DITHIAZIDE hydrochlorothiazide 25mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

dithiazide hydrochlorothiazide 25mg tablet bottle

phebra pty ltd - hydrochlorothiazide, quantity: 25 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; maize starch; magnesium stearate; calcium hydrogen phosphate dihydrate; sunset yellow fcf aluminium lake - hypertension: may be used alone or in combination with other antihypertensive drugs. oedema: associated with congestive heart failure, hepatic cirrhosis, nephrotic syndrome, acute glomerulonephritis, chronic renal failure (see precautions), premenstrual tension, and drug induced oedema.

BENZTROP benztropine mesilate 2mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

benztrop benztropine mesilate 2mg tablet bottle

phebra pty ltd - benzatropine mesilate, quantity: 2 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; pregelatinised maize starch; microcrystalline cellulose; magnesium stearate - indicated for the treatment of all forms of parkinsonism. the treatment of extrapyramidal reactions (except tardive dyskinesia [see contraindications and precautions]) due to neuroleptic drugs.

NARCAN naloxone hydrochloride (as dihydrate) 400 microgram/1 mL injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

narcan naloxone hydrochloride (as dihydrate) 400 microgram/1 ml injection ampoule

phebra pty ltd - naloxone hydrochloride dihydrate, quantity: 440 microgram (equivalent: naloxone hydrochloride?, qty 400 microgram) - injection - excipient ingredients: water for injections; sodium chloride; hydrochloric acid - narcan is indicated for the complete or partial reversal of narcotic depression, including respiratory depression, induced by opioids including natural and synthetic narcotics, propoxyphene, methadone and the narcotic antagonist analgesics: nalbuphine, pentazocine and butorphanol. narcan is also indicated for the diagnosis of suspected acute opioid overdosage.

Phebra SODIUM CHLORIDE 0.9% 900 mg in 100 mL solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

phebra sodium chloride 0.9% 900 mg in 100 ml solution for injection vial

phebra pty ltd - sodium chloride, quantity: 9 mg/ml - injection, solution - excipient ingredients: water for injections; hydrochloric acid; sodium hydroxide - indications as at 01 jan 1991 : prophylaxis of heat prostration or muscle cramps, chloride deficiency due to diuresis or salt restriction, prevention or treatment of extracellular volume depletion. parenteral - 0.9% (isotonic) nacl is used to restore sodium and chloride losses; to dilute or dissolve drugs for iv, im or sc use, flushing of iv catheters; extracellular fluid replacement; priming solution for hemodialysis; initiate and terminate blood transfusions so red blood cells will not hemolyze; metabolic alkalosis when there is fluid loss and mild sodium depletion. topical or irrigation - relief of inflamed, dry or crusted nasal membranes or as a topical irrigating or flush solution.

DROLEPTAN droperidol 2.5mg/1mL injection Australia - English - Department of Health (Therapeutic Goods Administration)

droleptan droperidol 2.5mg/1ml injection

phebra pty ltd - droperidol, quantity: 2.5 mg/ml - injection, solution - excipient ingredients: tartaric acid; mannitol; water for injections - in anaesthesia - drolepton is indicated to produce tranquillisation and to reduce the incidence of nausea and vomiting in surgical and diagnostic procedures; for premedication, induction, and as an adjunct in the maintenance of general and regional anaesthesia; in neuroleptanalgesia in which droleptan is given concurrently with a narcotic analgesic, to aid in producing tranquillity and decreasing anxiety and pain. in psychiatry - the management of severe agitation, hyperactivity, or agressiveness in psychotic disorders, including schizophrenic reaction and the manic type of manic depressive illness, or in disturbed states, such as some types of acute brain syndrome and in nonpsychotic acute excitation states.

BREVIBLOC Esmolol hydrochloride 100mg/10mL injection Australia - English - Department of Health (Therapeutic Goods Administration)

brevibloc esmolol hydrochloride 100mg/10ml injection

phebra pty ltd - esmolol hydrochloride, quantity: 100 mg - injection, solution - excipient ingredients: water for injections; hydrochloric acid; sodium acetate trihydrate; glacial acetic acid - supraventricular tachycardia - for the rapid control of ventricular rate in patients with atrial fibrillation or atrial flutter in perioperative, postoperative, or other emergent circumstances where short term control of ventricular rate with a short-acting agent is desirable. esmolol is also indicated in non-compensatory sinus tachycardia where, in the physician's judgement, the rapid heart rate requires specific intervention. esmolol is not intended for use in chronic settings where transfer to another agent is anticipated, or for treatment periods greater than 24 hours duration.

CARBOSORB XS activated charcoal 50 g/250 mL and sorbitol 70.75 g/250 mL suspension bottle Australia - English - Department of Health (Therapeutic Goods Administration)

carbosorb xs activated charcoal 50 g/250 ml and sorbitol 70.75 g/250 ml suspension bottle

phebra pty ltd - activated charcoal, quantity: 0.2 g/ml; sorbitol, quantity: 0.283 g/ml - suspension - excipient ingredients: propylene glycol; citric acid; sodium hydroxide; glycerol; purified water - for the treatment of poisoning and drug overdosage by oral ingestion.

RABIPUR rabies virus vaccine (Inactivated) 2.5 IU powder for injection vial with diluent pre-filled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

rabipur rabies virus vaccine (inactivated) 2.5 iu powder for injection vial with diluent pre-filled syringe

seqirus pty ltd - rabies virus, quantity: 2.5 iu - injection, powder for - excipient ingredients: monopotassium glutamate; trometamol; sodium chloride; disodium edetate; polygeline; sucrose - active immunisation against rabies virus, including a) pre-exposure immunisation b) post-exposure treatment following exposure to rabies virus.

ARAMINE metaraminol (as tartrate) 10 mg/1 mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

aramine metaraminol (as tartrate) 10 mg/1 ml injection vial

phebra pty ltd - metaraminol tartrate, quantity: 18.96 mg (equivalent: metaraminol, qty 10 mg) - injection - excipient ingredients: sodium metabisulfite; sodium chloride; water for injections; sodium hydroxide; tartaric acid - prevention and treatment of the acute hypotensive state occurring with spinal anaesthesia; adjunctive treatment of hypotension due to haemorrhage, reactions to medications, surgical complications, and shock associated with brain damage due to tumour or trauma.,it may also be useful as an adjunct in the treatment of hypotension due to cardiogenic shock or septicaemia.

METARAMINOL PHEBRA metaraminol (as tartrate) 10 mg/1 mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

metaraminol phebra metaraminol (as tartrate) 10 mg/1 ml injection vial

phebra pty ltd - metaraminol tartrate, quantity: 18.96 mg (equivalent: metaraminol, qty 10 mg) - injection - excipient ingredients: water for injections; sodium metabisulfite; sodium chloride; sodium hydroxide; tartaric acid - prevention and treatment of the acute hypotensive state occurring with spinal anaesthesia; adjunctive treatment of hypotension due to haemorrhage, reactions to medications, surgical complications, and shock associated with brain damage due to tumour or trauma.,it may also be useful as an adjunct in the treatment of hypotension due to cardiogenic shock or septicaemia.