 |
Human-based
formulation |
 |
IMOVAX®
Rabies is grown in MRC-5 human diploid-cell line and
contains phenol, betapropiolactone, and neomycin no
known specific contraindications for postexposure
treatment |
 |
Safe
and well tolerated |
 |
Only
supplier of both pre- and
postexposure rabies product |
 |
Round-the-clock
telephone contact |
 |
Special
delivery available
for emergency rooms |
Safety Information
IMOVAX® Rabies Adverse reactions due to administration
of the rabies vaccine may include pain, redness, swelling,
and itching at the injection site; headache, nausea, abdominal
pain, muscle aches, and dizziness are also possible. For
postexposure treatment, there are no known specific contraindications.
For pre-exposure immunization, the only known contraindication
is the development of febrile illness, etc.
IMOGAM® Rabies–HT Adverse reactions due to administration
of rabies immune globulin may include tenderness, pain,
soreness, and muscle stiffness at the injection site. Administration
of IMOGAM® |
Pre-exposure
immunization1...
| |
Vaccination
Schedule |
Treatment
Needed |
 |
| |
Day
0 |
IMOVAX®
Rabies |
 |
| |
Day
7 |
IMOVAX®
Rabies |
 |
| |
Day
21 or 28 |
IMOVAX®
Rabies |
 |
and postexposure treatment1
|
Postexposure
treatment for those who have received pre-exposure
vaccinations3 |
| |
Vaccination
Schedule |
Treatment
Needed |
 |
| |
Day
0 |
IMOVAX®
Rabies |
 |
| |
Day
3 |
IMOVAX®
Rabies |
 |
| |
Postexposure
treatment for those who have not received pre-exposure
immunization |
| |
Vaccination
Schedule |
Treatment
Needed |
 |
| |
Day
0 |
IMOVAX®
Rabies
IMOGAM® RabiesHT |
 |
| |
Day
3 |
IMOVAX®
Rabies |
 |
| |
Day
7 |
IMOVAX®
Rabies |
 |
| |
Day
14 |
IMOVAX®
Rabies |
 |
| |
Day
28 |
IMOVAX®
Rabies |
 |
|