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Sex - jemds
Sex - jemds

... in group B (52%). Salazar et al20 study also showed similar results in which seventy boys vomited sometime during treatment, 35 (51%) in the racecadotril group and 35 (52 percent) in the placebo group. Baumer et al23 in their study found that the frequency of symptoms associated with diarrhoea remai ...
Study protocol - BioMed Central
Study protocol - BioMed Central

... or two. In the reduction and simplification group (which consisted of 19 patients taking a mean of 3.7antipsychotic drugs at a mean dose of 2,067 mg CP at the time of enrollment), the mean dose reduction was 674 mg CP, and the mean reduction in the number of drugs was 1.0. Eleven patients succeeded ...
Solutions - Cynthia Bell
Solutions - Cynthia Bell

... (c) The authors concluded from the test that, “There is no evidence to support a beneficial effect of chelation therapy.” Explain how this conclusion agrees with inference based on the values in the confidence interval. We can also test that there is no true difference between the two therapies seei ...
DEPRESSION
DEPRESSION

REFERENCE GUIDE FOR THE PHARMACY LICENSING EXAM
REFERENCE GUIDE FOR THE PHARMACY LICENSING EXAM

... 5). Data from pregnancy registries indicate that infants exposed to Topiramate (Topamax) in utero have an increased risk for cleft lip and/or cleft palate (oral clefts). It is therefore classified under Pregnancy Category D. ...
co-guide
co-guide

... may cause undesirable adverse effects. Adverse drug reactions (ADRs) are the most common reasons for ART interruption among HIV infected patients and over 25% of these patients discontinue ART within the first year of treatment due to side effects2. Immune dysregulation, altered drug metabolism and ...
data sheet
data sheet

... exhibits antibacterial activity similar but not identical to the macrolide antibiotics (e.g. erythromycin). Some cross-resistance (with erythromycin) including a phenomenon known as dissociated cross-resistance or macrolide effect has been reported. Microorganisms have not developed resistance to LI ...
Controlled drug release
Controlled drug release

... conc that are produced. The ratio of max to minimum drug conc at steady state should not exceed the therapeutic index of the drug. ...
Controlled drug release
Controlled drug release

... conc that are produced. The ratio of max to minimum drug conc at steady state should not exceed the therapeutic index of the drug. ...
of patients
of patients

... 2012 American College of Rheumatology Guidelines for Management of Gout Significance & innovations (I) “The starting dosage of allopurinol should be no greater than 100 mg/day and less than that in moderate to severe chronic kidney disease (CKD), followed by gradual upward titration of the maintena ...
ANTHELMINTIC DRUGS
ANTHELMINTIC DRUGS

... alopecia ,elevation of liver enzymes .  used with caution under 2ys of age may cause convulsion in this group.  enzyme inducers and inhibitors affect plasma level of the drug.  hepatic parenchymal disease ...
OPIOID ANALGESICS
OPIOID ANALGESICS

... • Thus, glutaminergic NMDA receptors MAY regulate mureceptor mRNA, accounting for the development of tolerance to the continuous presence of opioid • Cross-tolerance is the condition where tolerance for one drug produces tolerance for another drug – person who is tolerant to morphine will also be to ...
Group 2 Food Toxicokinetics
Group 2 Food Toxicokinetics

... Should you keep or toss … ...
vitamin A (vye-ta-min A) - DavisPlus
vitamin A (vye-ta-min A) - DavisPlus

... sional. Explain that the best source of vitamins is a well-balanced diet with foods from the four basic food groups. ● Foods high in vitamin A include liver, fish liver oils, egg yolks, yellow-orange fruits and vegetables, dark green leafy vegetables, whole milk, vitamin A– fortified skim milk, butt ...
Colloids
Colloids

... • We’re Ok using Pentaspan, Voluven. • There is a dilutional effect, but this is only  relevant at very high doses.  ...
Pharmacogenomics and Personalized Medicine
Pharmacogenomics and Personalized Medicine

... Genetic Variance: Single Nucleotide Polymorphisms (SNPs) are differences in the DNA. They represent 90% of all human genetic variations. Genetically similar to a mutation, but distinct in that a SNP is not causal to a clinical disease or disorder. Genetic Inheritance: The appearance of deleterious m ...
immunosuppressed patients - Enlighten: Publications
immunosuppressed patients - Enlighten: Publications

... multiorgan failure rather than respiratory failure. ƒ Idiopathic pneumonia syndrome is a syndrome of diffuse lung injury that develops post HSCT where an infectious cause is not found. ƒ Bronchiolitis Obliterans Organising Pneumonia (BOOP) is related to GvsHD and usually responds to steroids. It has ...
Tarceva - Genentech
Tarceva - Genentech

... • If severe reactions occur with concomitant use of strong CYP3A4 inhibitors or with a combined CYP3A4 and CYP1A2 inhibitor. Avoid concomitant use if possible [see Drug Interactions (7)]. • When restarting therapy following withholding treatment for a dose-limiting toxicity that has resolved to base ...
Student Handout
Student Handout

... half-life remains constant at 2-3 hours; however, at higher doses, the enzymes responsible for metabolism become saturated and the apparent half-life can increase to 15-30 hours. Because of this, 5-7 days may be required before a steady-state concentration is reached. Salicylate and its metabolites ...
Product Information: Rifaximin
Product Information: Rifaximin

... conducted. There was no evidence of teratogenicity in pregnant rats or rabbits treated with rifaximin during the period of organogenesis at respective oral doses up to 300 and 1000 mg/kg/day. The dose in rats was about 4.5 times the clinical dose (600 mg/day) based on body surface area. Compared wit ...
Drug Nomenclature
Drug Nomenclature

... • Chemical name — identifies drug’s atomic and molecular structure • Generic name — assigned by the manufacturer that first develops the drug • Official name — name by which it is identified in official publications USP and NF • Trade name — brand name copyrighted by the company that sells the drug ...
TRIPTORELIN (Gonapeptyl Depot® or Decapeptyl
TRIPTORELIN (Gonapeptyl Depot® or Decapeptyl

... 1. The chronological age at the beginning of therapy should be under 9 years in girls and under 10 years in boys. 2. After finalising the therapy, development of puberty characteristics will occur. Information with regards to future fertility is still limited but at present no evidence suggests this ...
Surrogate End Points
Surrogate End Points

... outcomes”, are often very time consuming and expensive (but not impossible) to study. In a stroke prevention randomised controlled trail (RCT), for example, researchers would have to recruit 10,000 participants and wait for five years for the results. In comparison, surrogate endpoints are much fast ...
Contraindications of Vasoconstrictors in Dentistry
Contraindications of Vasoconstrictors in Dentistry

... these vasoconstrictors are used improperly. In spite of records of safety set by using these drugs, there is evidence to adverse reactions ranging from 2.5%11% and even death may take place12. As a dentist it is ones responsibility to have a thorough knowledge about the systemic diseases and the ind ...
A comparison of the tolerability of the direct renin inhibitor
A comparison of the tolerability of the direct renin inhibitor

... and 51 patients in the lisinopril-based treatment group) was considered sufficient to evaluate the overall tolerability profile of the aliskiren- and lisinopril-based regimens and to satisfy the regulatory requirement for the assessment of safety. Assuming a dropout rate of 15%, a total of X180 pati ...
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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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