Actilyse Cathflo 2 mg powder for solution for injection and infusion Ayalandi - Kiingereza - HPRA (Health Products Regulatory Authority)

actilyse cathflo 2 mg powder for solution for injection and infusion

boehringer ingelheim international gmbh - alteplase - powder and solvent for solution for injection/infusion - 2 milligram(s) - alteplase

ACTILYSE 20 MG Israeli - Kiingereza - Ministry of Health

actilyse 20 mg

boehringer ingelheim israel ltd. - alteplase - powder and solvent for solution for injection/infusion - alteplase 20 mg/vial - enzymes - acute myocardial infarction :actilyse is indicated for use in the management of acute myocardial infraction (ami) in adults for the lysis of thrombi obstructing coronary arteries, the reduction of infract size, improvement of ventricular function, the reduction of the incidence of congestive heart failure and the reduction of mortality associated with ami. treatment should be initiated as soon as possible after the onset of ami symptoms.acute massive pulmonary embolism with hemodynamic deprivation:actylise is indicated in the management of acute massive pulmonary embolism (pe) in adults:- for the lysis of acute pulmonary emboli, defined as obstruction of blood flow to a lobe or multiple segments of the lung, and- for the lysis of pulmonary emboli accompanied by unstable hemodynamics e.g. failure to maintain blood pressure without supportive measures. the diagnosis should be confirmed by objective means, such as pulmonary angiography or noninvasive procedures such as lung scanning. for fibrinolytic treatment of acute ischaemic stroke.treatment must be started as early as possible within 4.5 hours after onset of stroke symptoms and after exclusion of intracranial haemorrhage by appropriate imaging techniques (e.g. cranial computerised tomography or other diagnostic imaging method sensitive for the presence of haemorrhage). the treatment effect is time-dependent; therefore earlier treatment increases the probability of a favourable outcome. this treatment is restricted to a prescription by a specialist in neurology.

Actilyse 20 mg powder and solvent for solution for injection and infusion Ayalandi - Kiingereza - HPRA (Health Products Regulatory Authority)

actilyse 20 mg powder and solvent for solution for injection and infusion

boehringer ingelheim limited - alteplase - powder and solvent for solution for injection/infusion - 20 milligram(s) - enzymes; alteplase

Actilyse 10 mg powder and solvent for solution for injection and infusion Ayalandi - Kiingereza - HPRA (Health Products Regulatory Authority)

actilyse 10 mg powder and solvent for solution for injection and infusion

boehringer ingelheim limited - alteplase - powder and solvent for solution for injection/infusion - 10 milligram(s) - enzymes; alteplase

Actilyse Nyuzilandi - Kiingereza - Medsafe (Medicines Safety Authority)

actilyse

boehringer ingelheim (nz) limited - alteplase 10mg - injection with diluent - 10 mg - active: alteplase 10mg excipient: arginine nitrogen phosphoric acid polysorbate 80 water for injection - actilyse is indicated for fibrinolytic therapy in acute thrombotic artery occlusion to restore coronary artery patency, reduce infarct size, preserve ventricular function, prevent cardiac insufficiency and reduce mortality · 90 minutes (accelerated) dose regimen: for patients in whom treatment can be started within 6 h of symptom onset; · 3 hour dose regimen: for patients in whom treatment can be started between 6 - 12 hrs after symptom onset.

Actilyse Nyuzilandi - Kiingereza - Medsafe (Medicines Safety Authority)

actilyse

boehringer ingelheim (nz) limited - alteplase 20mg - injection with diluent - 20 mg - active: alteplase 20mg excipient: arginine nitrogen phosphoric acid polysorbate 80 water for injection - actilyse is indicated for fibrinolytic therapy in acute thrombotic artery occlusion to restore coronary artery patency, reduce infarct size, preserve ventricular function, prevent cardiac insufficiency and reduce mortality · 90 minutes (accelerated) dose regimen: for patients in whom treatment can be started within 6 h of symptom onset; · 3 hour dose regimen: for patients in whom treatment can be started between 6 - 12 hrs after symptom onset.

Actilyse 50 mg Powder for Solution for Infusion (IV Filipino - Kiingereza - FDA (Food And Drug Administration)

actilyse 50 mg powder for solution for infusion (iv

n/a; importer: boehringer ingelheim (philippines), inc.; distributor: boehringer ingelheim (philippines), inc. - alteplase - powder for solution for infusion (iv - 50 mg

ACTILYSE CATHFLO alteplase (rch) 2 mg powder for injection vial Australia - Kiingereza - Department of Health (Therapeutic Goods Administration)

actilyse cathflo alteplase (rch) 2 mg powder for injection vial

boehringer ingelheim pty ltd - alteplase, quantity: 2 mg - injection, powder for - excipient ingredients: phosphoric acid; polysorbate 80; arginine; nitrogen - actilyse cathflo is indicated for the thrombolytic treatment of occluded central venous access devices including those used for haemodialysis. the 2 mg strength of alteplase (actilyse cathflo) is the only recommended presentation for use in this indication. see also precautions - use in children.

METALYSE tenecteplase (rch) 50mg powder for injection vial plus prefilled syringe Australia - Kiingereza - Department of Health (Therapeutic Goods Administration)

metalyse tenecteplase (rch) 50mg powder for injection vial plus prefilled syringe

boehringer ingelheim pty ltd - tenecteplase, quantity: 50 mg - injection, powder for - excipient ingredients: arginine; phosphoric acid; polysorbate 20 - metalyse is indicated for the thrombolytic treatment of the acute phase of myocardial infarction (ami). treatment should be initiated as soon as possible after the onset of symptoms. treatment can be initiated within 12 hours of symptom onset.