KERASTASE PARIS K SYMBIOSE SERUM NUIT ANTIPELLICULAIRE INTENSIF ANTIDANDRUFF TREATMENT- salicylic acid liquid United States - English - NLM (National Library of Medicine)

kerastase paris k symbiose serum nuit antipelliculaire intensif antidandruff treatment- salicylic acid liquid

l'oreal usa products inc. - salicylic acid (unii: o414pz4lpz) (salicylic acid - unii:o414pz4lpz) - antidandruff - helps eliminate the symptoms of dandruff condition worsens or does not improve after regular use of this product as directed

KERASTASE PARIS K SYMBIOSE SCALP RENEWAL MICRO EXFOLIATING SCRUB ANTIDANDRUFF TREATMENT- salicylic acid shampoo United States - English - NLM (National Library of Medicine)

kerastase paris k symbiose scalp renewal micro exfoliating scrub antidandruff treatment- salicylic acid shampoo

productos capilares loreal sa - salicylic acid (unii: o414pz4lpz) (salicylic acid - unii:o414pz4lpz) - antidandruff - helps eliminate the symptoms of dandruff condition worsens or does not improve after regular use of this product as directed

BAIN EXFOLIANT HYDRATANT SHAMPOO Canada - English - Health Canada

bain exfoliant hydratant shampoo

kerastase paris canada - pyrithione zinc - shampoo - 1% - pyrithione zinc 1% - miscellaneous local anti-infectives

IntronA European Union - English - EMA (European Medicines Agency)

introna

merck sharp & dohme b.v. - interferon alfa-2b - carcinoid tumor; leukemia, hairy cell; lymphoma, follicular; hepatitis b, chronic; hepatitis c, chronic; leukemia, myelogenous, chronic, bcr-abl positive; melanoma; multiple myeloma - immunostimulants, - chronic hepatitis btreatment of adult patients with chronic hepatitis b associated with evidence of hepatitis-b viral replication (presence of dna of hepatitis-b virus (hbv-dna) and hepatitis-b antigen (hbeag), elevated alanine aminotransferase (alt) and histologically proven active liver inflammation and / or fibrosis.chronic hepatitis cbefore initiating treatment with introna, consideration should be given to the results from clinical trials comparing introna with pegylated interferon.adult patientsintrona is indicated for the treatment of adult patients with chronic hepatitis c who have elevated transaminases without liver decompensation and who are positive for hepatitis-c virus-rna (hcv-rna).the best way to use introna in this indication is in combination with ribavirin.children three years of age and older and adolescentsintrona is indicated, in a combination regimen with ribavirin, for the treatment of children three years of age and older and adolescents, who have chronic hepatitis c, not previously treated, without liver decompensation, and who are positive for hcv-rna. when deciding not to defer treatment until adulthood, it is important to consider that the combination therapy induced a growth inhibition that resulted in reduced final adult height in some patients.the decision to treat should be made on a case-by-case basis.hairy-cell leukaemiatreatment of patients with hairy cell leukaemia.chronic myelogenous leukaemiamonotherapytreatment of adult patients with philadelphia-chromosome- or bcr/abl-translocation-positive chronic myelogenous leukaemia.clinical experience indicates that a haematological and cytogenetic major / minor response is obtainable in the majority of patients treated. a major cytogenetic response is defined by < 34 % ph+ leukaemic cells in the bone marrow, whereas a minor response is ≥ 34 %, but < 90 % ph+ cells in the marrow.combination therapythe combination of interferon alfa-2b and cytarabine (ara-c) administered during the first 12 months of treatment has been demonstrated to significantly increase the rate of major cytogenetic responses and to significantly prolong the overall survival at three years when compared to interferon alfa-2b monotherapy.multiple myelomaas maintenance therapy in patients who have achieved objective remission (more than 50% reduction in myeloma protein) following initial induction chemotherapy.current clinical experience indicates that maintenance therapy with interferon alfa-2b prolongs the plateau phase; however, effects on overall survival have not been conclusively demonstrated.follicular lymphomatreatment of high-tumour-burden follicular lymphoma as adjunct to appropriate combination induction chemotherapy such as a chop-like regimen. high tumour burden is defined as having at least one of the following: bulky tumour mass (> 7 cm), involvement of three or more nodal sites (each > 3 cm), systemic symptoms (weight loss > 10 %, pyrexia > 38°c for more than eight days, or nocturnal sweats), splenomegaly beyond the umbilicus, major organ obstruction or compression syndrome, orbital or epidural involvement, serous effusion, or leukaemia.carcinoid tumourtreatment of carcinoid tumours with lymph node or liver metastases and with 'carcinoid syndrome'.malignant melanomaas adjuvant therapy in patients who are free of disease after surgery but are at high risk of systemic recurrence, e.g. patients with primary or recurrent (clinical or pathological) lymph-node.

OCTREOTIDE GH octreotide as acetate 50 micrograms/1 mL injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

octreotide gh octreotide as acetate 50 micrograms/1 ml injection ampoule

generic health pty ltd - octreotide, quantity: 50 microgram - injection, solution - excipient ingredients: mannitol; glycine; water for injections; dilute hydrochloric acid - for symptomatic control and reduction of growth hormone and igf-1 plasma levels in patients with acromegaly, including those who are inadequately controlled by surgery, radiotherapy, or dopamine agonist treatment. octreotide treatment is also indicated in acromegalic patients unfit or unwilling to undergo surgery, or in the interim period until radiotherapy becomes fully effective. for the relief of symptoms associated with the following functional tumours of the gastro-entero-pancreatic endocrine system: carcinoid tumours with features of the carcinoid syndrome; vasoactive intestinal peptide secreting tumours (vipomas). octreotide is not an antitumour therapy and is not curative in these patients. for reduction of the incidence of complications following pancreatic surgery.

OCTREOTIDE GH octreotide as acetate 500 micrograms/1 mL injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

octreotide gh octreotide as acetate 500 micrograms/1 ml injection ampoule

generic health pty ltd - octreotide, quantity: 500 microgram - injection, solution - excipient ingredients: glycine; mannitol; dilute hydrochloric acid; water for injections - for symptomatic control and reduction of growth hormone and igf-1 plasma levels in patients with acromegaly, including those who are inadequately controlled by surgery, radiotherapy, or dopamine agonist treatment. octreotide treatment is also indicated in acromegalic patients unfit or unwilling to undergo surgery, or in the interim period until radiotherapy becomes fully effective. for the relief of symptoms associated with the following functional tumours of the gastro-entero-pancreatic endocrine system: carcinoid tumours with features of the carcinoid syndrome; vasoactive intestinal peptide secreting tumours (vipomas). octreotide is not an antitumour therapy and is not curative in these patients. for reduction of the incidence of complications following pancreatic surgery.

OCTREOTIDE GH octreotide as acetate 100 micrograms/1 mL injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

octreotide gh octreotide as acetate 100 micrograms/1 ml injection ampoule

generic health pty ltd - octreotide, quantity: 100 microgram - injection, solution - excipient ingredients: glycine; dilute hydrochloric acid; mannitol; water for injections - for symptomatic control and reduction of growth hormone and igf-1 plasma levels in patients with acromegaly, including those who are inadequately controlled by surgery, radiotherapy, or dopamine agonist treatment. octreotide treatment is also indicated in acromegalic patients unfit or unwilling to undergo surgery, or in the interim period until radiotherapy becomes fully effective. for the relief of symptoms associated with the following functional tumours of the gastro-entero-pancreatic endocrine system: carcinoid tumours with features of the carcinoid syndrome; vasoactive intestinal peptide secreting tumours (vipomas). octreotide is not an antitumour therapy and is not curative in these patients. for reduction of the incidence of complications following pancreatic surgery.

XGEVA denosumab (rch) 70mg/mL (120mg/1.7mL) solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

xgeva denosumab (rch) 70mg/ml (120mg/1.7ml) solution for injection vial

amgen australia pty ltd - denosumab, quantity: 120 mg - injection, solution - excipient ingredients: sorbitol; sodium hydroxide; glacial acetic acid; water for injections; polysorbate 20 - prevention of skeletal related events in patients with multiple myeloma and in patients with bone metastases from solid tumours. treatment of giant cell tumour of bone in adults or skeletally mature adolescents that is recurrent, or unresectable, or resectable but associated with severe morbidity. treatment of hypercalcaemia of malignancy that is refractory to intravenous bisphosphonate.

OCTREOTIDE SUN octreotide (as acetate) 50 microgram/1 mL solution for injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

octreotide sun octreotide (as acetate) 50 microgram/1 ml solution for injection ampoule

sun pharma anz pty ltd - octreotide, quantity: 50 microgram - injection, solution - excipient ingredients: water for injections; sodium chloride; glacial acetic acid; sodium acetate trihydrate - for symptomatic control and reduction of growth hormone and igf-l plasma levels in patients with acromegaly, including those who are inadequately controlled by surgery, radiotherapy, or dopamine agonist treatment. octreotide treatment is also indicated in acromegalic patients unfit or unwilling to undergo surgery, or in the interim period until radiotherapy becomes fully effective.,for the relief of symptoms associated with the following functional tumours of the gastro-entero-pancreatic endocrine system: - carcinoid tumours with features of the carcinoid syndrome - vasoactive intestinal peptide secreting tumours [vipomas] octreotide is not curative in these patients.,for reduction of the incidence of complications following pancreatic surgery.

OCTREOTIDE SUN octreotide (as acetate) 100 microgram/1 mL solution for injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

octreotide sun octreotide (as acetate) 100 microgram/1 ml solution for injection ampoule

sun pharma anz pty ltd - octreotide, quantity: 100 microgram - injection, solution - excipient ingredients: water for injections; sodium chloride; sodium acetate trihydrate; glacial acetic acid - for symptomatic control and reduction of growth hormone and igf-l plasma levels in patients with acromegaly, including those who are inadequately controlled by surgery, radiotherapy, or dopamine agonist treatment. octreotide treatment is also indicated in acromegalic patients unfit or unwilling to undergo surgery, or in the interim period until radiotherapy becomes fully effective.,for the relief of symptoms associated with the following functional tumours of the gastro-entero-pancreatic endocrine system: - carcinoid tumours with features of the carcinoid syndrome - vasoactive intestinal peptide secreting tumours [vipomas] octreotide is not curative in these patients.,for reduction of the incidence of complications following pancreatic surgery.