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New search Medicine profile Montelukast / Levocetirizine

Clinical medicine profile

Montelukast / Levocetirizine

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

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

Precautions

  • [From component Montelukast] Monitoring of patient when systemic corticosteroid reduction is considered.
  • Combination therapy with bronchodilator.
  • Exercise-induced asthma.
  • Pregnancy and lactation
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

  • Therapeutic use is agent- and indication-specific within the class (Therapeutic agent (verify pharmacological class)).
  • Use according to culture results, national guidelines (Kenya STG/EML where applicable) and the current product SmPC.
  • Allergic rhinitis

Adverse effects

  • [From component Montelukast] Dream abnormalities, hallucinations, palpitations, drowsiness, irritability, restlessness, insomnia, increased sweating, headache
  • nausea, vomiting, dyspepsia, diarrhea, abdominal pain
  • myalgia including muscle cramps
  • increased bleeding tendency, bruising edema
  • tremor, dry mouth, vertigo, arthralgia.
  • Fixed-dose/multi-ingredient product.
  • Clinical details partially inherited from component monographs: Montelukast, Levocetirizine.
  • Confirm combination SmPC for exact dosing.
04 Pharmacology

Mechanism & disposition

Combination product.

Combination product.Component mechanism (Montelukast): Inhibit…The cysteinyl leukotrienes [LTC4, LTD4 and…
Read complete mechanism

Combination product. Component mechanism (Montelukast): Inhibits airway CysLT receptors. The cysteinyl leukotrienes [LTC4, LTD4 and LTE4] are products of arachidonic acid metabolism and are released from various cells, includ-ing mast cells and eosinophils. These eicosanoids bind to cysteinyl leukotriene [CysLT] receptors. The CysLT type-1 [CysLT1] receptor is found in the human airway including airway smooth muscle cells and airway macrophages and on other pro-inflammatory cells including eosinophils and certain myeloid stem cells. CysLTs contribute to the pathophysiology of asthma and allergic rhinitis].

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

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

Lactation

[Montelukast] Assess infant risk vs benefit of maternal therapy; prefer agents with lactation data. [Levocetirizine] [Levocetirizine] Assess infant risk vs benefit of maternal therapy; prefer agents with lactation data. [Montelukast] Assess infant risk vs benefit of maternal therapy; prefer agents with lactation data.

06 Kenya market

Brands & loaded prices

FromKES 335
MedianKES 335
Listings4
BrandManufacturerPackObserved price
MONTALLERG TABS 20*S Not recorded KES 953.72Daima Chemist price-list reference ↗ Source date not recorded · verify current price
MONTA PLUS TABS 10*S Not recorded UnavailableDaima Chemist price-list reference
Montecor Plus Signature mg / 10mg 30's Unavailable
MONTECOR PLUS TABLETS 10*S Not recorded KES 335.40Daima Chemist price-list reference ↗ Source date not recorded · verify current price
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; RxNorm (NLM RxNav); PubChem; Component monographs (multi-source pipeline)
Last reviewed14 Aug 2026
EvidenceGeneral guidance
Open source document ↗

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