Velogen 125 mg/5 ml (Powder for Suspension)
100 ml bottle: ৳ 82.56
Medicine Details
Category | Details |
---|---|
Generic | Cephradine |
Company | General pharmaceuticals ltd |
Also available as |
Therapeutic Class
- First generation Cephalosporins
Indications
- Treatment of infections caused by sensitive Gram-positive and Gram-negative bacteria
- Upper respiratory tract infections: sinusitis, pharyngitis, tonsillitis, laryngo-tracheo bronchitis, otitis media
- Lower respiratory tract infections: bronchitis (acute and chronic), lobar pneumonia, bronchopneumonia
- Urinary tract infections: cystitis, urethritis, pyelonephritis
- Skin and soft tissue infections: abscess, cellulitis, furunculosis, impetigo
- Susceptible microorganisms: Staphylococci, Streptococci, Streptococcus pyogenes, Streptococcus pneumonia, Escherichia coli, Klebsiella spp, Proteus mirabilis, Haemophilus influenza, Shigella spp, Salmonella spp (including Salmonella typhi), Neisseria spp
Pharmacology
- Semisynthetic broad spectrum bactericidal antibiotic
- Active against both gram-positive and gram-negative microorganisms
- Inhibits cross-linking process in the cell wall of bacteria
- Main site of action is the cell wall of bacteria
- Lysis of bacteria occurs due to external osmotic pressure
Dosage & Administration
- Variable dosage for adults based on infection type and severity
- Dosage for children based on total daily dose and specific infections
- Maximum daily dosage: 4 gm
- Dosage adjustment necessary in elderly and patients with impaired renal or hepatic function
- Usual dose for injectable administration in adults and children
Interaction
- Increased risk of kidney damage with concomitant use of nephrotoxic drugs like aminoglycosides
- Enhanced possibility of renal toxicity with diuretics (e.g. frusemide, ethacrynic acid) and probenecid
Contraindications
- Not to be used in patients with known or suspected hypersensitivity to cephalosporins
Side Effects
- Limited essentially to gastro-intestinal disturbances and on occasions to hypersensitivity phenomena
- Possible skin reactions and hypersensitivity reactions
- Rare occurrences of glossitis, heartburn, dizziness, nausea, vomiting, diarrhoea, abdominal pain, vaginitis, candida overgrowth
Pregnancy & Lactation
- Safety in pregnancy not established
- Excreted in breast milk, caution advised in lactating mothers
- Patients cautioned about operating hazardous machinery, including automobiles
Precautions & Warnings
- Prolonged use may result in the development of superinfection due to the emergence of resistant organisms
- Administered with care to patients hypersensitive to penicillins
- May cause a false positive urine glucose result with certain testing solutions
- Dosage adjustment necessary in renal impairment
- Contains lactose, not suitable for patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency, or glucose-galactose malabsorption
Use in Special Populations
- Recommended doses for patients with renal impairment not on haemodialysis based on creatinine clearance
- Additional dosing information for patients on chronic, intermittent haemodialysis
- Higher doses may be required for chronic or severe infections
- Paediatric dosages should not exceed those specified for adults, regardless of infection severity
Overdose Effects
- Non-specific symptoms such as nausea, vomiting, diarrhoea, and gastric upsets
- Supportive treatment recommended
- Gastric lavage may be necessary if a large amount has been ingested
Storage Conditions
- Velogen Suspension should be freshly prepared
- Reconstituted Suspension should be used within 7 days at room temperature or within 14 days in a refrigerator
- Velogen Injection solutions should be used within 2 hours at room temperature
- When stored at 5°C, solutions retain potency for 12 hours
- Reconstituted solutions may vary in colour; potency is not affected
- Do not use later than the date of expiry
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