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introduction – what is parkinson`s disease?
introduction – what is parkinson`s disease?

... • A drug cocktail is currently administered to increase the efficacy of these anti-Parkinson’s agents. • The objective is to synthesise new molecules that are more effective or have less side effects. ...
ThromboGenics Highlights Diabetic Eye Drug Developments at
ThromboGenics Highlights Diabetic Eye Drug Developments at

... This study is evaluating the efficacy and safety of multiple doses of THR-409 (ocriplasmin) in inducing total posterior vitreous detachment (PVD) in patients with non-proliferative diabetic retinopathy (NPDR). The trial is being conducted at centers in the US, Canada and Europe. ThromboGenics believ ...
CAP : Cyclophosphamide / Doxorubicin / Cisplatin in Malignant
CAP : Cyclophosphamide / Doxorubicin / Cisplatin in Malignant

... Hydration / fluid balance - Cisplatin Encourage oral hydration during treatment; for instance, drink a glass of water every hour during treatment, and at least a further 2 litres over the 24 hours following treatment. Weight should be recorded prior to and at the end of Cisplatin treatment, and a s ...
Questions for Review
Questions for Review

... Achieve steady-state more rapidly. Avoid drug toxicity seen at higher concentrations. Maximize drug accumulation with subsequent doses. Determine the most effective concentrations of drug in any given patient. Achieve therapeutic concentrations of drug more rapidly. ...
Ch. 18-Drugs used to Lower Lipids
Ch. 18-Drugs used to Lower Lipids

... 625mg tablets IMPLEMENTATION: see pg. 237 for adult dosages and preparation EVALUATION: report and record: -constipation, abdominal pain, bloating, fullness, nausea, flatulence. Mix drug with non-carbonated drink, no gulping air with swallowing, increase liquid intake, fiber ...
The statins: a drug class to celebrate
The statins: a drug class to celebrate

... a result of LDL-lowering is not clear. Of interest, lipid-lowering with resins, which are not systemically absorbed, can also increase transaminases. A greater than three-fold rise is usually taken as a significant increase. There is little evidence that these changes are associated with more seriou ...
Competitive advantage
Competitive advantage

The Doctor-Patient Relationship in Pharmacotherapy of Depression
The Doctor-Patient Relationship in Pharmacotherapy of Depression

... • Antidepressant nonadherence is a frequent problem that undermines treatment effectiveness. • Nonadherence can be addressed through attention to the medication regimen, treatment availability, and the therapeutic alliance. • Simple interventions such as use of motivational interviewing techniques, ...
DSUR Template - CTT55 - Leeds Teaching Hospitals NHS Trust
DSUR Template - CTT55 - Leeds Teaching Hospitals NHS Trust

... 7.2 Line listing of Serious Adverse Reactions (SARs) during the reporting period. The MHRA require information on any DRUG related Serious Adverse Events. This section should summarise how case reports were selected for inclusion in the line listings. A brief narrative of the SAE should occur here i ...
503 paper
503 paper

... tested 88 patients who were diagnosed with various tumor types.5 They found that higher doses ...
Male Sexual Dysfunction EAU Guidelines Pocket 2009
Male Sexual Dysfunction EAU Guidelines Pocket 2009

... were reported after 12 weeks of treatment by 67% and 81% of men taking 10 mg and 20 mg of tadalafil, respectively, compared to 35% of men taking placebo. The results were confirmed in post-marketing studies. Tadalafil also improved erections in difficult-to-treat subgroups. Vardenafil (Levitra™) Var ...
STADOL NS®
STADOL NS®

... is 1 mg IV or 2 mg IM with repeated doses every 3 to 4 hours, as necessary. This dosage regimen is likely to be effective for the majority of patients. Dosage adjustments of STADOL Injection should be based on observations of its beneficial and adverse effects. The initial dose in the elderly and in ...
Basics Pharmacology Review Part 2 - Dr. Halil
Basics Pharmacology Review Part 2 - Dr. Halil

... the VLDL effect; it can inhibit lipolysis and decrease subsequent hepatic fatty acid uptake as well as inhibit hepatic secretion of VLDL; together these actions decrease serum VLDL levels; increases HDL-cholesterol; the mechanism behind HDL elevation is currently unknown) ...
Core Aspects of Clinical Development and Trials in Chronic
Core Aspects of Clinical Development and Trials in Chronic

... newer secretagogues, such as linaclotide and plecanatide, are peptides that are unabsorbed and systemically inert (Harris & Cromwell, 2007; Shailubhai et al., 2010). The maximal tolerated dose (MTD) of a systemically available drug depends on many factors, including end-organ toxicities and drug int ...
Appendix 5 Notes on Cyclophosphamide Therapy in ILD
Appendix 5 Notes on Cyclophosphamide Therapy in ILD

... systemic sclerosis-associated ILD, oral therapy has been continued for up to 1 year1. Intravenous cyclophosphamide therapy is increasingly favoured over oral therapy due to a significantly better side-effect profile2. Pulsed intravenous treatment is usually given at a dose of 500-750mg/m2 with adjus ...
Alternatives for High Risk Medications in the Elderly
Alternatives for High Risk Medications in the Elderly

... 2. PQA. Use of High-Risk Medications in the Elderly: Review and Revision of Performance Measure. June 2012. 3. Lovell P, Vender RB. Management and Treatment of Pruritus. Skin Therapy Letter. 2007. 12(1). 4. Nadler SF. Non-pharmacologic Treatment of Pain. J Am Osteopath Assoc. 2004; 104(11 suppl): 6S ...
Idiopathic pulmonary fibrosis trials: recommendations for the jury EDITORIAL
Idiopathic pulmonary fibrosis trials: recommendations for the jury EDITORIAL

... fibroblastic focus, which might allow adequate levels of systemically delivered drug to deposit in these areas, thus targeting the arrest of these cells in an early stage of their differentiation [13]. To date, most IPF studies have included orally or subcutaneously administered medications. Drug de ...
Nebulized  or  intravenous  beta adrenoceptor  agonist G.K.
Nebulized or intravenous beta adrenoceptor agonist G.K.

... Departments of most British hospitals [2]. This treatment was recommended as the most effective in 1972 [3J. but after the advent of intravenous salbutamol and terbutaline the choice of administering these drugs in severe acute asthma by aerosol or by the intravenous route was considered to be conte ...
“Natural” Hormone Replacement Therapy
“Natural” Hormone Replacement Therapy

... MNatural progesterone (Prometriumâ) is well absorbed following oral administration but is ~90% metabolized after the hepatic first pass. This can limit the potential for once daily administration and results in high levels of progesterone metabolites which can cause dizziness and drowsiness. 9 Takin ...
Prescribing Information
Prescribing Information

... these reasons, in patients undergoing elective surgery, some authorities recommend gradual withdrawal of betaadrenergic receptor blocking agents. If necessary during surgery, the effects of beta-adrenergic blocking agents may be reversed by sufficient doses of adrenergic agonists. ...
A1991GA09000001
A1991GA09000001

... the early 1 960s was mostly performed using alfentanil. Carfentanil, the most potent anala classical test in mice, introduced by N.H. gesic known, has been selected for veterinary Eddy: inhibition of paw licking on a hot plate. use, more specifically for the immobilization With the introduction of n ...
No more graspiNg, sTrUggLiNg, sqUirmiNg, gaggiNg or growLiNg
No more graspiNg, sTrUggLiNg, sqUirmiNg, gaggiNg or growLiNg

... Suspension should be given for two (2) to three (3) days beyond the cessation of clinical signs. Antibiotic susceptibility of the pathogenic organism(s) should be determined prior to use of this preparation. Therapy with ORBAX® Oral Suspension may be initiated before results of these tests are known ...
Horses im dose 0.4-0.8 mg/kg give good sedation, muscle tremor
Horses im dose 0.4-0.8 mg/kg give good sedation, muscle tremor

... 0.10 to 0.40 mg/kg (0.05 to 0.2 mg/lb) iii)Increased dosages are NOT associated with an increase in analgesia (1)Doses exceeding 0.4 mg/kg (0.2 mg/lb) can cause undesirable excitatory effects iv)Routes of administration (1)IV, IM, or SC ...
Marijuana exposure in animals
Marijuana exposure in animals

... The prognosis is favorable for symptomatic animals with no secondary complications, such as aspiration pneumonia. unchanged in urine.1 THC’s plasma half-life is short because of lipid solubility, but its biologic half-life is long (i.e. 25 to 30 hours) because of adipose storage.1 By five days after ...
Shared care guideline for acamprosate
Shared care guideline for acamprosate

... − in patients with a known hypersensitivity to the drug − in pregnant women and lactating women − in cases of renal insufficiency (serum creatinine >120 micromol/L) − in cases with severe hepatic failure (Childs- Pugh Classification C) The severity of chronic liver disease is usually assessed by usi ...
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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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