VYVANSE CAPSULES 60 mg Singapura - Inggris - HSA (Health Sciences Authority)

vyvanse capsules 60 mg

takeda pharmaceuticals (asia pacific) pte. ltd. - lisdexamfetamine dimesylate - capsule - lisdexamfetamine dimesylate 60.0 mg

VYVANSE CAPSULES 70 mg Singapura - Inggris - HSA (Health Sciences Authority)

vyvanse capsules 70 mg

takeda pharmaceuticals (asia pacific) pte. ltd. - lisdexamfetamine dimesylate - capsule - lisdexamfetamine dimesylate 70.0 mg

GUANFACINE HYDROCHLORIDE tablet film coated extended release Amerika Serikat - Inggris - NLM (National Library of Medicine)

guanfacine hydrochloride tablet film coated extended release

mylan pharmaceuticals inc. - guanfacine hydrochloride (unii: pml56a160o) (guanfacine - unii:30omy4g3mk) - guanfacine 1 mg

GUANFACINE EXTENDED-RELEASE tablet Amerika Serikat - Inggris - NLM (National Library of Medicine)

guanfacine extended-release tablet

par pharmaceutical inc. - guanfacine (unii: 30omy4g3mk) (guanfacine - unii:30omy4g3mk) - guanfacine 1 mg

GUANFACINE EXTENDED-RELEASE- guanfacine tablet, extended release Amerika Serikat - Inggris - NLM (National Library of Medicine)

guanfacine extended-release- guanfacine tablet, extended release

sandoz inc - guanfacine hydrochloride (unii: pml56a160o) (guanfacine - unii:30omy4g3mk) - guanfacine 1 mg - guanfacine extended-release tablets are indicated for the treatment of attention deficit hyperactivity disorder (adhd) as monotherapy and as adjunctive therapy to stimulant medications [see clinical studies (14)]. guanfacine extended-release tablets are contraindicated in patients with a history of a hypersensitivity reaction to guanfacine extended-release tablets or its inactive ingredients, or other products containing guanfacine. rash and pruritus have been reported. pregnancy category b risk summary there are no adequate and well-controlled studies of guanfacine extended-release tablets in pregnant women. no fetal harm was observed in rats and rabbits with administration of guanfacine at 4 and 2.7 times, respectively, the maximum recommended human dose. because animal studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. animal data reproduction studies conducted in rats have shown that guanfacine crosses the placenta. however, administratio

GUANFACINE EXTENDED-RELEASE tablet Amerika Serikat - Inggris - NLM (National Library of Medicine)

guanfacine extended-release tablet

avera mckennan hospital - guanfacine (unii: 30omy4g3mk) (guanfacine - unii:30omy4g3mk) - guanfacine 2 mg

GUANFACINE tablet extended release Amerika Serikat - Inggris - NLM (National Library of Medicine)

guanfacine tablet extended release

avera mckennan hospital - guanfacine hydrochloride (unii: pml56a160o) (guanfacine - unii:30omy4g3mk) - guanfacine 1 mg

DEXTROAMPHETAMINE SULFATE tablet Amerika Serikat - Inggris - NLM (National Library of Medicine)

dextroamphetamine sulfate tablet

wilshire pharmaceuticals, inc. - dextroamphetamine sulfate (unii: jj768o327n) (dextroamphetamine - unii:tz47u051fi) - dextroamphetamine sulfate 5 mg - dextroamphetamine sulfate tablets, usp are indicated for: known hypersensitivity to amphetamine products. during or within 14 days following the administration of monoamine oxidase inhibitors (hypertensive crises may result). dextroamphetamine sulfate tablets are a schedule ii controlled substance. dextroamphetamine sulfate has a high potential for abuse and misuse which can lead to the development of a substance use disorder, including addiction (see warnings). dextroamphetamine sulfate can be diverted for non-medical use into illicit channels or distribution. abuse is the intentional non-therapeutic use of a drug, even once, to achieve a desired psychological or physiological effect. misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider or for whom it was not prescribed. drug addiction is a cluster of behavioral, cognitive, and physiological phenomena that may include a strong desire to take the drug, difficulties in con

ZENZEDI- dextroamphetamine sulfate tablet Amerika Serikat - Inggris - NLM (National Library of Medicine)

zenzedi- dextroamphetamine sulfate tablet

azurity pharmaceuticals, inc. - dextroamphetamine sulfate (unii: jj768o327n) (dextroamphetamine - unii:tz47u051fi) - dextroamphetamine sulfate 2.5 mg - zenzedi® (dextroamphetamine sulfate tablets, usp) is indicated for: known hypersensitivity to amphetamine products . during or within 14 days following the administration of monoamine oxidase inhibitors (hypertensive crises may result). zenzedi is a schedule ii controlled substance. dextroamphetamine sulfate has a high potential for abuse and misuse which can lead to the development of a substance use disorder, including addiction (see warnings). dextroamphetamine sulfate can be diverted for non-medical use into illicit channels or distribution. abuse is the intentional non-therapeutic use of a drug, even once, to achieve a desired psychological or physiological effect. misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider or for whom it was not prescribed. drug addiction is a cluster of behavioral, cognitive, and physiological phenomena that may include a strong desire to take the drug, difficulties in controlling drug u

DEXTROAMPHETAMINE SULFATE tablet Amerika Serikat - Inggris - NLM (National Library of Medicine)

dextroamphetamine sulfate tablet

aurolife pharma, llc - dextroamphetamine sulfate (unii: jj768o327n) (dextroamphetamine - unii:tz47u051fi) - dextroamphetamine sulfate 5 mg - dextroamphetamine sulfate tablets, usp are indicated for:   1.      narcolepsy . 2.      attention deficit disorder with hyperactivity , as an integral part of a total treatment program which typically includes other remedial measures (psychological, educational, social) for a stabilizing effect in pediatric patients (ages 3 to 16 years) with a behavioral syndrome  characterized  by  the  following  group  of  developmentally  inappropriate symptoms: moderate to severe distractibility, short attention span, hyperactivity, emotional lability, and impulsivity. the diagnosis of this syndrome should not be made with finality when these symptoms are only of comparatively recent origin. nonlocalizing (soft) neurological signs, learning disability, and abnormal eeg may or may not be present, and a diagnosis of central nervous system dysfunction may or may not be warranted. known hypersensitivity to amphetamine products. during or within 14 days following the administration of monoamine oxidase inhibitors (hypertensive crises may result). dextroamphetamine sulfate is a schedule ii controlled substance. abuse dextroamphetamine sulfate has a high potential for abuse and misuse which can lead to the development of a substance use disorder, including addiction (see warnings). dextroamphetamine sulfate can be diverted for non-medical use into illicit channels or distribution. abuse is the intentional non-therapeutic use of a drug, even once, to achieve a desired psychological or physiological effect. misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider or for whom it was not prescribed. drug addiction is a cluster of behavioral, cognitive, and physiological phenomena that may include a strong desire to take the drug, difficulties in controlling drug use (e.g., continuing drug use despite harmful consequences, giving a higher priority to drug use than other activities and obligations), and possible tolerance or physical dependence. misuse and abuse of amphetamines may cause increased heart rate, respiratory rate, or blood pressure; sweating; dilated pupils; hyperactivity; restlessness; insomnia; decreased appetite; loss of coordination; tremors; flushed skin; vomiting; and/or abdominal pain. anxiety, psychosis, hostility, aggression, and suicidal or homicidal ideation have also been observed with cns stimulants abuse and/or misuse. misuse and abuse of cns stimulants, including dextroamphetamine sulfate, can result in overdose and death (see overdosage), and this risk is increased with higher doses or unapproved methods of administration, such as snorting or injection. dependence physical dependence dextroamphetamine sulfate may produce physical dependence. physical dependence is a state that develops as a result of physiological adaptation in response to repeated drug use, manifested by withdrawal signs and symptoms after abrupt discontinuation or a significant dose reduction of a drug. withdrawal signs and symptoms after abrupt discontinuation or dose reduction following prolonged use of cns stimulants including dextroamphetamine sulfate include dysphoric mood; depression; fatigue; vivid, unpleasant dreams; insomnia or hypersomnia; increased appetite; and psychomotor retardation or agitation. tolerance dextroamphetamine sulfate may produce tolerance. tolerance is a physiological state characterized by a reduced response to a drug after repeated administration (i.e., a higher dose of a drug is required to produce the same effect that was once obtained at a lower dose).