Page last updated: 2024-10-28

ibuprofen and Cardiovascular Stroke

ibuprofen has been researched along with Cardiovascular Stroke in 63 studies

Midol: combination of cinnamedrine, phenacetin, aspirin & caffeine

Research Excerpts

ExcerptRelevanceReference
" Patients with symptomatic pericarditis were treated with indomethacin (group 1, n = 73) or ibuprofen (group 2, n = 49) and those without symptomatic pericarditis received neither drug (group 3, n = 99)."8.77Myocardial infarct expansion during indomethacin or ibuprofen therapy for symptomatic post infarction pericarditis. Influence of other pharmacologic agents during early remodelling. ( Basualdo, CA; Jugdutt, BI, 1989)
"The aim was to assess whether using LSPS matching would enable the evaluation of paracetamol, compared to ibuprofen, and increased risk of myocardial infarction, stroke, gastrointestinal (GI) bleeding, or acute renal failure."7.96Channeling Bias in the Analysis of Risk of Myocardial Infarction, Stroke, Gastrointestinal Bleeding, and Acute Renal Failure with the Use of Paracetamol Compared with Ibuprofen. ( Berlin, JA; Fife, D; Ryan, PB; Schuemie, MJ; Swerdel, J; Weinstein, RB, 2020)
"To determine whether patients taking aspirin for secondary prevention of myocardial infarction are at increased risk of recurrent disease when they take concomitant ibuprofen."7.73Ibuprofen may abrogate the benefits of aspirin when used for secondary prevention of myocardial infarction. ( Baron, M; Hudson, M; Pilote, L; Rahme, E, 2005)
"This study was designed to determine if non-aspirin non-steroidal anti-inflammatory drugs (NANSAIDs) are associated with lower odds of myocardial infarction (MI) and if NANSAIDs, particularly ibuprofen, interfere with aspirin's cardioprotective effect."7.72The effects of nonselective non-aspirin non-steroidal anti-inflammatory medications on the risk of nonfatal myocardial infarction and their interaction with aspirin. ( Berlin, JA; Chittams, J; Jaskowiak, J; Kimmel, SE; Kishel, L; Reilly, M; Strom, BL, 2004)
"There does not seem to be an increased risk of myocardial infarction among patients simultaneously consuming aspirin and ibuprofen compared with aspirin alone."7.72Use of aspirin and ibuprofen compared with aspirin alone and the risk of myocardial infarction. ( Goldberg, KC; Patel, TN, 2004)
"To assess the ability of ibuprofen to influence the extent of platelet aggregation and leukocyte infiltration during acute myocardial infarction, autologous indium-111 (111-In)-labeled platelets or leukocytes were injected before 60 minutes of left circumflex coronary artery (LCx) occlusion, followed by 24 hours of reperfusion in the canine heart."7.66The effect of ibuprofen on accumulation of indium-111-labeled platelets and leukocytes in experimental myocardial infarction. ( Hook, BG; Lucchesi, BR; Rigot, VH; Romson, JL; Schork, MA; Swanson, DP, 1982)
"Pre-treatment with ibuprofen (30, 60 and 90mg/kg p."5.43Inhibition of RhoA/Rho kinase by ibuprofen exerts cardioprotective effect on isoproterenol induced myocardial infarction in rats. ( Gandhi, T; Parikh, M; Patel, P; Shah, H, 2016)
"Celecoxib and rofecoxib were associated with different odds of MI."5.33Patients exposed to rofecoxib and celecoxib have different odds of nonfatal myocardial infarction. ( Berlin, JA; Chittams, J; Jaskowiak, J; Kimmel, SE; Kishel, L; Reilly, M; Strom, BL, 2005)
" Patients with symptomatic pericarditis were treated with indomethacin (group 1, n = 73) or ibuprofen (group 2, n = 49) and those without symptomatic pericarditis received neither drug (group 3, n = 99)."4.77Myocardial infarct expansion during indomethacin or ibuprofen therapy for symptomatic post infarction pericarditis. Influence of other pharmacologic agents during early remodelling. ( Basualdo, CA; Jugdutt, BI, 1989)
"In parallel with experimental research into methods for salvage of ischemic myocardium after acute myocardial infarction (AMI) over the last decade, there has been a growing interest in prostaglandins (PG) and their inhibition by aspirin-like drugs or nonsteroidal anti-inflammatory drugs (NSAID)."4.76Prostaglandin inhibition and myocardial infarct size. ( Becker, LC; Jugdutt, BI, 1981)
" We used a Mantel-Haenszel method to obtain odds ratios (ORs) of the association between NSAID use (ibuprofen, naproxen, or diclofenac) and MACE (myocardial infarction, ischemic stroke, heart failure, or all-cause death)."4.31Impact of Lifestyle and Socioeconomic Position on the Association Between Non-steroidal Anti-inflammatory Drug Use and Major Adverse Cardiovascular Events: A Case-Crossover Study. ( Bonnesen, K; Ehrenstein, V; Grønkjær, MS; Hallas, J; Lash, TL; Pedersen, L; Schmidt, M; Sørensen, HT, 2023)
" After applying these weights in a pooled logistic regression, we estimated hazard ratios (HRs) of the association between use of NSAIDs (ibuprofen, naproxen, or diclofenac) and cardiovascular events (a composite of myocardial infarction, ischemic stroke, congestive heart failure, atrial fibrillation or flutter, and all-cause death)."4.31Impact of hemoglobin A1c level on the association between non-steroidal anti-inflammatory drug use and cardiovascular events in patients with type 2 diabetes: A population-based cohort study. ( Bonnesen, K; Ehrenstein, V; Lash, TL; Pedersen, L; Schmidt, M; Sørensen, HT, 2023)
"The aim was to assess whether using LSPS matching would enable the evaluation of paracetamol, compared to ibuprofen, and increased risk of myocardial infarction, stroke, gastrointestinal (GI) bleeding, or acute renal failure."3.96Channeling Bias in the Analysis of Risk of Myocardial Infarction, Stroke, Gastrointestinal Bleeding, and Acute Renal Failure with the Use of Paracetamol Compared with Ibuprofen. ( Berlin, JA; Fife, D; Ryan, PB; Schuemie, MJ; Swerdel, J; Weinstein, RB, 2020)
"This was a post hoc analysis from the INternational VErapamil Trandolapril STudy (INVEST), which enrolled patients with hypertension and coronary artery disease."3.77Harmful effects of NSAIDs among patients with hypertension and coronary artery disease. ( Bavry, AA; Cooper-Dehoff, RM; Gong, Y; Handberg, EM; Khaliq, A; Pepine, CJ, 2011)
" Naproxen users had the lowest adjusted rates of serious coronary heart disease (myocardial infarction, coronary heart disease death) and serious cardiovascular disease (myocardial infarction, stroke)/death from any cause, with respective incidence rate ratios (relative to NSAID nonusers) of 0."3.75Cardiovascular risks of nonsteroidal antiinflammatory drugs in patients after hospitalization for serious coronary heart disease. ( Arbogast, PG; Castellsague, J; Chung, CP; Daugherty, JR; García-Rodríguez, LA; Murray, KT; Ray, WA; Stein, CM; Varas-Lorenzo, C, 2009)
"To investigate the risk of myocardial infarction (MI) with diclofenac, ibuprofen and naproxen, taking into account the exposure patterns."3.74Does the varied use of NSAIDs explain the differences in the risk of myocardial infarction? ( Leufkens, HG; Rietbrock, S; Setakis, E; van Staa, TP, 2008)
"To evaluate the association between rofecoxib, celecoxib, diclofenac, and ibuprofen and the risk of hospitalization for acute myocardial infarction (AMI) in an elderly population."3.74Association between nonnaproxen NSAIDs, COX-2 inhibitors and hospitalization for acute myocardial infarction among the elderly: a retrospective cohort study. ( Kong, SX; LeLorier, J; Rahme, E; Toubouti, Y; Watson, DJ, 2007)
"To determine whether patients taking aspirin for secondary prevention of myocardial infarction are at increased risk of recurrent disease when they take concomitant ibuprofen."3.73Ibuprofen may abrogate the benefits of aspirin when used for secondary prevention of myocardial infarction. ( Baron, M; Hudson, M; Pilote, L; Rahme, E, 2005)
"To simultaneously assess the short-term reduction in risk of gastrointestinal (GI) complications and increase in risk of acute myocardial infarction (MI) by celecoxib compared with rofecoxib and several nonselective nonsteroidal antiinflammatory drugs (NSAIDs) using instrumental variable analysis."3.73Simultaneous assessment of short-term gastrointestinal benefits and cardiovascular risks of selective cyclooxygenase 2 inhibitors and nonselective nonsteroidal antiinflammatory drugs: an instrumental variable analysis. ( Brookhart, MA; Rassen, J; Schneeweiss, S; Solomon, DH; Wang, PS, 2006)
"Patients suffering an acute myocardial infarction routinely receive morphine and nonsteroidal anti-inflammatory drugs (NSAIDs) alone or in combination."3.72Acute aspirin treatment abolishes, whereas acute ibuprofen treatment enhances morphine-induced cardioprotection: role of 12-lipoxygenase. ( Gross, ER; Gross, GJ; Hsu, AK, 2004)
"This study was designed to determine if non-aspirin non-steroidal anti-inflammatory drugs (NANSAIDs) are associated with lower odds of myocardial infarction (MI) and if NANSAIDs, particularly ibuprofen, interfere with aspirin's cardioprotective effect."3.72The effects of nonselective non-aspirin non-steroidal anti-inflammatory medications on the risk of nonfatal myocardial infarction and their interaction with aspirin. ( Berlin, JA; Chittams, J; Jaskowiak, J; Kimmel, SE; Kishel, L; Reilly, M; Strom, BL, 2004)
"There does not seem to be an increased risk of myocardial infarction among patients simultaneously consuming aspirin and ibuprofen compared with aspirin alone."3.72Use of aspirin and ibuprofen compared with aspirin alone and the risk of myocardial infarction. ( Goldberg, KC; Patel, TN, 2004)
"Non-aspirin, non-steroidal anti-inflammatory drugs (NANSAIDs) have complex effects that could either prevent or promote coronary heart disease."3.71Non-steroidal anti-inflammatory drugs and risk of serious coronary heart disease: an observational cohort study. ( Daugherty, JR; Griffin, MR; Hall, K; Ray, WA; Stein, CM, 2002)
"The prophylactic role of ibuprofen in experimental myocardial infarction has not been reported."3.68Failure to reduce experimental myocardial infarct size with ibuprofen pre-treatment in rats. ( Lal, A; Sharma, ML, 1992)
"To assess the ability of ibuprofen to influence the extent of platelet aggregation and leukocyte infiltration during acute myocardial infarction, autologous indium-111 (111-In)-labeled platelets or leukocytes were injected before 60 minutes of left circumflex coronary artery (LCx) occlusion, followed by 24 hours of reperfusion in the canine heart."3.66The effect of ibuprofen on accumulation of indium-111-labeled platelets and leukocytes in experimental myocardial infarction. ( Hook, BG; Lucchesi, BR; Rigot, VH; Romson, JL; Schork, MA; Swanson, DP, 1982)
" An increased risk was observed for diclofenac and rofecoxib, the latter one with a clear dose-response trend."2.43Non-steroidal antiinflammatory drugs and the risk of acute myocardial infarction. ( García Rodríguez, LA; Hernández-Díaz, S; Varas-Lorenzo, C, 2006)
"Pre-treatment with ibuprofen (30, 60 and 90mg/kg p."1.43Inhibition of RhoA/Rho kinase by ibuprofen exerts cardioprotective effect on isoproterenol induced myocardial infarction in rats. ( Gandhi, T; Parikh, M; Patel, P; Shah, H, 2016)
"Celecoxib and rofecoxib were associated with different odds of MI."1.33Patients exposed to rofecoxib and celecoxib have different odds of nonfatal myocardial infarction. ( Berlin, JA; Chittams, J; Jaskowiak, J; Kimmel, SE; Kishel, L; Reilly, M; Strom, BL, 2005)
"Naproxen was associated with an OR of 0."1.32Nonsteroidal antiinflammatory drugs and the risk of myocardial infarction in the general population. ( García Rodríguez, LA; González-Pérez, A; Maguire, A; Varas-Lorenzo, C, 2004)
"1."1.29Dissociation of the anti-ischaemic effects of cloricromene from its anti-platelet activity. ( Cirillo, R; Lidbury, PS; Vane, JR, 1993)
"Ibuprofen and verapamil treatment resulted in less myocardial damage after 48 h than placebo treatment but the differences were generally not statistically significant."1.27Evaluation of a rat model for assessing interventions to salvage ischaemic myocardium: effects of ibuprofen and verapamil. ( Evans, RG; Fischer, VW; Kulevich, J; Mueller, HS; Val-Mejias, JE, 1985)

Research

Studies (63)

TimeframeStudies, this research(%)All Research%
pre-199023 (36.51)18.7374
1990's4 (6.35)18.2507
2000's25 (39.68)29.6817
2010's6 (9.52)24.3611
2020's5 (7.94)2.80

Authors

AuthorsStudies
Baak, BN1
Jick, SS1
Bonnesen, K2
Pedersen, L2
Ehrenstein, V2
Grønkjær, MS1
Sørensen, HT2
Hallas, J2
Lash, TL2
Schmidt, M3
Ernst, MT1
Pottegård, A1
Weinstein, RB1
Ryan, PB1
Berlin, JA3
Schuemie, MJ1
Swerdel, J1
Fife, D1
Chen, YR1
Hsieh, FI1
Chang, CC1
Chi, NF1
Wu, HC1
Chiou, HY1
Bhala, N1
Emberson, J1
Merhi, A1
Abramson, S1
Arber, N1
Baron, JA1
Bombardier, C1
Cannon, C1
Farkouh, ME1
FitzGerald, GA1
Goss, P1
Halls, H1
Hawk, E1
Hawkey, C1
Hennekens, C1
Hochberg, M1
Holland, LE1
Kearney, PM1
Laine, L1
Lanas, A1
Lance, P1
Laupacis, A1
Oates, J1
Patrono, C1
Schnitzer, TJ1
Solomon, S1
Tugwell, P1
Wilson, K1
Wittes, J1
Baigent, C1
Patel, P1
Parikh, M1
Shah, H1
Gandhi, T1
van Staa, TP1
Rietbrock, S1
Setakis, E1
Leufkens, HG1
Ray, WA2
Varas-Lorenzo, C3
Chung, CP1
Castellsague, J1
Murray, KT1
Stein, CM2
Daugherty, JR2
Arbogast, PG1
García-Rodríguez, LA1
Schjerning Olsen, AM1
Fosbøl, EL1
Lindhardsen, J1
Folke, F1
Charlot, M1
Selmer, C1
Lamberts, M1
Bjerring Olesen, J1
Køber, L2
Hansen, PR1
Torp-Pedersen, C2
Gislason, GH2
Bavry, AA1
Khaliq, A1
Gong, Y1
Handberg, EM1
Cooper-Dehoff, RM1
Pepine, CJ1
He, B1
Tang, J1
Ding, Y1
Wang, H1
Sun, Y1
Shin, JH1
Chen, B1
Moorthy, G1
Qiu, J1
Desai, P1
Wild, DJ1
Brandt, KD1
Kimmel, SE3
Strom, BL3
Curtis, JP2
Wang, Y1
Portnay, EL1
Masoudi, FA1
Havranek, EP1
Krumholz, HM2
Gross, ER1
Hsu, AK1
Gross, GJ1
Reilly, M2
Jaskowiak, J2
Kishel, L2
Chittams, J2
Patel, TN1
Goldberg, KC1
García Rodríguez, LA2
Maguire, A1
González-Pérez, A1
Lee, RT1
Hudson, M1
Baron, M1
Rahme, E2
Pilote, L1
Hernández-Díaz, S1
Jacobsen, S1
Rasmussen, JN1
Rasmussen, S1
Buch, P1
Friberg, J1
Schramm, TK1
Abildstrom, SZ1
Madsen, M1
Schneeweiss, S1
Solomon, DH1
Wang, PS1
Rassen, J1
Brookhart, MA1
Watson, DJ1
Kong, SX1
Toubouti, Y1
LeLorier, J1
Singh, H1
Hennekens, CH1
Borzak, S1
Flynn, PJ1
Becker, WK1
Vercellotti, GM1
Weisdorf, DJ1
Craddock, PR1
Hammerschmidt, DE1
Lillehei, RC1
Jacob, HS1
Huval, WV1
Lelcuk, S1
Allen, PD1
Mannick, JA1
Shepro, D1
Hechtman, HB1
Jugdutt, BI6
Brown, EJ1
Kloner, RA2
Schoen, FJ1
Hammerman, H1
Hale, S1
Braunwald, E1
Becker, LC3
Kirlin, PC1
Romson, JL3
Pitt, B1
Abrams, GD1
Schork, MA2
Lucchesi, BR3
Hook, BG1
Rigot, VH1
Swanson, DP1
Darsee, JR1
Lefer, AM1
Crossley, K1
Hutchins, GM2
Bulkley, BH2
Maroko, PR1
Lidbury, PS1
Cirillo, R1
Vane, JR1
Schafer, A1
Hall, K1
Griffin, MR1
Miser, WF1
Lal, A1
Sharma, ML1
Bailey, KR2
Sinitsyn, SP1
Basualdo, CA1
Przyklenk, K1
Hess, ML1
Rowe, GT1
Caplan, M1
Lucchesi, B1
Reimer, KA1
Jennings, RB1
Cobb, FR1
Murdock, RH1
Greenfield, JC1
Schwartz, RP1
Spodick, DH1
Hasselstrøm, LJ1
Eliasen, K1
Mogensen, T1
Andersen, JB1
Evans, RG1
Val-Mejias, JE1
Kulevich, J1
Fischer, VW1
Mueller, HS1
Cannon, RO1
Rodríguez, ER1
Speir, E1
Yamaguchi, M1
Butany, J1
McManus, BM1
Bolli, R1
Ferrans, VJ1
Boden, WE1
Sadaniantz, A1

Clinical Trials (7)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
WilL LOWer Dose Aspirin be More Effective Following ACS? (WILLOW-ACS)[NCT02741817]Phase 420 participants (Actual)Interventional2016-06-26Completed
Astaxanthin Effects on Osteoarthritis Associated Pain and Inflammatory Indicators[NCT03664466]0 participants (Actual)Interventional2021-04-29Withdrawn (stopped due to Inadequate funding)
Analgesic Efficacy of Preoperative Oral Administration of Dexketoprofen Trometamol in Third Molar Surgery, Compared to Postoperative Administration[NCT02380001]Phase 460 participants (Actual)Interventional2015-01-31Completed
Treatment Efficacy of 'Shinbaro Capsule' in the Treatment of Hand Osteoarthritis: Randomized, Double-blinded, Placebo-controlled, Multicenter Investigator Initiated Trial.[NCT01910116]Phase 2/Phase 3220 participants (Actual)Interventional2013-09-30Completed
Effects on Omission of NSAIDs on the Consumption of Opioids in the Standard Analgesic Regimen After Elective Laparoscopic Colorectal Cancer Resection in an ERAS Setting. A Retrospective Single-center Cohort Study.[NCT04448652]502 participants (Actual)Observational [Patient Registry]2015-01-01Completed
A Phase IIa Randomized, Active-controlled, Double-blind, Dose-escalation Study in Patients With Vulvovaginal Candidiasis to Evaluate Dose Response Relationship of Clinical Efficacy, Safety and Tolerability of Topically Administered ProF-001[NCT03115073]Phase 2/Phase 384 participants (Actual)Interventional2017-04-04Completed
Single and Repeated Leech Therapy for the Treatment of Late Stage Knee Osteoarthritis. A Randomized, Placebo Controlled Comparative Trial[NCT00435773]Phase 2118 participants Interventional2004-02-29Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

AUSCAN Function Change at 12 Weeks From Baseline

"Change in AUSCAN function score at 12 weeks from baseline = Function score at 12 weeks (0-100)- Function score at baseline (0-100). AUSCAN Function score scale ranges from 0 (no functional limitation) to 100 (worst possible functional limitation).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 12 weeks

Interventionunits on a scale (Median)
Shinbaro-11
Placebo-2.9

AUSCAN Function Change at 16 Weeks From Baseline

"Change in AUSCAN function score at 16 weeks from baseline = Function score at 16 weeks (0-100)- Function score at baseline (0-100). AUSCAN Function score scale ranges from 0 (no functional limitation) to 100 (worst possible functional limitation).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 16 weeks

Interventionunits on a scale (Median)
Shinbaro-9.9
Placebo-4.8

AUSCAN Function Change at 4 Weeks From Baseline

"Change in AUSCAN function score at 4 weeks from baseline = Function score at 4 weeks (0-100)- Function score at baseline (0-100). AUSCAN Function score scale ranges from 0 (no functional limitation) to 100 (worst possible functional limitation).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Basline and 4 weeks

Interventionunits on a scale (Median)
Shinbaro-6.8
Placebo-3.7

AUSCAN Function Change at 8 Weeks From Baseline

"Change in AUSCAN function score at 8 weeks from baseline = Function score at 8 weeks (0-100)- Function score at baseline (0-100). AUSCAN Function score scale ranges from 0 (no functional limitation) to 100 (worst possible functional limitation).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 8 weeks

Interventionunits on a scale (Median)
Shinbaro-9.7
Placebo-4.8

AUSCAN Pain Change at 4 Weeks From Baseline

"Change in AUSCAN pain score at 4 weeks from baseline = Pain at 4 weeks (0-100) - Pain at baseline (0-100).~AUSCAN Pain scale ranges from 0 (no pain) to 100 (worst possible pain).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 4 weeks

Interventionunits on a scale (Median)
Shinbaro-9.0
Placebo-2.2

AUSCAN Pain Score at 12 Weeks From Baseline

"Change in AUSCAN pain score at 12 weeks from baseline = Pain at 12 weeks (0-100)- Pain at baseline (0-100). AUSCAN Pain scale ranges from 0 (no pain) to 100 (worst possible pain).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline, 12 weeks

Interventionunits on a scale (Median)
Shinbaro-14.6
Placebo-8.0

AUSCAN Pain Score at 16 Weeks From Baseline

"Change in AUSCAN pain score at 16 weeks from baseline = Pain at 16 weeks (0-100)- Pain at baseline (0-100). AUSCAN Pain scale ranges from 0 (no pain) to 100 (worst possible pain).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 16 weeks

Interventionunits on a scale (Median)
Shinbaro-15.6
Placebo-4.4

AUSCAN Pain Score at 8 Weeks From Baseline

"Change in AUSCAN pain score at 8 weeks from baseline = Pain at 8 weeks (0-100)- Pain at baseline (0-100). AUSCAN Pain scale ranges from 0 (no pain) to 100 (worst possible pain).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline, 8 weeks

Interventionunits on a scale (Median)
Shinbaro-13.4
Placebo-2.2

AUSCAN Stiffness at 12 Weeks Change From Baseline

"Change in AUSCAN stiffness score at 12 weeks from baseline = Stiffness at 12 weeks (0-100)- Stiffness at baseline (0-100). AUSCAN Stiffness scale ranges from 0 (no stiffness) to 100 (worst possible stiffness).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Basline and 12 weeks

Interventionunits on a scale (Median)
Shinbaro-14.0
Placebo-11.0

AUSCAN Stiffness at 16 Weeks Change From Baseline

"Change in AUSCAN stiffness score at 16 weeks from baseline = Stiffness at 16 weeks (0-100)- Stiffness at baseline (0-100). AUSCAN Stiffness scale ranges from 0 (no stiffness) to 100 (worst possible stiffness).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline, 16 weeks

Interventionunits on a scale (Median)
Shinbaro-10.0
Placebo-8.0

AUSCAN Stiffness at 4 Weeks Change From Baseline

"Change in AUSCAN stiffness score at 4 weeks from baseline = Stiffness at 4 weeks (0-100)- Stiffness at baseline (0-100). AUSCAN Stiffness scale ranges from 0 (no stiffness) to 100 (worst possible stiffness).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 4 weeks

Interventionunits on a scale (Median)
Shinbaro-9.0
Placebo-6.0

AUSCAN Stiffness at 8 Weeks Change From Baseline

"Change in AUSCAN stiffness score at 8 weeks from baseline = Stiffness at 8 weeks (0-100)- Stiffness at baseline (0-100). AUSCAN Stiffness scale ranges from 0 (no stiffness) to 100 (worst possible stiffness).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: baseline and 8 weeks

Interventionunits on a scale (Median)
Shinbaro-12.0
Placebo-6

Number of OMERACT-OARSI Responder

Number of patients who met OMERACT-OARSI criteria = significant clinical improvement in osteoarthritis symptom after treatment (NCT01910116)
Timeframe: Baselie and 16 weeks

Interventionparticipants (Number)
Shinbaro55
Placebo40

Patient Global Assessment, Change From Baseline

"Change in Patient global assessment (PGA) at 12 weeks from baseline = PGA at 12 weeks (0-100)- PGA score at baseline (0-100). GPA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 12 weeks

Interventionunits on a scale (Median)
Shinbaro-11.0
Placebo-6.0

Patient Global Assessment, Change From Baseline

"Change in Patient global assessment (PGA) at 16 weeks from baseline = PGA at 16 weeks (0-100)- PGA score at baseline (0-100). PGA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 16 weeks

Interventionunits on a scale (Median)
Shinbaro-10.0
Placebo-8.5

Patient Global Assessment, Change From Baseline

"Change in Patient global assessment (PGA) at 4 weeks from baseline = PGA at 4 weeks (0-100)- PGA score at baseline (0-100). PGA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 4 weeks

Interventionunits on a scale (Median)
Shinbaro-9.0
Placebo-3.0

Patient Global Assessment, Change From Baseline

"Change in Patient global assessment (PGA) at 8 weeks from baseline = PGA at 8 weeks (0-100)- PGA score at baseline (0-100). PGA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 8 weeks

Interventionunits on a scale (Median)
Shinbaro-10.0
Placebo-6.0

Physician Global Assessment, Change From Baseline

"Change in Physician global assessment (PhGA) at 12 weeks from baseline = PhGA at 12 weeks (0-100)- PhGA score at baseline (0-100). PhGA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 12 weeks

Interventionunits on a scale (Median)
Shinbaro-19.0
Placebo-13

Physician Global Assessment, Change From Baseline

"Change in Physician global assessment (PhGA) at 16 weeks from baseline = PhGA at 16 weeks (0-100)- PhGA score at baseline (0-100). PhGA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 16 weeks

Interventionunits on a scale (Median)
Shinbaro-12
Placebo-6.5

Physician Global Assessment, Change From Baseline

"Change in Physician global assessment (PhGA) at 4 weeks from baseline = PhGA at 4 weeks (0-100)- PhGA score at baseline (0-100). GPA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: baseline and 4 weeks

Interventionunits on a scale (Median)
Shinbaro-12
Placebo-7.0

Physician Global Assessment, Change From Baseline

"Change in Physician global assessment (PhGA) at 8 weeks from baseline = PhGA at 8 weeks (0-100)- PhGA score at baseline (0-100). PhGA scale ranges from 0 (excellent condition) to 100 (worst possible worse possible condition).~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 8 weeks

Interventionunits on a scale (Median)
Shinbaro-16.0
Placebo-11.5

Swollen Joint Count, Change From Baseline

"Change in Swollen joint count (SJC) at 12 weeks from baseline = SJC at 12 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 12 weeks

InterventionJoints (Median)
Shinbaro0
Placebo0

Swollen Joint Count, Change From Baseline

"Change in Swollen joint count (SJC) at 16 weeks from baseline = SJC at 16 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 16 weeks

InterventionJoints (Median)
Shinbaro0
Placebo0

Swollen Joint Count, Change From Baseline

"Change in Swollen joint count (SJC) at 4 weeks from baseline = SJC at 4 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 4 weeks

InterventionJoints (Median)
Shinbaro0
Placebo0

Swollen Joint Count, Change From Baseline

"Change in Swollen joint count (SJC) at 8 weeks from baseline = SJC at 8 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 8 weeks

InterventionJoints (Median)
Shinbaro0
Placebo0

Tender Joint Count, Change From Baseline

"Change in Tender joint count (TJC) at 12 weeks from baseline = TJC at 12 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 12 weeks

Interventionjoints (Median)
Shinbaro-2.0
Placebo-1.0

Tender Joint Count, Change From Baseline

"Change in Tender joint count (TJC) at 16 weeks from baseline = TJC at 16 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 16 weeks

Interventionjoints (Median)
Shinbaro-2.0
Placebo-1.0

Tender Joint Count, Change From Baseline

"Change in Tender joint count (TJC) at 4 weeks from baseline = TJC at 4 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 4 weeks

Interventionjoints (Median)
Shinbaro-1
Placebo0

Tender Joint Count, Change From Baseline

"Change in Tender joint count (TJC) at 8 weeks from baseline = TJC at 8 weeks - TJC at baseline..~Negative value means improvement from baseline~Positive value means deterioration from baseline" (NCT01910116)
Timeframe: Baseline and 8 weeks

InterventionJoints (Median)
Shinbaro-1.0
Placebo-1.0

Acetaminophen Rescue

yes = AAP rescue use, no = no AAP rescue use (NCT01910116)
Timeframe: 12 weeks and 16 weeks

,
Interventionparticipants (Number)
yesno
Placebo2104
Shinbaro4105

Acetaminophen Rescue

yes = AAP rescue use, no = no AAP rescue use (NCT01910116)
Timeframe: 4 weeks and 8 weeks

,
Interventionparticipants (Number)
yesno
Placebo799
Shinbaro1099

Acetaminophen Rescue

yes = AAP rescue use, no = no AAP rescue use (NCT01910116)
Timeframe: 8 weeks and 12 weeks

,
Interventionparticipants (Number)
yesno
Placebo4102
Shinbaro4105

Acetaminophen Rescue

yes = AAP rescue use, no = no AAP rescue use (NCT01910116)
Timeframe: Baseline 4 weeks

,
Interventionparticipants (Number)
yesno
Placebo4102
Shinbaro7102

Number of OMERACT-OARSI Responder

Number of patients who met OMERACT-OARSI criteria = significant clinical improvement in osteoarthritis symptom after treatment (NCT01910116)
Timeframe: Baseline and 12 weeks

,
Interventionparticipants (Number)
respondernonresponder
Placebo4363
Shinbaro6247

Number of OMERACT-OARSI Responder

Number of patients who met OMERACT-OARSI criteria = significant clinical improvement in osteoarthritis symptom after treatment (NCT01910116)
Timeframe: Baseline and 8 weeks

,
Interventionparticipants (Number)
respondernonresponder
Placebo3868
Shinbaro5653

Number of OMERACT-OARSI Responder

Outcome Measures in Rheumatology-Osteoarthritis Research Society International (OMERACT-OARSI) Number of patients who met OMERACT-OARSI criteria = significant clinical improvement in osteoarthritis symptom after treatment (NCT01910116)
Timeframe: Baseline and 4 weeks

,
Interventionparticipants (Number)
ResponderNonresponder
Placebo3274
Shinbaro4861

Reviews

5 reviews available for ibuprofen and Cardiovascular Stroke

ArticleYear
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials.
    Lancet (London, England), 2013, Aug-31, Volume: 382, Issue:9894

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Blood Vessels; Coronary Disease; Cyclooxygenase 2 Inhibitor

2013
Non-steroidal antiinflammatory drugs and the risk of acute myocardial infarction.
    Basic & clinical pharmacology & toxicology, 2006, Volume: 98, Issue:3

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Case-Control Studies; Cohort Studies; Diclofenac; Dose-Resp

2006
Prostaglandin inhibition and myocardial infarct size.
    Clinical cardiology, 1981, Volume: 4, Issue:3

    Topics: Acute Disease; Animals; Aspirin; Coronary Disease; Humans; Ibuprofen; Indomethacin; Models, Biologic

1981
Myocardial ischemia, reperfusion and free radical injury.
    The American journal of cardiology, 1990, May-22, Volume: 65, Issue:19

    Topics: Animals; Cell Adhesion Molecules; Chemotactic Factors; Complement Activation; E-Selectin; Free Radic

1990
Myocardial infarct expansion during indomethacin or ibuprofen therapy for symptomatic post infarction pericarditis. Influence of other pharmacologic agents during early remodelling.
    The Canadian journal of cardiology, 1989, Volume: 5, Issue:4

    Topics: Adrenergic alpha-Antagonists; Drug Therapy, Combination; Echocardiography; Ibuprofen; Indomethacin;

1989

Trials

1 trial available for ibuprofen and Cardiovascular Stroke

ArticleYear
Determinants of cardiovascular stability during abdominal aortic aneurysmectomy (AAA).
    Annals of surgery, 1984, Volume: 199, Issue:2

    Topics: Aged; Aorta, Abdominal; Aortic Aneurysm; Blood Platelets; Epoprostenol; Female; Heart; Hematologic T

1984

Other Studies

57 other studies available for ibuprofen and Cardiovascular Stroke

ArticleYear
Non-steroidal anti-inflammatory drugs and risk of myocardial infarction adjusting for use of proton pump-inhibitors in patients with no major risk factors: a nested case-control study in the UK Clinical Practice Research Datalink.
    European heart journal. Cardiovascular pharmacotherapy, 2022, 12-15, Volume: 9, Issue:1

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Case-Control Studies; Diclofenac; Humans; Ibuprofen; Myocar

2022
Impact of Lifestyle and Socioeconomic Position on the Association Between Non-steroidal Anti-inflammatory Drug Use and Major Adverse Cardiovascular Events: A Case-Crossover Study.
    Drug safety, 2023, Volume: 46, Issue:6

    Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Cardiovascular Diseases; Cross-Over Studies; Diclofe

2023
Impact of hemoglobin A1c level on the association between non-steroidal anti-inflammatory drug use and cardiovascular events in patients with type 2 diabetes: A population-based cohort study.
    Pharmacoepidemiology and drug safety, 2023, Volume: 32, Issue:11

    Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Cohort Studies; Diabetes Mellitus, Type 2; Diclofena

2023
Cardiovascular risks of continuing vs. initiating NSAIDs after first-time myocardial infarction or heart failure: a nationwide cohort study.
    European heart journal. Cardiovascular pharmacotherapy, 2023, 09-20, Volume: 9, Issue:6

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Cardiovascular Diseases; Cohort Studies; Diclofenac; Heart

2023
Channeling Bias in the Analysis of Risk of Myocardial Infarction, Stroke, Gastrointestinal Bleeding, and Acute Renal Failure with the Use of Paracetamol Compared with Ibuprofen.
    Drug safety, 2020, Volume: 43, Issue:9

    Topics: Acetaminophen; Acute Kidney Injury; Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Ag

2020
Effect on Risk of Stroke and Acute Myocardial Infarction of Nonselective Nonsteroidal Anti-Inflammatory Drugs in Patients With Rheumatoid Arthritis.
    The American journal of cardiology, 2018, 05-15, Volume: 121, Issue:10

    Topics: Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Arthritis, Rheumatoid; Celecoxib;

2018
Inhibition of RhoA/Rho kinase by ibuprofen exerts cardioprotective effect on isoproterenol induced myocardial infarction in rats.
    European journal of pharmacology, 2016, Nov-15, Volume: 791

    Topics: Animals; Antioxidants; Cardiotonic Agents; Electrocardiography; Gene Expression Regulation, Enzymolo

2016
Does the varied use of NSAIDs explain the differences in the risk of myocardial infarction?
    Journal of internal medicine, 2008, Volume: 264, Issue:5

    Topics: Adult; Age Factors; Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Diclofenac; Dr

2008
Cardiovascular risks of nonsteroidal antiinflammatory drugs in patients after hospitalization for serious coronary heart disease.
    Circulation. Cardiovascular quality and outcomes, 2009, Volume: 2, Issue:3

    Topics: Aged; Anti-Inflammatory Agents, Non-Steroidal; Cardiovascular Diseases; Celecoxib; Cohort Studies; C

2009
Duration of treatment with nonsteroidal anti-inflammatory drugs and impact on risk of death and recurrent myocardial infarction in patients with prior myocardial infarction: a nationwide cohort study.
    Circulation, 2011, May-24, Volume: 123, Issue:20

    Topics: Adrenergic beta-Antagonists; Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Cohor

2011
Harmful effects of NSAIDs among patients with hypertension and coronary artery disease.
    The American journal of medicine, 2011, Volume: 124, Issue:7

    Topics: Adult; Aged; Anti-Inflammatory Agents, Non-Steroidal; Antihypertensive Agents; Blood Pressure; Celec

2011
Mining relational paths in integrated biomedical data.
    PloS one, 2011, Volume: 6, Issue:12

    Topics: Algorithms; Computers; Data Collection; Data Mining; Databases, Factual; Humans; Hypoglycemic Agents

2011
Key questions concerning paracetamol and NSAIDs for OA.
    Annals of the rheumatic diseases, 2003, Volume: 62, Issue:3

    Topics: Acetaminophen; Analgesics, Non-Narcotic; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Humans; I

2003
Giving aspirin and ibuprofen after myocardial infarction.
    BMJ (Clinical research ed.), 2003, Dec-06, Volume: 327, Issue:7427

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Contraindications; Drug Interactions; Humans; Ibup

2003
Aspirin, ibuprofen, and mortality after myocardial infarction: retrospective cohort study.
    BMJ (Clinical research ed.), 2003, Dec-06, Volume: 327, Issue:7427

    Topics: Aged; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Cohort Studies; Contraindications; Drug Inte

2003
Acute aspirin treatment abolishes, whereas acute ibuprofen treatment enhances morphine-induced cardioprotection: role of 12-lipoxygenase.
    The Journal of pharmacology and experimental therapeutics, 2004, Volume: 310, Issue:1

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Arachidonate 12-Lipoxygenase; Aspirin; Blood Press

2004
The effects of nonselective non-aspirin non-steroidal anti-inflammatory medications on the risk of nonfatal myocardial infarction and their interaction with aspirin.
    Journal of the American College of Cardiology, 2004, Mar-17, Volume: 43, Issue:6

    Topics: Adult; Aged; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Case-Control Studies; Drug Interactio

2004
The case for an adverse interaction between aspirin and non-steroidal anti-inflammatory drugs: is it time to believe the hype?
    Journal of the American College of Cardiology, 2004, Mar-17, Volume: 43, Issue:6

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Drug Interactions; Humans; Ibuprofen; Myocardial I

2004
Painkillers appear to weaken aspirin's primary protection.
    Heart advisor, 2003, Volume: 6, Issue:11

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Drug Interactions; Humans; Ibuprofen; Myocardial I

2003
Use of aspirin and ibuprofen compared with aspirin alone and the risk of myocardial infarction.
    Archives of internal medicine, 2004, Apr-26, Volume: 164, Issue:8

    Topics: Aged; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Drug Therapy, Combination; Female; Humans; I

2004
Nonsteroidal antiinflammatory drugs and the risk of myocardial infarction in the general population.
    Circulation, 2004, Jun-22, Volume: 109, Issue:24

    Topics: Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Cardiotonic Agents; Case-

2004
Patients exposed to rofecoxib and celecoxib have different odds of nonfatal myocardial infarction.
    Annals of internal medicine, 2005, Feb-01, Volume: 142, Issue:3

    Topics: Aged; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Bias; Case-Control Studies; Celecoxib; Confo

2005
Ask the doctor. I am a 60-year-old man with several risk factors for heart disease. I take Aleve twice a day. Do I still need to take aspirin, or is the Aleve enough? I often take ibuprofen for my headaches or aching back. Now my doctor wants me to start
    Harvard heart letter : from Harvard Medical School, 2005, Volume: 15, Issue:6

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Cyclooxygenase Inhibitors; Drug Interactions; Huma

2005
Ibuprofen may abrogate the benefits of aspirin when used for secondary prevention of myocardial infarction.
    The Journal of rheumatology, 2005, Volume: 32, Issue:8

    Topics: Aged; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Cohort Studies; Contraindications; Drug Inte

2005
[Study results of routine clinical practice. Do rheumatism patients get substandard care?].
    MMW Fortschritte der Medizin, 2005, Nov-24, Volume: 147, Issue:47

    Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Arthritis, Rheumatoid; Cyclooxygenase 2 Inhibitors;

2005
Risk of death or reinfarction associated with the use of selective cyclooxygenase-2 inhibitors and nonselective nonsteroidal antiinflammatory drugs after acute myocardial infarction.
    Circulation, 2006, Jun-27, Volume: 113, Issue:25

    Topics: Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Confidence Intervals; C

2006
Simultaneous assessment of short-term gastrointestinal benefits and cardiovascular risks of selective cyclooxygenase 2 inhibitors and nonselective nonsteroidal antiinflammatory drugs: an instrumental variable analysis.
    Arthritis and rheumatism, 2006, Volume: 54, Issue:11

    Topics: Aged; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Cyclooxygenase 2 Inhibitors; Diclofenac; F

2006
Association between nonnaproxen NSAIDs, COX-2 inhibitors and hospitalization for acute myocardial infarction among the elderly: a retrospective cohort study.
    Pharmacoepidemiology and drug safety, 2007, Volume: 16, Issue:5

    Topics: Age Factors; Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Cohort Stu

2007
Take aspirin before ibuprofen, not after.
    Harvard heart letter : from Harvard Medical School, 2006, Volume: 17, Issue:3

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Drug Administration Schedule; Drug Interactions; H

2006
Treating osteoarthritis in the elderly: should recent data on NSAIDs change our way of practice?
    Southern medical journal, 2007, Volume: 100, Issue:8

    Topics: Aged; Anti-Inflammatory Agents, Non-Steroidal; Cyclooxygenase 2 Inhibitors; Databases, Factual; Dicl

2007
Cyclooxygenase-2 inhibitors and most traditional nonsteroidal anti-inflammatory drugs cause similar moderately increased risks of cardiovascular disease.
    Journal of cardiovascular pharmacology and therapeutics, 2008, Volume: 13, Issue:1

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Cardiovascular Diseases; Clinical Trials as Topic; Cyclooxy

2008
Ibuprofen inhibits granulocyte responses to inflammatory mediators. A proposed mechanism for reduction of experimental myocardial infarct size.
    Inflammation, 1984, Volume: 8, Issue:1

    Topics: Animals; Aspirin; Cats; Complement C5; Coronary Vessels; Female; Granulocytes; Ibuprofen; Ligation;

1984
Effect of PGE1, PGE2 and PGI2 on ventricular arrhythmias during myocardial infarction in conscious dogs: relation to infarct size.
    Prostaglandins and medicine, 1981, Volume: 7, Issue:5

    Topics: Alprostadil; Animals; Arrhythmias, Cardiac; Collateral Circulation; Dinoprostone; Dogs; Electrocardi

1981
Scar thinning due to ibuprofen administration after experimental myocardial infarction.
    The American journal of cardiology, 1983, Mar-01, Volume: 51, Issue:5

    Topics: Animals; Aspirin; Dogs; Female; Hydroxyproline; Ibuprofen; Male; Myocardial Infarction; Myocardium

1983
Ibuprofen-mediated infarct size reduction: effects on regional myocardial function in canine myocardial infarction in canine myocardial infarction.
    The American journal of cardiology, 1982, Volume: 50, Issue:4

    Topics: Animals; Arterial Occlusive Diseases; Blood Pressure; Coronary Disease; Dogs; Heart Rate; Ibuprofen;

1982
The effect of ibuprofen on accumulation of indium-111-labeled platelets and leukocytes in experimental myocardial infarction.
    Circulation, 1982, Volume: 66, Issue:5

    Topics: Animals; Blood Platelets; Dogs; Ibuprofen; Indium; Inflammation; Isotope Labeling; Leukocytes; Myoca

1982
Dependency of location of salvageable myocardium on type of intervention.
    The American journal of cardiology, 1981, Volume: 48, Issue:4

    Topics: Animals; Coronary Circulation; Coronary Disease; Dogs; Female; Flurbiprofen; Glycine; Heart; Ibuprof

1981
Mechanisms of the optimal protective effects of ibuprofen in acute myocardial ischemia.
    Advances in shock research, 1980, Volume: 3

    Topics: Animals; Blood Pressure; Cats; Central Venous Pressure; Coronary Vessels; Female; Heart Rate; Ibupro

1980
Salvage of ischemic myocardium by ibuprofen during infarction in the conscious dog.
    The American journal of cardiology, 1980, Volume: 46, Issue:1

    Topics: Animals; Blood Pressure; Coronary Circulation; Coronary Disease; Dogs; Electrocardiography; Heart Ra

1980
Experimental infarction studies.
    Clinical and investigative medicine. Medecine clinique et experimentale, 1980, Volume: 3, Issue:1-2

    Topics: Animals; Chlorpromazine; Dogs; Heart Rate; Ibuprofen; Morphine; Myocardial Infarction; Myocardium; P

1980
Dissociation of the anti-ischaemic effects of cloricromene from its anti-platelet activity.
    British journal of pharmacology, 1993, Volume: 110, Issue:1

    Topics: Animals; Blood Pressure; Chromonar; Coronary Vessels; Electrocardiography; Heart Rate; Ibuprofen; In

1993
My doctor recently recommended that I take low-dose aspirin to minimize the risk of a heart attack or stroke. I routinely take ibuprofen for arthritis pain. Do I need both, and is it safe to combine the two?
    Health news (Waltham, Mass.), 2000, Volume: 6, Issue:1

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Drug Interactions; Humans; Ibuprofen; Myocardial I

2000
Non-steroidal anti-inflammatory drugs and risk of serious coronary heart disease: an observational cohort study.
    Lancet (London, England), 2002, Jan-12, Volume: 359, Issue:9301

    Topics: Age Distribution; Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Bias; C

2002
An aspirin a day keeps the MI away (for some).
    American family physician, 2002, May-15, Volume: 65, Issue:10

    Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Cardiovascular Diseases; Drug Antagonism; H

2002
Failure to reduce experimental myocardial infarct size with ibuprofen pre-treatment in rats.
    Indian journal of physiology and pharmacology, 1992, Volume: 36, Issue:2

    Topics: Animals; Female; Heart; Ibuprofen; Isoproterenol; Male; Myocardial Infarction; Myocardium; Rats

1992
Detecting fabrication of data in a multicenter collaborative animal study.
    Controlled clinical trials, 1991, Volume: 12, Issue:6

    Topics: Animals; Data Interpretation, Statistical; Disease Models, Animal; Dogs; Ibuprofen; Multicenter Stud

1991
[Correction of metabolic disorders of the myocardium in acute myocardial infarct as an important factor in preventing the development of circulatory insufficiency].
    Kardiologiia, 1985, Volume: 25, Issue:7

    Topics: Animals; Aprotinin; Ascorbic Acid; Drug Therapy, Combination; Glutamates; Glutamic Acid; Heart Failu

1985
Effect of chronic ibuprofen therapy on early healing of experimentally induced acute myocardial infarction in dogs.
    The American journal of cardiology, 1989, May-01, Volume: 63, Issue:15

    Topics: Animals; Collagen; Dogs; Drug Administration Schedule; Ibuprofen; Myocardial Infarction; Myocardium;

1989
Identification of hydrogen peroxide and hydroxyl radicals as mediators of leukocyte-induced myocardial dysfunction. Limitation of infarct size with neutrophil inhibition and depletion.
    Advances in myocardiology, 1985, Volume: 5

    Topics: Adenosine Triphosphatases; Animals; Butylated Hydroxytoluene; Calcium; Catalase; Dogs; Free Radicals

1985
Effect of nitroglycerin and ibuprofen on left ventricular topography and rupture threshold during healing after myocardial infarction in the dog.
    Canadian journal of physiology and pharmacology, 1988, Volume: 66, Issue:4

    Topics: Animals; Dogs; Echocardiography; Heart; Heart Rupture; Hemodynamics; Hydroxyproline; Ibuprofen; Myoc

1988
Animal models for protecting ischemic myocardium: results of the NHLBI Cooperative Study. Comparison of unconscious and conscious dog models.
    Circulation research, 1985, Volume: 56, Issue:5

    Topics: Anesthesia; Animal Testing Alternatives; Animals; Arterial Occlusive Diseases; Coronary Circulation;

1985
Delayed effects of early infarct-limiting therapies on healing after myocardial infarction.
    Circulation, 1985, Volume: 72, Issue:4

    Topics: Animals; Collagen; Dogs; Epoprostenol; Hemodynamics; Hydroxyproline; Ibuprofen; Macrophages; Myocard

1985
Safety of ibuprofen for acute myocardial infarction pericarditis.
    The American journal of cardiology, 1986, Apr-01, Volume: 57, Issue:10

    Topics: Humans; Ibuprofen; Myocardial Infarction; Pericarditis

1986
Lowering pulmonary artery pressure in a patient with severe acute respiratory failure.
    Intensive care medicine, 1985, Volume: 11, Issue:1

    Topics: Blood Pressure; Humans; Hypertension, Pulmonary; Ibuprofen; Male; Middle Aged; Myocardial Infarction

1985
Evaluation of a rat model for assessing interventions to salvage ischaemic myocardium: effects of ibuprofen and verapamil.
    Cardiovascular research, 1985, Volume: 19, Issue:3

    Topics: Animals; Body Weight; Creatine Kinase; Disease Models, Animal; Ibuprofen; Male; Myocardial Infarctio

1985
Effect of ibuprofen on the healing phase of experimental myocardial infarction in the rat.
    The American journal of cardiology, 1985, Jun-01, Volume: 55, Issue:13 Pt 1

    Topics: Animals; Cell Count; Collagen; Hydroxyproline; Ibuprofen; Leukocytes; Male; Myocardial Infarction; R

1985
Ventricular septal rupture during ibuprofen therapy for pericarditis after acute myocardial infarction.
    The American journal of cardiology, 1985, Jun-01, Volume: 55, Issue:13 Pt 1

    Topics: Aged; Female; Heart Rupture; Heart Septum; Humans; Ibuprofen; Male; Middle Aged; Myocardial Infarcti

1985