RUBIFEN LA methylphenidate hydrochloride 10 mg modified release capsules blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

rubifen la methylphenidate hydrochloride 10 mg modified release capsules blister pack

aft pharmaceuticals pty ltd - methylphenidate hydrochloride, quantity: 10 mg - capsule, hard - excipient ingredients: strong ammonia solution; shellac; gelatin; purified talc; propylene glycol; iron oxide yellow; ammonio methacrylate copolymer; triethyl citrate; titanium dioxide; povidone; iron oxide red; methacrylic acid copolymer; potassium hydroxide; sucrose; maize starch - rubifen la modified release capsules are indicated for the treatment of attention-deficit hyperactivity disorder (adhd).,adhd adhd was previously known as attention-deficit disorder. other terms used to describe this behavioural syndrome include: minimal brain dysfunction in children, hyperkinetic child syndrome, minimal brain damage, minimal cerebral dysfunction, minor cerebral dysfunction and psycho-organic syndrome of children.,rubifen la modified release capsules are indicated as an integral part of a total treatment program for adhd that may include other measures (psychological, educational and social) for patients with this syndrome. stimulants are not intended for use in the patient who exhibits symptoms secondary to environmental factors and/or other primary psychiatric disorders, including psychosis.,special diagnostic considerations for adhd in children the aetiology of this syndrome is unknown and there is no single diagnostic test. adequate diagnosis requires the use, not only of medical, but also of psychological, educational and social resources. characteristics commonly reported include: chronic history of short attention span, distractibility, emotional lability, impulsivity, moderate to severe hyperactivity, minor neurological signs and an abnormal eeg. learning may or may not be impaired. the diagnosis must be based upon a complete history and evaluation of the child and not solely on the presence of one or more of these characteristics.,drug treatment is not indicated for all children with this syndrome. stimulants are not intended for use in children who exhibit symptoms secondary to environmental factors (e.g. child abuse in particular) or primary psychiatric disorders. appropriate educational placement is essential and psychosocial intervention is generally necessary. when remedial measures alone are insufficient, the decision to prescribe stimulant medicine will depend upon the physician's assessment of the chronicity and severity of the child's symptoms.,continuation of treatment in adolescent and special diagnostic considerations for adhd in adults there is limited information to guide clinicians about how long older adolescents should continue to receive treatment with drugs for attention deficit hyperactivity disorder (adhd). the decision should be based on the extent to which symptoms of adhd and social functioning have improved to a point that medication is no longer needed. if older adolescents have been largely symptom-free for a year and are functioning well, a trial without medication is warranted. this should be undertaken at times of low stress such as during holidays or in a period when a school routine is well established.,adhd needs to be considered in adults who present with longstanding symptoms suggestive of adhd (inattention, impulsivity, disorganisation) that appear to have started in childhood and are persisting into adult life. further, people with personality disorder and/or problems with drug use accompanied by a significant level of impulsivity and inattention should be referred for evaluation by a psychiatrist with the training and skills required to assess and treat adhd. this expertise is necessary due to the overlap of adhd symptoms with anxiety, mood and personality disorders.

RUBIFEN LA methylphenidate hydrochloride 30 mg modified release capsules blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

rubifen la methylphenidate hydrochloride 30 mg modified release capsules blister pack

aft pharmaceuticals pty ltd - methylphenidate hydrochloride, quantity: 30 mg - capsule, hard - excipient ingredients: iron oxide yellow; gelatin; titanium dioxide; iron oxide red; propylene glycol; strong ammonia solution; triethyl citrate; methacrylic acid copolymer; shellac; ammonio methacrylate copolymer; purified talc; potassium hydroxide; povidone; sucrose; maize starch - rubifen la modified release capsules are indicated for the treatment of attention-deficit hyperactivity disorder (adhd).,adhd adhd was previously known as attention-deficit disorder. other terms used to describe this behavioural syndrome include: minimal brain dysfunction in children, hyperkinetic child syndrome, minimal brain damage, minimal cerebral dysfunction, minor cerebral dysfunction and psycho-organic syndrome of children.,rubifen la modified release capsules are indicated as an integral part of a total treatment program for adhd that may include other measures (psychological, educational and social) for patients with this syndrome. stimulants are not intended for use in the patient who exhibits symptoms secondary to environmental factors and/or other primary psychiatric disorders, including psychosis.,special diagnostic considerations for adhd in children the aetiology of this syndrome is unknown and there is no single diagnostic test. adequate diagnosis requires the use, not only of medical, but also of psychological, educational and social resources. characteristics commonly reported include: chronic history of short attention span, distractibility, emotional lability, impulsivity, moderate to severe hyperactivity, minor neurological signs and an abnormal eeg. learning may or may not be impaired. the diagnosis must be based upon a complete history and evaluation of the child and not solely on the presence of one or more of these characteristics.,drug treatment is not indicated for all children with this syndrome. stimulants are not intended for use in children who exhibit symptoms secondary to environmental factors (e.g. child abuse in particular) or primary psychiatric disorders. appropriate educational placement is essential and psychosocial intervention is generally necessary. when remedial measures alone are insufficient, the decision to prescribe stimulant medicine will depend upon the physician's assessment of the chronicity and severity of the child's symptoms.,continuation of treatment in adolescent and special diagnostic considerations for adhd in adults there is limited information to guide clinicians about how long older adolescents should continue to receive treatment with drugs for attention deficit hyperactivity disorder (adhd). the decision should be based on the extent to which symptoms of adhd and social functioning have improved to a point that medication is no longer needed. if older adolescents have been largely symptom-free for a year and are functioning well, a trial without medication is warranted. this should be undertaken at times of low stress such as during holidays or in a period when a school routine is well established.,adhd needs to be considered in adults who present with longstanding symptoms suggestive of adhd (inattention, impulsivity, disorganisation) that appear to have started in childhood and are persisting into adult life. further, people with personality disorder and/or problems with drug use accompanied by a significant level of impulsivity and inattention should be referred for evaluation by a psychiatrist with the training and skills required to assess and treat adhd. this expertise is necessary due to the overlap of adhd symptoms with anxiety, mood and personality disorders.

RUBIFEN LA methylphenidate hydrochloride 20 mg modified release capsules blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

rubifen la methylphenidate hydrochloride 20 mg modified release capsules blister pack

aft pharmaceuticals pty ltd - methylphenidate hydrochloride, quantity: 20 mg - capsule, hard - excipient ingredients: potassium hydroxide; iron oxide red; gelatin; povidone; shellac; purified talc; methacrylic acid copolymer; titanium dioxide; propylene glycol; ammonio methacrylate copolymer; strong ammonia solution; triethyl citrate; sucrose; maize starch - rubifen la modified release capsules are indicated for the treatment of attention-deficit hyperactivity disorder (adhd).,adhd adhd was previously known as attention-deficit disorder. other terms used to describe this behavioural syndrome include: minimal brain dysfunction in children, hyperkinetic child syndrome, minimal brain damage, minimal cerebral dysfunction, minor cerebral dysfunction and psycho-organic syndrome of children.,rubifen la modified release capsules are indicated as an integral part of a total treatment program for adhd that may include other measures (psychological, educational and social) for patients with this syndrome. stimulants are not intended for use in the patient who exhibits symptoms secondary to environmental factors and/or other primary psychiatric disorders, including psychosis.,special diagnostic considerations for adhd in children the aetiology of this syndrome is unknown and there is no single diagnostic test. adequate diagnosis requires the use, not only of medical, but also of psychological, educational and social resources. characteristics commonly reported include: chronic history of short attention span, distractibility, emotional lability, impulsivity, moderate to severe hyperactivity, minor neurological signs and an abnormal eeg. learning may or may not be impaired. the diagnosis must be based upon a complete history and evaluation of the child and not solely on the presence of one or more of these characteristics.,drug treatment is not indicated for all children with this syndrome. stimulants are not intended for use in children who exhibit symptoms secondary to environmental factors (e.g. child abuse in particular) or primary psychiatric disorders. appropriate educational placement is essential and psychosocial intervention is generally necessary. when remedial measures alone are insufficient, the decision to prescribe stimulant medicine will depend upon the physician's assessment of the chronicity and severity of the child's symptoms.,continuation of treatment in adolescent and special diagnostic considerations for adhd in adults there is limited information to guide clinicians about how long older adolescents should continue to receive treatment with drugs for attention deficit hyperactivity disorder (adhd). the decision should be based on the extent to which symptoms of adhd and social functioning have improved to a point that medication is no longer needed. if older adolescents have been largely symptom-free for a year and are functioning well, a trial without medication is warranted. this should be undertaken at times of low stress such as during holidays or in a period when a school routine is well established.,adhd needs to be considered in adults who present with longstanding symptoms suggestive of adhd (inattention, impulsivity, disorganisation) that appear to have started in childhood and are persisting into adult life. further, people with personality disorder and/or problems with drug use accompanied by a significant level of impulsivity and inattention should be referred for evaluation by a psychiatrist with the training and skills required to assess and treat adhd. this expertise is necessary due to the overlap of adhd symptoms with anxiety, mood and personality disorders.

RUBIFEN LA methylphenidate hydrochloride 40 mg modified release capsules blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

rubifen la methylphenidate hydrochloride 40 mg modified release capsules blister pack

aft pharmaceuticals pty ltd - methylphenidate hydrochloride, quantity: 40 mg - capsule, hard - excipient ingredients: gelatin; strong ammonia solution; purified talc; potassium hydroxide; triethyl citrate; ammonio methacrylate copolymer; iron oxide red; propylene glycol; methacrylic acid copolymer; iron oxide yellow; titanium dioxide; povidone; shellac; sucrose; maize starch - rubifen la modified release capsules are indicated for the treatment of attention-deficit hyperactivity disorder (adhd).,adhd adhd was previously known as attention-deficit disorder. other terms used to describe this behavioural syndrome include: minimal brain dysfunction in children, hyperkinetic child syndrome, minimal brain damage, minimal cerebral dysfunction, minor cerebral dysfunction and psycho-organic syndrome of children.,rubifen la modified release capsules are indicated as an integral part of a total treatment program for adhd that may include other measures (psychological, educational and social) for patients with this syndrome. stimulants are not intended for use in the patient who exhibits symptoms secondary to environmental factors and/or other primary psychiatric disorders, including psychosis.,special diagnostic considerations for adhd in children the aetiology of this syndrome is unknown and there is no single diagnostic test. adequate diagnosis requires the use, not only of medical, but also of psychological, educational and social resources. characteristics commonly reported include: chronic history of short attention span, distractibility, emotional lability, impulsivity, moderate to severe hyperactivity, minor neurological signs and an abnormal eeg. learning may or may not be impaired. the diagnosis must be based upon a complete history and evaluation of the child and not solely on the presence of one or more of these characteristics.,drug treatment is not indicated for all children with this syndrome. stimulants are not intended for use in children who exhibit symptoms secondary to environmental factors (e.g. child abuse in particular) or primary psychiatric disorders. appropriate educational placement is essential and psychosocial intervention is generally necessary. when remedial measures alone are insufficient, the decision to prescribe stimulant medicine will depend upon the physician's assessment of the chronicity and severity of the child's symptoms.,continuation of treatment in adolescent and special diagnostic considerations for adhd in adults there is limited information to guide clinicians about how long older adolescents should continue to receive treatment with drugs for attention deficit hyperactivity disorder (adhd). the decision should be based on the extent to which symptoms of adhd and social functioning have improved to a point that medication is no longer needed. if older adolescents have been largely symptom-free for a year and are functioning well, a trial without medication is warranted. this should be undertaken at times of low stress such as during holidays or in a period when a school routine is well established.,adhd needs to be considered in adults who present with longstanding symptoms suggestive of adhd (inattention, impulsivity, disorganisation) that appear to have started in childhood and are persisting into adult life. further, people with personality disorder and/or problems with drug use accompanied by a significant level of impulsivity and inattention should be referred for evaluation by a psychiatrist with the training and skills required to assess and treat adhd. this expertise is necessary due to the overlap of adhd symptoms with anxiety, mood and personality disorders.

NO ROT GEL INDUSTRIAL INSECTICIDE/FUNGICIDE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

no rot gel industrial insecticide/fungicide

preschem pty. ltd. - boron present as disodium octaborate tetrahydrate; benzalkonium chloride; mono ethylene glycol - gel - boron present as disodium octaborate tetrahydrate mineral-boron active 111.0 g/l; benzalkonium chloride ammonium-quaternary active 13.2 g/l; mono ethylene glycol ungrouped other 739.0 g/l - wood preservative - brickwork and/or path | concrete | timber | painted concrete | unpainted concrete | wood - algae | borer | fungal decay | mould | termite - mastotermes spp. | decay fungi | giant northern termite | mastotermes darwiniensis

PLASMITE PATROL MASONRY & TIMBER INSECTICIDE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

plasmite patrol masonry & timber insecticide

creepy crawly pest control pty ltd - boron present as disodium octaborate tetrahydrate; benzalkonium chloride; ethylene glycol - liquid - boron present as disodium octaborate tetrahydrate mineral-boron active 111.0 g/l; benzalkonium chloride ammonium-quaternary active 13.2 g/l; ethylene glycol solvent other 739.0 g/l - mixed function pesticide - brick work | concrete | masonry | timber | brick structures | brick wall | bricks | painted concrete | path | paving | unpainted - decay prevention or preservation | insect | pre-conditioning treatment | gives longer life

TIMBERTREAT INSECTICIDE/FUNGICIDE PRESERVATIVE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

timbertreat insecticide/fungicide preservative

kop-coat australia pty ltd - boron present as disodium octaborate tetrahydrate; benzalkonium chloride; mono ethylene glycol - other liquids to be applied undiluted - boron present as disodium octaborate tetrahydrate mineral-boron active 52.0 g/l; benzalkonium chloride ammonium-quaternary active 12.0 g/l; mono ethylene glycol ungrouped other 886.0 g/l - mixed function pesticide - timber | wood - algae | borer | fungal decay | mould | termite - mastotermes spp. | decay fungi | giant northern termite | mastotermes darwiniensis

NO ROT GEL INSECTICIDE / FUNGICIDE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

no rot gel insecticide / fungicide

preschem pty. ltd. - boron present as disodium octaborate tetrahydrate; benzalkonium chloride; mono ethylene glycol - lotion - boron present as disodium octaborate tetrahydrate mineral-boron active 52.0 g/l; benzalkonium chloride ammonium-quaternary active 12.0 g/l; mono ethylene glycol ungrouped other 878.0 g/l - mixed function pesticide - brick work | concrete | masonry | timber | brick structures | brick wall | bricks | painted concrete | path | paving | unpainted - algae | decay prevention or preservation | fungus | insect pest of timber | mould | termite | woodborer | anobiid | borers | drywood termite | fungal leaf spots | fungi | fungus diseases | gives longer life | leaf spot diseases | leaf spots | lyctid | lyctids | quarantine timber insects | subterranean termite | termite | timber destroying insects

TWA WOODCARE DIFFUSIBLE WOOD PRESERVITIVE NO-ROT GEL INJECTION GRADE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

twa woodcare diffusible wood preservitive no-rot gel injection grade

preschem pty. ltd. - boron present as disodium octaborate tetrahydrate; benzalkonium chloride; mono ethylene glycol - gel - boron present as disodium octaborate tetrahydrate mineral-boron active 111.0 g/l; benzalkonium chloride ammonium-quaternary active 13.2 g/l; mono ethylene glycol ungrouped other 739.0 g/l - wood preservative - timber | wood - decay prevention or preservation | insect pest of timber | timber decay | borers | gives longer life | lyctids | quarantine timber insects | termite | timber destroying insects