Bortezomib Accord European Union - English - EMA (European Medicines Agency)

bortezomib accord

accord healthcare s.l.u. - bortezomib - multiple myeloma - antineoplastic agents - bortezomib accord as monotherapy or in combination with pegylated liposomal doxorubicin or dexamethasone is indicated for the treatment of adult patients with progressive multiple myeloma who have received at least 1 prior therapy and who have already undergone or are unsuitable for haematopoietic stem cell transplantation.bortezomib accord in combination with melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for high‑dose chemotherapy with haematopoietic stem cell transplantation.bortezomib accord in combination with dexamethasone, or with dexamethasone and thalidomide, is indicated for the induction treatment of adult patients with previously untreated multiple myeloma who are eligible for high‑dose chemotherapy with haematopoietic stem cell transplantation.bortezomib accord in combination with rituximab, cyclophosphamide, doxorubicin and prednisone is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma who are unsuitable for haematopoietic stem cell transplantation.

AZACITIDINE ACCORD azacitidine 100mg powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

azacitidine accord azacitidine 100mg powder for injection vial

accord healthcare pty ltd - azacitidine, quantity: 100 mg - injection, powder for - excipient ingredients: mannitol - azacitidine accord is indicated for the treatment of patients with,? intermediate-2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss), ,? chronic myelomonocytic leukemia (cmmol (10-29 percent marrow blasts without myeloproliferative disorder)), ,? acute myeloid leukemia (aml) with 20-30 percent blasts and multi-lineage dysplasia, according to world health organisation classification (who), ,in whom allogenic stem cell transplantation is not indicated.

Aripiprazole Accord Healthcare 10 mg tablets Ireland - English - HPRA (Health Products Regulatory Authority)

aripiprazole accord healthcare 10 mg tablets

accord healthcare ireland ltd. - aripiprazole - tablet - 10 milligram(s) - other antipsychotics; aripiprazole

Aripiprazole Accord Healthcare 15 mg tablets Ireland - English - HPRA (Health Products Regulatory Authority)

aripiprazole accord healthcare 15 mg tablets

accord healthcare ireland ltd. - aripiprazole - tablet - 15 milligram(s) - other antipsychotics; aripiprazole

Aripiprazole Accord Healthcare 30 mg tablets Ireland - English - HPRA (Health Products Regulatory Authority)

aripiprazole accord healthcare 30 mg tablets

accord healthcare ireland ltd. - aripiprazole - tablet - 30 milligram(s) - other antipsychotics; aripiprazole

Aripiprazole Accord Healthcare 5 mg tablets Ireland - English - HPRA (Health Products Regulatory Authority)

aripiprazole accord healthcare 5 mg tablets

accord healthcare ireland ltd. - aripiprazole - tablet - 5 milligram(s) - other antipsychotics; aripiprazole

Abacavir/Lamivudine Accord Healthcare 600mg/300mg film-coated Tablets Malta - English - Medicines Authority

abacavir/lamivudine accord healthcare 600mg/300mg film-coated tablets

accord healthcare ireland ltd euro house, euro business park, little island cork, t45 k857, ireland - abacavir, lamivudine - film-coated tablet - abacavir 600 mg lamivudine 300 mg - antivirals for systemic use

BORTEZOMIB ACCORD bortezomib 3.5 mg/1.4 mL solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

bortezomib accord bortezomib 3.5 mg/1.4 ml solution for injection vial

accord healthcare pty ltd - bortezomib, quantity: 3.5 mg - injection, solution - excipient ingredients: mannitol; water for injections - bortezomib accord, in combination with melphalan and prednisone is indicated for the treatment of patients with previously untreated multiple myeloma who are not candidates for high dose chemotherapy.,bortezomib accord, as part of combination therapy, is indicated for induction therapy prior to high dose chemotherapy with autologous stem cell rescue for patients under 65 years of age with previously untreated multiple myeloma.,bortezomib accord is also indicated for the treatment of multiple myeloma patients who have received at least one prior therapy, and who have progressive disease.,bortezomib accord in combination with rituximab, cyclophosphamide, doxorubicin and prednisone is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma.

BORTEZOMIB ACCORD bortezomib 2.5 mg/1 mL solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

bortezomib accord bortezomib 2.5 mg/1 ml solution for injection vial

accord healthcare pty ltd - bortezomib, quantity: 2.5 mg - injection, solution - excipient ingredients: mannitol; water for injections - bortezomib accord, in combination with melphalan and prednisone is indicated for the treatment of patients with previously untreated multiple myeloma who are not candidates for high dose chemotherapy.,bortezomib accord, as part of combination therapy, is indicated for induction therapy prior to high dose chemotherapy with autologous stem cell rescue for patients under 65 years of age with previously untreated multiple myeloma.,bortezomib accord is also indicated for the treatment of multiple myeloma patients who have received at least one prior therapy, and who have progressive disease.,bortezomib accord in combination with rituximab, cyclophosphamide, doxorubicin and prednisone is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma.

Dimethyl fumarate Accord European Union - English - EMA (European Medicines Agency)

dimethyl fumarate accord

accord healthcare s.l.u. - dimethyl fumarate - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosuppressants - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).