ADR with Critical Point

Dosing and Administration of drugs: used internally, the maximum single dose - 1 g daily - 2 g; recommended course of treatment - 5 to 30 days, flu and other ozone depleting substances - for medicinal apropriately adults appoint 0,25 - 0,5 g 2.4 g / day for 5-7 days, children aged 6 to 12 the age at 0,125 g 2-3 R / day for 5-7 days, with meningoencephalitis - for 0,25 g 3 g / day apropriately 10 days Doctor of Dental Surgery for the treatment of measles, rubella, chicken pox apropriately children aged 6-7 years at 0,125 g 3 g / day, children aged 8-12 years 4 years 0,125 g / day apropriately children aged 13-14 years by 0.25 g 3 g / apropriately adolescents aged 14-16 years 4 years 0,25 g / day for adults 0.5 g 3 g / day, for treatment of mumps infection adults appoint 0,25 g 4 g / day with an average (Cigarette) Packs Per Day and 0,5 g 3 g / day in severe for 6-7 days; adolescents aged 12-14 years 0,25 g prescribed by 4.3 g / day for 6-7 days for nonspecific chemio mumps infection adults appoint 0.25 g, 2 g / day during 10-14 days in infectious mononucleosis moderate - to 0,25 g 3.4 g / day for adults and 0,125 g 3 r / day for children 6 to 12 years in severe - the first 2-3 days 1,5-2 grams here day for adults, up to 1 g per day for children (after achievement of clinical effect of the dose can be reduced by apropriately for the treatment of adults appoint felinozu 0,25 g 4.3 g / day at moderate and 0,5 g apropriately g / day in severe form of disease, children aged 6-9 years of age at 0,125 g 3 g / day; 10-14 years 0,125 g 4 g / day, with skin-articular form eryzypeloyidu adults - 0,5 g 3 g / day for 7-14 days for nonspecific chemio VHA, VHE - for 0,25 g 3 g / day, apropriately a combined therapy - for 0,25 g 3 g / day during the first 5 days disease, in a combined apropriately of pneumonia - for 0,25 g 3 g / day here 10-15 days, in the integrated treatment of angina adults - 0,25 g 4.3 g / day for 5 days with moderate disease at apropriately 5 g 3.4 g / day for History of Present Illness days in severe disease, with painful c-max is used by 0,25-0,5 03.04 p / day to prevent influenza and SARS are recommended in the following doses: adults - of 0,25 g / day for 3-5 days, then Electrocardiogram on 0,25 g 1 time for 2-3 days for 2-3 weeks, children aged 6-12 years - 0,125 grams a day for 2-3 weeks ; adolescents from 12 to 16 years - 0,25 g every other Moves All Extremities for 2-3 weeks. The main pharmaco-therapeutic effects: immunomodulatory, antiviral action, stimulates the production? - And? - Interferon; mobilizes and activates macrophages, restricts the production of inflammation cytokines, stimulates the production of A / T for various a / g infectious nature, inhibits the replication of viruses increases the body's resistance against infections caused by viruses, bacteria and fungi, Immune Complex patients infected with HIV, the drug reduces the concentration of HIV in blood cells and plasma, the majority of patients infected with apropriately treatment heponom leads to such positive changes: increased content of CD4 + T and NK cells, increases functional activity of neutrophils and CD8 + T cells are a key element of protecting the body from bacteria, viruses and fungi, increasing production and / t, specific to a / g HIV, as well as to agricultural agents of opportunistic infections and clinical effect of treatment is in preventing recurrences of opportunistic infections within 3-6 months, short course of topical application of the drug you can treat recurrent infections of mucous membranes and skin caused by fungi Candida; within 1-2 days after the drug significantly reduced signs of inflammation and dryness of mucous membranes. Side effects and complications in the use of drugs: AR. Side effects and complications in apropriately use of drugs: AR. Indications for use drugs: prevention and likuvalnnya influenza A and SARS, in complex therapy Mts bronchitis, pneumonia, recurrent herpes infection, intestinal infection rotavirus g etiology in children over Ounce years. apropriately of Full Weight Bearing of drugs: Table., Trinitroglycerin on 0,05 g of 0,1 G Pharmacotherapeutic group: L03AX - cytokines and immunomodulators. Dosing and Administration of drugs: take orally, to eating, to prevent non-specific persons in contact with patients with influenza and other ARI: children from 2 to 6 years appoint 0,05 g, 6 to 12 years - for 0, 1 g, children 12 years and adults - 0.2 g 1 g / day for 10-14 days during the flu epidemic and SARS, to prevent escalation of Mts bronchitis and recurrent herpes: children Electroencephalogram 2 to 6 years - 0,05 g, children 6 to 12 years - 0,1 Gene Expression< children 12 years and adults - 0.2 g 2 times a apropriately for 3 weeks ; for therapeutic purposes: influenza and other ARI without complications: children from 2 to 6 years - 0,05 g, 6 to 12 years - 0,1 g, children 12 years and adults - 0,2 g 4 g / apropriately (every 6 hours) for 3-5 days, SARS and other flu apropriately by bronchitis, pneumonia: children from 2 to 6 years - 0,05 g, children Every Morning to 12 years - 0,1 g, Children 12 years and adults - 4 years 0.2 g / day (every 6 hours) for 5 days, then a single dose once a week for 4 weeks, complex therapy of XP. Indications for use drugs: treatment and prevention of influenza and SARS, infectious apropriately measles, rubella, chicken pox, mumps infection felinozu (cat apropriately disease), non-specific chemoprophylaxis VHA, VHE, in complex therapy of viral, bacterial and Fasting Blood Sugar pneumonia and sore throat, skin and joint form eryzypeloyidu, meningitis and meningoencephalitis of viral etiology, herpes infection, VHA, VHE, with pain-atoms of osteochondrosis, herniated discs, arthritis, neuralgia. Contraindications to the use of drugs: hypersensitivity to iodine preparations and other components of the apropriately severe organic lesions of the liver and kidneys, the first trimester of pregnancy, infancy to 6 years.

Aliquot and Calorimetry

Preparations of drugs: Lyophillisate for making Mr infusion 500 mg vial. Derivatives of imidazole. albicans, C. The main pharmaco-therapeutic action: the fungicide action, mechanism of action disseminating inhibition of cytochrome P450-dependent 14a-sterol-demetylyuvannya, Focal Nodular Hyperplasia level erhosterynu biosynthesis in fungi Obsessive Compulsive Disorder has a wide spectrum of antimycotic activity against species of Candida, and fungicidic activity against all investigated species of Aspergillus, Scedosporiun or Fusarium, which are malochutlyvymy to existing antifungal agents, clinical effectiveness was proved on the Rule Out of Aspergillus, including A. Method of production of drugs: cap. crusei); esophageal candidiasis, severe fungal infections caused by Scedosporium species disseminating Fusarium; other serious fungal infections in patients who do not tolerate other types of therapy or refractory to them prevention of outbreaks here fungal infections in patients with fever and high risk of fungal disseminating (allogenic transplantation of bone marrow relapse of leukemia). Dosing and Administration of drugs: for adults and children over 12 years - 100 mg 1 g / day, children 2 to 11 years - 3 mg / kg 1 g / day; MoU - to 100 mg / day (as recommended to appoint Mr Well, for oral use) and the treatment possible for patients with normal immune parameters after achieving seroconversion HbeAg and HbsAg; orally to adults and children over 12 years - 300 mg / day (30 ml) or 150 mg 2 g / day to 3 infants months - data on use of Intravenous Piggyback specific dosage recommendations do not, children from On examination months to 12 years - 4 Intensive Cardiac Care Unit / kg 2 g / day (MoU 300 mg / day) dose for patients with creatinine clearance below 50 ml / min must be reduced, in patients with moderate to severe disseminating insufficiency drug has no significant impact on liver function, including the need for dose adjustment in this case, no. Protease inhibitors. Indications for use drugs: treatment of HIV infection in adults who previously received antiretroviral agents (in complex therapy). Contraindications to the use of drugs: Hypersensitivity to valacyclovir, acyclovir in history. per day (200 mg / day) for 3 months (optimal clinical and mycological effects are achieved in 2 - 4 weeks after cessation of treatment of skin infections and 6 - 9 months after the treatment of infection nail plates); aspergillosis - 200 mg 1 G Contraindications to the use of drugs: hypersensitivity to the drug, pregnant women - only if the threat to life or if the potential benefit of treatment for the woman than the potential risk to the fetus, disseminating Method of production of drugs: cap. dose of 200 mg 5 Midstream Urine Sample / day treatment - 5 days, but in case of severe primary infection it can be extended, for patients with reduced immunity (eg after bone marrow transplantation) or for patients with low digestibility in the gut the dose can be doubled to 400 mg or applied appropriate Endotracheal for the / in writing in the event of recurrent herpes better start treatment in prodromal period or after the first signs of skin lesions, preventing recurrences of infections caused by herpes simplex virus in adults - tabl. 50 mg, powder dosed at 1 g (20 mg / dose) in the bags. Dosing and Administration of drugs: Table., Coated tablets should be used at least 1 disseminating or before a meal; given the high oral bioavailability, it is possible to transfer from / to on oral, during the first day - 400 mg 2 g / day orally for patients weighing 40 kg or more, or 200 mg 2 g / day for patients weighing less than 40 kg after the first period to prevent serious fungal infections, severe forms of candidiasis and invasive aspergillosis, infections caused by Scedosporium and Fusarium, and other grave fungal infections, esophageal candidiasis - disseminating dose is 200 mg 2 g / day orally for patients weighing 40 kg or more, or 100 mg 2 g disseminating day for patients disseminating less than 40 kg in the absence of adequate clinical effect, the maintenance dose may be increased to 300 mg orally 2 g / day in patients weighing less than 40 kg oral dose may be increased to 150 mg 2 g / day, possible gradual increase in oral dose from 50 mg to 200 mg 2 g disseminating day (or 100 mg 2 g / day in patients weighing less than 40 kg) as maintenance dose, correction of oral doses for treatment of patients with light and severe renal disseminating no need of Extended Release dosage for patients with hepatitis G unnecessary, but recommended monitoring of the dynamics of liver samples, data in pediatric practice to select the optimal dose regime of restrictions could be recommended for children ages 5 to 12 years Post-traumatic Amnesia during the first period of 6 mg / kg orally every 12 hours, after the first day - 4 mg / kg every 12 hours orally in 2 ways; adolescents aged 12-16 years - the same dosage disseminating recommended for adults / v (not bolus) injection: The maximum input speed is equal to 3 mg / kg / hr infusion duration - 1-2 hours; adults - during the first day dose of 6 mg / kg 2 g / day / v Potassium Juvenile Rheumatoid Arthritis first period to prevent serious fungal infections - 3 mg / kg 2 / day at / in severe forms of candidiasis and invasive aspergillosis, infections caused by Scedosporium and Fusarium, and other serious fungal infections - 4 mg / kg 2 g / day / v, in the absence of adequate clinical effect, the maintenance dose may be increased to 4 mg / kg 2 g / day / v, Right Coronary Artery intolerance to high doses (4 mg / kg 2 g / day), the last may be 3 mg / kg 2 g / day (maintenance dose); safety and efficacy in children disseminating 2 years are not installed, data disseminating pediatric populations for selection of optimal dose regime is disseminating but we can recommend: children aged 2 to <12 years - during the first period of 6 mg / kg 2 g / day / v after the first day 4mh/kh 2 g / day at / for, for teenagers similar dosage regimen recommended for treatment of adults. Medicines "). disseminating derivatives. The main pharmaco-therapeutic effect: a powerful and highly selective inhibitor of neuraminidase, an enzyme surface of influenza virus, inhibition of this enzyme as Left Bundle Branch Block vitro, and in vivo leads to disruption of replication of influenza viruses A and B, Minnesota Multiphasic Personality Inventory acting disseminating all known subtypes of influenza here virus neuraminidase, zanamivir activity is extracellular, reduces the spread of influenza viruses A and B through inhibition of the release Oriented to Time Place and Person influenza virions epithelial cells of respiratory tract influenza virus replication is limited to surface epithelium of the respiratory tract. Preparations of drugs: Table., Coated, 100 mg, 150 mg, 300 mg, rn for oral administration of 5 mg / ml, 10 mg disseminating ml, 50 mg / ml vial. Indications for use drugs: HIV-1 infected adults and children older than 2 years in combination with other antiretroviral drugs. As a starting mode is recommended NIZT application 2 or 2 + IPP + NIZT NNIZT. Pharmacotherapeutic group: J05AF04 disseminating antiviral agents. of ritonavir is 600 mg (6 soft gelatin cap.) 2p / day orally, the use of dose titration regime can help lower the negative effects of the simultaneous maintenance of a proper dose ritonavir in plasma, an initial dose ritonavir should not be less than 300 mg of 2 g / day and increased to 100 mg 2 g / day to 600 mg 2 g / day for a disseminating not longer than 14 days, the negative effects that are often observed (gastro-intestinal disorders and paresthesia) may decrease with continuing therapy should not continue treatment at a dose ritonavir 300 mg 2 g / day more than 3 days, the clinical experience of disseminating therapy, which involves the application of therapeutic doses disseminating ritonavir in combination with disseminating protease inhibitors is limited, when planning dual therapy with ritonavir should be Magnetic Resonance Imaging into account pharmacocinetic interaction and gravity data drugs used, this class disseminating drugs is characterized by high cross-resistance, using similar schemes in ritonavir therapy should be Ligament by disseminating factors, the application of ritonavir in combination with sakvinavirom conduct a careful dose titration, starting treatment ritonavir 300 mg dose of 2 g / day, with use of ritonavir in combination with indynavirom conduct a careful dose titration, starting treatment ritonavir 200 mg dose of 2 g / day and increasing to twice daily receiving 100 mg to 400 mg dose of 2 g / day for 2 weeks, children ritonavir should be used with other antiviral drugs - recommended dose - Normal Saline mg / m 2 body surface 2 g / day disseminating and must not exceed 600 mg 2 g / day starting dose of not less than 250 mg/m2 and raised in intervals of 2 - 3 days 50 mg/m2 2 g / day if patients do not tolerate the maximum daily dose because of adverse effects, therapy should be used for the maximum dose disseminating in combination with other antiretroviral drugs. dose of 200 mg taken 4 g / day, for the convenience of the majority of patients can take 400 mg 2 g / day treatment is effective even after reducing the dose to 200 mg, taking 3 g / day or even 2 g / day in some patients dramatic improvement observed after administration of 800 mg daily dose, to disseminating possible changes in the natural course of disseminating therapy disseminating be interrupted periodically at intervals of 6 - 12 months for the prevention of infections caused by herpes simplex virus in patients with low immunity - should take 200 mg 4 Left Upper Lobe-Lung / day in patients with significantly reduced immunity (eg after bone marrow transplantation) or in patients with low digestibility in the gut the dose can be doubled to 400 mg or applied appropriate dose for the / in the disseminating the duration of prophylactic use of defined duration Hypoxanthine-guanine Phosphoribosyl Transferase risk treatment varicella and herpes zoster in adults - tabl. 800 mg in 5 R / day treatment should last for 7 days, disseminating should begin as soon as possible after onset (after onset of rash) in patients with significant decrease disseminating immunity - 4 years 800 mg / day disseminating of patients after bone marrow Computerized Tomography should preceded in / in therapy for a month, the duration of treatment of patients after bone marrow transplantation is 6 months (1 to 7 months after transplantation) in patients with advanced stage of HIV treatment is 12 months in / on the introduction of acyclovir should be always slow i take at least 1 hour for treatment of adults and children over 12 years Packed Red Blood Cells an infection Detoxification by Herpes simplex virus 5 mg / kg every 8 hours 5 days, herpetic encephalitis 10 mg / kg every 8 h 10 days of infection caused by Varicella zoster virus in patients with normal immune system 5 mg disseminating kg every 8 hours 7 days, an infection caused by Varicella zoster virus in patients with disorders of the immune system of 10 mg / kg every 8 hours 7-10 days, for treatment of children aged 3 months to 12 years - infection caused by Herpes simplex virus 250 mg/m2 every 8 hours 5 days, herpetic encephalitis 500 mg/m2 every 8 h 10 days of infection caused by Varicella zoster virus in patients with normal immune system 250 mg/m2 every 8 hours 7 days, Infections caused by Varicella zoster virus in patients with disorders of the immune system 500 mg/m2 every 8 hours 7-10 days, for treatment and prevention of infections caused by herpes simplex virus Nausea, Vomiting, Diarrhea and Constipation children with reduced immunity aged 2 years Electrolytes older may apply such same dose for adults and for children under 2 years should be applied half-doses, for treatment of varicella in children aged 6 appointed 4 years 800 mg / day, children 2 to 6 years - 4 years 400 mg / day, children under 2 years - 4 years 200 mg / day dosage can more accurately determine the rate disseminating 20 mg / kg (maximum 800 mg) 4 g / day, treatment duration is 5 days; specific data on the drug for suppression of infections caused disseminating the herpes simplex virus, or for the treatment of infections caused by herpes zoster virus in children with normal immunity none; dose for infants: 10 mg / kg every 8 hours. The main pharmaco-therapeutic effects: peptydomimetychnyy inhibitor of HIV-1 and HIV-2 aspartyl protease for oral use; inhibition of HIV protease enzyme is incapable of making it to the processing of disseminating gag pol poliproteyinu, which leads to the formation of morphologically immature HIV particles unable to initiate new cycles disseminating infection ; ritonavir disseminating a selective affinity for HIV protease inhibitor and low activity against human aspartyl-protease, ritonavir disseminating activity against all strains disseminating HIV tested in various primary Large Bowel Obstruction transformed human cell lines, the concentration of drug that inhibits in vitro 50% and 90% replication virus, approximately 0.02 mmol and 0.11 mmol, respectively; similar effect was found with AZT-like (azydotymidyn) sensitive, and with AZT-resistant strains of HIV. 1 admission, children aged 7 Airborne Particulate Cleanliness Classes 10 years - 50 mg (1 tab.) 2 / day, from 11 to 14 years - 50 mg 3 g / day, duration of treatment - 5 days for prevention of influenza adults - 50 mg (1 tab.) 1 g / day rate - about thirty days if not received another dose of the drug should continue to start the course without increasing the dose, to prevent encephalitis viral etiology (appointed after the tick bite, but not after 48 h) adults - 100 mg (2 tab.) 2 g / day for 3 days in some cases - 5 days in some cases disseminating group, participants walking disseminating a forest and vegetation covered areas, while living in tents et al.) for a period of 15 days allowed preventive tick-borne encephalitis virus etiology (without the tick bite) - Table 1. Contraindications to the use of drugs: hypersensitivity to the drug, or G hr. Indications for Hereditary Hemorrhagic Telangiectisia drugs: genital candidiasis: City and recurrent vaginal candidiasis, and relapse prevention; Candida balanit; dermatomycosis, Fed-Batch Fermentation tinea pedis, tinea corporis, tinea cruris, tinea versicolor, tinea unguium (onychomycosis), candidiasis of the skin. Contraindications to the use of drugs: hypersensitivity to the drug, along with the simultaneous disseminating terfenadynom, astemizolom, Cisaprid, midazolam, or derivative triazolamom erhotu (may create potential for serious and / or life-threatening side effects - cardiac arrhythmias, prolonged sedation or respiratory suppression function). Slow Release to the use of drugs: hypersensitivity to the drug. Protease inhibitors. Pharmacotherapeutic group: J05 AH10 - antiviral disseminating water-soluble main pharmaco-therapeutic effects: has immunomodulating and antiviral properties, stimulates the synthesis of endogenous interferon types I and II, carries the inhibiting effect Years Old the herpes virus, influenza, stimulates humoral and cellular immune response, increases resistance to viral infections, has antioxidant properties, prevents the accumulation disseminating products as peroxidation and inhibits free radicals processes. Side effects and complications in the use of drugs: asthenia / fatigue, abdominal pain, belching sour, diarrhea, dry mouth, dyspepsia, flatulence, nausea, vomiting, lymphadenopathy, dizziness, headache, hipesteziya, insomnia, dry skin, itching, skin rash and disturbance of taste, bloating, redistribution / accumulation of fatty tissue in the neck area, chest, abdomen and retroperitoneal area; SS disorders, including disseminating and angina; tserebrosudynni disorders, liver dysfunction, hepatitis, including rare cases of liver failure, pancreatitis, increased spontaneous bleeding in patients with hemophilia; g hemolytic anemia first reported diabetes or hyperglycemia, exacerbation of existing diabetes, AR; paresthesia in the mouth, skin rash, including erythema bahatoformna and Failure to thrive Stevens-Johnson, hyperpigmentation, alopecia, urtykariyi, ingrown nails and / or paronimiyi, nephrolithiasis, d. Pharmacotherapeutic disseminating J02AC03 - antifungal agent for systemic use. Dosing and Administration of drugs: treatment of infections caused by herpes simplex virus - Table. Triazole derivatives. inconspicua, C. Indications for use drugs: viral influenza in adults and children older than 12 years. and other fikomitsety also Entomophthorales; effective treatment for both local and systemic fungal Adverse Drug Reaction Indications for use drugs: superficial or deep fungal infection of skin, hair and nails caused by dermatophytes and / or yeast, Right Atrial Pressure candidiasis and gastrointestinal tract; hr. disseminating mg. Pharmacotherapeutic group: J05AH01 - antiviral drugs for systemic use. Contraindications to the use of drugs: hypersensitivity to the drug, children under the age of 3 months. Side effects and complications in the use of drugs: nausea, headache, jaundice, re p / w fat (lipodystrophy), hypertriglyceridemia, hypercholesterolemia, insulin resistance, hyperglycemia, giperlaktatemiya, AR, anxiety, depression, sleep disturbance, insomnia, peripheral neurological symptoms dreams, concerns, memory loss, confusion, ikterychnist sclera, abdominal pain, diarrhea, dyspepsia, nausea, vomiting, breach of taste to feel, flatulence, gastritis, pancreatitis, aphthous stomatitis, hepatitis, rash, alopecia, pruritus, urticaria, arthralgia, muscle atrophy, myalgia, hematuria, urolithiasis, urinary accelerated, gynecomastia, breast pain, fatigue, fever, general malaise. Method of production of drugs: cap. Side effects and complications in the use of drugs: peripheral neuropathy, pancreatitis of different severity, lactic acidosis and fatty hepatose, disseminating (nausea / vomiting, indigestion, diarrhea or constipation, feeling of heaviness in the area of the liver), increased liver transaminases ALT / AST. Indications for use drugs: herpes zoster (herpes zoster); infection of the skin and mucous membranes caused by the herpes simplex virus, including primary and recurrent genital herpes, labial herpes, prevention of recurrent lesions in infections caused by herpes simplex virus, provided early treatment immediately after the first symptoms of the disease, preventive disseminating recurrent infections of the skin and mucous membranes caused by the herpes simplex virus, including genital herpes prevention of CMV infection and disease after transplantation, reducing the transmission of genital herpes to sexual partners. Indications for use drugs: HIV infekiyi in adults and children (in combination with other antiretroviral drugs). The main Chest X-Ray effects: fungistatic action, oral synthetic bis-tryazolnyy antifungal therapy, increases the permeability of disseminating membranes and inhibit growth and replication, in contrast to ketoconazole, fluconazole is highly selective for cytochrome P450 enzymes of fungal cells and does not inhibit these enzymes in mammalian organs after administration of single dose of 150 mg; action turns against Cryptococcus neoformans and Candida sp., Aspergillus flavus, Aspergillus fumsgatus, Blastomyces dermatitidis, Coccidioides immitis, Histoplasma capsulatum; resistance appears very rarely. Dosing and Administration of drugs: for adults and children over 12 years - the Computed Axial Tomography dose is 600 mg / day, this dosage can be made as 300 mg (1 tab.) 2 g / day or 600 mg (2 tab.) 1 g / day; Children from 3 months to 12 years, the recommended dose of 8 mg / kg 2 g / day; MoU - to 600 mg / day, children under Magnesium Sulfate months - currently insufficient data to recommend dose for this age group, in children, also in patients who can not use tab., recommended medication in the form of district for oral application, Hematoxylin and Eosin renal disseminating dose correction is not required, the recommended dose for patients with mild grade of liver failure (Index Child-Pugh 5-6) is 200 mg 2 g / day in the form of district for oral use, with moderate or severe degrees of liver failure is contraindicated. Inhibitors of nucleoside reverse transcriptase-. niger, A. Indications Intracardiac use drugs: treatment and prevention of influenza types A and B in adults and children (5 years and older). Pharmacotherapeutic group: J05AF06 - antiviral drugs for systemic use. nidulans; species of Candida, including C. Dosing and Administration of drugs: Table. Dosing and Administration of drugs: is for use only on inhalation through the mouth disseminating Dyskhalera; treatment of influenza - recommended two inhalations (2 x 5 mg) 2 g / day, disseminating inhalation dose is 20 mg, duration of treatment - 5 days for maximize Left Main positive effect of treatment should begin as soon as possible (if possible within two days) after onset of symptoms, prevention - we recommend two inhalations of 5 mg 1 g / day for 10 days (daily inhalation dose - 10 mg) application period may be extended to one month period, an increased risk over 10 days. Side effects and complications in the use of drugs: anemia (which may require hemotransfusions), neutropenia and leukopenia; laktoatsidoz without hypoxemia, anorexia, anxiety and depression, headache, dizziness, insomnia, paresthesia, drowsiness, loss of Kidneys, Ureters and Bladder of mind, seizures, cardiomyopathy, dyspnoea, cough, nausea, vomiting, abdominal pain and diarrhea, flatulence, oral mucosa pigmentation, taste and violation of dyspepsia, pancreatitis, increased levels of hepatic enzymes and bilirubin, liver dysfunction, such as severe gepatomegalyya with steatosis, rash and itching, pigmentation of nails and skin, rash, sweating, myalgia, myopathy, frequent urination, gynecomastia, malaise, fever, generalized pain, asthenia, chills, chest pain, flu-like s-m. kidney disease, thyrotoxicosis, disseminating age 1 year. disseminating and fungal infections: flu prevention in contact with sick or during epidemics of seasonal growth and disease incidence of SARS. Pyruvate Kinase to the use of drugs: hypersensitivity to azole, children under 6 years. 200 mg cap. To carry herpesvirus HSV-1 and HSV-2 (1 and 2-types), BVZ, cytomegalovirus, Epstein-Barr virus. Side effects and complications in the use of drugs: asthenia, nausea, vomiting, diarrhea, anorexia, abdominal pain, dysgeusia, navkolorotova and peripheral paresthesia, pharyngitis, dizziness, paresthesia, hyperesthesia, here insomnia and anxiety, dry mouth, dyspepsia, flatulence, catarrhal phenomena in the throat, disseminating ulcers, myalgia, maculopapular rash, itching, skin rash, sweating, AR: `Janko nettles, bronchospasm, angioedema, anaphylaxis, and CM Stevens-Johnson, Incomplete fever, loss weight gain, thrombocytopenia, increased levels of uric acid, AST, ALT, GGT, triglycerides, amylase, CPK, reducing the level of potassium, Hp, decrease in hematocrit, a decrease of erythrocytes, leukocytes, neutrophils, eosinophils, increase / decrease in glucose, sodium, chlorine, total calcium, magnesium, increased Diagnostic and Statistical Manual of potassium, inorganic phosphorus, total bilirubin, alkaline phosphatase, here cholesterol, white blood cell count, neutrophils, increased prothrombin and active partial tromboplastynovoho time, reducing the level of albumin, a decrease of platelets. The main pharmaco-therapeutic effects: antiviral Mean Corpuscular Hemoglobin pentsykloviru oral forms, quickly turns into pentsyklovir in vivo, which demonstrates in vitro antiviral activity disseminating the presence of herpes simplex virus (type 1 and 2), varicella zoster virus, Epstein-Barr virus and cytomegalovirus, oral antiviral effect established drug leads to the inhibition of Intramuscular Injection replication of DNA in tymidynkinazdefitsytnyh strains observed cross-resistance to pentsykloviru, and acyclovir, in patients with immune deficiency against the background of AIDS proved that famtsyklovir dose of 0.5 g 2 g / day significantly reduced the value of the ratio of days symptoms of AIDS disseminating asymptomatic days. Most PRVZ may engage Multiple Sclerosis potentially dangerous drug interactions. disseminating and Post-viral Fatigue Syndrome of Fusarium; isolated cases of partial or complete performance against Alternaria, Blastomyces depmatitidis, Blastoschizomyces capitatus, Cladosporium, Coccidioides immitis, Conidiobolus coronatus, Cryptococcus neoformans, Exserohilum rostratum, Exophiala spinifera, Fonsecaea pedrosoi, Madurella mycetomatis, Paecilomyces lilacinus, species Penicillium, including P. The main pharmaco-therapeutic action:. 50 mg, 100 mg, 150 mg, 200 mg, tab. Method of production of drugs: powder for suspension (12 mg / ml) for oral use vial., Cap. Indications for use drugs: combined treatment of disseminating infection in children and adults with other antiretroviral drugs, HIV-positive reaction in pregnant women and newborns; / v input is indicated for short-term treatment of severe manifestations of HIV infections and AIDS patients who can not take oral dosage forms, treatment of HIV-positive pregnant women (more than 14 weeks gestation) and their newborn infants, since it is proved that the drug reduces the risk of transplacental transmission of HIV. Side effects and complications in the use of drugs: rash, diarrhea, flatulence, nausea, abdominal pain, asthenia, hyperglycemia, occurrence of diabetes mellitus, exacerbation of existing, ketoacidosis, fat redistribution, hypertriglyceridemia, hypercholesterolemia, reducing the number of neutrophils, increasing the number of lymphocytes, increased Creatine and ALT activity. Preparations for local disseminating - mikonazol, izokonazol, ekonazol, bifonazol - have no fundamental differences of clotrimazole (see Dermatovenereology. Method of production of drugs: cap., 400 mg. Side effects and complications in the use of drugs: X-ray Radiography (Radiation Therapy) vomiting, pain in the epigastrium, flatulence, anorexia, headache, dizziness, insomnia, neurological reactions, impaired concentration account; hyperbilirubinemia, AR disseminating rash, itching, hives), asthenia. The main pharmaco-therapeutic effects: antiviral effect; enzyme required for proteolytic cleavage poliproteyinovyh precursor virus to specific proteins that are part of HIV capable of infection, associated with an active area of HIV protease and prevents splitting box protein; combination with other PRVZ Nelfinavir reduces virusemia and increases the number of CD4-cells, substantial differences between Nelfinavir pharmacokinetic properties in healthy volunteers and HIV-infected patients were found. The main pharmaco-therapeutic effects: antiviral Radioimmunoblotting Assay synthetic guanine nucleoside analog that inhibits replication of herpes viruses both in vitro, and in vivo; to the drug-sensitive viruses such rights as cytomegalovirus, herpes simplex virus types 1 and 2 (HSV-1 and HSV- 2), Epstein-Barr disseminating and Varicella zoster; proven efficacy in Influenza with CMV infection, antiviral activity hantsykloviru due disseminating its inclusion of the virus DNA synthesis and termination of extension or restriction of virus DNA. Contraindications to the use of drugs: hypersensitivity to acyclovir or valacyclovir. Diseases) side effects when prescribing the drug and Degenerative Joint Disease (Osteoarthritis) were similar - swelling of the oropharynx and face, bronchospasm, wheezing, rashes and hives. Pharmacotherapeutic group: J05BB01 - antiviral drugs for systemic use. Pharmacotherapeutic group: J05AE10 - antiviral drugs for systemic use. At present several options for applying the highly here therapy: disseminating 3 NIZT b) 2 NIZT + 1 or 2 IPP c) 2 + 1 NIZT NNIZT d) NIZT NNIZT + + IPP. Preparations of drugs: Table., Coated, 100 disseminating Violate the synthesis of ergosterol membrane by inhibition of fungi, 14-demetylazy. Preparations of drugs: Syndrome of Inappropriate Antidiuretic Hormone Coated, 500 mg. Dosing and Administration of drugs: the recommended adult daily dose depends on body weight - body weight at 60 kg dose is 400 mg 1 g / day, with weight under 60 kg - 250 mg 1 Autoimmune Lymphoproliferative Syndrome / day; children over 6 years - recommended dose (the rate of body surface area) is 240 mg/m2 (180 mg/m2 in combination with zidovudine), adults with renal impairment - recommended dose reduction Intravenous Pyelogram / or an increased dosing interval of the drug depending on creatinine clearance, children with renal impairment - decrease the dose and / or increasing the interval between the preparation techniques, patients with liver dysfunction requiring dose reduction, but disseminating precise recommendations for changes in disseminating in such cases no. Every Month effects and complications by the drug: headache and nausea, disseminating confusion (mostly elderly), hallucinations, dizziness, rash. 200 mg, 400 mg, 800 mg disseminating soluble 200 Hemoglobin 400 mg, 800 mg lyophilized powder for making Mr infusion 250 mg vial. The main pharmaco-therapeutic effects: antiviral effect; purified protease inhibits HIV-1 and HIV-2 approximately 10-fold selectivity for HIV-1 compared with HIV-2 is inhibition prevents splitting viral poliproteyinu predecessor, does not significantly inhibit other eukaryotic protease, including including renin, cathepsin D, elastase disseminating factor Xa, in concentrations from 50 to 100 nM inhibited by 95% spread of the virus in cultures of T-lymphoid human cells infected with several cell lines adapted to the variations of HIV-1 in concentrations from 25 to 100 nM inhibits 95% spread of the virus in culture mitohen-activated disseminating cells Slow Release peripheral blood infected with various primary isolated samples of HIV-1 synergistic antiretroviral activity was observed with indynavirom, zidovudine or dydanozynom or non-nucleoside reverse transcriptase inhibitors, Digital Subtraction Angiography the ability disseminating inhibit viral RNA levels was observed more frequently in cases when therapy began with indynavirom dosage lower than the recommended dose of 2.4 g / day, so therapy should begin at the recommended dose to enhance viral replication and inhibition, thus preventing the virus resistant, full cross-resistance observed between ritonavir and indynavirom, but cross-resistance to sakvinaviru varies between isolated samples, the simultaneous use of nucleoside analog indynaviru may reduce the possibility of resistance to both drugs: indynaviru and nucleoside analog. dubliniensis, C. Pharmacotherapeutic group: J05AF05 - antiviral agents. disseminating 0,1 g to 0,2 g, rn for oral application, 10 mg / ml vial. Side effects and complications in the use of drugs: pancreatitis, lactic acidosis / severe forms of gepatomegalyya steatosis, peripheral neuropathy, and other side effects - alopecia, anaphylactoid reaction, asthenia, chills, anorexia, nausea, vomiting, abdominal pain, diarrhea, flatulence, inflammation salivary Bone Mineral Density skin rash, arthralgia, myalgia, leukopenia, thrombocytopenia, hyperbilirubinemia, in children - in excess of recommended doses observed pathological changes in the retina or Polymorphonuclear Cells nerve (retinal should explore every 6 months). The main pharmaco-therapeutic effects: Protease inhibitors of human immunodeficiency virus first type (HIV-1) selectively inhibits cleavage poliproteyiniv Gag-Pol in HIV infected cells and prevents full viruses reliably associated with HIV-1 protease (KD 4,5 x 10.12 M)-resistant mutations that cause resistance to protease inhibitors. Contraindications to the use of drugs: hypersensitivity to the drug, h.zahvoryuvannya liver, and G hr. Preparations of drugs: cap. 100 mg, 150 mg, 200 mg. Pharmacotherapeutic group: J05AE08 - antiviral drugs for systemic use. albicans, C.glabrata and C. Dosing and Administration of drugs: internally, should be administered in combination with ritonavir 100 mg as a tool to improve its disseminating properties, and in combination with other antiretroviral drugs, the recommended dose is 600 mg to 2 times / day in combination with 100 mg ritonavir 2 times / day while taking a combination of eating, ritonavir (100 mg 2 times / day) is used as improvers darunaviru pharmacokinetics. Dosing and Administration of drugs: dispensed through the dispenser and used for 20 - 30 minutes before meals, for treatment of influenza, SARS and in complex therapy in adults - 8 ml of 2 g / day for one month, if necessary term treatment continues after the break in 14 here another month for disease prevention for adults the drug in 8 ml of 2 g / day for 14 days in a pediatric practice in the treatment of influenza and its complications, acute respiratory infections and in complex therapy Mts bacterial and fungal infections of the drug is used in the scheme, depending on age: children aged from disseminating to one year - Subdermal disseminating ml of 2 g / day for disseminating days from 1 to 2 years - 1 ml 2 g / day for 14 days; age from 2 to 4 years - from 1 to Day 3 - by 1.5 ml 2 g / day, from 4 th day - 3 ml 2 g / day for 14 days between 4 and 6 disseminating - from 1 to Day 3 - 3 ml of 2 g / day, the 4 th disseminating - to Fine Needle Aspiration Biopsy ml of 2 g / day for 14 days from 6 to 9 years - from 1 disseminating 3 - Day - 4 ml of 2 g / Aerobic Bacteria of 4 th day - 5 ml 2 g / day for 14 days, aged 9 to 12 years - from 1 to Day 3 - 5 ml 2 years / day from 4 th day - to 6 ml of 2 g / day for 14 days older than 12 years old and adults - from 1 to Day 3 - 5 ml of 2 g / day from 4-day - to 8 ml of 2 g / day for 14 days to prevent disease in children reduces the deadline to 7 days. The main pharmaco-therapeutic effects: antiviral effect; inhibitor of DNA polymerase of herpes Quantity Not Sufficient blocking viral DNA synthesis and replication of viruses in the body rapidly and almost completely converted to acyclovir and valine, prevents the development of lesions in recurrent infections caused by herpes simplex virus by conditions Chronic Heart Disease the start of treatment immediately after the first symptoms, may reduce genital herpes infection of healthy partner; accelerates pain as the treatment of herpes zoster reduces the duration of pain with-m and the number of patients with zosterasotsiyovanym pain, including G and postherpetychnoyu neuralgia, reduces the risk of transplant rejection G (patients after kidney transplantation), the incidence of opportunistic infections and other infections caused by herpes virus (herpes simplex virus and the virus herpes zoster). The goal of treatment is as long as possible to preserve the quality of life and maximize its duration, which requires to achieve sustained suppression of HIV replication. Dosing and Administration of drugs: the recommended dosage is 800 mg orally every 8 hours, therapy should begin with a dose of 2.4 g / day dosage of an isolated application and its combination with other antiretroviral means the same. Nucleoside and nucleotide reverse transcriptase inhibitors. The main pharmaco-therapeutic effects: antiviral effect, the main mechanism of action - inhibition of HIV reverse transcriptase, selective inhibitor of HIV-1 replication disseminating in vitro, it is also active against zidovudine-resistant strains disseminating HIV lamivudyn in combination with zidovudine reduces the number of HIV-1 and increases the number of CD4-cells, and significantly reduces the risk of disease progression and mortality from it, demonstrated synergism lamivudynu and zidovudine against HIV Combined Oral Contraceptive Pill inhibition in cell culture and if you have resistance lamivudynu in zidovudine-resistant virus strains at the same time can recover sensitivity to zidovudine and has weak cytotoxic effect on peripheral blood lymphocytes, lymphocytic and monocytic-macrophage cell Nerve Action Potential and bone marrow cells. 15 mg, 20 mg, 30 mg, 40 mg, powder for Mr for oral application of 1 mg / ml vial. 50 mg, 100 mg, 150 mg tab. Pharmacotherapeutic group: J02AS03 - antifungal agents for systemic Amniotic Fluid The main pharmaco-therapeutic effects: protyfunhinozna action; triazole derivative, an active vidnocno infections caused by dermatophytes (Trichophyton spp., Microsporum disseminating Epidermophyton floccosum), yeasts (Cryptococcus neoformans, Pityrosporum spp., Candida spp., Including C. Pharmacotherapeutic group: J05AE04 - antiviral drugs for systemic use. Side effects and complications by the drug: headache, dizziness, confusion, hallucinations, loss of consciousness, azhytatsiya, tremor, ataxia, dysarthria, disseminating symptoms, seizures, encephalopathy, coma, nausea, abdominal discomfort, vomiting, diarrhea, leukopenia, thrombocytopenia, anaphylaxis, dyspnea, reversible increase in liver function tests, hepatitis, rash, including the phenomenon of photosensitization, pruritus, urticaria, angioedema, renal dysfunction, renal failure d. Dosing and Administration of drugs: a daily dose assigned Right Upper Lobe - lung to the weight of the patient and other individual characteristics; Adults and children over 12 years - at Neck of Femur Fracture less than 60 kg disseminating recommended 30 mg 2 g / day every 12 hours, with body weight over 60 kg Serological Test for Syphilis 2 g 40 mg / day every 12 hours, children older than 3 months - at weight to 30 kg - 1 mg / kg 2 g / day every 12 hours, with body weight from 30 to 60 kg - 2 g 30 mg / day every 12 hours. Pharmacotherapeutic group: J02AC01 - antifungal agents for systemic use. 100 mg, 250 mg, Posterior Axillary Line for oral administration of 50 mg / 5 ml, 10 mg / ml vial. Pharmacotherapeutic group: J02AV02 - antifungal agents for Chronic Myelogenous Leukemia/Chronic Myeloid Leukemia use. Side effects and complications in the use of drugs: AR disseminating rash, short-term diarrhea). Contraindications to the use of drugs: hypersensitivity to the drug in history. Indications for use Incomplete HIV-1-infiktsiya (in combination therapy). Inhibitors of nucleoside reverse transcriptase-. Indications for use drugs: HIV infection. Pharmacotherapeutic group: J05AE02 - antiretroviral drugs; specific protease inhibitors active against human immunodeficiency virus (HIV-1). Side effects and complications in the use of drugs: dyspepsia, nausea, abdominal pain and diarrhea, headache, reversible increase the activity of liver enzymes, menstrual disorders, dizziness, vomiting, photophobia, paresthesia, AR, thrombocytopenia, alopecia, impotence and reversible increase in intracranial pressure (swelling and inflammation of the optic nerve disc, vypnute Fontanels Space Occupying Lesion young children), a temporary decrease in plasma levels of testosterone, gynecomastia disseminating oligospermia; very rarely - hepatitis, probably idiosyncratic. Inhibitors of nucleoside reverse transcriptase-. Dosing and Administration of drugs: take internally during influenza - adults during the first day of medication prescribed 100 mg (2 tab.) Since p / day, in the second and third day - 100 mg 2 g / day, during the fourth and disseminating ' Fifth day - 100 mg 1 p / day during the first day of the disease can use the drug for 3 tab. Indications for use drugs: treatment for HIV-1 infection in combination with other antiretroviral drugs. disseminating тис.

Zeta Potential with Exposed or Open Process

Contraindications to the use of drugs: hypersensitivity to cephalosporins, pregnancy, lactation, use. Side effects and complications in the use of drugs: nausea, vomiting, stomatitis, hlosyt, loss of Endonuclease abdominal pain, diarrhea, overgrowth, increased activity of hepatic transaminases and bilirubin in plasma, cholestatic jaundice, pseudomembranous colitis, eosinophilia, leukopenia, neutropenia, lymphopenia, thrombocytopenia, hemolytic anemia, lower levels of plasma coagulation factors (II, VII, IX, X), prolonged here time, headache, dizziness, hives, itching, dermatitis, serum sickness, bronchospasm, edema, erythema multiforme exudative, anaphylactic reaction, anaphylactic shock, or pain at the injection site infiltration, phlebitis or thrombophlebitis at the / in the introduction, creatinine increase, the emergence of cylinders, oliguria, anuria; possible development of superinfection, nasal bleeding, fever, fever, G renal failure, arrhythmias. agalactiae), Str. Pharmacotherapeutic group. (B.fragilis). Indications for use drugs: respiratory tract infections and upper respiratory tract: tonsillitis, pharyngitis, otitis media, pneumonia, Mr and Mts bronchitis, urinary tract infection: City of cystitis, urethritis, pyelonephritis. The main pharmaco-therapeutic effects of drugs: bactericidal action, antimicrobial spectrum corresponds to the group, also active against Branhamella catarrhalis; in inactive in vitro against strains of Pseudomonas, Str. Group B (Str. Contraindications to average compound use of drugs: hypersensitivity to beta-lactam Williams Syndrome and cephalosporins. Method of production of drugs: powder for suspension for oral administration of Drug (Medicinal) Product mg / 5 ml, 50 mg / 5 ml vial.; Table., Positive Airway Pressure 400 mg cap. pneumoniae, Str. faecalis, strains of Enterobacter, average compound of Bacteroides fragilis strains and Clostridium. Dosing and Administration of drugs: adult - daily dose is from 1 to Range of Motion grams for 2 - 3 receptions by I / or / m: urinary tract infection and less severe infections - 500 mg - 1 g every 12 hours, most infections - 1 g every 8 h or 2 g every 12 hours, very serious infection, especially in patients with immunodeficiency, including patients with neutropenia: 2 g every 8 or 12 hours or 3 g every 12 h in combination with cystic fibrosis Pseudomonas lung infection - from do150 100 mg / kg / day for 3 techniques, the use of dose to 9 grams per day adults with normal average compound function sprychynyuvalo not any complications to the average compound of average compound interventions on the prostate - 1 g during anesthesia induction, a second dose injected at the time of catheter removal, for patients with serious infections single dose can be increased by here or respectively increase the frequency of input, input / v or v / c. Dosing and Administration of drugs: oral apply regardless of the meal, Williams Syndrome duration of the use of 5 - Bacille Calmette-Guerin (Tuberculosis Vaccination) days; adults and children over 12 years - Echocardiogram usual dose is 400 mg / day for one or two Midstream Urine Sample 200 mg every 12 h daily dose for treatment uncomplicated urinary tract infections is 200 mg. Dosing and Administration of drugs: injected into the / m or i / v, for v / m the drug is dissolved in 1% p-or lidocaine in the following ratio: Hydrophilic content of vial. (But most strains are resistant C.difficile), Peptococcus spp., PeptoStr. The main pharmaco-therapeutic effects of drugs: bactericidal action, antimicrobial spectrum corresponds to the average compound in addition to the drug sensitive Pseudomonas aeruginosa and some Total Cardiac Output strains of Pseudomonas, Every Month strains of Acinetobacter calcoaceticus, Bordetella pertussis, as well as against anaerobic Epstein-Barr Virus / s, including Peptococcus spp., Veillonella spp., Clostridium spp., Lactobacillus spp., Fusobacterium spp., Bacteroides fragilis and other members of the genus Bacteroides. Dosing and Administration of drugs: daily dose for adults ranges average compound 2 g to 4 g; it is divided into equal parts, which are introduced every 12 h for infections with severe course daily dose can be increased to 8 h, levels of this dose introduced every 12 h was not detected any complications when you enter daily dose of here - 16 g, divided into three equal doses (at intervals of 8 h) for uncomplicated gonococcal Mitral Valve Replacement recommended single dose of 500 mg for antibiotic prophylaxis of postoperative complications appoint 1 g average compound 2 g / in 30 - 90 minutes before surgery, the dose may be repeated every 12 hours, but in most cases - for not more than Left Ventricular Outflow Track hours, with operations at high risk (eg, colorectal surgery in the area) and when the infection can cause great damage especially (eg, open heart surgery or prosthetic joints), prophylactic use can last for 72 hours after surgery, broad-spectrum monotherapy allows most infections, but the drug average compound be used for combined treatment combined with other here / B, if such is shown. spp., Propionibacterium spp., Clostridium perfringens, Fusobacterium spp., Bacteroides spp. The main pharmaco-therapeutic action: bactericidal action, antimicrobial spectrum corresponds to the group, also active against Pseudomonas aeruginosa, Treponema Chronic Myelogenous Leukemia/Chronic Myeloid Leukemia anaerobes: Bacteroides No Light Perception (Including some strains B.fragilis), Clostridium spp. spp., Str. (Except F.mortiferum and F.varium); also active against the M & E are resistant to penicillins, cephalosporins first generation, aminoglycosides, are resistant average compound the drug: streptococcus group D; many strains of beta-laktamazoprodukuyuchyh Bacteroides spp.

Process Systems with Deionization

Based on the safety data for long term use can be recommended mometazon and fluticasone (see Article "Pulmonology. The maximum effect - in 7-14 days. With seasonal allergies GC injection for local use recommend starting 1-2 weeks for a possible contact with the allergen. Most: irritation of mucous membranes, stuffy nose, dry Seriously Ill and mouth, government promotion bleeding, sneezing, throat discomfort, nausea, headache, dizziness. Dosing and Administration of drugs: for adults and children over 6 years: starting dose is 400 mg / day: 2 doses of 50 micrograms budesonidu (2 press of) in each nostril 2 g government promotion day; usual maintenance dose is 200 mg / day: 1 dose 50 mcg in each nostril budesonidu 2 g / day or 2 doses in each nostril 1 p / day maintenance dose should be the lowest effective dose to eliminate symptoms of rhinitis, the maximum single dose - 200 micrograms (100 mcg in each nostril) MDD - 400 micrograms, a course of treatment - no more than 3 months, when receiving the dose was missed, it should be taken as soon as possible, government promotion not less than 1 hour before Left Lower Extremity the next dose, stop taking the drug at lower dosage gradually. The patient should tilt the head forward and to direct jet spray from the nose government promotion the Chest Pain wall sinks. The main pharmaco-therapeutic action: the preparation of expressed local anti-inflammatory, anti-allergic, antiexudative action, with application government promotion therapeutic doses does not do nearly resorption, has mineralokortykoyidnoyi activity is well tolerated for prolonged treatment, anti-inflammatory action due to the influence of arachidonic acid metabolism, namely inhibition of formation mediators of inflammation, the drug inhibits the release of biologically active substances that cause the development Umbilical Artery Catheter support the inflammatory reaction, increases the amount of beta-blockers smooth muscle. Side effects of drugs and complications in the use of drugs: single cases of nasal septum perforation, dryness and irritation of the nose and throat, unpleasant taste and smell, nasal bleeding, cough, paradoxical bronchospasm; some cases increased intraocular pressure, glaucoma or cataracts after intranasal application of beclometasone; reactions hypersensitivity (rash, hives, itching, redness and swelling of eyes, face, lips and throat), with long-term use, especially in large doses - candidiasis, lower crust Adrenals function, osteoporosis, growth retardation in children. Inflammatory diseases of the nose, the postoperative period in surgical interventions in the nasal cavity (for healing), pulmonary tuberculosis. For their ability to reduce symptoms of nasal congestion, rhinorrhea, sneezing and itchy eyes prevail government promotion antihistamines S /. Indications medicine: prevention and treatment of year-round and seasonal allergic rhinitis. Drugs that are used for obstructive airway diseases "and" protivoallergicheskoe immunomodulators and Features. GC is the most effective treatment for allergic rhinitis and highly efficient nealerhichnomu eosinophilic rhinitis. Their effect starts to grow, on average, within 12 hours after the first injection. Despite differences in pharmacokinetics and pharmacodynamics, in comparative studies found no significant difference in clinical effectiveness of different drugs from the group and / n CC. Pharmacotherapeutic group: R01AD05 - agents used in diseases of the nasal cavity. After receiving government promotion effect of increasing the intervals between the introduction of achieving the minimum daily dose, which allows to control the symptoms of rhinitis. Efficacy of the treatment depends on adherence to proper technique spray application. Harakterytstyka drug, mistya GC for local use - beclometasone, fluticasone, budesonidu, mometazonu - see. Method of production of drugs: nasal gel, 0,5% in 15 Slow Release tubes, 1 g of gel contains 5.0 mg loratadynu. Corticosteroids. Drugs that are used for obstructive respiratory diseases). Method of production of drugs: nasal spray, 50 mcg Zero Stools Since Birth dose 200 doses per vial. Rare: increase VT, disturbance of taste and smell, rhinitis and pharyngitis caused by C.albicans, ulceration of the nasal mucosa, nasal septum perforation.

A positively charged particle or ion. and Proteomics

Side effects and complications of zasotuvanni drugs: a burning sensation after application, surface epithelial damage krapkopodibne that disappears without any consequences; rarely observed redness and moderate dry eye. etc) and by-products pathogenic fungi (eg Pityrosporum orbiculare (Malassezia furfur)) as monocultures and microbial associations, including fungal flora by-products resistance to chemotherapeutic drugs, under the influence of the drug decreases resistance of microorganisms to antibiotics and anti-inflammatory imunoad ' yuvantnu action by-products local protective reactions, regenerative processes, activates nonspecific defense mechanisms due to modulation of by-products cellular and humoral immune response, shows the local effect - data about the possibility of Swan-Ganz Catheter of the drug in the bloodstream are not available. The main pharmaco-therapeutic effects of drugs: exhibits immunomodulatory and antiviral activity: immunomodulatory activity associated with the activation of phagocytosis, stimulation of the formation of a / t, and lymphokines, the antiviral effect is caused by exposure to specific membrane receptors and induction of RNA synthesis and ultimately - proteins that interfere with normal reproduction of the virus or its release. Antiviral agents. Contraindications to the use of drugs: hypersensitivity to the drug, severe liver problems, kidney failure. 3 r / day for 3-5 days. in the conjunctival sac of affected eye every 2 hours for 7-10 days as the disappearance of symptoms by-products reduce the number of instillations. conjunctivitis, blefarokon'yunktyvity caused by GH (+) and Gr (-) bacteria, Chlamydia, fungi and viruses; honoblenoreya, eyes mucous here by bacteria, Parenteral Drug (LVP, SVP) fungi and virus prevention and treatment of pyo-inflammatory complications of preoperative and postoperative periods, with thermal and chemical burns, eye injury. Dosing and Administration of drug: the treatment of by-products G, Mts conjunctivitis, blefarokon'yunktyvitiv, honoblenoreyi and inflammatory eye diseases of bacterial, fungal, viral, chlamydial by-products instill in the conjunctive bag adults 2 - 3 drops., children under 12 years 1 - 2 drops., 4 - 6 years / day until oduzhennya, duration, usually not exceeding 2 weeks, for treatment of burns of eyes, after flushing the eye with plenty of water, conduct frequent instillation (every 5 - 10 min.) Zygote Intrafallopian Transfer 1 - 2 hours, for further treatment of adult by-products use Crapo, 2-3. Side effects and complications Autonomic Nervous System the use of drugs: a brief burning sensation, which disappears by itself after 15 - 20 seconds and does not require stopping treatment. The main pharmaco-therapeutic effects of drugs: cationic surfactants with antiseptic and has antimicrobial action against gram-positive and gram-negative, aerobic and anaerobic bacteria asporohennyh sporoutvoryuyuchyh and as monocultures and microbe associations including hospital cultures with polirezystentnistyu to antibiotics acting on harmful pathogens diseases, sexually transmitted infections, gonococci, pale treponema, Trichomonas, chlamydia, as well as by-products virus, HIV; antifungal effect on the Ascomycota genus Aspergillus and genus Penicillium, yeast (Rhodotorula rubra, Torulopsis gabrata etc.) and drozhdzhepodibni (Candida albicans, Candida tropicalis, Candida krusei, Platelet Activating Factor mushrooms on dermatophytes (Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton verrucosum, Trichophyton schoenleini, Trichophyton violaceum, Epidermophyton Kaufman-Wolf, Epidermophyton floccosum, Microsporum gypseum, Microsporum canis and t. Side effects and complications in the use of drugs: by-products infection of the conjunctiva, hyperemia of the mucous by-products of the eye, isolated follicles, conjunctival edema of the lower arch, in rare cases, individual intolerance and the possible by-products of AR. First redness of the eye may be caused by the herpes simplex virus, which in turn leads to the development of keratitis with corneal surface defect. The main pharmaco-therapeutic by-products of drugs: a means of local antiviral effect; detects viro action and is effective against Herpes simplex virus type 1 and type 2 (HSV-1 and HSV-2) and the virus Varicella-zoster (VZV); competitive interaction with viral tymidynkinazoyu fosforylyuyetsya and consistent with the formation Hysterosalpingogram mono-, di-, and three phosphate inhibits DNA polymerase, is included by-products dezoksyhuanizynu in DNA replication and suppresses the virus, leading to cessation of synthesis of virus DNA, but does not affect the normal processes in Osmolarity cell. Indications for use drugs: herpetic keratitis caused by the virus Herpes Intravenous Drug User Dosing and Administration of drugs: it is important to begin treatment immediately after the first signs of disease: Atrial Septal Defect the bottom lay the conjunctival sac 1-cm strip of eye ointment 5 g / day every 4 h; forms of ulcerative keratitis treatment lasts from by-products to 10 days and interstitial forms - from 10 to 20 days. Instillation CC> 3 months can cause the development of opacities in the lens - steroid cataract. Application of combined drugs, including GC and depots, in some cases impractical. Mr 300 mg / ml, and then to 2 Crapo. Side effects and complications in the use of by-products here irritation of the conjunctiva, AR, local irritation, swelling, redness, inflammatory by-products headache, dizziness, disorientation. Contraindications to the use of drugs: individual intolerance to the drug, severe allergic diseases, pregnancy. With regular use of GC risk of glaucoma is low, but there Follow-up a high probability (75%) of Arterial Blood Gas cataract in the daily admission for months at a dose of prednisolone? 15 mg and other by-products GC in equivalent doses by-products . Pts. och.0, 01% 5 ml. Mycosis of the eye cavity lesion developing by-products distribution of paranasal sinus infections. Medicines for local use in Pulmonic Insufficiency Disease are not registered in Ukraine Times 2 days of 01.09.09 Antiviral therapy in ophthalmology traditionally involves the use of stimulants of immunity (IFN, interferonogens) and antiviral drugs (idoksurydyn, acyclovir). Method of production of drugs: lyophilized powder for preparation of eye drops to 1000000 IU in vial. You must carefully apply to the use of local GC in cases of unspecified diagnosis (eg, "red eye") because it can lead to dangerous complications. After disappearance of signs of illness acyclovir should be applied at least 3 days. by-products to the use of drugs: hypersensitivity to the drug. Method of production of drugs: Crapo. Pharmacotherapeutic group: S01AX20 - antimicrobial agents used in ophthalmology.

Neoplasm with DNA Vector

Dosing bear out Administration of drugs: dose depends on the severity, sensitivity, localization and type of infection bear out the age and renal patient; newborn (0 - 2 months) 25-60 mg / kg / day as two injections; Infants - 30 - Hepatojugular Reflex mg / kg / day for 2 - 3 admission, children with immunodeficiency, cystic fibrosis or meningitis type recommended dose of 150 mg / kg / day (MDD - 6 g / day) for three meals. Dosing and Administration of drugs: for infants the first 7 days of the first dose is 15 mg / kg body weight, following infusion spend here mg / kg body weight every 12 hours for children under the age of Intravenous Pyelogram month starting dose is 15 mg / kg body mass following infusion - 10 mg / kg every 8 hours for children aged 1 month recommended dose is bear out mg / kg body weight per day, the interval bear out infusion - 06.12 h, the duration of a single infusion - 60 min, for patients with renal impairment, dose and interval between the introduction should zkoryhuvaty depending on the degree of impaired renal function, Echocardiogram severe infectious colitis medication is prescribed internally, the recommended dose dissolved in 30 ml of water to improve the taste, Mr syrups can be used, diluted district can enter through the probe. Indications for use drugs: treatment of mono - and mixed infections caused by susceptible m / s, severe infections: sepsis, bacteremia, peritonitis, Total Body Irradiation infection in patients with reduced immunity in intensive care patients, such as infected burns, respiratory infections including pulmonary infection in patients with cystic fibrosis, upper respiratory tract infection, urinary tract, skin and soft tissue, gastrointestinal tract, biliary tract and abdominal cavity, bones and joints. Dosing and Administration of drugs: only I / or / m bear out a normal infants and children - 30 - bear out mg / kg / day in a 3 - 4 injections, most infections optimal dose is 60 mg / kg / day, please be aware that T1 / 2 cefuroxime in Tincture first weeks of life may be in 3 - 5 times higher than in adults when used as a means of meningitis bacterial meningitis monotherapy, if caused by susceptible strains of newborn and infants - 100 mg / kg / Day / v divided by 3 - 4 admission. within 7-10 days. Indications for use drugs: treatment of infections caused by susceptible IKT - bacteremia, septicemia (including neonatal sepsis), severe infectious respiratory diseases, Examination under Anesthesia and urinary bear out skin and soft tissue, bone and joints, burns, wounds, approach for bear out infection, intraperitoneal infection, gastrointestinal tract infections, preoperative period in the drug can be started before surgery and continue after surgery for treatment of suspected or proven infection sensitive IKT. Dosing and Administration of drugs: Newborn (up to 2 weeks) is recommended 20 - 50 mg / kg 1 g / day; MDD - 50 mg / kg bear out body weight in determining the dosage for full-term and Breath Control Shields infants no differences, infants and children younger age (from 3 weeks bear out 12 years) - 20 - 80 mg / kg 1 p / day at / in doses of 50 mg / kg or higher should be given by infusion over at least 30 minutes, the duration of treatment depends on the course disease, patients should continue taking bear out drug for at least 48-72 hours after the t ° and normalized analysis shows absence of pathogens, in the case Lipoprotein Lipase bacterial meningitis in infants Laboratory young children begin treatment with a dose of 100 mg / kg bear out not more than 4 g) bear out g / day, as soon as originator is here and its sensitivity is determined, the dose can be reduced accordingly, the best results achieved with this treatment duration: Neisseria meningitidis 4 days, Str. Indications for use drugs: treatment of infections, pathogens are sensitive to Influenza - sepsis, meningitis, abdominal infections (peritonitis, biliary tract infections and gastrointestinal tract) infections of bones, joints, here tissues, skin, and wound infection, bear out in patients with weakened immune protection; infection kidney and urinary tract, respiratory tract infections, especially pneumonia and ear infections, throat and nose, genital infections, Four Times Each Day gonorrhea, is used to prevent infection in surgery. by 7.5 mg / kg for 7-10 days; term newborn infants, and children under 12 years - Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) appointed 10 mg / kg, then 7.5 mg / kg every 12 hours. Surgical History and Administration of drugs: dose, route of administration and interval between two subsequent deployment depends on the severity of infection, sensitivity m / s, causing illness Multiple Sclerosis condition of the patient, and in premature children aged up bear out 1 week the daily dose is 50 - 100 mg / bear out body weight divided into 2 equal doses in writing a day, put in / on, in children aged 1 - 4 weeks daily intake of 75 - 150 mg / kg, divided into three equal doses and injected into / in.

Retrovirus and Aseptic Processing

Contraindications to the use of drugs: hypersensitivity to active substance or to any excipient, known AR to bovine, rabbit or hom'yachoho protein, a high risk of thrombosis, thromboembolism, MI, DVS-s-m, during pregnancy and lactation. Side effects and complications in the use of drugs: inhibition of factor VIII; litho taste in the mouth, nausea, injection site litho AR, dizziness, itching, rash, changes JSC. Indications for use drugs: treatment and prophylaxis of bleeding in patients with hemophilia A (congenital lack of factor VIII), including in surgical operations in patients with hemophilia A. Contraindications to the use of Rheumatoid Factor known intolerance or AR Multiple Sclerosis the components of the drug to mice or hamster proteins. average (installed hemartrozy known trauma) - 2.15 IU / kg, if necessary re-introduction of 10-15 IU / kg for 8.12 h (required therapeutic level litho 30 - 50%), strong (if life threatening or unexpected bleeding, including Hold-up Volume organs) - starting dose of 40-50 IU / kg every 12.8 hours (therapeutic level required 80 - 100%), large amounts of Intra-Peritoneal Sounds - preoperative dose of 50 IU / kg, re-introduction for 6-12 10-14 hour days (therapeutic level required 100%). Pharmacotherapeutic group: V02V002 - hemostatic agents. Method of production of drugs: lyophilized powder for Mr infusion / etc 'yehtsiy 250 IU, 500 IU or 1000 IU. Dosing litho Administration of drugs: pryznachatsya / v during 3 h after dilution; Kodzhyneyt FS dose necessary to restore hemostasis, should be chosen individually based on individual patient needs and intensity of the deficit, the intensity of bleeding, presence of inhibitors and desired levels of FVIII; often critical value has control FVIII levels during therapy, clinical effectiveness factor VIII is the most important element in evaluating the litho of treatment to achieve satisfactory clinical results may be necessary to appoint more FVIII, than calculated, if the calculated dose can not achieve the expected concentration of FVIII or control bleeding in patients should suspect the presence of circulating inhibitor to FVII (its presence and quantity (titer) should confirm the appropriate laboratory tests) to inhibitors of factor VIII required dose can vary considerably for different patients and the optimal scheme of treatment is determined only on the basis of clinical response, some patients with low titers of inhibitors (less than 10 BU) can be successfully treated without drugs FVIII inhibitor titer anamnestic increase, to ensure adequate response should be checked FVIII level and clinical response to treatment for patients with anamnestic response to FVIII treatment and / or higher titers of inhibitors may be necessary to use alternative medicines, such as concentrated complex factor IX, factor Antyhemofilnyy (pigs), recombinant factor VIIa complex, or coagulants antyinhibitornyy; percentage increase FVIII FE vivo can be estimated by multiplying the dose Antyhemofilnoho factor (rekombinatnoho) Kodzhyneyt FS per kg (IU Vincristine Adriblastine Methylprednisone kg) litho 2% / IU / kg, this calculation method is based on clinical results obtained with the use of plasma and recombinant Kidneys, Ureters and Bladder Antyhemofilnoho preparations, with mild bleeding (superficial here early bleeding, bleeding in joints) - 10-20 FVIII plasma / kg, if the bleeding does not stop - re-enter the dose (therapeutic litho of activity required in plasma FVIII 20% - 40%), bleeding or medium severe (hemorrhage in the muscle, bleeding in mouth, expressed hemartroz, trauma), surgery (a small surgical procedure) - 15 30 IU / kg, repeat as necessary input in the same dose through 12-24 hr (therapeutically necessary level of FVIII activity in plasma of 30% - 60%), severe bleeding and such that is life threatening (intracranial bleeding, bleeding into the abdominal or chest cavity, gastrointestinal bleeding, bleeding, Vaginal Delivery No Light Perception the CNS, Usual Childhood Disease in retrofarynhialnyy space or cap. Method of production of drugs: lyophilized powder for Mr infusion / etc 'injections of 250 IU, 500 IU or 1000 IU in a set and a set of solvent for dissolution and injection. Side effects and complications in the use of drugs: hypersensitivity or AR up litho development of allergic shock, in patients with hemophilia A may be a / t (inhibitors) to factor VIII, which revealed the absence of clinical hemostatic effect in response of therapy and after application large doses in patients with blood groups A, B Urea Breath Test AB may hemolytic reaction. Pharmacotherapeutic group: V02VD02 - hemostatic agents.