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New search Medicine profile L-Ornithine-L-Aspartate

Clinical medicine profile

L-Ornithine-L-Aspartate

Insulin (antidiabetic hormone)

High alert POM
Evidence state Source not available Reviewed 14 Aug 2026
Route
SC / IV (soluble in critical care)
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
Verification required

This profile needs source confirmation

A traceable source link is not attached to this profile. 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.

High-alert medicine — use an independent double-check during prescribing, preparation, and dispensing.

Contraindications

  • Hypoglycaemia.
  • Hypersensitivity to specific formulation.

Precautions

  • HIGH-ALERT medication.
  • Dose double-checks.
  • Educate hypo recognition/treatment.
  • Adjust for renal failure (reduced clearance), illness, steroids, exercise.
  • Never share pens.
  • Rotate sites.
02 Point of care

Dosing matrix

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

Adult

Dose: 1-2 sachets or tablets TID, dissolved in liquid with or after a meal.

Paediatric

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

Renal

Reduced insulin clearance — lower doses often needed in advanced CKD.

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

Impaired gluconeogenesis increases hypo risk.

03 Clinical use

Use, effects & interactions

Indications

  • High ammonia levels
  • severe liver impairment
  • end-stage cirrhosis Clinical selection for L-Ornithine-L-Aspartate should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Insulin (antidiabetic hormone).
  • Confirm site-specific dose, duration and monitoring before prescribing.

Adverse effects

  • Hypoglycaemia, weight gain, injection-site reactions, lipodystrophy.
  • Rare: severe allergy, hypokalaemia (shift).
  • ISMP high-alert.
  • Write units in full.
  • Confirm concentration (U-100 vs U-200/U-300/U-500).
  • Sick-day rules and ketone advice for type 1.
  • Structured education improves outcomes.
04 Pharmacology

Mechanism & disposition

Insulin binds insulin receptors, promoting GLUT4-mediated glucose uptake in muscle/adipose tissue, stimulating glycogenesis, inhibiting glycogenolysis/gluconeogenesis and lipolysis — lowers blood glucose.

Insulin binds insulin receptors, promoting…
Read complete mechanism

Insulin binds insulin receptors, promoting GLUT4-mediated glucose uptake in muscle/adipose tissue, stimulating glycogenesis, inhibiting glycogenolysis/gluconeogenesis and lipolysis — lowers blood glucose.

Onset

Minutes–hours (formulation-dependent)

Duration

Hours–>40 h (basal analogues)

Route

SC / IV (soluble in critical care)

Absorption

varies by site, temperature, lipohypertrophy. Analogues engineered for prandial vs basal profiles. IV soluble insulin used in DKA/HHS protocols.

05 Special populations

Pregnancy, lactation & diet

Pregnancy

Insulin is preferred pharmacological therapy for diabetes in pregnancy when needed.

Lactation

Compatible; may need dose adjustment postpartum.

06 Kenya market

Brands & loaded prices

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

Sources & review state

Primary sourceLocal active-ingredient clinical extract; Professional class pharmacology (Insulin (antidiabetic hormone))
Last reviewed14 Aug 2026
EvidenceSource not available

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