- Home
- Automated
- List of product information
- CRAVIT TABLET 250 MG [SIN11633P]
CRAVIT TABLET 250 MG [SIN11633P]
Active ingredients: CRAVIT TABLET 250 MG
Product Info
CRAVIT TABLET 250 MG
[SIN11633P]
Product information
Active Ingredient and Strength | LEVOFLOXACIN - 250 MG |
Dosage Form | TABLET, FILM COATED |
Manufacturer and Country | PT KALBE FARMA TBK - INDONESIA REP OF |
Registration Number | SIN11633P |
Licence Holder | RANBAXY (MALAYSIA) SDN. BHD. |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | J01MA12 |
INDICATIONS AND USAGE
CRAVIT® Tablets are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible strains of the designated microorganisms in the conditions listed below. Please see DOSAGE AND ADMINISTRATION for specific recommendations.
Acute bacterial sinusitis due to Streptococcus pneumoniae, Haemophilus influenzae, or Moraxella catarrhalis.
Acute bacterial exacerbation of chronic bronchitis due to Staphylococcus aureus, Streptococcus pneumoniae, Haemophilus influenzae, Haemophilus parainfluenzae, or Moraxella catarrhalis.
Community-acquired pneumonia due to Staphylococcus aureus, Streptococcus pneumoniae (including penicillin-resistant strains, MIC value for penicillin ≥2mcg/mL), Haemophilus influenzae, Haemophilus parainfluenzae, Klebsiella pneumoniae, Moraxella catarrhalis, Chlamydia pneumoniae, Legionella pneumophila, or Mycoplasma pneumoniae. (See CLINICAL STUDIES – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information.)
Nosocomial pneumonia due to methicillin-susceptible Staphylococcus aureus, Pseudomonas aeruginosa, Serratia marcescens, Escherichia coli, Klebsiella pneumoniae, Haemophilus influenzae, Streptococcus pneumoniae. Adjunctive therapy should be used as clinically indicated. Where Pseudomonas aeruginosa is a documented or presumptive pathogen, combination therapy with an anti-pseudomonal β-lactam is recommended.
Complicated skin and skin structure infections due to methicillin-sensitive Staphylococcus aureus, Enterococcus faecalis, Streptococcus pyogenes, or Proteus mirabilis.
Uncomplicated skin and skin structure infections (mild to moderate) including abscesses, cellulitis, furuncles, impetigo, pyoderma, wound infections due to Staphylococcus aureus, or Streptococcus pyogenes.
Complicated urinary tract infections (mild to moderate) due to Enterococcus faecalis, Enterobacter cloacae, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, or Pseudomonas aeruginosa.
Acute pyelonephritis (mild to moderate) caused by Escherichia coli.
Uncomplicated urinary tract infections (mild to moderate) due to Escherichia coli, Klebsiella pneumoniae, or Staphylococcus saprophyticus.
Chronic bacterial prostatitis due to Escherichia coli, Enterococcus faecalis, or methicillin-susceptible Staphylococcus epidermidis.
Appropriate culture and susceptibility tests should be performed before treatment in order to isolate and identify organisms causing the infection and to determine their susceptibility to levofloxacin. Therapy with levofloxacin may be initiated before results of these tests are known; once results become available, appropriate therapy should be selected.
As with other drugs in this class, some strains of Pseudomonas aeruginosa may develop resistance fairly rapidly during treatment with levofloxacin. Culture and susceptibility testing performed periodically during therapy will provide information about the continued susceptibility of the pathogens to the antimicrobial agent and also the possible emergence of bacterial resistance.
DOSAGE AND ADMINISTRATION
The usual dose of CRAVIT® Tablets is 250 mg or 500 mg administered orally, as indicated by infection and described in the following dosing chart. These recommendations apply to patients with normal renal function (i.e., creatinine clearance > 80 mL/min). For patients with altered renal function see the Patients with Impaired Renal Function subsection. Oral doses should be administered at least two hours before or two hours after antacids containing magnesium, aluminum, as well as sucralfate, metal cations such as iron, and multivitamin preparations with zinc or Videx® (Didanosine), chewable/buffered tablets or the pediatric powder for oral solution.

Table caption
Patients with Impaired Renal Function | ||
Renal Status | Initial Dose | Subsequent Dose |
Acute Bacterial Exacerbation of Chronic Bronchitis / | ||
CLCR from 50 to 80 mL/min | No dosage adjustment required | |
CLCR from 20 to 49 mL/min | 500 mg | 250 mg q24h |
CLCR from 10 to 19 mL/min | 500 mg | 250 mg q48h |
Hemodialysis | 500 mg | 250 mg q48h |
CAPD | 500 mg | 250 mg q48h |
Complicated SSSI | ||
CLCR from 50 to 80 mL/min | No dosage adjustment required | |
CLCR from 20 to 49 mL/min | 750 mg | 750 mg q48h |
CLCR from 10 to 19 mL/min | 750 mg | 500 mg q48h |
Hemodialysis | 750 mg | 500 mg q48h |
CAPD | 750 mg | 500 mg q48h |
Complicated UTI / Acute Pyelonephritis | ||
CLCR ≥20 mL/min | No dosage adjustment required | |
CLCR from 10 to 19 mL/min | 250 mg | 250 mg q48h |
Uncomplicated UTI | No dosage adjustment required | |
CLCR = creatinine clearances | ||
CAPD = chronic ambulatory peritoneal dialysis |
When only the serum creatinine is known, the following formula may be used to estimate creatinine clearance.

The serum creatinine should represent a steady state of renal function.
CONTRAINDICATIONS
Levofloxacin is contraindicated in persons with a history of hypersensitivity to levofloxacin, quinolone antimicrobial agents, or any other components of this product.
