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Strengths available for Silodyx:

Silodyx 4mg
Silodyx 8mg

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Latest news releases on Silodyx:

VIDAL - SILODYX 4 mg gél - Indications - VIDAL - La base ...

SILODYX 4 mg gél : Synthèse, Formes et présentations, Composition, Indications, Posologie et mode d'administration, Contre-indications, Mises en garde et ...

VIDAL - SILODYX 4 mg gél - Synthèse - VIDAL - La base de ...

SILODYX 4 mg gél : Synthèse, Formes et présentations, Composition, Indications, Posologie et mode d'administration, Contre-indications, Mises en garde et ...

Silodyx bijsluiter | Exmedica

Silodyx Download: Bijsluiter Werkzame stoffen: silodosine Afleverstatus: Uitsluitend recept Registratiedatum: 29 januari 2010 Nummer Omschrijving Houder EU/1/09/607 ...

SILODYX - Silodosine - Posologie, Effets secondaires ...

SILODYX : Traitement des signes et symptômes de l'hypertrophie bénigne de la prostate (HBP) chez l'homme adulte.

Silodyx | Medicijn ervaringen en bijwerkingen | mijnmedicijn

Silodyx: 17 ervaringen met effect en bijwerkingen. Man, 52: voorafgaandelijk verschillende keren moeten opstaan s'nachts en hoge aandrang... tests laten...

Silodyx | Farmaci: Esperienze ed effetti collaterali ...

Silodyx: 1 esperienze e le reazioni avverse. Uomo, 44: Buongiorno, sono 10 giorni che assumo il suddetto farmaco, come già anticipato dal medico...

UROREC Cáps. dura 8 mg - Datos generales

UROREC aa Cáps. dura 8 mg,efectos secundarios, efectos adversos, precio (Silodosina) de CASEN RECORDATI S.L. es indicado para Hiperplasia prostática benigna.

DUODART Cáps. dura 0,5 mg/0,4 mg - Datos generales

DUODART aa Cáps. dura 0,5 mg/0,4 mg,efectos secundarios, efectos adversos, precio (Dutasterida,Tamsulosina hidrocloruro) de DIFARMED S.L. es indicado para ...

Silodosin - Wikipedia

Silodosin; Clinical data; Synonyms: KAD-3213, KMD-3213: License data ... US: B (No risk in non-human studies) Not approved for use in women

Generics applications under review by EMA – June 2018 ...

According to EMA’s list of applications for new human medicines under evaluation by the Committee for Medicinal Products for Human Use (CHMP) released on 6 June ...

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