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Tetanus Antitoxin Refined 1500 I.U Subcutaneous/I.V. Injection Medicine for treatment and prevention of tetanus

Wuhan uni-pharma bio-tech co.,ltd
Wuhan uni-pharma bio-tech co.,ltd
Province/State: Hubei
Country/Region: China
Tel: 86-27-82316816

Tetanus Antitoxin Refined 1500 I.U Subcutaneous/I.V. Injection Medicine for treatment and prevention of tetanus

Brand Name : Uni-pharma
Model Number : 15000 I.U.
Certification : GMP
Place of Origin : China
MOQ : 500000Amps
Payment Terms : L/C, D/A, D/P, T/T
Delivery Time : After packaging confirmed 30 days
Packaging Details : 10 Amps/Box
Applications : Internal Medicine
Usage method : Injectable
Applicable people : Adults/Children
Form : Liquid
Shape : Injection
Type : Organic Chemcials
Pharmaceutical methods : Chemical Synthesis
Specification : 1.0mg
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Western Medicine Tetanus Antitoxin Refined 1500 I.U (Used for the treatment and prevention of tetanus.)

Modified Globulin from Antitetanus Horse Serum

It is prepared from immunized plasma of healthy horses through the process of ammonium sulphate fractionation and ultra-filtration after being digested with pepsin.

[Indication & Use]


For those started with tetanus symptoms or in suspicion. Tetanus antitoxin should be given immediately together with surgical and other clinical administration at the same time.

For those openly wounded,especially those wounded deeply and contaminated seriously,and in danger of being infected with tetanus,prophylactic injection of Tetanus antitoxin should be given at once. Patient who have had previous injection of Tetanus toxoid should be boosted with one more injection of Tetanus toxoid (but not Tetanus antitoxin). To those who haven't had previous Tetanus toxoid injection or without a clear history of immunization, both antitoxin and toxoid should be given for prophylaxis and permanent immunocompetence.


The right site for subcutaneous injection of the Tetanus antitoxin is around the deltoid muscle of the upper arm. If Tetanus toxoid is to be given at the same time,seperate sites are desirable. The right site for intramuscular injection is the center area of the deltoid muscle or the lateral upper pare of the gluteus maximum

Intravenous route should not be used until no untowards reaction occurs after intramuscular or subcutancous injection. Intravenous injection should be done slowly enough:not more than 1ml/min at the beignning and don't exceed 4ml/min afterward.
The total volume for a single dose should be no more than 40ml for adults and no more than 0.8ml/kg body weight for children. Tetanus antitoxin may be diluted with dextrose solution or physiological saline for intravenous drip. The drip must be stopped at once if any untoward reaction occurs.

[Recommended Dosage]

1.Prophylactic Use: 1500-3000IU both for adults and children injection should be repeated after six days when infections still persists.

In those cases who have been immunized previously with tetanus toxoid,it is advisable to give a booster dose dose of tetanus toxoid only.

For prophylactic use the antitoxin may be given by subcutaneous or intramuscular route.

2.Therapeutic use: Tetanus antitoxin should be administered as early as possible. A case usually requires about 100,000-200,00IU on average.

A. Usually, 50,000IU of Antitoxin should be given on the first and the following day of illness,and 10,000IU is repeated on the third,fourth and eighth day respectively.

B. The neonates with tetanus should receive 20,000-100,000IU Antitoxin within 24 hours of illness either single or separate dose.

[Adverse effects]

1.Type I hypersensitivity reaction:anaphylaxis shick may suddenly occur during or after the injection of equine antitoxin with symptoms of gloominess or dysphoria,pale or flush face,chest depression or asthma,cold sweat,nausea or abdominal pain,weak and rapid pulses,hypotension or collapse in severe case. The patient will die soon if wthout emergent treatment.

2. Serum sickness (Type III hypersensitivity reaction) may occur,frequently 7 to 10 days after the injection. The main symptoms are urticaria,high fever,lymphadenopathy,local swelling and occasional albuminuria,vomiting,join pain as well as erythema,itch and edema at the vaccination site.

[Precautions & warnings]

Before use the ampoule package must be examined with care, Any broken ampoules, or ampoules containing un-dispersive precipitates or particles must be discarded.

Before injectiong antisera,information should be obtained whenver possible as to whether previous injections of antisera have been received and whether the patient is subject to hypersensitivity disorders. Sensitivity testing should be performed before the administration of antisera. Adrenaline injection and resuscitation facilities should be available.

A sensitivity test should be done by:Dilute the antitoxin to be 1:10 with physiological ssaline (i.e.0.1ml antitoxin + 0.9ml saline), and injec 0.05ml of the flexor surface of the forearm. A positive reaction characterized by erythema,edema or infiltration appearing in 15-30 minutes denotes hypersensitiveness to horses serum preparation.

A negative reactor may be treated in the usual manner, A positive reactor must be desensitized when antitoxin administration is indispensable.

The following desensitization producedure may be recommended: dilute the antitoxin to be 1:10 with sterile physiological saline. Inject subcutaneously 0.2ml at first,observe for 30 minutes, If no reaction occurs,give another injection with increase dose. If noreaction occurs,give the third injection,and so forth. If still no reaction occurs then the administration od undiluted antitoxin can be started.

Adrenaline should always be at hangd. In case od anaphylaxis,adrenaline should be give at once. All patients developed hypersensitive reactions following injections should be handled peoperly.

[Package and Storage]

Package for prophylactic use,each ampoule contains 1500IU;3000IU. or 5000IU

Package for therapeutic use,each ampoule contains 10000IU or 20000IU.

Store in dark at 2-8°C, and not allowed to be frozen.

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