Bss - Balanced Salt Solution 6.4mg + 1.7mg + 3.9mg + 0.75mg + 0.48mg + 0.30mg Sterile Intraocular Irrigating Solution Filipíny - angličtina - FDA (Food And Drug Administration)

bss - balanced salt solution 6.4mg + 1.7mg + 3.9mg + 0.75mg + 0.48mg + 0.30mg sterile intraocular irrigating solution

alcon laboratories (phils.), inc. - intraocular irrigating solution - sterile intraocular irrigating solution - 6.4mg + 1.7mg + 3.9mg + 0.75mg + 0.48mg + 0.30mg

SINTETICA BACLOFEN INTRATHECAL baclofen 40 mg/20 mL injection solution ampoule Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

sintetica baclofen intrathecal baclofen 40 mg/20 ml injection solution ampoule

boucher & muir pty ltd - baclofen, quantity: 2 mg/ml - injection, solution - excipient ingredients: sodium chloride; water for injections - sintetica baclofen intrathecal is indicated in patients with severe chronic spasticity of spinal origin (associated with injury, multiple sclerosis, or other spinal cord diseases) or of cerebral origin who are unresponsive to orally administered antispastics (including oral baclofen) and/or who experience unacceptable side effects at effective oral doses.

SINTETICA BACLOFEN INTRATHECAL baclofen 10 mg/5 mL injection solution ampoule Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

sintetica baclofen intrathecal baclofen 10 mg/5 ml injection solution ampoule

boucher & muir pty ltd - baclofen, quantity: 2 mg/ml - injection, solution - excipient ingredients: sodium chloride; water for injections - sintetica baclofen intrathecal is indicated in patients with severe chronic spasticity of spinal origin (associated with injury, multiple sclerosis, or other spinal cord diseases) or of cerebral origin who are unresponsive to orally administered antispastics (including oral baclofen) and/or who experience unacceptable side effects at effective oral doses.

SINTETICA BACLOFEN INTRATHECAL baclofen 10 mg/20 mL injection solution ampoule Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

sintetica baclofen intrathecal baclofen 10 mg/20 ml injection solution ampoule

boucher & muir pty ltd - baclofen, quantity: 0.5 mg/ml - injection, solution - excipient ingredients: sodium chloride; water for injections - sintetica baclofen intrathecal is indicated in patients with severe chronic spasticity of spinal origin (associated with injury, multiple sclerosis, or other spinal cord diseases) or of cerebral origin who are unresponsive to orally administered antispastics (including oral baclofen) and/or who experience unacceptable side effects at effective oral doses.

SINTETICA BACLOFEN INTRATHECAL baclofen 50 microgram/1 mL injection solution ampoule Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

sintetica baclofen intrathecal baclofen 50 microgram/1 ml injection solution ampoule

boucher & muir pty ltd - baclofen, quantity: 50 microgram/ml - injection, solution - excipient ingredients: sodium chloride; water for injections - sintetica baclofen intrathecal is indicated in patients with severe chronic spasticity of spinal origin (associated with injury, multiple sclerosis, or other spinal cord diseases) or of cerebral origin who are unresponsive to orally administered antispastics (including oral baclofen) and/or who experience unacceptable side effects at effective oral doses.

SMOFlipid (lipid emulsion) 20% emulsion for intravenous infusion 250 mL bag Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

smoflipid (lipid emulsion) 20% emulsion for intravenous infusion 250 ml bag

fresenius kabi australia pty ltd - olive oil, quantity: 50 g; fish oil - rich in omega-3 acids, quantity: 30 g; medium chain triglycerides, quantity: 60 g; soya oil, quantity: 60 g - injection, intravenous infusion - excipient ingredients: glycerol; sodium oleate; dl-alpha-tocopherol; water for injections; egg lecithin; sodium hydroxide - supply of energy and essential fatty acids to patients, as part of a parenteral nutrition regimen, when oral or enteral nutrition is impossible, insufficient or contra-indicated.

SMOFlipid (lipid emulsion) 20% emulsion for intravenous infusion 100 mL bag Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

smoflipid (lipid emulsion) 20% emulsion for intravenous infusion 100 ml bag

fresenius kabi australia pty ltd - olive oil, quantity: 50 g; fish oil - rich in omega-3 acids, quantity: 30 g; medium chain triglycerides, quantity: 60 g; soya oil, quantity: 60 g - injection, intravenous infusion - excipient ingredients: glycerol; sodium oleate; dl-alpha-tocopherol; water for injections; egg lecithin; sodium hydroxide - supply of energy and essential fatty acids to patients, as part of a parenteral nutrition regimen, when oral or enteral nutrition is impossible, insufficient or contra-indicated.

B. BRAUN MIDAZOLAM midazolam (as hydrochloride) 50 mg/50 mL Injection, Intravenous Infusion bottle Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b. braun midazolam midazolam (as hydrochloride) 50 mg/50 ml injection, intravenous infusion bottle

b braun australia pty ltd - midazolam hydrochloride, quantity: 1.112 mg/ml (equivalent: midazolam, qty 1 mg/ml) - injection, intravenous infusion - excipient ingredients: hydrochloric acid; sodium chloride; water for injections - iv as an agent for conscious sedation prior to short surgical, diagnostic, therapeutic or endoscopic procedures, such as bronchoscopy, gastroscopy, cystoscopy, coronary angiography and cardiac catheterisation, either alone or in conjunction with a narcotic; iv for induction of anaesthesia, preliminary to administration of other anaesthetic agents. with the use of a narcotic premedicant, induction of anaesthesia can be attained with a narrower dose range and in a shorter period of time; iv for sedation in intensive care units; intermittent administration or continuous infusion; im for preoperative sedation (induction of sleepiness or drowsiness and relief of apprehension) and to impair memory of perioperative events.

B. BRAUN MIDAZOLAM midazolam (as hydrochloride) 100 mg/100 mL Injection, Intravenous Infusion bottle Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b. braun midazolam midazolam (as hydrochloride) 100 mg/100 ml injection, intravenous infusion bottle

b braun australia pty ltd - midazolam hydrochloride, quantity: 1.112 mg/ml (equivalent: midazolam, qty 1 mg/ml) - injection, intravenous infusion - excipient ingredients: hydrochloric acid; sodium chloride; water for injections - iv as an agent for conscious sedation prior to short surgical, diagnostic, therapeutic or endoscopic procedures, such as bronchoscopy, gastroscopy, cystoscopy, coronary angiography and cardiac catheterisation, either alone or in conjunction with a narcotic; iv for induction of anaesthesia, preliminary to administration of other anaesthetic agents. with the use of a narcotic premedicant, induction of anaesthesia can be attained with a narrower dose range and in a shorter period of time; iv for sedation in intensive care units; intermittent administration or continuous infusion; im for preoperative sedation (induction of sleepiness or drowsiness and relief of apprehension) and to impair memory of perioperative events.

BAXTER POTASSIUM CHLORIDE 40 mmol and 0.9% SODIUM CHLORIDE 100 mL intravenous infusion bag Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

baxter potassium chloride 40 mmol and 0.9% sodium chloride 100 ml intravenous infusion bag

baxter healthcare pty ltd - potassium chloride, quantity: 29.8 g/l; sodium chloride, quantity: 9 g/l - injection, intravenous infusion - excipient ingredients: water for injections - the baxter potassium chloride and sodium chloride intravenous infusion is indicated as a source of water and to restore electrolyte balance as required by the patient's clinical condition, such as hypokalaemia.