Nauseamine

Nauseamine^®

COMPOSITION :
Each tablet contains :
– Diphenhydramine HCl……………………….50 mg
– Excipients : q.s. …………………..…….One tablet
THERAPEUTIC PROPERTIES :
 H1 antihistamine
 Antiemetic
INDICATIONS :
Prevention and treatment of motion sickness.

CONTRAINDICATIONS :

 Hypersensitivity to antihistamines.
 Children under 2 years old.
 Due to anticholinergic properties:

Risk of angle-closure glaucoma.
Risk of urinary retention related to uroprostatic disorders.

EN CAS DE DOUTE , IL EST INDISPENSABLE DE DEMANDER

L’AVIS DE VOTRE MÉDECIN OU DE VOTRE PHARMACIEN.

WARNING AND PRECAUTION :

In children under 6 years of age, due to the risk of choking associated with the pharmaceutical form, the tablets should be crushed before administration.
Breastfeeding women (see Pregnancy/Breastfeeding).
In cases of severe hepatic and/or renal insufficiency, due to the risk of accumulation.

The consumption of alcoholic beverages and medications containing alcohol during treatment is strongly discouraged (see Interactions).

EFFETS INDÉSIRABLES :

Sedation or drowsiness;
Anticholinergic effects such as dry mucous membranes, constipation, palpitations, and a risk of urinary retention;

Balance disturbances, dizziness, memory or concentration impairment, which are more frequent in the elderly: mental confusion and hallucinations.

DOSAGE :

Motion sickness:

Children:
- From 2 to 5 years: ½ tablet.
- From 5 to 13 years: 1 tablet. Take half an hour before departure, repeat if necessary.
Adults and children over 13 years:
- 1 to 2 tablets, half an hour before departure, repeat if necessary.

Nausea and vomiting:

1 to 2 tablets, repeat if necessary. Do not exceed 12 tablets per day.

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.