Vaxelis 0.5 ml
As listed in the register: Vaxelis 0.5 ml, Injektionssuspension
·
- Prescription only
- Antibiotics, antivirals and antifungals taken into the body
- Made by
- Future Health Pharma GmbH
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
- Grundimmunisierung und Auffrischimpfung bei Säuglingen und Kleinkindern ab einem Alter von 6 Wochen bis 4 Jahre (vor dem 5. Geburtstag) gegen Diphtherie, Tetanus, Pertussis, Hepatitis B, Poliomyelitis und durch Haemophilus influenzae Typ b (Hib) verursachte invasive Krankheiten.
From the official label · 2026-09-30 · Swissmedic
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
European UnionNo exact match for this strength and form
SpainNo exact match for this strength and form
NetherlandsNo exact match for this strength and form
Details
| Made by | Future Health Pharma GmbH |
|---|---|
| Active substance | Polysaccharida haemophili influenzae typus B conjugata cum proteino neisseriae meningitidis B + Hepatitidis B viri antigenum ADNr + Toxoidum pertussis + Haemagglutininum filamentosum + Pertactinum + Fimbriae Typ 2 und 3 + Toxoidum diphtheriae + Toxoidum tetani + Virus poliomyelitis typus 1 inactivatus (Mahoney) + Virus poliomyelitis typus 2 inactivatus (MEF-1) + Virus poliomyelitis typus 3 inactivatus (Saukett) |
| Used in | Antibiotics, antivirals and antifungals taken into the body |
| Classification | J07CA09 · Antibiotics, antivirals and antifungals taken into the body |
| Dispensing (as stated by the register) | Abgabekategorie B |
| Name in the register | Vaxelis 0.5 ml, Injektionssuspension |
| Packs | 1 Fertigspritze(n) · 10 Fertigspritze(n) · 10 Fertigspritze(n) · 1 Fertigspritze(n) |
| Zulassungsnummer | 66940 |
| Dosisstärke | 1 |
Source: Zugelassene Packungen Humanarzneimittel · 2026-09-30 · not reviewed by a clinician
Quelle: Swissmedic. The publisher’s terms do not grant reproduction, so text is shortened and linked. Publisher’s terms.