levocetirizine reference
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(levocetirizine · DailyMed)
Registered Malawi · PMRA

FITIN 2.5MG/5ML SYRUP

LEVOCETIRIZINE DIHYDROCHLORIDE

PMPB/PL177/28 SYRUP respiratory system INN generic

What it does

Levocetirizine is an antihistamine that helps relieve allergy symptoms.

Commonly used for: allergic rhinitis (hay fever), chronic urticaria (hives)

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
PMPB/PL177/28
Registration date
14/03/2017
Expiry date
30/06/2019
Status
Registered
Active ingredient
LEVOCETIRIZINE DIHYDROCHLORIDE
Dosage form
SYRUP
Strength
-
Pack size
-
Therapeutic class
-
ATC class (WHO)
R06AE - Piperazine derivatives
Drug group
RESPIRATORY SYSTEM
RxNorm RxCUI
356887
Manufacturer / MAH
-
Applicant / LTR
-
Country of origin
-

Source: Pharmacy and Medicines Regulatory Authority · fetched 2026-04-21 17:37:38 · updated 2026-09-15 04:32:43

Disclaimer: This information is sourced from Pharmacy and Medicines Regulatory Authority (Malawi). Always consult a qualified healthcare professional before using any medication.

About this medicine

Levocetirizine is an antihistamine that helps relieve allergy symptoms.

What it treats

  • allergic rhinitis (hay fever)
  • chronic urticaria (hives)

How it works

It works by blocking the effects of histamine, a substance in the body that causes allergic symptoms.

Who it's for

It is for adults and children who suffer from allergies.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: levocetirizine

BNF-referenced

Levocetirizine is a second-generation antihistamine primarily used to alleviate symptoms associated with allergic reactions, such as allergic rhinitis and chronic urticaria. It is known for its selectivity for the H1 histamine receptor, resulting in fewer sedative effects compared to first-generation antihistamines. Levocetirizine is typically administered once daily due to its long duration of action.

Indications

  • Allergic rhinitis
  • Chronic urticaria

Dosage

Children: For children aged 6 to 11 years, the recommended dose is 5 mg once daily. For children aged 2 to 5 years, the dose is 1.25 mg once daily.

Adults: The usual dose for adults is 5 mg once daily.

Mechanism of action

Levocetirizine selectively inhibits histamine H1 receptors. This action prevents histamine from activating the receptor and causing effects such as smooth muscle contraction, increased permeability of vascular endothelium, histidine uptake in basophils, stimulation of cough receptors, and stimulation of flare responses in the nervous system.

Pharmacodynamics

As a second-generation histamine H1 antagonist, levocetirizine effectively reduces various allergic symptoms. It possesses a long duration of action, allowing for once-daily dosing. The therapeutic index is favorable, with studies showing that the maximal nonlethal dose is significantly higher than the therapeutic dose. Caution is advised for activities requiring full alertness and in patients predisposed to urinary retention.

Pharmacokinetics

Levocetirizine is well absorbed after oral administration, with peak plasma concentrations typically reached within approximately 1 hour. It has a volume of distribution of about 0.4 L/kg and is primarily excreted unchanged in the urine. The elimination half-life is approximately 8 to 9 hours, allowing for once-daily dosing.

Contra-indications

  • Hypersensitivity to levocetirizine or any of its components
  • Severe renal impairment

Adverse effects

  • Drowsiness
  • Fatigue
  • Dry mouth
  • Headache
  • Gastrointestinal disturbances

Interactions

  • CNS depressants may enhance sedative effects
  • Alcohol may increase sedation

Precautions

  • Caution in patients with a history of urinary retention
  • Caution in patients with severe renal impairment
  • Avoid operating machinery or driving until you know how levocetirizine affects you

Pregnancy

Levocetirizine should be used in pregnancy only if the potential benefit justifies the potential risk to the fetus.

Breast-feeding

Levocetirizine is excreted in breast milk; caution should be exercised when administering to nursing mothers.

Storage

Store at room temperature, away from moisture and heat.

Formulations

  • Tablets
  • Oral solution

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Clinical monograph: Levocetirizinehydrochloride

BNF-referenced

Levocetirizine hydrochloride is a third-generation antihistamine primarily used for the symptomatic relief of allergic conditions such as seasonal allergic rhinitis and chronic idiopathic urticaria. It is known for its non-sedating properties, making it preferable for patients who require management of allergy symptoms without significant sedation or psychomotor impairment.

Indications

  • Seasonal allergic rhinitis
  • Chronic idiopathic urticaria

Dosage

Children: For children aged 6 to 11 years, the dose is 30 mg twice daily. For children aged 12 to 17 years, the dose is 120 mg once daily.

Adults: For adults, the recommended dose is 180 mg once daily.

Mechanism of action

Levocetirizine is an active enantiomer of cetirizine and functions as a selective antagonist of the peripheral H1 receptor. By blocking the action of histamine, a key mediator in allergic responses, it reduces symptoms such as sneezing, itching, and runny nose. It also prevents the activation of sensory neurons, thereby mitigating pruritus and swelling associated with allergic reactions.

Pharmacodynamics

Levocetirizine exhibits antihistaminic effects with a rapid onset of action. Its affinity for peripheral H1 receptors allows it to effectively reduce the symptoms of allergic rhinitis and urticaria. While it is termed 'non-sedating', some degree of sedation may still occur in sensitive individuals, although this is generally minimal compared to first-generation antihistamines.

Pharmacokinetics

Levocetirizine is well absorbed after oral administration, with peak plasma concentrations typically reached within 0.9 hours. The drug has a volume of distribution of approximately 0.4 L/kg and is primarily excreted unchanged in urine. It has a half-life of about 8 hours, allowing for once-daily dosing. In patients with renal impairment, dose adjustments may be necessary due to altered drug clearance.

Contra-indications

  • Acute porphyrias

Adverse effects

  • Asthenia
  • Constipation
  • Drowsiness
  • Dry mouth
  • Abdominal pain
  • Aggression
  • Agitation
  • Angioedema
  • Appetite increased
  • Arthralgia
  • Depression
  • Diarrhoea
  • Dizziness
  • Fatigue
  • Hallucination
  • Hepatitis
  • Myalgia
  • Nausea
  • Oedema
  • Palpitations
  • Paraesthesia
  • Seizure
  • Skin reactions
  • Sleep disorders
  • Suicidal ideation
  • Syncope
  • Tachycardia
  • Taste altered
  • Tremor
  • Urinary disorders
  • Vertigo
  • Vision disorders
  • Vomiting
  • Weight increased

Interactions

  • Other antihistamines
  • Alcohol (may increase sedation)
  • CNS depressants

Precautions

  • Caution in renal impairment
  • Patients should be advised about potential drowsiness affecting driving and skilled tasks

Pregnancy

Most manufacturers of antihistamines advise avoiding their use during pregnancy; however, there is no evidence of teratogenicity.

Breast-feeding

Most antihistamines are present in breast milk in varying amounts; although not known to be harmful, most manufacturers advise avoiding their use in mothers who are breastfeeding.

Storage

Store in a cool, dry place away from light. Keep out of reach of children.

Formulations

  • Oral suspension
  • Oral solution
  • Tablets
BNF 85 (British National Formulary) p.326 BNF for Children 2019-2020 p.200 PubChem / pathway

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Molecular reference: levocetirizine

PubChem CID 1549000

Molecular formula: C21H25ClN2O3

Mechanism of action

Levocetirizine selectively inhibits histamine H<sub>1</sub> receptors. This action prevents histamine from activating this receptor and causing effects like smooth muscle contraction, increased permeability of vascular endothelium, histidine uptake in basophils, stimulation of cough receptors, and stimulation of flare responses in the nervous system.

Pharmacodynamics

Levocetirizine is a second generation histamine H<sub>1</sub> antagonist used to treat various allergic symptoms. It has a long duration of action as it is generally taken once daily, and a wide therapeutic window as animal studies show the maximal nonlethal dose is over 100x a normal dose. Patients are cautioned to avoid tasks that require complete alertness, avoid alertness, and use caution in patients with factors predisposing urinary retention.

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

Molecular reference: Levocetirizinehydrochloride

PubChem CID 67336450

Molecular formula: C21H26Cl2N2O3

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.