藥品名稱
drug name
Poliovirus Vaccine Inactivated (Imovax Polio Injection, 巴斯德小兒麻痺注射疫苗) 0.5 mL/syringe (旅遊醫學門診專用)
藥檔狀態使用中 (需冷藏)
成  份
Ingredient
Poliovirus Vaccine Inactivated
單位含量0.5 mL/syringe
Dosage FormsSuspension for Injection: 0.5 ml [Suspension of 3 types of poliomyelitis virus cultured on the Vero continuous cell line and inactivated with formol]
外觀描述 針劑/注射
AppearanceIM, SC
標  示
outward
廠商名稱
Manufacturer
賽諾菲股份有限公司
製 造 商
Manufacturer
SANOFI PASTEUR, FRANCE
字  號
Product ID
衛署菌疫輸字第000440號
藥理分類
Pharmacologic Category
BIOLOGIC AND IMMUNOLOGIC AGENTS/ Immunizations/ Vaccines-Virus (Inactivated)
作用機轉
Mechanism of action
As an inactivated virus vaccine, poliovirus vaccine induces active immunity against poliovirus types 1, 2, and 3 infection
用途/適應症小兒麻痺疫苗
Use Poliovirus prevention:

Active immunization of infants (≧6 weeks [US labeling]; ≧2 months [Canadian labeling]), children, adolescents, and adults for prevention of poliomyelitis caused by poliovirus types 1, 2, and 3.

ACIP recommends routine vaccination for the following:
All infants and children (first dose given at 2 months of age) (CDC/ACIP, 58[30] 2009)

衛福部核准適用症狀
MOHW approved indications
預防小兒麻痺症。
Dose Administration: IM, SC

【Adults】:
Un-vaccinated and increased risk of exposure: 3 doses at 0, 1-2, 6-12 months.

Incompletely vaccinated: with at least 1 previous dose of OPV, <3 doses of IPV, or a combination of OPV and IPV equaling <3 doses, administer at least one 0.5 mL dose of IPV. Additional doses to complete the series may be given if time permits.

Completely vaccinated and at increased risk of exposure: One 0.5 mL dose


【Children & infants, IPV regimen】: 4 doses at 2, 4, 6-18 m/o and booster dose at 4-6 y/o.
懷孕分級
Pregnancy Risk Factor
C

禁忌症 對疫苗中之主成分或其他成分、neomycin、steptomycin和polymyxine B過敏,或先前施打本疫苗後有過敏反應。
有發燒或急性疾病時,應延後使用疫苗。
Contraindications Defer vaccination for persons with acute febrile illness until recovery
常見副作用注射部位泛紅/疼痛、發燒、疲倦、食慾不振、嘔吐、躁動。
Common adverse drug reactionsTenderness or swelling of injection site, fever, tiredness, anorexia, vomiting, irritability.
Adverse Reactions Percentages noted with concomitant administration of DTP or DTaP vaccine and observed within 48 hours of injection.

>10%:
Central nervous system: Irritability (7% to 65%; most common in infants 2 months of age), tiredness (4% to 61%)
Gastrointestinal: Anorexia (1% to 17%)
Local: Injection Site: Tenderness (≦ 29%), swelling (≦11%)

1% to 10%:
Central nervous system: Fever >39°C (≦ 4%)
Gastrointestinal: Vomiting (1% to 3%)
Local: Injection site: Erythema (≦ 3%)
Miscellaneous: Persistent crying (≦ 1% reported within 72 hours)
Postmarketing and/or case reports (Limited to important or life-threatening): Allergic reaction, anaphylactic shock, anaphylaxis, febrile seizures, hypersensitivity reactions, lymphadenopathy, seizures; Guillain-Barre syndrome has been temporally related to another inactivated poliovirus vaccine
監測
Monitoring
Monitor for syncope for 15 minutes following administration (NCIRD/ACIP 2011). If seizure-like activity associated with syncope occurs, maintain patient in supine or Trendelenburg position to reestablish adequate cerebral perfusion.
警語與注意事項冷藏保存;不可口服
Warnings & precautionsStore under refrigeration 2°C to 8°C.
針劑溶解條件
針劑稀釋條件
針劑不相容性
針劑施打條件
針劑保存安定性 應冷藏(2-8℃)且避光儲存。請勿冷凍。(1050815仿單資料)
最近修改日期時間
Updated
9/27/2019 10:51:11 AM
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