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New search Medicine profile Faropenem

Clinical medicine profile

Faropenem

Therapeutic agent (verify pharmacological class)

POM
Evidence state General guidance Reviewed 14 Aug 2026
Route
See product SmPC
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
Verification required

This profile needs source confirmation

Some sections contain general class guidance rather than medicine-specific evidence. Confirm prescribing decisions against the current SmPC and Kenya STG/EML.

01 Risk first

Safety essentials

The information most likely to change a prescribing or dispensing decision.

Contraindications

  • Hypersensitivity to the active substance or excipients.
  • Additional absolute contraindications are indication- and product-specific — consult SmPC.

Precautions

  • Obtain allergy and medication history.
  • Adjust for renal/hepatic impairment, pregnancy, lactation, extremes of age and interacting drugs.
  • Use the lowest effective dose for the shortest appropriate duration.
  • Monitor for expected class adverse effects.
02 Point of care

Dosing matrix

Population and organ-function guidance, shown together for faster comparison.

Adult

Dosing is indication-, age-, weight- and organ-function-specific for this INN. Do not use class averages for high-risk patients. Confirm the exact regimen in the current SmPC and Kenya Standard Treatment Guidelines. Typical professional workflow: (1) confirm indication, (2) check renal/hepatic function, (3) screen interactions/allergies, (4) select dose/route/duration, (5) define monitoring.

Paediatric

Paediatric dosing is weight- and age-based; use a paediatric formulary / SmPC. Do not extrapolate adult tablets without calculation.

Renal

Review renal impairment dosing; many agents need CrCl/eGFR adjustment.

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

Review hepatic impairment dosing; monitor LFTs if agent is hepatically cleared or hepatotoxic.

03 Clinical use

Use, effects & interactions

Indications

  • Community-acquired pneumonia, bacterial sinusitis, chronic bronchitis and skin infections.
  • Clinical selection for Faropenem should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Therapeutic agent (verify pharmacological class).
  • Confirm site-specific dose, duration and monitoring before prescribing.

Adverse effects

  • Shock, pseudoanaphylactic symptoms (e.g. wheezing, breathing problems), dizziness, feeling a need to evacuate the bowel, tinnitus, sweating, flushing of the whole body, vascular edema, hypotension, renal impairment, pseudomembranous colitis, Stevens-Johnson syndrome, Lyell syndrome, pneumonia, pyrexia, cough, hepatic disorders.
  • Agranulocytosis, triated muscle softening, muscular pain, feeling of exhaustion, increase, hypersensitivity reactions, vitamin deficiency, symptoms of vitamin K deficiency, low prothrombin and tendency of hemorrhage.
  • Symptoms of vitamin B-group deficiency.
  • GIT disorders.
  • Burning sensation, headache, dizziness, drowsiness, edema, dryness of the mouth and lips, change in nail color, and a washed-out feeling.
  • An orally-active penem group beta-lactam antibiotic that is resistant to some forms of extended-spectrum beta-lactamase.
  • An orally-active penem group beta-lactam antibiotic that is resistant to some forms of extended-spectrum beta-lactamase.
04 Pharmacology

Mechanism & disposition

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

Inhibits synthesis of bacterial cell wall,…Mechanism is agent-specific.At receptor, enzyme, ion channel, transpor…
Read complete mechanism

Inhibits synthesis of bacterial cell wall, causing cell death, hence bactericidal. Mechanism is agent-specific. At receptor, enzyme, ion channel, transporter or microbial target level, the drug alters a physiological or pathological pathway to produce its therapeutic effect. Confirm precise molecular mechanism in current SmPC / pharmacology reference for this INN before high-stakes decisions.

Onset

Product-specific

Duration

Product-specific

Route

See product SmPC

Elimination

are product-specific. Consider food effects, protein binding, hepatic CYP/UGT

Half-life

when adjusting for organ impairment, age and drug interactions. Verify parameters in the current SmPC.

05 Special populations

Pregnancy, lactation & diet

Pregnancy

Use only if potential benefit justifies potential risk; prefer agents with better reproductive data when alternatives exist.

Lactation

Assess infant risk vs benefit of maternal therapy; prefer agents with lactation data.

06 Kenya market

Brands & loaded prices

From
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Listings0
BrandManufacturerPackObserved price
No reviewed brand listings are linked yet.
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; Professional class pharmacology (Therapeutic agent (verify pharmacological class))
Last reviewed14 Aug 2026
EvidenceGeneral guidance

Decision support only. Confirm patient-specific decisions against the current product SmPC, Kenya STG/EML, and professional judgement.