NANSTAR 500

NANSTAR 500

COMPOSITION
Each capsule contains :
Tetracycline hydrochloride : …………………………………………………….500 mg
Excipients : q.s…………………………………………………………………One capsule
THERAPEUTIC PROPERTIES :
Antibiotique de la classe cycline.
INDICATIONS
Elles sont indiquées dans les maladies suivantes :
– Respiratoires
– Génito-urinaire
– Indication particulière : Acné
CONTRAINDICATIONS
Ce médicament ne doit pas être utilisé dans les cas suivants :
– Allergie aux antibiotiques de la famille des tétracyclines.
– L’emploi de ce médicament doit être évité chez l’enfant de moins de
8 ans en raison du risque de coloration permanente des dents et
hypoplasie de l’émail dentaire.
– GROSSESSE ET ALLAITEMENT : Risque d’anormalie de bourgeon
dentaire ou de dyschromie dentaire chez l’enfant.
IN CASE OF DOUBT, IT IS ESSENTIAL TO SEEK
THE ADVICE OF DOCTOR OR PHARMACIST.
WARNING AND PRECAUTION
-In case of hepatic or renal insufficiency.
Overdose may lead to a risk of hepatotoxicity.
-Due to the risk of photosensitivity, it is advised to avoid
direct exposure to the sun and UV rays during treatment
(which may cause skin manifestations such as erythema).
SIDE EFFECTS
-Dental discoloration or enamel hypoplasia when
administered to children under 8 years old.
-Digestive disorders: diarrhea, nausea, epigastric
discomfort.
-Allergic reactions: urticaria, rash, pruritus.
-Photosensitivity reaction.
DOSAGE
Voie orale
Adult: The usual dosage is 1.5 to 2g per day, to be
taken on an empty stomach, in 2 to 4 evenly spaced
doses.
Treatment of acne: a gradually decreasing
dosage, starting from 750mg to 1g/day, down to
250mg/day.
Children older than 8 years: 50mg/kg/24 hours in 2 to 4 doses.
CONSERVATION
-Store at a temperature below 30°C, away from light and humidity.
-Keep out of the reach and sight of children.
-Do not use after the expiration date on the box.