BECOTIDE 50 INHALER* South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

becotide 50 inhaler*

sekpharma (pty) ltd - inhaler - each metered dose contains beclomethasone dipropionate 50 ug

BECOTIDE ROTACAPS 100 ug Inhaler South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

becotide rotacaps 100 ug inhaler

sekpharma (pty) ltd - inhaler - each capsule contains beclomethasone dipropionate equivalent to beclomethasone 100,0 ug

BECOTIDE ROTACAPS 200 ug Inhaler South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

becotide rotacaps 200 ug inhaler

sekpharma (pty) ltd - inhaler - each capsule contains beclomethasone dipropionate equivalent to beclomethasone 200,0 ug

BECOTIDE 100 Inhaler South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

becotide 100 inhaler

sekpharma (pty) ltd - inhaler - each metered dose contains beclomethasone dipropionate solvate equivalent to 200 g beclomethasone dipropionate

Becotide 100 Namibia - English - Namibia Medicines Regulatory Council

becotide 100

glaxosmithkline (sa) (pty) ltd - beclomethasone dipropionate - inhaler - 100?g beclomethasone dipropionate

Becotide 50 Inhaler Namibia - English - Namibia Medicines Regulatory Council

becotide 50 inhaler

glaxosmithkline (sa) (pty) ltd - beclomethasone dipropionate - inhaler - 50?g beclomethosone propionate

HUMATROPE somatropin 18IU (6mg) powder for injection cartridge with diluent syringe Australia - English - Department of Health (Therapeutic Goods Administration)

humatrope somatropin 18iu (6mg) powder for injection cartridge with diluent syringe

eli lilly australia pty ltd - somatropin, quantity: 6 mg (equivalent: somatropin, qty 18 iu) - injection, solution - excipient ingredients: water for injections; sodium hydroxide; glycerol; hydrochloric acid; metacresol - humatrope is indicated for the long-term treatment of children who have growth failure due to inadequate secretion of normal endogenous growth hormone.,humatrope is also indicated for the treatment of growth disturbances associated with gonadal dysgenesis (turner syndrome).,humatrope is also indicated for the treatment of adults with severe growth hormone deficiency defined as patients with known hypothalamic-pituitary pathology and at least one known deficiency of a pituitary hormone not being prolactin. these patients should undergo a single dynamic test in order to diagnose or exclude a growth deficiency. in patients with childhood onset isolated gh deficiency (no evidence of hypothalamic-pituitary disease or cranal irradiation), two dynamic tests should be recommended, except for those having low igf-i concentrations less than or equal to 2 sds who may be considered for one test. the cut-off point of the dynamic test should be strict.,humatrope is also indicated for the treatment of growth retardation in prepubertal children with chronic renal insufficiency whose height is on or less than the twenty-fifth percentile and whose growth velocity is on or less than the twenty-fifth percentile for bone age. chronic renal insufficiency is defined as glomerular filtration rate of less than 30 ml/min/1.73 m2.,humatrope is also indicated for the treatment of growth failure in children born small for gestational age (sga) who fail to demonstrate catch-up growth by age two to four years (see clinical trials). humatrope is also indicated for the treatment of growth failure in children born small for gestational age (sga) who fail to demonstrate catch-up growth by age two to four years. (see clinical trials)