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2012 פברואר ה
2012 פברואר ה

... Plasma concentrations decline slowly thereafter and were still measurable in most subjects 96 hours post-dose. A second dose administered 48 hours later resulted in a plasma profile similar to that of the first dose. Distribution: Absorbed miconazole is bound to plasma proteins (88.2%) and red blood ...
Fentanyl citrate - Therapeutic Goods Administration
Fentanyl citrate - Therapeutic Goods Administration

... In a published literature report, continuous infusion of fentanyl for 24 h had no effect on blood pressure, heart rate, cardiac output and left ventricular function in conscious rats at a dose of 20 µg/kg/h intravenous (IV).3 In subsequent experiments carried out after animal sacrifice, there was no ...
5-7 days - FertilityCenter
5-7 days - FertilityCenter

... = 19), ovulatory disorder (n = 7), other (n = 19) and combined factors (n = 86). Pregnancy rates (% per couple, % per cycle) [overall (31.58, 12.7)] [<36 years (38.10, 15.69)] [>36 years (18.75, 7.23)] were greater in the <36 years group (P < 0.025). The probability of conception after three treatme ...
Deutsche Bank 36th Annual Health Care Conference
Deutsche Bank 36th Annual Health Care Conference

...  Patients with chronic lymphocytic leukemia, who have not responded to or have become refractory to previous therapies ...
TOBI® (nebulised tobramycin)
TOBI® (nebulised tobramycin)

... Centre Cardiff state that these patients would also be expected to have had 4 exacerbations requiring IV antibiotics in 1 year. The 2003 Cochrane Collaboration review1 of nebulised anti-pseudomonal antibiotics for CF concluded that, “Nebulised anti-pseudomonal antibiotic treatment improves lung func ...
The drugs discussed in this chapter are used to alter an individual`s
The drugs discussed in this chapter are used to alter an individual`s

... Related to the CNS stimulation: nervousness, insomnia, dizziness, headache, blurred vision ...
PMB Dept of Internal medicine : Presentation: ARV Therapy
PMB Dept of Internal medicine : Presentation: ARV Therapy

... • When to change treatment – When the treatment has stopped working – When the treatment has caused harm – When there is a better treatment to try ...
T HE   C HE MIS T R Y ... IS CHOCOLATE AN APHRODISIAC?
T HE C HE MIS T R Y ... IS CHOCOLATE AN APHRODISIAC?

FDA Issues Complete Response Letter to
FDA Issues Complete Response Letter to

... Alimera conducted two Phase 3 pivotal clinical trials (collectively known as the FAME Study) for ILUVIEN involving 956 patients in sites across the United States, Canada, Europe and India to assess the efficacy and safety of ILUVIEN with two doses, a high and low dose, for the treatment of DME. The ...
Prescribing Matters Please circulate to all prescribers, including
Prescribing Matters Please circulate to all prescribers, including

... Newsletter archive can be found at: http://nww.hastingsandrothergpinfo.nhs.uk/gp/prescribing/index.asp http://nww.esdwgpinfo.nhs.uk/prescribing/index.asp ...
Symax DuoTab - Capellon Pharmaceuticals
Symax DuoTab - Capellon Pharmaceuticals

... hydrolyzed to tropic acid and tropine but the majority of the drug is excreted in the urine unchanged within the first 12 hours. Only traces of this drug are found in breast milk. Hyoscyamine sulfate passes the blood brain barrier and the placental barrier. Symax™ Duotab releases 0.125 mg hyoscyamin ...
HIGHLIGHTS OF PRESCRIBING INFORMATION -------------------------------CONTRAINDICATIONS------------------------------
HIGHLIGHTS OF PRESCRIBING INFORMATION -------------------------------CONTRAINDICATIONS------------------------------

... In vitro studies have shown that rifaximin did not inhibit cytochrome P450 isoenzymes 1A2, 2A6, 2B6, 2C9, 2C19, 2D6, 2E1 and CYP3A4 at concentrations ranging from 2 to 200 ng/mL [see Clinical Pharmacology (12.3)]. Rifaximin is not expected to inhibit these enzymes in clinical use. An in vitro study ...
Effects
Effects

... (an individual dose for supporting a therapeutic effect during long-term treatment) ...
Treatment of Tuberculosis: Standard Therapy for Active Disease in
Treatment of Tuberculosis: Standard Therapy for Active Disease in

... • Tuberculosis treatment should always be undertaken in consultation with a physician who is well-versed and experienced in its management. • All patients should be initially started on a 4-drug regimen of Isoniazid (INH), Rifampin (RIF), Pyrazinamide (PZA), and Ethambutol (EMB). Following the initi ...
E-Prescribing Form
E-Prescribing Form

... and contractors (collectively, “Pharmacy”), to use and disclose all of my individually identifiable health information; protected health information including but not limited to records that may contain information created by other persons or entities, including physicians and other health care prov ...
Seventh Report of the Joint National Committee on Prevention
Seventh Report of the Joint National Committee on Prevention

... doses of the component agents, resulting in fewer side effects.129,130 ...
QA50_8_Hypersalivationgeneral
QA50_8_Hypersalivationgeneral

... Glycopyrronium (glycopyrrolate) is slower in onset and produces less tachycardia than atropine or hyoscine (16). Benefits of using glycopyrronium include its long duration of action and its inability to cross the blood-brain barrier thus reducing central adverse effects (e.g. sedation, restlessness) ...
Main Title Slide — Always use Title Case on
Main Title Slide — Always use Title Case on

Department of Pharmacy
Department of Pharmacy

... 1. Ensures that only manufacturer’s unit-dose syringes are procured whenever available; otherwise, unit-dose and barcoded packaging is provided before LMWH is dispensed. 2. References medical staff approved dose rounding chart for enoxaparin and modifies ordered dose in a manner that allows dispensi ...
Introduction
Introduction

... transmission and reduces the ability of cholinesterase inhibitors to reverse the action. Pancuronium is a long acting aminosterodial nondepolarzing NMBA with a peak effect occurring within 2-3 minutes and duration of action of 60-90 minutes.3 Approximately, 30-45% of the drug is metabolized in the l ...
excipient-related adverse drug reactions: a clinical approach
excipient-related adverse drug reactions: a clinical approach

... but concluded that no change in legislation was needed. It is known that some individuals are in fact prone to hyperactivity following the intake of colouring agents or dyes, whether it is in the food that they eat or in the medicine that they drink.10 It was also found that not only do colouring ag ...
shands - UF Health Professionals
shands - UF Health Professionals

... prolactin and blood glucose). However, there are limited comparative data published on the efficacy and safety of ziprasidone compared with other atypical agents. The limited data that are available are poor quality. The weight gain effects of ziprasidone appear to be similar to haloperidol. It also ...
Sedation & Analgesia - Pediatric Critical Care Education
Sedation & Analgesia - Pediatric Critical Care Education

... Onset of action: 10-20 minutes Peak action: 60 minutes Duration 4-8 hours No reversal agent Unreliable in children over 3 years of age (Krauss Lancet 2006) ...
COUGHING AND YOUR PET
COUGHING AND YOUR PET

... is via the urine. The absorption and elimination characteristics beyond this point are unknown. In cats, no oral absorption information is available at other than 2.5 mg/kg, administered orally as a single dose. Saturable absorption and/or elimination processes may occur at greater doses. When satur ...
Possible Test Questions
Possible Test Questions

... Common Neurotransmitter Receptors found in Psych. Drugs and their effects - SERT – Serotonin Transporter – Serotoin Reuptake Inhibitors (SRI’s or SSRI’s) – i.e. some drugs, particularly the SSRIs, blockade (antagonize) the SERT  leading to ↓ reuptake of serotonin back into the presynaptic neurons a ...
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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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