Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Timecef
Synonyms :
cefodizime
Class :
Cephalosporins
Dosage Forms & StrengthsÂ
Intravenous/Intramuscular infusionÂ
1gÂ
2gÂ
Administer 1 to 2 g once or twice a day intramuscularly or intravenous infusion.
Maximum dose-4 g/day.
Renal impairment
CrCl 10 to 30ml/min-Administer 1 to 2 g every day.
CrCl<10ml/min- Administer 0.5 to 1 g every day.
Lower Respiratory Tract InfectionsÂ
Administer 1 to 2 g once or twice a day intramuscularly or intravenous infusion.
Maximum dose-4 g/day.
Renal impairment
CrCl 10 to 30ml/min-Administer 1 to 2 g every day.
CrCl<10ml/min- Administer 0.5 to 1 g every day.
Administer 0.25 to 0.5 g intramuscularly or intravenous infusion as a single dose.
Safety and efficacy not establishedÂ
Refer adult dosingÂ
Actions and Spectrum:Â
cefodizime exerts its antibacterial effects by interfering with bacterial cell wall synthesis. Bacterial cell walls are essential for maintaining the structural integrity of the cell. cefodizime works through the following mechanism:Â
cefodizime has a broad spectrum of activity against Gram-positive and Gram-negative bacteria, including some beta-lactamase-producing strains.Â
Frequency not definedÂ
VomitingÂ
Hypersensitivity reactionsÂ
CNS toxicityÂ
Hepatic dysfunctionÂ
Pain at the injection site Â
NauseaÂ
DiarrhoeaÂ
NephrotoxicityÂ
Pseudomembranous colitisÂ
Haematologic disordersÂ
Black box warning:Â
NoneÂ
Contraindications/caution:Â
Contraindications:Â
Hypersensitivity reactionsÂ
Caution:Â
Pregnancy consideration: N/AÂ
Lactation: N/AÂ
Pregnancy category:Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.Â
<b>Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.   Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: There is no data available for the drug under this categoryÂ
Pharmacology:Â
cefodizime exerts its antibacterial effects by interfering with bacterial cell wall synthesis. Bacterial cell walls are essential for maintaining the structural integrity of the cell. Like other cephalosporin antibiotics, cefodizime achieves its bactericidal action by binding to penicillin-binding proteins (PBPs) in the bacterial cell wall. This binding interferes with the enzymes responsible for cross-linking the peptidoglycan chains in the cell wall. Disruption of the peptidoglycan cross-linking process weakens the cell wall, making it more susceptible to osmotic pressure. This eventually leads to cell lysis (rupture) and bacterial death.Â
Pharmacodynamics:Â Â
Pharmacokinetics:Â
AbsorptionÂ
cefodizime is administered parenterally through intravenous (IV) or intramuscular (IM) injection. When administered through these routes, it bypasses the gastrointestinal tract, and its absorption is nearly complete and rapid. It exhibits high bioavailability when administered via parenteral routes because it is directly introduced into the bloodstream.Â
DistributionÂ
cefodizime is widely distributed throughout the body, allowing it to reach various tissues and fluids. This extensive distribution contributes to its ability to treat infections at different anatomical sites. While cefodizime can penetrate various tissues, it has limited penetration across the blood-brain barrier. It may reach therapeutic levels in the cerebrospinal fluid under certain conditions.Â
MetabolismÂ
cefodizime undergoes minimal metabolism in the body. It is primarily excreted unchanged, which is typical for most cephalosporin antibiotics.Â
Elimination and ExcretionÂ
The primary route of excretion for cefodizime is renal (through the kidneys). The drug is primarily eliminated unchanged in the urine. The terminal elimination half-life of cefodizime is relatively short, approximately 4 hours. It is mainly excreted in its unchanged form through the kidneys.
Administration:Â
Intramuscular/Intravenous administrationÂ
cefodizime is often administered as an intravenous infusion over a specified period, typically 30 minutes to one hour.Â
Patient information leafletÂ
Generic Name: cefodizimeÂ
Why do we use cefodizime?Â
cefodizime is an antibiotic medication used to treat various bacterial infections. It belongs to the cephalosporin class of antibiotics and is effective against a wide range of both Gram-positive and Gram-negative bacteria. Here are some common uses of cefodizime:Â
Pneumonia: Caused by susceptible bacteria.Â
Bronchitis: In some cases, when a bacterial infection is suspected.Â
Sinusitis: Caused by susceptible bacteria.Â
Pharyngitis and Tonsillitis: Caused by Streptococcus pyogenes (Group A Streptococcus).Â