Quinupristin And Dalfopristin (Synercid)

Trade Name : Synercid

Pfizer Laboratories Div Pfizer Inc

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Strength 150350 mg/5mLmg/5mL

QUINUPRISTIN; DALFOPRISTIN Streptogramin Antibacterial [EPC],Streptogramins [CS],Streptogramin Antibacterial [EPC],Streptogramins [CS]

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Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Quinupristin And Dalfopristin (Synercid) which is also known as Synercid and Manufactured by Pfizer Laboratories Div Pfizer Inc. It is available in strength of 150; 350 mg/5mL; mg/5mL per ml. Read more

Quinupristin And Dalfopristin (Synercid) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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  • No data
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of and other antibacterial drugs, should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.
  • Synercidn
  • Quinupristin is a white to very slightly yellow, hygroscopic powder. It is a combination of three peptide macrolactones. The main component of quinupristin (> 88.0%) has the following chemical name: N-[(6,9,10,13,15,18,22,24 )-22-[-(dimethylamino)benzyl]-6-ethyldocosahydro-10,23-dimethyl-5,8,12,15,17,21,24-heptaoxo-13-phenyl-18-[[(3 )-3-quinuclidinylthio] methyl]-12-pyrido[2,1- ]pyrrolo-[2,1- ][1,4,7,10,13,16] oxapentaazacyclononadecin-9-yl]-3-hydroxypicolinamide.
  • The main component of quinupristin has an empirical formula of CHNOS, a molecular weight of 1022.24 and the following structural formula:
  • Dalfopristin is a slightly yellow to yellow, hygroscopic, powder. The chemical name for dalfopristin is: (3,4,5,10,12,14,26,26a)-26-[[2-(diethylamino)ethyl]sulfonyl]-8,9,14,15,24,25,26,26a-octahydro-14-hydroxy-3-isopropyl-4,12-dimethyl-3-21,18-nitrilo-1,22-pyrrolo[2,1- ][1,8,4,19]-dioxadiazacyclotetracosine-1,7,16,22(4,17)-tetrone.
  • Dalfopristin has an empirical formula of CHNOS, a molecular weight of 690.85 and the following structural formula:
  • No data
  • To reduce the development of drug-resistant bacteria and maintain the effectiveness of and other antibacterial drugs, should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.
  • Synercidn- susceptible
  • Complicated skin and skin structure infectionsn- Staphylococcus aureusn- susceptiblen- Streptococcus pyogenesn- .
  • No data
  • In vitro
  • Synercid
  • Synercid
  • Therapeutic level monitoring of cyclosporine should be performed when cyclosporine must be used concomitantly with Synercid
  • It is reasonable to expect that the concomitant administration of Synercid and other drugs primarily metabolized by the cytochrome P450 3A4 enzyme system may likely result in increased plasma concentrations of these drugs that could increase or prolong their therapeutic effect and/or increase adverse reactions. (See below.) Therefore, coadministration of Synercid with drugs which are cytochrome P450 3A4 substrates and possess a narrow therapeutic window requires caution and monitoring of these drugs (, cyclosporine), whenever possible. Concomitant medications metabolized by the cytochrome P450 3A4 enzyme system that may prolong the QTc interval should be avoided.
  • Concomitant administration of and nifedipine (repeated oral doses) and midazolam (intravenous bolus dose) in healthy volunteers led to elevated plasma concentrations of these drugs. The C increased by 18% and 14% (median values) and the AUC increased by 44% and 33% for nifedipine and midazolam, respectively.
  • Clostridium difficile
  • Synercid
  • C. difficile
  • C. difficile
  • C. difficile
  • If CDAD is suspected or confirmed, ongoing antibiotic use not directed against may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of , and surgical evaluation should be instituted as clinically indicated.
  • No data
  • The safety of was evaluated in 1099 patients enrolled in 5 comparative clinical trials. Additionally, 4 non-comparative clinical trials (3 prospective and 1 retrospective in design) were conducted in which 1199 patients received for infections due to Gram-positive pathogens for which no other treatment option was available. In non-comparative trials, the patients were severely ill, often with multiple co-morbidities or physiological impairments, and may have been intolerant to or failed other antibacterial therapies.
  • There are four reports of patients receiving doses at up to three times that recommended (7.5 mg/kg). No adverse events were considered possibly or probably related to overdose. Signs of acute overdosage may include dyspnea, emesis, tremors, and ataxia as seen in animals given extremely high doses (50 mg/kg) of . Patients who receive an overdose should be carefully observed and given supportive treatment. is not removed by peritoneal dialysis or by hemodialysis.
  • WARNINGS
  • NOTE: As for other parenteral drug products, should be inspected visually for particulate matter prior to administration.
  • DO NOT DILUTE WITH SALINE SOLUTIONS BECAUSE SYNERCID IS NOT COMPATIBLE WITH THESE AGENTS. Synercid
  • If is to be given concomitantly with another drug, each drug should be given separately in accordance with the recommended dosage and route of administration for each drug.
  • With intermittent infusion of and other drugs through a common intravenous line, the line should be flushed before and after administration with 5% Dextrose in Water solution.
  • Before Reconstitution
  • Because contains no antibacterial preservative, it should be reconstituted under strict aseptic conditions (., Laminar Air Flow Hood). The reconstituted solution should be diluted within 30 minutes. Vials are for single use. The storage time of the diluted solution should be as short as possible to minimize the risk of microbial contamination. Stability of the diluted solution prior to the infusion is established as 5 hours at room temperature or 54 hours if stored under refrigeration 2 to 8u00b0C (36 to 46u00b0F). The solution should not be frozen.
  • Synercid
  • No data
  • This product's label may have been updated. For current full prescribing information, please visit www.pfizer.com
  • LAB-0591-9.07/2018
  • NDC 61570-260-01
  • Synercid I.V.
  • (quinupristin 150mg and dalfopristin 350mg)for Injection
  • 500 mg
  • Single Dose Vial, For I.V. Use Only-Not For Direct Infusion1 Sterile Vial
  • PfizerInjectables
  • Rx only
  • NDC 61570-260-10Contains 10 of NDC 61570-260-01
  • REFRIGERATE
  • Synercid I.V.
  • (quinupristin 150mg anddalfopristin 350mg) for Injection
  • 500 mg
  • For I.V. Use Only. n n n n Single Dose Vials
  • PfizerInjectables
  • Rx only

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