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

stada arzneimittel ag - apomorfina hidrocloruro - soluciÓn para perfusiÓn - 5 mg/ml inyectable 10 ml - apomorfina hidrocloruro 5 mg - apomorfina

Unión Europea - español - EMA (European Medicines Agency)

stada arzneimittel ag - teriparatida - osteoporosis - homeostasis del calcio - movymia está indicado en adultos. tratamiento de la osteoporosis en mujeres posmenopáusicas y en hombres con mayor riesgo de fractura. en mujeres posmenopáusicas, se ha demostrado una reducción significativa en la incidencia de fracturas vertebrales y no vertebrales, pero no fracturas de cadera. el tratamiento de la osteoporosis asociada con sostenido sistémica de glucocorticoides terapia en las mujeres y los hombres en mayor riesgo de fractura.

Unión Europea - español - EMA (European Medicines Agency)

stada arzneimittel ag - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - agentes antineoplásicos - oyavas in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. oyavas in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. para obtener más información sobre el estado del receptor 2 del factor de crecimiento epidérmico humano (her2), consulte la sección 5. oyavas in combination with capecitabine is indicated for first line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with oyavas in combination with capecitabine. para más información sobre el estado de her2, consulte la sección 5. oyavas, in addition to platinum based chemotherapy, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non small cell lung cancer other than predominantly squamous cell histology. oyavas, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. oyavas in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. oyavas, in combination with carboplatin and paclitaxel is indicated for the front line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. oyavas, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents. oyavas, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents (see section 5. oyavas, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.

Unión Europea - español - EMA (European Medicines Agency)

stada arzneimittel ag - budesonide, micronised - glomerulonephritis, iga - antidiarreicos, antiinflamatorio intestinal / contra la infección de los agentes - kinpeygo is indicated for the treatment of primary immunoglobulin a (iga) nephropathy (igan) in adults at risk of rapid disease progression with a urine protein-to-creatinine ratio (upcr) ≥1. 5 g/gram.

Unión Europea - español - EMA (European Medicines Agency)

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - oftalmológicos - ximluci is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

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

laboratorio stada s.l. - lamotrigina - comprimido dispersable - 100 mg - lamotrigina 100 mg - lamotrigina

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

laboratorio stada s.l. - lamotrigina - comprimido dispersable - 200 mg - lamotrigina 200 mg - lamotrigina

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

laboratorio stada s.l. - lamotrigina - comprimido dispersable - 25 mg - lamotrigina 25 mg - lamotrigina

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

laboratorio stada s.l. - lamotrigina - comprimido dispersable - 50 mg - lamotrigina 50 mg - lamotrigina

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

laboratorio stada s.l. - pioglitazona hidrocloruro - comprimido - 15 mg - pioglitazona hidrocloruro 15 mg - pioglitazona