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Brand Name :
Rapitus, Mewell
Synonyms :
levodropropizine
Class :
Antitussives
Dosage Forms & Strengths
Tablet
60 mg
Syrup
30 mg/5ml
60 mg/5ml
60 mg orally taken thrice a day for not more than a week
Dose Adjustments
Dosage modifications
Hepatic impairment: Contraindicated in Severe cases
Dosage Forms & Strengths
Tablet
60 mg
Syrup
30 mg/5ml
60 mg/5ml
Above 2 years: 1 mg/kg thrice a day;
Above 12 years: 60 mg orally taken thrice a day for Not more than a week
Dose Adjustments
Dosage modifications
Hepatic impairment: Contraindicated in Severe cases
Refer to the adult dosing regimen
Actions and spectrum:
levodropropizine is an antitussive medication primarily used to relieve coughing. It acts by suppressing cough reflex in the central nervous system. It is used to alleviate dry, non-productive coughs that can be caused by various respiratory conditions, such as bronchitis or the common cold. levodropropizine’s spectrum is specific to its antitussive action and is not used for other purposes.
Frequency not defined
drowsiness
Palpitations
Nausea
diarrhoea
heartburn
Fatigue
Dizziness
numbness
altered consciousness
Vomiting
abdominal distress
headache
Black Box Warning:
levodropropizine does not have a black box warning.
Contraindication/Caution:
Contraindication:
Caution:
Comorbidities:
Pregnancy consideration: pregnancy category: not assigned
Lactation: excreted into human milk: unknown
Pregnancy category:
Pharmacology:
levodropropizine is a medication used primarily to relieve cough symptoms. Its pharmacology involves suppressing the cough reflex by acting on the peripheral sensory nerves in the respiratory tract.
It exerts its effect by inhibiting the release of substances like histamine and prostaglandins, which can trigger coughing. levodropropizine does not possess significant sedative or antihistamine properties, making it a well-tolerated cough suppressant.
Its mechanism of action is primarily local, affecting the respiratory tract’s cough reflex without causing significant central nervous system effects. This targeted action helps alleviate coughing while minimizing the risk of drowsiness or other systemic side effects commonly associated with some cough medications.
Pharmacodynamics:
Pharmacokinetics:
Absorption
levodropropizine is well-absorbed from the gastrointestinal tract after oral administration. It is rapidly absorbed, and peak blood concentrations are usually reached within 1 to 2 hours after ingestion. The absorption is not affected by food, so it can be taken with or without meals.
Distribution
levodropropizine is distributed throughout the body, but it exerts its effects in the respiratory tract. It has a low binding affinity to plasma proteins, which means it can easily move from the bloodstream to the target tissues, such as the respiratory mucosa. This distribution allows it to act locally in the airways to suppress coughing.
Metabolism
levodropropizine undergoes hepatic (liver) metabolism. It is metabolized into various metabolites, although the specific enzymes and pathways involved in its metabolism may not be well-documented. The metabolites are less active than the parent drug.
Elimination and excretion
The elimination of levodropropizine and its metabolites occurs primarily through the urine. The exact details of the excretion process, including the extent of renal (kidney) excretion and the elimination half-life, may vary among individuals. In general, the drug and its metabolites are eliminated quickly from the body.
Administration:
Patient information leaflet
Generic Name: levodropropizine
Pronounced: (lee-voe-dro-PRO-pi-zeen)
Why do we use levodropropizine?