Xylometazoline apteo med

Poland
Brand name Xylometazoline apteo med
Form drops, nasal solution
Active substance / Dosage
Prescription type Over-the-counter
ATC code
Registration number 100400245
Xylometazoline apteo med drops, nasal solution

Package leaflet: Information for the patient

Xylometazolin APTEO MED
1 mg/ml, nasal drops, solution
Xylometazolini hydrochloridum
Please read the entire leaflet carefully before use, as it contains
important information for the patient.
This medicine should always be used exactly as described in this patient leaflet or as directed by
the doctor or pharmacist.

  • Keep this leaflet, so that you can read it again if necessary.
  • If you need advice or further information, please contact your pharmacist.
  • If you experience any adverse reactions, including any possible adverse reactions not listed in this leaflet, inform your doctor or pharmacist. See section 4.
  • If there is no improvement after 7 days of treatment, or if symptoms worsen, consult your doctor.

Table of contents of the leaflet:

  1. What Xylometazolin APTEO MED is and what it is used for
  2. Important information before using Xylometazolin APTEO MED
  3. How to use Xylometazolin APTEO MED
  4. Possible side effects
  5. How to store Xylometazolin APTEO MED
  6. Contents of the pack and other information

1. What Xylometazolin APTEO MED is and what it is used for

The active substance in Xylometazolin APTEO MED is xylometazoline hydrochloride.
Xylometazolin APTEO MED is a locally acting medicine that reduces nasal mucosal congestion and swelling, as well as nasal discharge, by constricting blood vessels.
It helps patients with a stuffy nose to breathe more easily through the nose.
The effect of Xylometazolin APTEO MED begins within 2 minutes after administration and lasts up to 10 hours.
Xylometazolin APTEO MED is indicated for use in adults and adolescents over 12 years of age.
Indications
Excessive nasal mucosal congestion occurring during colds, hay fever, allergic rhinitis, and sinusitis. The medicine facilitates drainage of secretions from inflamed paranasal sinuses. By reducing congestion of the nasopharyngeal mucosa, it may be used as supportive treatment in acute otitis media. Xylometazolin APTEO MED facilitates nasal speculum examination (examination of the nasal cavity).

2. Information before using Xylometazolin APTEO MED

When not to use Xylometazolin APTEO MED:

  • if the patient is allergic to xylometazoline hydrochloride or any of the other ingredients of this medicine (listed in section 6),
  • if the patient has undergone surgery performed through the nose, e.g. removal of the pituitary gland or surgery involving exposure of the dura mater (brain surgery performed through the nose or mouth),
  • if the patient has narrow-angle glaucoma (increased pressure in the eye),
  • if the patient has very dry nasal mucosa (atrophic rhinitis or drying inflammation of the nasal mucosa).

Warnings and precautions
Before using Xylometazolin APTEO MED, consult a doctor in case of:

  • high blood pressure,
  • heart disease (e.g. long QT syndrome),
  • hyperthyroidism,
  • diabetes,
  • benign prostatic hyperplasia,
  • a benign adrenal gland tumour producing large amounts of adrenaline and noradrenaline (pheochromocytoma),
  • taking certain antidepressant medicines known as monoamine oxidase inhibitors (MAOIs) or having taken them within the last 2 weeks,
  • hypersensitivity to substances with effects similar to xylometazoline. In sensitive patients, Xylometazolin APTEO MED may cause insomnia, dizziness, irregular heartbeat, high blood pressure or tremor.

Do not use Xylometazolin APTEO MED for longer than 7 consecutive days. If symptoms persist, consult a doctor.
Using the medicine for longer than 7 days or in doses higher than recommended may worsen or cause recurrence of symptoms, or lead to atrophy of the nasal mucosa.
Do not use Xylometazolin APTEO MED in the eyes or in the mouth.
Do not exceed the recommended dose.

Children and adolescents
Xylometazolin APTEO MED must not be used in children under 12 years of age.

Xylometazolin APTEO MED with other medicines
Tell your doctor or pharmacist about all medicines the patient is currently taking or has recently taken, as well as any medicines the patient plans to take.
Do not use Xylometazolin APTEO MED if taking certain medicines used to treat depression. These are:

  • monoamine oxidase inhibitors (MAOIs): DO NOT use Xylometazolin APTEO MED if taking MAOIs simultaneously or if such medicines have been taken within the last 14 days,
  • tricyclic and tetracyclic antidepressants.

If taking any of the above medicines, consult a doctor before using Xylometazolin APTEO MED.

Pregnancy and breastfeeding
If the patient is pregnant or breastfeeding, suspects she may be pregnant, or is planning to have a child, she should consult a doctor or pharmacist before using this medicine.
Do not use Xylometazolin APTEO MED during pregnancy.
During breastfeeding, Xylometazolin APTEO MED may be used only after consultation with a doctor.

Driving and operating machinery
Xylometazolin APTEO MED, when used at recommended doses, has no effect or has negligible effect on the ability to drive vehicles or operate machinery.

Xylometazolin APTEO MED contains benzalkonium chloride, which may cause irritation of mucous membranes.

3. How to use Xylometazolin APTEO MED

This medicine should always be used exactly as described in this patient leaflet or as directed by
your doctor. If in doubt, consult your doctor or pharmacist.
Xylometazolin APTEO MED should be used for the nose only (including in cases of middle ear
infection).
To avoid spreading infection, the medicine container should be used by only one patient.

Adults and adolescents over 12 years of age:
2 to 4 drops of Xylometazolin APTEO MED solution into each nostril three times daily.
Do not use more than 3 doses per nostril per day.
It is recommended that the last dose be taken immediately before bedtime.
Xylometazolin APTEO MED should not be used for longer than 7 consecutive days.
Xylometazolin APTEO MED should not be used in children under 12 years of age.

Instructions for use

  1. Clear the nose.
  2. Unscrew the cap containing the dropper.
  3. Tilt the head backward.
  4. Instill drops into both nostrils and keep the head tilted for a while to allow the drops to spread throughout the nasal cavity.
Schematic line drawing showing a person's facial profile, with hands gently supporting the head while another hand holds an applicator at the nose
  1. After using the medicine, carefully wipe the dropper tip with a clean paper tissue and then replace the cap on the bottle.

Overdose of Xylometazolin APTEO MED
If more than the recommended dose has been used, seek immediate advice from a doctor or
pharmacist.
Symptoms of overdose include severe dizziness, excessive sweating, significantly lowered body
temperature, headache, slow heart rate, breathing difficulties, coma, convulsions, high blood
pressure (hypertension), which may be followed by low blood pressure.
Symptomatic treatment should be administered.

Missed dose of Xylometazolin APTEO MED
Do not use a double dose to make up for a missed dose.
If you have any further questions about the use of this medicine, consult your doctor or pharmacist.

4. Possible adverse reactions

Like all medicines, this product may cause adverse reactions, although not everyone experiences them.
You should DISCONTINUE using Xylometazolin Apteo Med and immediately consult a doctor if any of the following adverse symptoms occur, as they may indicate an allergic reaction:

  • difficulty breathing or swallowing,
  • swelling of the face, lips, tongue or throat,
  • itching with red rash or blisters.
    These symptoms are very rare (occurring in fewer than 1 in 10,000 people using the medicine).

Common adverse reactions (occur in 1 to 10 out of 100 patients):
nasal mucosa dryness or irritation, nausea, headache, burning sensation at the site of administration.

Uncommon adverse reactions (occur in 1 to 10 out of 1,000 patients):
nosebleed

Very rare adverse reactions (occur in fewer than 1 in 10,000 patients):
allergic reaction (skin rash, itching), transient visual disturbances, arrhythmia or increased heart rate.

Reporting of adverse reactions
If any adverse reactions occur, including any not listed in this leaflet, inform your doctor, pharmacist or nurse.
Adverse reactions can be reported directly to the Department of Monitoring Adverse Drug Reactions, Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, phone: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl.
Adverse reactions can also be reported to the responsible entity.
Reporting adverse reactions helps to provide more information on the safety of the medicine.

5. How to store Xylometazolin APTEO MED

Keep this medicine out of sight and reach of children.
Store below 25 °C.
Do not use this medicine after the expiry date stated on the carton and bottle after "EXP". The expiry date refers to the last day of the stated month.
The abbreviation "LOT" on the packaging indicates the batch number.
Discard the bottle 4 weeks after first opening, even if some solution remains.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer in use. This will help protect the environment.

6. Contents of the pack and other information

What Xylometazolin APTEO MED contains

  • The active substance in Xylometazolin APTEO MED is xylometazoline hydrochloride. One ml of solution contains 1 mg of xylometazoline hydrochloride, corresponding to 0.024–0.032 mg of xylometazoline hydrochloride per drop of solution (0.028 ± 15%).
  • The other ingredients of the medicine are: sodium chloride, benzalkonium chloride solution, disodium phosphate dihydrate, potassium dihydrogen phosphate, purified water.

What Xylometazolin APTEO MED looks like and contents of the pack
Xylometazolin APTEO MED is a nasal drop solution, a colourless, transparent liquid.
The medicine is packaged in an LDPE bottle with an LDPE dropper and an HDPE screw cap with a tamper-evident seal, containing 10 ml of solution, in a cardboard carton.
Marketing Authorisation Holder and Manufacturer:
Marketing Authorisation Holder:
Synoptis Pharma Sp. z o.o.
ul. Krakowiaków 65
02-255 Warsaw
tel. 22 321 62 40
Manufacturer:
Jadran-Galenski laboratorij d.d.
Svilno 20
51000 Rijeka
Croatia