What Is the Connection Between Tetanus, Diphtheria and Pertussis?

This strain is made from pertussis vaccine stock solution, refined diphtheria toxoid and refined tetanus toxoid by aluminum hydroxide adsorption. It is a milky white suspension containing preservatives. The adjuvant sinks after standing and shakes to form a uniform suspension.

Adsorption of pertussis, diphtheria and tetanus

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This strain is made from pertussis vaccine stock solution, refined diphtheria toxoid and refined tetanus toxoid by aluminum hydroxide adsorption. It is a milky white suspension containing preservatives. The adjuvant sinks after standing and shakes to form a uniform suspension.

Chinese name

Adsorption of pertussis, diphtheria and tetanus

Use

Prevention of pertussis, diphtheria and tetanus

Inoculation object

3 months-6 years old

Storage

Store and transport at 2-8 ° C, protected from light, do not freeze

After the vaccination, the body can produce

This product is produced and tested according to the 2000 edition of "Chinese Biological Product Regulations", and the quality meets the requirements.

Children from 3 months to 6 years.

1. Intramuscular injection after disinfecting the skin at the upper 1/4 of the outer buttock or the upper deltoid muscle attachment site.

2. Immunization has started from 3 months of age, and 3 shots of immunization have been completed to 12 months of age, with each shot separated by 4-6 weeks, and the fourth shot is injected at 18-24 months of age. Each injection is 0.5ml.

1. People with a history of epilepsy, neurological disorders and convulsions are prohibited.

2. For patients with acute infectious diseases (including recovery period) and fever, suspend the injection.

After injection of this product, there may be redness, swelling, pain, itching, or low fever, fatigue, headache, etc., which usually subsides without treatment. If serious reactions occur, diagnose and treat in time.

1. Shake well during use. If there is a clot, foreign matter, cracks in the ampoule, the product has been frozen, the label is unclear and expired can not be used.

2. There may be induration after injection, which can be gradually absorbed. The other site should be replaced when the second needle is injected.

3. Adrenaline should be prepared for emergency use in case of shock. In case of abnormalities such as high fever and convulsions after the first injection, the second injection will not be given.

Store and transport at 2-8 ° C, protected from light, do not freeze.