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Suggestion from clinicians
Suggestion from clinicians

... “Domperidone and metoclopramide were equally effective in alleviating symptoms of diabetic gastroparesis. Elicited adverse CNS effects were more severe and more common with metoclopramide. Somnolence was acknowledged by 49% of patients (mean severity score, 1.03) after 4 wk of metoclopramide compare ...
Treatment of ACS Objectives “Early Invasive
Treatment of ACS Objectives “Early Invasive

... More on Lytic Use • Goal is 30 minutes from initial emergency system presentation to lytic administration • Most effective if used within 12 hours of symptom onset • Small benefit between 12-24 hours of symptom onset • Not beneficial if > 24 hours of symptom onset • No need to wait for biochemical c ...
Anti-anemics
Anti-anemics

Thrombolytic Medications
Thrombolytic Medications

... International Normalized Ration (INR): therapeutic range for oral anticoagulant therapy  Defined as patient prothombin time/mean of normal prothrombin time for the lab  Prothrombin time determined from a fasting blood sample obtained 8-14 hours after the last dose of an oral anticoagulant o Toxici ...
Drugs For The Treatment Of Heroin Addiction
Drugs For The Treatment Of Heroin Addiction

... metabolites get stored in fatty tissue. When the fatty tissue is broken down, the metabolites are released and act on the brain again, causing a craving. ...
Excess mortality in patients with asthma on long-acting b -agonists 2
Excess mortality in patients with asthma on long-acting b -agonists 2

... increase in either the primary end-point or asthma-related death. The termination criterion was defined as an RR of 1.4 for the primary end-point and an RR of 3.0 for asthma-related deaths. This interim analysis was performed in 2002 after 25,858 patients had been recruited. SMART was prematurely te ...
Pharmacological Treatment of Bulimia Nervosa
Pharmacological Treatment of Bulimia Nervosa

cv risk reduction in canada 2009
cv risk reduction in canada 2009

... LDL-C is causally linked to atherosclerosis and CHD events. Statins effectively and predictably reduce coronary events in proportion to the extent to which they reduce LDL-C, as evidenced by the reduction in CHD events in statin treated patients who achieve LDL-C treatment goals in long-term statin ...
Study title: A series of N-of-1 trials to assess therapeutic
Study title: A series of N-of-1 trials to assess therapeutic

... vasoconstriction of blood vessels, resulting in an increase in blood pressure. After absorption, effective inhibition occurs in 2-4 hours after oral administration. Onset of antihypertensive activity is at 1 hour, with peak reduction of blood pressure achieved by 4-6 hours after administration. The ...
6/28/2012
6/28/2012

... Discuss key features of available antifungal agents, including spectrum and common toxicities Provide a brief overview of adjunctive treatment measures for certain fungal infections ...
The “Magic Bullet” idea
The “Magic Bullet” idea

... the trial earlier. Typical results were often a statistically significant but clinically meaningless improvement, largely due to the fact that only a few patients responded well. WHY? • Phase 4: Post-marketing studies: investigate rare side effects not captured by Phase 3 studies under real-life con ...
Dopaminergic agents 拟多巴胺药levodopa, (L
Dopaminergic agents 拟多巴胺药levodopa, (L

... decreases dose of Levodopa by 75%; ...
Product Monograph - Sanofi Genzyme Canada
Product Monograph - Sanofi Genzyme Canada

... symptoms develop, patients should be closely monitored, promptly investigated, and appropriately treated. Interruption of JEVTANA therapy is recommended until diagnosis is available. Early use of supportive care measures may help improve the condition. The benefit of resuming JEVTANA treatment must ...
traditional use of swarnamrita prashana as a preventive measure
traditional use of swarnamrita prashana as a preventive measure

... play as drug delivery system with immunomodulatoy effect.34 In a study conducted among school going children of Kolkata of low income group showed that underweight and overweight were found to be the risk factors for diseases.35 This public health initiative is an example of health economics involve ...
Does my study require an Investigational New Drug Application (IND
Does my study require an Investigational New Drug Application (IND

... A food is considered to be a drug if it is “intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease,” except that a food may bear an authorized health claim about reducing the risk of a disease without becoming a drug. The FDA regulates conventional foods (including ...
drl_DAIDS_NVP_final_ risk_list_7_2010
drl_DAIDS_NVP_final_ risk_list_7_2010

... The drugs used in this study may have side effects, some of which are listed below. Please note that these lists do not include all the side effects seen with these drugs. These lists include the more serious or common side effects with a known, or possible relationship. If you have questions concer ...
Dr. Brian Feagan
Dr. Brian Feagan

... • Rare immune-mediated reactions (e.g. 1 in 10,000 patientyears) will only become apparent through robust postmarketing surveillance The immunogenicity profile of biopharmaceuticals and biosimilars can only come from clinical trials and robust post-marketing programmes Schellekens H. Nat Rev Drug Di ...
Crominet eyedrops, solution ENG SmPC
Crominet eyedrops, solution ENG SmPC

... sensitised mast cells which occurs after exposure to specific antigens. Sodium cromoglicate acts by inhibiting the release of histamine and various membrane derived mediators from the mast cell. Sodium cromoglicate has demonstrated the activity in vitro to inhibit the degranulation of non-sensitised ...
DENS 521 5th S - Home - KSU Faculty Member websites
DENS 521 5th S - Home - KSU Faculty Member websites

Milk Thistle: Hepatoprotection at its Best
Milk Thistle: Hepatoprotection at its Best

... defined inclusion criteria. While effect sizes are small or not statistically significant in some, there does appear to be benefits, although higher quality and long term studies need to be done. A systematic review of studies on the effectiveness of milk thistle in liver disease identified 16 rando ...
Antidepressant drugs - Dr Lynch
Antidepressant drugs - Dr Lynch

... Main postulated action re-uptake inhibition, but have effects on 5HT1a, 5HT2 and NA ß receptors Relatively little effect on dopamine Have membrane stabilising effects Anticholinergic, antiadrenergic and quinidine effects. ...
Evaluation of Multiple Dosing Regimens in Phase 2 Studies of
Evaluation of Multiple Dosing Regimens in Phase 2 Studies of

... symptoms were maintained throughout randomization and open label phase Shaded Area shows Open Label period, all subjects on sapropterin. p-value is mean change difference from baseline for the differences between placebo and sapropterin. Mean change difference from placebo (SE); SE = standard error ...
Depression and Suicide
Depression and Suicide

... Main postulated action re-uptake inhibition, but have effects on 5HT1a, 5HT2 and NA ß receptors Relatively little effect on dopamine Have membrane stabilising effects Anticholinergic, antiadrenergic and quinidine effects. ...
ANS Review+Qs
ANS Review+Qs

... receptor X. When the drug is applied to cells expressing receptor X, there is an immediate change in transmembrane sodium and potassium flow thought secondary to the opening of receptorcoupled transmembrane ion channels. Receptor X is most likely which type of receptor? A. a1adrenoreceptor B. β1 adr ...
IN VIVO COMPARATIVE BIOAVAILABILITY STUDY OF TWO VALPROIC ACID SYRUP
IN VIVO COMPARATIVE BIOAVAILABILITY STUDY OF TWO VALPROIC ACID SYRUP

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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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