FEXOFENADINE-DRLA fexofenadine hydrochloride 180 mg film coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

fexofenadine-drla fexofenadine hydrochloride 180 mg film coated tablet blister pack

dr reddys laboratories australia pty ltd - fexofenadine hydrochloride, quantity: 180 mg - tablet, film coated - excipient ingredients: mannitol; magnesium stearate; croscarmellose sodium; powdered cellulose; colloidal anhydrous silica; maize starch; titanium dioxide; hypromellose; allura red ac aluminium lake; iron oxide black; macrogol 400 - seasonal allergic rhinitis, urticaria in adults and children aged 12 years and over.

FEXOFENADINE-DRLA fexofenadine hydrochloride 120 mg film coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

fexofenadine-drla fexofenadine hydrochloride 120 mg film coated tablet blister pack

dr reddys laboratories australia pty ltd - fexofenadine hydrochloride, quantity: 120 mg - tablet, film coated - excipient ingredients: colloidal anhydrous silica; maize starch; magnesium stearate; mannitol; croscarmellose sodium; powdered cellulose; titanium dioxide; hypromellose; allura red ac aluminium lake; iron oxide black; macrogol 400 - seasonal allergic rhinitis, in adults and children aged 12 years and over.

IVABRADINE MYLAN Ireland - English - HPRA (Health Products Regulatory Authority)

ivabradine mylan

mcdermott laboratories ltd t/a gerard laboratories - ivabradine oxalate - film coated tablet - 5 milligram - ivabradine

IVABRADINE MYLAN Ireland - English - HPRA (Health Products Regulatory Authority)

ivabradine mylan

mcdermott laboratories ltd t/a gerard laboratories - ivabradine oxalate - film coated tablet - 7.5 milligram - ivabradine

RIMANTADINE HYDROCHLORIDE tablet, film coated United States - English - NLM (National Library of Medicine)

rimantadine hydrochloride tablet, film coated

amneal pharmaceuticals of new york llc - rimantadine hydrochloride (unii: jei07oos8y) (rimantadine - unii:0t2ef4jqtu) - rimantadine hydrochloride 100 mg - rimantadine hydrochloride tablet is indicated for the prophylaxis and treatment of illness caused by various strains of influenza a virus in adults (17 years and older). rimantadine hydrochloride tablet is indicated for prophylaxis against influenza a virus in children (1 year to 16 years of age). in controlled studies of children (1 year to 16 years of age), healthy adults (17 years and older), and elderly patients (65 years of age and older), rimantadine hydrochloride has been shown to be safe and effective in preventing signs and symptoms of infection caused by various strains of influenza a virus. since rimantadine 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 outbreak, rimantadine hydrochloride prophylaxis should be considered for the 2 to 4 week time period required to develop an antibody response. however, the safety and effectiveness of rimantadine hydrochloride prophylaxis have not been demonstrated for longer than 6 weeks. rimantadine hydrochloride therapy should be considered for adults (17 years and older) who develop an influenza-like illness during known or suspected influenza a infection in the community. when administered within 48 hours after onset of signs and symptoms of infection caused by influenza a virus strains, rimantadine hydrochloride has been shown to reduce the duration of fever and systemic symptoms. the following points should be considered before initiating treatment or prophylaxis with rimantadine hydrochloride: - rimantadine hydrochloride is not a substitute for early vaccination on an annual basis as recommended by the centers for disease control and prevention advisory committee on immunization practices. - influenza viruses change over time. emergence of resistance mutations could decrease drug effectiveness. other factors (for example, changes in viral virulence) might also diminish clinical benefit of antiviral drugs. prescribers should consider available information on influenza drug susceptibility patterns and treatment effects when deciding whether to use rimantadine hydrochloride. rimantadine hydrochloride tablet is contraindicated in patients with known hypersensitivity to drugs of the adamantane class, including rimantadine and amantadine.

RIMANTADINE HYDROCHLORIDE tablet, film coated United States - English - NLM (National Library of Medicine)

rimantadine hydrochloride tablet, film coated

h.j. harkins company, inc. - rimantadine hydrochloride (unii: jei07oos8y) (rimantadine - unii:0t2ef4jqtu) - rimantadine hydrochloride 100 mg - rimantadine hydrochloride tablet is indicated for the prophylaxis and treatment of illness caused by various strains of influenza a virus in adults (17 years and older). rimantadine hydrochloride tablet is indicated for prophylaxis against influenza a virus in children (1 year to 16 years of age). in controlled studies of children (1 year to 16 years of age), healthy adults (17 years and older), and elderly patients (65 years of age and older), rimantadine hydrochloride has been shown to be safe and effective in preventing signs and symptoms of infection caused by various strains of influenza a virus. since rimantadine 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 outbreak, rimantadine hydrochloride prophylaxis should be considered for the 2 to 4 week

RIMANTADINE HYDROCHLORIDE tablet, film coated United States - English - NLM (National Library of Medicine)

rimantadine hydrochloride tablet, film coated

stat rx usa llc - rimantadine hydrochloride (unii: jei07oos8y) (rimantadine - unii:0t2ef4jqtu) - rimantadine hydrochloride 100 mg - rimantadine hydrochloride tablet is indicated for the prophylaxis and treatment of illness caused by various strains of influenza a virus in adults (17 years and older). rimantadine hydrochloride tablet is indicated for prophylaxis against influenza a virus in children (1 year to 16 years of age). in controlled studies of children (1 year to 16 years of age), healthy adults (17 years and older), and elderly patients (65 years of age and older), rimantadine hydrochloride has been shown to be safe and effective in preventing signs and symptoms of infection caused by various strains of influenza a virus. since rimantadine 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 outbreak, rimantadine hydrochloride prophylaxis should be considered for the 2 to 4 week

AMANTADINE HYDROCHLORIDE tablet United States - English - NLM (National Library of Medicine)

amantadine hydrochloride tablet

newgen pharmaceuticals llc - amantadine hydrochloride (unii: m6q1eo9td0) (amantadine - unii:bf4c9z1j53) - amantadine hydrochloride 100 mg - amantadine hydrochloride tablets are indicated for the prophylaxis and treatment of signs and symptoms of infection caused by various strains of influenza a virus. amantadine hydrochloride tablets are also indicated in the treatment of parkinsonism and drug-induced extrapyramidal reactions. amantadine hydrochloride tablets are indicated for chemoprophylaxis against signs and symptoms of influenza a virus infection. because amantadine hydrochloride tablets do 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 tablets prophylaxis should be considered for the 2- to 4-week time period required to develop an antibody response. amantadine hydrochloride tablets are also indicated in the treatment of uncomplicated respiratory tract illness caused

AMANTADINE HYDROCHLORIDE tablet United States - English - NLM (National Library of Medicine)

amantadine hydrochloride tablet

cipla usa inc. - amantadine hydrochloride (unii: m6q1eo9td0) (amantadine - unii:bf4c9z1j53) - amantadine hydrochloride 100 mg - amantadine hydrochloride tablets are indicated for the prophylaxis and treatment of signs and symptoms of infection caused by various strains of influenza a virus. amantadine hydrochloride tablets are also indicated in the treatment of parkinsonism and drug-induced extrapyramidal reactions. amantadine hydrochloride tablets are indicated for chemoprophylaxis against signs and symptoms of influenza a virus infection.  because amantadine hydrochloride tablets do 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 tablets prophylaxis should be considered for the 2- to 4-week time period required to develop an antibody response. amantadine hydrochloride tablets are also indicated in the treatment of uncomplicated respiratory tract illness cause