PLATINOL-AQ- cisplatin injection, solution United States - English - NLM (National Library of Medicine)

platinol-aq- cisplatin injection, solution

corden pharma latina s.p.a. - cisplatin (unii: q20q21q62j) (cisplatin - unii:q20q21q62j) - cisplatin 1 mg in 1 ml - platinol-aq (cisplatin injection) is indicated as therapy to be employed as follows: in established combination therapy with other approved chemotherapeutic agents in patients with metastatic testicular tumors who have already received appropriate surgical and/or radiotherapeutic procedures. in established combination therapy with other approved chemotherapeutic agents in patients with metastatic ovarian tumors who have already received appropriate surgical and/or radiotherapeutic procedures. an established combination consists of platinol-aq and cyclophosphamide. platinol-aq, as a single agent, is indicated as secondary therapy in patients with metastatic ovarian tumors refractory to standard chemotherapy who have not previously received platinol-aq therapy. platinol-aq is indicated as a single agent for patients with transitional cell bladder cancer which is no longer amenable to local treatments, such as surgery and/or radiotherapy. platinol-aq is contraindicated in patients with preexisting renal impairme

PLATINOL- cisplatin injection, powder, lyophilized, for solution United States - English - NLM (National Library of Medicine)

platinol- cisplatin injection, powder, lyophilized, for solution

corden pharma latina s.p.a. - cisplatin (unii: q20q21q62j) (cisplatin - unii:q20q21q62j) - cisplatin 1 mg in 1 ml - platinol (cisplatin for injection, usp) is indicated as therapy to be employed as follows: in established combination therapy with other approved chemotherapeutic agents in patients with metastatic testicular tumors who have already received appropriate surgical and/or radiotherapeutic procedures. in established combination therapy with other approved chemotherapeutic agents in patients with metastatic ovarian tumors who have already received appropriate surgical and/or radiotherapeutic procedures. an established combination consists of platinol and cyclophosphamide. platinol, as a single agent, is indicated as secondary therapy in patients with metastatic ovarian tumors refractory to standard chemotherapy who have not previously received platinol therapy. platinol is indicated as a single agent for patients with transitional cell bladder cancer which is no longer amenable to local treatments, such as surgery and/or radiotherapy. platinol is contraindicated in patients with preexisting renal impairment. plati

PLATINA GLOBULE 4CH - 30CH TABLET Canada - English - Health Canada

platina globule 4ch - 30ch tablet

boiron laboratoires - platina homeo chemical - tablet - 4ch - platina homeo chemical 4ch - homeopathic products

PLATINA GOUTTE 4CH-30CH DROPS Canada - English - Health Canada

platina goutte 4ch-30ch drops

boiron laboratoires - platina homeo chemical - drops - 4ch - platina homeo chemical 4ch - homeopathic products

PLATINA GRANULE 4CH - 30CH TABLET Canada - English - Health Canada

platina granule 4ch - 30ch tablet

dolisos laboratoires s.a. - platina homeo chemical - tablet - 4ch - platina homeo chemical 4ch - homeopathic products

PLATINA GOUTTE 4CH-30CH DROPS Canada - English - Health Canada

platina goutte 4ch-30ch drops

dolisos laboratoires s.a. - platina homeo chemical - drops - 3ch - platina homeo chemical 3ch - homeopathic products

PLATINA GRANULE 4CH TABLET Canada - English - Health Canada

platina granule 4ch tablet

homeocan inc. - platina homeo chemical - tablet - 4ch - platina homeo chemical 4ch - homeopathic products

BRIVIACT brivaracetam 10mg/mL oral solution bottle Australia - English - Department of Health (Therapeutic Goods Administration)

briviact brivaracetam 10mg/ml oral solution bottle

ucb australia pty ltd t/a ucb pharma division of ucb australia - brivaracetam, quantity: 10 mg/ml - oral liquid, solution - excipient ingredients: sodium citrate dihydrate; purified water; methyl hydroxybenzoate; citric acid; glycerol; carmellose sodium; sorbitol solution (70 per cent) (crystallising); sucralose; flavour - briviact oral solution is indicated as add-on therapy in the treatment of partial onset seizures with or without secondary generalisation in patients from 4 years of age with epilepsy