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Product Monograph - Ask Novartis Pharma
Product Monograph - Ask Novartis Pharma

... incidence of atrial fibrillation in isolated studies with some bisphosphonates, including AREDIA®, is unknown. Effects on ability to drive or use machines Somnolence and/or dizziness may occur following AREDIA® infusion, in which case the patient should not drive, operate potentially dangerous machi ...
PDF - Bentham Open
PDF - Bentham Open

... adopted in the next phase II clinical trials. It is generally assumed for cancer therapy that toxicity is a prerequisite for optimal anti-tumour activity [8]. While the new treatment regimen may produce therapeutic benefits to patients, it may also have toxic reactions. Higher therapeutic outcomes c ...
Product Monograph Template - Standard
Product Monograph Template - Standard

... the most part, seen in post-marketing clinical use and epidemiologic studies, and not in clinical trials. Diabetic ketoacidosis (DKA) has occurred in patients treated with antipsychotics with no reported history of hyperglycemia. In clinical trials, hyperglycemia or exacerbation of pre-existing diab ...
KEPPRA (levetiracetam) Rx only 250 mg, 500 mg, 750 mg, and
KEPPRA (levetiracetam) Rx only 250 mg, 500 mg, 750 mg, and

... Pharmacokinetics of levetiracetam were evaluated in 16 elderly subjects (age 61-88 years) with creatinine clearance ranging from 30 to 74 mL/min. Following oral administration of twice-daily dosing for 10 days, total body clearance decreased by 38% and the half-life was 2.5 hours longer in the elder ...
Cyclosporin Nephrotoxicity
Cyclosporin Nephrotoxicity

... Reduced GFR , Reduced renal blood flow, Rise in serum creatinine, Decrease in renal clearance, Rise in RAS, Arteriolopathy of afferent ateriole, Vascular dysfunction and ...
Buccal Midazolam (Epistatus) Training
Buccal Midazolam (Epistatus) Training

... administer rescue medication, by experienced qualified staff • The protocol must be shared with those who will need to follow it • The individual must be included whenever possible in the decision making process around deciding on the use of rescue medication – (consent to its use sought and recorde ...
Workshop 2: Adverse Drug Reactions
Workshop 2: Adverse Drug Reactions

... Sodium valproate is a medicine originally developed to treat epilepsy. Some doctors have carried out clinical trials that show sodium valproate can help people with migraine. However, it does not have a license for use in this way. In the meantime, doctors are allowed to prescribe sodium valproate f ...
milk thistle in liver diseases: past, present, future
milk thistle in liver diseases: past, present, future

... blocked the translocation of NF-κB p65 protein (through phosphorylation) to the nucleus without affecting its ability to bind the DNA (Manna et al., 1999). Silymarin also inhibited the TNF-α- induced activation of mitogen-activated protein kinase and c-Jun N-terminal kinase and abrogated TNF-α-induc ...
Running head: PERSONAL DRUGS PERSONAL DRUGS Personal
Running head: PERSONAL DRUGS PERSONAL DRUGS Personal

... renal tubular damage, leukopenia, neutropenia, seizure, thrombocytopenia Monitor: Renal, hepatic, and hematologic function with long term use ...
Healthcare Professional Guide
Healthcare Professional Guide

... • A potentially fatal symptom complex sometimes referred to as Neuroleptic Malignant Syndrome (NMS) has been reported in association with XENAZINE. Clinical manifestations of NMS are hyperpyrexia, muscle rigidity, altered mental status, and evidence of autonomic instability (irregular pulse or bloo ...
July 2012 - Kaiser Permanente
July 2012 - Kaiser Permanente

... from a clinical study suggests ondansetron (Zofran) may prolong the QT interval in a dose-dependent manner, which could predispose patients to develop an abnormal and potentially fatal heart rhythm, torsades de pointes  GlaxoSmithKline announced changes to ondansetron drug label to remove the 32mg ...
PRODUCT MONOGRAPH PrSALAZOPYRIN® Sulfasalazine tablets
PRODUCT MONOGRAPH PrSALAZOPYRIN® Sulfasalazine tablets

... About 20% of SALAZOPYRIN (sulfasalazine) is absorbed in the small intestine after oral administration. A small percentage of the absorbed sulfasalazine is excreted in the urine and the rest via the bile into the small intestine (enterohepatic circulation). This portion together with the unabsorbed s ...
Consumer Safety Officer,  Division  of  Dietary Supplement... Nutritional  Products, Labeling and Dietary Supplements, MFS-8 10
Consumer Safety Officer, Division of Dietary Supplement... Nutritional Products, Labeling and Dietary Supplements, MFS-8 10

... has not been chemically altered must submit to FDA, at least 75 days before the dietary ingredient’is introduced or delivered for introduction into interstate eornmerce, information that is the basis on which the manufacturer or distributor has concluded that a dietary-supplementcontaining such new ...
The Top 6 June specials 2015
The Top 6 June specials 2015

... also licensed for use in several EU countries, such as Germany, France, Ireland, Italy and Spain. In line with guidance from the General Medical Council (GMC), it is the responsibility of the prescriber to determine the clinical need of the patient and the suitability of using midodrine as an unlice ...
Suggestion from clinicians
Suggestion from clinicians

... newer antihistamines is usually sufficient. Although sedation and anticholinergic side effects are common with the older antihistamines (also known as first-generation or sedating antihistamines), these side effects are usually not seen with newer agents (second-generation or nonsedating antihistami ...
Acute pain management for opioid tolerant patients - e
Acute pain management for opioid tolerant patients - e

... treatment of neuropathic pain. A number of meta-analyses on non-opioid tolerant patients have shown that perioperative gabapentinoids lead to improved analgesia and reduced postoperative opioid consumption, but can also lead to increased sedation scores when compared to placebo. There may ...
Afeksin
Afeksin

... concerning long-term effect on safety in children and adolescents, including effects on growth, sexual maturation and cognitive, emotional and behavioural developments. In a 19-week clinical trial, decreased height and weight gain was observed in children and adolescents treated with fluoxetine (see ...
Tobramycin_Dexamethasone Tubilux Pharma eye drops
Tobramycin_Dexamethasone Tubilux Pharma eye drops

... Methicillin-susceptible (S), Methicillin-resistant (R). The beta-lactam (i.e., methicillin; penicillin) resistance phenotype is unrelated to the aminoglycoside resistance phenotype and both are unrelated to the virulence phenotypes. Some methicillin-resistant (R) S. aureus strains (MRSA) are suscept ...
Pharmacokinetics, Pharmacodynamics, and
Pharmacokinetics, Pharmacodynamics, and

... aggressive fluid resuscitation may lead to increases in total body water, which results in a larger Vd and lower serum concentrations. That effect of aggressive fluid management has also been demonstrated among aminoglycosides and other β-lactam antibiotics (Dasta 1988,Triginer 1990). In summary, cr ...
FAQ Slide no.
FAQ Slide no.

... Why gel and ointment and not tablets and ampoules? This study aimed to compare topical preparations only Further studies have demonstrated the efficacy of oral and systemic administration of Traumeel Traumeel has previously been reported to be well tolerated and without treatment-related adverse ef ...
and B
and B

... modelling of distribution in several tissues and blood circulation ...
Basics Pharmacology Review
Basics Pharmacology Review

... amount of time in preparation for LMCC • List the four steps of rational prescribing • Understand the pharmacological classes, generic examples and mechanisms of action of important tools in the practice of medicine. • Understand how the kinetics and dynamics of these agents can affect their use • H ...
Lidocaine with Epinephrine
Lidocaine with Epinephrine

... aspiration. Allow a 5-minute interval between sides. Nursing Mothers: It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when lidocaine is administered to a nursing woman. Pediatric Use: Dosages in pediatric patient ...
INTRAVENOUS INFUSION (not for IV Bolus Injection)
INTRAVENOUS INFUSION (not for IV Bolus Injection)

... who received CANCIDAS 70 mg on Days 1 through 10, and also received two 3 mg/kg doses of cyclosporine 12 hours apart on Day 10, developed transient elevations of alanine transaminase (ALT) on Day 11 that were 2 to 3 times the upper limit of normal (ULN). In a separate panel of adult subjects in the ...
Invega PI
Invega PI

... caused a slight increase in the free fraction of paliperidone at 50 ng/mL. These changes are not expected to be of clinical significance. Metabolism and Elimination: One week following administration of a single oral dose of 1 mg immediate-release 14C-paliperidone, 59% (range 51% - 67%) of the dose ...
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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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