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Panic Disorder
Panic Disorder

... alprazolam acts very quickly to control the attacks. Patient is relieved of his panic symptoms in a day or two. ...
Comparison of the efficacy and safety of mometasone furoate dry
Comparison of the efficacy and safety of mometasone furoate dry

... the baseline visit, patients eligible for participation in the study discontinued use of their previous inhaled corticosteroid and were randomly assigned to one of the following treatments: MF DPI 100, 200, or 400 mg b.i.d; or BUD Turbuhaler1 400 mg b.i.d. All treatments were taken twice a day, in t ...
SUPRAX® CEFIXIME TABLETS USP, 400 mg Rx only To reduce the
SUPRAX® CEFIXIME TABLETS USP, 400 mg Rx only To reduce the

... Lifetime studies in animals to evaluate carcinogenic potential have not been conducted. Cefixime did not cause point mutations in bacteria or mammalian cells, DNA damage, or chromosome damage in vitro and did not exhibit clastogenic potential in vivo in the mouse micronucleus test. In rats, fertilit ...
shands - UF Health Professionals
shands - UF Health Professionals

... Formulary. One approach is to designate these drugs not available. These drugs will not be obtained through the nonformulary system. However, it is preferable to use education to discourage the use of these products. Benzonatate (Tessalon® Perles) is an example of a nonformulary drug with questionab ...
PRINCIPLES OF PHARMACOKINETICS Learning Objectives
PRINCIPLES OF PHARMACOKINETICS Learning Objectives

... group is dependent on urinary pH; raising the pH promotes excretion of acids, impairs excretion of bases), renal disease (creatinine clearance or its estimate from serum creatinine provides a useful clinical indicator of impaired renal function and is approximately proportional to drug renal clearan ...
1- Rheumatoid arthritis
1- Rheumatoid arthritis

Guidelines for Conducting Clinical Trials
Guidelines for Conducting Clinical Trials

... PHASE II  The purpose of a phase II trial is to demonstrate activity of the drug and to obtain further safety data. It also aims at the determination of effective dose ranges and regimens and provides an optimal background for the design of future therapeutic trials.  This phase may be an open tri ...
PPT
PPT

... Parkinson’s Disease and remains the “gold standard” after so many years. • It definitely provides dramatic benefits in terms of alleviating many symptoms thus allowing patients afflicted with this disease to enjoy their routine activities as well as prolong their life span. • In the early stages of ...
Long-acting inhaled bronchodilators in COPD: how many drugs do we need? EDITORIAL
Long-acting inhaled bronchodilators in COPD: how many drugs do we need? EDITORIAL

... [12, 17–19] and, as anticipated, there was a significant improvement in mean trough FEV1 of ,100 mL after this drug. This is comparable with other studies and was significantly greater than that after formoterol (b.i.d.). There was further significant improvement in spirometry over the first 12 h af ...
(PSD) July 2016 PBAC Meeting - (Word 56KB)
(PSD) July 2016 PBAC Meeting - (Word 56KB)

... The PBAC rejected the submission for denosumab in March 2016 on the basis of low quality clinical data that did not support the claim of superior efficacy over zoledronic acid, and the lack of a clear clinical place for denosumab. The PBAC considered that the clinical place of denosumab had not been ...
Document
Document

Hallucinogens - People Server at UNCW
Hallucinogens - People Server at UNCW

... Spontaneous recurrence of trip after period of normalcy • can occur after long periods of abstinence • more common after multiple high dose use • prolonged afterimages for days and weeks after – mechanism unknown ...
Asthma Update
Asthma Update

renal impairment studies in early development services
renal impairment studies in early development services

... Table 2: Drugs Administered to Subjects with Renal Impairment ...
phenytoin - DavisPlus
phenytoin - DavisPlus

... Absorption: Absorbed slowly from the GI tract. Bioavailability differs among products; the Dilantin and Phenytek preparations are considered to be “extended” products. Other products are considered to be prompt release. Distribution: Distributes into CSF and other body tissues and fluids. Enters bre ...
Newer Weight Loss Medications: Worth the Weight
Newer Weight Loss Medications: Worth the Weight

... and weight maintenance for at least one year and that studies also assess effects on weight-related comorbidities. Additionally, medications must demonstrate either a mean change in baseline body weight between placebo-treated groups of ≥ 5% or that the proportion of patients losing at least 5% of t ...
Substance Related Disorders - California Association for Alcohol
Substance Related Disorders - California Association for Alcohol

... Intoxication: severe dissociative reactions – paranoid delusions, hallucinations, can become very agitated/ violent with decreased awareness of pain. Cerebellar symptoms - ataxia, dysarthria, nystagmus (vertical and horizontal) ...
HYPNOTIC - SEDATIVE DRUGS Dra. Ma. Shiela C
HYPNOTIC - SEDATIVE DRUGS Dra. Ma. Shiela C

... > Methohexital ( Brevital ) > Thiamylal (Surital) ...
Rosuvastatin Stada 5 mg film-coated tablets Rosuvastatin
Rosuvastatin Stada 5 mg film-coated tablets Rosuvastatin

... There is no experience in subjects with severe hepatic impairment (Child-Pugh scores above 9). Animal studies provided limited evidence of reproductive toxicity. If a patient becomes pregnant during use of this product, treatment should be discontinued immediately. Rosuvastatin is excreted in the mi ...
Complexities of Warfarin Therapy May Lead to Increased Resource
Complexities of Warfarin Therapy May Lead to Increased Resource

... UNSAFE INR LEVELS ~44% of INR values were unsafe in a study with anticoagulation clinIc patients (INR <2.0 or >4.0 prior to study enrollment)†10 ...
Gabapentin (300mg) Information and Advice for Users with Chronic
Gabapentin (300mg) Information and Advice for Users with Chronic

... a low dose and will build up gradually over days and weeks. Should you have any troublesome side-effects, stay on a low dose for a few more days before starting to build it up again. This reduces the sideeffects and makes it possible for you to carry on with the treatment. If you cannot tolerate the ...
highlights of prescribing information
highlights of prescribing information

... compared to placebo (p<0.0001). Eleven percent (11%) of patients treated with LOTRONEX 1 mg twice daily withdrew from the studies due to constipation. Although the number of patients with IBS treated with LOTRONEX 0.5 mg twice daily is relatively small (n = 243), only 11% of those patients reported ...
Ch 4 lec 1
Ch 4 lec 1

... Distribution of Drugs Within the Body  Lipid Solubility – ease with drug molecules are soluble in fat.  Heroin more lipid soluble than morphine so gets to brain faster; more intense ”rush”  Depot Binding – binding of a drug with various tissues of the body or with proteins in the blood.  If drug ...
European Experience on the Practical Use of Levosimendan in
European Experience on the Practical Use of Levosimendan in

... view of the long-lasting hemodynamic improvement because of a long-acting metabolite (half-life, approximately 80 hours),16 levosimendan appears to be a suitable drug for repetitive treatment of patients with advanced HF as a bridge to cardiac transplantation. Large-scale trials including comparison ...
PRODUCT INFORMATION JONCIA 25, 50, 100 mg Capsules NAME
PRODUCT INFORMATION JONCIA 25, 50, 100 mg Capsules NAME

... plasma concentration (Cmax) is reached 2 to 4 hours hours after dosing. Plasma concentrations are dose-proportional up to 300 mg twice daily. After repeated administration, the steady-state is reached within 2 to 3 days. In these conditions, the Cmax is about 250 ng/mL after a 100 mg daily dose give ...
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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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