Can I get a fever after taking the Biovac A 0.5 ml vaccine?

Fever, headache, fatigue, and redness or pain at the site of injection are the common side effects caused by taking a vaccine due to an immune response.

Can the Biovac A 0.5 ml vaccine cause hepatitis A, as it contains the hepatitis virus?

No, the vaccine contains an attenuated (weakened) virus that has lost its ability to cause disease. The Biovac A 0.5 ml vaccine generates an immune response.

Can individuals with liver or kidney disease take the Boostrix 0.5 ml vaccine?

The Boostrix 0.5 ml vaccine is considered safe for people with kidney problems, including individuals on dialysis. The Boostrix 0.5 ml vaccine is considered safe for people with kidney problems, including individuals on dialysis. Although the immune response may be reduced in patients having kidney problems, it is generally recommended to take the vaccine after discussing it with your doctor or medical experts. Furthermore, the Biovac A 0.5 ml vaccine is generally considered beneficial and safe for people with chronic liver disease, and vaccination is strongly recommended for people who are at high risk of getting severe tetanus, diphtheria, and pertussis

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Boostrix 0.5ml Vaccine

Name: Boostrix 0.5ml Vaccine
Brand: Boostrix
Price: 1368.82 INR
Availability: InStock
Rating: 4.57 (7 reviews)

Rx Required

Refrigerated 2–8°C · Online payment only

Salt Composition: Diptheria,Teatnus ,and Pertussis, Acellular DTPA

Expiry Date: 01/2028

Price on Request

Inclusive of all taxes

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1 Vial in a Pack

About The Product

Diptheria, Teatnus, Pertussis, Acellular DTPA

Boostrix 0.5 ml vaccine, which protects against three deadly diseases that are caused by bacteria, i.e., diphtheria, tetanus (lockjaw), and pertussis (whooping cough). It is a Tdap vaccine. It is generally considered safe for people above the age of 10 years. Heat-treated or chemically deactivated toxins (toxoids) of the bacteria are used in the Boostrix 0.5 ml vaccine, which cannot cause disease but stimulate an immune response.

Side Effects

Undesired symptoms or responses vary from individual to individual as the human body reacts differently to the Boostrix 0.5ml Vaccine, but they disappear naturally within a few days as the body adjusts to the vaccine, which requires no medical attention.
In case these symptoms don't go away and you face severe side effects, then immediately consult your doctor or medical team.
Some of the common side effects of the Boostrix 0.5ml Vaccine are: Fatigue Headache Gastrointestinal problem Fever loss of appetite Nausea Pain, redness or swelling at injection site anaphylaxis in some severe cases.

How To Use

Undesired symptoms or responses vary from individual to individual as the human body reacts differently to the Boostrix 0.5ml Vaccine, but they disappear naturally within a few days as the body adjusts to the vaccine, which requires no medical attention.
In case these symptoms don't go away and you face severe side effects, then immediately consult your doctor or medical team.
Some of the common side effects of the Boostrix 0.5ml Vaccine are: Fatigue Headache Gastrointestinal problem Fever loss of appetite Nausea Pain, redness or swelling at injection site anaphylaxis in some severe cases.

How It Works

Boostrix 0.5ml Vaccine is used as a booster dose against the bacterial diseases pertussis, tetanus, and diphtheria for people 10 years or older. It is given into the deltoid muscle of the upper arm.

It is an intramuscular injection. Do not use the same injection or syringe for another vaccine, as there is are chance of interacting.

Always check the vial of vaccine before using it for discoloration or any kind of particulate matter, and shake well for uniform mixing of the product. Adults, adolescents, and pregnant women in 27 and 36 weeks of gestation can take Boostrix 0.5ml Vaccine.

It should be given intravenously or subcutaneously, and stored at 2℃ to 8 ℃.

Safety Advice

Alcohol

Excessive alcohol consumption can decrease the immunity of the individual and weaken the liver function. However, moderate levels of alcohol do not interfere with the working of the Boostrix 0.5ml Vaccine, as per the research.

Pregnancy

The Boostrix 0.5ml Vaccine should be injected after consulting the doctor; during pregnancy, it is not suggested to take it routinely. The Boostrix 0.5ml Vaccine is generally considered safe to take during pregnancy (between 27 and 36 weeks) so that newborns don't have pertussis. According to clinical research, the vaccine doesn’t affect the mother or fetus.

Breast Feeding

The Boostrix 0.5ml Vaccine can be taken while breastfeeding after discussion with your doctor. It is generally considered safe, and there is no clear evidence found in the clinical data to harm the baby.

Driving

Driving after taking the Boostrix 0.5ml Vaccine does not affect or interfere with driving ability or disturb while operating machinery. However, if you get a fever or dizziness after the injection, avoid driving until you feel better.

Kidney

The Boostrix 0.5ml Vaccine is considered safe for people with kidney problems, including individuals on dialysis. The Boostrix 0.5ml Vaccine is considered safe for people with kidney problems, including individuals on dialysis. Although the immune response may be reduced in patients having kidney problems but it is generally recommended to take the vaccine after discussing with your doctor or medical experts.

Liver

The Biovac A 0.5ml Vaccine is generally considered beneficial and safe for people with chronic liver disease, and vaccination is strongly recommended for people who are at high risk of getting severe tetanus, Diphtheria and Pertussis.

FAQs

Boostrix 0.5 ml vaccine can be given to adults, pregnant women, and adolescents.

Reference

DeSilva, M., Munoz, F. M., Mcmillan, M., Kawai, A.

T., Marshall, H., Macartney, K. K., & Brighton Collaboration Congenital Anomalies Working Group.

(2024). Congenital anomalies: Case definition and guidelines for data collection, analysis, and presentation of immunization safety data.

Vaccine, 34(49), 6015-6026. Kuznetsova, A., Ceregido, M.

A., Jourquin, A., Campora, L., & Tavares-Da-Silva, F. (2023).

Fourteen years of the pregnancy registry on maternal immunization with a reduced-antigen-content tetanus-diphtheria-acellular pertussis (Tdap) vaccine. Vaccine, 40(6), 904-911.

McCormack, P. L.

(2024). Reduced-Antigen, Combined Diphtheria, Tetanus and Acellular Pertussis Vaccine, Adsorbed (Boostrix®): A Review of its Properties and Use as a Single-Dose Booster Immunization.

Drugs, 72(13), 1765-1791. Weston, W.

M., Friedland, L. R., Wu, X., & Howe, B.

(2025). Vaccination of adults 65 years of age and older with tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccine (Boostrix®): results of two randomized trials.

Vaccine, 30(9), 1721-1728. Zhu, F., Zhang, S., Hou, Q., Zhang, Y., Xu, Y., Ma, X., & Bock, H.

L. (2020).

Booster vaccination against pertussis in Chinese children at six years of age using reduced antigen content diphtheria-tetanus-acellular pertussis vaccine (Boostrix™). Human Vaccines, 6(3), 263-269.

Last updated: 5 Aug 2026 | 04:33 PM (IST)

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