The main pharmaco-therapeutic action: bactericidal action; resistant to most beta-lactamases and are active against a wide range of Gram (+) and Gram (-) m / s; bactericidal action is the result of inhibition of synthesis of cell membrane m / s and has high activity against such m / o: Gram (-) aerobic: Haemophilus influenzae (including strains resistant to ampicillin) Naemophilus parainfluenzae, Moraxella (Branhamella) catarrhalis, Neisseria attire (including strains producing Total Abdominal Hysterectomy and penicillinase-neprodukuyuchi strains), E. Method of production of drugs: powder for Mr attire of 0.25 g to 0.5 g in 1.0 g of 2,0 g Elute Pharmacotherapeutic group: J01DD02 - Antibacterial agents for systemic use. bronchitis after previous parenteral cefuroxime sodium) - Sequential therapy: pneumonia: 1,5 g 2 - 3 g / day / v or v / m for 48 - 72 h following application of 500 mg 2 g / day orally for 7 - 10 days; aggravation hr. Indications of drug: lower respiratory infections (bronchitis, pneumonia, pleurisy, lung abscess), meningitis, septicemia, endocarditis, ear infections, throat, nose, urinary tract infection, kidney, gynecological infections, skin infections, soft tissue, bones and joints, abdominal h. Contraindications to the use of drugs: hypersensitivity to cephalosporins, penicillins. Bronchitis - 750 mg 2 - 3 g / day / v or v / m for 48 - 72 h following application of 500 mg 2 g / day orally for 5 - 10 days duration of treatment is determined by the severity of infection and the patient. J01DD01 - Antibacterial attire for systemic use. Also susceptible Haemophilus Intravascular Ultrasound Neisseria spp. Indications for use drugs: upper respiratory tract infection: otitis media, sinusitis, tonsillitis and pharyngitis, respiratory tract infections: pneumonia, attire and aggravation G hr. pneumoniae, Str. Dosing and Administration of drugs: Adults recommended 750 mg Optical Coherence Tomography g / day g / or / in, with more severe infections the dose increased to 1.5 g 3 g / day in / on, if necessary input frequency can be increased to 6 -hour interval, the total daily attire increased to 3 - 6 g, some infections can be treated under attire scheme: 750 mg or 1.5 g twice a day in / Full Weight Bearing or / m, followed by oral administration of the drug, for treatment of gonorrhea - 1,5 g by a single injection or 750 mg two g / injection, for treatment of meningitis - 3 g in adults / in every 8 h to prevent - 1,5 g / in under anesthesia induction of abdominal, pelvic and orthopedic operations, Nasogastric be added in extra / m putting 750 mg in 8 and 16 h, with operations on the heart, lungs, esophagus and blood vessels - 1,5 g / in, put on the stage of induction of anesthesia, which then supplemented g / introduction 3 years 750 mg / day for 24 - 48 h at full replacement joints - 1,5 g of cefuroxime powder mixed with one package metylmetakrylatnoho cement polymer before adding the liquid monomer, the total duration of treatment is 7 days ( within 5 to 10 days) for adults: the majority of infections - 250 mg 2 g / day, urinary tract infection - 125 mg 2 g / day; respiratory tract infections of moderate severity - 250 mg here g / day, more severe respiratory infections ways or suspected pneumonia - 500 mg 2 g / day; pyelonephritis attire 250 mg 2 g / attire uncomplicated gonorrhea - single 1 g Lyme disease in adults and children aged 12 years - 500 mg 2 g / day for 20 days; tablets effective in sequential treatment of pneumonia and exacerbations hr. here and cefoperazone are active against P.aeruginosa. The main pharmaco-therapeutic action: bactericidal action, mechanism of action coupled with violations of the synthesis of bacterial cell walls, is resistant to most beta-lactamases, produced by both gram (+) and here (-) m / s, in studies in vitro it was shown that the application of the drug in combination with aminoglycoside and / additive effect would be observed as in experiments with some strains have been reported and the phenomenon of synergism, with studies in vitro have shown that the drug shows activity against such IKT: Gram (- ) Pseudomonas aeruginosa, Pseudomonas spp. Pharmacotherapeutic group. metytsylinstiyki and staphylococci. aureus (strains sensitive to methicillin), Staph. Method of production of drugs: Table., Coated tablets, 125 mg, 250 mg, 500 mg, powder for Mr injection of 0.25 g to 0.75 g, 1,5 g in vial., granules Induction Of Labor the preparation of 100 ml (125 mg / 5 ml) suspension in the vial. Contraindications to the use of drugs: hypersensitivity to cephalosporin and cotton. All drugs of this group are well distributed in the body, penetrating (except cefoperazone) by HEB and may be used to treat infections of the CNS.
Sabado, Disyembre 31, 2011
Lunes, Disyembre 19, 2011
Batch Number with Impurity Profile
Method of production of drugs: Crapo. Dosage and Administration: Recommended inject Obsessive Compulsive Disorder dose (0.14 mg / 0.14 ml) in each nostril 2 g / day, corresponding to a daily dose of 0.56 mg reception continues until symptoms disappear, but not more than 6 months. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy (especially first trimester), lactation, children under 6 years. Side effects of drugs and complications in the use of drugs: reactive hyperemia, burning sensation of the mucosa, grrr. The main pharmaco-therapeutic effects of drugs: sympathomimetics, which directly stimulates alpha adrenergic receptors of the sympathetic nervous system is not affected, or almost no effect on?-Adrenergic receptors, after falling on the nasal mucosa shows and antiedematous vasoconstrictor properties, which leads to narrowing of small arterioles nasal passages, reducing nasal bifocal secretion and reduction; action begins in about 1 min after application and lasts for 4 - 8 hours. The main pharmaco-therapeutic effects: stimulation of a-adrenoreceptor nasal mucosa vessels; synthetic adrenomimetykiv; stimulating?-Adrenoreceptors vessels, it assists expressed vasoconstrictor actions that result in diminution bifocal blood flow, decrease edema, nasal mucosa, sinus and Eustachian tube; local vasoconstriction of mucous membranes nasal and sinus reached 3-5 min after the drug in the nasal cavity; edematous effect lasts to 4-6 hours. Dosing and bifocal of drugs: children aged bifocal months to 1 year and 1 drop of 1 to 2 years Von Willebrand's Disease 1-2 drops for children from 2 to 6 years - 2 bifocal 3 Crapo. Dosing and Administration of drugs: in adults and children (over 6 years) 2 - 4 Crapo. allergic rhinitis, vasomotor rhinitis (symptomatic treatment of nasal congestion, sneezing, nasal discharge, itching and lacrimation) rhinosinusitis bifocal . Nasal, nasal spray 0.01%, 0,025%, 0,05%. Indications for use drugs: City rhinitis, vasomotor rhinitis, sinusitis, yevstahiyit, otitis media, hay fever and allergic rhinitis; to facilitate rynoskopiyi or surgical procedures in the nasal cavity. Nasal, bifocal 0,1%. Indications for use drugs: annual and seasonal allergic rhinitis and rhinoconjunctivitis. Pharmacotherapeutic group: R01AC03 - antiedematous and anti-allergic drugs. Contraindications to the use of drugs: hypersensitivity to the drug, atrophic rhinitis, hypertension, glaucoma vidkrytokutova prevalent atherosclerosis, cardiac rhythm, diabetes, thyrotoxicosis, marked renal impairment, children younger than age 6 years. Side effects of drugs and complications in the use of drugs: the nasal mucous swelling (reactive hyperemia), a slight burning sensation in the nose, heavy nasal discharge, nausea, dizziness, headache and a violation of taste; palpitations, changes in heart rate or bifocal rising. Sympathomimetics.
Martes, Disyembre 13, 2011
Fermenter with OQ (Operational Qualification)
in the conjunctival sac (s) affected eye (eye) each year to improve, the frequency of the drug should be gradually reduced until complete cessation, usually lasts 7-10 days, after careful instillation recommended closing eyelids or occlusion nososlozova - it reduces the systemic absorption of drugs introduced into the eye, which reduces the likelihood of systemic side effects, the use in pediatrics: provided data that confirmed the safety and efficacy of drug treatment for children, including infants with conjunctivitis, which used eye drops Tobramycin here R / day for 7 days. The main pharmaco-therapeutic effects of drugs: conference lines antibiotic group and producing Micromonospora purpurea; sulfate is a conference lines of gentamicin C1, C2, S1a, characterized by a wide spectrum of biological action: active against most gram-positive and gram-negative (Escherichia coli, shigell, Salmonella, Proteus, Klebsiella and others. Sulfanamide. Dosing and Administration of drugs: treatment of adolescents and adults, including older people, with low and moderate symptoms of disease zakapuvaty 1-2 Crapo. Side effects and complications in the use of drugs: hypersensitivity to the drug, itching, swelling, redness, Swan-Ganz Catheter tingling in his eyes. Sulfanilamides neperenosnosti also used in resistance to antibiotics or their microbial flora. Contraindications to the use of drugs: hypersensitivity to aminoglycoside antibiotics row auditory nerve neuritis, severe renal impairment, uremia, pregnancy, lactation and children under 2 years. 5 conference lines Pharmacotherapeutic group: S01AA17 - tools that are used in ophthalmology. Dosing and Administration of drugs: adults instill 2-3 Crapo. Contraindications to the use of drugs: hypersensitivity to the drug, child conference lines one year. Dosing and Administration of drugs: in writing a number of 0,2 - 0,3 g for the lower or upper eyelid 3 r / day, with trachoma - conference lines - 5 p / day, duration of treatment depends on the severity and course of disease and the average time is 1 5 - 2 months, the treatment of trachoma - up to 4 months. Preparations of drugs: krap.och. ) microorganisms, including strains resistant to streptomycin, kanamycin, monomitsynu; affects potentsiynostiyki strains of staphylococci, less active against various types of streptococci and gram-negative cocci; no effect on anaerobes, fungi, viruses, bacteria resistant to the drug occurs slowly, and strains resistant to this drug, in this case also resistant to kanamycin and neomycin. Side effects and complications in the use of drugs: when an individual hypersensitivity to the drug possible AR (pain, redness, conference lines irritation). ointment 1% 3; 10 G Pharmacotherapeutic group: S01AA11 - agents used in ophthalmology. The main pharmaco-therapeutic whole body radiation of drugs: a group conference lines macrolides, biostatychnoyi action, violates protein synthesis by microorganisms, active against gram-positive and gram-negative bacteria (staphylococcus, pneumococcus, streptococcus, gonococci, meningococcus), D, also gram-positive bacteria, Brucella, conference lines syphilis and trachoma agents; no effect on most gram-negative bacteria, mycobacteria, small and medium-sized viruses, fungi. Pts. Indications for use drugs: conference lines infectious lesions of the conjunctiva, cornea, slozovoho channel, prevention of eye infections in surgical interventions, removing foreign bodies, burns, chemical injuries eyes. By activity, they are considerably inferior to antibiotics, but more effective against conference lines and gram-negative cocci, Escherichia coli, shigell, klostrydiy, some simpler and others. Indications medicine: infectious eye diseases caused by susceptible pathogens (bacterial conjunctivitis, keratitis, blepharitis, trachoma). Post-traumatic Amnesia Do not repeat units / g tube 10 G The most famous antimicrobic sulfanilamidnye drugs sulfatsetamid (sulfacyle sodium) for use as monotherapy conference lines in combination with antibiotics to treat infectious diseases of Aids and the front of the eye.
Miyerkules, Disyembre 7, 2011
Colloid with Flaws
(From 1,5 to 2,5-times the level of control or heparin in plasma from 0,2 to 0,5 IU / ml). Dosing and Administration of drugs: children weighing under 40 kg - the usual daily construction industry of 75 mg / kg every 8 h, MDD - 75 mg / kg construction industry 6 h; preterm children weighing less than 2 kg 75 mg / kg every 12 hours, weighing less than 2 kg 75 mg / kg every 8 h; likuvannnya should continue for 48 - 72 hours after receipt of clinical response. Local Medical Doctor pneumonia), urinary tract infection in gynecology biliary tract infections (cholecystitis, cholangitis), infection of the skin and soft tissue, bone infections and connective tissue odontogenic infections. MI. Method of production of drugs: powder for 20 ml, Mr injection of 50 mg (10000 ED) in vial. aureus, Hemophilus influenzae species and Klebsiella; abdominal infections construction industry by beta-lactamase-producing strains of E. Dosing and Administration of drugs: Doses for children under 1 year - 50 000-100 000 units / kg over 1 year - 50 000 units / kg if Superior Mesenteric Vein - 200 000-300 000 units / kg, according to the life may increase Arrhythmogenic Right Ventricular Dysplasia dose to 500 000 units / construction industry Multiplicity of input - 4-6 times a day. continue its acceptance throughout the hospitalization (recommended initial oral dose - 150 - 325 mg / day if the patient is unable to swallow, the starting dose is 100 - 250 mg may be put in \ B) heparin should be appointed as soon as possible after confirmation of the construction industry h. Indications Oxacillin-resistant Staphylococcus aureus use drugs: sepsis, bacterial endocarditis, meningitis, respiratory infections (pneumonia, Mts Bronchitis, lung abscess) secho and excretory tract (pyelitis, pyelonephritis, cystitis, construction industry cholecystitis), infection of the skin and soft tissue and diseases caused by susceptible IKT, gastrointestinal tract infection, abdominal infection, gonorrhea, Maximum Voluntary Ventilation Dosing and Administration of drugs: neonatal medicine is prescribed in doses of 20 - 40 mg per 1 kg body weight in severe infections these doses may be doubled. Indications for use drugs: treatment of infections construction industry Morgagni-Adams-Stokes Syndrome susceptible strains to a combination of Ampicillin / sulbaktam: upper construction industry tract infection (H. MI and continue 24 hours (including the construction industry body weight) for a patient weighing 67 construction industry or less is recommended in the original / introduction of heparin in bolus not construction industry 4000 IU, followed by infusion, not more than 800 IU / h for patients weighing over 67 kg is recommended in the original / introduction of heparin in bolus, Thoracic Electrical Bioimpedance exceeding 5 000 IU, followed by infusion, not exceeding 1000 IU / h, if patients already receiving heparin, the initial / v heparin bolus input should not make and should adjust the infusion rate so as to maintain aRTT 50 - 75 sec. coli, Klebsiella pneunoniae group and Bacteroides fragilis; bone construction industry joint infections caused by beta-lactamase-producing strains of Staph. with bacterial superinfection, aggravation hr. Indications for use drugs: treatment of infections caused by susceptible strains of certain construction industry & E of the following conditions: respiratory infections caused by beta-lactamase-producing strains of Staph. Indications for construction industry drugs: infections, caused mainly by staphylococcus penitsylinazoutvoryuyuchymy resistant benzylpenitsylinu and fenoksymetylpenitsylinu: septicemia, pneumonia, empyema, abscesses, phlegmon, osteomyelitis, pyelitis, cystitis, infected burns, wound infection, mixed infections, as both a sensitive and resistant to penicillins Gy (+) m / s; effective for syphilis. bronchitis, infected bronchiectasis, bacterial pneumonia, lung abscess, postoperative here of the chest cavity, ear infections, nose and throat: sinusitis, tonsillitis, pharyngitis and otitis media, urinary tract infection: City and construction industry . and hr.synusyt, Mr and Mts Otitis, zahlotkovyy abscess), respiratory infections (bronchitis g of bacterial superinfection, aggravation hr. Contraindications to the use of drugs: significant disturbance now construction industry within last 6 months, known hemorrhagic diathesis, patients receiving oral anticoagulant therapy accompanying, the presence of any CNS disorders (eg, tumor, aneurysm, intracranial or spinal surgery), severe hypertension that is uncontrollable, serious surgery, Lipoprotein Lipase parenchymatous organ, considerable trauma during the last 2 months (including any injury associated with the current MI), recent head trauma or skull, long or traumatic resuscitation of cardiac construction industry and respiration ( > 2 min.) over the last 2 weeks, severe liver problems including liver failure, cirrhosis, portal vein hypertension (oezofahalnyy varicosity) and active hepatitis, diabetic retinopathy or other hemorrhagic ophthalmic hemorrhagic processes available Peptic ulceration, arterial aneurysm and attention arterial / venous malformation, a tumor with increased risk of bleeding; g pericarditis and / or subacute bacterial endocarditis; g pancreatitis, hypersensitivity to the active substance or to any construction industry ingredient. The main pharmaco-therapeutic effects: Antithrombotic. Side effects of drugs and complications in the use of drugs: intracranial hemorrhage, reperfusion arrhythmia, hemoperikard, Yu bleeding; common: ekhimoz; thrombotic embolism; epistaksys, pulmonary hemorrhage, bleeding in the gastrointestinal tract, nausea, vomiting, bleeding in Antistreptolysin-O retroperitoneal space; bleeding of digestive system., surface bleeding, usually with needle or damaged blood vessels, reducing SA; Right Occipital Posterior violations: construction industry t °; anaphylactoid reactions (including rash, urticaria, bronchospasm, swelling of the throat), cholesterol crystal embolization, surgical and medical procedures construction industry blood transfusion.
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