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redsmile
RobertMrთარიჭი: Вторник, 22.04.2014, 03:11 | შეტყობინება # 256
თანამდებობა: Гости






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Tannerkrთარიჭი: Четверг, 24.04.2014, 17:32 | შეტყობინება # 257
თანამდებობა: Гости






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lisimthmruთარიჭი: Суббота, 26.04.2014, 19:10 | შეტყობინება # 258
თანამდებობა: Гости





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heiyetwoთარიჭი: Пятница, 11.07.2014, 15:28 | შეტყობინება # 259
თანამდებობა: Гости





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woowssafთარიჭი: Воскресенье, 31.08.2014, 18:37 | შეტყობინება # 260
თანამდებობა: Гости





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Russell Campolongoთარიჭი: Воскресенье, 21.09.2014, 06:54 | შეტყობინება # 261
თანამდებობა: Гости





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jueiwqoquთარიჭი: Пятница, 28.11.2014, 12:29 | შეტყობინება # 262
თანამდებობა: Гости





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jueiwqorkთარიჭი: Пятница, 05.12.2014, 09:02 | შეტყობინება # 263
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fmyykjpთარიჭი: Пятница, 13.02.2015, 13:16 | შეტყობინება # 264
თანამდებობა: Гости





Tacrolimus (also FK-506 or fujimycin, swop names Prograf, Advagraf, Protopic) is an immunosuppressive drug that is primarily employed after allogeneic medium transfer to subdue the vocation of the passive's exempt system and so bring the imperil of medium rejection. It is also used in a local preparation in the treatment of atopic dermatitis (eczema), harsh refractory uveitis after bone marrow transplants, exacerbations of slightest change complaint, and the husk condition vitiligo.
It is a 23-membered macrolide lactone discovered in 1984 from the fermentation stock of a Japanese soil sampling that contained the bacteria Streptomyces tsukubaensis. It reduces interleukin-2 (IL-2) making beside T-cells.
History
Tacrolimus was discovered in 1984; it was middle the maiden macrolide immunosuppressants discovered, preceded near the development of rapamycin (sirolimus) on Rapa Nui (Easter Eyot) in 1975.[1 - It is produced during a type of soil bacterium,Streptomyces tsukubaensis.[2 - The high regard tacrolimus is derived from 'Tsukuba macrolide immunosuppressant'.[3 -
Tacrolimus was fundamental approved by the Comestibles and Downer Administration (FDA) in 1994 someone is concerned end in liver transplantation; this has been extended to number kidney, middle, reduced bowel, pancreas, lung, trachea, overlay, cornea, bone marrow, and limb transplants.
Availability
The branded manifestation of the dull is owned by Astellas Pharma, and is sold below the marketing names Prograf given twice daily,Advagraf, a continual releasing formulation allowing a single time finally constantly dosing, and Protopic (Eczemus in Pakistan past Brookes Pharma), the up to date formulation.[4 - Advagraf is handy in 0.5, 1, 3 and 5 mg capsules, the ointment is concentrations of 0.1% and 0.03%.
A jiffy once-daily formulation of tacrolimus is in Aspect 3 clinical trials in the U.S. and Europe. This formulation also has a smoother pharmacokinetic limn gross that reduces the peak-to-trough assortment in blood levels compared to twice-daily tacrolimus.[5 - Data from the to begin Configuration 3 litigation in stable kidney transplant patients showed that this once-daily formulation was non-inferior in efficacy and sanctuary compared to twice-daily tacrolimus.[6 - A next Condition 3 effort in de novo patients is ongoing.[7 -
Logical positivism of strength
Tacrolimus is chemically known as a macrolide. In T-cells, activation of the T-cell receptor normally increases intracellular calcium, which acts via calmodulin to turn on calcineurin. Calcineurin then dephosphorylates the transcription go-between NF-AT (atomic part of activated T-cells), which moves to the core of the T-cell and increases the undertaking of genes coding to save IL-2 and tied up cytokines. Tacrolimus prevents the dephosphorylation of NF-AT.[8 - In charge, Tacrolimus reduces peptidyl-prolyl isomerase vocation via binding to the immunophilin FKBP12 (FK506 binding protein) creating a up to date complex. This FKBP12-FK506 complex interacts with and inhibits calcineurin wise inhibiting both T-lymphocytesignal transduction and IL-2 transcription.[9 - Although this action is correspond to to ciclosporin, studies secure shown that the degree of shrewd rejection is reduced about tacrolimus use done with ciclosporin.[10 - Although short-term immunosuppression anent patient and extortion survival is develop to be nearly the same between the two drugs, tacrolimus results in a more favorable lipid good, and this may eat substantial long-term implications given the prognostic play of renunciation on graft survival.[11 -
From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.
 
fmyykjuთარიჭი: Понедельник, 23.02.2015, 17:03 | შეტყობინება # 265
თანამდებობა: Гости





Moxidectin (Milbemycin B[1 - ) kills parasites, so is acclimated to because of the mitigation and manage of heartworm and intestinal worms, and can be create in treatments prescribed for animals such as dogs, cats, horses, livestock and sheep. Diligence methods towards moxidectin change by treatment, and group vocalized, timely, and injectable solutions. Cydectin Spurt On is a barter choose for a formulation for capitalize on on cows and red deer.
Moxidectin is a semisynthetic imitative of nemadectin [2 - which is produced during fermentation next to Streptomyces cyano-griseus. This Streptomyces species was discovered in a soil cross-section from Australia in the past due 1980s collected during an agronomist working for the American Cyanamid company.
Moxidectin treats and controls some of the most unrefined internal and external parasites by way of selectively binding to parasites’ glutamate-gated chloride ion channels. These channels are mandatory to the r搇e of invertebrate tenacity and muscle cells; when moxidectin binds to the channels, it disrupts neurotransmission, resulting in paralysis and death of the parasite.
Studies of moxidectin posture the side effects remodel at hand animalistic and may be fake by the product’s formulation, appositeness method and dosage. The products are most often recommended about a veterinarian to ensure chasten speak and application. Herding dogs may be avermectin-sensitive, but avermectin-sensitive dogs can turn a blind eye to measure doses for heartworm prevention. Moxidectin is manifestly unharmed after collie breeds. As a heartworm preventative, moxidectin can be injected in a wink every six months at the beck the brand name big cheese Proheart6, or every 12 months lower than drunk the trade-mark name Proheart SR 12.
Moxidectin is the rationale of a misery to assess its suitability, as an alternative to ivermectin, to doctor onchocerciasis in humans.[3 -

From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.
 
tcsgroupnთარიჭი: Среда, 04.03.2015, 13:06 | შეტყობინება # 266
თანამდებობა: Гости





Docetaxel (as generic or underneath the trade eminence Taxotere) is a clinically well-established anti-mitotic chemotherapy medication (medication which interferes with apartment division). It is used mostly to the treatment of breast, ovarian, prostate, and non-small chamber lung cancer.[1 - [2 - [3 - Docetaxel has an FDA approved allege after treatment of patients who arrange locally advanced, or metastatic titty or non small-cell lung cancer who have undergone anthracycline-based chemotherapy and failed to impede cancer advance or relapsed[4 - and a European subscribe to to licence in hormone-refractory prostate cancer.[5 -
According to a 2005 article in the quarterly Drugs, docetaxel administered as a one-hour infusion every three weeks generally in excess of a ten recur track, docetaxel is considered as or more basic than doxorubicin, paclitaxel and fluorouracil as a cytotoxic agent.[1 - Extent the effectiveness of docetaxel versus paclitaxel and other taxanes is still controversial. Several more brand-new articles father build "no evidence that regimens containing docetaxel cry quits greater benefits than those including paclitaxel."[6 - Additionally, the optimal scheduling of docetaxel and other taxanes remains unconfirmed. A three-week distribution register used to be and is stationary considered efficient but new studies are indicating a weekly plan effect be better. A 2010 article in Accepted Clinical Pharmacology states, "weekly application has emerged as the optimal schedule." Docetaxel is marketed worldwide comprised in the name Taxotere during Sanofi-Aventis.[7 - Annual sales in 2010 were Euro 2.122 billion ($US 3.1 billion). The franchise expired in 2010.[citation
Nature
Docetaxel is of the chemotherapy drug type; taxane, and is a semi-synthetic analogue of paclitaxel (Taxol), an distillate from the bark of the rare Pacific yew tree Taxus brevifolia.[2 - Fitting to paucity of paclitaxel, vast scrutiny was carried peripheral exhausted leading to the formulation of docetaxel – an esterified product of 10-deacetyl baccatin III, which is extracted from the renewable and promptly at one's disposal European yew tree.
Docetaxel differs from paclitaxel at two positions in its chemical structure. It has a hydroxyl useful dispose on carbon 10, whereas paclitaxel has an acetate ester, and a tert-butyl carbamate ester exists on the phenylpropionate side sequence in place of of the benzyl amide in paclitaxel. The carbon 10 going group exchange causes docetaxel to be more water soluble than paclitaxel.[2 -
Formulations and compositions
Docetaxel is a snowy coat capacity and is the active ingredient available in 20 mg and 80 mg Taxotere single-dose vials of concentrated anhydrous docetaxel in polysorbate 80.[2 - [8 - The solution is a readable brown-yellow containing 40 mg docetaxel and 1040 mg polysorbate 80 per mL.[8 - 20 mg Taxotere is distributed in a blister carton containing whole single-dose vial of Taxotere (docetaxel) preparation in 0.5 mL infecund pyrogen-free anhydrous polysorbate 80, and a single dose Taxotere debt-free vial containing 1.5 mL 13% ethanol in saline to be combined and diluted in a 250 mL infusion shopping bag containing 0.9% sodium chloride or 5% glucose after administration.[8 - 80 mg Taxotere is supplied identically but with 2.0 mL polysorbate 80 and 6.0 mL 13% ethanol in saline. The docetaxel and financially sound vials are combined to bestow a solution of 10 mg/mL and the required measure is tense from this solution. Vials be suffering with an overfill to compensate for solvent impoverishment during preparation, foaming, adhesion to vial walls and the dead volume. 20 mg vials may be stored looking for 24 months in this world 25 °C away from understanding and 80 mg vials as far as something 26 months in the anyhow conditions.[8 -
Recently Sanofi has got sanction for one-vial formulation.[citation needed - With this one-vial formulation, the preparation of the infusion solution is simplified during eliminating the blue ribbon dilution step. The two-vial and one-vial formulations restrict the unaltered panacea pith, docetaxel trihydrate, and the word-for-word excipients (ethanol, polysorbate 80 and citric acid). The one-vial formulation is administered as an aqueous intravenous result that contains the same tranquillizer theme in the unchanged concentration as the already approved two-vial formulation. The same form, status, and volume of polysorbate 80 are closest in the infusion revelation of both formulations. The at best argument between these two formulations is the quantity of ethanol.
From http://www.tcsindustry.com - TCS INDUSTRY LTD
 
famuyiyaoiთარიჭი: Вторник, 14.04.2015, 14:59 | შეტყობინება # 267
თანამდებობა: Гости





Varenicline (employment name Chantix in the USA and Champix in Canada, Europe and other countries, marketed sooner than Pfizer, chiefly in the tone of varenicline tartrate), is a prescription medication occupied to treat nicotine addiction. Varenicline is a nicotinic receptor unfair agonist—it stimulates nicotine receptors more weakly than nicotine itself does. In this respect it is nearly the same tocytisine and distinct from the nicotinic enemy, bupropion, and nicotine replacement therapies (NRTs) like nicotine patchesand nicotine gum. As a partial agonist it both reduces cravings looking for and decreases the pleasurable effects of cigarettes and other tobacco products. Inclusive of these mechanisms it can assist some patients to relinquish smoking.
Medical uses
Varenicline is indicated for smoking cessation. In a 2006 randomized controlled trial sponsored through Pfizer, after inseparable year the figure of unremitting abstinence was 10% in the interest placebo, 15% an eye to bupropion and 23% to go to varenicline.[1 - In a 2009 meta-analysis of 101 studies funded via Pfizer, varenicline was found to be more powerful than bupropion (odds proportion 1.40) and NRTs (odds proportion 1.56).[2 -
A Cochrane planned review concluded that varenicline improved the strong of successfully quitting smoking by two- to three-fold relative to pharmacologically unassisted attempts. Varenicline was more serviceable than bupropion in this refer to but not statistically upper to NRT.[3 -
The FDA has approved the utilize of varenicline on up to twelve weeks. If smoking cessation has been achieved it may be continued in requital for another twelve weeks.[4 -
Varenicline has not been tested in those directed 18 years old or preggers women and thus is not recommended for use aside these groups.
Adverse effects
Nausea occurs commonly in people engaging varenicline. Other less worn out side effects include trouble, gordian knot embarrassment sleeping, and irregular dreams. Rare side effects reported close people winning varenicline compared to placebo encompass change in drop, vomiting,abdominal woe, flatulence, and constipation. In a modern meta-analysis ownership papers past Leung et al., it has been estimated that in place of every five subjects taking varenicline at maintenance doses (1 mg twice common), there determination be an event of nausea, and for every 24 and 35 treated subjects, there will-power be an event of constipation and flatulence respectively. Gastrointestinal side-effects are signal factors compromising the compliance of varenicline.[5 - [6 -
Despair and suicide
In November 2007, the FDA announced it had received post-marketing reports that patients using varenicline as a service to smoking cessation had knowledgeable not too pensive side-effects, including suicidal ideation and random suicidal behavior, bizarre behavior, and drowsiness. On February 1, 2008 the FDA issued an alert to in addition clarify its findings, noting that "it appears increasingly like as not that there is an combine between Chantix and serious neuropsychiatric symptoms". It is anonymous whether the psychiatric symptoms are linked to the cure or to nicotine withdrawal symptoms,[citation needed - although not all patients had stopped smoking. The FDA also recommended that condition vigilance professionals and patients ready for quest of behavioral and mood changes.[7 - In May 2008, Pfizer updated the safety information associated with varenicline, noting that "some patients keep reported changes in behavior, stimulation, depressed feeling ready, suicidal thoughts or actions."[8 -
As of July 1, 2009, the US Sustenance and Hypnotic Direction requires Chantix (varenicline) to lug a negro package trap notice, the medium's strongest safety warning, precisely to free reports of side effects including concavity, suicidal thoughts, and suicidal actions.[9 -
From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.
 
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