Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - influenza virus a (h1n1) haemagglutinin 15ug (a/wisconsin/67/2022 (h1n1)pdm09-like virus (a/georgia/12/2022 (cvr-167))); influenza virus a (h3n2) haemagglutinin 15ug (a/massachusetts/18/2022 (h3n2)-like virus (a/sydney/1304/2022)); influenza virus b (victoria) haemagglutinin 15ug (b/austria/1359417/2021-like virus (b/victoria lineage) (b/singapore/wuh4618/2021)); influenza virus b (yamagata) haemagglutinin 15ug (b/phuket/3073/2013-like virus (b/yamagata lineage) (b/singapore/inftt-16-0610/2016)) - suspension for injection - 60 mcg/0.5ml - active: influenza virus a (h1n1) haemagglutinin 15ug (a/wisconsin/67/2022 (h1n1)pdm09-like virus (a/georgia/12/2022 (cvr-167))) influenza virus a (h3n2) haemagglutinin 15ug (a/massachusetts/18/2022 (h3n2)-like virus (a/sydney/1304/2022)) influenza virus b (victoria) haemagglutinin 15ug (b/austria/1359417/2021-like virus (b/victoria lineage) (b/singapore/wuh4618/2021)) influenza virus b (yamagata) haemagglutinin 15ug (b/phuket/3073/2013-like virus (b/yamagata lineage) (b/singapore/inftt-16-0610/2016)) excipient: dibasic sodium phosphate dihydrate magnesium chloride hexahydrate monobasic potassium phosphate potassium chloride sodium chloride water for injection - flucelvax quad is indicated for the prevention of influenza caused by influenza virus types a and b contained in the vaccine. the vaccine is indicated for use in individuals 6 months of age and above. for full details regarding recommendations for influenza vaccination, please refer to the relevant national immunisation guidelines.

Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - influenza virus a (h1n1) haemagglutinin 15ug (a/victoria/4897/2022 (h1n1)pdm09-like virus (a/victoria/4897/2022 (ivr-238))); influenza virus a (h3n2) haemagglutinin 15ug (a/thailand/8/2022 (h3n2)-like virus (a/thailand/8/2022 (ivr-237))); influenza virus b (victoria) haemagglutinin 15ug (b/austria/1359417/2021(b/victoria lineage)-like virus (b/austria/1359417/2021 (bvr-26))); influenza virus b (yamagata) haemagglutinin 15ug (b/phuket/3073/2013-like virus (b/phuket/3073/2013 bvr-1b)) - suspension for injection - 60 mcg/0.5ml - active: influenza virus a (h1n1) haemagglutinin 15ug (a/victoria/4897/2022 (h1n1)pdm09-like virus (a/victoria/4897/2022 (ivr-238))) influenza virus a (h3n2) haemagglutinin 15ug (a/thailand/8/2022 (h3n2)-like virus (a/thailand/8/2022 (ivr-237))) influenza virus b (victoria) haemagglutinin 15ug (b/austria/1359417/2021(b/victoria lineage)-like virus (b/austria/1359417/2021 (bvr-26))) influenza virus b (yamagata) haemagglutinin 15ug (b/phuket/3073/2013-like virus (b/phuket/3073/2013 bvr-1b)) excipient: calcium chloride dihydrate citric acid monohydrate dibasic sodium phosphate dihydrate magnesium chloride hexahydrate monobasic potassium phosphate polysorbate 80 potassium chloride sodium chloride sodium citrate dihydrate sorbitan trioleate squalene water for injection - active immunisation against influenza in persons 65 years of age and older.

Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - diphtheria toxoid, adsorbed 2 [iu] (not less than 2iu/0.5ml); tetanus toxoid, adsorbed 20 [iu] (not less than 20iu/0.5ml) - suspension for injection - 2iu/20iu - active: diphtheria toxoid, adsorbed 2 [iu] (not less than 2iu/0.5ml) tetanus toxoid, adsorbed 20 [iu] (not less than 20iu/0.5ml) excipient: aluminium hydroxide sodium chloride sodium hydroxide water for injection - vaccination of children (not less than 5 years of age) and adults who have previously received at least 3 doses of a vaccine for primary immunisation against diphtheria and tetanus. adt booster is not intended for primary immunisation against diphtheria and tetanus.

Австралия - английски - Department of Health (Therapeutic Goods Administration)

seqirus pty ltd - diphtheria toxoid, quantity: 4 iu/ml; tetanus toxoid, quantity: 40 iu/ml - injection, suspension - excipient ingredients: water for injections; sodium hydroxide; aluminium hydroxide hydrate; sodium chloride - vaccination of children (greater than or equal to 5 years of age) and adults who have previously received at least 3 doses of a vaccine for primary immunisation against diphtheria and tetanus. adt booster is not intended for primary immunisation against diphtheria and tetanus. use of adt booster should be scheduled in accordance with official national recommendations.

Австралия - английски - Department of Health (Therapeutic Goods Administration)

seqirus pty ltd - tetanus toxoid, quantity: 40 iu/ml; diphtheria toxoid, quantity: 4 iu/ml - injection, suspension - excipient ingredients: water for injections; sodium chloride; aluminium hydroxide hydrate; sodium hydroxide - vaccination of children (greater than or equal to 5 years of age) and adults who have previously received at least 3 doses of a vaccine for primary immunisation against diphtheria and tetanus. adt booster is not intended for primary immunisation against diphtheria and tetanus. use of adt booster should be scheduled in accordance with official national recommendations.

Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - tramadol hydrochloride 50mg; tramadol hydrochloride 50mg; tramadol hydrochloride 50mg - capsule - 50 mg - active: tramadol hydrochloride 50mg excipient: colloidal silicon dioxide gelatin indigo carmine ink iron oxide yellow magnesium stearate microcrystalline cellulose sodium starch glycolate titanium dioxide active: tramadol hydrochloride 50mg excipient: colloidal silicon dioxide gelatin indigo carmine ink iron oxide yellow magnesium stearate microcrystalline cellulose sodium starch glycolate titanium dioxide active: tramadol hydrochloride 50mg excipient: colloidal silicon dioxide gelatin iron oxide yellow magnesium stearate microcrystalline cellulose sodium laurilsulfate sodium starch glycolate titanium dioxide - relief of moderate to severe pain.

Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - tramadol hydrochloride 50 mg/ml - solution for injection - 100 mg/2ml - active: tramadol hydrochloride 50 mg/ml excipient: sodium acetate trihydrate water for injection - relief of moderate to severe pain.

Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - tramadol hydrochloride 50 mg/ml - solution for injection - 50 mg/ml - active: tramadol hydrochloride 50 mg/ml excipient: sodium acetate trihydrate water for injection - relief of moderate to severe pain.

Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - tramadol hydrochloride 100 mg/ml - oral solution - 100 mg/ml - active: tramadol hydrochloride 100 mg/ml excipient: aniseed flavour (87122) glycerol mint oil, partially dementholised polyethylene glycol hydrogenated castor oil potassium sorbate propylene glycol purified water saccharin sodium sodium cyclamate sucrose - relief of moderate to severe pain.

Нова Зеландия - английски - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - tramadol hydrochloride 100mg - modified release tablet - 100 mg - active: tramadol hydrochloride 100mg excipient: colloidal silicon dioxide hypromellose   lactose monohydrate macrogol 6000 magnesium stearate microcrystalline cellulose propylene glycol purified talc titanium dioxide - relief of moderate to severe pain.