-28%

Zaditen SRO 2mg (Ketotifen Fumarate)

$39 $28

Pack30 tabs (2mg/tab)
Active Ingredient: Ketotifen Fumarate
Manufacturer: Novartis

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Description

Zaditen SRO 2 mg: general information

This treatment is recommended in the treatment of the symptoms of rhinoconjunctivitis allergic.

Zaditen SRO 2 mg: dosage

Reserved for adults and children over 6 years old.

Adult and child over 6 years old:

One tablet of Zaditen SRO 2 mg daily, preferably in the evening, at mealtimes.

The compressed form is not suitable for children under 6 years of age because of the risk of a wrong road.

In the child of 4 to 6 years the form oral solution is preferable.

IN ALL CASES, COMPLY STRICTLY WITH THE ORDER OF YOUR DOCTOR.

Method and route of administration
Oral way.

Duration of treatment
Comply with your doctor’s prescription.

Contraindications for Zaditen SRO 2 mg

Do not take ZADITEN SRO 2 mg prolonged-release film-coated tablets in the following circumstances:

  • have a history of allergy to any of the components of this medication.

IN CASE OF DOUBT, IT IS ESSENTIAL TO ASK THE ADVICE OF YOUR DOCTOR OR PHARMACIST.

Precautions for use of Zaditen SRO 2 mg

Warnings

Taking this medicine with alcohol or drugs containing alcohol is to be avoided.

Due to the presence of lactose, this drug is not recommended for galactosemia, glucose-galactose malabsorption syndrome or lactase deficiency (rare metabolic diseases).

IN CASE OF DOUBT, IT IS ESSENTIAL TO ASK THE ADVICE OF YOUR DOCTOR OR PHARMACIST.

Precautions for use

IF IN DOUBT, DO NOT HESITATE TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.

Known side effects of Zaditen SRO 2 mg

Like all medicines, ZADITEN SRO 2 mg Extended-Release Tablet may cause side effects, although not everybody gets them.

  • At the beginning of treatment, possibility of drowsiness, dryness of the mouth, feelings of vertigo, digestive disorders such as nausea, appetite disturbance, gastralgia, constipation. These side effects usually disappear with continued treatment.
  • Rarely have been described especially in children, nervousness, irritability, excitement and insomnia. Nevertheless these signs can also be related to the disease in question, ask the advice of your doctor.
  • Very rarely have been reported, especially in children, convulsions.
  • Rarely possibility of occurrence of skin reactions. If skin or mouth lesions appear (swelling, redness or vesicles) stop treatment and contact your doctor.
  • Very rarely has a slight increase in mammary glands been reported as a result of treatment without a clear direct relationship with taking the product. If this type of effect occurs, seek the advice of your doctor.
  • Very rarely have been described hepatitis.

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

Keep out of the reach and sight of children.

Interactions of Zaditen SRO 2 mg with other medicines

Taking alcoholic beverages or drugs containing alcohol during treatment is not recommended.

TO AVOID POSSIBLE INTERACTIONS BETWEEN SEVERAL MEDICINES, ALWAYS HAVE ANY OTHER CURRENT TREATMENT TO YOUR DOCTOR OR PHARMACIST, especially certain tranquilizing medications, antidepressants acting on the nervous system and atropine-based medicines.

Use of Zaditen SRO 2 mg during pregnancy and lactation

Pregnancy

It is best not to use this medicine during pregnancy.

If you discover that you are pregnant, consult your doctor because only he can judge the need to continue the treatment.

Brestfeeding

In the absence of data on passage into breast milk, treatment is not recommended during breastfeeding.

Ask your doctor or pharmacist for advice before taking any medicine.

Effects of Zaditen SRO 2 mg on the driving and use of cars

The attention of vehicle drivers and machine users is drawn to the risks of drowsiness associated with the use of this medication.

Zaditen SRO 2 mg: composition

Active substance

Ketotifen Fumarate: 2.75 mg

Quantity corresponding to Ketotifen base: 2.00 mg

For a film-coated tablet.

Other components

Anhydrous colloidal silica, magnesium stearate, ethylcellulose, povidone, corn starch, glycerol palmitostearate, lactose, macrogol 6000, talc, hypromellose, yellow iron oxide, anhydrous colloidal silica, titanium dioxide.

Components with known effect of Zaditen SRO 2 mg

lactose.

What should you do if you forget to take Zaditen SRO 2 mg?

Take the next dose at the usual time regardless of the missed dose.

What to do in case of overdose of Zaditen SRO 2 mg?

See a doctor.

Storage conditions

Store at a temperature not exceeding 25 ° C.

Expiry date of Zaditen SRO 2 mg

Do not use ZADITEN SRO 2 mg prolonged-release film-coated tablets after the expiry date which is stated on the carton.

Laboratory (s) owner (s), manufacturer (s) or operator (s) of Zaditen SRO 2 mg

Holder

DEFIANTE FARMACEUTICA SA

RUA DOS FERREIROS, 260

9000-082 FUNCHAL

PORTUGAL
exploiting

SIGMA TAU France

Building B says “Zeneo”

14, boulevard des Freres Voisin

92130 ISSY LES MOULINEAUX
Maker

NOVARTIS PHARMA SPA

VIA PROVINCIALE SCHITO, 131

80058 TORRE ANNUNZIA TA (NA)

ITALY

or

MIPHARM SPA

VIA BERNARDO QUARANTA 12

20141 MILANO (MI)

ITALY

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