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BCG vaccine live (BCG Vaccine (Tice strain))

 

Classes: Vaccines, Live, Bacterial

Dosing and uses of BCG Vaccine (Tice strain) (BCG vaccine live)

 

Adult dosage forms and strengths

suspension reconstituted

  • 50mg (Tice BCG)
  • 81mg (TheraCys)

 

Tuberculosis Immunization

Used as TB immunization, primarily in developing countries

ACIP recommended use: TB exposed health care workers in high risk settings

0.2-0.3 mL percutaneous

Conduct tuberculin test 2-3 months after percutaneous administration; if test negative repeat vaccination

 

Immunotherapy for Bladder Cancer

Initiate treatment 7-14 days after biopsy

TheraCys: Instill one dose into bladder; retain for 2 hr; repeat dose once weekly for 6 weeks followed by 1 treatment at 3, 6, 12, 18, and 24 months after initial treatment

TICE BCG: Instill one dose into blatter; retain for 2 hr; repeat dose once weekly for 6 weeks (may repeat cycle once) followed by once monthly for 6-12 months

 

Administration

Okay to give Hib, DTP, OPV, IPV, MMR, influenza, and hepatitis B at same time

 

Pediatric dosage forms and strengths

suspension reconstituted

  • 50mg (Tice BCG)
  • 81mg (TheraCys)

 

Tuberculosis Immunization

Used as TB immunization, primarily in developing countries

ACIP recommended use: TB exposed TB skin test-negative infants and children

<1 month

  • Half-strength (reconstitute with 2 mL instead of 1 mL sterile water)
  • 0.2-0.3 mL percutaneous
  • Conduct tuberculin test 2-3 months after percutaneous administration; if test negative repeat vaccination after 1 year

>1 month

  • 0.2-0.3 mL percutaneous
  • Conduct tuberculin test 2-3 months after percutaneous administration; if test negative repeat vaccination

 

Additional Information

Okay to give Hib, DTP, OPV, IPV, MMR, influenza, and hepatitis B at same time

 

BCG Vaccine (Tice strain) (BCG vaccine live) adverse (side) effects

>10%

Malaise (7-40%)

Fever (17-38%)

Pain (17%)

Chills (9-34%)

Nausea/vomiting (3-16%)

Dysuria (52-60%)

Hematutia (26-39%)

Urinary urgency (6-18%)

Infection (2-18%)

Anemia (21%)

Flu-lik syndrome (24-33%)

 

1-10%

Rash (2-3%)

Diarrhea (6%)

Abdominal pain (2-3%)

Headache (2%)

Leukopenia (6%)

Genital inflammation /abscess (2%)

Renal toxicity (10%)

Hemorrhagic cystitis (9%)

Nocturia (5%)

Urinary incontinence (2-6%)

Arthralgia/myalgia (3-7%)

Pulmonary infection (3%)

 

<1%

Urea nitrogen in blood increased

Creatinine increased

Disseminated sepsis

Hepatitis

Coagulopathy

Myoglobinuria

Nephritis

Uveitis

 

Warnings

Black Box Warning

Intravesical administration may cause disseminated infections

Contains live attenuated mycobacteria (handle with care and dispose properly)

 

Contraindications

Hypersensitivity, immunosuppression (corticosteroids)

Acquired immune deficiencies

Active tuberculosis

HIV infected patients

Bladder

  • Febrile illness
  • Urinary tract infection
  • Gross hematuria
  • Biopsy
  • Transurethral resection
  • Traumatic catherization

 

Cautions

Bacillus Calmette-Guérin strain of Mycobacterium bovis

Patient should have Mantoux skin test prior to vaccine administration

Following vaccination, Mantoux skin test usually positive; this is not a sensitive indicator of degree of protection

Immunity not permanent; duration unpredictable

Treat anaphylactoid reactions immediately

Intravesical administration may cause symptoms of bladder irritability 4-6 hr after instillation and increase in severity following each instillation; may last 24-72 hr

Use caution in patients with small bladder capacity

Postpone intravesical instillation during antibiotic therapy

Vaccination not recommended for patients with positive PPD reaction

Not for the treatment of active tuberculosis or prevention of cancer

May not result in effective immunity in all patients

Packaging may contain latex

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

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

 

Pregnancy and lactation

Pregnancy category: C

Lactation: Not known if excreted in breast milk, not recommended

 

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.

 

Pharmacology of BCG Vaccine (Tice strain) (BCG vaccine live)

Mechanism of action

M. bovis strain in the vaccine, immunologically similar to M. tuberculosis, produces cell-mediated immunity and simulates M. tuberculosis infection

May 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)

In bladder cancer a local inflammatory reaction may lead to destruction of superficial tumor cells of the endothellium; stimulates the host's immune system to reject the tumor