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INN monograph

Cloxacillin

Beta-lactam antibiotic — penicillin · POM

PPB Registered POM

Verified · Updated 01 Aug 2026 · Source: Local active-ingredient clinical extract; Professional class pharmacology (Beta-lactam antibiotic — penicillin)

Class
Beta-lactam antibiotic — penicillin
Schedule
POM
Route
ORAL / PARENTERAL (agent-dependent)
Onset
Within 1 hour (oral); faster IV
Duration
4–8 hours typical (agent/formulation dependent)
Pregnancy
Penicillins are generall...
Renal
Renal excretion dominant...
High-alert
No

Kenya market

Wholesale / list prices where loaded

From
Median
Brands
5

Risk first

Contraindications

  • History of serious immediate hypersensitivity (e.g. anaphylaxis, angioedema, urticaria) to any penicillin.
  • Caution with prior severe cephalosporin reaction (cross-reactivity risk).
  • Avoid in infectious mononucleosis if using aminopenicillins (rash risk).

Precautions

  • Risk of kernicterus in jaundiced neonates when high doses are given parenterally.
  • Serious and occasionally fatal immediate hyper- sensitivity reactions may occur

Point of care

Dosing

Adult

Orally: Adult; 500mg QID [orally]. Children; 25-50mg/kg/day. I.M: Adult; 250mg every 4-6 hours. I.V inj or inf. 500mg every 4-6 hours. Children; 25-50mg/kg/day. In severe case doses may be doubled.

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Renal excretion dominant — reduce dose or extend interval in significant renal impairment; risk of accumulation and seizures at high levels.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.

Hepatic

Low intrinsic hepatotoxicity; cholestatic hepatitis rare (notably flucloxacillin/co-amoxiclav patterns for related agents).

Strengths

250mg

Forms

Capsule

Safety

Drug interactions

Open checker →
  • For professionals: select agent by suspected pathogen and local resistance.
  • Natural penicillins remain first-line for many streptococcal infections when susceptibility expected.
  • Do not use penicillin alone for beta-lactamase-producing staphylococci.
  • Document allergy phenotype (immediate vs delayed).
  • De-escalate once cultures allow.

Safety

Adverse effects

  • Allergic reactions that include skin rashes and immediate anaphylaxis
  • sterile inflammationca at the site of intramuscular injec- tion
  • peripheral nerve pain and dysfunction
  • Nephropathy manifested as interstitial nephritis has been reported neutropenia and thrombocytopenia

Use

Indications

  • Infections, especially those due to penicillinase-producing staphylococci.
  • Clinical selection for Cloxacillin should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Beta-lactam antibiotic — penicillin.
  • Confirm site-specific dose, duration and monitoring before prescribing.

Pharmacology

Mode of action

Inhibits synthesis of bacterial cell wall, causing cell death, hence bactericidal.

Bind PBPs Block wall cross-linking Osmotic lysis Bactericidal
Full mechanism text

Inhibits synthesis of bacterial cell wall, causing cell death, hence bactericidal. Penicillins bind penicillin-binding proteins (PBPs) and inhibit the final transpeptidation step of peptidoglycan synthesis, weakening the bacterial cell wall. Osmotic lysis follows; activity is bactericidal against susceptible organisms in the growth phase. Spectrum and beta-lactamase stability vary by agent (narrow natural penicillins vs aminopenicillins vs antipseudomonal/anti-staphylococcal agents).

ADME

Pharmacokinetics & PD

Onset Within 1 hour (oral); faster IV
Duration 4–8 hours typical (agent/formulation dependent)
Route ORAL / PARENTERAL (agent-dependent)
Elimination is predominantly renal (glomerular filtration and tubular secretion). Dose adjustment is often required in severe renal impairment. Probenecid reduces tubular secretion and prolongs levels.
Half-life differ by agent and salt/ester. Most penicillins distribute widely into extracellular fluid; CSF penetration is poor unless meninges are inflamed.
Full PK/PD text

Absorption, protein binding and half-life differ by agent and salt/ester. Most penicillins distribute widely into extracellular fluid; CSF penetration is poor unless meninges are inflamed. Elimination is predominantly renal (glomerular filtration and tubular secretion). Dose adjustment is often required in severe renal impairment. Probenecid reduces tubular secretion and prolongs levels.

Kenya

Brands & prices

5 listed
Brand Company Pack KES
Cloxisel Distributed by Medisel (K) Limited Standard Commercial Pack
Dawaclox Dawa Limited Standard Commercial Pack
Dawaflox Dawa Limited 250mg [Vial]
Floxapen GSK Kenya (GlaxoSmithKline) 250mg [1000s]
Kloxy Laboratory & Allied Ltd. Standard Commercial Pack

Special populations

Pregnancy & lactation

Pregnancy

Penicillins are generally considered compatible in pregnancy when clearly indicated (decades of clinical use). Prefer agents with the best safety record for the indication; confirm current SmPC.

Lactation

Usually compatible with breastfeeding; small amounts excreted in milk. Monitor infant for diarrhoea, thrush or rash.

Diet

Food & alcohol

  • Food
  • Food

Trust

Sources & disclaimer

Source: Local active-ingredient clinical extract; Professional class pharmacology (Beta-lactam antibiotic — penicillin)

Last reviewed: 01 Aug 2026

Decision support only — not a substitute for clinical judgment, product SmPC, or Kenya STG/EML.

Kenya Verified Health Registry