MEDICATION GUIDE Abacavir, Lamivudine and Zidovudine Tablets
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Eparate Formulations According to the Prescribed Dosing Recommendations for These Products
ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS 1 1. NAME OF THE MEDICINAL PRODUCT Lamivudine/Zidovudine Teva 150 mg/300 mg film-coated tablets 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each film-coated tablet contains 150 mg lamivudine and 300 mg zidovudine. For the full list of excipients see section 6.1. 3. PHARMACEUTICAL FORM Film-coated tablet White, capsule shaped, biconvex, film-coated scored tablet – engraved with “L/Z” on one side and “150/300” on the other side. The tablet can be divided into equal halves. 4. CLINICAL PARTICULARS 4.1 Therapeutic indications Lamivudine/Zidovudine Teva is indicated in antiretroviral combination therapy for the treatment of Human Immunodeficiency Virus (HIV) infection (see section 4.2). 4.2 Posology and method of administration Therapy should be initiated by a physician experienced in the management of HIV infection. Lamivudine/Zidovudine Teva may be administered with or without food. To ensure administration of the entire dose, the tablet(s) should ideally be swallowed without crushing. For patients who are unable to swallow tablets, tablets may be crushed and added to a small amount of semi-solid food or liquid, all of which should be consumed immediately (see section 5.2). Adults and adolescents weighing at least 30 kg: the recommended oral dose of Lamivudine/Zidovudine Teva is one tablet twice daily. Children weighing between 21 kg and 30 kg: the recommended oral dose of Lamivudine/Zidovudine Teva is one-half tablet taken in the morning and one whole tablet taken in the evening. Children weighing from 14 kg to 21 kg: the recommended oral dose of Lamivudine/Zidovudine Teva is one-half tablet taken twice daily. -
TRIZIVIR® (Abacavir Sulfate, Lamivudine, and Zidovudine) Tablets
NDA 21-205/S-011 Page 4 PRESCRIBING INFORMATION TRIZIVIR® (abacavir sulfate, lamivudine, and zidovudine) Tablets WARNINGS TRIZIVIR contains 3 nucleoside analogues (abacavir sulfate, lamivudine, and zidovudine) and is intended only for patients whose regimen would otherwise include these 3 components. Hypersensitivity Reactions: Serious and sometimes fatal hypersensitivity reactions have been associated with abacavir sulfate, a component of TRIZIVIR. Hypersensitivity to abacavir is a multi-organ clinical syndrome usually characterized by a sign or symptom in 2 or more of the following groups: (1) fever, (2) rash, (3) gastrointestinal (including nausea, vomiting, diarrhea, or abdominal pain), (4) constitutional (including generalized malaise, fatigue, or achiness), and (5) respiratory (including dyspnea, cough, or pharyngitis). Discontinue TRIZIVIR as soon as a hypersensitivity reaction is suspected. Permanently discontinue TRIZIVIR if hypersensitivity cannot be ruled out, even when other diagnoses are possible. Following a hypersensitivity reaction to abacavir, NEVER restart TRIZIVIR or any other abacavir-containing product because more severe symptoms can occur within hours and may include life-threatening hypotension and death. Reintroduction of TRIZIVIR or any other abacavir-containing product, even in patients who have no identified history or unrecognized symptoms of hypersensitivity to abacavir therapy, can result in serious or fatal hypersensitivity reactions. Such reactions can occur within hours (see WARNINGS and PRECAUTIONS: Information -
ZIAGEN Safely and Effectively
HIGHLIGHTS OF PRESCRIBING INFORMATION • Patients With Hepatic Impairment: Mild hepatic impairment – 200 mg These highlights do not include all the information needed to use twice daily; moderate/severe hepatic impairment – contraindicated. (2.3) ZIAGEN safely and effectively. See full prescribing information for --------------------- DOSAGE FORMS AND STRENGTHS -------------- ZIAGEN. Tablets: 300 mg; Oral Solution: 20 mg/mL (3) ZIAGEN® (abacavir sulfate) Tablets and Oral Solution -------------------------------CONTRAINDICATIONS------------------------ Initial U.S. Approval: 1998 • Previously demonstrated hypersensitivity to abacavir. (4, 5.1) • Moderate or severe hepatic impairment. (4) WARNING: HYPERSENSITIVITY REACTIONS/LACTIC ACIDOSIS AND SEVERE HEPATOMEGALY ----------------------- WARNINGS AND PRECAUTIONS ---------------- • Hypersensitivity: Serious and sometime fatal hypersensitivity reactions See full prescribing information for complete boxed warning. have been associated with ZIAGEN and other abacavir-containing • Serious and sometimes fatal hypersensitivity reactions have been products. Read full prescribing information section 5.1 before associated with ZIAGEN (abacavir sulfate). (5.1) prescribing ZIAGEN. (5.1) • Hypersensitivity to abacavir is a multi-organ clinical syndrome. • Lactic acidosis and severe hepatomegaly with steatosis have been (5.1) reported with the use of nucleoside analogues. (5.2) • Patients who carry the HLA-B*5701 allele are at high risk for • Immune reconstitution syndrome (5.3) and redistribution/accumulation -
Package Leaflet: Information for the Patient Lamivudine/Zidovudine 150
Package Leaflet: Information for the patient Lamivudine/Zidovudine 150 mg/300 mg Film-coated Tablets (lamivudine/zidovudine) Read all of this leaflet carefully before you start taking this medicine because it contains important information for you. Keep this leaflet. You may need to read it again. If you have any further questions, ask your doctor or pharmacist. This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. What is in this leaflet: 1. What Lamivudine/Zidovudine is and what it is used for 2. What you need to know before you take Lamivudine/Zidovudine 3. How to take Lamivudine/Zidovudine 4. Possible side effects 5. How to store Lamivudine/Zidovudine 6. Contents of the pack and other information 1. What Lamivudine/Zidovudine is and what it is used for Lamivudine/Zidovudine is used to treat HIV (human immunodeficiency virus) infection in adults and children. Lamivudine/Zidovudine contains two active substances that are used to treat HIV infection: lamivudine and zidovudine. Both of these belong to a group of anti-retroviral medicines called nucleoside analogue reverse transcriptase inhibitors (NRTIs). Lamivudine/Zidovudine does not completely cure HIV infection; it reduces the amount of HIV virus in your body, and keeps it at a low level. It also increases the CD4 cell count in your blood. CD4 cells are a type of white blood cell that are important in helping your body to fight infection. -
Managing Drug Interactions in the Treatment of HIV-Related Tuberculosis
Managing Drug Interactions in the Treatment of HIV-Related Tuberculosis National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention Division of Tuberculosis Elimination Managing Drug Interactions in the Treatment of HIV-Related Tuberculosis Centers for Disease Control and Prevention Office of Infectious Diseases National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention Division of Tuberculosis Elimination June 2013 This document is accessible online at http://www.cdc.gov/tb/TB_HIV_Drugs/default.htm Suggested citation: CDC. Managing Drug Interactions in the Treatment of HIV-Related Tuberculosis [online]. 2013. Available from URL: http://www.cdc.gov/tb/TB_HIV_Drugs/default.htm Table of Contents Introduction 1 Methodology for Preparation of these Guidelines 2 The Role of Rifamycins in Tuberculosis Treatment 4 Managing Drug Interactions with Antivirals and Rifampin 5 Managing Drug Interactions with Antivirals and Rifabutin 9 Treatment of Latent TB Infection with Rifampin or Rifapentine 10 Treating Pregnant Women with Tuberculosis and HIV Co-infection 10 Treating Children with HIV-associated Tuberculosis 12 Co-treatment of Multidrug-resistant Tuberculosis and HIV 14 Limitations of these Guidelines 14 HIV-TB Drug Interaction Guideline Development Group 15 References 17 Table 1a. Recommendations for regimens for the concomitant treatment of tuberculosis and HIV infection in adults 21 Table 1b. Recommendations for regimens for the concomitant treatment of tuberculosis and HIV infection in children 22 Table 2a. Recommendations for co-administering antiretroviral drugs with RIFAMPIN in adults 23 Table 2b. Recommendations for co-administering antiretroviral drugs with RIFAMPIN in children 25 Table 3. Recommendations for co-administering antiretroviral drugs with RIFABUTIN in adults 26 ii Introduction Worldwide, tuberculosis is the most common serious opportunistic infection among people with HIV infection. -
DESCOVY, and Upon Diagnosis of These Highlights Do Not Include All the Information Needed to Use Any Other Sexually Transmitted Infections (Stis)
HIGHLIGHTS OF PRESCRIBING INFORMATION once every 3 months while taking DESCOVY, and upon diagnosis of These highlights do not include all the information needed to use any other sexually transmitted infections (STIs). (2.2) DESCOVY safely and effectively. See full prescribing information • Recommended dosage: for DESCOVY. • Treatment of HIV-1 Infection: One tablet taken once daily with or ® without food in patients with body weight at least 25 kg. (2.3) DESCOVY (emtricitabine and tenofovir alafenamide) tablets, for • HIV-1 PrEP: One tablet taken once daily with or without food in oral use individuals with body weight at least 35 kg. (2.4) Initial U.S. Approval: 2015 • Renal impairment: DESCOVY is not recommended in individuals with WARNING: POST-TREATMENT ACUTE EXACERBATION OF estimated creatinine clearance below 30 mL per minute. (2.5) HEPATITIS B and RISK OF DRUG RESISTANCE WITH USE ----------------------DOSAGE FORMS AND STRENGTHS-------------------- OF DESCOVY FOR HIV-1 PRE-EXPOSURE PROPHYLAXIS Tablets: 200 mg of FTC and 25 mg of TAF (3) (PrEP) IN UNDIAGNOSED EARLY HIV-1 INFECTION See full prescribing information for complete boxed warning. -------------------------------CONTRAINDICATIONS------------------------------ DESCOVY for HIV-1 PrEP is contraindicated in individuals with Severe acute exacerbations of hepatitis B (HBV) have been unknown or positive HIV-1 status. (4) reported in HBV-infected individuals who have discontinued products containing emtricitabine (FTC) and/or tenofovir -----------------------WARNINGS AND PRECAUTIONS----------------------- disoproxil fumarate (TDF), and may occur with • Comprehensive management to reduce the risk of sexually discontinuation of DESCOVY. Hepatic function should be transmitted infections (STIs), including HIV-1, when DESCOVY is monitored closely in these individuals. -
Dolutegravir-Abacavir-Lamivudine (Triumeq)
© National HIV Curriculum PDF created September 24, 2021, 7:23 pm Dolutegravir-Abacavir-Lamivudine (Triumeq) Table of Contents Dolutegravir-Abacavir-Lamivudine Triumeq Summary Drug Summary Key Clinical Trials Resistance Key Drug Interactions Drug Summary Dolutegravir-abacavir-lamivudine is a single-tablet regimen that is used primarily for treatment-naïve individuals. It has high potency, a relatively robust barrier to resistance (due to the dolutegravir component), and few drug interactions. It may be especially advantageous for individuals with renal insufficiency or risk factors for renal disease or osteoporosis, as it avoids the use of tenofovir DF. In certain treatment- experienced individuals, dolutegravir-abacavir-lamivudine may provide an option for switch or simplification of therapy. Abacavir can cause a life-threatening hypersensitivity reaction in individuals who are HLA-B*5701 positive; all patients need to undergo testing for HLA-B*5701 prior to receiving dolutegravir-abacavir- lamivudine and those who test positive for HLA-B*5701 should not receive this single tablet regimen. Dolutegravir blocks tubular secretion of creatinine and therefore causes a small increase in serum creatinine in the first 4 to 8 weeks of use; this increase is benign and does not indicate a change in true creatinine clearance. Key Clinical Trials In antiretroviral-naïve individuals, dolutegravir plus abacavir-lamivudine demonstrated superior virologic responses when compared with efavirenz-tenofovir disoproxil fumarate (DF)-emtricitabine [SINGLE], with superiority largely driven by the greater tolerability of the dolutegravir plus abacavir-lamivudine regimen. In a comparison of 2 NRTIs plus either dolutegravir or raltegravir in treatment-naïve patients, virologic responses in the subset of patients who received dolutegravir plus abacavir-lamivudine were equivalent to those receiving raltegravir plus either tenofovir DF-emtricitabine or abacavir-lamivudine [SPRING-2]. -
Bictegravir-Tenofovir Alafenamide-Emtricitabine (Biktarvy)
© National HIV Curriculum PDF created September 25, 2021, 12:10 pm Bictegravir-Tenofovir alafenamide-Emtricitabine (Biktarvy) Table of Contents Bictegravir-Tenofovir alafenamide-Emtricitabine Biktarvy Summary Drug Summary Key Clinical Trials Key Drug Interactions Figures Drug Summary Bictegravir-tenofovir alafenamide-emtricitabine is a single-tablet regimen that is comprised of an integrase strand transfer inhibitor (bictegravir) combined with two nucleoside reverse transcriptase inhibitors (tenofovir alafenamide and emtricitabine). Bictegravir, which is not FDA-approved as an individual antiretroviral medication, has a high barrier to resistance, is well tolerated, and, extrapolating from the phase 3 data, has virologic efficacy comparable to dolutegravir. Bictegravir levels can be reduced with medications or oral supplement that contain polyvalent cations (e.g. Ca, Mg, Al, Fe). Bictegravir blocks tubular secretion of creatinine and typically raises serum creatinine by about 0.1 mg/dL, but without affecting renal glomerular function. Phase 3 trials in antiretroviral-naïve persons as well as switch trials in persons with virologic suppression have shown excellent efficacy with bictegravir-tenofovir alafenamide-emtricitabine. Available data suggest that bictegravir has a high genetic barrier to resistance. Key Clinical Trials In a phase 3 trial, 629 antiretroviral-naïve adults were randomized to receive bictegravir-tenofovir alafenamide-emtricitabine or dolutegravir-abacavir-lamivudine; after 48 weeks, there was no significant difference -
Image-Guided Focused Ultrasound: Endless Possibilities for Non-Invasive Therapy in the 21St Century
Central JSM Biotechnology & Biomedical Engineering Review Article Corresponding author Sha Jin, Department of Biomedical Engineering, College of Engineering, University of Arkansas, 700 Therapeutic Potential of Research Center Blvd., 3912 ENRC, Fayetteville, AR 72701, USA, Tel: 479-575-5298; Fax: 479-575-7696; Email: [email protected] Natural Catechins in Antiviral Submitted: 09 July 2013 Accepted: 29 July 2013 Activity Published: 31 July 2013 Copyright Sha Jin* © 2013 Jin Department of Biomedical Engineering, College of Engineering, University of Arkansas Fayetteville, AR 72701, USA OPEN ACCESS Keywords Abstract • Epigallocatechin-3-gallate Natural compounds have been discovered to be effective in many disease • Epicatechin-3-gallate treatments. Among these compounds are epigallocatechin-3-gallate (EGCG) and • Antiviral treatment epicatechin-3-gallate (ECG), two abundant polyphenolic catechins in green tea. • Viral infection They have been found to be able to interfere with many disease-related biochemical processes in vitro. They are capable of suppressing inflammation, tumor growth, bacterial infection, and virus infection. Thus, EGCG and ECG have drawn great attention on the potential effects on disease prevention and treatment of carcinogenic, obesity, diabetic, and Alzheimer’s diseases. In this review, the potential of EGCG and ECG on anti-viral infection is elucidated in detail with an overview of research achievements in this field. The highlight will provide in depth knowledge on new drug discovery and contribute to the design and development of novel anti-virus agents. INTRODUCTION of the virus developing drug resistance against Bevirimat [5]. Other therapeutic compounds from plants are catechin Current strategies for the treatment of various viral components. The evergreen plant Camellia sinensis produces infections highly depend upon the virus type. -
Pdf 738.02 K
DOI:http://dx.doi.org/10.7314/APJCP.2014.15.3.1219 Inhibition of NF-ΚB/MMP-9 by Epigallocatechin-3-Gallate in HTLV-1 Positive Cells RESEARCH ARTICLE Epigallocatechin-3-gallate Inhibits Tax-dependent Activation of Nuclear Factor Kappa B and of Matrix Metalloproteinase 9 in Human T-cell Lymphotropic Virus-1 Positive Leukemia Cells Steve Harakeh1*, Mona Diab-Assaf2, Rania Azar2, Hani Mutlak Abdulla Hassan3, Safwan Tayeb1, Khalil Abou-El-Ardat4, Ghazi Abdullah Damanhouri3, Ishtiaq Qadri3, Adel Abuzenadah3, Adeel Chaudhary3, Taha Kumosani3,5, Aleksandra Niedzwiecki6, Mathias Rath6, Haitham Yacoub3,7, Esam Azhar1,3,8, Elie Barbour9 Abstract Epigallocatechin-3-gallate (EGCG) is the most abundant polyphenol molecule from green tea and is known to exhibit antioxidative as well as tumor suppressing activity. In order to examine EGCG tumor invasion and suppressing activity against adult T-cell leukemia (ATL), two HTLV-1 positive leukemia cells (HuT-102 and C91- PL) were treated with non-cytotoxic concentrations of EGCG for 2 and 4 days. Proliferation was significantly inhibited by 100 μM at 4 days, with low cell lysis or cytotoxicity. HTLV-1 oncoprotein (Tax) expression in HuT- 102 and C91-PL cells was inhibited by 25 μM and 125 μM respectively. The same concentrations of EGCG inhibited NF-kB nuclearization and stimulation of matrix metalloproteinase-9 (MMP-9) expression in both cell lines. These results indicate that EGCG can inhibit proliferation and reduce the invasive potential of HTLV-1- positive leukemia cells. It apparently exerted its effects by suppressing Tax expression, manifested by inhibiting the activation of NF-kB pathway and induction of MMP-9 transcription in HTLV-1 positive cells. -
Emtricitabine and Tenofovir Alafenamide
HIGHLIGHTS OF PRESCRIBING INFORMATION ------------------------DOSAGE AND ADMINISTRATION---------------------- These highlights do not include all the information needed to use • Testing: Prior to initiation of DESCOVY, patients should be tested for DESCOVY safely and effectively. See full prescribing information hepatitis B virus infection, and estimated creatinine clearance, urine for DESCOVY. glucose and urine protein should be obtained. (2.1) • ® Recommended dosage: One tablet taken once daily with or without DESCOVY (emtricitabine and tenofovir alafenamide) tablets, for food in patients with body weight at least 25 kg and a creatinine oral use clearance greater than or equal to 30 mL per minute. (2.2) Initial U.S. Approval: 2015 • Renal impairment: DESCOVY is not recommended in patients with WARNING: POST TREATMENT ACUTE EXACERBATION OF estimated creatinine clearance below 30 mL per minute. (2.3) HEPATITIS B ----------------------DOSAGE FORMS AND STRENGTHS-------------------- See full prescribing information for complete boxed warning. Tablets: 200 mg of FTC and 25 mg of TAF (3) • DESCOVY is not approved for the treatment of chronic -------------------------------CONTRAINDICATIONS------------------------------ hepatitis B virus (HBV) infection. Severe acute None. exacerbations of hepatitis B have been reported in patients who are coinfected with HIV-1 and HBV and have -----------------------WARNINGS AND PRECAUTIONS----------------------- discontinued products containing emtricitabine (FTC) • Immune reconstitution syndrome: May necessitate further evaluation and/or tenofovir disoproxil fumarate (TDF), and may occur and treatment.(5.2) with discontinuation of DESCOVY. Hepatic function should • New onset or worsening renal impairment: Assess creatinine be monitored closely in these patients. If appropriate, clearance, urine glucose, and urine protein in all patients before initiation of anti-hepatitis B therapy may be warranted. -
Zidovudine (Azt)
ZIDOVUDINE (AZT) 1. Exposure Data 1.1 Chemical and physical data Zidovudine is an analogue of thymidine in which the 3-hydroxyl group is replaced by an azido group. 1.1.1 Nomenclature Chem. Abstr. Serv. Reg. No.: 30516-87-1 Chem. Abstr. Name: 3′-Azido-3′-deoxythymidine IUPAC Systematic Name: 3′-Azido-3′-deoxythymidine Synonyms: 1-(3-Azido-2,3-dideoxy-β-D-ribofuranosyl)-5-methylpyrimidine-2,4- (1H,3H)-dione; azidothymidine; 3′-azidothymidine; AZT; 3′-deoxy-3′-azido- thymidine; ZDV [Note: The abbreviation AZT is also used for another drug, azathioprine (Royal Pharmaceutical Society of Great Britain, 1999).] 1.1.2 Structural and molecular formulae and relative molecular mass O CH3 HN O N HO O N3 C10H13N5O4 Relative molecular mass: 267.25 1.1.3 Chemical and physical properties of the pure substance (a) Description: White to off-white crystals or needles (Gennaro, 1995; American Hospital Formulary Service, 1997) –73– 74 IARC MONOGRAPHS VOLUME 76 (b) Melting-point: 106–112 °C (from petroleum ether); 120–122 °C (from water) (Budavari, 1996) (c) Spectroscopy data: Infrared, ultraviolet, nuclear magnetic resonance (proton) and mass spectral data have been reported (National Cancer Institute, 1989). (d) Solubility: Soluble in water (25 mg/mL at 25 °C) and ethanol (67 mg/mL) (Gennaro, 1995; Budavari, 1996) α 25 ° (e) Optical rotation: [ ]D , +99 (c = 0.5 in water) (Budavari, 1996) (f) Dissociation constant: pKa, 9.68 (Gennaro, 1995) 1.1.4 Technical products and impurities Zidovudine is available as a 300-mg tablet, a 100- or 250-mg capsule, a 50-mg/ 5 mL syrup and a 200-mg/20 mL injection solution; it is also available as a tablet in combination with lamivudine.