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OPTIMOX

Moxifloxacin

 

Description:

Optimox (Moxifloxacin) is a synthetic broad-spectrum antibacterial agent for oral administration. Optimox (Moxifloxacin) has in vitro activity against wide range of Gram-positive and Gram-negative microorganisms. The bacterial action of Optimox (Moxifloxacin) results from inhibition of the topoisomerase II (DNA gyrase) and topoisomerase IV required for bacterial DNA replication, transcription, repair, and recombination. US FDA approved Moxifloxacin for the treatment of acute exacerbations of chronic bronchitis, acute sinusitis, and pneumonia.

Composition:    

Each film-coated tablet contains Moxifloxacin HCl INN equivalent to Moxifloxacin 400 mg.

Indications:

Moxifloxacin is indicated for the treatment of infections caused by susceptible microorganisms in the conditions listed below in adults:

  1. Acute bacterial sinusitis

  2. Acute bacterial exacerbation of chronic bronchitis

  3. Mild to moderate community acquired pneumonia

  4. Uncomplicated skin and skin structure infections

Dosage & administration:

The usual dose of Optimox (Moxifloxacin) tablet is 400 mg once a day. The specific dosage and duration of Optimox in specific indications are as follows:

Infections

Dose

Duration

Acute bacterial sinusitis

400 mg once a day

10 days

Acute bacterial exacerbations of chronic bronchitis

400 mg once a day

5 days

Community–acquired pneumonia

400 mg once a day

10 days

Uncomplicated skin and skin structure infections

400 mg once a day

7 days

Contraindications:

Optimox (Moxifloxacin) is contraindicated in the patients with known hypersensitivity to Moxifloxacin, or any members of the quinolone class of antimicrobial agents.  

Side-effects:

Most side effects reported with Moxifloxacin treatment are mild to moderate in severity and required no treatment. Side effects include nausea, vomiting, diarrhea, dizziness, headache, abdominal pain, anorexia, anxiety, constipation, dry mouth, leukopenia, eosinophilia, myalgia, confusion, vertigo, insomnia, hallucination, palpitation, hypotension, hypertension, tachycardia, etc.

Precautions:

Moxifloxacin has been shown to prolong the QT interval of the ECG in some patients. It should be avoided in patients with known prolongation of QT interval, patients with uncorrected hypokalemia, and patients receiving Class IA (e.g. quinidine), or Class III (e.g. Amidarone), antiarrythmic agents, due to lack of clinical experience with the drug in these patients populations.

Use in Pregnancy:

There are no adequate and well-controlled studies in pregnant women. So, Moxifloxacin should only be given during pregnancy if the potential benefit justifies the potential risk to the fetus.

Use in Lactation:

Moxifloxacin may be excreted in the human breast milk. Because of the potential for serious adverse in reaction infants nursing from mothers taking Moxifloxacin, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Paediatric Use:

Safety and effectiveness in pediatric patients and adolescents less than 18 years of age have not been established.

Drug Interaction: 

Antacids containing aluminum, magnesium, or calcium, sucralfate, metal cations such as iron, multivitamins containing iron or zinc preparations containing divalent & trivalent cations, etc. may interfere with the absorption of quinolones, resulting in lower systemic concentration than desired. So, Moxifloxacin should be given at least 4 hours before or 8 hours after taking any of such drugs.

No clinically significant drug interactions between theophylline, warfarin, digoxin, or glyburide have been observed with Moxifloxacin.

Storage:

  • Store in a cool and dry place (at 25º C) protected from light.

  • Keep out of the reach of children.

Packing:

Optimox Tablet: Box containing 1 x 10’s tablets in Alu-Alu blister pack.

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