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Profile Documents Logout
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PDF Article
PDF Article

... The optimal dose of aspirin in vascular diseases remains controversial. Although low aspirin doses (⬍100 mg daily) have potential advantages over higher doses, a recent meta-analysis has shown that in patients at high risk for vascular events, there was a similar reduction of events over a dose rang ...
Hypoglycemic Drug Interactions
Hypoglycemic Drug Interactions

... Alcohol – can cause a disulfiram-like reaction when taken in combination with oral sulfonylureas, particularly chlorpropamide. Persons experience flushing, sensations of warmth, dizziness, nausea and tachycardia. Alcohol is best avoided since the amount consumed does not necessarily correlate with o ...
buprenorphine oxycodone table
buprenorphine oxycodone table

... Antitussive, antimotility agent and traditionally for head injury patients (no evidence – lack resp and neuro depressive effects) ...
Paediatric Review March 2006
Paediatric Review March 2006

... • Forms have been revised and enhanced with embedded tools to support and facilitate the new request process DOSE INTERVALS: • A clinical or logistical rationale must be provided if intervals between doses are too short – i.e. less than 21 days between the first and second dose and less than 30 days ...
Absorption, Metabolism& Excretion
Absorption, Metabolism& Excretion

... Rapidly absorbed from stomach and small intestine. Widely distributed to tissues and body fluids ( including CNS, CSF ), placenta and fetus. Absorbed sulfonamides bind to serum protein ( approx. 70% ). Metabolized in the liver by the process of acetylation. Eliminated in the urine, partly as such an ...
azaCITIDine - Cancer Care Ontario
azaCITIDine - Cancer Care Ontario

... Dosage with Renal Impairment: Monitor patients with renal impairment closely as azacitidine and its metabolites are primarily excreted renally. Azacitidine can be administered to patients with renal impairment without initial dose adjustment. Subsequent dosage modifications should be made if reducti ...
Attachment 1. Product Information for Ruxolitinib
Attachment 1. Product Information for Ruxolitinib

... effects of ruxolitinib treatment over time. In a thorough QT study in healthy subjects, there was no indication of a QT/QTc prolonging effect of ruxolitinib in single doses up to a supratherapeutic dose of 200 mg indicating that ruxolitinib has no effect on cardiac repolarization. Pharmacokinetics A ...
VIEW PDF - Retina Today
VIEW PDF - Retina Today

... side effects such as retinal detachment, vitreous hemorrhage, and endophthalmitis.5,6 Furthermore, while intravitreal administration of corticosteroids has been shown to reduce edema and improve or at least stabilize visual acuity, these effects are often transient.3 For example, a systemic review o ...
Report on New Patented Drugs — Olmetec Application of the
Report on New Patented Drugs — Olmetec Application of the

... review the prices of patented drug products sold in Canada to ensure that such prices are not excessive. The PMPRB reserves the right to exclude from the therapeutic class comparison test any drug product it has reason to believe is being sold at an excessive price. In Summary Reports under the pre- ...
My STIVARGA® (regorafenib):
My STIVARGA® (regorafenib):

... condition precedent of the co-payment support provided under this program, e.g., co-pay refunds, participating patients and pharmacies are obligated to inform insurance companies and third-party payors of any benefits they receive and the value of this program, as required by contract or otherwise. ...
Phase I Trials
Phase I Trials

... neutropenia ≥ 1 week; febrile neutropenia; grade 4 thrombocytopenia; grade 3 thrombocytopenia with bleeding; QTcF prolongation to > 500 msec, or an increase of > 60 msec from baseline QTcF to a QTcF value > 480 msec, confirmed on repeat EKG; grade 3 or 4 nausea, vomiting, or diarrhea despite use of ...
Florinef - Medsafe
Florinef - Medsafe

... abortion. These findings do not seem to be relevant to humans. Reduced placental and birthweight have been recorded in animals and humans after long-term treatment. Since the possibility of suppression of the adrenal cortex in the newborn infant after long-term treatment must be considered, the nee ...
Radiopharmaceutical Details: 18F-FDG 1. Name
Radiopharmaceutical Details: 18F-FDG 1. Name

drug master file: [18f]fdg
drug master file: [18f]fdg

... The product is delivered in a sterile multi-dose vial. No addition of liquid or aliquotting to another storage container is permitted. Individual doses are removed from this vial using aseptic techniques and only by trained pharmacy staff or nuclear medicine technicians. During preclinical studies t ...
Neurodegenerative Disorders - London Metropolitan University
Neurodegenerative Disorders - London Metropolitan University

... • Selegiline preferentially inhibits MAO-B (in doses < 10mg day-1) • Therefore preserves small amounts of DA present • Slows down progression of disease ...
Dawn Krauskopf
Dawn Krauskopf

... a plastic button in the kneecap. Total knee replacements are usually performed on people suffering from severe arthritic conditions. Most patients who have artificial knees are over age 55, but the procedure is performed in younger people. The prosthesis may be metallic or polyethylene (or a combina ...
management of congenital adrenal hyperplasia in
management of congenital adrenal hyperplasia in

... very high levels early in the morning. Androstenedione and testosterone do not change rapidly and are therefore better at monitoring overall long-term control. ACTH is the hormone that stimulates the adrenal gland, and is raised in untreated CAH (that is the effect of the “RAC men” ordering more ca ...
Number 6 - Laboratory Animal Boards Study Group
Number 6 - Laboratory Animal Boards Study Group

... SUMMARY: Wild caught and conventionally raised baboons have many indigenous viruses, bacteria and parasites. Pathologies occurring in infected animals, many of these agents can influence the results of biomedical research using baboons. Additionally, zoonotic agents may pose an occupational risk to ...
20810 AlleRx DF.indd
20810 AlleRx DF.indd

... motor vehicles should be cautioned accordingly. Methscopolamine nitrate should be used with caution in the elderly and all patients with autonomic neuropathy, hepatic or renal disease, or ulcerative colitis. Drug Interactions: Additive anticholinergic effects may result from concomitant use with ant ...
Reviewer`s report
Reviewer`s report

... what they are often describing, or alluding to, is notification of adverse events rather than "studies" which implies pharmacoepidemiology. I suggest changing "Pharmacovigilance studies" to "Pharmacovigilance activities". Suggestion acknowledged. The authors have changed the term “Pharmacovigilance ...
Back_to_basics_pharmacology 1, 2 and 3 2011
Back_to_basics_pharmacology 1, 2 and 3 2011

... – all opioids have the potential to cause skin itchiness which is not considered an allergic reaction – in all cases, monitor patient for possible cross-allergic reactions ...
New developments in the treatment of acute bacterial skin and skin
New developments in the treatment of acute bacterial skin and skin

... poor oral absorption and therefore requires IV administration.6 The pharmacokinetics of dalbavancin, including tissue distribution, was initially studied in rat models. Findings included a terminal half-life of 187.4 hours due to extensive protein binding (93%–98%), a volume of distribution of 0.52  ...
Pregabalin (Lyrica™) - A new treatment option for neuropathic pain
Pregabalin (Lyrica™) - A new treatment option for neuropathic pain

... cancer-related neuropathic pain, postherpetic neuralgia, HIV-related neuropathy, spinal cord injury, trigeminal neuralgia and other pain syndromes. 1 ...
Document
Document

... Having one or even two doesn’t confer clinical resistance Mostly different from other PI mutations C. Loveday study: DRV mutations in 14% of patients failing PIs: only 1.5% with ≥ 3: only 2 patients (out of 885) with 5 Did not occur before 2000 so other PIs can generate the DRV failure = failure to ...
Medivir
Medivir

... –Next step: selection of Candidate Drug Renin - Hypertension –IP compiled for three distinct and potent inhibitor series –Next step: studies in a pre-clinical efficacy model Cathepsin S – RA, MS and pain –Potent and selective inhibitors –Efficacious in preclinical disease models –Fine-tuning of PK p ...
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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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