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File: 970107_sep96_decls51_0004.txt
Subject: ADMINISTRATION OF ANTHRAX VACCINE
Unit: OTSG
Parent Organization: HSC
Box ID: BX003201
Folder Title: BOTULINUM VACCINATION PROGRAM
Document Number: 190001
Folder Seq #: 190000
ADMINISTRATION Of ANTM= VACCINZ
PURPOSZ: To provide the necessary information for the safe
administration of the anthrax vaccine.
BACKGROUND: An alum-precipitated, inactivated, anthrax.vaccine has
been approved and licensed for human use by the Food and Drug
Administration since 1972. It has been shown to be safe and
effective in protecting occupationally exposed individuals.
STORAGZ: The anthrax vaccine should be kept refrigerated or on wet
ice. Freezing or excess heat will inactivate the anthrax vaccine.
SCHEDULE:- Two doses of anthrax vaccine should be given two weeks
apart. A third dose of anthrax vaccine should be given two or more
weeks after the second as additional anthrax vaccine becomes
available.
SIDZ ZFFZCTS: Up to 6% of recipients will experience mild
discomfort (tenderness, redness, swelling, or itching) at the
inoculation site for up to 72 hours. Less than 1% will have more
severe local reaction potentially limiting the use of the arm for
I to'2 days. Mild systemic reactions (muscle aches, fatigue, or
fever) are uncommon and severe systemic reaction are rare. A few
vaccinees will develop small, firm, painless nodules at the
injection site which will persist for several weeks.
ADt4lNISTRATION: The anthrax vaccine should be
-given as follows:
1. Shake the vaccine bottle immediately
before use. Even after thorough shaking
anthrax vaccine has a milky texture.
2. Clean the rubber stopper with an
alcohol pad.
3. Use the alcohol pad to clean an area
of skin on the back side of the upper arm (see
g).
4. Draw up 0.5 cc of vaccine into the
syringe. muscle
5. Using a 25 gauge, 5/811 needle, subcutan
administer the vaccine subcutaneously at a 45 tissue
degree angle into a pinch of skin on backside skin
of the upper arm (see drawing). Do not give
this vaccine intramuscularly.
6, Use separate arms when administering
anthrax and botulinum vaccine simultaneously.
7. Warn the patient to expect a burning
sensation at the vaccine site approximately 30
seconds after'vaccination lasting 1-2 minutes.
SUBCUTANEOUS
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Document 5 f:/Week-36/BX003201/BOTULINUM VACCINATION PROGRAM/administration of anthrax vaccine:01029715474052
Control Fields 17
File Room = sep96_declassified
File Cabinet = Week-36
Box ID = BX003201
Unit = OTSG
Parent Organization = HSC
Folder Title = BOTULINUM VACCINATION PROGRAM
Folder Seq # = 190000
Subject = ADMINISTRATION OF ANTHRAX VACCINE
Document Seq # = 190001
Document Date =
Scan Date =
Queued for Declassification = 01-JAN-1980
Short Term Referral = 01-JAN-1980
Long Term Referral = 01-JAN-1980
Permanent Referral = 01-JAN-1980
Non-Health Related Document = 01-JAN-1980
Declassified = 02-JAN-1997