iverQuest duo Pasta Oral Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

iverquest duo pasta oral

agrovet market animal health - ivermectina; praziquantel - pasta oral - ivermectina 1.78 g;praziquantel 22.29 g;excipientes c.s.p , ivermectina 1.78 g; praziquantel 22.29 g; excipientes c.s.p - antiparasitarios internos: gastrointestinales (nematodos), pulmonares – traqueales, tenias (cestodos). antiparasitarios de uso externo: cutáneos (microfilarias, larvas, gusaneras, nuches), piojos. - equinos - endectocida de amplio espectro, efectivo en el control de parasitosis internas (nemátodes gastrointestinales, pulmonares y tenias) y externas como piojos y problemas de miasis en equinos. contiene praziquantel, el antiparasitario de mayor efectividad contra formas inmaduras y adultas, de todo tipo de tenias. la fórmula especial de iverquest®duo le confiere un agradable sabor a manzana, lo que lo hace una pasta muy palatable facilitando completamente la dosificación.

Triverfén 10.1 Suspensión Oral Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

triverfén 10.1 suspensión oral

agrovet market animal health - fenbendazol; ivermectina; triclabendazol - suspensión oral - fenbendazol 5 g;ivermectina 0.1 g;triclabendazol 5 g;excipientes c.s.p , fenbendazol 5 g; ivermectina 0.1 g; triclabendazol 5 g; excipientes c.s.p - antiparasitarios internos: gastrointestinales (nematodos), hepáticos (trematodos-fasciola), pulmonares – traqueales. antiparasitarios de uso externo: cutáneos (microfilarias, larvas, gusaneras, nuches), reguladores del crecimiento (larvas/huevos), garrapatas, piojos. - camelidos, caprinos, ovinos - indicado para el tratamiento y control simultáneo de todas las parasitosis internas (nemátodes gastrointestinales, pulmonares, incluyendo casos de fasciolasis aguda, subaguda y crónica, tenias y nemátodes resistentes a los benzimidazoles y a la ivermectina); así como para el tratamiento y control de ectoparásitos chupadores (ayudando además en el control de moscas).

Keytruda Unión Europea - español - EMA (European Medicines Agency)

keytruda

merck sharp & dohme b.v. - pembrolizumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; endometrial neoplasms - agentes antineoplásicos - melanomakeytruda as monotherapy is indicated for the treatment of adults and adolescents aged 12 years and older with advanced (unresectable or metastatic) melanoma. keytruda as monotherapy is indicated for the adjuvant treatment of adults and adolescents aged 12 years and older with stage iib, iic, or with stage iii melanoma and lymph node involvement who have undergone complete resection. non small cell lung carcinoma (nsclc)keytruda as monotherapy is indicated for the adjuvant treatment of adults with non-small cell lung carcinoma who are at high risk of recurrence following complete resection and platinum based chemotherapy (for selection criteria, see section 5. keytruda as monotherapy is indicated for the first line treatment of metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 50% tumour proportion score (tps) with no egfr or alk positive tumour mutations. keytruda, in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of metastatic non squamous non small cell lung carcinoma in adults whose tumours have no egfr or alk positive mutations. keytruda, in combination with carboplatin and either paclitaxel or nab paclitaxel, is indicated for the first line treatment of metastatic squamous non small cell lung carcinoma in adults. keytruda  as monotherapy is indicated for the treatment of locally advanced or metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 1% tps and who have received at least one prior chemotherapy regimen. los pacientes con egfr o alk positivo tumor mutaciones debe también han recibido terapia dirigida antes de recibir keytruda. classical hodgkin lymphoma (chl)keytruda as monotherapy is indicated for the treatment of adult and paediatric patients aged 3 years and older with relapsed or refractory classical hodgkin lymphoma who have failed autologous stem cell transplant (asct) or following at least two prior therapies when asct is not a treatment option. urothelial carcinomakeytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who have received prior platinum containing chemotherapy. keytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who are not eligible for cisplatin containing chemotherapy and whose tumours express pd l1 with a combined positive score (cps) ≥ 10. head and neck squamous cell carcinoma (hnscc)keytruda, as monotherapy or in combination with platinum and 5 fluorouracil (5 fu) chemotherapy, is indicated for the first line treatment of metastatic or unresectable recurrent head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a cps ≥ 1. keytruda as monotherapy is indicated for the treatment of recurrent or metastatic head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a ≥ 50% tps and progressing on or after platinum containing chemotherapy. renal cell carcinoma (rcc)keytruda, in combination with axitinib, is indicated for the first line treatment of advanced renal cell carcinoma in adults. keytruda  as monotherapy is indicated for the adjuvant treatment of adults with renal cell carcinoma at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions (for selection criteria, please see section 5. microsatellite instability high (msi-h) or mismatch repair deficient (dmmr) cancerscolorectal cancer (crc)keytruda as monotherapy is indicated for theadults with msi-h or dmmr colorectal cancer in the following settings:first line treatment of metastatic microsatellite instability high (msi h) or mismatch repair deficient (dmmr) colorectal cancer in adults;treatment of unresectable or metastatic colorectal cancer after previous fluoropyrimidine based combination therapy.  non-colorectal cancerskeytruda as monotherapy is indicated for the treatment of the following msi h or dmmr tumours in adults with:advanced or recurrent endometrial carcinoma, who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation;unresectable or metastatic gastric, small intestine, or biliary cancer, who have disease progression on or following at least one prior therapy. oesophageal carcinomakeytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic carcinoma of the oesophagus or her-2 negative gastroesophageal junction adenocarcinoma, in adults whose tumours express pd l1 with a cps ≥ 10. triple negative breast cancer (tnbc)keytruda, in combination with chemotherapy as neoadjuvant treatment, and then continued as monotherapy as adjuvant treatment after surgery, is indicated for the treatment of adults with locally advanced, or early stage triple negative breast cancer at high risk of recurrence. keytruda, in combination with chemotherapy, is indicated for the treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express pd l1 with a cps ≥ 10 and who have not received prior chemotherapy for metastatic disease. endometrial carcinoma (ec)keytruda, in combination with lenvatinib, is indicated for the treatment of advanced or recurrent endometrial carcinoma in adults who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation. cervical cancerkeytruda, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express pd l1 with a cps ≥ 1. gastric or gastro-oesophageal junction (gej) adenocarcinomakeytruda, in combination with trastuzumab, fluoropyrimidine and platinum-containing chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic her2-positive gastric or gastro-oesophageal junction adenocarcinoma in adults whose tumours express pd-l1 with a cps ≥ 1.

DUODOPA 20mg/ml + 5mg/ml gel intestinal España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

duodopa 20mg/ml + 5mg/ml gel intestinal

abbvie as - levodopa, carbidopa - excipientes: carmelosa sodica - agentes dopaminÉrgicos - dopa y derivados de la dopa - levodopa con inhibidor de la descarboxilasa

ARPON CONCENTRADO PARA EMULSIÓN PARA PULVERIZACIÓN CUTÁNEA España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

arpon concentrado para emulsión para pulverización cutánea

laboratorios zotal s.l.u. - cipermetrina - concentrado para emulsiÓn para pulverizaciÓn cutÁnea - cipermetrina 100 - cipermetrina - bovino; caballos no destinados a consumo humano

BUTASYL SOLUCIÓN INYECTABLE España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

butasyl solución inyectable

zoetis spain s.l. - salicilato sodio - soluciÓn inyectable - salicilato sodio 50 - otros antiinflamatorios/antirreumáticos en combinación con otros medicamentos - caballos no destinados a consumo humano

CIPER – PULVIZOO 100 mg/ml # CIPER-PULVIZOO CONCENTRADO PARA EMULSIÓN PARA PULVERIZACIÓN CUTÁNEA España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

ciper – pulvizoo 100 mg/ml # ciper-pulvizoo concentrado para emulsión para pulverización cutánea

laboratorios calier s.a. - cipermetrina - concentrado para emulsiÓn para pulverizaciÓn cutÁnea - cipermetrina 100 - cipermetrina - bovino; caballos no destinados a consumo humano

CHANAZONE 1 g POLVO ORAL PARA CABALLOS España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

chanazone 1 g polvo oral para caballos

chanelle pharmaceuticals manufacturing limited - fenilbutazona - polvo oral - fenilbutazona 1 - fenilbutazona - caballos no destinados a consumo humano

CALMO NEOSAN 5 mg/ml SOLUCION INYECTABLE # CALMO NEOSAN SOLUCION INYECTABLE España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

calmo neosan 5 mg/ml solucion inyectable # calmo neosan solucion inyectable

boehringer ingelheim animal health espaÑa s.a.u. - acepromazina maleato - soluciÓn inyectable - - acepromazina - perros; gatos; caballos no destinados a consumo humano