mResvia Respiratorisches-Synzytial-Virus (RSV) Vakzin 0.10 mg/ml, Injektionsdispersion

7680699950010 CH-69995 J07BX 08.08.
mResvia Respiratorisches-Synzytial-Virus (RSV) Vakzin 0.10 mg/ml, Injektionsdispersion
mResvia Respiratorisches-Synzytial-Virus (RSV) Vakzin 0.10 mg/ml, Injektionsdispersion
mResvia Respiratorisches-Synzytial-Virus (RSV) Vakzin 0.10 mg/ml, Injektionsdispersion
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Details

Product number
6999501
CPT
-
Packaging group
1
Unit
Fertigspritze(n)
Composition
Suspension: mRNA-1345 0.10 mg/ml, heptadecan-9-ylis 8-((2-hydroxyethyl)(6-oxo-6-(undecyloxy)hexyl)amino)-octanoas, cholesterolum, 1,2-distearoyl-sn-glycero-3-phosphocholinum, 1,2-dimyristoyl-rac-glycero-3-polyethylenglycoli 2000 aether methylicus, trometamolum, trometamoli hydrochloridum, acidum aceticum glaciale, natrii acetas trihydricus, saccharum, aqua ad iniectabile, 1 ml corresp., natrium 0.017 mg pro dosi.

Articles (1)

mResvia Respiratorisches-Synzytial-Virus (RSV) Vakzin 0.10 mg/ml, Injektionsdispersion
Injektionsdispersion
1
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Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Professional SmPC
Allemand
02/09/2025
Professional SmPC
Français
02/09/2025
Professional SmPC
Italien
02/09/2025
Patient information leaflet
Allemand
26/04/2025
Patient information leaflet
Français
26/04/2025
Patient information leaflet
Italien
26/04/2025

Detailed composition

Substance Quantity Type Category
SUS
0.1 MGML Substance Wirkstoff (Principe actif)
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
- Substance HNIDK
SUS
0.017 MG Substance HBESI

Authorization holder

Moderna Switzerland GmbH

4052 Basel

Authorization information

Swissmedic authorization number
69995
Drug name
mResvia Respiratorisches-Synzytial-Virus (RSV) Vakzin, Injektionsdispersion
Galenic form
DISII
ATC Code
J07BX
Authorization status
Z
Dispensation category
B
First authorization
17/04/2025
Authorization expiration date
16/04/2030
IT number
08.08.
Domain
Human medicine
Field of application
mRESVIA ist indiziert zur aktiven Immunisierung von Erwachsenen im Alter von 60 Jahren und älter zur Prävention von durch das Respiratorische Synzytial-Virus verursachten Erkrankungen der unteren Atemwege (lower respiratory tract disease, LRTD)

Packaging details

Description (FR)
mRESVIA Vaccin à ARNm contre le VRS
Description (DE)
mRESVIA RSV mRNA Impfstoff
Market launch
15/08/2025
Narcotic (BTM)
No

Application methods

IMU

Other packaging sizes