BARACLUDE TABLET 0.5mg Singapore - English - HSA (Health Sciences Authority)

baraclude tablet 0.5mg

bristol-myers squibb (singapore) pte. ltd. - entecavir - tablet, film coated - 0.5 mg - entecavir 0.5 mg

BARACLUDE TABLET 1mg Singapore - English - HSA (Health Sciences Authority)

baraclude tablet 1mg

bristol-myers squibb (singapore) pte. ltd. - entecavir - tablet, film coated - 1 mg - entecavir 1 mg

BARACLUDE ORAL SOLUTION 0.05mg/mL Singapore - English - HSA (Health Sciences Authority)

baraclude oral solution 0.05mg/ml

bristol-myers squibb (singapore) pte. ltd. - entecavir - solution - 0.05mg/ml

NIVOLUMAB BMS CONCENTRATE FOR SOLUTION FOR INFUSION 10MGML Singapore - English - HSA (Health Sciences Authority)

nivolumab bms concentrate for solution for infusion 10mgml

bristol-myers squibb (singapore) pte. ltd. - nivolumab - infusion, solution concentrate - nivolumab 10 mg/ml

SPRYCEL TABLETS 20MG Singapore - English - HSA (Health Sciences Authority)

sprycel tablets 20mg

bristol-myers squibb (singapore) pte. ltd. - dasatinib - tablet, film coated - 20 mg - dasatinib 20 mg

SPRYCEL TABLETS 50MG Singapore - English - HSA (Health Sciences Authority)

sprycel tablets 50mg

bristol-myers squibb (singapore) pte. ltd. - dasatinib - tablet, film coated - 50mg per tab - dasatinib 50mg per tab

SPRYCEL TABLETS 70MG Singapore - English - HSA (Health Sciences Authority)

sprycel tablets 70mg

bristol-myers squibb (singapore) pte. ltd. - dasatinib - tablet, film coated - 70mg/tab - dasatinib 70mg/tab

ORENCIA 250MG/VIAL Singapore - English - HSA (Health Sciences Authority)

orencia 250mg/vial

bristol-myers squibb (singapore) pte. ltd. - abatacept - injection, powder, lyophilized, for solution - 262.5mg

ORENCIA Injection 125mg/ml in Prefilled Syringe Singapore - English - HSA (Health Sciences Authority)

orencia injection 125mg/ml in prefilled syringe

bristol-myers squibb (singapore) pte. ltd. - abatacept - injection - 125mg

OPDIVO nivolumab 100 mg in 10 mL (10 mg/mL) concentrated solution for IV infusion vial Australia - English - Department of Health (Therapeutic Goods Administration)

opdivo nivolumab 100 mg in 10 ml (10 mg/ml) concentrated solution for iv infusion vial

bristol-myers squibb australia pty ltd - nivolumab, quantity: 107 mg - injection, concentrated - excipient ingredients: sodium citrate dihydrate; pentetic acid; mannitol; sodium chloride; polysorbate 80; sodium hydroxide; water for injections; hydrochloric acid - melanoma,opdivo, as monotherapy, is indicated for the adjuvant treatment of adults and adolescent patients 12 years and older with completely resected stage iib, iic, iii or iv melanoma.,opdivo, as monotherapy, is indicated for the treatment of patients with unresectable or metastatic melanoma.,opdivo, in combination with ipilimumab, is indicated for the treatment of patients with unresectable or metastatic melanoma. the approval of this indication is based on a pre-specified comparison to ipilimumab monotherapy. all analyses comparing nivolumab monotherapy with the nivolumab/ipilimumab combination are descriptive.,non-small cell lung cancer (nsclc),opdivo, in combination with platinum-doublet chemotherapy, is indicated for the neoadjuvant treatment of patients with resectable non-small cell lung cancer (nsclc).,opdivo, in combination with ipilimumab and 2 cycles of platinum-doublet chemotherapy, is indicated for the first-line treatment of patients with metastatic or recurrent non-small cell lung cancer (nsclc) with no egfr or alk genomic tumour aberrations.,opdivo, as monotherapy, is indicated for the treatment of locally advanced or metastatic squamous non-small cell lung cancer (nsclc) with progression on or after prior chemotherapy.,opdivo, as monotherapy, is indicated for the treatment of locally advanced or metastatic non-squamous non-small cell lung cancer (nsclc) with progression on or after prior chemotherapy. in patients with tumour egfr or alk genomic aberrations, opdivo should be used after progression on or after targeted therapy.,malignant pleural mesothelioma (mpm),opdivo, in combination with ipilimumab, is indicated for the first-line treatment of patients with unresectable malignant pleural mesothelioma.,renal cell carcinoma (rcc),opdivo, in combination with ipilimumab, is indicated for the treatment of patients with intermediate/poor-risk, previously untreated advanced renal cell carcinoma.,opdivo, in combination with cabozantinib, is indicated for the first-line treatment of patients with advanced renal cell carcinoma.,opdivo, as monotherapy, is indicated for the treatment of patients with advanced clear cell renal cell carcinoma after prior anti-angiogenic therapy.,classical hodgkin lymphoma (chl),opdivo, as monotherapy, is indicated for the treatment of patients with relapsed or refractory classical hodgkin lymphoma (chl) after autologous stem cell transplant and treatment with brentuximab vedotin. the approval of this indication is based on objective response rate in a single arm study.,squamous cell carcinoma of the head and neck (scchn),opdivo, as monotherapy, is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in patients progressing on or after platinum based therapy.,urothelial carcinoma (uc),opdivo, as monotherapy, is indicated for the adjuvant treatment of patients with muscle invasive urothelial carcinoma (miuc) who are at high risk of recurrence after undergoing radical resection of miuc.,opdivo, as monotherapy, is indicated for the treatment of patients with locally advanced unresectable or metastatic urothelial carcinoma after prior platinum-containing therapy. the approval of this indication is based on objective response rate and duration of response in a single arm study.,hepatocellular carcinoma (hcc),opdivo, as monotherapy, is indicated for the treatment of patients with hepatocellular carcinoma after prior sorafenib therapy. this indication is approved based on objective response rate and duration of response in a single arm study. an improvement in survival or disease-related symptoms has not been established.,oesophageal squamous cell carcinoma (oscc),opdivo in combination with ipilimumab is indicated for the first-line treatment of patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ? 1% as determined by a validated test.,opdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first-line treatment of patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ? 1% as determined by a validated test.,opdivo, as monotherapy, is indicated for the treatment of patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine and platinum based chemotherapy.,adjuvant oesophageal cancer (oc) or gastro-oesophageal junction cancer (gojc),opdivo, as monotherapy, is indicated for the adjuvant treatment of resected oesophageal or gastro-oesophageal junction cancer in patients who have received neoadjuvant chemoradiotherapy. gastric cancer (gc), gastro-oesophageal junction cancer (gojc), or oesophageal adenocarcinoma (oac),opdivo, in combination with fluoropyrimidine- and platinum-based combination chemotherapy, is indicated for the first-line treatment of patients with her2 negative advanced or metastatic gastric or gastro-oesophageal junction or oesophageal adenocarcinoma.