Glycerol Suppositories Malta - English - Medicines Authority

glycerol suppositories

lab. chimico farmaceutico a sella s.r.l via vicenza 67, schio, italy - glycerol - suppository - glycerol - drugs for constipation

Glycerol Sella Children 1375 mg suppositories Malta - English - Medicines Authority

glycerol sella children 1375 mg suppositories

laboratorio chimico farmaceutico a. sella s.r.l. via vicenza 67 - 36015 schio (vi), italy - suppository - glycerol 1375 mg - drugs for constipation

Lynparza European Union - English - EMA (European Medicines Agency)

lynparza

astrazeneca ab - olaparib - ovarian neoplasms - antineoplastic agents - ovarian cancerlynparza is indicated as monotherapy for the:maintenance treatment of adult patients with advanced (figo stages iii and iv) brca1/2-mutated (germline and/or somatic) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy.maintenance treatment of adult patients with platinum sensitive relapsed high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.lynparza in combination with bevacizumab is indicated for the:maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy in combination with bevacizumab and whose cancer is associated with homologous recombination deficiency (hrd) positive status defined by either a brca1/2 mutation and/or genomic instability (see section 5.1).breast cancerlynparza is indicated as:monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline brca1/2-mutations who have her2-negative, high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy (see sections 4.2 and 5.1).monotherapy for the treatment of adult patients with germline brca1/2-mutations, who have her2 negative locally advanced or metastatic breast cancer. patients should have previously been treated with an anthracycline and a taxane in the (neo)adjuvant or metastatic setting unless patients were not suitable for these treatments (see section 5.1). patients with hormone receptor (hr)-positive breast cancer should also have progressed on or after prior endocrine therapy, or be considered unsuitable for endocrine therapy.adenocarcinoma of the pancreaslynparza is indicated as:monotherapy for the maintenance treatment of adult patients with germline brca1/2-mutations who have metastatic adenocarcinoma of the pancreas and have not progressed after a minimum of 16 weeks of platinum treatment within a first-line chemotherapy regimen.prostate cancerlynparza is indicated as:monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer (mcrpc) and brca1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent.in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with mcrpc in whom chemotherapy is not clinically indicated (see section 5.1).

Zejula European Union - English - EMA (European Medicines Agency)

zejula

glaxosmithkline (ireland) limited - niraparib (tosilate monohydrate) - fallopian tube neoplasms; peritoneal neoplasms; ovarian neoplasms - antineoplastic agents - zejula is indicated: , as monotherapy for the maintenance treatment of adult patients with advanced epithelial (figo stages iii and iv) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy., as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

Shingrix European Union - English - EMA (European Medicines Agency)

shingrix

glaxosmithkline biologicals sa - recombinant varicella zoster virus glycoprotein e - herpes zoster - vaccines - shingrix is indicated for prevention of herpes zoster (hz) and post-herpetic neuralgia (phn), in:adults 50 years of age or older;adults 18 years of age or older at increased risk of hz.the use of shingrix should be in accordance with official recommendations.

ODONTOCAINA 3 % MEPIVACAINA 3 % SOLUCION INYECTABLE POR INFILTRACION DENTAL Panama - English - Ministerio de Salud (Dirección Nacional de Farmacia Y Drogas)

odontocaina 3 % mepivacaina 3 % solucion inyectable por infiltracion dental

productora y comercializadora odontolÓgica new stetic, s.a. - mepivacaina hydrocloruro - mepivacaina hydrocloruro....54,000 mg

PROLOPA 200MG + 50MG  COMPRIMIDOS Panama - English - Ministerio de Salud (Dirección Nacional de Farmacia Y Drogas)

prolopa 200mg + 50mg comprimidos

produtos roche quimicos e farmacÊuticos s.a. - clorhidrato de benserazida - clorhidrato de benserazida....57,000 mg (2% exceso: 58,140 mg) / levodopa....200,000 mg

Airexar Spiromax European Union - English - EMA (European Medicines Agency)

airexar spiromax

teva b.v. - salmeterol, fluticasone propionate - pulmonary disease, chronic obstructive; asthma - drugs for obstructive airway diseases, - airexar spiromax is indicated for use in adults aged 18 years and older only.asthmaairexar spiromax is indicated for the regular treatment of patients with severe asthma where use of a combination product (inhaled corticosteroid and long-acting β2 agonist) is appropriate:- patients not adequately controlled on a lower strength corticosteroid combination productor- patients already controlled on a high dose inhaled corticosteroid and long-acting β2 agonist.chronic obstructive pulmonary disease (copd)airexar spiromax is indicated for the symptomatic treatment of patients with copd, with a fev1