. May increase anticoagulant effect of coumarin derivatives. May reduce serum levels of mycophenolate. Didanosine, sevelamer, sucralfate and quinalapril may reduce the absorption of orally-administered moxifloxacin. Potentially Fatal: Risk of torsade de pointes with QT prolonging drugs e.g. class Ia or class III antiarrythmics, terfenadine, cisapride, astemizole. See Below for More moxifloxacin Drug Interactions |
Mechanism of Actions |
Moxifloxacin inhibits the topoisomerase II (DNA gyrase) and topoisomerase IV required for bacterial DNA replication, transcription, repair and recombination. Absorption: Well absorbed from GI tract. Distribution: Widely distributed throught the body. 30-50% protein bound. Metabolism: Metabolised via glucuronide and sulfate conjugation. Excretion: Excreted in urine and faeces as unchanged drug and metabolite. Elimination half life of around 12 hr. |
Administration |
May be taken with or without food. |
Storage Conditions |
Intravenous: Store at 25°C. Ophthalmic: Store at 2-25°C. Oral: Store at 25°C. |
ATC Classification |
J01MA14 - moxifloxacin ; Belongs to the class of fluoroquinolones. Used in the systemic treatment of infections. S01AX22 - moxifloxacin ; Belongs to the class of other antiinfectives. Used in the treatment of eye infections. |
Storage |
Intravenous: Store at 25°C. Ophthalmic: Store at 2-25°C. Oral: Store at 25°C. |
Available As |
|
Moxifloxacin
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Moxifloxacin Containing Brands
Moxifloxacin is used in following diseases
Drug - Drug Interactions of Moxifloxacin
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