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  2. Keyword: simvastatin
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IJCS
Original Article

Drug Interactions and Adverse Events in a Cohort of Warfarin Users Attending Public Health Clinics

Christiane de Fátima Colet et al. Tania Alves Amador Isabela Heineck

Abstract

Background:

Warfarin is an oral anticoagulant involved in important interactions with foods and other drugs.

Objectives:

To evaluate the occurrence of adverse events reported by warfarin users and their relationship with drug interactions.

Methods:

This was an open cohort, prospective study conducted in an 18-month period with warfarin users attending public health clinics of the city of Ijuí, Brazil. Data were collected by means of interviews administered at patients’ home every month. Patients’ responses were confirmed by review of medical records when patients sought medical care. Data were analyzed by descriptive statistics. Potential drug interactions were evaluated in a database and vitamin K consumption was quantified using a validated method.

Results:

A total of 68 patients were followed-up; 63 completed the study and 5 died in the study period. Mean number of medications taken by the patients was 9.6 ± 4.5, and mean number of interactions involving warfarin was 2.91 ± 1.52. Most potential interactions increased the risk of bleeding, 61 of them severe interactions and 116 moderate interactions. Eighty-seven episodes of bleeding and 4 episodes of thrombosis were reported by a total of 37 and 4 patients, respectively. At the occurrence of these events, 56.5% of warfarin users were also taking omeprazole, 35.9% were taking simvastatin and 25.0% paracetamol. Most patients had a low vitamin K intake.

Conclusions:

A high frequency of potential interactions between warfarin and other drugs was detected, but a low intake of foods that could possibly affect the effects of warfarin was observed. Based on our results, it seems prudent to follow patients on warfarin therapy for drug-drug interactions, aiming to control adverse effects and to promote a safe and effective therapy.

  • Acetaminophen
  • Anticoagulants / adverse effects
  • Delivery Health Care/statistics & numeral data
  • Drug Incompatibility
  • drug interactions
  • Omeprazole
  • Pharmacovigilance
  • simvastatin
  • Vitamin K
  • Warfarin
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Creative Commons Attribution (CC BY) Creative Commons license
17/12/2018 DOI: 10.5935/2359-4802.20180091 Views 2
ABC
Original Article

Evaluation of Sexual Dimorphism in the Efficacy and Safety of Simvastatin/Atorvastatin Therapy in a Southern Brazilian Cohort

Lisiane Smiderle et al. Luciana O. Lima Mara Helena Hutz Cézar Roberto Van der Sand … Luiz Carlos Van der Sand Maria Elvira Wagner Ferreira Renan Canibal Pires Silvana Almeida Marilu Fiegenbaum

Background:

Dyslipidemia is the primary risk factor for cardiovascular disease, and statins have been effective in controlling lipid levels. Sex differences in the pharmacokinetics and pharmacodynamics of statins contribute to interindividual variations in drug efficacy and toxicity.

Objective:

To evaluate the presence of sexual dimorphism in the efficacy and safety of simvastatin/atorvastatin treatment.

Methods:

Lipid levels of 495 patients (331 women and 164 men) were measured at baseline and after 6 ± 3 months of simvastatin/atorvastatin treatment to assess the efficacy and safety profiles of both drugs.

Results:

Women had higher baseline levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) compared with men (p < 0.0001). After treatment, women exhibited a greater decrease in plasma TC and LDL-C levels compared with men. After adjustment for covariates, baseline levels of TC and LDL-C influenced more than 30% of the efficacy of lipid-lowering therapy (p < 0.001), regardless of sex. Myalgia [with or without changes in creatine phosphokinase (CPK) levels] occurred more frequently in women (25.9%; p = 0.002), whereas an increase in CPK and/or abnormal liver function was more frequent in in men (17.9%; p = 0.017).

Conclusions:

Our results show that baseline TC and LDL-C levels are the main predictors of simvastatin/atorvastatin therapy efficacy, regardless of sex. In addition, they suggest the presence of sexual dimorphism in the safety of simvastatin/atorvastatin. The effect of sex differences on receptors, transporter proteins, and gene expression pathways needs to be better evaluated and characterized to confirm these observations.

  • Atorvastatin
  • Lipids
  • Sexual Dimorphism
  • simvastatin
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Creative Commons Attribution (CC BY) Creative Commons license
27/06/2014 DOI: 10.5935/abc.20140085 Views 2
Lack of clopidogrel-statin interaction in patients undergoing coronary stent implantation
ABC
Artigo Original

Lack of clopidogrel-statin interaction in patients undergoing coronary stent implantation

Carlos Vicente Serrano Júnior et al. Alexandre de Matos Soeiro Leila Fernandes Araújo Bruna Jabot … Fabiana Rached Noemia Mie Orii José Carlos Nicolau Alberto J. Duarte José Antonio F. Ramires

BACKGROUND: Some studies have suggested reduced activity of clopidogrel on platelet activation and adherence in patients using statins. OBJECTIVE: To assess whether platelet activation and aggregation decrease with clopidogrel, and whether there is a reduction of the action of clopidogrel when associated with atorvastatin or simvastatin. METHODS: This prospective study included 68 patients with stable angina with previous use of simvastatin, atorvastatin, or no statin (control group), with previous elective indication of percutaneous coronary intervention (PCI). Platelet activation was analyzed by means of platelet count, levels of P-selectin and glycoprotein IIb/IIIa (with and without ADP stimulation) by flow cytometry. The findings were analyzed before and after percutaneous coronary intervention and the administration of clopidogrel. RESULTS: We observed reduction in platelet activity with use of clopidogrel. Furthermore, no differences were found between the variables analyzed to prove reduced activity of clopidogrel when combined with statins. We observed levels of p-selectin (pre-angioplasty: 14.23 ± 7.52 x 8.83 x 11.45 ± 7.65 ± 7.09; after angioplasty: 21.49 ± 23.82 x 4 37 ± 2.71 x 4.82 ± 4.47, ρ < 0.01) and glycoprotein IIb/IIIa (pre-angioplasty: 98.97 ± 0.43 ± 1.25 x 98.79 x 99.21 ± 0.40 after angioplasty: 99.37 ± 0.29 ± 1.47 x 98.50 x 98.92 ± 0.88, ρ = 0.52), respectively, in the control, atorvastatin and simvastatin groups. CONCLUSION: We concluded that platelet activation decreases with administration of clopidogrel, and clopidogrel has no antiplatelet effect reduced in the presence of simvastatin or atorvastatin.

  • Angioplasty transluminal percutaneous coronary
  • Hidroxymethylglutaryl-CoA reductase inhibitors
  • simvastatin
  • Stents
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Creative Commons Attribution (CC BY) Creative Commons license
13/08/2010 DOI: 10.1590/S0066-782X2010005000106 Views 1

How to cite this article

EndNote RIS

Electronic Document Format (Vancouver)

Colet CF, Amador TA, Heineck I. Drug Interactions and Adverse Events in a Cohort of Warfarin Users Attending Public Health Clinics. International Journal of Cardiovascular Sciences 2018;32(2):110-7.

Electronic Document Format (ABNT)

Colet, Christiane de Fátima; Amador, Tania Alves; Heineck, Isabela. Drug Interactions and Adverse Events in a Cohort of Warfarin Users Attending Public Health Clinics. International Journal of Cardiovascular Sciences, v. 32, n. 2, p. 110-117, Dec. 2018.

Electronic Document Format (APA)

Colet, C. F., Amador, T. A., & Heineck, I. (2018). Drug Interactions and Adverse Events in a Cohort of Warfarin Users Attending Public Health Clinics. International Journal of Cardiovascular Sciences, 32(2), 110-117.

Electronic Document Format (ISO)

Colet, Christiane de Fátima and Amador, Tania Alves and Heineck, Isabela. Drug Interactions and Adverse Events in a Cohort of Warfarin Users Attending Public Health Clinics. International Journal of Cardiovascular Sciences [online]. 2018, vol. 32, n. 2, [cited 2026-10-15], pp. 110-117. Available from: <https://journals.cardiol.br/en/article/drug-interactions-and-adverse-events-in-a-cohort-of-warfarin-users-attending-public-health-clinics/>. ISSN 2359-4802

EndNote RIS

Electronic Document Format (Vancouver)

Smiderle L, Lima LO, Hutz MH, Sand CRV, Sand LCV, Ferreira MEW, Pires RC, et al. Evaluation of Sexual Dimorphism in the Efficacy and Safety of Simvastatin/Atorvastatin Therapy in a Southern Brazilian Cohort. Arquivos Brasileiros de Cardiologia 2014;103(1):33-40.

Electronic Document Format (ABNT)

Smiderle, Lisiane; Lima, Luciana O.; Hutz, Mara Helena; Sand, Cézar Roberto Van der; Sand, Luiz Carlos Van der; Ferreira, Maria Elvira Wagner; Pires, Renan Canibal; Almeida, Silvana; Fiegenbaum, Marilu. Evaluation of Sexual Dimorphism in the Efficacy and Safety of Simvastatin/Atorvastatin Therapy in a Southern Brazilian Cohort. Arquivos Brasileiros de Cardiologia, v. 103, n. 1, p. 33-40, Jun. 2014.

Electronic Document Format (APA)

Smiderle, L., Lima, L. O., Hutz, M. H., Sand, C. R. V. , Sand, L. C. V. , Ferreira, M. E. W., Pires, R. C., Almeida, S., & Fiegenbaum, M. (2014). Evaluation of Sexual Dimorphism in the Efficacy and Safety of Simvastatin/Atorvastatin Therapy in a Southern Brazilian Cohort. Arquivos Brasileiros de Cardiologia, 103(1), 33-40.

Electronic Document Format (ISO)

Smiderle, Lisiane and Lima, Luciana O. and Hutz, Mara Helena and Sand, Cézar Roberto Van der and Sand, Luiz Carlos Van der and Ferreira, Maria Elvira Wagner and Pires, Renan Canibal and Almeida, Silvana and Fiegenbaum, Marilu. Evaluation of Sexual Dimorphism in the Efficacy and Safety of Simvastatin/Atorvastatin Therapy in a Southern Brazilian Cohort. Arquivos Brasileiros de Cardiologia [online]. 2014, vol. 103, n. 1, [cited 2026-10-15], pp. 33-40. Available from: <https://journals.cardiol.br/en/article/evaluation-of-sexual-dimorphism-in-the-efficacy-and-safety-of-simvastatin-atorvastatin-therapy-in-a-southern-brazilian-cohort/>. ISSN 0066-782X

EndNote RIS

Electronic Document Format (Vancouver)

Serrano Júnior CV, Soeiro AM, Araújo LF, Jabot B, Rached F, Orii NM, Nicolau JC, et al. Lack of clopidogrel-statin interaction in patients undergoing coronary stent implantation. Arquivos Brasileiros de Cardiologia 2010;95(3):321-7.

Electronic Document Format (ABNT)

Serrano Júnior, Carlos Vicente; Soeiro, Alexandre de Matos; Araújo, Leila Fernandes; Jabot, Bruna; Rached, Fabiana; Orii, Noemia Mie; Nicolau, José Carlos; Duarte, Alberto J.; Ramires, José Antonio F.. Lack of clopidogrel-statin interaction in patients undergoing coronary stent implantation. Arquivos Brasileiros de Cardiologia, v. 95, n. 3, p. 321-327, Aug. 2010.

Electronic Document Format (APA)

Serrano Júnior, C. V., Soeiro, A. M., Araújo, L. F., Jabot, B., Rached, F., Orii, N. M., Nicolau, J. C., Duarte, A. J., & Ramires, J. A. F. (2010). Lack of clopidogrel-statin interaction in patients undergoing coronary stent implantation. Arquivos Brasileiros de Cardiologia, 95(3), 321-327.

Electronic Document Format (ISO)

Serrano Júnior, Carlos Vicente and Soeiro, Alexandre de Matos and Araújo, Leila Fernandes and Jabot, Bruna and Rached, Fabiana and Orii, Noemia Mie and Nicolau, José Carlos and Duarte, Alberto J. and Ramires, José Antonio F.. Lack of clopidogrel-statin interaction in patients undergoing coronary stent implantation. Arquivos Brasileiros de Cardiologia [online]. 2010, vol. 95, n. 3, [cited 2026-10-15], pp. 321-327. Available from: <https://journals.cardiol.br/en/article/lack-of-clopidogrel-statin-interaction-in-patients-undergoing-coronary-stent-implantation/>. ISSN 0066-782X

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