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poliovirus vaccine inactivated (Rx)Brand and Other Names:IPOL, IPV, more...Poliovax

 
 
 

Dosing & Uses

AdultPediatric

Dosage Forms & Strengths

IM/SC Solution

  • 5mL/vial
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Poliovirus Prophylaxis

Routine vaccination not recommended for adults (18 years or older) residing in the US; however, unimmunized or incompletely immunized adults exposed to wild poliovirus should be vaccinated with a 3-dose series

0.5 mL SC/IM 2 doses 1-2 months apart with 3rd dose 6-12 months later, OR

3 doses >1 months apart or enough to complete total 3 doses

Completely vaccinated adults can receive 1 booster dose if traveling to polio endemic areas or to areas where the risk of exposure is high

Risk of exposure to wild polioviruses

  • Travelers to regions or countries where poliomyelitis is endemic or epidemic
  • Healthcare workers in close contact with patients who may be excreting polioviruses
  • Laboratory workers handling specimens that may contain polioviruses
  • Members of communities or specific population groups with disease caused by wild polioviruses

Additional Information

Up-to-date vaccination schedules available at www.cdc.gov/nip/publications

Poliovirus Prophylaxis

<6 weeks old: Safety and efficacy not established

0.5 mL SC/IM; 2 doses 1-2 months apart (at 2 and 4 months old), 3rd dose 18 months later; and 4th dose at age 4-6 years old before entering school

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Interactions

Interaction Checker

poliovirus vaccine inactivated and

No Results

     
     activity indicator 
    No Interactions Found
    Interactions Found

    Contraindicated

      Serious - Use Alternative

        Significant - Monitor Closely

          Minor

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            Adverse Effects

            Suspected adverse events after administration of any vaccine may be reported to Vaccine Adverse Events Reporting System (VAERS), 1-800-822-7967

            >10%

            Irritability (7-65%)

            Tiredness (4-61%)

            Fever >39 degrees C (38%)

            Injection site tenderness (29%)

            Injection site pain (13%)

            Injection site swelling (11%)

            1-10%

            Erythema at inj site (3%), induration (1%)

            Vomiting (1-3%)

            Crying (1%)

            Postmarketing Reports

            Guillain-Barre syndrome

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            Warnings

            Contraindications

            Hypersensitivity to neomycin, streptomycin, polymixin B

            Defer if acute febrile illness

            Concomitant methotrexate

            Cautions

            Do not administer additional doses if anaphylaxis to previous dose

            Immunosuppressed patients may not develop immunity

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            Pregnancy & Lactation

            Pregnancy Category: C

            Lactation: not known if excreted in breast milk

            Pregnancy Categories

            A:Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

            B:May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

            C:Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

            D:Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

            X:Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

            NA:Information not available.

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            Pharmacology

            Mechanism of Action

            Inactivated virus of 3 strains; elicits antibody response following immunization

            These products convey active immunity via stimulation of production of endogenously produced antibodies

            The onset of protection from disease is relatively slow, but duration is long lasting (years)

            Duration: Not established

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            Images

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            Formulary

            FormularyPatient Discounts

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            The above information is provided for general informational and educational purposes only. Individual plans may vary and formulary information changes. Contact the applicable plan provider for the most current information.

            Tier Description
            1 This drug is available at the lowest co-pay. Most commonly, these are generic drugs.
            2 This drug is available at a middle level co-pay. Most commonly, these are "preferred" (on formulary) brand drugs.
            3 This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs.
            4 This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs or specialty prescription products.
            5 This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs or specialty prescription products.
            6 This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs or specialty prescription products.
            NC NOT COVERED – Drugs that are not covered by the plan.
            Code Definition
            PA Prior Authorization
            Drugs that require prior authorization. This restriction requires that specific clinical criteria be met prior to the approval of the prescription.
            QL Quantity Limits
            Drugs that have quantity limits associated with each prescription. This restriction typically limits the quantity of the drug that will be covered.
            ST Step Therapy
            Drugs that have step therapy associated with each prescription. This restriction typically requires that certain criteria be met prior to approval for the prescription.
            OR Other Restrictions
            Drugs that have restrictions other than prior authorization, quantity limits, and step therapy associated with each prescription.
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