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... DISCLAIMER: The content of this newsletter represents the research, experience and opinions of the authors and not those of the Board or Administration of Saskatoon Health Region (SHR). Neither the authors nor Saskatoon Health Region nor any other party who has been involved in the preparation or pu ...
- Minapharm Pharmaceuticals
- Minapharm Pharmaceuticals

... been used medicinally for centuries as a herbal medicine for the treatment of liverrelated disorders. It is widely prescribed by herbalists and has almost no known side effects. The plant is native to the Mediterranean and grows throughout Europe and North America. [1],[2] It also grows in India, Ch ...
Evidence-Based Perspectives on Contemporary Approaches to
Evidence-Based Perspectives on Contemporary Approaches to

... produce minimal, moderate or deep sedation or general anesthesia” • “Supplemental dosing is a single additional dose” for “prolonged procedures” and “should not exceed ½ the initial dose” (not until the “clinical half-life of the initial dose has ...
INTUNIV XR PRODUCT MONOGRAPH
INTUNIV XR PRODUCT MONOGRAPH

... Sedative events were commonly reported adverse reactions in clinical studies (38% for INTUNIV XR vs. 12% for placebo in monotherapy studies and 18% for INTUNIV XR vs. 7% for placebo in the adjunctive study), especially during initial use. INTUNIV XR should be dosed based on clinical response and tol ...
Slide 1
Slide 1

... domestic spoons are used by patients, prescribers ignore this diversity by reducing it to 3 sizes only. (5) Although pediatricians have a good knowledge of domestic spoon capacities, many GPs and most of the pharmacists overestimate them, leading to underdosage for adults, especially in cough prepar ...
VIEW PDF - Practical Dermatology
VIEW PDF - Practical Dermatology

... causative in three cases. All three of those patients experienced renal failure, and two of those three patients died. Based on their analysis of these cases and other databases, the authors recommend that minocycline be considered a “higher risk” medication.12 Although predictive and prognostic fac ...
2012 פברואר ה
2012 פברואר ה

... oral use. In the event of accidental ingestion of large quantities of GYNODAKTARIN products, an appropriate method of gastric emptying may be used, if considered necessary. See also Section 4.5, Interactions with other medicinal products and other forms of interaction. ...
Here - RxPATROL
Here - RxPATROL

... Accidental exposure/ingestion of ER/LA opioids, especially in children, can result in death. A positive­controlled study of the effects of transdermal buprenorphine on the QTc interval in healthy subjects demonstrated no clinically meaningful effect at a transdermal buprenorphine dose of 10 mcg/hour ...
Revised: January 2016 AN. 01318/2015 SUMMARY OF PRODUCT
Revised: January 2016 AN. 01318/2015 SUMMARY OF PRODUCT

... studies have shown that it crosses the placenta and diffuses into breast milk. The drug also crosses the blood brain barrier and enters the central nervous system. The apparent volume of distribution of theophylline in man ranges from 300 to 700 ml/kg and in dogs, 500 to 800 ml/kg. In humans, it is ...
PDR® entry for Naphcon-A Ophthalmic Solution (Alcon)
PDR® entry for Naphcon-A Ophthalmic Solution (Alcon)

... Zinc sulphate is an ocular astringent, which by precipitating proteins helps to clear mucus from the outer surface of the eye. The effectiveness of OCUREST-Z in temporarily relieving conjunctival hyperemia and eye discomfort due to pollen, dust and ragweed has been clinically demonstrated. In one do ...
A randomised, double-blind comparison of the angiotensin
A randomised, double-blind comparison of the angiotensin

... Irbesartan (BMS-186295; SR 47436; Bristol-Myers Squibb/Sanofi) is a potent, long-acting AII receptor antagonist, with high selectivity for the AT1 receptor subtype.14,15 Results of recent clinical studies show that irbesartan safely and effectively lowers blood pressure within 1 week in patients wit ...
pdf - Journal of Global Trends in Pharmaceutical Sciences
pdf - Journal of Global Trends in Pharmaceutical Sciences

... The EEGM did not exhibit any toxic effects up to 5000 mg/kg body weight on oral administration. Body weight before and after administration were noted and any changes in skin, eyes, mucous membrane, respiratory, circulatory, autonomic, central nervous system, behavioral pattern were observed, sign o ...
Proton pump inhibitor side effects and drug interactions Much ado
Proton pump inhibitor side effects and drug interactions Much ado

... been using PPIs for at least 1 year than in those who had not. The risk appeared to increase with Lon increased odds ratio for PPI use in patients with spine fractures as well as in patients with any type of fracture. Interestingly, this study found a lower risk of fracture in patients using a hista ...
Amiodarone - pharminfotech
Amiodarone - pharminfotech

... No, increasing the oral maintenance dose above 200mg is not recommended. Another antiarrhythmic medication can be added as the next step to achieve sinus rhythm. Occasionally, after cardiologist consultation, amiodarone levels can be measured and the dose increased if necessary. What if the patient ...
Asmanex® HFA (mometasone furoate)
Asmanex® HFA (mometasone furoate)

... is a cap-activated, inhalation-driven dry powder inhaler, for the maintenance treatment of asthma as prophylactic therapy in patients 4 years of age and older. • The safety and efficacy of Asmanex HFA were based on placebo-controlled trials in patients 12 years of age and older with persistent asthm ...
HEPATOPROTECTIVE ACTIVITY OF AN ETHANOLIC EXTRACT OF STEMS OF ANISOCHILUS  CARNOSUS AGAINST CARBON TETRACHLORIDE INDUCED HEPATOTOXICITY IN RATS 
HEPATOPROTECTIVE ACTIVITY OF AN ETHANOLIC EXTRACT OF STEMS OF ANISOCHILUS  CARNOSUS AGAINST CARBON TETRACHLORIDE INDUCED HEPATOTOXICITY IN RATS 

... Way ANOVA. The level of significance was found out by Dunnett’s test  wherein all the groups are compared against toxicant group.   ...
Orally Effective Drugs for Kala-azar
Orally Effective Drugs for Kala-azar

... Indian epidemic in Bihar (the epicentrre) but also life-threatening cardiotoxicity in 7-10% and treatmentrelated deaths in 5-10% cases, besides being unsuccessful at times. Parenteral amphotericin B is used as a secondary agent that shows 95% effectiveness but its toxicity and high cost of even the ...
NUCYNTA® ER: Full Prescribing Information
NUCYNTA® ER: Full Prescribing Information

... Use of NUCYNTA ER in Patients who are not Opioid Tolerant The starting dose for patients who are not opioid tolerant is NUCYNTA ER 50 mg orally twice daily (approximately every 12 hours). Use of higher starting doses in patients who are not opioid tolerant may cause fatal respiratory depression. Co ...
Rationale and design of ACTIVE
Rationale and design of ACTIVE

... reduced the risk of total cardiovascular events (hazard ratio [HR] 0.71, 95% CI 0.29 - 0.85, P b .001) and of stroke (HR 0.55, 95% CI 0.43 - 0.71, P b .001). Major bleeding (excluding the trials with combination ASA and low-intensity warfarin) was increased (HR 1.93, 95% CI ...
Endocrine draft for consultation
Endocrine draft for consultation

... initial body weight in 6 months) Gastric emptying may be delayed. Therefore the rate and extent of absorption of other oral drugs administered at the same time may be affected Doses of concomitant sulfonylurea may need to be reduced when a GLP-1 mimetic is started Upper gastrointestinal side effects ...
Dose-response  and  pharmacokinetic  study  with ... bismesylate  after  single  oral  administrations ...
Dose-response and pharmacokinetic study with ... bismesylate after single oral administrations ...

... almitrine also stimulates external ventilation through stimulation of peripheral chemoreceptors [1, 3]. Our study shows that almitrine causes a submaximal Pao~ improvement 2 and 3 h after a single lOO mg oral dose in COPD patients, but also that there are large inter-individual variations in the res ...
Pilot Bioavailability Study
Pilot Bioavailability Study

... treatments are bisphosphonates by intravenous route with sales above $ 1 billion. There is therefore an unmet medical need for patients treated by regular infusions at hospitals / clinics as no oral formulation is available. Bisphosphonates have very poor oral bioavailabilities, 0.6% in average. Des ...
PPI - Amazon Web Services
PPI - Amazon Web Services

... • Clinically significant bleeds in adult studies have shown increase in morbidity and mortality with increased relative risk of 4.1 • Also shown to increase length of ICU stay by 4-8 days • Meta-analysis in pediatric population suggest prophylaxis may be beneficial in preventing GI bleed but no chan ...
Change in Glomerular Filtration Rate and Renal Biomarkers in
Change in Glomerular Filtration Rate and Renal Biomarkers in

... *One subject experienced SAE of jaundice (considered related to study drug); one subject experienced anemia (unrelated) **AEs rated as severe included: jaundice and anemia (same as SAEs noted above); upper abdominal pain Note: One subject has 2 AEs missing ‘Severity, Relationship, and Seriousness’ i ...
Creatinine Clearance When Does It Matter?
Creatinine Clearance When Does It Matter?

... MUST be made in conjunction with the patients clinical status (ie: creatinine must be at steady state, etc.) U.S. FDA. Center for Drug Evaluation and Research. Guidance for Industry: March 2010 Am J Kidney Dis. 2015; 65(2): 177-205 NKDEP. Chronic Kidney Disease nd Drug Dosing: Information for Provid ...
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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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