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ZELBORAF Prescribing Information
ZELBORAF Prescribing Information

... the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not predict the rates observed in a broader patient population in clinical practice. This section describes adverse drug reactions (ADRs) identified from analyses of Trial 1 and Trial ...
November 2014 PBAC Meeting
November 2014 PBAC Meeting

... The PBAC noted that the minor submission sought PBS listing of the mercaptopurine oral suspension 20 mg/mL at a higher price (DPMQ ''''''''''''''''''''' for 100 mL) than the tablet. The PBAC further noted that the cost of liquid formulations in general are typically higher (per mg), than solid dose ...
Comparison of Fesoterodine, Tolterodine, Oxybutynin
Comparison of Fesoterodine, Tolterodine, Oxybutynin

... most frequently prescribed drugs. The aim of this review was to compare these five antimuscarinic agents in order to recommend a therapy for overactive bladder. Methods: We performed a systematic review using PubMed search. We searched on January 11th, 2011. Six studies were included. Our inclusion ...
Injectable Anesthetics - Dr. Roberta Dev Anand
Injectable Anesthetics - Dr. Roberta Dev Anand

...  Continuous or repeated dosing may lead to “full” muscle and fat and increased brain levels = prolonged recovery and possible ...
Registration Form Details Agenda
Registration Form Details Agenda

... and administration: Recommended dose: 50μg once daily using only the Breezhaler inhaler. Do not swallow the capsules.* Contraindications: Hypersensitivity to any ingredients, galactose intolerance, severe lactase deficiency or glucose-galactose malabsorption. Precautions: Acute use: should not be us ...
lamisil® tablets
lamisil® tablets

... Studies in animals suggest that in a high dose situation, such as accidental overdose, central nervous symptoms (CNS) may appear. The relevance of those effects to man is unknown. However, these effects can be monitored. Central Nervous System: headache and dizziness Gastrointestinal system: nausea, ...
Pharmcokinetics in Critical Care
Pharmcokinetics in Critical Care

... Pharmacogenetics genetic polymorphisms in drug metabolizing enzymes, transporters or receptors can cause clinically relevant effects on efficacy & toxicity of drugs individuals respond differently to drugs there are poor, intermediate, & ultra-rapid metabolizers ...
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... – Thrombocytopenia(血小板减少症) is the most common manifestation (seen in approximately 3% of treatment courses), particularly when the drug is administered for longer than 2 weeks. – Neutropenia may also occur, most commonly in patients with a predisposition to or underlying bone marrow suppression. ...
dosage guide - Veterinary Medicines Directorate
dosage guide - Veterinary Medicines Directorate

... Dogs should be dosed orally, starting with a dose of 2.5 - 5.0 mg/kg (0.06 0.125ml per kg) bodyweight per day. The dose should be divided and ...
BEXTRA® valdecoxib tablets
BEXTRA® valdecoxib tablets

... bleeding and who use NSAIDs, have a greater than 10-fold higher risk for developing a GI bleed than patients with neither of these risk factors. In addition to a past history of ulcer disease, pharmacoepidemiological studies have identified several other co-therapies or co-morbid conditions that may ...
DICLOFENAC-GA PRODUCT INFORMATION DICLOFENAC-GA
DICLOFENAC-GA PRODUCT INFORMATION DICLOFENAC-GA

... there was no evidence of the drugs accumulation in plasma. In a study in 16 patients with rheumatoid arthritis and knee joint effusions it was found that diclofenac enters the synovial fluid where maximum concentrations were measured 2 to 4 hours after oral administration. The apparent half-life for ...
Use of nonsteroidal antiinflammatory drugs in dental practice. A review
Use of nonsteroidal antiinflammatory drugs in dental practice. A review

... vasodilating action, resulting in increased vascular permeability, with the extravasation of fluids and white blood cells – all these phenomena contributing to inflammation. Consequently, the inhibition of cyclooxygenase synthesis exerts a clear anti-inflammatory effect. Of particular importance in ...
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L1- Final Ocular pha..

... Dr.Abdul latif Mahesar Department of Medical Pharmacology College of Medicine ...
RT101 Basic Therapeutics
RT101 Basic Therapeutics

... Tolerance: A condition in which the dose of a drug must be increased (over time) to obtain the desired effect -or- a decreasing intensity of responsiveness to a drug over time Tachyphylaxis: Rapidly developing tolerance to a drug -or- a rapid decrease in responsiveness to a drug. Additive effects: T ...
antibiotics - US Elsevier Health Bookshop
antibiotics - US Elsevier Health Bookshop

... from mild rash to anaphylaxis. Superinfections may result from alteration of bacterial environment. Ototoxicity and nephrotoxicity are potential adverse reactions of a number of antibiotics, esp. the aminoglycosides. Tetracyclines combine with calcium in forming teeth and may produce discoloration. ...
Pharm Profil-PANNARELLA-Apr PV
Pharm Profil-PANNARELLA-Apr PV

... tissues.1 Drug residues are near the lowest level of detection by 2 days after dosing, but residual quantities are still detectable in the liver 14 days later.1 FBZ should not be administered to animals with a known hypersensitivity to the drug or to horses intended for food.12 ...
The features and management of poisoning with drugs used to treat
The features and management of poisoning with drugs used to treat

... because of the depressant action of orphenadrine on myocardial excitation. Orphenadrine concentrations can be measured using GLC or HPLC,22'23 but are of no help in management. ...
HIGHLIGHTS OF PRESCRIBING INFORMATION Peripheral vascular disease (4) •
HIGHLIGHTS OF PRESCRIBING INFORMATION Peripheral vascular disease (4) •

... The recommended starting dose of ZOMIG is 1.25 mg or 2.5 mg. The 1.25 mg dose can be achieved by manually breaking the functionally-scored 2.5 mg tablet in half. The maximum recommended single dose of ZOMIG is 5 mg. In controlled clinical trials, a greater proportion of patients had headache respons ...
Sustained-Release Bupropion Overdose: A Case Report
Sustained-Release Bupropion Overdose: A Case Report

... Fortunately, the majority of these patients had self-limited seizures and recovered without any permanent damage like how our patient. Seizures were more common when patients had co-ingested stimulants or alcohol, which may resulted in a further lower threshold. Although seizures often occur early, ...
BHF Factfile: The Use of Digoxin
BHF Factfile: The Use of Digoxin

... randomized trial, showed that digoxin had no effect on mortality and only led to a small reduction in the number of hospital admissions. Since digoxin is hard to use without avoiding toxicity, its minimal efficacy in heart failure in sinus rhythm does not justify its use as a first-line drug. It sho ...
PICO Paper - Professional Portfolio
PICO Paper - Professional Portfolio

... uncomplicated UTI due to drug resistance and poor choice of antibiotics will lead to serious consequences. Such consequences may include development of pyelonephritis, repeat office visit, hospitalization, and financial expenditure. Because of the aforementioned, it is very important to tailor the g ...
phentermine HCl - Citius Pharmaceuticals
phentermine HCl - Citius Pharmaceuticals

... Dosage should be individualized to obtain an adequate response with the lowest effective dose. Use caution in patients with even mild hypertension (risk of increased blood pressure). A reduction in dose of insulin or oral hypoglycemic medication may be required in patients with diabetes mellitus. Ph ...
Diacol PI - 040610 Name Chnage clean
Diacol PI - 040610 Name Chnage clean

... Administration of the sodium phosphate-containing products, such as enemas or non-prescription liquid purgatives has resulted in fatalities due to significant fluid shifts, severe electrolyte abnormalities, and cardiac arrhythmias. These have been observed in patients with renal insufficiency or bow ...
7. Calculation of Doses- General considerations.ppt [相容模式]
7. Calculation of Doses- General considerations.ppt [相容模式]

... is the quantitative amount administered or taken by a patient for the intended medicinal effect. may be expressed as: n a single dose, the amount taken at one time; n a daily dose; n a total dose, the amount taken during the time-course of therapy. may be subdivided and taken in divided doses, two o ...
Endep - Medicines.org.au
Endep - Medicines.org.au

... Clinical Worsening and Suicide Risk associated with Psychiatric Disorders. The risk of suicide attempt is inherent in depression and may persist until significant remission occurs. This risk must be considered in all depressed patients. Patients with depression, both adult and paediatric, may experi ...
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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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