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What can we do now and what are the gaps in our knowledge?
What can we do now and what are the gaps in our knowledge?

... *Indication approved in Japan only [Edoxaban 30 mg (15 mg if CrCl 30-50 ml/min)]. †In selected patients at high risk of recurrence, according to clinical practice guidelines. ‡ Maximum treatment duration tested in Hokusai-VTE was 12 months. No experience beyond this period is available. §Potent P-gp ...
Hrvatsko društvo za kliničku psihijatriju
Hrvatsko društvo za kliničku psihijatriju

... environmental factors. Because of these factors there are much interindividual variabilities in the treatment with antipsychotics. Genetic determination of patients’ metabolic status is expected to bring clinical benefits by helping to adjust therapeutic doses and reduce adverse reactions (Arranz an ...
Gastrointestinal pro..
Gastrointestinal pro..

... The small intestine generates a wide variety of motor patterns in various spatial and temporal patterns to meet motility requirements in different situations. These contractions are to mix and agitate the luminal contents as well as slowly propel the food distally. All parts of the small bowel have ...
Patient Case - Vanderbilt University Medical Center
Patient Case - Vanderbilt University Medical Center

... – PPI therapy in combination with MMF does not appear to have a significant impact on early MPA exposure Kiberd BA, et al. Ther Drug Monit. 2011;33:120-123 ...
Product Monograph
Product Monograph

... response and metabolic effect should be closely monitored. Hepatitis (hepatocellular and/or cholestatic), elevations of liver enzymes and/or serum bilirubin have occurred during therapy with ACE inhibitors in patients with or without pre-existing liver abnormalities. In most cases the changes were r ...
Principles of Clinical Trials Introduction and Learning Objectives
Principles of Clinical Trials Introduction and Learning Objectives

... Clinical Trial Phases in Drug Development1 (continued) ...
First-time  treatment  with  steroids  in ... comparison  of  the  effects  of ...
First-time treatment with steroids in ... comparison of the effects of ...

... with inhaled BDP and oral prednisone have been compared to each other in 12 asthmatics. It should be pointed out that the study is not placebo-controlled. Based on the analysis for each individual, possible carry-over effects between the treatment periods were not found. The chosen doses of the drug ...
Dupixent - Regeneron
Dupixent - Regeneron

... There are no data on the presence of dupilumab in human milk, the effects on the breastfed infant, or the effects on milk production. Human IgG is known to be present in human milk. The effects of local gastrointestinal and limited systemic exposure to dupilumab on the breastfed infant are unknown. ...
2869 Galliprant PI 12.4015x7.75.indd
2869 Galliprant PI 12.4015x7.75.indd

... Grapiprant is a prostaglandin E2 (PGE2) EP4 receptor antagonist; a non-cyclooxygenase inhibiting, non-steroidal, anti-inflammatory drug. Grapiprant has a canine EP4 receptor binding affinity (Ki) of 24 nM. Prostaglandins have a wide variety of physiologic effects. Prostaglandin E2 (PGE2) is a prosta ...
1 ALLERGIES IN ORAL CAVITY,CLINICAL SYMPTOMS CAUSING
1 ALLERGIES IN ORAL CAVITY,CLINICAL SYMPTOMS CAUSING

... keratinization of hard palate(inhibits resorption of nickel ions) ...
Emergency Pharmacology
Emergency Pharmacology

... prove drug’s safety and to identify tolerable dosages  Phase II – limited controlled evaluation. Designed to test drug’s effect on the specific illness it was designed for. After completion of this phase, a new drug application can be submitted to the FDA. If approved, we move to phase III  Phase ...
Basic pharmacology
Basic pharmacology

... Routes of Administration # To be effective a drug must : – Be present in an active form – At the correct site – At the right concentration – For the right duration of time # The formulation of the product for each delivery route is vital to ensure optimal activity and consistent delivery # Thus cho ...
Slide 1
Slide 1

... codeine, hydrocodone, dihydrocodeine ...
Ciclosporin - Wolverhampton Formulary
Ciclosporin - Wolverhampton Formulary

... Ciclosporin is indicated for the prophylaxis of organ rejection in adults at low to moderate immunological risk receiving a renal transplant. Dosage and Administration Ciclosporin is available as capsules containing 10mg, 25mg, 50mg or 100mg or oral solution containing 100mg per ml. The total daily ...
Clinical Evaluation of Tentex Royal in Erectile Dysfunction
Clinical Evaluation of Tentex Royal in Erectile Dysfunction

... centuries. Tribulus terrestris has been clinically proven to improve sexual desire and enhance erection (Adimoelja, 2000). The pharmacological properties of Tribulus terrestris extracts have been studied on the rabbit corpus cavernosum muscles. The extract showed increase in relaxation of cavernosum ...
Adrenochromes Pink Adrenaline
Adrenochromes Pink Adrenaline

... It is believed that during World War II, supplies of adrenaline ran short. In medical emergencies, patients were given adrenaline from old stock that had been sitting around. This adrenaline had time to sit out and react with the air, causing it to be oxidized and making it appear pink. This oxidize ...
Praluent - Sanofi
Praluent - Sanofi

... The following adverse reactions are also discussed in the other sections of the labeling: • Allergic Reactions [See Warnings and Precautions (5.1).] ...
Improved delivery of fenoterol plus ipratropium bromide using
Improved delivery of fenoterol plus ipratropium bromide using

... patients. All F/I doses produced greater increases in FEV1 than placebo. A log-linear dose-response was obtained for the average increase in FEV1 up to 6 h (AUC0 – 6 h) and peak FEV1 across the dose range administered by Respimat1. Statistically, therapeutic equivalence was not demonstrated between ...
Brain Injury - Dr. John Lavelle
Brain Injury - Dr. John Lavelle

... Comatose receiving greater therapy intensity (by 60%) demonstrated a 31% decrease in length of stay. Blackerby:Brain Injury 1989;4:167-73 ...
The Drug development process
The Drug development process

... • Furthermore, not all patients respond positively to a specific drug (e.g. IFN-β is of clinical benefit to only one in three multiple sclerosis patients. • The range and severity of adverse effects induced by a drug can also vary significantly within a patient population base, genetic variation amo ...
TB Review (Click Here)
TB Review (Click Here)

... Early case detection of primary MDR cases. Education of medical and paramedical professionals in all aspects to be maintained or reemphasized. Free treatment and other incentives for the patients. ...
Antifungal Agents
Antifungal Agents

... specificity than the triazoles, accounting for their higher incidence of drug interactions and side effects. ...
zontivity pi
zontivity pi

... ZONTIVITY was evaluated for safety in 13,186 patients, including 2,187 patients treated for more than 3 years, in the Phase 3 study TRA 2°P TIMI 50 (Thrombin Receptor Antagonist in Secondary Prevention of Atherothrombotic Ischemic Events). The overall study population, patients who had evidence or a ...
Pr TECFIDERA™ - Biogen Canada
Pr TECFIDERA™ - Biogen Canada

... Nursing Women: It is not known whether dimethyl fumarate or its metabolites are excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when TECFIDERA is administered to a nursing woman. Pediatrics (< 18 years of age): The safety and efficacy of TECFIDERA ...
Children’s Advil Suspension Ibuprofen 100 mg (NSAID) per 5 mL Drug Facts
Children’s Advil Suspension Ibuprofen 100 mg (NSAID) per 5 mL Drug Facts

... ■ the child does not get any relief within first day (24 hours) of treatment ■ fever or pain gets worse or lasts more than 3 days ■ redness or swelling is present in the painful area ■ any new symptoms appear Keep out of reach of children. In case of overdose, get medical help or contact a Poison Co ...
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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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