Brompheniramine, Pseudoephedrine, Dextromethorphan

Prescription

Handelsnamen: Brompheniramine, Pseudoephedrine, Dextromethorphan

Darreichungsform

Liquid/Solution

Applikationsweg

ORAL

Hersteller

Ascend Laboratories, LLC

About This Medication

DESCRIPTION Brompheniramine maleate, pseudoephedrine hydrochloride and dextromethorphan hydrobromide syrup is a clear, light pink syrup with a butterscotch flavor. Each 5 mL (1 teaspoonful) contains: Brompheniramine Maleate, USP ----------------- 2 mg Pseudoephedrine Hydrochloride, USP -------- 30 mg Dextromethorphan Hydrobromide, USP ------ 10 mg Alcohol ------------------------------------------- 0.95% v/v In a palatable, aromatic vehicle. Inactive Ingredients: dehydrated ethanol, glycerin, sucrose, citric acid anhydrous, spectracol dual FD&C Red No 40, artificial butterscotch flavour, methylparaben, sodium benzoate, propylene glycol, sodium citrate anhydrous and purified water. It may contain 10% sodium citrate solution for pH adjustment. The pH range is between 3.0 and 6.0. Antihistamine/Nasal Decongestant/Antitussive syrup for oral administration. bpd-01.jpg bpd-02.jpg bpd-03

Wirkstoffe

Wirkstoff	Stärke
Brompheniramine Maleate	-
Dextromethorphan Hydrobromide	-
Pseudoephedrine Hydrochloride	-

Indikationen und Anwendung

INDICATIONS & USAGE For relief of coughs and upper respiratory symptoms, including nasal congestion, associated with allergy or the common cold.

Dosierung und Verabreichung

DOSAGE & ADMINISTRATION Adults and pediatric patients 12 years of age and over: 10 mL (2 teaspoonfuls) every 4 hours. Children 6 to under 12 years of age: 5 mL (1 teaspoonful) every 4 hours. Children 2 to under 6 years of age: 2.5 mL (½ teaspoonful) every 4 hours. Infants 6 months to under 2 years of age: Dosage to be established by a physician. Do not exceed 6 doses during a 24-hour period.

Side Effects Overview

ADVERSE REACTIONS The most frequent adverse reactions to brompheniramine maleate, pseudoephedrine hydrochloride and dextromethorphan hydrobromide syrup are: sedation; dryness of mouth, nose and throat; thickening of bronchial secretions; dizziness. Other adverse reactions may include: Dermatologic: Urticaria, drug rash, photosensitivity, pruritus. Cardiovascular System: Hypotension, hypertension, cardiac arrhythmias, palpitation. CNS: Disturbed coordination, tremor, irritability, insomnia, visual disturbances, weakness, nervousness, convulsions, headache, euphoria, and dysphoria. G.U. System : Urinary frequency, difficult urination. G.I. System : Epigastric discomfort, anorexia, nausea, vomiting, diarrhea, constipation. Respiratory System: Tightness of chest and wheezing, shortness of breath. Hematologic System: Hemolytic anemia, thrombocytopenia, agranulocytosis.

Warnhinweise und Vorsichtsmaßnahmen

WARNINGS Especially in infants and small children, antihistamines in overdosage may cause hallucinations, convulsions, and death. Antihistamines may diminish mental alertness. In the young child, they may produce excitation.

Kontraindikationen

CONTRAINDICATIONS Hypersensitivity to any of the ingredients. Do not use in the newborn, in premature infants, in nursing mothers, or in patients with severe hypertension or severe coronary artery disease. Do not use dextromethorphan in patients receiving monoamine oxidase (MAOI) inhibitors (see PRECAUTIONS - Drug Interactions ). Antihistamines should not be used to treat lower respiratory tract conditions including asthma.

Frequently Asked Questions

INDICATIONS & USAGE For relief of coughs and upper respiratory symptoms, including nasal congestion, associated with allergy or the common cold.

DOSAGE & ADMINISTRATION Adults and pediatric patients 12 years of age and over: 10 mL (2 teaspoonfuls) every 4 hours. Children 6 to under 12 years of age: 5 mL (1 teaspoonful) every 4 hours. Children 2 to under 6 years of age: 2.5 mL (½ teaspoonful) every 4 hours. Infants 6 months to under 2 years of age: Dosage to be established by a physician. Do not exceed 6 doses during a 24-hour period.

WARNINGS Especially in infants and small children, antihistamines in overdosage may cause hallucinations, convulsions, and death. Antihistamines may diminish mental alertness. In the young child, they may produce excitation.

CONTRAINDICATIONS Hypersensitivity to any of the ingredients. Do not use in the newborn, in premature infants, in nursing mothers, or in patients with severe hypertension or severe coronary artery disease. Do not use dextromethorphan in patients receiving monoamine oxidase (MAOI) inhibitors (see PRECAUTIONS - Drug Interactions ). Antihistamines should not be used to treat lower respiratory tract conditions including asthma.

Brompheniramine, Pseudoephedrine, Dextromethorphan is a prescription medication. You will need a valid prescription from a licensed healthcare provider.

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References & Data Sources

• DailyMed — Brompheniramine, Pseudoephedrine, Dextromethorphan drug label (National Library of Medicine)
• openFDA — Brompheniramine, Pseudoephedrine, Dextromethorphan label data (U.S. Food & Drug Administration)
• RxNorm — RXCUI 1357010 (NLM Normalized Drug Names)
• NDC Directory — Brompheniramine, Pseudoephedrine, Dextromethorphan (FDA National Drug Code)

Medizinischer Haftungsausschluss

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Datenquellen: DailyMed (NLM), openFDA, MFDS