NOVO-BENZYDAMINE SOLUTION

País: Canadá

Idioma: inglés

Fuente: Health Canada

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Ficha técnica Ficha técnica (SPC)
20-06-2008

Ingredientes activos:

BENZYDAMINE HYDROCHLORIDE

Disponible desde:

NOVOPHARM LIMITED

Código ATC:

A01AD02

Designación común internacional (DCI):

BENZYDAMINE

Dosis:

1.5MG

formulario farmacéutico:

SOLUTION

Composición:

BENZYDAMINE HYDROCHLORIDE 1.5MG

Vía de administración:

BUCCAL

Unidades en paquete:

100ML/250ML

tipo de receta:

Prescription

Área terapéutica:

NONSTEROIDAL ANTI-INFLAMMATORY AGENTS

Resumen del producto:

Active ingredient group (AIG) number: 0113801001; AHFS:

Estado de Autorización:

CANCELLED POST MARKET

Fecha de autorización:

2018-05-17

Ficha técnica

                                1
PRODUCT MONOGRAPH
Pr
NOVO-BENZYDAMINE
(Benzydamine Hydrochloride Oral Rinse 0.15% w/v)
Local Analgesic
Novopharm Limited
30 Novopharm Court
Toronto, Ontario
M1B 2K9
Submission Control No: 121722
Date of Preparation:
May 14, 2008
2
PRODUCT MONOGRAPH
PR
NOVO-BENZYDAMINE
(Benzydamine Hydrochloride Oral Rinse 0.15% w/v)
THERAPEUTIC CLASSIFICATION
Local Analgesic
ACTIONS AND CLINICAL PHARMACOLOGY
Animal studies using parenteral route have shown that benzydamine
hydrochloride
possesses properties of an analgesic/anti-inflammatory agent. This
effect is not mediated
through the pituitary-adrenal axis. Studies using the topical route
have demonstrated local
anesthetic properties of benzydamine hydrochloride. In controlled
studies in humans with
oro-pharyngeal mucosity due to radiation therapy, benzydamine
hydrochloride oral rinse
use has provided relief through reduction of pain and edema. Similar
studies in patients
with acute sore throat demonstrated relief from pain.
Benzydamine hydrochloride has been detected in blood and urine after
gargling four
times for 20 2seconds, in rapid succession, each time with a volume
equivalent to 25.5
mg benzydamine per 70 kg body weight (approximately 17 mL per gargle).
The average
maximum plasma level of 59 ng/mL (range 17 to 173) was obtained 2
hours after
gargling. For comparison, one dose of 17 mL, when swallowed, yielded
an average
maximum plasma level of 180 ng/ mL (range 102 to 324), also at 2 hours
after ingestion.
Benzydamine was still detectable 24 hours later in 7 out of 10
subjects after the gargling
(average plasma level of 7 ng/mL) and in 9 out of 10 subjects after
the ingestion (average
32 ng/mL).
The urinary excretion was completed within 3-4 days after the single
dose in both groups;
about 46% of the dose was recovered in garglers, about 26% in
ingestors. Repeated
administration for 7 days did not result in a significant accumulation
of benzydamine
hydrochloride in plasma.
INDICATIONS AND CLINICAL USE
NOVO-BENZYDAMINE (benzydamine hydrochloride) Oral Rinse is indicat
                                
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Ficha técnica Ficha técnica francés 14-05-2008

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