M-M-RVAXPRO
ItalyThe vaccine is used to stimulate the body to produce antibodies to protect against infections from the measles, mumps, and rubella viruses, helping to prevent the transmission of these infectious agents.
Frequently asked questions
What are the most common side effects?
Very common side effects include fever (38.5 °C or higher), redness, pain, or swelling at the injection site. The appearance of rashes (including measles-like rashes) and bruising at the injection site is also common.
What other side effects may occur?
Uncommon side effects reported include nasal congestion, sore throat, runny nose, diarrhea, vomiting, urticaria, crying, and upper respiratory tract infections. Less frequent or unknown frequency side effects have also been reported, ranging from headache and joint pain to severe allergic reactions, nervous system disorders, or eye inflammation.
How is the vaccine administered?
The vaccine is administered via injection. In younger children, the thigh area is preferred, while in others, the outer thigh or the arm is used.
What should I do with medicines I no longer use?
Do not throw the vaccine down the drain or in household waste. It is necessary to ask a pharmacist how to dispose of unused vaccines to help protect the environment.
Instructions for use
Patient Information Leaflet: Information for the User
What it is
What it is
the body) will produce antibodies against the measles virus,
exposure, or for use in
infection with mumps and rubella.
treatment for asthma or replacement therapy).
a medical history
a viral infection from the
hepatitis A during the same vaccination session, at different injection sites (e.g. the other arm or
the other leg).
some routine childhood vaccines that must
“ ”
“potassium”
’
’
in the area
arm. For intramuscular injections, the area
The interval
have been reported with the use of
| Frequency | Adverse Reaction |
| Very common (may occur in more than 1 in 10 vaccinated individuals) |
|
| Common (may occur in up to |
|
| 1 in 10 vaccinated individuals) |
|
| Uncommon (may occur in up to 1 in 100 vaccinated individuals) |
|
| Not known (frequency cannot be estimated from the available data)* |
|
have been reported with the
following use after marketing authorization
not reported in the
expiry refers to the last
–
the outer packaging
Do not dispose of any vaccine via wastewater or household waste. Ask your pharmacist how
to dispose of vaccines no longer required. This will help protect the environment.
Description of the appearance of
Marketing Authorization Holder
of the Authorization
България
Merck Sharp & Dohme Bulgaria EOOD
Tel.: +359 2 819 3737
Česká republika
Merck Sharp & Dohme s.r.o.
Tel.:
Ελλάδα
MSD A.E.E.
Tel: +30 210 98 97 300
Κύπρος
Tel
Other sources of information
are available on the website of the Agency
to prevent transmission of infectious agents from one individual to another.
a new separate needle and syringe for injection.
Withdraw the entire
for injection. Inject the entire contents of the syringe into the vial containing the powder. Shake
the appearance of the solvent, powder or reconstituted vaccine differs from that described above.
withdraw the entire contents of the reconstituted vaccine from the vial, change the needle, and
inject the entire volume
illustrative: information for the user
What is
What is
organism) will produce antibodies against measles, mumps and rubella viruses. The
exposure, or for use in
infection with mumps and rubella.
therapy for asthma or replacement therapy).
a family history of congenital immunodeficiency
an infection with irus of
hepatitis A during the same vaccination session, at different injection sites (e.g. the other arm or
the other leg).
some routine childhood vaccines that should
“ ”
“ potassium”
’
’
in the outer area of the thigh or in the
upper arm. For intramuscular injections, the thigh area is generally preferred in younger children
should be administered according to the physician's recommendations. The interval between 2
have been reported with the use of
| Frequency | Adverse reaction |
| Very common (may occur in more than 1 in 10 vaccinated subjects) |
|
| Common (may occur in up to 1 in 10 vaccinated subjects) |
|
| Uncommon (may occur in up to 1 in 100 vaccinated subjects) |
|
| Not known (frequency cannot be estimated from the available data)* |
|
have been reported with
prior to use following marketing authorization
the national reporting system outlined in section
expiry refers to the last day of that month.
–
’packaging
in the water of
which you no longer use. This will help protect the environment
Description of the appearance of
Marketing Authorization Holder
of the Marketing Authorization
България
Merck Sharp & Dohme Bulgaria EOOD
Tel.: +359 2 819 3737
Česká republika
Merck Sharp & Dohme s.r.o.
Tel.:
Ελλάδα
MSD A.E.E.
Tel: +30 210 98 97 300
Κύπρος
Tel
Other sources of information
are available on the website of the Agency
to prevent transmission of infectious agents from one individual to another.
for reconstitution and a separate new needle for injection.
For administration, the needle must be firmly placed on the tip of the syringe and secured
Inject the entire contents of the solvent syringe into the
the appearance of the solvent, powder or reconstituted vaccine differs from that described above.
withdraw the entire vaccine content from the vial, change the needle and
inject the entire volume
The original data is available in the language of the country of manufacture.
Data source: Italian Medicines Agency (AIFA)
Data last verified: September 21, 2026