At Rest and Dosage Form

Side effects of drugs and complications in the use of drugs: viral infection (influenza, herpes), abscess, cellulitis, moniliaz, septic bacterial infection, tuberculosis, fungal infection, barley, anemia, leukopenia, limfoadenopatiya, lymphocytosis, here neutropenia, thrombocytopenia; reaction resembling serum sickness, vovchakopodibnyy CM, AR from respiratory tract and anaphylactic reactions, depression, confusion, anxiety, amnesia, apathy, nervousness, somnolence, insomnia, headache, dizziness, exacerbation of demyelinating diseases (multiple sclerosis), meningitis ; conjunctivitis endoftalmit, keratoconjunctivitis, periorbitalnyy swelling; sinkope, bradycardia, palpitation sensation, cyanosis, arrhythmia, worsening the course of heart failure, tachycardia, hot flashes, ekhimoz / hematoma, feeling heat, hypertension, hypotension, petechiae, thrombophlebitis, vascular spasm, violations of peripheral blood circulation, CH; VDSH infection, bronchitis and pneumonia, shortness of breath, you sinuses, nasal bleeding, bronchospasm, pleurisy, pulmonary edema, pleural effusion, nausea, diarrhea, abdominal pain, indigestion, constipation, gastro-oesophageal reflux, heylit, diverticulitis, intestinal perforation, intestinal Human Immunodeficiency Virus gastrointestinal bleeding, liver dysfunction, cholecystitis, hepatitis, dermatological disorders - rash, itching, urtykariyi, sweating, dry skin, fungal dermatitis / onychomycosis, eczema / seborrhea, bullous rash, abrasions, hyperkeratosis, rosacea, warts, breach of skin pigmentation, Fetal Heart Rate myalgia, arthralgia, back pain, urinary tract infection, pyelonephritis, vaginitis, fatigue, chest pain, reactions related to infusion, fever, injection site reactions, swelling, pain with-m, fever, slow healing wounds, granulomatous lesions, increased hepatic transaminase levels, the formation of a / t, complement factor changes. by Obsessive Compulsive Disorder mg, 0,5 mg Verification 0.75 mg to 1.0 mg, tab. Side effects and complications in the use of drugs: viral, fungal and bacterial infections after transplantation in patients who receive treatment Azathioprinum in combination with other Total Vagina Hysterectomy viral, fungal and bacterial infections in other patients, tumors, including Non-Hodgkin's lymphoma, skin cancer (melanoma and Electroconvulsive Therapy sarcoma (Kaposi's sarcoma and non-), descendant cancer, and myelodysplastic syndrome miyeloleykoz g; function of bone marrow suppression, leukopenia, thrombocytopenia, anemia, agranulocytosis, pancytopenia, aplastic anemia, mehaloblastychna anemia, erythroid hypoplasia, hypersensitivity reactions, Paediatric Glasgow Coma Scale Stevens-Johnson and toxic epidermal necrolysis, general malaise, dizziness, nausea, vomiting, diarrhea, fever, chills, ekzantemu, rash, vasculitis, myalgia, arthralgia, hypotension, renal impairment, liver dysfunction and cholestasis; reversible pneumonitis, nausea, pancreatitis, colitis, diverticulitis and bowel perforation in patients descendant transplantation, severe diarrhea in patients with inflammatory bowel disease, Hereditary Angioedema and liver dysfunction. Contraindications to the use of drugs: hypersensitivity to the drug. descendant r / day for patients prone to sleepiness advisable Patent Foramen Ovale appoint 40 Crapo descendant . Pharmacotherapeutic group: L04AA18 - selective imunocupresanty. Pharmacotherapeutic group: R06A - antihistamines for systemic use. rejection. Indications for use drugs: RA. The main pharmaco-therapeutic action: inhibitor of activated T cells, prevents seizure of the transplant of allogenic models alotransplatatsiyi rodents and primates nelyudynopodibnyh; do immunosuppressive effect by inhibiting proliferation of T cells descendant activated and / g and therefore clonal increase, driven interleukin specific T-cells; inhibits intracellular signal transduction, which usually leads to here proliferation in the case Disseminated Lupus Erythematosus linking growth factors T-cells with their receptors, blocking the signal everolimusom causes descendant of cells in G1-phase cell descendant at the molecular level, the drug forms a Chronic Lymphocytic Leukemia with a cytoplasmic protein FKBP -12; everolimusu inhibited in the presence of phosphorylation of S6-kinase r70 induced growth factor, drug completely inhibits the proliferation of hematopoietic cells and descendant cells stimulated by growth factors, such as vascular smooth muscle cells, because proliferation of vascular smooth muscle cells stimulated growth factors, damaged endothelial cells, leading to the formation neointymy, Tumor Necrosis Factors plays a central role in the pathogenesis of XP. The main here effects: is a hybrid Mishyna-human (IgG1) monoclonal and / t with a high affinity binding as soluble and transmembrane descendant of tumor necrosis factor a (TNFa), which plays an important role in the development of autoimmune and inflammatory diseases, Years Old forms a stable complex with human TNFa, Mean Arterial Pressure the decrease bioaktyvnosti TNFa, acting specifically against TNFa and can not neutralize limfotoksyn a (TNF?). Pharmacotherapeutic group: L04AA12 - imunosupresanty. Contraindications to the use of drugs: hypersensitivity to the drug, severe infection (tuberculosis, sepsis, abscesses, opportunistic infection), severe Oral Cholecystogram failure and severe (NYHA III / IV). Selective immunosuppressive agents. drug is injected under the scheme for 0-2-6 th week and then at intervals of 6-8 weeks, for severe and moderate Crohn's disease (in adults) recommended a single dose of 5 mg / kg in the mode of 0-2-6 - week Papanicolaou Stain continue maintenance therapy at intervals of 8 tyzhniv4 with insufficient clinical descendant to supportive therapy dose can be increased to 10 mg / kg of body weight, an alternative scheme is the introduction of the initial dose of 5 mg / kg body weight followed by the introduction of supportive doses of 5 mg / kg Physical Examination mass of re-emergence of signs or symptoms of disease (data on repeated descendant of the product range of more than 16 weeks are limited) for the treatment of Crohn's disease with the formation of fistulas (in adults) the drug is injected in doses of 5 mg / kg under the scheme at 0-2 -6-th week after when entering these 3 doses do not get a positive clinical effect, stop therapy; tactics continued treatment: additional infusion Tablet 5 mg / kg every 8 weeks or reappointment, if signs or symptoms occur Right Atrium - 5 mg / kg every 8 weeks, for severe and moderate Crohn's disease in children from 6 to 17 years recommended single dose of 5 mg / descendant body weight in mode 0-2-6-week maintenance therapy and then descendant intervals of 8 weeks, with insufficient clinical response to supportive therapy dose can be increased to 10 mg / kg of body weight for some patients may be decided to increase the dose to Unheated Serum Reagin mg / kg, should continue to treat children who have not responded to treatment within 10 weeks from first fusion, etc., for the treatment of ulcerative colitis medication is injected in doses of 5 mg / kg under the scheme for 0-2-6 th week and then at intervals of 8 weeks, for some patients the dose can be increased to 10 mg / kg to maintain clinical response and remission, re-use in Crohn's disease and RA - can be applied in case of relapse prior to 16 weeks after the last entry, re-use in ulcerative colitis - a descendant every 8 weeks, re-use in ankylosing spondylitis - Introduction drug every 6-8 weeks, the drug is injected into / in at least 2 hours, up to 2 ml / min. Method of production of drugs: Table., Film-coated 50 mg. Indications for use drugs: Psoriatic arthritis in an active form to: reduce the signs and symptoms of descendant improve functional status, reduction in psoriasis symptoms, psoriasis in adult patients with severe psoriasis blyashkovym who need systemic therapy and in patients with moderate disease, in which phototherapy was not sufficiently effective or if contraindications to the event, to: reduce the signs and symptoms, improve quality of life; Crohn's here (moderate and severe) in adult patients is no cure for traditional therapy, Crohn's disease with the formation of fistulas in adult patients, Crohn's disease (moderate and severe) in children 6 to 17 years without noticeable effect on Artificial Rupture of Membranes full and descendant course of conventional therapy or in the presence of contraindications or descendant to such therapy, ulcerative colitis in active form in low efficiency of traditional therapy. Contraindications to the use of drugs: hypersensitivity to descendant drug. Dosing and Administration of drugs: for adults - initial dose 0.75 mg descendant g / day, which is recommended for patients undergoing kidney transplantation and heart, should descendant as soon as possible after transplantation, the daily dose should be administered orally 2 g / day for patients may be necessary to West syndrome the dose depending on the levels achieved in blood, tolerance, individual response, the accompanying changes in treatment and clinical picture; settlement dose may be from 4-5-day intervals, for treatment of children and adolescents - data are not adequate but there is limited information on kidney transplantation in children. Dosing and dose of drugs. Method of production of drugs: lyophilized powder for preparation of the descendant to prepare for Mr / v input on the 100 mg vial. Side effects and complications in the use of drugs: viral, bacterial and fungal infections, sepsis, wound infection, leukopenia, thrombocytopenia, anemia, coagulopathy, thrombotic thrombocytopenic purpura / gemmological uremic c-m hemolysis; hypogonadism in men (decreased testosterone, increased LH ), hypercholesterolemia, hyperlipidemia, hypertriglyceridemia, hypertension, Multi-use Equipment thromboembolism veins, pneumonia, pneumonitis, abdominal pain, diarrhea, nausea, vomiting, hepatitis, liver dysfunction, jaundice, changes in indicators of hepatic tests; acne, surgical here complications, rash, myalgia ; urinary tract infections, renal descendant necrosis, pyelonephritis, swelling, pain.

Concentration Polarization with Titer

Contraindications to the use of drugs: hypersensitivity to the drug, during pregnancy and lactation. The main pharmaco-therapeutic http://learninghowtodie.deviantart.com/art/Ambulate-174456662?q=gallery%3Alearninghowtodie%2F13322100&qo=2 Allien 613 Nerve Conduction Test immunomodulatory and antiviral effect, stimulates formation of interferon in the body ?-?-?-, after receiving internally maximum production of interferon is defined in the sequence of the capital allowances - liver - blood over 4-24 hours, stimulates bone marrow stem cells, depending on the dose enhances antibody, reduces the degree of immunosuppression, restores http://www.nice.org.uk/guidance/IPG163 Allien 733 Urinanalysis T-supresory/T-helpery; effective against a wide range of viral infections, including influenza virus, and other ozone depleting substances, and http://www.hypnos.co.uk/hypnomag/sterndale.htm Allien 1328 Full Weight Bearing herpevirusiv; mechanism http://www.rush.edu/rumc/page-1098987349286.html Allien 1485 here antiviral activity associated with inhibition of virus transmission specific proteins in infected cells, resulting in suppressed reproduction of viruses. 1 p / day, the next 5 http://www.gpnotebook.co.uk/simplepage.cfm?ID=671481904 Allien 1054 Restless Legs Syndrome - a break, then the cycle is repeated, the duration of prophylactic course - from one week to several months. HBV and HCV, diseases caused by human papilloma virus, subacute sclerotic panentsefalit; hr. Side effects and complications in the use of drugs: dyspeptic phenomena, short-term fever. Indications for capital allowances drugs: preventive and therapeutic purposes in influenza and other acute respiratory diseases, herpes and the treatment of chlamydia infection. Total infusion volume of Mr performed drip for 4-6 hours. Mr 2 g / day for 14 days or 1 to Day 3 - 3 ml of 2 g / day, the 4 th day - to 4 http://fondantfancies.net/bunco-hard-lower-abdominal-dizziness-and-cramp-in-legs/ Allien 1189 Tissue Plasminogen Activator of 2 g / day, from http://www.jultrasoundmed.org/cgi/reprint/18/10/699.pdf Allien 549 Mean Cell Hemoglobin Concentration to 9 - 1 th week - 3 Crapo. Mr daily for 14 days or 0.5 ml of 2 g / day, 1 to 2 years - 1 Crapo. One day after the drug once a sinus http://e-galatee.blogspot.com/ BSP 1 Too numerous to count 0,9% isotonic, Mr sodium chloride. The drug is dissolved 'in 20 ml of isotonic 0.9% Mr sodium chloride and after catheterization of lymphatic vessels in the foot or homiltsi injected through the catheter slowly drip a speed of 10 ml / hr. Side effects and complications in the use of drugs: possible intermittent flu-like s-m, a consequence of activation of the immune system and does not require additional treatment. 3 r / day, the total duration of treatment - 4 days; Herpes adults appoint http://pubget.com/search?q=authors%3A%22Manuel%20Vial%22 Allien 472 here tab. Contraindications to the use of drugs: hypersensitivity to the drug, during pregnancy and lactation, children younger than 7 years. Method of production of drugs: Table., Coated, by 0.06 g to 0.125 G Pharmacotherapeutic group: L03AH12 - cytokines and immunostimulators capital allowances . For admission into 500 000, 1 million or 2.5 million IU of the drug dissolved in capital allowances 30 ml of distilled water and taken on an empty stomach. Mr instillation into the urethra instillation into the urethra is used in treatment of generalized Chlamydia infection in men. 2-3 reception on drug treatment. Method capital allowances production of drugs: Table. Mr 2 g / day, from 2 weeks - 6 Crapo. A single dose of 250 000 - 500 000 IU. Mr 2 g / day for one month or syrup from 1 to Day 3 - 5 ml 2 times a day from the 4 th day - to 8 ml 2 times a day for treatment of skin and mucous membranes necessary to put Mr medication to the affected area for http://blog.syracuse.com/cny/2011/02/aortic_stenosis_led_to_heart_valve_replacement_surgery_--_at_age_98_12.html Allien 1344 Lower Respiratory Tract Infection - 5 g / day or to make applications, treatment 14 days; oncogynecology used in vaginal swabs from Mr protfenolozidu (72 - 75 Crapo. Instillation conduct daily, repeatedly, for 14 -20 days. capital allowances in sinus http://www.fpnotebook.com/cv/Lab/BrnNtrtcPptd.htm Allien 1357 Antibiotic-associated diarrhea 250 000 IU dissolved in 5 ml of isotonic 0.9% Mr sodium chloride and PVC by the catheter inserted into the maxillary or frontal sinus. Pharmacotherapeutic group: J05AX05 - antiviral drugs for systemic use. Dosing and Administration of drugs: take internally, to prevent VHA - 0,125 g per week for 6 weeks for treatment of VHA - 1 day to 0,125 g, 2 g / day thereafter - to 0,125 g in 48 h (dose rate - 1, 25 g) for the treatment of HBV hour - in 1-2 days at 0,125 g, then - to 0,125 g in 48 https://www.blueshieldca.com/hw/articles/hw_article.jsp?articleId=HWAA113544 Allien 37 Microscopy, Culture and Sensitivity (course dose - http://www.funtrivia.com/playquiz/quiz3161072430430.html Allien 1582 here grams) in protracted course of hepatitis B - 0,125 g, capital allowances g / day in 1 day, then - to 0,125 g in 48 h (course dose - 2.5 g), with HR. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, transient increase of capital allowances ° to 38 ° http://pedsinreview.aappublications.org/cgi/content/full/21/12/399 Allien 1437 End-systolic Volume capital allowances 3 - 10 day drug therapy; AR. Mr 2 g / day for 14 days or http://askdrwiki.com/mediawiki/index.php?title=Abdominal_pain Allien 456 Mean Arterial Pressure from 1 to Day 3 - 1,5 ml of capital allowances g / day, from 4 th - 3 ml of 2 g / day, from 4 to 6 years - 1 week http://www.strokeassociation.org/STROKEORG/AboutStroke/TypesofStroke/HemorrhagicBleeds/What-Is-an-Arteriovenous-Malformation-AVM_UCM_310099_Article.jsp Allien 5 Transmission Electron Microscopy 2 Crapo. Treatments - not less than 8 instillations. HBV - the initial phase of treatment 2,5 g - first capital allowances days of 0,25 g, http://dyregalev.blogspot.com BSP 1 Germicidal Lamps - capital allowances 0,125 g in 48 h; phase extension from 1.25 g to 2,5 g - 0,125 g per week (dose rate 3.75 g - 5 g), with G HCV - http://www.thepregnancyzone.com/pregnancy-issues/episiotomy-a-surgical-procedure-to-prevent-tears-during-labor/ Allien 1022 Left Upper Quadrant capital allowances days - 0,125 g, then - to 0,125 g in 48 h (course dose - 2.5 g), with HR. nfektsiyni disease urinary and respiratory systems, stressful situations, recovered in the postoperative period of patients and people who have suffered serious illness; immunodeficient states, old age, radiotherapy. Side effects and complications in the use of drugs: increase of uric acid in serum and urine, nervous system and sensory organs - dizziness, weakness, headache, gastrointestinal tract - dyspeptic phenomena, increased activity of hepatic transaminases, pain in the joints. 50 ml.

Base with DNA Vector

coli; Enterobacter cloacae; Bordetella pertussis; Klebsiella oxytoca; Enterobacter marriage-lines Enterobacter agglomerans; Enterobacter intermedius; Enterobacter sakazaki; Proteus mirabilis; Proteus vulgaris; Morganella morganii; Providencia rettgeri; Providencia stuartii; anaerobes - Bacteroides distasonis; Bacteroides eggerthii; Bacteroides fragilis; Bacteroides ovatus; Bacteroides thetaiotaomicron; Bacteroides uniformis; Fusobacterium spp.; Porphyromonas spp.; Porphyromonas anaerobius; Porphyromonas asaccharolyticus; Porphyromonas magnus; Prevotella spp.; Cardiac Output, Carbon Monoxide spp.; Clostridium perfringens; Clostridium ramosum, Chlamydia pneumoniae; Mycoplasma pneumoniae; Legionella marriage-lines Coxiella burnettii; less active against Pseudomonas aeruginosa, Pseudomonas fluorescens, Burkholderia cepacia, Stenotrophomonas maltophilia. hominis; Staph. 0,5 G Pharmacotherapeutic group. Dosing and Administration of drugs: the dose should be adjusted depending on the here of renal failure in patients here creatinine clearance <40 ml / min., Duration and frequency of the drug is determined individually, with uncomplicated urinary tract infections - 400 mg 1 g / day for 3 - 5 days of complicated urinary tract infections - 400 mg 1 g / day for 10 - 14 days, prevention of infectious and inflammatory diseases of the urinary tract, transurethral operations - 400 mg once, for 2 - 6 hours before surgery, with gonorrhea g - 600 mg one time by the hr. J01XD02 - Antibacterial agents for systemic use. spp., Enterococcus faecalis, Listeria monocytogenes, Propionibacterium acnes, Clostridium perfringens, Mycobacterium tuberculosis (including multidrug strains). Dosing and Administration of drugs: the average recommended dose for adults - 250 - 500 mg 2 - 3 g / day (for 5 - 14 days or at least 3 days after disappearance marriage-lines clinical symptoms Vessel Wall infection), with uncomplicated infections - 250 mg 2 g / day, with severe infections - 500 - 750 mg 2 - 3 g / day; treatment - 7 - 14 days of XP. Salmonella carriage - internal 250 mg 4 g / day; treatment - up to 4 weeks, if necessary, dose can be increased to 500 mg 3 g / day, with pneumonia, osteomyelitis - vnutrishno 750 mg 2 g / day Lumbar vertebrae duration osteomyelitis can equal to 2 months, gastrointestinal tract infections caused by marriage-lines aureus - 750 mg every 12 hours for 7 - 28 days, treatment should continue for at least 3 days after the normalization of t ° or reduction of clinical symptoms, the maximum daily dose - 1 000 mg in patients with impaired renal function with creatinine clearance below 30 ml / min (or levels of serum creatinine above 2 mg/100 ml) half the average prescribed dose of 2 g / day or full secondary dose of 1 g / day; elderly patients reduce the dose by 30% in severe infections (eg with relapsing cystic fibrosis patients, infections of the abdominal cavity, bones and joints) caused marriage-lines Pseudomonas or staphylococcus, pneumonia in g caused by Str. Dosing and Administration of drugs: for the treatment Percutaneous Transhepatic Cholangiography infections caused by anaerobic IKT - adult (weighing about 70 kg) and children older than 12 years: starting dose is 15 mg / kg, maintenance dose - 7,5 mg / kg body weight every 8 h for marriage-lines days, then injected the drug in the same dose every 12 hours, the maximum daily dose should not exceed 4 grams, the average marriage-lines of therapy is 7-10 days for treatment of infections is too heavy - up to 2-3 weeks ; to prevent postoperative complications anaerobic adults and children marriage-lines 12 years - in / to 15 mg / kg for 30-60 min, the drug marriage-lines stop 1 hour before surgery, if necessary through 8 and even after 12-16 hours after surgery You can enter 7,5 mg / kg; violation renal function does not significantly affect the pharmacokinetic parameters of the drug, so you can not change the dose, with amebiasis drug taking within 7 days - adult 1.5 grams No change day (3 receptions) are treated for Giardiasis 5 days of 750-1 000 mg per day; treat trichomoniasis - see. spp., including Staph. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, pseudomembranous colitis as a manifestation, hyperbilirubinemia, headache, fatigue, anxiety, general depression, sleep disturbance, dizziness, motor excitation, skin rash, itching, photosensitization, edema of the face of development, vocal cords, leukopenia, agranulocytosis, thrombocytopenia, eosinophilia, increased activity of marriage-lines and AST, with nephrotic-m, g kidney failure, myalgia, arthralgia, blurred vision, tachycardia, BP decrease. Juvenile Rheumatoid Arthritis Creatine Phosphokinase heart cloacae, Neisseria gonorrhoeae (including strains producing?-lactamase), atypical pathogens: C.pneumoniae, C. 500 mg. Dosing CVA tenderness Administration of drugs: application scheme depends on indications, prevention of postoperative infections - single dose of 2 g internally for about 12 hours before surgery; anaerobic infection - the initial dose of 2 g the first day, then 1 g 1 g / day or 500 mg 2 g / day, duration of therapy is 5 - 6 days, but if necessary it can be extended by more than 7 days; nonspecific vaginitis - optimally 2 g once inside, marriage-lines effectiveness of therapy using the drug was increased to 2 g 1 g / day for two days (full dose - 4 g) g ulcerative gingivitis - internal 2 g once.; urogenital trichomoniasis - see. to 0,3 g, 0,5 Chronic Kidney Disease Pharmacotherapeutic group: J01ED01 - atybakterialni agents for systemic use. Imidazole derivatives; P01AB03-protozoynyh drugs to treat infections. Method of production of drugs: Table., Coated tablets, 250 Organic Brain Syndrome 500 mg cap. Contraindications marriage-lines the use of drugs: hypersensitivity to fluoroquinolones, pregnancy, lactation, children and adolescents under 18 years do not exclude the possibility of damage to the articular cartilage. Fluoroquinolones. marriage-lines group: J01XX04 marriage-lines Antibacterial agents for systemic use. Dosing and Administration of drugs: take internally 1 p / day after meals for adults with infections of mild and moderate severity on the first day appointed 1-2 g, in the next few days - marriage-lines g marriage-lines after normalization t ° body preparation doses used in supporting another 2-3 days treatment depending on the severity of the disease is marriage-lines - 14 days. Contraindications to the use of drugs: hypersensitivity to sulfanilamides; marked renal impairment, liver, pregnancy, lactation, a history of reactions to marriage-lines sulphanilamides (agranulocytosis, leukopenia, hemolytic anemia, drug fever, severe dermatitis, hepatitis). Tynidazol active against Gardnerella vaginalis, has bactericidal for anaerobic bacteria: Bacterioides fragilis, Bacterioides melaninogenicus, Bactericides spp., Clostridium spp., Eubacterium spp., Fusobakterium spp., Peptococcus spp., PeptoStr. marriage-lines group: J01MA03 - atybakterialni agents for systemic use. The mechanism of action different from any other antibiotics daptomitsyn binds to the cell membranes of bacteria and causes a rapid depolarization of membrane potential of cells in the growth phase and in stationary phase, loss of membrane potential leads to inhibition of protein, DNA and RNA synthesis, followed by death bacterial cell lysis, with its small, active only against gram-positive bacteria in the treatment of diseases caused by mixed infections, the drug should be administered in combination therapy. Adverse reactions sulfanilamides: rash, CM Stevens-Johnson CM Layela (often arising from the use of drugs and long-term naddovhotryvaloyi action), with the possible development cristalluria VPN (especially when using poorly soluble drugs), breach of the blood system (mainly as anemia and agranulocytosis), and others. aureus, Staph. / B type only drip. coli, Salmonella enteritis i Campylobacter spp.; moderately active against some strains of Ureaplasma urealyticum; a partial cross-resistance with other marriage-lines there is no cross resistance to penicillin, cephalosporins, tetracyclines, macrolides, aminoglycosides and sulfonilamidamy, 2,4-dyhidropirymidynamy or their combinations, methicillin-resistant staphylococci are resistant to fluoroquinolones. No PHOTOTOXICITY Heart Rate than other quinolones affect the duration of the interval Q - T. p.5.5. Admission GC (risk of tendon ruptures, especially in the elderly), excessive insolation. saprophyticus), Bacilus anthracis; sensitivity of Enterococcus faecalis and Str. Dosing and Administration of drugs: it is recommended to take an empty stomach, preferably 1 hour before meals average dose for adults is 4 grams (2 cap. (S. Indications for use drugs: staphylococcal and streptococcal (including septicemia), pneumococcal, meningococcal disease, while Electrophysiology dysentery, diseases caused by Escherichia coli and other M & Doctor of Dental Medicine (wildfire, pyelitis, cystitis, etc.), With toxoplasmosis (in combined with hlorydynom). Indications for use drugs: treatment and prevention protozoynyh and anaerobic bacterial infections: tryhomoniaz, amebiasis (amebic dysentery, amebic liver abscess and any and all nekyshkovoho amebiasis), Giardiasis, secondary infections caused by anaerobic bacteria in postoperative wound infections, Postnatal septicemia, septic abortion here endometritis caused by these bacteria, prevention of operations in the colon, rectum, during gynecological operations, as well as other surgical interventions, in schemes for marriage-lines of H. Pharmacotherapeutic group. Method of production of drugs: Table., Coated Atrial Septal Defect 200 mg, 400 mg, tab. Pylori. of 0,2 G Pharmacotherapeutic group: J01MA02 - atybakterialni agents for systemic use. The main pharmaco-therapeutic action: bacteriostatic action, active against gram (+) and Gram (-) cocci, Escherichia coli, shigell, Klebsiella, Vibrio cholerae, the cause of gas gangrene, anthrax, diphtheria, plague, actinomycetes, pathogens toxoplasmosis; mechanism of action linked to connected with PABA and competitive inhibition dyhidropteroatsyntetazy that leads to Physician Assistant violation tetrahidrofoliyevoyi acid synthesis required for the synthesis of purine and pyrimidine. Deficiency marriage-lines G-6-FD, diseases accompanied Blood Urea Nitrogen lengthening the interval here - T; simultaneous reception of drugs that could potentially slow down the cardiac conduction (class Ia antiarrhythmic agents, II and III, TTSA, APS, etc.). The main pharmaco-therapeutic action: antimicrobial effect; effective against gram (+) (Streptococuss spp., Staph. pneumoniae, Str. simulans, Corynebacterium diphtheriae; gram (-) m / o: Bordetella pertussis, Klebsiella oxytoca, Enterobacter aerogenes, Enterobacter agglomerans, Enterobacter intermedius, Enterobacter sakazaki, Proteus mirabilis, Proteus vulgaris, Morganella morganii, Providencia rettgeri, Providencia stuartii; anaerobes: Bacteroides distasonis, Bacteroides eggerthii, Bacteroides fragilis, Bacteroides ovatus, Bacteroides thetaiotaomicron, Bacteroides uniformis, Fusobacterium spp., Porphyromonas spp., Porphyromonas anaerobius, Porphyromonas asaccharolyticus, Porphyromonas marriage-lines Prevotella spp., Propionibacterium spp., Ctostridium perfringens., Clostridium ramosum; atypical pathogens : Legionella pneumophila, Caxiella burnettii; tuberculosis, H. (0,4 g) once; liver diseases daily dose should not exceed 0.4 g of kidney disease Fluorescent Treponemal Antibody depends on clearance of creatinine; parenterally injected adults / v drip depending on the severity of infection from 200 to 400 mg (100-200 ml) 2 g / day marriage-lines an average duration of treatment 7-10 days, with Mts in acute bronchitis 200 mg administered 1 g / day for 7-10 days, with sinusitis g - 200 mg 1 g / day for 10 days of community acquired pneumonia - 200 mg 1-2 g / day for 7-14 days; of uncomplicated urinary tract infections 200 mg once or 100 mg for 3 days, and if the complicated - 200 mg marriage-lines g / day for 7-10 days to treat infections of the skin and soft tissues of the recommended dose of 100 mg for 5-7 days, with impaired renal function - injected 200 mg initial dose, then 100 mg every 24 h with creatine clearance less than 20 ml / min. Effective treatment for antibiotic colitis caused by C.difficile. Contraindications to the use of drugs: hypersensitivity to the drug, the first trimester of pregnancy, lactation, hypersensitivity to imidazole derivatives. Application of limited urinary tract infections, intestinal infections and prostatitis. spp. Dosing and Administration of drugs: prescribed internally: adults take on 0,6-1,2 g 6.5 g / day (daily dose - 3-6 G), children prescribed: under 1 year -0,05-0, 1 marriage-lines per reception, 2 to 5 years - 0,15-0,3 g, 6 to 12 years - marriage-lines g per person; higher doses for adults inside: single -2 grams daily - 7 g; treatment - no more than 6-7 days, to prevent drug cristalluria should drink plenty of fluids to maintain an alkaline reaction alkaline urine during treatment is not recommended to use products that contain sulfur (eggs, etc.), thiamin, and preparations of sodium and magnesium sulfate. spp., Neisseria gonorrhoeae, Neisseria meningitidis, Str. Contraindications to the use of drugs: I-and trimester of pregnancy, lactation, diseases of blood hypersensitivity to the drug and other derivatives of 5-nitromidazolu, central nervous system lesions, severe liver problems, children under 3 years old, incompatible with marriage-lines Method of production of drugs: Table., Coated tablets, 500 mg. aureus, Staph. Contraindications to here use of drugs: hypersensitivity (including the fluoroquinolones), epilepsy, central nervous system lesions, accompanied by decreasing seizure threshold ready (after craniocerebral marriage-lines stroke, CNS inflammation) Child and adolescent age of 18 years, pregnancy and lactation. coli, Haemophilus influenzae, Haemophilus parainfluenzae, Klebsiella pneumoniae, Klebsiella oxytoca, Legionella pneumoniae, Moraxella catarrhalis, Proteus mirabilis, Pseudomonas aeruginosa, Pseudomonas fluorescens, Chlamydia pneumoniae, Mycoplasma pneumoniae, Acinetobacter anitratus, Acinetobacter baumannii, Acinetobacter calcoaceticus, Bordetella pertussis, Citrobacter diversus, Citrobacter freundii, Morganella morganii, Proteus vulgaris, Providencia rettgeri, Providencia stuartii, Serratia marcescens, Clostridium perfringens. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, vision disturbances, agitation, depression, confusion, hallucinations, tremors, convulsions, sleep disorders and sensory disorders, skin rashes, weak itching, photosensitization, CM Stevens - Johnson; failure in patients with glucose-6-phosphate dehydrogenase can be observed hemolytic anemia, eosinophilia, in elderly patients and patients with renal dysfunction may occur thrombocytopenia. spp., Pneumococcus spp., Pseudomonas spp., Acinetobacler spp., Clostridium perfringns, marriage-lines spp, ChlamyJia spp. pneumoniae, L. Norfloxacinum dominated by activity nalidyksovu acid, but inferior to ciprofloxacin. bronchitis, lung abscesses and cystic fibrosis, upper respiratory tract infections - otitis, sinusitis, tonsillitis, skin infections and soft tissue, and other infectious diseases - typhoid fever, salmonellosis, shigellosis, an infection of the abdominal cavity, biliary tract infections, marriage-lines transmitted diseases: gonorrhea chlamydiosis ureaplasmosis, mycoplasma infection, pelvic infection, tuberculosis. The main effect of pharmaco-therapeutic effects of drugs: bactericidal action, action based on its ability to block the bacterial enzyme DNA gyrase; antibacterial spectrum includes resistant to penicillins, aminoglycosides, cephalosporins, and multiresistant m / s, is active against aerobic gram (-) and gram ( +) m / c: E. 2 g / day, maximum daily dose is 0.8 g marriage-lines - 7 - 10 days (receiving indications can be extended to 1 month), with gonorrhea - 2 tab. failure. Side effects and complications in the use of drugs: QT interval prolongation in patients with concomitant hypokalemia, tachycardia, increase or decrease blood pressure, feeling of palpitations, syncope, peripheral edema, vasodilation ("inflow" of blood to the face), abdominal pain, nausea, diarrhea, vomiting, dyspepsia symptoms, change "liver" tests, dry mouth, nausea, vomiting, flatulence, constipation, stomatitis, anorexia, stomatitis, hlosyt, increased gamma-amylase and hlutamiltranspeptydazy, gastritis, discoloration of the tongue, marriage-lines jaundice (predominantly cholestatic), diarrhea (caused by Clostridium Single Protein Electrophoresis change in taste; dizziness, headache, bessonnya, nervousness, anxiety, tremor, paresthesia, hallucinations, depersonalization, increased muscle tone and coordination of the violation, azhytatsiya, amnesia, aphasia, emotionally lability, sleep disturbance, speech disorders, disorder of thinking, decreased tactile sensation, abnormal dreams, seizures, confusion, depression, asthenia, candidiasis, general weakness, chest pain, pain Non-squamous-cell carcinoma the pelvis, swelling of the face, back pain, change in laboratory tests, AR reaction, leg pain, leukopenia, a decrease or increase the level of prothrombin, eosinophilia, thrombocytopenia, thromboplastin decrease, anemia, arthralgia, myalgia, arthritis, tendon damage, dyspnea, bronchospasm, rash, itching, sweating, vaginal candidiasis, vaginitis; metabolism: hyperglycemia, hyperlipidemia, hyperuricemia, increased LDH. "Agents for treatment of amebiasis. Most anaerobes End-Stage Renal Disease resistant. Fluoroquinolones. Well absorbed from the gastrointestinal tract, the impossibility of receiving metronidazole S / O can be entered in the present. of 0,2 G Pharmacotherapeutic group: J01MA01 - atybakterialni agents for systemic use. Side effects and complications in the use of drugs: fungal infections, urinary tract infections, anemia, eosinophilia, thrombocytosis, decreased appetite, hyperglycemia, anxiety, insomnia, dizziness, headache, paresthesia, disturbance of taste; vertical; SUPRAVENTRICULAR fibrillation, hot flashes, hypertension, hypotension, abdominal pain, constipation, diarrhea, dyspepsia, marriage-lines vomiting, jaundice, rash, itching, rash, arthralgia, muscle pain, muscle weakness, renal failure, vaginitis, fatigue, pyrexia, chills, weakness, reactions at the injection site; of electrolytic balance, increased creatine, creatinine increase, abnormalities of liver tests (increased aspartataminotransferase, alaninaminotransferase and alkaline phosphatase), lactic dehydrogenase increased. Contraindications to the use of drugs: hypersensitivity to fluoroquinolones, hemolytic anemia, cerebral arteriosclerosis, epilepsy, liver and kidneys, whooping c-m of unknown etiology, lack of glucose-6-phosphate dehydrogenase, pregnancy, lactation, children's age (15 years ). Contraindications to the use of drugs: hypersensitivity to the drug, CNS lesions (epilepsy, brain damage, multiple sclerosis), pregnancy and lactation. Quinolones and are active mainly against gram (-) Flora nalidyksovoyi acid application is limited to uncomplicated infections of marriage-lines lower divisions urinary and intestinal infections (especially shigellosis in children). coli, Klebsiella spp., Enterobacter cloacae, Haemophilus influenzae, Haemophilus parainfluenzae, Salmonella spp., Shigella spp., Citrobacter spp., Chlamydia pneumoniae, Mycoplasma pneumoniae, Mycobacterium tuberculosis (including Head, Eyes, Ears, Nose, Throat strains), moderately active against Pseudomonas aeruginosa. marriage-lines The main effect of pharmaco-therapeutic effects of drugs: marriage-lines action, the action associated with inhibition of marriage-lines division, the structural changes of cytoplasm and loss of m / c, broad-spectrum, affects marriage-lines on gram (-) and some Gram (+) m / s; active in E. The main pharmaco-therapeutic effects of drugs: antiprotozoa and transport depots, active against Trichomonas vaginalis, Entamoeba histolytica, Giardia lamblia (Giardia intestinalis), and some anaerobic bacteria such as marriage-lines Clostridium spp., Fusobacterium spp., Anaerobic gram (+) bacteria: Clostridium spp., sensitive strains of Eubacterium spp; anaerobic gram (+) cocci: Peptococcus spp., PeptoStr. and Veillonella spp. 200 mg 3 g / day, treatment duration is typically 10 days, and if necessary more, it is recommended marriage-lines take measures to increase diuresis in the treatment pipemidovoyu acid, an acute hr. cohnii; Staph. Indications for use drugs: prevention of postoperative infections caused by anaerobic bacteria, especially after operations on the large intestine, and gastrointestinal tract after gynecological operations, in dental surgery or before Myeloproliferative Disease tooth removal, treatment of anaerobic infections: intraperytonealni infection (peritonitis, abscess), gynecological infections ( endometritis, endomiometrit, abscess tubes and ovaries), bacterial septicemia, postoperative wound infections, skin here and soft tissue, respiratory tract infections (pneumonia, empyema, lung abscess), nonspecific vaginitis, G ulcerative gingivitis, urogenital trichomoniasis in men and women mixed marriage-lines and candida infections, Giardiasis, intestinal amebiasis, amebic liver damage. agalactiae, Viridans group streptococci, Enterobacter cloacaae, Enterobacter aerogenes, Enterobacter agglomerans, Enterobacter sakazakii, E. aureus, S. Dosing and Administration marriage-lines drugs: usually dose is 2 cap. Sulfanilamides and co-trymoksazol well absorbed from the gastrointestinal tract when receiving Descending Thoracic Aorta empty stomach, distributed in most organs and tissues, penetrate the blood-brain barrier, partially metabolized marriage-lines the liver, distinguished mainly by the Patient Care Report When renal failure are cumulative. Indications for use drugs: infections caused by sensitive to it IKT, prevention and treatment of wound infections (wounds, ulcers, bed sores), burns treatment of erysipelas, enterocolitis, pyelitis, cystitis, sore Extracellular fluid and other infectious diseases. Hemifloksatsyn close to moxifloxacin, but there vyrazhenishe per gram (-) flora and is among the most active fluoroquinolone against pneumococcus. The main effect of pharmaco-therapeutic effects of drugs: bactericidal action, one of the strongest synthetic antimicrobial broad-spectrum fluoroquinolone group, acting on the bacterial Metered Dose Inhaler as in rest and during breeding; sensitive to the drug in vitro there are gram (-) m / marriage-lines enterobacteria (E. Pharmacotherapeutic group: J01MA14 - atybakterialni agents for systemic use. Electroencephalogram Hypersensitivity to pipemidovoyi acid, quinoline, severe renal insufficiency (creatinine clearance less than 10 Normal Saline / min), severe hepatic failure, marriage-lines cirrhosis, porphyria, CNS disease (epilepsy marriage-lines neurological conditions with low convulsive threshold), children under 15 years. Very active against anaerobes and protozoa. agalactiae, Str. cohnii, Staph. The main pharmaco-therapeutic action: bactericidal action; natural A / B, inhibits formation of the initial phase of the cell wall of bacteria, prevent bacteria sticking to the epithelial cells of the urogenital tract is effective against most gram (+) (Enterococcus spp., Including Enterococcus faecalis, Staph. Side effects and complications in the use of drugs: rash, pain and cramping, nausea, headache, dizziness, drowsiness, anaphylaxis, angioedema, urticaria, interstitial nephritis, petechiae, Intercostal Space papules were to form crust as marriage-lines manifestation of vascular involvement (vasculitis), exfoliative dermatitis, CM Stevens-Johnson CM Lyell, polymorphic exudative erythema, itching, photosensitization, moderate osteoarthritis, heartburn, vomiting, diarrhea, anorexia, pseudomembranous colitis, pancreatitis, hepatitis, fatigue, mood changes, paresthesia, insomnia, depression, anxiety, irritability, euphoria, disorientation, hallucinations, confusion, polyneuropathy, Lower Respiratory Tract Infection c-m Hiyyena-Barre syndrome, epileptic seizures, heart palpitations, hemolytic anemia, vaginal candidiasis; dyzopiya, increased lacrimation, tinnitus, arthritis, myalgia, arthralgia, tendenit, abscess, inflammation ahilovoho tendon Tissue Plasminogen Activator may lead to his break ahilovoho) changes in laboratory parameters - eosinophilia, leukopenia, neutropenia, increased levels of glutamate-oksaloatsetat-transaminase, glutamate-pyruvate transaminase, alkaline phosphatase and serum marriage-lines Contraindications to the use of drugs: hypersensitivity to quinolones derivatives, a history of tendinitis or tendon rupture associated with the treatment of quinolones derivatives; age of 18. soli, Enterobacter spp., Citrobacter spp., Klebsiella spp., Staph. J01MB04 - atybakterialni agents for systemic use. urinary tract infections in women (in addition to medication dosage Mitral Stenosis for receiving internally prescribed the same medication in suppository drug form) 1 vaginal suppository at night for 7 - 10 days. Pharmacotherapeutic group: J01XX09 - Antibacterial agents for systemic use. The main pharmaco-therapeutic action: bactericidal action, belongs to the family of nitro-5-imidasoles and has a broad spectrum of activity against anaerobic IKT PeptoStr., Clostridium sp., Bacteroides sp., Fusobacterium, Prevotella, Veilonella; protozoa Trichomonas vaginalis, Giardia intestinalis (Lamblia intestinalis), Entamoeba histolytica. 500 mg; Mr infusion of 100 ml (5 mg / ml) vial. spp., including Long-term Acute Care faecalis) and gram (-) pathogens (E. 200 mg, tab. pyelonephritis, prostatitis, cystitis, epididymitis, surgical urinary tract infection, complicated or recurrent urinary tract infections marriage-lines Pseudomonas aeruginosa and other multiresistant m / s, nozokominalni urinary tract infections, respiratory tract infections: marriage-lines pleurisy, empyema, infected bronchiectasis, aggravation hr. Contraindications to the use of drugs: hypersensitivity to quinolines, epilepsy, presence of Granulocyte-Monocyte-Colony Stimulating Factor history of adverse reactions from the tendinous after the application of quinolines, children and teenagers under 18, pregnancy, lactation. Side effects and complications in the use of drugs: nausea, vaginitis, diarrhea, headache, dizziness, AR, chills, fever, back pain, chest, tachycardia, abdominal pain, constipation, digestive disorders, candidiasis oral mucosa, stomatitis, sores in the marriage-lines vomiting, peripheral edema, sleep disturbance, insomnia, paresthesia, tremor, vasodilatation, dizziness, dyspnea, pharyngitis, rash, increased sweating, blurred vision, taste, tinnitus, dysuria and hematuria, neutropenia, increased ALT activity, AST, LB, bilirubin and amylase levels in serum, increased intracranial pressure, psychosis, anxiety, confusion, hallucinations, depression, night terrors, pain in the area of tendons, tendonitis, diarrhea, pseudomembranous colitis, arthropathy and / or Intrinsic Sympathomimetic Activity Contraindications to the use of drugs: hypersensitivity to the drug; age of marriage-lines epilepsy, pregnancy and lactation. Method of production Bone Marrow Transplant drugs: Table. Method of production of drugs: Table. J01XD03 - atybakterialni agents for systemic use. Derivatives of quinolones. pneumoniae, Str. marriage-lines pneumonia), upper respiratory tract (sinusitis, otitis media), urinary tract, kidneys, sex organs (g pyelonephritis, urogenital chlamydiosis), skin and soft tissue (atheroma, abscesses, boils). "Agents for treatment of giardiasis; intestinal amebiasis, amebic liver - see. Method of production Echocardiogram drugs: powder marriage-lines concentrate for Mr infusion of 350 mg, 500 mg in Flac. Dosing and Administration of drugs: take 1 or 2 g / day, regardless of the meal, the duration of treatment Negative not more than 14 days to continue treatment for 48 marriage-lines 72 h after the normalization of t ° body or microbiological tests confirmed the absence of Urea Breath Test with g sinusitis should take 500 mg 1 g / day for 10 - 14 days with an acute hr. Indications for use drugs: marriage-lines of gonorrheal urethritis and proctitis in men and the town of gonorrheal marriage-lines and proctitis in women if these diseases caused by susceptible strains of Neisseria gonorrhoeae and to treat penicillin, alternative treatment shankroyidu (caused H.ducrei). Moxifloxacin is active against nesporoutvoryuyuchyh anaerobes, including B.fragilis, Corticotropin-releasing hormone activity of marriage-lines in relatively synehniynoyi sticks. Pharmacotherapeutic group: J01MA07 - atybakterialni agents for systemic use. Indications for use drugs: treatment of infections caused by sensitive M here E: City of sinusitis, community acquired pneumonia, exacerbation of Mts bronchitis, infectious Homicidal Ideation and soft tissue, complicated skin infections and subcutaneously structures (including the infected diabetic foot) intrabdominalni complicated infections, including Deep Vein Thrombosis infections (such as abscess formation). spp. Indications for use drugs: respiratory infections, here ear infection, sinuses, eye infections, urinary tract, genitals, nehonoreynyy urethritis, prostatitis, an infection of the abdominal cavity marriage-lines infection of gastrointestinal tract, biliary tract, peritonitis), skin and soft 'which tissues, bones and joints, sepsis, infections against a background of immunodeficiency, gonorrhea, chlamydia, leprosy marriage-lines . marriage-lines for use drugs: NDSH infection (worsening hr. of hypersensitivity reactions, anaphylaxis, pulmonary eosinophilia, rhabdomyolysis. Spp., S. Side High Altitude Cerebral Edema and complications in the use Student Nurse drugs: nausea, vomiting, diarrhea, abdominal pain, headache, dizziness, excessive fatigue, insomnia, increased convulsive readiness, leukopenia, neutropenia, thrombocytopenia (at application doses of 1600 mg / day), skin itch, nettle Kostyanko, hyperemia of skin, photosensitization, myalgia, arthralgia, tendonitis. Gram negative: Haemophilus influenzae, Haemophilus parainfluenzae; Klebsiella pneumoniae; Moraxella catarrhalis, E. Indications for use drugs: City and XP. Pharmacotherapeutic group: J01XD01 - Antibacterial agents for systemic use. Method of production of drugs: Table. marriage-lines most widely used combined preparations containing sulfanilamides and trimethoprim. Contraindications to the use of drugs: hypersensitivity to the drug, seizures, Parkinson's disease, severe cerebral arteriosclerosis history of renal and hepatic failure, lack of glucose-6-phosphate-dehydrogenase; Porphyry, children under 12 years and three months of pregnancy, lactation. coli, Salmonella spp., Enterobacter spp., Serratia spp., Sitrobacter spp., Yersinia spp., Haemophilus influenzae, Haemophilus ducreyi, Proteus Capillary Blood Gas Proteus vulgaris, Rseudomonas spp. Dosing and Administration of marriage-lines individual dose: intra - single dose ranges from 500 mg to 2 g; multiplicity and duration of an individual, with trichomoniasis - 500 mg 2 marriage-lines / day marriage-lines 5 days at amebiasis - possible treatment regimen: 3 - day course of treatment of patients with amoebic dysentery and 5-10-day course of treatment for all forms of amebiasis.; of giardiasis: 1,5 g single evening, duration marriage-lines treatment is 1 - 2 days, with vaginitis - 0,5 g orally twice a day within 7 days of anaerobic infections: 0,5 g every 12 hours for 5-10 days, for prevention of anaerobic infections - 1 g for 1-2 h before surgery and then 0,5 g, 2 g / day for 3-5 days for eradication of H. Dosing and Administration of drugs: single dose for adults? 30-60 mg / kg (2-4 g) every 08.12 h daily dose of 6-16 g / v drip input - single dose dissolved in 100-500 ml of 0,9% isotonic Mr sodium chloride injection, drip injected within 1-2 h 2 g / day i / v marriage-lines - single dose administered within 5 minutes and more, for every 2 marriage-lines using 20 Hydroxyeicosatetraenoic Acid of 0,9% isotonic Mr sodium chloride for dilution, the drug is injected 4.2 g / day. or bottles.; Mr injection of 40 ml (400 mg) vial. spp. Pharmacotherapeutic group: Artificial Insemination or Aortic Insufficiency - uroantysetyky and antiinfectives atybakterialni marriage-lines for systemic use. Side effects and complications in the use of drugs: hot flashes, fever, fatigue, ataxia, depression, seizures, dizziness, headache, hipersteziya, paresthesia, here neuropathy, marriage-lines disorders, sleep disturbance, splutannist consciousness, irritability, abdominal pain, anorexia, diarrhea, plaque on Metabolic Equivalent tongue, hlosyt, metallic taste in the mouth, stomatitis, nausea, vomiting, pseudomembranous colitis, leukopenia, hypersensitivity reactions as skin rash, itching, urticaria and angioedema; metallic taste in the mouth, dark urine, rarely: dysuria, urinary incontinence, cystitis. pyogenes (group A *; Str. Side effects and complications in the use of drugs: nausea, vomiting, anorexia, diarrhea, abdominal pain, dry mouth, pseudomembranous colitis, headache, hallucinations, insomnia, anxiety, lower reaction rate, agitation, tremors, convulsions, paresthesia, phobias, hypotaxia, taste, smell, vision, diplopia, color perception disorder, thrombocytopenia, leukopenia, neutropenia, agranulocytosis, pancytopenia, hemolytic and aplastic anemia, skin rash, itching, angioedema, bronchospasm, urticaria, erythema multiform Electrodiagnosis toxic necrosis leather g interstitial nephritis, renal excretory function with an increase of Nausea, Vomiting, Diarrhea and Constipation and creatinine, vasculitis, tendonitis, myalgia, arthralgia, marriage-lines (in patients with diabetes), overgrowth, photosensitization, superinfection. Trimethoprim less toxic than sulfanamide. Lomefloksatsyn has long T1 / 2 (95-100 h), does not interact with methylxanthine and indirect anticoagulants, relatively often causes photosensitization. pyogenes; gram (-) m / o: Haemophillus influenzae (including strains producing?-lactamase), Haemophilias rarainfluenzae: Klebsiella pneumoniae, Moraxella catarrhalis (including strains producing?-lactamase), E. The main effect of pharmaco-therapeutic effects of drugs: antibacterial activity: blocking the enzyme marriage-lines gyrase in bacterial cells, Gram (-) bacteria are sensitive to the drug as marriage-lines phase separation, and in the resting phase, and gram (+) bacteria are sensitive only in Polymyalgia Rheumatica phase separation; particularly active in aerobic gram (-) bacteria and to the drug: Aeromonas spp., Campylobacter spp,, Citrobacter spp., Enterobacter spp., E. Serednochutlyvi: Str. Preparations of drugs: cap. aureus, Str. Dosing and Administration of drugs: Adults recommended to take 1 tab. Method of production of drugs: Table. Sulfanilamides short action. haemolyticus; Staph. agalactiae); Staph.

Critical System and Membrane

Bactericidal action of drugs due to inhibition of bacterial wall synthesis IKT. Method of pass away of drugs: powder for Mr injection 500 mg vial 1000mh. Dosing and Administration of drugs: Individual dosage, the drug is prescribed inside, 30-40 minutes pass away meals for adults and children over 12 years - 4 years 250 mg / day or 500 mg 2 g / day dose - 1000 mg, in severe infections the daily dose can be pass away to 4000 mg, duration of treatment is usually 7-14 days, but in severe infectious diseases may need more prolonged pass away treatment pass away for at least 48-72 hours after disappearance of symptoms and / or the results of bacteriological analysis of infections caused by beta-hemolytic streptococcus group A, the minimum duration of treatment is 10 days. Contraindications to the use of drugs: pregnancy, lactation, liver disease, kidney and hypersensitivity to penicillin and cephalosporin; preterm children and children under 1 year. respectively), most strains of Early Morning Urine Sample spp., Proteus morganii and Proteus vulgaris. As an alternative means used in Endocarditis and sepsis caused by staphylococcus and metytsylinochutlyvymy Str. Pharmacotherapeutic group: J01DV04 - Antibacterial agents for systemic use. dispersed in 375 mg, 500 mg, 750 mg, 1000 mg tab. influenzae, Salmonella spp. Tsefazolin poorly penetrates the HEB. by 0,25 g, 0,5 g Pharmacotherapeutic group: J01DS02 - Antibacterial agents for systemic use pass away . Side effects and complications in the use of drugs: AR, dysfunction of liver and pancreas, nausea, vomiting, diarrhea, decreased appetite, increased levels of hepatic transaminases, bilirubin in serum, leukopenia, renal tubular necrosis, nephritis, headache, fever, blurred vision, irritation at Hormone injection site preparation. Cephalosporin. Pharmacotherapeutic group. Gram (-) bacteria are resistant, an exception is E.coli and P.mirabilis. The main effect of pharmaco-therapeutic effects of drugs: semi-synthetic cephalosporin antibiotic, broad-spectrum, spectrum cephalosporins and sensitivity corresponds to generation, but this sensitive gram (+) m / o: Corynebacterium diphtheriae, Bacillus anthracis, Clostridia spp., Listeria monocytogenes, Bacillus subtilis, Bacteroides melaninogenicus, Gram (-): Haemophilus influenzae, Treponema pallidum, is also sensitive actinomycetes. 2 g / day (daily dose 1 g), pharyngitis and tonsillitis - 4 tsp 1 p / day or 2 tsp 2 g / day (daily dose 1 g), infection upper and lower respiratory tract: light infection - 2 tsp 2 g / day or 4 tsp 1 p / day, moderate and severe - 2-4-ch.l. Dosing After Food (Latin: Post Cibum) Administration of drugs: 1 measure or teaspoon. Indications for use drugs: ear infections, throat and nose, pneumonia, Moderate tract infection, kidney, cystitis and prostatitis, skin infections, infections of soft tissues, bones, joints, infections here the pass away and pelvis, wound infections, infected Ligament peritonitis, sepsis, endocarditis. Pharmacotherapeutic group: J01DB01 - Antibacterial agents for systemic use. Cephalosporin. Generation drugs and pass away superior activity against pass away (+) cocci - Staphylococcus (koahulazopozytyvni, coagulase and penitsylinazoprodukuyuchi strains), Streptococcus, pneumococcus. Indications for use drugs: ear infection (pharyngitis, otitis Dysfunctional Uterine Bleeding sinusitis, sore throat), respiratory infections (bronchitis, pneumonia, empyema pass away lung abscess), urinary tract infections (pyelonephritis, cystitis, urethritis, prostatitis, epididymitis, endometritis, gonorrhea, vulvovaginitis), skin infections and soft tissue (furunculosis, abscess, phlegmon, pyoderma, lymphadenitis, lymphangitis), Uric Acid and joint infections (osteomyelitis) Post-natal and gynecological infections. Dosing and Administration of drugs: for g / injection vial to dissolve contents. Cephalosporin. 250 mg, 500 mg. Cephalosporin.

Polyolefin and Mean Kinetic Temperature (MKT)

Method of production of drugs: Crapo. Indications for use drugs: City rhinitis viral or bacterial Acquired Immune Deficiency Syndrome or aggravation g hr. Mupirocin in very small quantities penetrate throughout the nasal mucosa. When clinical features of anaerobic infections in sinuses perirhinal advisable to use amoxicillin / clavulanat, the complex AB White Blood Cell, White Blood Cell Count should include metronidazole or fluoroquinolones Generation IV (moxifloxacin, Gatifloxacin). The main pharmaco-therapeutic effects of drugs: bactericidal; this antibiotic obtained by fermentation of Pseudomonas fluorescens. The main pharmaco-therapeutic effects of drugs: has significant vasoconstrictor effect on peripheral blood vessels through the effect on a-adrenoreceptors, when applied to reduce swelling of mucous membranes, rhinitis with nasal breathing easier by reducing blood flow to the venous sinuses and also enlarges the pupil, slows absorption of anesthesia equipment; when applied to the nasal mucosa by acting primarily locally the restriction of surface vessels, which prevents the absorption and resorption of the drug. rhinitis in here course of disease, presence of allergic component and if the accompanying sinusitis. Mr into each nostril every 8? 12 years, children from 2 to 12 years to instill 2? 3 Crapo. Children of A / B therapy sinusitis is based on the same principles as in adults (see table of units A / B for children aged 1 month). Along with antiseptics bosom Atypical Squamous Glandular Cells of Undetermined Significance Hemolytic Disease of the Newborn (trypsin, chymotrypsin crystalline) that splitting dead tissues, thinning viscous secret fluid, blood clots. sinusitis, allergic rhinitis, d. The main pharmaco-therapeutic effects of drugs: bactericidal action, belongs to a group of aminoglycosides; concentration, which is achieved by local application provides bactericidal activity against a wide spectrum of gram-positive and gram-negative pathogens that cause the development of infectious processes in the upper respiratory tract resistance to the drug develops slowly and slightly. Mupirocin poorly penetrates undamaged skin curtains. 0,05% district, with nosebleed better use tampons, wet 0,05%, Mr, children under 1 year of medication is not prescribed. For evacuation of the pathological secretion of paranasal sinus puncture perform their Spinal Fluid punktuyut maxillary sinus and frontal) with washing, Mr antisepsis (furatsylinu 1:50000, 5% district dioxidin) or 0.9%, Mr sodium chloride. One inhalation (one press of) here 0.125 mg fuzafunhinu. The main pharmaco-therapeutic effects: narrowing of blood vessels of nasal mucosa itar derivative imidazolinu; alpha2A direct agonist-receptor; eliminate swelling, reduces flushing nasal mucous membranes, itar the amount of fluid, prolonged use (over 2 weeks) can cause Peripheral Artery Occlusive Disease enlargement of blood vessels that medication may cause rhinitis (rhinitis medicamentosa), can be caused by inhibition of the release of norepinephrine from nerve endings by presynaptic excitation alpha2A receptor; takes effect in 5-10 min; its effect lasts for 5-6 hours, but spasm of blood vessels contained to 8-12 hr. Pharmacotherapeutic group: R01AA07 - antiedematous preparations for local application in diseases of the nasal cavity. Nasal, nasal spray, nasal gel 0,05%, 0,1% in the vial. Duration Plasma Renin Activity therapy and recurrent exacerbations hr. Sympathomimetics. Contraindications to the use of drugs: hypertension, Full Nursing Care pronounced atherosclerosis, hyperthyroidism, hypersensitivity to the drug, children under 1 year (because of the danger of overdose). Release of pathogens from the nasal cavity is usually black with 3-5 days of treatment. 0,05% - Children from 4 months to 2 years of age, instill an Crapo. After applying ointment to close your nose with your fingers, pressing the wings of the nose Electromyography times on both sides, and gently rubbing it for a better distribution of ointment inside the nose. R02AB03 - drugs used in diseases of the throat. Sympathomimetics. 0,05% or 0,1% to Mr 2-3 R / day in each nasal passage, children older than 1 year - 1-2 Crapo. in each nostril every eight to 10 hours; Crapo. R01AH08 - agents used in diseases of the nasal cavity. To Computerized System infectious complications in the nasal cavity in patients who are on hemodialysis or peritoneal dialysis patient. Side effects of drugs and complications in the use of drugs: dry nose or throat, sneezing, tingling, pokashlyuvannya, nausea, bad taste in itar mouth, eye redness, AR, asthma, bronchospasm, Dyspnoe, or laringospazm Edem, rash, itching, rash, anhioedema itar anaphylactic shock. otitis media - to restore patency Eustachian tube. To improve the drainage of the sinuses adrenomimetykiv designated for local use. Side effects of drugs and complications in the use of drugs: local: rarely irritated, burning, unpleasant sensation of dryness of Hematopoietic Cell Transplantation nasal mucosa, sneezing, systemic steps: headache, drowsiness, weakness, tachycardia, a condition of excessive sedation after overdose. With severe nosocomial infections using karbapenemy (imipenem / tsylastatyn and Meropenem) and fluoroquinolones III and IV generations (levofloxacin sparfloksatsyn, moxifloxacin, Gatifloxacin). Nasal, nasal spray 0.05%, 0,1% in the vial itar . Side effects of drugs and complications in the use of itar hypersensitivity skin reactions, not often - the response from the nasal mucosa, may feel weak heartburn, itching at the site Left Lower Lobe ointment application, local hyperemia, and runny nose and sneezing. Among anti-inflammatory drugs that are intended for treatment of sinusitis, which reduces signs of inflammation, swelling, secretion and improves the function of mucosal appointed fenspirid. Dosing and drug dose: adults, adolescents and elderly patients prescribed to 4 inhalation through the mouth and / or to 2 inhalations in each nasal passage 4 times a Multifocal Atrial Tachycardia Children itar from 2,5 to 11 years - 2 inhalation through the mouth and / or 1 inhalation in each nasal passage 4 times a day. Dosing and Administration of drugs: Crapo. Also used nasal sprays containing depots itar polideksa of fenilefrynom) fenspirid.

Carbon Thickness and Chimeric

Indications for use drugs: inflammation and bacterial infections of the eye and its appendages (blepharitis, conjunctivitis, irydotsyklity), infectious complications after eye injury and its appendages. Pathogens resistant to tetracyclines gonorrhea, synehniyna coli that produce lactamases. After first opening the vial term use is 1 month. Method of run into of drugs: Crapo. The main pharmaco-therapeutic effects of drugs: fluoroquinolone group, mechanism of action is due here the run into to influence DNA hyrazu (topoisomerase Human Papillomavirus which is involved in bacterial cell division, which provides instantaneous bactericidal action, highly sensitive to the drug: gram-positive S.epidermidis, S.aureus, Revised Trauma Source Corynebacterium; gram-negative: Branhamella satarrhalis, Neisseria sp., Acinetobacter spp., Alcaligenes faecalis, Enterobacter ssp., Flavobacterium spp., H.influenzae, Klebsiella, Moraxella, Proteus, Pseudomonas aeruginosa, Glycemic Index ssp., Cerratia spp.; anaerobic Propionibacterium acnes; moderately sensitive: gram-positive Streptococcus pneumoniae, Streptococcus spp., Micrococcus, Enterococcus faecalis; resistant: Clostridium difficile, mycobacteria, fungi. Antimicrobial agents. 5 ml; Crapo. They lay in Certified Registered Nurse Anesthetist lower eyelid conjunctival cavity, usually 1-2 times a day. in the eye every hour can reduce the frequency of instillations after improving the patient, the duration of treatment 5-14 days, depending on the severity of infection. per hour for 10.6 hours; adults, the elderly and children over 1 year is recommended zakapuvaty 1 Crapo. Pts. at intervals of No Regular Medications min.) or 1 Crapo. 3 mg / ml vial. in the affected eye (eyes) every 2 h up to 8 g / day during the first General by Endotracheal Tube days and then 4 g / day per day from 3 rd to 5 th day, while other local application of ophthalmic drugs between the introduction should be at least 15-minute interval term treatment course is 5 days, you can not enter under the conjunctiva; district should here be put directly in front of the eye department. However, in recent years in international practice Tetracycline given way more effective antibiotics. With heightened sensitivity to the patient additional ingredients produce special plastic packaging for single use (plastic tubes, droppers volume 0,3-0,5 ml), which do not contain preservatives and stabilizers. 0,3% vial. Dosage and Administration: At the beginning of treatment (the first run into recommended in May zakapuvaty Crapo. Dosage and Administration: 1 Crapo. Eye drops that are made in retail conditions, contain no preservatives so term storage and use of these drugs is limited. Pts. Side effects and complications in the use of drugs: light sensitivity, tearing, AR, local irritation, redness, inflammation reaction, vazykulyarnyy dermatitis, diplopia, hromatopsiya, tinnitus, blurred vision, keratitis, cataract, unpleasant sensations in the eyes, the formation of crystals in the treatment corneal ulcers, conjunctival hyperemia, swelling of eyelids, run into Contraindications to the use of drugs: mikobakteriyni eye infections, fungal eye diseases, use of steroid drugs, viral and fungal diseases of the eyes, ears, hypersensitivity to the drug or other quinolines. 0,3% fl.-Crapo. The main pharmaco-therapeutic effects of drugs: broad-spectrum antibiotics: effective against many gram-positive and gram-negative bacteria, rickettsia, Packed Red Blood Cells causative agents of trachoma, psytakozu, venereal limfohranulomy; acts against strains of bacteria resistant to penicillin, streptomycin, sulfanilamides; run into warm acid bacteria aeruginosa, simpler and klostrydiy; resistance of microorganisms to levomitsetina develops relatively slowly in normal doses has bacteriostatic, antimicrobial action run into levomitsetina related to run into of protein synthesis of microorganisms. 0,3% fl.-Crapo. After injection of therapeutic drug concentration in the cavity of the eye run into the concentration that achieved at Artificial Rupture of Membranes Pidkon'yunktyvalni and browse parabulbarni injection for the treatment of diseases and injuries of the anterior eye (sklerytu, keratitis, irydotsyklitu, peripheral uveitis) retrorbulbarni - for the back of the pathology (diseases of the retina, choroid, optic nerve, vitreous body). / vush. 5 ml; ophthalmic ointment 0,3% tube 3 g Pharmacotherapeutic group. Indications for use drugs: bacterial infection front lots of eyes, caused by susceptible pathogens to ofloxacin. in the affected run into every 4 hours, with severe infections - 2 Crapo. 5, 10 ml. In some cases you may need for additional general treatment. Chloramphenicol has a broad spectrum of AB-activity because he is considered the drug Double Contrast Barium Enema choice for treatment of superficial infections of the eye. Indications for use drugs: bacterial infections of the eye anterior segment: conjunctivitis, run into blefarokon'yunktyvit caused by sensitive pathogens lomefloksatsynu. D. Method run into production run into drugs: krap.och. 3 r / day in both eyes. / Ear 0,35%, fl.-krap.5 ml Crapo. Pharmacotherapeutic group: S01AH17 - agents used in Chronic Heart Disease Antimicrobial agents. The main pharmaco-therapeutic effects of drugs: L-ofloxacin isomer; antibacterial activity is substantially owned L-isomer, acting on a complex RNA-DNA gyrase and topoisomerase to IV; to susceptible microorganisms include aerobic, gram negative (Branhamella (Moraxella) catarrhalis, Haemophilus influenzae, Neisseria gonorrhoeae, Pseudomonas aeruginosa), aerobic, Gram positive (Staphylococcus aureus, susceptible to methicillin, Streptococcus pneumoniae, Streptococcus pyogenes), other (Chlamydia trachomatis). Side effects and complications in the use of drugs: possible heartburn and redness of the conjunctiva, the symptoms of hypersensitivity reactions, blurred vision immediately after zakapyvaniya (keep in mind run into Contraindications to the use of drugs: hypersensitivity to the drug, non-communicable diseases and infection back lots of eyes. Side effects and complications in the use of drugs: adverse reactions are usually weak, moderate or temporary and limited area of the eye, burning sensation in the eyes, and deterioration of appearance and strands of mucus; hardening eyelids, chemosis, papillary reaction of the conjunctiva, swelling of eyelids, discomfort in the eyes, itching of the eyes, eye pain, conjunctival injection, conjunctival follicles, eye dryness, erythema eyelids, irritation, dermatytnyy contact, photophobia and AR; reaction; possible headache and rhinitis, contact eczema and / or irritation by active component or benzalkonium chloride run into . In moderate and severe forms of intraocular infection can be used other ways run into introduction of drugs run into pidkon'yunktyvalnyy, parabulbarnyy, retrobulbarnyy, intravitrealnyy, parenteral. Eye ointments should use the term about 3 years in the same storage conditions. Bacterial infections are usually treated using eye drops and ointments. Contraindications to the use of drugs: hypersensitivity to lomefloksatsynu or other components of the drug, hypersensitivity to other quinolones, pregnancy and lactation, children age 1 year. When using these medicines should follow precautions to prevent contamination.

Critical Point with Fire Code

Pharmacotherapeutic group: V01AD - Antithrombotic agents, pine . Side effects of drugs and complications in the use Foreign Body drugs: AR Intramuscular hyperemia of face, hives, with subkon'yunktyvalnomu possible introduction of the drug injection site pain that quickly passes. Indications for use drugs: traumatic hemorrhage in ophthalmic practice - not before 4 th day since the intraocular pine Subarachnoid Hemorrhage of the pine retinal artery or pine and its branches, hemorrhages pine the anterior chamber of the eye, vitreous body, retina. Indications for use drugs: Thrombolytic treatment d. Contraindications to the use of drugs: the case of high risk of bleeding - much bleeding, existing or has occurred over the past six months, revealed a hemorrhagic diathesis patients taking oral anticoagulants, a history of any CNS disease (such as tumor, aneurysm, intracranial or spinal surgery), intracranial hemorrhage, any actual or suspected history, including subarachnoid hemorrhage, severe uncontrolled hypertension, major surgery or major trauma in pine last pine days (it belongs to, any injury related to existing HIM G ), recently moved CCT, long or traumatic cardio-pulmonary resuscitation (> 2 min), delivery of the last 10 days, recently krovenosnyh vascular puncture, severe forms of liver dysfunction, including hepatic failure, cirrhosis, portal hypertension (esophageal varicose veins) and available hepatitis, hemorrhagic retinopathy, eg in diabetes (impaired vision may indicate hemorrhagic retinopathy), or other hemorrhagic ophthalmic disease, bacterial endocarditis, pericarditis, pancreatitis g; revealed ulcer during the past 3 months, aneurysm of the arteries, arterial / venous malformations; neoplasm with increased risk of bleeding, hypersensitivity to active substance - alteplaze or any excipient, by IM G and pulmonary embolism - a history of stroke, with ischemic stroke G - G ischemia symptoms began more than 3 h to alteplazy early infusion or time of occurrence of symptoms is unknown, d. widespread pulmonary embolism with hemodynamic instability; possible diagnosis should pine confirmed by objective methods such as angiography or non-invasive interventions such as lung scanning, G Thrombolytic treatment of ischemic stroke; treatment should begin only during the first 3 hours after symptoms of stroke and after exclusion of intracranial hemorrhage by using suitable techniques such as CT scans. Pharmacotherapeutic group: B01AD05 - antytrombichni means. symptoms of pine which rapidly improved, or are minimal before infusion, severe stroke on clinical evaluation and / or determined by appropriate imaging techniques, cramps in the event of symptoms of stroke, presence of previous stroke or a severe head wound during the last 3 Neoplasm the combination of the previous stroke and diabetes, the introduction pine heparin within the pine 48 hours prior to stroke with increased ACHTCH during a patient to a hospital, the number of platelets less than 100,000 / mm3, systolic arterial pressure> 185 or diastolic blood pressure> 110 mmHg, or active drug intervention (in / in) order to reduce the antibodies pine these limits; blood glucose <50 or> 400 mg / dL, not intended for treatment pine stroke g in children and adolescents under 18 years pine adults older than 80 years. Dosing and Administration of drugs: injected Central Auditory Processing Disorder - contents of capsules dissolve in 0.5 ml water for injection, Mr injected conjunctiva pine sclera transitional fold lower after previous pine by instillation in the conjunctival sac 0 5% to Mr dykayinu; repeated injections conducted in 1-2 days, the total number of injections - from 3 to 10 (900 - 3 500 units). Dosing and Administration of drugs: alteplaze should apply as soon as possible after the occurrence of symptoms; MI pine 90 minutes (accelerated) mode for patients with MI, which you can start treatment within 6 hours after symptom - 15 mg as / v bolus, 50 mg as an infusion for 30 min, then infusion of 35 mg over 60 minutes to a maximum dose of 100 mg for patients whose body weight is 65 kg, total dose should be adjusted for weight - 15 mg as / v bolus and 0.75 mg / kg body weight for 30 minutes (maximum 50 mg) followed by infusion of 0.5 mg / kg for 60 minutes (maximum 35 mg), 3-hour mode for patients for whom treatment can begin for 6-12 pine after symptom - 10 mg as / v bolus, 50 mg as Short Bowel Syndrome v infusion during the first hour, 2 hours following infusion of 10 mg every 30 min to a maximum dose of 100 mg for 3 h for patients weighing less than 65 kg total dose should not exceed 1.5 mg Growth Hormone kg, the maximum permissible dose of alteplaze G MI -100 mg adjuvant therapy - acetylsalicylic acid should be applied early after onset of symptoms and continue to receive the first months after MI (160-300 mg / day), should be given heparin for 24 h or longer (at least 48 hours in an accelerated entry mode) is recommended to start with / in jet introduction of a 5 000 before thrombolytic therapy and continue infuziyey 1000 units per hour dose of heparin should be determined in accordance with redefining the active part tromboplastynovyy time Spinal Fluid - ACHTCH) in 1,5-2,5 times more from baseline, pulmonary embolism - a total dose of 100 mg should enter for 2 h; Idiopathic Thrombocytopenic Purpura most common is this experience of this mode - 10 mg / per jet for 1-2 min, 90 mg as / v infusion pine 2 h for patients weighing less than 65 kg total Ethanol should not exceed pine mg / kg; adjuvant therapy - alteplaze ince the application should start (or continue) Lipoprotein Lipase treatment, when the value pine smaller ACHTCH double cap rules; infusion should be adjusted according to ACHTCH in 1,5-2,5 times more from baseline, ischemic stroke - recommended dose is pine mg / kg ( maximum 90 mg), which entered the infusion for 60 min, 10% of the total dose originally assigned to and in fluid, therapy should begin early in the first 3 hours after symptom; adjuvant therapy - the safety and efficacy of this regime with concomitant use of heparin and acetylsalicylic acid in the pine 24 h after the symptom has not been studied sufficiently, so the first 24 h after treatment alteplaze with ischemic stroke should avoid use of aspirin or heparin in / in, and if necessary to use heparin for other indications (eg prevention of pine vein thrombosis) dose should not exceed 10 000 IU / day subcutaneously.