Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Suprax
Synonyms :
cefixime
Class :
Third generation cephalosporins
Dosage Forms & Strengths
capsule
400mg
tablet, chewable
100mg
200mg
oral suspension
100mg/5mL
200mg/5mL
500mg/5mL
Indicated for Acute Exacerbations of Chronic Bronchitis:
400
mg/day
Orally 
Single dose or divided every 12hr
400
mg/day
Orally 
Single dose or divided every 12hr
400 mg/day orally in single daily dose or divided every 12hr
Indicated for Uncomplicated Gonorrhea:
400 mg orally once along with azithromycin 1g orally once or doxycycline
100mg orally every 12hhr for 7days as alternate therapy
Dosage Forms & Strengths
capsule
400mg
tablet, chewable
100mg
200mg
oral suspension
100mg/5mL
200mg/5mL
500mg/5mL
Refer to the adult dosing
Actions and spectrum:
cefixime is a third-generation cephalosporin antibiotic that is used to treat a variety of bacterial infections, including respiratory tract infections, urinary tract infections, and sexually transmitted infections.
The mechanism of action of cefixime involves inhibition of bacterial cell wall synthesis. cefixime interferes with the formation of peptidoglycan, a complex molecule that provides structural integrity to the bacterial cell wall. By inhibiting the formation of peptidoglycan, cefixime disrupts the normal structure of the cell wall and leads to bacterial cell death.
Spectrum
The spectrum of cefixime refers to the range of bacteria that it is effective against. Cefixime is a broad-spectrum antibiotic that is used to treat a variety of bacterial infections.
cefixime has activity against both gram-negative and gram-positive bacteria. It is particularly effective against gram-negative bacteria, such as Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, Proteus mirabilis, and Neisseria gonorrhoeae. It is also active against some gram-positive bacteria, such as Streptococcus pneumoniae.
Frequency defined:
>10%
Diarrhea (16%)
Frequency not defined:
Abdominal pain
Elevated transaminases
Increased creatinine
Prolonged prothrombin time (PT)
Serum sickness-like reaction
Thrombocytopenia
Vaginitis
Candidiasis
Dyspepsia
Flatulence
Leukopenia
Pruritus
Rash
Thrombocytopenia
Stevens-Johnson syndrome
Vomiting
Contraindications/caution:
Contraindication
Pregnancy consideration: USFDA pregnancy category A
Lactation: safety and efficacy not established
Pregnancy category:
Category A: Satisfactory and well-controlled studies show no risk to the fetus in the first or later trimester.
Category B: There is no evidence of risk to the fetus found in animal reproduction studies and there are not enough studies on pregnant women.
Category C: Adverse effects on the fetus found with evidence in animal reproduction studies and no adequate evidence for an effect in humans, care must be taken for potential risks in pregnant women
Category D: There is adequate data available with sufficient evidence of human fetal risk from various platforms, but despite potential risks may be used only in emergency cases for potential benefits.
Category X: Drugs listed in this category outweigh risks over benefits These category drugs should be prohibited for pregnant women.
Category N: There is no data available for the drug under this category.
Pharmacology:
The mechanism of action of cefixime involves binding the drug to specific penicillin-binding proteins (PBPs) in the bacterial cell wall. PBPs are enzymes involved in the synthesis and maintenance of the cell wall, and by binding to these proteins, cefixime interferes with the normal functioning of the cell wall. This weakens the cell wall, making it more susceptible to damage and eventually causing the bacterial cell to lyse or break apart.
Pharmacodynamics
cefixime acts by binding to penicillin-binding proteins (PBPs) located on the bacterial cell wall, thereby preventing the formation of cross-links between the peptidoglycan chains. This leads to a destabilization of the bacterial cell wall, resulting in its lysis and death of the bacterium.
Pharmacokinetics
Absorption
cefixime is rapidly absorbed from the gastrointestinal tract after oral administration. Peak plasma concentrations are achieved approximately 2-3 hours after dosing. The bioavailability of cefixime is approximately 50-70%, which means that a significant portion of the drug is absorbed by the body.
Distribution
cefixime is widely distributed in the body and has good penetration into many tissues and body fluids, including the respiratory tract, urinary tract, and bone. The drug is also able to cross the blood-brain barrier, making it effective for the treatment of central nervous system infections.
Metabolism
cefixime is not metabolized in the body and is excreted unchanged in the urine.
Excretion:
cefixime is mainly excreted unchanged in the urine, with approximately 70-80% of an oral dose being excreted in the urine within 24 hours. The remaining drug is excreted in the feces.The half-life of cefixime is approximately 2-3 hours, meaning that the drug is rapidly eliminated from the body.
Administration:
Patient information leaflet
Generic Name: cefixime
Pronounced: (sef-IX-eem)
Why do we use cefixime?
cefixime is a third-generation cephalosporin antibiotic that is used to treat a variety of bacterial infections.