Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

swisse wellness pty ltd - folic acid, quantity: 71.43 microgram/g; pyridoxine hydrochloride, quantity: 34.76 microgram/g (equivalent: pyridoxine, qty 28.57 microgram/g); cyanocobalamin, quantity: 85.7 ng/g; retinol acetate, quantity: 46.89 microgram/g (equivalent: vitamin a, qty 4.57 microgram/g); ascorbic acid, quantity: 1.71 mg/g; d-alpha-tocopheryl acid succinate, quantity: 299.28 microgram/g (equivalent: d-alpha-tocopherol, qty 242.86 microgram/g); selenomethionine, quantity: 5.36 microgram/g (equivalent: selenium, qty 2.14 microgram/g); zinc citrate dihydrate, quantity: 912.86 microgram/g (equivalent: zinc, qty 285.71 microgram/g); ferrous fumarate, quantity: 3.48 mg/g (equivalent: iron, qty 1.14 mg/g); calcium carbonate, quantity: 50 mg/g (equivalent: calcium, qty 20 mg/g); potassium iodide, quantity: 28.07 microgram/g (equivalent: iodine, qty 21.43 microgram/g); inositol, quantity: 571.43 mg/g; fructooligosaccharides, quantity: 114.29 mg/g; colecalciferol, quantity: 1.4333 microgram/g - powder, oral - excipient ingredients: maltodextrin; silicon dioxide; maize starch; acacia; dl-alpha-tocopherol; sucrose; medium chain triglycerides - fertility conception support supports normal ovulation in healthy women help moms-to-be on their journey of reproductive wellness by supporting a healthy cycle in healthy women.

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp - tretinoin (unii: 5688utc01r) (tretinoin - unii:5688utc01r) - tretinoin 0.1 mg in 1 g - tretinoin gel and cream are indicated for topical application in the treatment of acne vulgaris. the safety and efficacy of the long-term use of this product in the treatment of other disorders have not been established. use of the product should be discontinued if hypersensitivity to any of the ingredients is noted.

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp. - amantadine hydrochloride (unii: m6q1eo9td0) (amantadine - unii:bf4c9z1j53) - amantadine hydrochloride 100 mg - amantadine hydrochloride capsules, usp are indicated for the prophylaxis and treatment of signs and symptoms of infection caused by various strains of influenza a virus. amantadine hydrochloride capsules, usp are also indicated in the treatment of parkinsonism and drug-induced extrapyramidal reactions. amantadine hydrochloride capsules, usp are indicated for chemoprophylaxis against signs and symptoms of influenza a virus infection. because amantadine hydrochloride does not completely prevent the host immune response to influenza a infection, individuals who take this drug may still develop immune responses to natural disease or vaccination and may be protected when later exposed to antigenically related viruses. following vaccination during an influenza a outbreak, amantadine hydrochloride capsules, usp prophylaxis should be considered for the 2- to 4-week time period required to develop an antibody response. amantadine hydrochloride capsules, usp are also indicated in the treatment of uncomplicated respirat

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp. - propylthiouracil (unii: 721m9407iy) (propylthiouracil - unii:721m9407iy) - propylthiouracil 50 mg - propylthiouracil is indicated: - in patients with graves' disease with hyperthyroidism or toxic multinodular goiter who are intolerant of methimazole and for whom surgery or radioactive iodine therapy is not an appropriate treatment option. - to ameliorate symptoms of hyperthyroidism in preparation for thyroidectomy or radioactive iodine therapy in patients who are intolerant of methimazole. propylthiouracil is contraindicated in patients who have demonstrated hypersensitivity to the drug or any of the other product components.

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp - varenicline tartrate (unii: 82269asb48) (varenicline - unii:w6hs99o8zo) - varenicline 0.5 mg - chantix is indicated for use as an aid to smoking cessation treatment. chantix is contraindicated in patients with a known history of serious hypersensitivity reactions or skin reactions to chantix pregnancy category c. there are no adequate and well-controlled studies of chantix use in pregnant women. in animal studies, chantix caused decreased fetal weights, increased auditory startle response, and decreased fertility in offspring. chantix should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. in reproductive and developmental toxicity studies, pregnant rats and rabbits received varenicline succinate during organogenesis at oral doses up to 15 and 30 mg/kg/day, respectively. these exposures were 36 (rats) and 50 (rabbits) times the human exposure (based on auc) at the maximum recommended human dose (mrhd) of 1 mg bid. while no fetal structural abnormalities occurred in either species, reduced fetal weights occurred in rabbits at the highest dose (exposures 5

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp - varenicline tartrate (unii: 82269asb48) (varenicline - unii:w6hs99o8zo) - varenicline 0.5 mg - chantix is indicated for use as an aid to smoking cessation treatment. chantix is contraindicated in patients with a known history of serious hypersensitivity reactions or skin reactions to chantix pregnancy category c. there are no adequate and well-controlled studies of chantix use in pregnant women. in animal studies, chantix caused decreased fetal weights, increased auditory startle response, and decreased fertility in offspring. chantix should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. in reproductive and developmental toxicity studies, pregnant rats and rabbits received varenicline succinate during organogenesis at oral doses up to 15 and 30 mg/kg/day, respectively. these exposures were 36 (rats) and 50 (rabbits) times the human exposure (based on auc) at the maximum recommended human dose (mrhd) of 1 mg bid. while no fetal structural abnormalities occurred in either species, reduced fetal weights occurred in rabbits at the highest dose (exposures 5

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp - mirtazapine (unii: a051q2099q) (mirtazapine - unii:a051q2099q) - mirtazapine 15 mg - mirtazapine tablets usp are indicated for the treatment of major depressive disorder. the efficacy of mirtazapine in the treatment of major depressive disorder was established in six week controlled trials of outpatients whose diagnoses corresponded most closely to the diagnostic and statistical manual of mental disorders-3rd edition (dsm-lll) category of major depressive disorder (see clinical pharmacology ). a major depressive episode (dsm-lv) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed or dysphoric mood that usually interferes with daily functioning, and includes at least five of the following nine symptoms: depressed mood, loss of interest in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a suicide attempt or suicidal ideation. the effectiveness of mirtazapine in hospitalized dep

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp - eszopiclone (unii: uzx80k71oe) (eszopiclone - unii:uzx80k71oe) - eszopiclone 2 mg - lunesta is indicated for the treatment of insomnia. in controlled outpatient and sleep laboratory studies, lunesta administered at bedtime decreased sleep latency and improved sleep maintenance. the clinical trials performed in support of efficacy were up to 6 months in duration. the final formal assessments of sleep latency and maintenance were performed at 4 weeks in the 6-week study (adults only), at the end of both 2-week studies (elderly only) and at the end of the 6-month study (adults only). none known. lunesta is a schedule iv controlled substance under the controlled substances act. other substances under the same classification are benzodiazepines and the nonbenzodiazepine hypnotics zaleplon and zolpidem. while eszopiclone is a hypnotic agent with a chemical structure unrelated to benzodiazepines, it shares some of the pharmacologic properties of the benzodiazepines. abuse and addiction are separate and distinct from physical dependence and tolerance. abuse is characterized by misuse of the drug for

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp - diclofenac epolamine (unii: x5f8ekl9zg) (diclofenac - unii:144o8ql0l1) - diclofenac epolamine 180 mg - carefully consider the potential benefits and risks of flector® patch and other treatment options before deciding to use flector® patch. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (seewarnings ). flector® patch is indicated for the topical treatment of acute pain due to minor strains, sprains, and contusions. flector® patch is contraindicated in patients with known hypersensitivity to diclofenac. flector® patch should not be given to patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (seewarnings - anaphylactoid reactions , andprecautions - preexisting asthma ). flector® patch is contraindicated for the treatment of peri-operative pain in the setting of coronary artery bypass graft (cabg) surgery (seewarnings ). flector® patch should not be applied to non-intact or damaged skin resulting fr

Hoa Kỳ - Tiếng Anh - NLM (National Library of Medicine)

rebel distributors corp - etodolac (unii: 2m36281008) (etodolac - unii:2m36281008) - etodolac 400 mg - carefully consider the potential benefits and risks of etodolac tablets and other treatment options before deciding to use etodolac tablets. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). etodolac tablets are indicated: - for acute and long-term use in the management of signs and symptoms of the following:   1. osteoarthritis   2. rheumatoid arthritis - for the management of acute pain etodolac tablets are contraindicated in patients with known hypersensitivity to etodolac or other ingredients in etodolac tablets. etodolac tablets should not be given to patients who have experienced asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings , anaphylactoid reactions and precautions , preexisting asthma). etodolac tablets are contraindicated for the treatment of peri-operative pain in the settin