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ProQuad

ProQuad

Manufacturer:

MSD

Distributor:

Zuellig Pharma
Concise Prescribing Info
Contents
Per 0.5 mL MMR & varicella (Oka/Merck) virus vaccine (live)
Indications/Uses
Vaccination against MMR & varicella in individuals 12 mth-12 yr.
Dosage/Direction for Use
IM/SC Individual 12 mth-12 yr Single dose. Administer 2nd dose of measles-containing vaccine according to Singapore's national immunization program. At least 1 mth should elapse between a dose of M-M-R II & a dose of ProQuad. Min of 3-mth dose interval, if 2nd dose of varicella-containing vaccine is administered.
Contraindications
Hypersensitivity to any component of vaccine (MMR & varicella) including gelatin. History of anaphylactoid reaction to neomycin. Blood dyscrasias, leukemia, lymphomas of any type or other malignant neoplasms affecting the bone marrow or lymphatic system. Immunosuppressive therapy (including high-dose corticosteroids). Primary & acquired immunodeficiency states including immunosuppression in association w/ AIDS or other clinical manifestations of infection w/ HIV; cellular immune deficiencies; & hypogammaglobulinemic & dysgammaglobulinemic states. Family history of congenital or hereditary immunodeficiency. Active untreated TB. Any active febrile illness w/ fever >38.5°C. Pregnancy.
Special Precautions
Hypersensitivity to eggs (low risk for anaphylactic reactions in childn). Adequate treatment provisions including epinephrine inj should be available for immediate use if anaphylactic or anaphylactoid reaction occur. Do not inj intravascularly. Obtain vaccination history & determine previous reactions to any vaccine, including ProQuad, Varivax, or any MMR-containing vaccines prior to administration. History of convulsions, cerebral injury or any other condition in which stress due to fever should be avoided. HIV w/ or w/o evidence of immunosuppression. May not protect all vaccine recipients. Avoid close association w/ high-risk individuals (eg, immunocompromised, pregnant women w/o documented +ve history of varicella or lab evidence of prior infection & their newborns) susceptible to varicella for up to 6 wk following vaccination. Administer vaccine subcutaneously to individuals w/ thrombocytopenia or any coagulation disorder; bleeding may occur following IM administration. Post-exposure prophylaxis. May result in temporary depression of tuberculin skin sensitivity; administer tuberculin test any time before, simultaneously w/ or at least 4-6 wk after ProQuad. Concomitant vaccination w/ diphtheria, tetanus & acellular pertussis. Not to be given concomitantly w/ Ig or varicella-zoster Ig. Avoid pregnancy for 3 mth following vaccination in females of childbearing age. Lactation. Not recommended for infant <12 mth. Childn w/ untreated TB. Adolescents & adults. Not indicated for elderly >65 yr.
Adverse Reactions
Fever ≥38.9°C, erythema or pain/tenderness/soreness at the inj site. Upper resp infection; irritability; diarrhea, vomiting; rash, measles-like & varicella-like rash; ecchymosis or swelling at inj site, inj site rash.
Drug Interactions
May interfere w/ the expected immune response w/ Ig. Defer vaccination at least 3 mth following blood/plasma transfusion or Ig administration. Risk of Reye syndrome w/ salicylates; avoid salicylate use for 6 wk after vaccination. Concomitant use w/ inactivated poliovirus, pneumococcal conjugate & meningococcal C conjugate vaccines.
MIMS Class
Vaccines, Antisera & Immunologicals
ATC Classification
J07BD54 - measles, combinations with mumps, rubella and varicella, live attenuated ; Belongs to the class of measles vaccines.
Presentation/Packing
Form
ProQuad lyo powd for soln for inj
Packing/Price
(+ diluent (syringe, vial)) 0.5 mL x 1's
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