QUETIA XR quetiapine (as fumarate) 50mg modified release tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

quetia xr quetiapine (as fumarate) 50mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - quetiapine fumarate, quantity: 57.565 mg (equivalent: quetiapine, qty 50 mg) - tablet, modified release - excipient ingredients: povidone; titanium dioxide; carrageenan; light magnesium oxide; lactose monohydrate; magnesium stearate; iron oxide red; macrogol 400; microcrystalline cellulose; iron oxide yellow - bipolar disorder - maintenance treatment of bipolar 1 disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes. treatment of depressive episodes associated with bipolar disorder (see dosage and administration). treatment of acute mania associated with bipolar i disorder as monotherapy or incombination with lithium or sodium valproate. efficacy of quetiapine in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine immediate release tablets. schizophrenia - treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder (mdd)- treatment of recurrent major depressive disorde in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder (gad). treatment of generalised anxiety disorder.

APX-QUETIAPINE XR quetiapine (as fumarate) 200mg modified release tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

apx-quetiapine xr quetiapine (as fumarate) 200mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - quetiapine fumarate, quantity: 230.26 mg (equivalent: quetiapine, qty 200 mg) - tablet, modified release - excipient ingredients: lactose monohydrate; magnesium stearate; iron oxide yellow; povidone; carrageenan; macrogol 400; light magnesium oxide; titanium dioxide; microcrystalline cellulose - bipolar disorder - maintenance treatment of bipolar 1 disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes. treatment of depressive episodes associated with bipolar disorder (see dosage and administration). treatment of acute mania associated with bipolar i disorder as monotherapy or incombination with lithium or sodium valproate. efficacy of quetiapine in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine immediate release tablets. schizophrenia - treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder (mdd)- treatment of recurrent major depressive disorde in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder (gad). treatment of generalised anxiety disorder.

QUETIA XR quetiapine (as fumarate) 300mg modified release tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

quetia xr quetiapine (as fumarate) 300mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - quetiapine fumarate, quantity: 345.39 mg (equivalent: quetiapine, qty 300 mg) - tablet, modified release - excipient ingredients: carrageenan; titanium dioxide; macrogol 400; microcrystalline cellulose; povidone; lactose monohydrate; magnesium stearate; iron oxide yellow; light magnesium oxide - bipolar disorder - maintenance treatment of bipolar 1 disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes. treatment of depressive episodes associated with bipolar disorder (see dosage and administration). treatment of acute mania associated with bipolar i disorder as monotherapy or incombination with lithium or sodium valproate. efficacy of quetiapine in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine immediate release tablets. schizophrenia - treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder (mdd)- treatment of recurrent major depressive disorde in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder (gad). treatment of generalised anxiety disorder.

QUETIA XR quetiapine (as fumarate) 200mg modified release tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

quetia xr quetiapine (as fumarate) 200mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - quetiapine fumarate, quantity: 230.26 mg (equivalent: quetiapine, qty 200 mg) - tablet, modified release - excipient ingredients: carrageenan; macrogol 400; magnesium stearate; povidone; lactose monohydrate; light magnesium oxide; microcrystalline cellulose; iron oxide yellow; titanium dioxide - bipolar disorder - maintenance treatment of bipolar 1 disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes. treatment of depressive episodes associated with bipolar disorder (see dosage and administration). treatment of acute mania associated with bipolar i disorder as monotherapy or incombination with lithium or sodium valproate. efficacy of quetiapine in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine immediate release tablets. schizophrenia - treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder (mdd)- treatment of recurrent major depressive disorde in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder (gad). treatment of generalised anxiety disorder.

APX-QUETIAPINE XR quetiapine (as fumarate) 400mg modified release tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

apx-quetiapine xr quetiapine (as fumarate) 400mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - quetiapine fumarate, quantity: 460.52 mg (equivalent: quetiapine, qty 400 mg) - tablet, modified release - excipient ingredients: microcrystalline cellulose; magnesium stearate; povidone; macrogol 400; lactose monohydrate; light magnesium oxide; titanium dioxide; carrageenan - bipolar disorder - maintenance treatment of bipolar 1 disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes. treatment of depressive episodes associated with bipolar disorder (see dosage and administration). treatment of acute mania associated with bipolar i disorder as monotherapy or incombination with lithium or sodium valproate. efficacy of quetiapine in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine immediate release tablets. schizophrenia - treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder (mdd)- treatment of recurrent major depressive disorde in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder (gad). treatment of generalised anxiety disorder.

APX-QUETIAPINE XR quetiapine (as fumarate) 300mg modified release tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

apx-quetiapine xr quetiapine (as fumarate) 300mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - quetiapine fumarate, quantity: 345.39 mg (equivalent: quetiapine, qty 300 mg) - tablet, modified release - excipient ingredients: magnesium stearate; macrogol 400; lactose monohydrate; light magnesium oxide; carrageenan; titanium dioxide; microcrystalline cellulose; iron oxide yellow; povidone - bipolar disorder - maintenance treatment of bipolar 1 disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes. treatment of depressive episodes associated with bipolar disorder (see dosage and administration). treatment of acute mania associated with bipolar i disorder as monotherapy or incombination with lithium or sodium valproate. efficacy of quetiapine in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine immediate release tablets. schizophrenia - treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder (mdd)- treatment of recurrent major depressive disorde in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder (gad). treatment of generalised anxiety disorder.

Balance Mat Model 1 - Balance/mobility management system platform Australia - engelsk - Department of Health (Therapeutic Goods Administration)

balance mat model 1 - balance/mobility management system platform

balance mat pty ltd - 43114 - balance/mobility management system platform - the device consists of a rubber mat, embedded with an optical fibre mesh and a single sensor, which is connected by a usb cable to a personal computer running windows10. the usb cable provides power to the mat and also transmits commands and data between the mat and the computer. the device gives healthcare and medical practitioners an indication through a graphical display of a person?s postural sway whilst they are standing on the mat. the degree of postural sway shown on the graphical display can assist the practitioner to assess a person's balance ability.

RIVOTRIL clonazepam 0.5mg tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

rivotril clonazepam 0.5mg tablet blister pack

pharmaco australia ltd - clonazepam, quantity: 0.5 mg - tablet, uncoated - excipient ingredients: iron oxide red; magnesium stearate; pregelatinised potato starch; purified talc; maize starch; iron oxide yellow; lactose monohydrate - tablets: most types epilepsy in infants and children, especially absences (petit mal), myoclonic seizures and tonic-clonic fits, whether due to primary generalised epilepsy, or to secondary generalisation of partial epilepsy. in adults all varieties of generalised epilepsy (including myoclonic, akinetic, tonic and tonic-clonic seizures), and in partial epilepsy (including psychomotor seizures).

CORTIMENT PROLONGED RELEASE TABLETS 9 MG Singapore - engelsk - HSA (Health Sciences Authority)

cortiment prolonged release tablets 9 mg

ferring pharmaceuticals private limited - (tablet core) budesonide micronized - tablet, film coated, extended release - (tablet core) budesonide micronized 9.0 mg

KALURIL amiloride hydrochloride dihydrate 5mg tablet bottle Australia - engelsk - Department of Health (Therapeutic Goods Administration)

kaluril amiloride hydrochloride dihydrate 5mg tablet bottle

alphapharm pty ltd - amiloride hydrochloride dihydrate, quantity: 5 mg - tablet, uncoated - excipient ingredients: maize starch; povidone; lactose monohydrate; microcrystalline cellulose; magnesium stearate - indications as at 15 july 1998 : kaluril's main indication is as concomitant therapy with diuretics to conserve potassium during periods of vigorous diuresis and during long-term maintenance therapy with thiazides or other more potent diuretics. kaluril when used alone, has mild diuretic and antihypertensive activity. oedema of cardiac origin. although kaluril alone may provide adequate diuresis for some patients with oedema of cardiac origin, it is primarily indicated for concomitant use in patients receiving thiazides or more potent saluretic diuretic agents. in these patients it may provide increased sodium, chloride and water excretion and decreased potassium excretion. the positive effect of kaluril on potassium balance may be especially important for digitalised cardiac patients, in whom potassium depletion sensitises or exaggerates the response of the heart to the toxic effects of digitalis (e.g. increased ventricular irritability), which may precipitate digitalis intoxication with potentially seriou