MANNITOL 20 %  IMUNA SOLUTION FOR INFUSION Israel - English - Ministry of Health

mannitol 20 % imuna solution for infusion

a.l. medi-market ltd. - mannitol - solution for infusion - mannitol 200 g / 1000 ml - mannitol - mannitol 20% imuna, solution for infusion is indicated for: - the promotion of diuresis, in the prevention and/or treatment of the oliguric phase of acute renal failure before irreversible renal failure becomes established;- the reduction of intracranial pressure and treatment of cerebral edema by reducing brain mass; - the reduction of elevated intraocular pressure when the pressure cannot be lowered by other means, and promoting the urinary excretion of toxic substances.

GLUCOSE 5 % IMUNA SOLUTION FOR INFUSION Israel - English - Ministry of Health

glucose 5 % imuna solution for infusion

a.l. medi-market ltd. - glucose as monohydrate - solution for infusion - glucose as monohydrate 5 % - glucose - glucose 5 % intravenous infusion is indicated for the treatment of carbohydrate and fluid depletion. glucose 5 % is also used as a vehicle and diluent for compatible medicinal products for parenteral administration.

SODIUM CHLORIDE 0.9% IMUNA Israel - English - Ministry of Health

sodium chloride 0.9% imuna

a.l. medi-market ltd. - sodium chloride - solution for infusion - sodium chloride 9 mg/ml - sodium chloride - short- term intravascular volume substitution. hypotonic dehydration or isotonic dehydration. vehicle solution for supplementary medication.fluid and electrolyte replacement, hypochloremic alkalosis and chloride losses.

PHEBRA GLUCOSE 50% intravenous infusion 25g/50mL vial Australia - English - Department of Health (Therapeutic Goods Administration)

phebra glucose 50% intravenous infusion 25g/50ml vial

phebra pty ltd - glucose, quantity: 500 mg/ml - injection, intravenous infusion - excipient ingredients: hydrochloric acid; water for injections; sodium bicarbonate - glucose 50% intravenous infusion is strongly hypertonic and may be used to reduce increased cerebrospinal pressure and/or oedema due to delirium tremens or acute alcoholic intoxication. it may also be used to treat severe hypoglycaemia due to an excess of insulin and to provide concentrated calories in total parenteral nutrition regimes.

GLUCOSE IV INFUSION BP (5% W/V) Kenya - English - Pharmacy and Poisons Board

glucose iv infusion bp (5% w/v)

questa care inc. c/o surgilinks ltd 4251 s. higuera st. suite 800 san luis obispo ca - glucose iv infusion bp - infusion - glucose iv infusion bp 5%w/v - other i.v. solution additives

RINGER LACTATE IMUNA Israel - English - Ministry of Health

ringer lactate imuna

a.l. medi-market ltd. - calcium chloride dihydrate; potassium chloride; sodium chloride; sodium lactate - solution for infusion - sodium lactate 3.2 mg / 1 ml; sodium chloride 6 mg / 1 ml; potassium chloride 0.4 mg / 1 ml; calcium chloride dihydrate 0.27 mg / 1 ml - electrolytes - ringer lactate imuna is indicated for source of water and electrolytes. regulation or maintenance of metabolic acidosis ( except lactic acidosis).

PRECEDEX READY TO USE dexmedetomidine hydrochloride 400 micrograms/100 mL injection for intravenous infusion bottle Australia - English - Department of Health (Therapeutic Goods Administration)

precedex ready to use dexmedetomidine hydrochloride 400 micrograms/100 ml injection for intravenous infusion bottle

pfizer australia pty ltd - dexmedetomidine hydrochloride, quantity: 4.72 microgram/ml (equivalent: dexmedetomidine, qty 4 microgram/ml) - injection, intravenous infusion - excipient ingredients: sodium chloride; water for injections - intensive care unit (icu) sedation: for sedation of initially intubated adult patients during treatment in an intensive care setting. the use of precedex ready to use by continuous infusion in these patients should not exceed 24 hours.,procedural sedation: for sedation of non-intubated adult patients prior to and/or during surgical and other procedures.

PRECEDEX READY TO USE dexmedetomidine hydrochloride 200 micrograms/50 mL injection for intravenous infusion bottle Australia - English - Department of Health (Therapeutic Goods Administration)

precedex ready to use dexmedetomidine hydrochloride 200 micrograms/50 ml injection for intravenous infusion bottle

pfizer australia pty ltd - dexmedetomidine hydrochloride, quantity: 4.72 microgram/ml (equivalent: dexmedetomidine, qty 4 microgram/ml) - injection, intravenous infusion - excipient ingredients: sodium chloride; water for injections - intensive care unit (icu) sedation: for sedation of initially intubated adult patients during treatment in an intensive care setting. the use of precedex ready to use by continuous infusion in these patients should not exceed 24 hours.,procedural sedation: for sedation of non-intubated adult patients prior to and/or during surgical and other procedures.

PRECEDEX READY TO USE dexmedetomidine hydrochloride 80 micrograms/20 mL injection for intravenous infusion vial Australia - English - Department of Health (Therapeutic Goods Administration)

precedex ready to use dexmedetomidine hydrochloride 80 micrograms/20 ml injection for intravenous infusion vial

pfizer australia pty ltd - dexmedetomidine hydrochloride, quantity: 4.72 microgram/ml (equivalent: dexmedetomidine, qty 4 microgram/ml) - injection, intravenous infusion - excipient ingredients: sodium chloride; water for injections - intensive care unit (icu) sedation: for sedation of initially intubated adult patients during treatment in an intensive care setting. the use of precedex ready to use by continuous infusion in these patients should not exceed 24 hours.,procedural sedation: for sedation of non-intubated adult patients prior to and/or during surgical and other procedures.

LEVETIRACETAM IV ARX levetiracetam 500mg/5mL concentrate solution for IV infusion vial Australia - English - Department of Health (Therapeutic Goods Administration)

levetiracetam iv arx levetiracetam 500mg/5ml concentrate solution for iv infusion vial

arrotex pharmaceuticals pty ltd - levetiracetam, quantity: 100 mg/ml - injection, intravenous infusion - excipient ingredients: sodium acetate trihydrate; sodium chloride; water for injections; glacial acetic acid - levetiracetam concentrate solution for iv infusion after dilution is an alternative for patients when oral administration is temporarily not feasible. use in epileptic patients aged 4 years and older, initially as add on therapy, in the treatment of partial onset seizures with or without secondary generalisation; monotherapy in the treatment of partial onset seizures, with or without secondary generalisation, in patients from 16 years of age with newly diagnosed epilepsy; add on therapy in the treatment of myoclonic seizures in adults and adolescents from 12 years of age with juvenile myoclonic epilepsy (jme); and, add on therapy in the treatment of primary generalized tonic-clonic seizures in adults and children from 4 years of age with idiopathic generalized epilepsy (ige).