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Pharmacokinetics-Pharmacodynamics
Pharmacokinetics-Pharmacodynamics

... – A drug that is more efficacious (effective) can produce a greater peak, or maximum, effect than a drug that is less efficacious. ...
5-Parkinson Disease
5-Parkinson Disease

... The dose of amantadine in early PD is 200 to 300 mg daily; there is no evidence that larger doses are of additional benefit. The main advantage of this agent is a low incidence of side effects. • It is excreted unchanged in the urine and should be used with caution in the presence of renal failure. ...
bisoprolol - DavisPlus
bisoprolol - DavisPlus

... Advise patient to carry identification describing disease process and medication regimen at all times. Hypertension: Reinforce the need to continue additional therapies for hypertension (weight loss, sodium restriction, stress reduction, regular exercise, moderation of alcohol consumption, and smoki ...
No Slide Title
No Slide Title

... negative symptoms – would not respond to drugs but rather was brain damage as a consequence of whatever schizophrenia did to the brain ...
Laminil Investigational Drug
Laminil Investigational Drug

... using retrograde venous therapy. We tested other routes such as systemic intravenous injection, oral, and topically with a patch, but at this date, retrograde venous therapy shows superior efficacy. Protein binding: The drug is approximately 89 percent protein bound in human plasma. No data is avail ...
5HT6 receptors AVN-211 (CD-008
5HT6 receptors AVN-211 (CD-008

... was administered 60 min prior to the testing (volume of injection was 10 mL/kg). Apomorphine was administered s.c. 20 min before the testing (volume of injection was 1 mL/kg.). AVN-211 was administered i.p. 5 min before the testing (volume of injection was 10 mL/kg). The results demonstrated about 5 ...
ATTACHMENT I Regulatory Information Number (RIN) :  RIN 0910-AF14
ATTACHMENT I Regulatory Information Number (RIN) : RIN 0910-AF14

... The same comment applies in this case and critical drug shortages may occur_ 2 .4 Larger Populations, Treatment YND = No Change The evidence for al.l.owingn a large-scale treatment IND is such that the drua supply issue identified in l. and 2 above is less likely. These treatment lNbs appear to be b ...
1- Systemic antifungals
1- Systemic antifungals

... for one day OR 200 mg daily for 3 days • Oral candidiasis: 100 mg daily for two weeks • Tinea unguium: 200 mg/day for 6-8 weeks (fingernails) or 3-4 months (toenails), OR 200 mg twice daily for 7 days, repeated monthly for 2 months (fingernails) or 3-4 months ...
EU Core Safety Profile
EU Core Safety Profile

... Use with PDE-5 inhibitors: Concomitant administration of doxazosin with phosphodiesterase-5-inhibitors (eg sildenafil, tadalafil, and vardenafil) should be done with caution as both drugs have vasodilating effects and may lead to symptomatic hypotension in some patients. To reduce the risk of orthos ...
PROF. Rosita Aniuliene LITHUANIAN UNIVERSITY OF HEALTH
PROF. Rosita Aniuliene LITHUANIAN UNIVERSITY OF HEALTH

...  Conservative therapy is indicated as primary treatment  Antimuscarinic agents are most commonly used drugs  Limited by tolerability and efficacy  Significant effect on compliance and resistance  Newer bladder specific agents may offer advantages  Possible to individualise treatment for each p ...
L9-rhinitis and coug..
L9-rhinitis and coug..

...  firing from internal ear to vomiting center 2. Anti-emetic ...
spironolactone (speer-oh-no-lak-tone) - DavisPlus
spironolactone (speer-oh-no-lak-tone) - DavisPlus

... ions by antagonizing aldosterone. Therapeutic Effects: Increased survival in patients with severe heart failure (New York Heart Association class II-IV). Weak diuretic and antihypertensive response when compared with other diuretics. Conservation of potassium. ...
Study Results Published in Journal of Clinical Infectious Diseases
Study Results Published in Journal of Clinical Infectious Diseases

... - First Head-to-Head, Blinded Safety Comparison of Lipid-Based Amphotericin B Agents Deerfield, IL and Foster City, CA -- November 17, 2000 Fujisawa Healthcare, Inc. (FHI) and Gilead Sciences, Inc. (Nasdaq: GILD) today announced the publication of results of a multicenter head-to-head study comparin ...
Pirlimycin - American Academy of Veterinary Pharmacology and
Pirlimycin - American Academy of Veterinary Pharmacology and

... (milk samples should be tested three weeks after treatment with pirlimycin is discontinued; mastitis is not considered bacteriologically cured until samples show an absence of the mastitis-causing organism; for refractory Staphylococcus aureus mastitis, in which control, but not elimination, is achi ...
No such thing as a free lunch - or a leather
No such thing as a free lunch - or a leather

... around 300mg per day and our own dosage which is nearer to 200 mg per day. With the experience of around 70 patients in the community on clozapine I would say that these patients were probably receiving clozapine at too high a dosage. Apart from the case of neuroleptic malignant syndrome, and of neu ...
mg/kg/day
mg/kg/day

... Deferasirox (DFX) ...
HYPERTENSION
HYPERTENSION

... angiotensin I to angiotensin II and are usually well tolerated. They should be used with particular care in patients with impaired renal function or renal artery stenosis because they can reduce the filtration pressure in the glomeruli and precipitate renal failure. Electrolytes and creatinine shoul ...
Respiratory Drugs 2 - Suny-perfusion
Respiratory Drugs 2 - Suny-perfusion

... anaphlaxis(SRSA). ...
DICLOGENTA Composition Pharmacology Indications
DICLOGENTA Composition Pharmacology Indications

... Diclofenac sodium is one of a series of phenylacetic acids that has demonstrated antiinflammatory and analgesic properties in pharmacological studies. It inhibits the enzyme cyclooxygenase, which is essential in the biosynthesis of prostaglandins (PGs). PGs have been shown in many animal models to b ...
Drugs That Require Gradual Dose Reduction (GDR)
Drugs That Require Gradual Dose Reduction (GDR)

... “a response to a drug that is noxious and unintended and occurs at doses normally used for prophylaxis, diagnosis or therapy of a disease, or for the modification of psychological function.”15 Serious ADEs are defined by the Food and Drug Administration as events caused by a drug that result in a pa ...
Clincial Pharmacology of Analgesic Medications
Clincial Pharmacology of Analgesic Medications

... Significant first-pass metabolism, reducing effect of oral administration Very lipophilic, quick onset, seconds to minutes, short half-life due to redistribution Don’t get on hands – it is absorbed IV use in anesthesia Delivery systems include patch, buccal tablet, nasal spray and lozenge ...
EU Core Safety Profile Active Substance: Cabergoline Brand Names
EU Core Safety Profile Active Substance: Cabergoline Brand Names

... In a twelve year observational study on pregnancy outcomes following cabergoline therapy, information is available on 256 pregnancies. Seventeen of these 256 pregnancies (6.6%) eventuated in major congenital malformations or abortion. Information is available on 23/258 infants who had a total of 27 ...
HIGHLIGHTS OF PRESCRIBING INFORMATION Clostridium difficile
HIGHLIGHTS OF PRESCRIBING INFORMATION Clostridium difficile

... clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The safety of DEXILANT was evaluated in 4548 patients in controlled and uncontrolled clinical studies, including 863 patients treated for at least ...
Anti-Emetic Guidelines For Chemotherapy Patients
Anti-Emetic Guidelines For Chemotherapy Patients

... consultation with medical staff. Anti-emetics should be given prior to chemotherapy and for at least 3-days following treatment if delayed nausea and vomiting are expected (as with cisplatin). 3. Give psychological support to prevent and reduce the stress of anticipatory nausea and vomiting. The use ...
Phase I Clinical Trials
Phase I Clinical Trials

... • DLT and MTD are used for the purposes of making decisions about dose escalation. • The occurrence of DLT in the first course of therapy is what limits dose escalation. • The phase II dose should incorporate multiple-cycle toxicity (including DLT), tolerability, dose reductions, and dose delays. • ...
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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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