Quest for the right Drug
הבריקס 720 ג'וניור HAVRIX 720 JUNIOR (HEPATITIS A VIRUS ANTIGEN, INACTIVATED)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-שרירי : I.M
צורת מינון:
תרחיף להזרקה : SUSPENSION FOR INJECTION
עלון לרופא
מינוניםPosology התוויות
Indications תופעות לוואי
Adverse reactions התוויות נגד
Contraindications אינטראקציות
Interactions מינון יתר
Overdose הריון/הנקה
Pregnancy & Lactation אוכלוסיות מיוחדות
Special populations תכונות פרמקולוגיות
Pharmacological properties מידע רוקחי
Pharmaceutical particulars אזהרת שימוש
Special Warning עלון לרופא
Physicians Leaflet
Adverse reactions : תופעות לוואי
4.8 Undesirable effects Summary of the safety profile The most common local undesirable effects, both in children and adults, are pain and redness at the injection site. The most common general undesirable effects are, in children, irritability and in adults, fatigue and headache. Tabulated list of adverse reactions Clinical trial data The safety profile presented in the table below is based on data from 5 331 subjects including 1 664 children (up to 18 years of age) vaccinated with Havrix 720 Junior and 3 667 adults (from 16 years of age) vaccinated with Havrix 1440 Adult, in clinical trials (total vaccinated cohort). A total of 3 193 doses of Havrix 720 Junior and 7 131 doses of Havrix 1440 Adult were administered during clinical trials. A total number of 3 971 doses of Havrix 1440 Adult were administered concomitantly with Engerix-B in 2 064 adult subjects. Adverse reactions reported are listed according to the following frequency: Very common (≥1/10) Common (≥1/100 to <1/10) Uncommon (≥1/1 000 to <1/100) Rare (≥1/10 000 to <1/1 000) Very rare (<1/10 000) Within each frequency grouping the adverse reactions are presented in the order of decreasing seriousness. System organ class Frequency Adverse reactions Upper respiratory tract infection (2), Infections and infestations Uncommon rhinitis Metabolism and nutrition disorders Common Appetite lost Psychiatric disorders Very common Irritability (1) Very common Headache (3) Common Drowsiness (1) Nervous system disorders Uncommon Dizziness (2) Rare Hypoaesthesia (2), paraesthesia (2) Gastrointestinal signs and symptoms (2) (5), Common Gastrointestinal disorders diarrhoea (4), nausea Uncommon Vomiting Uncommon Rash (1) Skin and subcutaneous tissue disorders Rare Pruritus (2) Musculoskeletal and connective tissue Uncommon Myalgia (2), musculoskeletal stiffness (2) disorders Injection site pain and injection site Very common erythema, fatigue (2) Malaise, fever (≥37.5 C), injection site General disorders and administration Common reaction (such as injection site site conditions induration (4) and injection site swelling) Uncommon Influenza like illness (2) Rare Chills (2) (1) only with Havrix 720 Junior (2) only with Havrix 1440 Adult (3) reported with a frequency of common with Havrix 720 Junior (4) reported with a frequency of uncommon with Havrix 720 Junior (5) gastrointestinal = including nausea, vomiting, diarrhoea (symptoms not separately recorded) Post-marketing data The following additional adverse reactions have been identified during post-marketing surveillance with both Havrix 720 Junior and Havrix 1440 Adult. System organ class Frequency Adverse reactions Anaphylaxis, allergic reactions including Immune system disorders Rare anaphylactoid reactions and serum sickness-like reaction Nervous system disorders Rare Convulsions Vascular disorders Rare Vasculitis Angioneurotic oedema, erythema Skin and subcutaneous tissue disorders Rare multiforme, urticaria Musculoskeletal and connective tissue Rare Arthralgia disorders Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Any suspected adverse events should be reported to the Ministry of Health according to the National Regulation by using an online form https://sideeffects.health.gov.il/ Additionally, you should also report to GSK Israel (il.safety@gsk.com).
שימוש לפי פנקס קופ''ח כללית 1994
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תאריך הכללה מקורי בסל
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הגבלות
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מידע נוסף