Esto*Im Iv 3f 1000mg/4ml PREPARAZIONE INIETTABILE

Esto*Im Iv 3f 1000mg/4ml Principio attivo: GLICEROFOSFORILETANOLAMINA MONOIDRATA
Forma: PREPARAZIONE INIETTABILE
Fornitore: ANGELINI SPA *
Conservazione: NESSUNA PARTICOLARE CONDIZIONE DI CONSERVAZIONE
Degrassi: SPECIALITA' MEDICINALI CON PRESCRIZIONE MEDICA
Categoria merceologica: FARMACO ETICO

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Foglietto illustrativo Esto*Im Iv 3f 1000mg/4ml

Il e la relativa posologia di questo prodotto sono indicazioni generali, soggette a cambiamenti.
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DENOMINAZIONE
ESTO
CATEGORIA FARMACOTERAPEUTICA
Psicoanalettici.
PRINCIPI ATTIVI
L-alfa-glicerofosforil-etanolamina monoidrata.
ECCIPIENTI
Compresse: amido pregelatinizzato 70 mg; cellulosa microcristallina 66mg; silice precipitata 45 mg; croscarmellosa sodica 35 mg; magnesio stearato 14 mg. Flaconi: Glicerolo 750 mg; sodio citrato 15 mg; acido citrico monoidrato 8 mg; saccarina sodica 2,5 mg; metile paraidrossibenzoato 6,6 mg; propile paraidrossibenzoato 0,7 mg; aroma lampone 4,7 mg; acqua demineralizzata q.b. a 5 ml. Fiale: acqua per prep. iniettabili q.b. 4 ml.
INDICAZIONI
Trattamento coadiuvante delle sindromi involutive cerebrali dell'anziano.
CONTROINDICAZIONI/EFF.SECONDAR
Ipersensibilita' individuale accertata verso i componenti.
POSOLOGIA
Compresse: una compressa due volte al giorno. Fiale: una fiala per viaintramuscolare o endovenosa al giorno. Flaconi orali: un flacone duevolte al giorno.
CONSERVAZIONE
Compresse: conservare a temperatura non superiore a 30 gradi C. Soluzione iniettabile e Soluzione orale: nessuna speciale precauzione per laconservazione.
AVVERTENZE
Nessuna.
INTERAZIONI
Durante gli studi non sono emerse interazioni negative con altri farmaci.
EFFETTI INDESIDERATI
Come precursore di sostanze biologiche la somministrazione anche protratta di l-alfa-GFE non pone particolari problemi di tollerabilita'. Molto raramente sono stati segnalati episodi di nausea e/o vomito o di leggera sonnolenza, tendenti peraltro a scomparire spontaneamente.
GRAVIDANZA E ALLATTAMENTO
Gli studi nell'animale non hanno evidenziato effetti teratogeni, ne' sulla capacita' procreativa. Tuttavia, l'alfa-GFE va somministrata durante la gravidanza e l'allattamento solo in caso di effettiva necessita'.


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