APPENDIX I: BW Agents: Vaccines, Therapeutics and Prophylactics
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DISEASE |
VACCINE |
CHEMOTHERAPY (Rx) |
CHEMOPROPHYLAXIS (Px) |
COMMENTS |
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Anthrax |
Bioport vaccine (licensed) 0.5 mL SC @ 0, 2, 4 wk, 6, 12, 18 mo then annual boosters |
Ciprofloxacin 400 mg IV q 8-12 h |
Ciprofloxacin 500 mg PO bid x 4 wk If unvaccinated, begin initial doses of vaccine |
Potential alternates for Rx: gentamicin, erythromycin, and chloramphenicol |
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Doxycycline 200 mg IV, then 100 mg IV q 8-12 h |
Doxycycline 100 mg PO bid x 4 wk plus vaccination |
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Penicillin 2 million units IV q 2 h |
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PCN for sensitive organisms only |
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Cholera |
Wyeth-Ayerst Vaccine 2 doses 0.5 mL IM or SC @ 0, 7-30 days, then boosters Q 6 months |
Oral rehydration therapy during period of high fluid loss |
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Vaccine not recommended for routine protection in endemic areas (50% efficacy, short term) |
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Tetracycline 500 mg q 6 h x 3 d |
Alternates for Rx: erythromycin, |
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Doxycycline 300 mg once, or 100 mg q 12 h x 3 d |
trimethoprim and sulfamethoxazole, and furazolidone |
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Ciprofloxacin 500 mg q 12 h x 3 d |
Quinolones for tetra/doxy resistant strains |
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Norfloxacin 400 mg q 12 h x 3 d |
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Q Fever |
IND 610 - inactivated whole cell vaccine given as single 0.5 ml s.c. injection |
Tetracycline 500 mg PO q 6 h x 5-7 d |
Tetracycline start 8-12 d post-exposure x 5 d |
Currently testing vaccine to determine the necessity of skin testing prior to use. |
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Doxycycline 100 mg PO q 12 h x 5-7 d |
Doxycycline start 8-12 d post-exposure x 5 d |
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Glanders |
No vaccine available |
Sulfadiazine 100 mg/kg in divided doses x 3 weeks may be effective TMP-SMX may be effective |
Post-exposure prophylaxis may be tried with TMP-SMX |
No large therapeutic human trials have been conducted owing to the rarity of naturally occurring disease. |
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DISEASE |
VACCINE |
CHEMOTHERAPY (Rx) |
CHEMOPROPHYLAXIS (Px) |
COMMENTS |
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Plague |
Greer inactivated vaccine (FDA licensed): 1.0 mL IM; 0.2 mL IM 1-3 mo later; 0.2 mL 5-6 mo after dose 2; 0.2 mL boosters @ 6,12, 18 mo after dose 3 then q 1-2 years |
Streptomycin 30 mg/kg/d IM in 2 divided doses x 10 d (or gentamicin) |
Doxycycline 100 mg PO bid x 7 d or duration of exposure Ciprofloxacin 500 mg PO bid x 7 d |
Plague vaccine not protective against aerosol challenge in animal studies |
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Doxy 200 mg IV then 100 mg IV bid x 10-14 d |
Doxycycline 100 mg PO bid x 7 d Tetracycline 500 mg PO qid x 7 d |
Alternate Rx: trimethoprim-sulfamethoxazole |
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Chloramphenicol 1 gm IV qid x 10-14 d |
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Chloramphenicol for plague meningitis |
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Tularemia |
IND - Live attenuated vaccine: one dose by scarification |
Streptomycin 30 mg/kg IM divided BID x 10-14 d |
Doxycyline 100 mg PO bid x 14 d |
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Gentamicin 3-5 mg/kg/d IV x 10-14 d |
Tetracycline 500 mg PO QID x 14 d |
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Brucellosis |
No human vaccine available |
Doxycycline 200 mg/d PO plus rifampin 600-900 mg/d PO x 6 wk |
Doxycycline and rifampin x 3 wk |
Trimethoprim-sulfamethoxazole may be substituted for rifampin; however, relapse may reach 30% |
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Ofloxacin 400/rifampin 600 mg/d PO x 6 wks |
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Viral encephalitides |
VEE DOD TC-83 live attenuated vaccine (IND): 0.5 mL SC x1 dose |
Supportive therapy: analgesics and anticonvulsants prn |
NA |
TC-83 reactogenic in 20% No seroconversion in 20% Only effective against subtypes 1A, 1B, and 1C |
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VEE DOD C-84 (formalin inactivated TC-83) (IND): 0.5 mL SC for up to 3 doses |
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C-84 vaccine used for non-responders to TC-83 |
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EEE inactivated (IND): 0.5 mL SC at 0 & 28 d |
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EEE and WEE inactivated vaccines are poorly |
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WEE inactivated (IND): 0.5 mL SC at 0, 7, and 28 d |
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Immunogenic. Multiple immunizations are required |
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DISEASE |
VACCINE |
CHEMOTHERAPY (Rx) |
CHEMOPROPHYLAXIS (Px) |
COMMENTS |
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Viral Hemorrhagic Fevers |
AHF Candid #1 vaccine (x-protection for BHF) (IND) |
Ribavirin (CCHF/arenaviruses) 30 mg/kg IV initial dose 15 mg/kg IV q 6 h x 4 d 7.5 mg/kg IV q 8 h x 6 d |
NA |
Aggresive supportive care and management of hypotension very important |
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RVF inactivated vaccine (IND) |
Passive antibody for AHF, BHF, Lassa fever, and CCHF |
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Smallpox |
Wyeth calf lymph vaccinia vaccine (licensed): 1 dose by scarification |
Cidofovir (effective in vitro) |
Vaccinia immune globulin 0.6 mL/kg IM (within 3 d of exposure, best within 24 h) |
Pre and post exposure vaccination recommended if > 3 years since last vaccine |
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Botulism |
DOD pentavalent toxoid for serotypes A - E (IND): 0.5 ml deep SC @ 0, 2 & 12 wk, then yearly boosters |
DOD heptavalent equine despeciated antitoxin for serotypes A-G (IND): 1 vial (10 mL) IV |
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Skin test for hypersensitivity before equine antitoxin administration |
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CDC trivalent equine antitoxin for serotypes A, B, E (licensed) |
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Staphylococcus Enterotoxin B |
No vaccine available |
Ventilatory support for inhalation exposure |
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Ricin |
No vaccine available |
Inhalation: supportive therapy G-I : gastric lavage, superactivated charcoal, cathartics |
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T-2 Mycotoxins |
No vaccine available |
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Decontamination of clothing and skin |
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Nuclear |
Biological
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Chemical![]() |
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UVA
Nuclear Reactor Facility FEMA Fact Sheet:
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History of Biological Warfare and Current Threat Medical Aspects of the Biological Threat Bacterial
Agents Viruses Biological
Toxins Appendix
A: Appendix
B: Appendix
C: Appendix
D: Appendix
E: Appendix
F: Appendix
G: Appendix
H: Appendix
I: Appendix
J: |
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