EVRYSDI pdr 0.75 mg/ml sol fl 80 ml + 1 ml ser

7680672510026 CH-67251 M09AX10 01.99.0.

Reimbursement limitations:

EVRYSDI.01

EVRYSDI ne peut être prescrit que par un médecin spécialiste en neurologie/neuropédiatrie dans des centres …

EVRYSDI pdr 0.75 mg/ml sol fl 80 ml + 1 ml ser
EVRYSDI pdr 0.75 mg/ml sol fl 80 ml + 1 ml ser
EVRYSDI pdr 0.75 mg/ml sol fl 80 ml + 1 ml ser
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Details

Product number
6725101
CPT
-
Packaging group
80
Unit
ml
Composition
risdiplamum 60 mg, mannitolum, isomaltum 237.25 mg, aromatica (Erdbeere) cum maltodextrinum et E 1450, acidum tartaricum, natrii benzoas 30 mg, macrogolum 6000, sucralosum, E 300, dinatrii edetas, ad pulverem pro 2 g corresp. solutio reconstituta 80 ml corresp. natrium 7.21 mg corresp. risdiplamum 0.75 mg/1 ml.

Articles (1)

Evrysdi 0.75 mg/ml, Pulver zur Herstellung einer Lösung zum Einnehmen
Pulver zur Herstellung einer Lösung zum Einnehmen
80
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
10/06/2025
Patient information leaflet
Français
10/06/2025
Patient information leaflet
Italien
10/06/2025
Professional SmPC
Allemand
10/06/2025
Professional SmPC
Français
10/06/2025
Professional SmPC
Italien
10/06/2025

Detailed composition

Substance Quantity Type Category
(N/A)
60.0 MG Substance Wirkstoff (Principe actif)
(N/A)
- Substance HNIDK
(N/A)
237.25 MG Substance HBESI
(N/A)
- Substance AROMA
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
30.0 MG Substance HBESI
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance ANTON
(N/A)
- Substance HNIDK
(N/A)
7.21 MG Substance HBESI
(N/A)
- Substance WIZUS

Reimbursement information

Public price
CHF 8471.35
Specialties list
Yes
Generic
No

Reimbursement limitation

SL addition date: 01/12/2021

Authorization holder

Roche Pharma (Schweiz) AG

4058 Basel

Authorization information

Swissmedic authorization number
67251
Drug name
Evrysdi, Pulver zur Herstellung einer Lösung zum Einnehmen
Galenic form
PULO
ATC Code
M09AX10
Authorization status
Z
Dispensation category
A
First authorization
06/05/2021
Authorization expiration date
05/05/2026
IT number
01.99.0.
Domain
Human medicine
Field of application
Spinale Muskelatrophie (SMA)

Packaging details

Description (FR)
EVRYSDI pdr 0.75 mg/ml sol fl 80 ml + 1 ml ser
Description (DE)
EVRYSDI Pulv 0.75 mg/ml Lös Fl 80 ml + 1 ml Spr
Market launch
06/05/2021
Narcotic (BTM)
No

Other packaging sizes