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Building Stewardship: A Team Approach 1
Building Stewardship: A Team Approach 1

... Treatment failures with both metronidazole and vancomycin Increasing rates of recurrence with both vancomycin and metronidazole Risk of VRE colonization with both agents ADRs with current treatments especially, metronidazole ...
Product Monograph - AstraZeneca Canada
Product Monograph - AstraZeneca Canada

... In patients requiring concomitant treatment with BRICANYL TURBUHALER and a betablocker, it is recommended that a beta-blocker (e.g., metoprolol) with less predominant β2blocking effects be considered. If concomitant treatment is necessary, patients should be monitored carefully for possible deterior ...
Oral Medications
Oral Medications

... • If tube connected to suction, disconnect and allow 20-30 mins for absorption of med before reconnecting • Disconnect continuous feed prior to giving meds and leave off according to agency ...
Is there still a place for metoclopramide as a prokinetic drug in
Is there still a place for metoclopramide as a prokinetic drug in

... associated with the use of metoclopramide. The side effects in non-ICU patients are as follows1: 1. Neurological adverse reactions, including extrapyramidal disorders, dyskinesia, dystonia, convulsion, hypertonia and tremor. The reported occurrence of tardive dyskinesia ranges from <0.01% to 23%. Hi ...
Anticonvulsive Effect of Seed Extract of Caesalpinia bonducella
Anticonvulsive Effect of Seed Extract of Caesalpinia bonducella

... in the forebrain while the brain stem is involved in the network of tonic PTZ induced convulsions. The antiepileptic drug should abolish or increase the threshold for clonic and tonic convulsions. The mechanism by which PTZ exert its convulsive action is by acting as an antagonist at the GABAA recep ...
Evening Primrose Oil
Evening Primrose Oil

... insufficient to make a reliable assessment of effectiveA systematic review of treatments for cyclical mastal- ness.14 EPO is applied vaginally by many midwives to gia found only three double-blind, placebo-controlled accelerate cervical ripening, shorten labor, and decrease trials of EPO and one m ...
Current Therapy in Ocular Disease -The Vision Institute of Canada-
Current Therapy in Ocular Disease -The Vision Institute of Canada-

... emphasis in original; underlined emphasis added) This claim is misleading because it implies that AzaSite delivers anti-inflammatory effects, when this has not been demonstrated by substantial evidence or substantial clinical experience ...
English - Micromedex
English - Micromedex

... c. May result in increased dasatinib plasma concentrations d. A and C above are correct e. May result in decreased dasatinib plasma concentrations ...
(continued): Many commercially available liquid preparations are
(continued): Many commercially available liquid preparations are

... 8-, 12-, or 24-hours. Crushing or breaking these products can cause an immediate release of a potentially harmful dose of medication sometimes referred to as dose dumping. Besides increasing the risk of adverse events, altering these products reduces their therapeutic benefits by producing wide vari ...
Otomax Label - MSD Animal Health New Zealand
Otomax Label - MSD Animal Health New Zealand

... UNDESIRABLE EFFECTS Gentamicin: While aminoglycosides are absorbed poorly from skin, intoxication may occur when aminoglycosides are applied topically for prolonged periods of time to large wounds, burns or any denuded skin, particularly if there is renal insufficiency. All aminoglycosides have the ...
COO (CHOH)2•2½H2O COOH CH2 CH2 OCH3 O O HN±CH3 CH3
COO (CHOH)2•2½H2O COOH CH2 CH2 OCH3 O O HN±CH3 CH3

... is excreted in the urine, 50% to 60% as metabolites and approximately 15% as unchanged drug and conjugate. The plasma half-life is 2.2 hours. Special Populations No significant pharmacokinetic differences based on age or gender have been demonstrated. The pharmacokinetics of hydrocodone and ibuprofe ...
Lutinus vaginal tablet ENG SmPC
Lutinus vaginal tablet ENG SmPC

... Adults The dose of Lutinus is 100 mg administered vaginally three times daily starting at oocyte retrieval. The administration of Lutinus should be continued for 30 days, if pregnancy has been confirmed. Paediatric population There is no relevant use of Lutinus in the paediatric population. Elderly ...
Chapter 9. Comparing Two Population Means
Chapter 9. Comparing Two Population Means

...  A  B contains zero ? ...
Scott Shannon, , is an assistant clinical professor in the
Scott Shannon, , is an assistant clinical professor in the

... SJW to tricyclic antidepressants, the outcomes were roughly equivalent but the side effect profile of SJW was quite superior (all side effects: 19.8% vs 52.8%). In the 15 placebo-controlled trials, SJW demonstrated significantly better clinical outcomes. There have been 3 studies in children. In one ...
June 26, 2006 Office of Special Nutritionals (HFS-450) Food and Drug Administration
June 26, 2006 Office of Special Nutritionals (HFS-450) Food and Drug Administration

... literature to convert via the aromatase enzyme to estrogens (1). In addition, DHEA has been shown to convert to more potent 5-alpha reduced metabolites. 19-norandrostanes, including 19-norDHEA, are known to convert to less potent metabolites through 5-alpha reduction. In addition, the lack of a carb ...
Extract from Clinical Evaluation Report: Riociguat
Extract from Clinical Evaluation Report: Riociguat

... these patients medical therapy is warranted. There are currently no approved pharmacotherapies for CTEPH and patients are frequently treated off-label. Anticoagulation may prevent further embolism and in situ thrombosis but not necessarily disease progression. There are no effective primary therapie ...
Antimalarial drug discovery: efficacy models for compound
Antimalarial drug discovery: efficacy models for compound

... order to determine whether the same ED5 0 and ED9 0 values are observed in drug-resistant strains of rodent malaria when compared to P. berghei ANKA. In vivo generation of drug resistance: It may also be helpful to determine the potential of parasites to develop resistance to a new compound in vivo, ...
- Journal of Hepatology
- Journal of Hepatology

... trials of AIH difficult. This is important because achieving a biochemical remission influences long term outcome and the combination of normal transaminases and normal IgG/gammaglobulins may best predict the lack of histological activity [3,16,17]. Obviously, the major weakness of the study is the la ...
Moxacil - Square Pharmaceuticals Ltd.
Moxacil - Square Pharmaceuticals Ltd.

Child Psychiatric Medications 101
Child Psychiatric Medications 101

... • any other action is a side effect – side effects may be adverse, beneficial, or innocuous – adverse drug reactions include  toxic effects due to overmedication  common side effects that appear at therapeutic dosages  idiosyncratic side effects (e.g., allergic reactions) that are not  clearly re ...
毒物与吸毒Poisons and drug abuse Department of Forenxic
毒物与吸毒Poisons and drug abuse Department of Forenxic

IOPIDINE ® Solution
IOPIDINE ® Solution

... (Apraclonidine Hydrochloride) Ophthalmic Solution. The possibility of an additive or potentiating effect with CNS depressants (alcohol, barbiturates, opiates, sedatives, anesthetics) should be borne in mind. Tricyclic antidepressants have been reported to blunt the hypotensive effect of systemic clo ...
The dose-related effects of bolus esmolol on heart rate and blood
The dose-related effects of bolus esmolol on heart rate and blood

... esmolol by IV bolus involved giving 100 or 200 mg of esmolol or placebo 90 seconds before intubation. Forty-five patients were studied using a rapidsequence induction with thiopental, 3 to 5 mg/kg; succinylcholine, 1.5 mg/kg, also was used. Esmolol was ineffective at protecting all cardiovascular re ...
Iodine and Tyrosine
Iodine and Tyrosine

... 2 capsules per day, in divided doses, with meals. ...
Prinivil - Merck.com
Prinivil - Merck.com

... adequately to diuretics and digitalis [see Clinical Studies (14.2)]. 1.3 Acute Myocardial Infarction PRINIVIL is indicated for the reduction of mortality in treatment of hemodynamically stable patients within 24 hours of acute myocardial infarction. Patients should receive, as appropriate, the stand ...
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Bilastine



Bilastine (trade name Bilaxten) is a second generation antihistamine drug for the treatment of allergic rhinoconjunctivitis and urticaria (hives).It exerts its effect as a selective histamine H1 receptor antagonist, and has a effectiveness similar to cetirizine, fexofenadine and desloratadine. It was developed in Spain by FAES Farma.Bilastine is approved in the European Union for the symptomatic treatment of allergic rhinoconjunctivitis and urticaria, but it is not approved by the U.S. Food and Drug Administration for any use in the United States. Bilastine meets the current European Academy of Allergy and Clinical Immunology (EAACI) and Allergic Rhinitis and its Impact of Asthma (ARIA) criteria for medication used in the treatment of allergic rhinitis.Bilastine has been effective in the treatment of ocular symptoms and diseases of allergies, including rhinoconjuctivitis. Additionally, bilastine has been shown to improve quality of life, and all nasal and ocular symptoms related to allergic rhinitis.
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