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Polypharmacy, Adverse Drug Reactions, and Geriatric
Polypharmacy, Adverse Drug Reactions, and Geriatric

... nonprescription medications.9 The average older adult filled 31 prescriptions per year in 2009, twice as many as all other age groups combined.10 Similar disproportionate use has been reported in Canada and the United Kingdom.11,12 The prevalence of polypharmacy reported in the literature, ranging f ...
Percocet® (oxycodone hydrochloride 5 mg / acetaminophen 325 mg)
Percocet® (oxycodone hydrochloride 5 mg / acetaminophen 325 mg)

... benzodiazepines, centrally-active anti-emetics and other CNS depressants. Respiratory depression, hypotension and profound sedation, coma or death may result. Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mort ...
PACLitaxel - Cancer Care Ontario
PACLitaxel - Cancer Care Ontario

... Intravenous: 100 mg/m² over 3 hours every 2 weeks  Dosage with Toxicity: Dosage in myelosuppression:  Modify according to protocol by which patient is being treated; if no guidelines available, refer to Appendix 6 "Dosage Modification for Hematologic and NonHematologic Toxicities." ...
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)

... addition of clonidine to bupivacaine.xiii In a study, Patil KN et al reported shortened time by addition of clonidine to ropivacaine.xiv Similar results were also noted by Singh and Aggarwal xv in their study. The mean duration of sensory block in clonidine group RC was prolonged significantly (p <0 ...
Standard 4 PPT
Standard 4 PPT

... Australian studies have shown that administration errors occur in up to 18% of cases - furthermore, up to 70% of intravenously administered drugs have one or more clinical errors (ACSQHC 2012). ...
Document
Document

... • Interfering drugs or lifestyle • White coat effect ...
PART II - Veterinary Medicines Directorate
PART II - Veterinary Medicines Directorate

... relation to its anti-inflammatory and analgesic potency. The precise mode of action of carprofen is not clear. ...
details - Global Pharmaceuticals Pakistan
details - Global Pharmaceuticals Pakistan

... carefully during treatment. As with any potent systemic agent. It is advisable to check periodically for organ system dysfunction during extended therapy; this includes renal, hepatic, and hematopoietic systems, this is particularly important in neonates, especially when premature, and other infants ...
The Stimulus Properties of Para-Methoxyamphetamine
The Stimulus Properties of Para-Methoxyamphetamine

... A nonessential serotonergic component. PHARMACOL BIOCHEM BEHAV 20(2) 201-203, 1984.--A group of six rats was trained to discriminate the effects of paramethoxyamphetamine (PMA; 3 mg/kg, i5 rain pretreatment time) and saline in a two-lever choice task using a fixed ratio I0 schedule of water reinforc ...
NOVEL NANOEMULSION AS VEHICLES FOR TRANSDERMAL DELIVERY OF CLOZAPINE: IN VITRO
NOVEL NANOEMULSION AS VEHICLES FOR TRANSDERMAL DELIVERY OF CLOZAPINE: IN VITRO

Modulating the cystic fibrosis transmembrane regulator – breaking
Modulating the cystic fibrosis transmembrane regulator – breaking

... promote ribosomal read-through of nonsense mutations is under review, designated PTC124 and also known as Ataluren.34 Ataluren binds to eukaryotic ribosomes and suppresses PTCs in cell- and animal-based disease models. There have been three randomised open-label dose-ascending Phase II trials in CF. ...
Management of sodium-channel blocker poisoning: the role of
Management of sodium-channel blocker poisoning: the role of

... and imipramine. The effect of sodium bicarbonate is entirely due to alkalinization in case of imipramine, but both increase in pH and rise in Na+ concentration contribute to the interaction with flecainide26. Timing of Administration In clinical practice, hypertonic sodium salts are administered whe ...
PRODUCT INFORMATION METHADONE SYRUP
PRODUCT INFORMATION METHADONE SYRUP

... ratios from other opiods are not static, but are a function of previous opioid exposure. Incomplete cross-tolerance between μ-opioid agonists makes determination of dosing during opioid conversion complex. It is recommended that use of this drug should only be undertaken by prescribers familiar with ...
-. - ” .~, ,1_11 _ _, IX-X,““.
-. - ” .~, ,1_11 _ _, IX-X,““.

... doses are between 70 and 75% of the index ...
Asthma
Asthma

... – Studied in children as young as 5 – Avoid food 1 hour before and 2 hours after taking: Food decreases the bioavailability of Accolate – Metabolism: Metabolized through the CY P450 2C9 and 3A4 pathways • Major pathways in the body • Numerous other medications use this same pathway ...
CORE MODULES & FORMS OF TOBACCO
CORE MODULES & FORMS OF TOBACCO

Imatinib - BC Cancer Agency
Imatinib - BC Cancer Agency

... CYP3A4 inhibitors may decrease metabolism and increase imatinib plasma concentrations. Concurrent administration of drugs that inhibit CYP3A4 (eg, clarithromycin, erythromycin, grapefruit juice, itraconazole) may significantly increase exposure of imatinib.28 Drugs that have high oral bioavailabilit ...
florida health care plan, inc
florida health care plan, inc

... when used in combination with paclitaxel for the treatment of patients who have not received chemotherapy for metastatic HER2-negative breast cancer and the dose is either 10 mg/kg every 2 weeks or 15 mg/kg every 3 weeks Nonsquamous non-small cell lung cancer in combination with carboplatin and pacl ...
PACIFIC BUSPIRONE Presentation NEW ZEALAND DATA SHEET
PACIFIC BUSPIRONE Presentation NEW ZEALAND DATA SHEET

... none of the subjects was able to distinguish between buspirone and placebo. By contrast, subjects showed a statistically significant preference for methaqualone and diazepam. Short term studies in monkeys, mice and rats have shown that buspirone lacks potential for abuse. Patients with a history of ...
HIV Treatment Failure - Forum for Collaborative HIV Research
HIV Treatment Failure - Forum for Collaborative HIV Research

... There have been significant changes in clinical trial design over the past few years, including: (1) the use of virologically based entry criteria, (2) shorter length of follow-up time, (3) the use of virological, rather than clinical endpoints. Most reports of successful treatment of individuals wh ...
Clinical pharmacokinetic equations and calculations
Clinical pharmacokinetic equations and calculations

... patients with normal renal function is approximately 8 hours, a one compartment model intravenous bolus equation can be used to compute concentrations in the postinfusion, postdistribution phase without a large amount of error. ...
Pharmacokinetic Drug Interactions of Antimicrobial Drugs: A
Pharmacokinetic Drug Interactions of Antimicrobial Drugs: A

... and did not inhibit the activities of human CYP isoforms 1A2, 2C9, 2C19, 2D6, 2E1, or 3A4 [3]. Based on these observations along with the fact that RIF is a well-known P-gp inducer, the authors suggest LZD to be a P-gp substrate [2]. This hypothesis was further supported by a case report of a patien ...
appendix – iii
appendix – iii

Psychotropic Medication and Interaction with Alcohol
Psychotropic Medication and Interaction with Alcohol

... and recorded. Medical staff and shift coordinator should agree what actions need to be taken and the frequency of physical observation.’ (1) To help decide whether to administer or omit medication in a patient who is apparently acutely intoxicated two factors can be taken into account: 1. The Alcome ...
Sub chronic Evaluation of Ciprofloxacin and Perfloxacin on Sperm
Sub chronic Evaluation of Ciprofloxacin and Perfloxacin on Sperm

... treatment of bacterial prostatitis and epididymitis infection in humans. They are known to have high concentration in semen, prostate, epididymis, vesicle gland, and tissues of testis in human. Studies showed that they are safe for therapeutic use but there are reports that the impaired spermatogene ...
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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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