AGRIPPAL GS1 不活化流感疫苗 (2014/2015 季節) 2. 組成 每0.5 ml 劑量含以下流感病毒株的表面抗原( 血球凝集素和神經胺酶)*： A/California/7/2009 (H1N1)pdm09– nlike strain (A/California/7/2009, NYMC X-181 ...
15/8/2020 · Agrippal S1 Injection is used in the treatment of Influenza (flu). View Agrippal S1 Injection (vial of 1 ml Injection) uses, composition, side-effects, price, substitutes, drug interactions, precautions, warnings, expert advice and buy online at ...
Agrippal S-1 is a suspension containing highly purified surface antigens of Influenza Virus Types A and B propagated in chick embryo cell cultures and inactivated with Betapropiolactone. Each 0,5 mL dose contains inactivated influenza virus ...
- Dosage Form, Composition and Packaging
- Pharmacological Action
- Side Effect
- Pregnancy and Lactation
- Drug Interactions
- Terms and Conditions of Storage
Suspension for the m and s/to the introduction *as a colorless, a transparent liquid. Excipients: sodium chloride, potassium chloride, potassium phosphate dwuzameshchenny, sodium phosphate dwuzameshchenny two-water, magnesium chloride, calcium chloride, water d / and. * hemahhlyutynyn. ** the antigenic composition of vaccines in line with the recommendations of who the current epidemic season and annually updated according to who recommendations. 0.5 ml – glass syringes with needles (1) – blisters (1) – packs cardboard.
A vaccine for the prevention of influenza. A protective level of antibodies usually develops through 2-3 weeks after inoculation, duration of immunity varies from 6 to 12 Months.
Vaccine Agrippal S1 is designed for the prevention of influenza from 6 months of age. Immunization is particularly suitable for adults and children of the following risk groups: — adults and children with concomitant diseases of the cardiovascular system, chronic respiratory diseases, chronic kidney disease, with diabetes and other chronic metabolic diseases, chronic anemias, congenital and acquired immunodeficiency; -persons over 60 years; -persons with high occupational risk of infection and persons, which, because of their professional activities can be a source of infection. In times of epidemics or pandemics, it is recommended that vaccination of all population groups.
The vaccine should not be administered in /! The vaccine is injected in/m, mainly in the deltoid muscle, or deep-n/a. In young children the vaccine can be administered in front of the lateral part of the thigh. Before use, the contents of the syringe should be brought to room temperature. Carefully shake. Babies with 6 Months before 35 Monthsappointed 0.25 ml (half dose). Babies, that have not been previously vaccinated, recommended vaccination dvukratnaya at intervals 4 of the week. Children from 35 Months, adolescents and adults appointed 0.5 ml. When you use a syringe, contains 0.5 ml of the vaccine for the immunization of children, which shows the introduction of half-dose (0.25 ml), you need to remove half of its content, pushing the plunger, to special risks. You then enter the remaining number of vaccines. Vaccination should be carried out, if possible, before the start of flu season (in autumn and winter). However, depending on the epidemiological situation may need to condu...
Normal (≥1/100, <1/10) Local reactions:redness, bruise, packing, soreness and swelling at the injection site. Common reactions:temperature rise, malaise, chills, weakness, headache, Sweating, myalgia, arthralgia. These side effects usually disappear on their own through the 1-2 day. Unusual (≥1/1000, <1/100) Dermatological reactions: General skin reactions, including itching, krapivnicu, nonspecific skin irritation. Few (≥1/10 000, <1/1000) From the nervous system: neuralgia, paraesthesia (burning sensation, numbness), convulsions. From the hematopoietic system:short thrombocytopenia. Allergic reactions were noted, in rare cases, lead to the development of shock, symptoms of a serious allergic reactions up to and including anaphylactic reaction: a sudden sharp fall in HELL, increase or drop in HEART RATE, unusual weakness or malaise, anxiety, nervousness, loss of consciousness, difficulty breathing and swallowing, itch (especially on the feet and palms), urticaria with swelling or w...
-hypersensitivity to chicken egg protein; — history of allergic reactions to other components, included in vaccines, or preceding the drug vaccination. Vaccination of persons, survivors of acute infectious disease, is done through 1 months after convalescence. In light forms disease vaccination may be carried out after the normalization of the temperature.
Experience of using the vaccine among pregnant women revealed, Agrippal S1 that has no teratogenic or toxic effects on the body. This vaccine can be applied from the second trimester of pregnancy. Pregnant women, medically at risk of developing complications after influenza infection, vaccination is recommended for any pregnancy. Vaccination may be carried out during the entire lactation period (breast-feeding).
As is the case with the other injectable vaccines, should always be available funds, applicable in the case of rare anaphylactic reactions. The vaccine may contain residual formaldehyde, cetiltrimetilammonija bromide and polisorbata 80, used in the production of vaccines (can cause hypersensitivity).
The application of vaccines Agrippal S1 within a calendar preventive vaccination in case and inactivated vaccines national calendar of preventive vaccination may be simultaneously subject to the introduction of different needles in different parts of the body or with an interval of one month. This should take into account the possibility of strengthening the intensity of adverse reactions. Patients, receiving immunosuppressive therapy, as well as in patients with congenital and acquired immunodeficiency vaccination may be less effective. After influenza vaccination were marked by false positive results of antibody by ELISA against HIV infection (HIV1), hepatitis c and especially against the t-cell to grow human virus (HTLV1). To exclude false positive result it is necessary to undertake a study on the method of WesternBlot. Transient absorption results can be linked with the advent of the immunoglobulin IgM, as a response to vaccination. Vaccine Agrippal S1 must not be mixed with ot...
The vaccine should be stored in the dark, reach of children, at a temperature of from 2 ° to 8 ° C.; Do not freeze. The vaccine should be transported in accordance with the SP 220.127.116.118-03 all kinds of covered transport at a temperature from 2° to 8° c; Do not freeze. Shelf life – 12 Months. Do not use the vaccine after the expiration date, indicated on the label and outer package.
AGRIPPAL S1 Suspension for injection 本藥須由醫師處方使用 1. 品名 AGRIPPAL S1 不活化流感疫苗 (2017/2018 季節) 2. 組成 每0.5 ml 劑量含以下流感病毒株的表面抗原(血球凝集素和神經胺酶)*： A/Michigan/45/2015 (H1N1)pdm09 - like
What does agrippal S-1 influenza vaccine stand for?
Is it safe to inject agrippal S-1 intravenously?
Can you take agrippal if you have a fever?
AGRIPPAL S1 用藥指導單張 ATC7藥理類別 J07BB02 influenza, purified antigen 孕婦用藥分級 C 級： 在對照的動物研究試驗中顯示該藥學物對胚胎有不良反應（致畸胎性或殺胚胎性或其他），但未進行人體懷孕婦女研究；或者尚無對照的人體懷孕婦女或動物
Agrippal S1-Novartis Vaccines and Diagnostics S.r.l. PIL -GB June 2008 Confidential Page 1 of 3 AGRIPPAL S1 J07BB02 Influenza Vaccine, Surface Antigen, Inactivated Suspension for injection in pre-filled syringe 2008/2009 Season Composition. ...
Agrippal is indicated for the prevention of influenza caused by Influenza Virus, Types A and B. Immunization Guideline Adults and children from 36 months: 0.5 mL. Children 6 months to 35 months of age: 0.25 mL. For children less than 9 years of ...
Agrippal should under no circumstances be administered intravascularly. Anxiety-related reactions, including vasovagal reactions (syncope), hyperventilation or stress-related reactions can occur following, or even before, any vaccination as a ...
AGRIPPAL® 2015 Published by MIMS June 2015 2 Having other vaccines Tell your doctor if you have had any vaccines in the last 4 weeks. Your doctor will tell you if Agrippal vaccine can be given at the same visit as another vaccine. Your doctor ...