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ALLERGOZOL-DF

nasal spray 0.06%, 0.03%, 10 ml

Dispensing conditions: NO PRESCRIPTION 

Category: Nasal preparations

THERAPEUTIC INDICATIONS:

  • acute rhinitis;

  • allergic rhinosinusitis;

  • allergic vasomotor rhinitis;

  • hyperemia and swelling of mucous membranes of the upper respiratory tract after surgery;

  • facilitation of rhinoscopy..

dwldDownload instructions for use

Composition

10 ml of the product contains 0,03% 0,06%
active substances:    
- naphazoline nitrate 3,0 mg 6,0 mg
- diphenhydramine hydrochloride 5,0 mg 10,0 mg
excipients: boric acid, water for injection

Pharmaceutical form

Nasal spray, 0.03% and 0.06%, 10 ml

Pharmacotherapeutic group

Respiratory system. Nasal preparations. Decongestants and other topical medications. Sympathomimetics, combinations, excluding corticosteroids. Naphazoline.

ATC code  R01АВ02

Indications

  • acute rhinitis;
  • allergic rhinosinusitis;
  • allergic vasomotor rhinitis;
  • hyperemia and swelling of mucous membranes of the upper respiratory tract after surgery;
  • facilitation of rhinoscopy.

Contraindications

  • hypersensitivity to the components of the product;
  • closed angle glaucoma;
  • severe eye diseases;
  • arterial hypertension, tachycardia, pronounced atherosclerosis;
  • hyperthyroidism;
  • diabetes mellitus;
  • chronic rhinitis;
  • hypertrophy of the prostate gland;
  • concomitant use of monoamine oxidase inhibitors and a period of up to 14 days after the end of their use%
  • children under 2 years of age (for Allergozol-DF 0.03%);
  • children under 15 years of age (for Allergozol-DF 0.06%).

Precautions for use:

  • The product has a resorptive effect, so it should be used for a short time - no more than 1 week, then take a break for a few days.

Drug interactions:

Concomitant use with tricyclic antidepressants may increase the vasoconstrictor effect of naphazoline. Concomitant use of naphazoline with monoamine oxidase inhibitors and for 14 days after its withdrawal may lead to a hypertensive crisis.

The product slows down absorption of local anesthetic agents (prolongs their effect during surface anesthesia).

Posology and method of administration

Intranasally.

0.06% spray for adults and adolescents over 15 years of age:

  • 1 injection into each nasal passage 3 times a day.

0.03% spray for children:

  • 2 to 6 years of age - 1 injection into each nasal passage 1-2 times a day;
  • 6 to 15 years of age - 1 injection into each nasal passage 3 times a day.

The course of treatment is not more than 1 week.

Adverse reactions

Rare:

  • if used for more than 1 week - edema of the mucous membranes, atrophic rhinitis.

Very rare:

  • nausea, headache;
  • increased blood pressure, tachycardia;
  • irritation of the nasal mucosa;
  • reactive hyperemia of the nasal mucosa - dry mouth.

Overdose

Symptoms: decreased body temperature, bradycardia, arterial hypertension, dry mouth, difficulty in breathing, agitation, confusion.

Treatment: withdrawal of the product, symptomatic treatment.

Use during pregnancy or breastfeeding

Use of the product during pregnancy and lactation is possible only when the estimated benefit to the mother exceeds the potential risk to the child and fetus.

Pediatric population

Approved for children over 2 years of age.

Special warnings

The product has a resorptive effect, so it should be used for a short time - no more than 1 week, then take a break for a few days.

Presentation and package

10 ml of the product in polypropylene bottles with a spray lid and a protective cap. One bottle is with instruction for use in Kazakh and Russian language are placed in a carton pack.

Storage conditions

Store in a place protected from light, at a temperature below 25°С.

Keep out of the reach of children.

Shelf life

3 years

Manufacturer

"DOSFARM" LLP, 3 Chaplygin street, Almaty city, 050034, Kazakhstan, tel.: (727) 253-03-88.

Marketing authorization holder

"DOSFARM" LLP, 3 Chaplygin street, Almaty city, 050034, Kazakhstan.

Name, address, contact information of the organization accepting claims (proposals) against quality of products from consumers in the territory of the Republic of Kazakhstan, which is responsible for post-authorization safety surveillance of the medicine:

"DOSFARM" LLP, 3 Chaplygin street, Almaty city, 050034, Kazakhstan,

Tel./Fax: (727) 253-07-07, 253-03-88, e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

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