Sanorin 0.1% 10 ml emuls.naz.
- $6.10
The instruction
for medical use
of SANORIN medicine
the Trade name
Sanorin
the International unlicensed
name Naphazoline Dosage Form
of the Drop nasal (emulsion) of 0.1%
Structure
of 10 ml of an emulsion contain
active agent: naphazoline of nitrate of 0.01 g
excipients: boric acid, methylparahydroxybenzoate, cetyl alcohol, eucalyptus oil, polysorbate 80, cholesterol, liquid paraffin, ethylene diamine, the water purified.
The description
the White, easily stirred up emulsion
Pharmacotherapeutic group
Drugs for treatment of diseases of a nose. Sympathomimetics.
The code of automatic telephone exchange R01AA08
the Pharmacological
Pharmacokinetics Data properties about distribution, metabolism and elimination of naphazoline are not known. At topical administration the vasoconstrictive effect occurs in 5-10 minutes and proceeds from 4 to 6 hours. It is absorbed in a system blood stream and can have systemic action.
The pharmacodynamics
Sanorin contains the naphazoline which is a sympathomimetic with direct promoting effect on alpha 2адренорецепторы. Owing to sosudosuzhivayushchegosya actions puffiness, hyperaemia, exudation decreases. At instranazalny use promotes opening and expansion of output channels of adnexal bosoms of a nose and release of Eustachian tubes. It promotes outflow of a secret and prevents sedimentation of bacteria.
Indications
- acute rhinitis
- sinusitis
- an eustachitis
- laryngitis
- for simplification of carrying out a rinoskopiya
- need of a stop of nasal bleeding
the Route of administration and
Intranazalno's doses: 2-3 times a day on 1-3 drops of an emulsion in each nasal course. Between receptions the interval has to be not less than 4 hours.
Drug is used limited time, no more than 5 days. If nasal breath is facilitated, then use can be finished earlier.
Repeated use of drug is possible only in several days.
About 3-4 drops of drug in each nasal course are applied to simplification of carrying out a rinoskopiya with the diagnostic purpose.
In nasal bleeding to place the cotton plug moistened with drug in the nasal course.
Side effects
At use in the recommended doses drug usually well is transferred.
Appearance of a headache, tachycardia, increase in blood pressure, feeling of dryness and burning mucous a nose is in rare instances possible
At prolonged and frequent use, more than 1 week is at adults, accustoming which is shown by disturbance of passability of the nasal courses and dryness mucous at once after burying is possible.
Contraindications
- hypersensitivity to drug components
- an arterial hypertension, tachycardia, the profound atherosclerosis
- a serious illness of eyes
- a hyper thyroidism
- diabetes
- closed-angle glaucoma
- chronic rhinitis (atrophic type)
- children's age up to 15 years
Medicinal interactions
it is not necessary to use Drug along with MAO inhibitors or earlier, than in 14 days after the end of their use as there can be a disturbance of a warm rhythm and increase in blood pressure.
Special instructions
Patients who accept high doses of drug have to be under observation, in connection with possible emergence of cardiovascular and neurologic by-effects (hypertensia, arrhythmia, heartbeat, headaches, dizziness, drowsiness or insomnia).
Pregnancy and the period of a lactation
Are not present enough data on use of drug for pregnant women and the nursing women therefore it should be applied with care and only when the expected advantage of its use exceeds potential risk.
Features of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms.
Sanorin does not affect control of vehicles and activity which demands the increased concentration of attention.
Overdose
Symptoms: irritability, the increased perspiration, weakness, tachycardia, increase in blood pressure. Further emergence of drowsiness, decrease in body temperature, bradycardia is possible.
Treatment: symptomatic. Specific antidote is absent.
A form of release and packing
On 10 ml in bottles of orange glass with a dropper.
On 1 bottle together with the instruction for medical use in the state and Russian languages place in a cardboard box.
To Store storage conditions in original packing, at a temperature not above 25ºС.
To store out of children's reach!
4 years
not to apply a period of storage after an expiration date.
Prescription status
Without prescription
Tev's Producer the Czech Enterprises of neuter of the lake,
Ostravsk 29747 70 Opava Mosquitoes,
the Czech Republic
the Name and the country of the owner of the registration certificate
Tev the Czech Enterprises of neuter of the lake, the Czech Republic
the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products (goods): Representative office Teva Chesh Indastriyez of neuter of the lake in PK050000 Republic of Kazakhstan Almaty, Al-Farabi Avenue 13, Biness Nurla Tau's center 1v office 305, 306 Phone number, fax (727) 311-10-66, 311-10-68 E-mail of teva@teva.co.il
for medical use
of SANORIN medicine
the Trade name
Sanorin
the International unlicensed
name Naphazoline Dosage Form
of the Drop nasal (emulsion) of 0.1%
Structure
of 10 ml of an emulsion contain
active agent: naphazoline of nitrate of 0.01 g
excipients: boric acid, methylparahydroxybenzoate, cetyl alcohol, eucalyptus oil, polysorbate 80, cholesterol, liquid paraffin, ethylene diamine, the water purified.
The description
the White, easily stirred up emulsion
Pharmacotherapeutic group
Drugs for treatment of diseases of a nose. Sympathomimetics.
The code of automatic telephone exchange R01AA08
the Pharmacological
Pharmacokinetics Data properties about distribution, metabolism and elimination of naphazoline are not known. At topical administration the vasoconstrictive effect occurs in 5-10 minutes and proceeds from 4 to 6 hours. It is absorbed in a system blood stream and can have systemic action.
The pharmacodynamics
Sanorin contains the naphazoline which is a sympathomimetic with direct promoting effect on alpha 2адренорецепторы. Owing to sosudosuzhivayushchegosya actions puffiness, hyperaemia, exudation decreases. At instranazalny use promotes opening and expansion of output channels of adnexal bosoms of a nose and release of Eustachian tubes. It promotes outflow of a secret and prevents sedimentation of bacteria.
Indications
- acute rhinitis
- sinusitis
- an eustachitis
- laryngitis
- for simplification of carrying out a rinoskopiya
- need of a stop of nasal bleeding
the Route of administration and
Intranazalno's doses: 2-3 times a day on 1-3 drops of an emulsion in each nasal course. Between receptions the interval has to be not less than 4 hours.
Drug is used limited time, no more than 5 days. If nasal breath is facilitated, then use can be finished earlier.
Repeated use of drug is possible only in several days.
About 3-4 drops of drug in each nasal course are applied to simplification of carrying out a rinoskopiya with the diagnostic purpose.
In nasal bleeding to place the cotton plug moistened with drug in the nasal course.
Side effects
At use in the recommended doses drug usually well is transferred.
Appearance of a headache, tachycardia, increase in blood pressure, feeling of dryness and burning mucous a nose is in rare instances possible
At prolonged and frequent use, more than 1 week is at adults, accustoming which is shown by disturbance of passability of the nasal courses and dryness mucous at once after burying is possible.
Contraindications
- hypersensitivity to drug components
- an arterial hypertension, tachycardia, the profound atherosclerosis
- a serious illness of eyes
- a hyper thyroidism
- diabetes
- closed-angle glaucoma
- chronic rhinitis (atrophic type)
- children's age up to 15 years
Medicinal interactions
it is not necessary to use Drug along with MAO inhibitors or earlier, than in 14 days after the end of their use as there can be a disturbance of a warm rhythm and increase in blood pressure.
Special instructions
Patients who accept high doses of drug have to be under observation, in connection with possible emergence of cardiovascular and neurologic by-effects (hypertensia, arrhythmia, heartbeat, headaches, dizziness, drowsiness or insomnia).
Pregnancy and the period of a lactation
Are not present enough data on use of drug for pregnant women and the nursing women therefore it should be applied with care and only when the expected advantage of its use exceeds potential risk.
Features of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms.
Sanorin does not affect control of vehicles and activity which demands the increased concentration of attention.
Overdose
Symptoms: irritability, the increased perspiration, weakness, tachycardia, increase in blood pressure. Further emergence of drowsiness, decrease in body temperature, bradycardia is possible.
Treatment: symptomatic. Specific antidote is absent.
A form of release and packing
On 10 ml in bottles of orange glass with a dropper.
On 1 bottle together with the instruction for medical use in the state and Russian languages place in a cardboard box.
To Store storage conditions in original packing, at a temperature not above 25ºС.
To store out of children's reach!
4 years
not to apply a period of storage after an expiration date.
Prescription status
Without prescription
Tev's Producer the Czech Enterprises of neuter of the lake,
Ostravsk 29747 70 Opava Mosquitoes,
the Czech Republic
the Name and the country of the owner of the registration certificate
Tev the Czech Enterprises of neuter of the lake, the Czech Republic
the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products (goods): Representative office Teva Chesh Indastriyez of neuter of the lake in PK050000 Republic of Kazakhstan Almaty, Al-Farabi Avenue 13, Biness Nurla Tau's center 1v office 305, 306 Phone number, fax (727) 311-10-66, 311-10-68 E-mail of teva@teva.co.il
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