Yanimo Respimat 2.5 microgram/2.5 microgram,  inhalation solution Ireland - English - HPRA (Health Products Regulatory Authority)

yanimo respimat 2.5 microgram/2.5 microgram, inhalation solution

boehringer ingelheim international gmbh - tiotropium; olodaterol - inhalation solution - 2.5 µg/2.5 microgram(s) - anticholinergics; anticholinergics - drugs for obstructive airway diseases, adrenergics in combination with anticholinergics - it is indicated as a maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (copd).

Cilostazol Sandoz 100mg Tablets Malta - English - Malta Medicines Authority

cilostazol sandoz 100mg tablets

hexal pharma gmbh stella-klein-low-weg 17, 1020 wein, austria - cilostazol - tablet - cilostazol 100 mg - antithrombotic agents

Ceftriaxone 500mg Powder for Solution for injection United Kingdom - English - myHealthbox

ceftriaxone 500mg powder for solution for injection

midas pharma gmbh - ceftriaxone sodium - powder for solution for injection - 0.596g - antibacterials for systemic use, third generation cephalosporins - it is indicated for the treatment of the following infections in adults and children including term neonates (from birth): • bacterial meningitis • community acquired pneumonia • hospital acquired pneumonia • acute otitis media • intra-abdominal infections • complicated urinary tract infections (including pyelonephritis) • infections of bones and joints • complicated skin and soft tissue infections • gonorrhoea • syphilis • bacterial endocarditis

Ceftriaxone 2g Powder for Solution for infusion United Kingdom - English - myHealthbox

ceftriaxone 2g powder for solution for infusion

midas pharma gmbh - ceftriaxone sodium - powder for solution for infusion - 2.38g - antibacterials for systemic use, third generation cephalosporins - it is indicated for the treatment of the following infections in adults and children including term neonates (from birth): • bacterial meningitis • community acquired pneumonia • hospital acquired pneumonia • acute otitis media • intra-abdominal infections • complicated urinary tract infections (including pyelonephritis) • infections of bones and joints • complicated skin and soft tissue infections • gonorrhoea • syphilis • bacterial endocarditis

Ceftazidime 1g, powder for solution for injection/infusion United Kingdom - English - myHealthbox

ceftazidime 1g, powder for solution for injection/infusion

mip pharma gmbh - ceftazidime - powder for solution for injection/infusion - 1g - antibacterials for systemic use. third-generation cephalosporins - it is indicated for the treatment of the infections listed below in adults and children including neonates (from birth). - nosocomial pneumonia - broncho-pulmonary infections in cystic fibrosis - bacterial meningitis - chronic suppurative otitis media - malignant otitis externa - complicated urinary tract infections - complicated skin and soft tissue infections - complicated intra-abdominal infections - bone and joint infections - peritonitis associated with dialysis in patients on capd

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

biograstim

abz-pharma gmbh - filgrastim - neutropenia; hematopoietic stem cell transplantation; cancer - colony stimulating factors - biograstim is indicated for the reduction in the duration of neutropenia and the incidence of febrile neutropenia in patients treated with established cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes) and for the reduction in the duration of neutropenia in patients undergoing myeloablative therapy followed by bone-marrow transplantation considered to be at increased risk of prolonged severe neutropenia. the safety and efficacy of filgrastim are similar in adults and children receiving cytotoxic chemotherapy.biograstim is indicated for the mobilisation of peripheral blood progenitor cells (pbpc).in patients, children or adults, with severe congenital, cyclic, or idiopathic neutropenia with an absolute neutrophil count (anc) of 0.5 x 109/l, and a history of severe or recurrent infections, long-term administration of biograstim is indicated to increase neutrophil counts and to reduce the incidence and duration of infection-related events.biograstim is indicated for the treatment of persistent neutropenia (anc less than or equal to 1.0 x 109/l) in patients with advanced hiv infection, in order to reduce the risk of bacterial infections when other options to manage neutropenia are inappropriate.

Clopidogrel 1A Pharma European Union - English - EMA (European Medicines Agency)

clopidogrel 1a pharma

acino pharma gmbh  - clopidogrel - peripheral vascular diseases - antithrombotic agents - clopidogrel is indicated in adults for the prevention of atherothrombotic events in:patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease.patients suffering from acute coronary syndrome:- non st segment elevation acute coronary syndrome (unstable angina or non q wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa).- st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy.for further information please refer to section 5.1.

Clopidogrel Acino Pharma European Union - English - EMA (European Medicines Agency)

clopidogrel acino pharma

acino pharma gmbh - clopidogrel - peripheral vascular diseases; stroke; myocardial infarction - antithrombotic agents - clopidogrel is indicated in adults for the prevention of atherothrombotic events in:patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease.for further information please refer to section 5.1.

Clopidogrel DURA European Union - English - EMA (European Medicines Agency)

clopidogrel dura

mylan dura gmbh - clopidogrel (as hydrochloride) - peripheral vascular diseases; stroke; myocardial infarction - antithrombotic agents - clopidogrel is indicated in adults for the prevention of atherothrombotic events in:patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease.

Clopidogrel Hexal European Union - English - EMA (European Medicines Agency)

clopidogrel hexal

acino pharma gmbh - clopidogrel - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - antithrombotic agents - clopidogrel is indicated in adults for the prevention of atherothrombotic events in:patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease;patients suffering from acute coronary syndrome:- non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa);- st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy.for further information please refer to section 5.1.