LOSARTAN POTASSIUM TABLETS, 25 MG- losartan potassium tablet
LOSARTAN POTASSIUM TABLETS, 50 MG- losartan potassium tablet
LOSA Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

losartan potassium tablets, 25 mg- losartan potassium tablet losartan potassium tablets, 50 mg- losartan potassium tablet losa

jubilant cadista pharmaceuticals inc. - losartan potassium (unii: 3st302b24a) (losartan - unii:jms50mpo89) - losartan potassium 25 mg - losartan potassium is indicated for the treatment of hypertension in adults and pediatric patients 6 years of age and older, to lower blood pressure. lowering blood pressure lowers the risk of fatal and nonfatal cardiovascular (cv) events, primarily strokes and myocardial infarction. these benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including losartan. control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. many patients will require more than 1 drug to achieve blood pressure goals. for specific advice on goals and management, see published guidelines, such as those of the national high blood pressure education program’s joint national committee on prevention, detection, evaluation, and treatment of high blood pressure (jnc). numerous antihypertensive drugs, f

VORICONAZOLE- voriconazole tablet Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

voriconazole- voriconazole tablet

appco pharma llc - voriconazole (unii: jfu09i87tr) (voriconazole - unii:jfu09i87tr) - voriconazole 50 mg - voriconazole is indicated for use in patients 12 years of age and older in the treatment of the following fungal infections: in clinical trials, the majority of isolates recovered were aspergillus fumigatus. there was a small number of cases of culture-proven disease due to species of aspergillus other than a. fumigatus [see clinical studies (14.1), and clinical pharmacology (12.4)]. [see clinical studies (14.2), and clinical pharmacology (12.4)] [see clinical studies (14.3), and clinical pharmacology (12.4)] [see clinical studies (14.4), and clinical pharmacology (12.4)] specimens for fungal culture and other relevant laboratory studies (including histopathology) should be obtained prior to therapy to isolate and identify causative organism(s). therapy may be instituted before the results of the cultures and other laboratory studies are known. however, once these results become available, antifungal therapy should be adjusted accordingly. - voriconazole is contraindicated in patients with known hypersensitiv

CUTIVATE- fluticasone propionate ointment Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

cutivate- fluticasone propionate ointment

pharmaderm a division of fougera pharmaceuticals inc. - fluticasone propionate (unii: o2gmz0lf5w) (fluticasone - unii:cut2w21n7u) - fluticasone propionate 0.05 mg in 1 g - pregnancy category c

NYSTATIN ointment Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

nystatin ointment

zydus pharmaceuticals (usa) inc. - nystatin (unii: bdf1o1c72e) (nystatin - unii:bdf1o1c72e) - nystatin ointment is indicated in the treatment of cutaneous or mucocutaneous mycotic infections caused by candida albicans and other susceptible candida species. nystatin ointment is not indicated for systemic, oral, intravaginal or ophthalmic use. nystatin ointment is contraindicated in patients with a history of hypersensitivity to any of their components.

TRIAMCINOLONE ACETONIDE ointment Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

triamcinolone acetonide ointment

macleods pharmaceuticals limited - triamcinolone acetonide (unii: f446c597ka) (triamcinolone acetonide - unii:f446c597ka) - triamcinolone acetonide ointment is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparations.

CHLORTHALIDONE tablet Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

chlorthalidone tablet

unichem pharmaceuticals (usa), inc. - chlorthalidone (unii: q0mqd1073q) (chlorthalidone - unii:q0mqd1073q) - diuretics such as chlorthalidone are indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effect of other antihypertensive drugs in the more severe forms of hypertension. chlorthalidone is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. chlorthalidone has also been found useful in edema due to various forms of renal dysfunction, such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. the routine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unnecessary hazard. diuretics do not prevent development of toxemia of pregnancy, and there is no satisfactory evidence that they are useful in the treatment of developed toxemia. edema during pregnancy may arise from pathologic causes or from the physiologic and mechanical consequences of pregnancy. chlorthalidone is indicated in pregnancy when edema is due to

WARFARIN SODIUM tablet Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

warfarin sodium tablet

camber pharmaceuticals - warfarin sodium (unii: 6153cwm0cl) (warfarin - unii:5q7zvv76ei) - warfarin sodium 1 mg - warfarin sodium tablets, usp are indicated for: limitations of use warfarin sodium tablets, usp have no direct effect on an established thrombus, nor does it reverse ischemic tissue damage. once a thrombus has occurred, however, the goals of anticoagulant treatment are to prevent further extension of the formed clot and to prevent secondary thromboembolic complications that may result in serious and possibly fatal sequelae. warfarin sodium tablets are contraindicated in women who are pregnant except in pregnant women with mechanical heart valves, who are at high risk of thromboembolism [see warnings and precautions (5.5) and use in specific populations (8.1)] . warfarin sodium tablets can cause fetal harm when administered to a pregnant woman. warfarin sodium tablets exposure during pregnancy causes a recognized pattern of major congenital malformations (warfarin embryopathy and fetotoxicity), fatal fetal hemorrhage, and an increased risk of spontaneous abortion and fetal mortality. if warfarin sodium tablets

FLUOXETINE- fluoxetine hydrochloride capsule Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

fluoxetine- fluoxetine hydrochloride capsule

avpak - fluoxetine hydrochloride (unii: i9w7n6b1kj) (fluoxetine - unii:01k63sup8d) - fluoxetine 10 mg - fluoxetine capsules are indicated for the treatment of: - acute and maintenance treatment of major depressive disorder [see clinical studies (14.1)] . -  acute and maintenance treatment of obsessions and compulsions in patients with obsessive compulsive disorder (ocd) [see clinical studies (14.2)] . -  acute and maintenance treatment of binge-eating and vomiting behaviors in patients with moderate to severe bulimia nervosa [see clinical studies (14.3)] . - acute treatment of panic disorder, with or without agoraphobia [see clinical studies (14.4)] . fluoxetine capsules and olanzapine in combination are indicated for the treatment of: - acute treatment of depressive episodes associated with bipolar i disorder. - treatment resistant depression (major depressive disorder in patients, who do not respond to 2 sep

CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE cream Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

clotrimazole and betamethasone dipropionate cream

rebel distributors corp - clotrimazole (unii: g07gz97h65) (clotrimazole - unii:g07gz97h65), betamethasone dipropionate (unii: 826y60901u) (betamethasone - unii:9842x06q6m) - clotrimazole 10 mg in 1 g - clotrimazole and betamethasone dipropionate cream and lotion are indicated in patients 17 years and older for the topical treatment of symptomatic inflammatory tinea pedis, tinea cruris, and tinea corporis due to epidermophyton floccosum, trichophyton mentagrophytes and trichophyton rubrum. effective treatment without the risks associated with topical corticosteroid use may be obtained using a topical antifungal agent that does not contain a corticosteroid, especially for noninflammatory tinea infections. the efficacy of clotrimazole and betamethasone dipropionate cream or lotion for the treatment of infections caused by zoophilic dermatophytes (e.g. microsporum canis ) has not been established. several cases of treatment failure of clotrimazole and betamethasone dipropionate cream, usp in the treatment of infections caused by microsporum canis have been reported. clotrimazole and betamethasone dipropionate cream or lotion is contraindicated in patients who are sensitive to clotrimazole, betamethasone dipr

DAPSONE tablet Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

dapsone tablet

alvogen inc. - dapsone (unii: 8w5c518302) (dapsone - unii:8w5c518302) - dapsone 25 mg - dermatitis herpetiformis: (d.h.) leprosy: all forms of leprosy except for cases of proven dapsone resistance. hypersensitivity to dapsone and/or its derivatives.