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Profile Documents Logout
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Knowledge
Knowledge

... happens. This includes not just the cellular and molecular aspects, but also the relevant clinical laboratory or instrumental parameters. Correct prescribing – includes using the right medication, at the right dose, with the right way and frequency of administration and stopping the drug use at the ...
et al. - Deep learning for chemoinformatics
et al. - Deep learning for chemoinformatics

... • Concerned with the study of drug action on a molecular and chemical level • Seek to discover and validate new therapeutic strategies to improve human health • Draw from ideas across multiple fields of study: ...
P. aeruginosa
P. aeruginosa

... Cefaclor, cefuroxime axetil, and cefprozil, can be given orally. The usual dosage for adults is 10 to 15 mg/kg/d in 2 to 4 divided doses; children should be given 20 to 40 mg/kg/d up to a maximum of 1 g/d. Except for cefuroxime axetil, these drugs are not predictably active against penicillin-resis ...
Product Information - Therapeutic Goods Administration
Product Information - Therapeutic Goods Administration

... integrase strand transfer inhibitor raltegravir depending on the type and number of mutations. Viruses expressing the T66I/A mutations maintain susceptibility to raltegravir, while most other patterns showed reduced susceptibility to raltegravir. Pharmacodynamics Effects on Electrocardiogram The ele ...
Ezetimibe (Zetia): a new type of lipid-lowering
Ezetimibe (Zetia): a new type of lipid-lowering

... to the addition of ezetimibe may have an effect on LDL cholesterol reduction. Also, the duration of the study could have been longer. Most studies have used a time period of at least 12 weeks to observe changes in LDL cholesterol reductions. However, this study was conducted for a period of only 8 w ...
Pharmacological treatments for fatigue associated with palliative care
Pharmacological treatments for fatigue associated with palliative care

... studies if they met the selection criteria. If we identified two or more studies that investigated a specific drug with the same dose in a population with the same disease and using the same assessment instrument or scale, we conducted meta-analysis. In addition, we compared the type of drug investi ...
YOUR COMPLETE SOURCE FOR PARENTERAL NUTRITION
YOUR COMPLETE SOURCE FOR PARENTERAL NUTRITION

... thrombocytopenia in neonates occurred (less than 1%). Geriatric Use Clinical studies of Nutrilipid® 20% did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differenc ...
Doctor Discussion Guide
Doctor Discussion Guide

... Have there been any major changes in your life or health recently? ___________________________________________________________________ _________________________________________________________________________________________________________________________ Are you taking GEODON each day as prescribe ...
2009 internal medicine course - final
2009 internal medicine course - final

... one or more of the sites of defect in Type 2 DM - what about: Efficacy Side effects Actually improve outcomes or make them worse Decrease mortality or kill people ...
The features and management of poisoning with drugs used to treat
The features and management of poisoning with drugs used to treat

... L-dopa is converted by dopa decarboxylase to dopamine, an active catecholamine with prominent alphaand beta-adrenergic effects, and toxicity appears to be a direct effect and also receptor-mediated.31 There are few reports of acute overdose in the literature. A 61-year-old man (on 7.5 g levodopa dai ...
FLAVERIA TRINERVIA HEPATOTOXICITY USING RATS Research Article
FLAVERIA TRINERVIA HEPATOTOXICITY USING RATS Research Article

Population Pharmacokinetics
Population Pharmacokinetics

... and elimination is a specific feature of very young paediatric patients, therefore changes in dose may be necessary for a patient over time, based on individual maturation.  Pharmacokinetic studies in the paediatric population reveal which dose will produce blood levels similar to those observed in ...
PUBLIC ASSESSMENT REPORT of the Medicines Evaluation Board
PUBLIC ASSESSMENT REPORT of the Medicines Evaluation Board

... pharmacovigilance system at their disposal, which is based on the current European legislation. Routine pharmacovigilance activities are sufficient to identify actual or potential risks and a detailed European Risk Management Plan is not necessary for this product. Withdrawal of 0.5 mg/ml nasal spra ...
DRUG NAME: Hydroxyurea
DRUG NAME: Hydroxyurea

... not recommended due to risk of serious toxicities, namely pancreatitis, hepatotoxicity, and peripheral neuropathy; if the combination is used, monitor for toxicities.3 Previous or current chemotherapy: increased risk of bone marrow suppression; dose adjustment may be ...
How Much Tylenol is Too Much Tylenol
How Much Tylenol is Too Much Tylenol

... time standby remedy has been Tylenol (Acetaminophen, APAP; N-Acetyl-PAminophenol). This medication is marketed not only for its medicinal quality, but for NOT causing stomach upset and risks of stomach ulceration; this medicine is noted for being well tolerated. With this quality, it seems obvious t ...
Patient-Controlled Analgesia
Patient-Controlled Analgesia

... Parenteral opioids have three profiles of ␮ opiatereceptor binding capacity: pure agonists, agonistantagonists, and partial agonists (Table 3). Pure agonists are mainstays of acute pain management because they provide full ␮-receptor binding, i.e., there is no analgesic ceiling (e.g., titration of m ...
Supreme Court Rejects Bright
Supreme Court Rejects Bright

... "companies can control what they have to disclose…by controlling what they say to the market." Slip op. at 16. The Court considered Matrixx's public statements as part of the "total mix" of information, and concluded that if the complaint's allegations were true, the information Matrixx had about Z ...
Feline Dosing Chart
Feline Dosing Chart

... after dexmedetomidine could lead to adverse cardiovascular effects (secondary tachycardia, prolonged hypertension, and cardiac arrhythmias1, 2, 3). However, an anticholinergic drug may be administered to dogs at least 10 minutes before dexmedetomidine for the prevention of the dexmedetomidine-induce ...
RISPERDAL
RISPERDAL

... than lower doses, were associated with more extrapyramidal symptoms and other adverse effects, and are generally not recommended. In a single study supporting once-daily dosing, the efficacy results were generally stronger for 8 mg than for 4  mg. The safety of doses above 16  mg per day has not bee ...
Differentiating neuropathic pain, opioid
Differentiating neuropathic pain, opioid

... neurological structures and could not be described with dermatomes. The pain gradually increased and very high doses of morphine were administered. The patient reported that each dose increase gave some relief for a short while, which was why the dose of morphine increased so swiftly. The patient wa ...
Michigan Medical Marijuana
Michigan Medical Marijuana

... patient's primary caregiver, if any, were collectively in possession of a quantity of marihuana that was not more than was reasonably necessary to ensure the uninterrupted availability of marihuana for the purpose of treating or alleviating the patient's serious or debilitating medical condition.” • ...
QA415_2_Mistletoe_cancer2015
QA415_2_Mistletoe_cancer2015

... The conclusion of the Cochrane Review is that the evidence to support use of mistletoe in cancers is weak, and until more high quality research is available, the true efficacy and safety of the products are unknown.7 Osterman et al, 2009 Osterman et al attempted a systematic review and meta-analysis ...
Drug-induced oral lichenoid reactions. A literature review
Drug-induced oral lichenoid reactions. A literature review

...  Well defined, mainly lymphocytic band infiltration in the most superficial zone of the connective tissue.  Signs of degenerative liquefaction in epithelial basal layer.  Absence of epithelial dysplasia. The term “histologically compatible with” is to be used in application to all histopatholo ...
Bioidentical Hormone Therapy
Bioidentical Hormone Therapy

... is the predominant circulating estrogen before menopause, with 80 times the activity of estriol but making up only 10% to 20% of the formulation. In addition to 17β-estradiol and estriol, the compounded drug tri-estrogen (tri-est) contains estrone (at a ratio of 8:1:1) and is the predominant circula ...
, English, Pages 303
, English, Pages 303

... found unchanged (without worsening, but without any benefit) at two consecutive checkups, the next therapy option was initiated. A remission was declared when patients were clinically normal, and skin scrapings from three sites where mites had been previously identified were negative. An animal was ...
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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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