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Dr. Pressman`s PowerPoint slides
Dr. Pressman`s PowerPoint slides

... seizures: integrated analysis of three pivotal controlled trials. Epilepsy Res. 2012;101:103–112. 17. Ng YT, Conry JA, Drummond R, Stolle J, Weinberg MA. Randomized, phase III study results of clobazam in Lennox-Gastaut syndrome. Neurology. 2011;77:1473–1481. 18. Buck ML. Clobazam: a new option for ...
dose - Recherche Clinique Paris Centre
dose - Recherche Clinique Paris Centre

... ● Effect of the IP on a drug’s PK which is a substrate of CYP3A4 ● Depends on in vitro in human liver microsomes investigations ● Midazolam is exclusively metabolized by CYP3A4/3A5; after oral administration, its clearance reflects combined intestinal and hepatic CYP3A activity. ● The aim of this st ...
Piroxicam Capsules USP, 10 mg 100 count
Piroxicam Capsules USP, 10 mg 100 count

... NSAIDs, including Piroxicam Capsules USP, can lead to onset of new hypertension or worsening of pre-existing hypertension, either of which may contribute to the increased incidence of CV events. Patients taking thiazides or loop diuretics may have impaired response to these therapies when taking NSA ...
Mucomist ® DT Prescribing information
Mucomist ® DT Prescribing information

... Mucomist ® DT: The dispersible tablet should be dissolved in 1/2 glass of water before use (preferably in the evening). The duration of treatment should be 5 to 10 days in the acute phase. It may be continued in the chronic state for up to 6 months or according to the advice of the physician. As a m ...
For patients with severe COPD associated with chronic bronchitis
For patients with severe COPD associated with chronic bronchitis

... has at least 4 hours of bedtime remaining. It should not be taken if alcohol has been consumed or with any other sleep aid. The recommended and maximum dose of Intermezzo is 1.75 mg for women and 3.5 mg for men, taken once per night. The recommended dose for women is lower because women clear zolpid ...
JB-D - Pharmaceutical Press
JB-D - Pharmaceutical Press

... Most drugs are taken orally and typical measures for the dose are then mg/kg or µmol/kg body weight (or per cm2 body surface area for interspecies comparisons). The same measures are used for intravenous injections and any other type of bolus dose. For inhalation experiments using sprays, it is not ...
How Toxic is Amiodarone to the Liver?
How Toxic is Amiodarone to the Liver?

... The histological changes that occur in the liver of patients ingesting alcohol are remarkably similar to those in patients receiving amiodarone [1, 4]. Like alcohol, amiodarone, to varying degrees, can produce microsteatosis, apoptosis and necrosis of the hepatocytes. Therefore, it is worth pausing ...
Data Sheet
Data Sheet

... There have been rare reports in which this residue has caused the lumen to occlude. Patients treated with anti-arrhythmic drugs class III (e.g. amiodarone) should be kept under close surveillance and ECG monitoring considered, since cardiac effects may be additive. If the dose or administration is l ...
Advertising - Journal - American College of Chest Physicians
Advertising - Journal - American College of Chest Physicians

... Teratogenic Effects: Pregnancy Category C. There are no adequate and well-controlled studies of ESBRIET in pregnant women. Pirfenidone was not teratogenic in rats and rabbits. Because animal reproduction studies are not always predictive of human response, ESBRIET should be used during pregnancy onl ...
Aripiprazole LAI Prescribing Guidelines
Aripiprazole LAI Prescribing Guidelines

... 6. Oral aripiprazole at 10mg-20mg per day must continue for two weeks after the first injection to maintain therapeutic aripiprazole concentrations during initiation of therapy. 7. As aripiprazole LAI requires oral supplementation for the first 2 weeks (as point 6 above), consideration must be made ...
Antiretroviral-associated Hepatotoxicity
Antiretroviral-associated Hepatotoxicity

... commonly used NNRTI, efavirenz. Most cases of nevirapine-associated hepatotoxicity have been reported to occur within the first 6 to 12 weeks of therapy. Nevirapineinduced hepatotoxicity may often present as part of a systemic hypersensitivity-type reaction characterized by rash, fever, and eosinoph ...
cyanide - Utah Poison Control Center
cyanide - Utah Poison Control Center

... hours. Adverse effects following hydroxocobalamin were evaluated in healthy volunteers and were felt to tolerable given the ...
DOSAGE FORMS AND STRENGTHS
DOSAGE FORMS AND STRENGTHS

... as a single agent for the prevention of exercise-induced bronchospasm may be clinically indicated in patients who do not have persistent asthma. In patients with persistent asthma, use of FORADIL AEROLIZER for the prevention of exerciseinduced bronchospasm may be clinically indicated, but the treatm ...
new zealand data sheet pred forte
new zealand data sheet pred forte

... and abortion. These findings do not seem to be relevant to humans. Reduced intrauterine growth and lower birth weight have been recorded in animals and humans after long-term or high dose treatment. Suppression of the adrenal cortex in the newborn baby, infants and children may occur after frequent ...
Rivaroxaban and Dabigatran for the prevention of stroke and
Rivaroxaban and Dabigatran for the prevention of stroke and

... Warfarin should be stopped and treatment with rivaroxaban initiated when the INR is ≤ 3.0. When converting patients from warfarin, INR values will be falsely elevated after the intake of rivaroxaban. The INR is not valid to measure the anticoagulant activity of rivaroxaban and therefore should not b ...
anoro ellipta
anoro ellipta

... possibly through intracellular shunting, which has the potential to produce adverse cardiovascular effects. The decrease in serum potassium is usually transient, not requiring supplementation. Beta-agonist medicines may produce transient hyperglycemia in some patients. In 4 clinical trials of 6-mont ...
product monograph
product monograph

... normal therapeutic doses of this product ordinarily deliver amounts of benzyl alcohol that are substantially lower than those reported in association with the “gasping syndrome”, the minimum amount of benzyl alcohol at which toxicity may occur is not known. The risk of benzyl alcohol toxicity depen ...
PDF Version - Cardiological Society of India
PDF Version - Cardiological Society of India

... •• Rapid onset of action: Peak onset 1–4 hours; all of them thus act more or less immediately over the same time course as the low-molecular-weight heparin (LMWH). •• Fixed dose: They can be given in fixed doses. There is no effect of dietary vitamin K intake on the pharmacological activities of the ...
Revised: December 2016 AN: 00745/2016 SUMMARY OF
Revised: December 2016 AN: 00745/2016 SUMMARY OF

... solution per kg) and should initially be administered daily. The frequency of administration should subsequently be reduced depending on the response. The veterinary medicinal product can be given either mixed with food or directly into the mouth. If given with food, the solution should be mixed wit ...
AusPAR: Eltrombopag
AusPAR: Eltrombopag

... This work is copyright. You may reproduce the whole or part of this work in unaltered form for your own personal use or, if you are part of an organisation, for internal use within your organisation, but only if you or your organisation do not use the reproduction for any commercial purpose and reta ...
Prescribing Information including Medication Guide
Prescribing Information including Medication Guide

... Prior to injection, reconstitute each vial of XEOMIN with sterile, preservative-free 0.9% Sodium Chloride Injection, USP [see Dosage Form and Strengths (3)]. A 2027 gauge short bevel needle is recommended for reconstitution. Draw up an appropriate amount of preservative-free 0.9% Sodium Chloride Inj ...
Drug Therapy Protocols: Atropine
Drug Therapy Protocols: Atropine

... International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/. ...
Statement on the use of EFV in children less than 3 years of age
Statement on the use of EFV in children less than 3 years of age

... compared to older children and adults and therefore require higher doses in order to maintain therapeutic plasma drug concentrations similar to adults. In the case of EFV, it has been found that some children (and adults) are genetically slow metabolisers of EFV and higher doses may result in toxici ...
HIGHLIGHTS OF PRESCRIBING INFORMATION ----------------------- WARNINGS AND PRECAUTIONS -----------------------
HIGHLIGHTS OF PRESCRIBING INFORMATION ----------------------- WARNINGS AND PRECAUTIONS -----------------------

... disorders. In trials of treatment-experienced HIV-1-infected subjects, approximately 6% of subjects were co-infected with hepatitis B and approximately 6% were co-infected with hepatitis C. Due to the small number of co-infected subjects studied, no conclusions can be drawn regarding whether they ar ...
Document
Document

... Distribution in extracellular space Elimination unchanged in kidney Variable elimination kinetics and therefore variable half-lives of elimination ranging from hours to days. ...
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Ofloxacin



Ofloxacin is a synthetic antibiotic of the fluoroquinolone drug class considered to be a second-generation fluoroquinolone.Ofloxacin was first patented in 1982 (European Patent Daiichi) and received approval from the U.S. Food and Drug Administration (FDA) on December 28, 1990. Ofloxacin is sold under a wide variety of brand names as well as generic drug equivalents, for oral and intravenous administration. Ofloxacin is also available for topical use, as eye drops and ear drops (marketed as Ocuflox and Floxin Otic respectively in the United States and marketed as Optiflox, eylox respectively in Jordan and Saudi Arabia).Ofloxacin is a racemic mixture, which consists of 50% levofloxacin (the biologically active component) and 50% of its “mirror image” or enantiomer dextrofloxacin.Ofloxacin has been associated with adverse drug reactions, such as tendon damage (including spontaneous tendon ruptures) and peripheral neuropathy (which may be irreversible); tendon damage may manifest long after therapy had been completed, and, in severe cases, may result in lifelong disabilities.
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