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Fatimah Al-Shehri,journal club presentation of amplfy study NGH
Fatimah Al-Shehri,journal club presentation of amplfy study NGH

... should be taken consistently ,interact with many drugs. ...
Nebulisers
Nebulisers

... A nebuliser is a powerful drug delivery system. It converts liquid into aerosol droplets suitable for inhalation. It should only be used if recommended by the doctor, and if you would benefit from this form of treatment and even then, only under careful medical supervision. Their use is declining bu ...
Approach to Self poisoning: common pharmaceuticals Risk
Approach to Self poisoning: common pharmaceuticals Risk

Anti depressant drugs
Anti depressant drugs

... Inhibition of this recptors=antidepressant and anti anxiety effects . Lsd ( lysergic acid diethylamide) and mescaline = agonists to ...
Effects of a branched-chain amino acid drink in mania
Effects of a branched-chain amino acid drink in mania

... Fig. 1 Mean scores on the Beigel Manic State Rating Scale (measured as change from baseline) following a branched-chain amino acid (BCAA) drink (^ (^) (n (n¼13) 13) and placebo (& (&) (n (n¼12) ...
Prescribing Information as of XXXX ALLEGRA (fexofenadine hydrochloride)
Prescribing Information as of XXXX ALLEGRA (fexofenadine hydrochloride)

... Mechanism of Action Fexofenadine hydrochloride is an antihistamine with selective peripheral H1-receptor antagonist activity. Both enantiomers of fexofenadine hydrochloride displayed approximately equipotent antihistaminic effects. Fexofenadine inhibited histamine release from peritoneal mast cells ...
About the ATLAS ACS Clinical Trial Program
About the ATLAS ACS Clinical Trial Program

... HealthCare and Johnson & Johnson Pharmaceutical Research & Development, L.L.C. In clinical studies, rivaroxaban has been shown to be effective in preventing VTE in adult patients following elective hip or knee replacement surgery. It has a rapid onset of action with a predictable dose response and h ...
PARKINSON*S DISEASE
PARKINSON*S DISEASE

... – Trihexyphenidyl: 2-15 mg/day – Benztropine: 1-8 mg/day • Side effects: – Dry mouth, sedation, delirium, confusion, hallucinations, constipation, urinary retention ...
Oral Small Molecule GLP-1 Receptor (GLP
Oral Small Molecule GLP-1 Receptor (GLP

... Proof of Concept ...
Angiotensin Receptor Blockers - Advantages of the
Angiotensin Receptor Blockers - Advantages of the

... by the cytochrome P-450 system, drugs that induce, inhibit, or are metabolized by this enzyme do not appear to interact with it. Clinical Efficacy : Seven placebo-controlled studies involved 2,693 patients with essential hypertension; 2,145 patients received olmesartan medoxomil, and 548 patients re ...
More Dosage calculations 2
More Dosage calculations 2

... 5 ml solution. How many mL should patient received? ______________________ 3. Insulin is usually administered in a syringe (U-50 or U-100) that corresponds to the concentration of the insulin stock solution of 100U / mL (U-100). If an insulin syringe is not available, a tuberculin syringe may be use ...
ALLEGRON
ALLEGRON

... antidepressant may be compromised in these patients as cimetidine is discontinued. Several of the tricyclic antidepressants have been cited in these reports. There have been greater than two-fold increases in previously stable plasma levels of other antidepressants, including nortriptyline, when PRO ...
Erythropoiesis-stimulating agents: When good turns evil
Erythropoiesis-stimulating agents: When good turns evil

... disorders. Desvenlafaxine’s efficacy is thought to be related to potentiation of serotonin and norepinephrine in the central nervous system. The labeled dosage is 50 mg once daily. Daily doses up to 400 mg have been used in clinical studies, although no additional benefit was demonstrated at doses g ...
July/August 2008, Number 7
July/August 2008, Number 7

... Salmon calcitonin is produced chemically (Miacalcin®) or using recombinant DNA technology (Fortical®). It is more potent than human calcitonin and has a longer duration of action than the endogenous hormone. The P&T Committee approved therapeutic interchange of these products using the same dosage. ...
djimbe
djimbe

... - C) quinine: 500 mg per day, for five consecutive days (IDA, The Netherlands). Assignment to protocol A, B, or C was made on the basis of every arrival to the hospital. Randomization consisted of assignment of the one treatment every other three eligible patients and so on. Patients gave informed c ...
Ursodex - The IBN SINA Pharmaceutical Industry Ltd.
Ursodex - The IBN SINA Pharmaceutical Industry Ltd.

... mg/kg/day administered in two to four divided doses with food. Dissolution of gallstones: The recommended adult dose is 6-12 mg/kg/day as a single dose at bedtime. Dosing regimen should be adjusted according to each patient's need at the discretion of the physician. Contraindication: Non-functioning ...
administration of decorporation drugs
administration of decorporation drugs

... When accidents occur involving radiation workers, one knows right away what radionuclide(s) is (are) involved. With an RDD event, the radionuclides used will have to be determined by radiologic health experts, either locally or through the Department of Energy (DOE). While some radionuclides are rat ...
Medication Alternatives for the Elderly
Medication Alternatives for the Elderly

... No preferred agents exist within the drug class. Perform risk-benefit determination prior to use. Lower doses should be used and patients should be monitored due to the increased potential for side effects. ...
Link - Lundbeck
Link - Lundbeck

... population in clinical trials with some atypical antipsychotics. The mechanism for this increased risk is not known. There is insufficient data to know if there is an increased risk of cerebrovascular events associated with zuclopenthixol. An increased risk however cannot be excluded. Zuclopenthixo ...
Bob-Holland-Presentation
Bob-Holland-Presentation

... drugs in your countries (and may not be the approved interpretation of the data by regulatory authorities). Nothing in this presentation should be construed as promotional material and I am not advocating the use of any test or any medicine outside of the approved label texts. All drugs and diagnost ...
A PRIMER OF DRUG ACTION
A PRIMER OF DRUG ACTION

... • Absorbed through the skin (usually as a drugh-containing skin patch) • Absorbed through mucous membranes (from snorting or sniffing drug) ...
Half-Life
Half-Life

...  Half-Life is a good predictor of how long a substance will exist.  Drug Half-Life: The time required for the total amount of a drug in blood to diminish by half, once the drug reaches its peak concentration. See PDR  How to construct a half-life curve for a drug. ...
Montelukast
Montelukast

... Asthma: Overall, the use of montelukast has been shown to reduced the use of “as needed” betaagonist use, decrease the incidence of nocturnal awakenings. When compared to placebo, montelukast decreased the incidence of asthma attacks requiring medical intervention, reduced the need for oral corticos ...
Tuberculosis: A Global Epidemic
Tuberculosis: A Global Epidemic

... Special Considerations  Children  Guided by the source-case susceptibility results.  If source unknown and circumstances suggest an increased risk of drug resistance, treat with standard four-drug initial-phase regimen until susceptibility pattern known.  Ethambutol (EMB) can be used safely (15 ...
DOC
DOC

... - Medical treatment and/or dose can be optimized according to the patient’s genotype. - Personalized treatment is a cost-effective method for improving the quality of life and managing risk. Details: Biotransformation of xenobiotics is carried out in the liver through various phase-I, and phase-II r ...
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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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