BYETTA 5 ug INJECTION South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

byetta 5 ug injection

astrazeneca pharmaceuticals (pty) ltd - injection - see ingredients - each dose contains exenatide 5,0 ug

BYETTA 10 ug INJECTION South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

byetta 10 ug injection

astrazeneca pharmaceuticals (pty) ltd - injection - see ingredients - each dose contains exenatide 10,0 ug

BYDUREON BCISE INJECTION South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

bydureon bcise injection

astrazeneca pharmaceuticals (pty) ltd - injection - 2,0 mg - each dose (0,85 ml) contains exenatide 2,0 mg

Saxenda New Zealand - English - Medsafe (Medicines Safety Authority)

saxenda

novo nordisk pharmaceuticals ltd - liraglutide 6 mg/ml;   - solution for injection - 6 mg/ml - active: liraglutide 6 mg/ml   excipient: dibasic sodium phosphate dihydrate hydrochloric acid phenol propylene glycol sodium hydroxide water for injection - saxenda is indicated as an adjunct to a reduced-calorie diet and increased physical activity for weight management in adult patients with an initial body mass index (bmi) of · 30 kg/m2 or greater (obese) or · 27 kg/m2 or greater (overweight) in the presence of at least one weight related comorbidity, such as dysglycaemia (pre-diabetes and type 2 diabetes mellitus), hypertension, dyslipidaemia, or obstructive sleep apnoea. treatment with saxenda should be discontinued after 12 weeks on the 3.0 mg/day dose if a patient has not lost at least 5% of their initial body weight.