ticlopidine has been researched along with Adverse Drug Event in 36 studies
Ticlopidine: An effective inhibitor of platelet aggregation commonly used in the placement of STENTS in CORONARY ARTERIES.
ticlopidine : A thienopyridine that is 4,5,6,7-tetrahydrothieno[3,2-c]pyridine in which the hydrogen attached to the nitrogen is replaced by an o-chlorobenzyl group.
Excerpt | Relevance | Reference |
---|---|---|
" This study aimed to assess the risk of bleeding complications in patients receiving clopidogrel at the time of cardiac device surgery." | 7.78 | Clopidogrel increases bleeding complications in patients undergoing heart rhythm device procedures. ( Acheré, C; Boulé, S; Brigadeau, F; Goéminne-Boulé, C; Guédon-Moreau, L; Kacet, S; Klug, D; Kouakam, C; Lacroix, D; Marquié, C; Vanesson-Bricout, C, 2012) |
"Clinicians will be able to understand the safety profile of using different doses of clopidogrel and the incidence of bleeding when used alone or in combination with other antiplatelet agents." | 4.87 | The safety of clopidogrel. ( Kleiman, NS; Mangalpally, KK, 2011) |
"Sarpogrelate-containing triple antiplatelet therapy demonstrated comparable rates of MACCE prevention to the conventional dual antiplatelet therapy after PCI without significantly increasing bleeding risk during the two-year follow-up period." | 3.83 | Antiplatelet Therapy of Cilostazol or Sarpogrelate with Aspirin and Clopidogrel after Percutaneous Coronary Intervention: A Retrospective Cohort Study Using the Korean National Health Insurance Claim Database. ( Bae, SK; Kim, GJ; Kim, JH; Lee, J; Lee, S; Lim, HS; Noh, Y; Oh, E; Shin, S, 2016) |
"This ecological comparison of bleeding reports and dispensed prescriptions showed a signal towards a higher prevalence of bleeding reports in women on clopidogrel treatment while the opposite was found for low-dose aspirin." | 3.80 | Sex differences in spontaneous reports on adverse bleeding events of antithrombotic treatment. ( Holm, L; Loikas, D; Malmström, RE; Mejyr, S; Rydberg, DM; Schenck-Gustafsson, K; von Euler, M; Wettermark, B, 2014) |
" This study aimed to assess the risk of bleeding complications in patients receiving clopidogrel at the time of cardiac device surgery." | 3.78 | Clopidogrel increases bleeding complications in patients undergoing heart rhythm device procedures. ( Acheré, C; Boulé, S; Brigadeau, F; Goéminne-Boulé, C; Guédon-Moreau, L; Kacet, S; Klug, D; Kouakam, C; Lacroix, D; Marquié, C; Vanesson-Bricout, C, 2012) |
" Bleeding caused by some combination of nonsteroidal antiinflammatory drugs (NSAIDs), cyclooxygenase-2-selective NSAIDS, aspirin, and clopidogrel was the most common reason for ADR-related MICU admissions." | 3.74 | Admissions to a medical intensive care unit related to adverse drug reactions. ( Rivkin, A, 2007) |
" Secondly, the efficacy and safety disparity of clopidogrel, statins and irinotecan each among races and genetic variants are discussed to illustrate that pharmacogenetic knowledge is important for the interpretation and prediction of drug interaction-induced adverse events, whereas drug interaction -induced adverse events are equally informative for identifying genes-based mechanisms involved." | 2.46 | Ongoing challenges in drug interaction safety: from exposure to pharmacogenomics. ( Bai, JP, 2010) |
"Patients in nursing homes are often treated with many drugs concurrently (polypharmacy), which increases the risk of drug-drug interactions." | 1.40 | [Drug-drug interactions in nursing home patients]. ( Slørdal, L; Spigset, O; Staurset, HB; Søraas, IA, 2014) |
" We proposed a systematic classification scheme using FDA-approved drug labeling to assess the DILI potential of drugs, which yielded a benchmark dataset with 287 drugs representing a wide range of therapeutic categories and daily dosage amounts." | 1.37 | FDA-approved drug labeling for the study of drug-induced liver injury. ( Chen, M; Fang, H; Liu, Z; Shi, Q; Tong, W; Vijay, V, 2011) |
"Bupropion is an atypical antidepressant that is biotransformed in humans to its major active metabolite hydroxybupropion by cytochrome P450 2B6 (CYP2B6)." | 1.37 | Drug interaction study between bupropion and ticlopidine in male CF-1 mice. ( Hassan, HE; Moeller, BM; Molnari, JC; Myers, AL, 2011) |
"We assessed the safety of thrombolysis under APs in 11,865 patients compliant with the European license criteria and recorded between 2002 and 2007 in the Safe Implementation of Treatments in Stroke (SITS) International Stroke Thrombolysis Register (SITS-ISTR)." | 1.36 | Safety of intravenous thrombolysis for acute ischemic stroke in patients receiving antiplatelet therapy at stroke onset. ( Ahmed, N; Diedler, J; Ford, GA; Lees, KR; Luijckx, GJ; Overgaard, K; Ringleb, P; Soinne, L; Sykora, M; Uyttenboogaart, M; Wahlgren, N, 2010) |
" It is concluded that MEGX test widens opportunities for personalization and safe pharmacotherapy." | 1.36 | [Individual pharmacotherapy safety in the assessment of cytochrome P-450 3A4 (CYP3A4) isoenzyme activity]. ( Kukes, IV; Paukov, SV; Ruvinov, IuV; Sivkov, AS, 2010) |
"Ticlopidine has a relative high rate of side-effects." | 1.34 | Incidence of side-effects of ticlopidine after sirolimus-eluting stent implantation. ( Fukushima, K; Kobayashi, Y; Komuro, I; Kuroda, N; Miyazaki, A; Nakamura, Y; Nakayama, T; Okuno, T; Sakakibara, M; Shimizu, Y, 2007) |
"5 million adverse drug reaction (ADR) reports for 8620 drugs/biologics that are listed for 1191 Coding Symbols for Thesaurus of Adverse Reaction (COSTAR) terms of adverse effects." | 1.32 | Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling. ( Benz, RD; Contrera, JF; Kruhlak, NL; Matthews, EJ; Weaver, JL, 2004) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 7 (19.44) | 29.6817 |
2010's | 28 (77.78) | 24.3611 |
2020's | 1 (2.78) | 2.80 |
Authors | Studies |
---|---|
Matthews, EJ | 1 |
Kruhlak, NL | 1 |
Weaver, JL | 1 |
Benz, RD | 1 |
Contrera, JF | 1 |
Chen, M | 1 |
Vijay, V | 1 |
Shi, Q | 2 |
Liu, Z | 2 |
Fang, H | 2 |
Tong, W | 2 |
Dawson, S | 1 |
Stahl, S | 1 |
Paul, N | 1 |
Barber, J | 1 |
Kenna, JG | 1 |
Ding, D | 1 |
Kelly, R | 1 |
Sakatis, MZ | 1 |
Reese, MJ | 1 |
Harrell, AW | 1 |
Taylor, MA | 4 |
Baines, IA | 1 |
Chen, L | 1 |
Bloomer, JC | 1 |
Yang, EY | 1 |
Ellens, HM | 1 |
Ambroso, JL | 1 |
Lovatt, CA | 1 |
Ayrton, AD | 1 |
Clarke, SE | 1 |
Godwin, AC | 3 |
Hoque, S | 3 |
Bennett, CL | 3 |
Parker, WA | 1 |
Bhatt, DL | 1 |
Prats, J | 1 |
Day, JRS | 1 |
Steg, PG | 1 |
Stone, GW | 1 |
Hamm, CW | 1 |
Mahaffey, KW | 1 |
Price, MJ | 1 |
Gibson, CM | 1 |
White, HD | 1 |
Storey, RF | 1 |
Martin, AC | 1 |
Houssany-Pissot, S | 1 |
Zlotnik, D | 1 |
Taylor, G | 1 |
Godier, A | 1 |
Tan, SSN | 1 |
Fong, AYY | 1 |
Mejin, M | 1 |
Gerunsin, J | 1 |
Kong, KL | 1 |
Chin, FYY | 1 |
Tiong, LL | 1 |
Lim, MSH | 1 |
Asri, S | 1 |
Khiew, NZ | 1 |
Voon, CY | 1 |
Mohd Amin, NH | 1 |
Cham, YL | 1 |
Koh, KT | 1 |
Oon, YY | 1 |
Ong, TK | 1 |
Kim, SG | 1 |
Shim, KS | 1 |
Lee, DW | 1 |
Kim, EJ | 1 |
Lee, SG | 1 |
Lee, JH | 1 |
An, JH | 1 |
Blais, DM | 1 |
Zukkoor, SM | 1 |
Hayes, C | 1 |
Pickworth, KK | 1 |
Porter, K | 1 |
Firstenberg, MS | 1 |
Rydberg, DM | 1 |
Holm, L | 1 |
Mejyr, S | 1 |
Loikas, D | 1 |
Schenck-Gustafsson, K | 1 |
von Euler, M | 1 |
Wettermark, B | 1 |
Malmström, RE | 1 |
Søraas, IA | 1 |
Staurset, HB | 1 |
Slørdal, L | 1 |
Spigset, O | 1 |
Tong, V | 1 |
Raynor, DK | 1 |
Blalock, SJ | 1 |
Aslani, P | 1 |
Koziolova, NA | 1 |
Nishimura, AA | 1 |
Shirts, BH | 1 |
Salama, J | 1 |
Smith, JW | 1 |
Devine, B | 1 |
Tarczy-Hornoch, P | 1 |
Noh, Y | 1 |
Lee, J | 1 |
Shin, S | 1 |
Lim, HS | 1 |
Bae, SK | 1 |
Oh, E | 1 |
Kim, GJ | 1 |
Kim, JH | 1 |
Lee, S | 1 |
Payne, CD | 1 |
Li, YG | 1 |
Brandt, JT | 1 |
Jakubowski, JA | 1 |
Small, DS | 1 |
Farid, NA | 1 |
Salazar, DE | 1 |
Winters, KJ | 1 |
Heer, T | 1 |
Juenger, C | 1 |
Gitt, AK | 1 |
Bauer, T | 1 |
Towae, F | 1 |
Zahn, R | 1 |
Senges, J | 1 |
Zeymer, U | 1 |
Mirabella, F | 1 |
Francaviglia, B | 1 |
Capodanno, D | 1 |
Di Salvo, ME | 1 |
Galassi, AR | 1 |
Ussia, GP | 1 |
Capranzano, P | 1 |
Tamburino, C | 1 |
Diedler, J | 1 |
Ahmed, N | 1 |
Sykora, M | 1 |
Uyttenboogaart, M | 1 |
Overgaard, K | 1 |
Luijckx, GJ | 1 |
Soinne, L | 1 |
Ford, GA | 1 |
Lees, KR | 1 |
Wahlgren, N | 1 |
Ringleb, P | 1 |
Kramer, E | 1 |
Hadad, E | 1 |
Westreich, M | 1 |
Shalom, A | 1 |
Bai, JP | 1 |
Hassan, AE | 1 |
Zacharatos, H | 1 |
Vazquez, G | 1 |
Rodriguez, GJ | 1 |
Suri, MF | 1 |
Tummala, RP | 1 |
Taylor, RA | 1 |
Qureshi, AI | 1 |
Donohue, MM | 1 |
Tirschwell, DL | 1 |
Mangalpally, KK | 1 |
Kleiman, NS | 1 |
Sivkov, AS | 1 |
Paukov, SV | 1 |
Ruvinov, IuV | 1 |
Kukes, IV | 1 |
Machado-Alba, JE | 1 |
Giraldo-Giraldo, C | 1 |
Moncada-Escobar, JC | 1 |
Molnari, JC | 1 |
Hassan, HE | 1 |
Moeller, BM | 1 |
Myers, AL | 1 |
Messinger-Rapport, BJ | 1 |
Morley, JE | 1 |
Thomas, DR | 1 |
Gammack, JK | 1 |
Dolgin, E | 1 |
Miyaji, Y | 1 |
Makino, C | 1 |
Kurihara, A | 1 |
Suzuki, W | 1 |
Okazaki, O | 1 |
Boulé, S | 1 |
Marquié, C | 1 |
Vanesson-Bricout, C | 1 |
Kouakam, C | 1 |
Brigadeau, F | 1 |
Guédon-Moreau, L | 1 |
Acheré, C | 1 |
Goéminne-Boulé, C | 1 |
Lacroix, D | 1 |
Klug, D | 1 |
Kacet, S | 1 |
Fukushima, K | 1 |
Kobayashi, Y | 1 |
Okuno, T | 1 |
Nakamura, Y | 1 |
Sakakibara, M | 1 |
Nakayama, T | 1 |
Kuroda, N | 1 |
Miyazaki, A | 1 |
Shimizu, Y | 1 |
Komuro, I | 1 |
Rivkin, A | 1 |
Gallagher, P | 1 |
Ryan, C | 1 |
Byrne, S | 1 |
Kennedy, J | 1 |
O'Mahony, D | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Clinical Trial Comparing Cangrelor to Clopidogrel Standard of Care Therapy in Subjects Who Require Percutaneous Coronary Intervention (CHAMPION PHOENIX)[NCT01156571] | Phase 3 | 11,145 participants (Actual) | Interventional | 2010-09-30 | Completed | ||
A Clinical Trial Comparing Cangrelor to Clopidogrel in Subjects Who Require Percutaneous Coronary Intervention (PCI).[NCT00305162] | Phase 3 | 8,882 participants (Actual) | Interventional | 2006-04-30 | Terminated (stopped due to Insufficient evidence of the clinical effectiveness of cangrelor) | ||
A Clinical Trial Comparing Treatment With Cangrelor (in Combination With Usual Care) to Usual Care, in Subjects Who Require Percutaneous Coronary Intervention (PCI).[NCT00385138] | Phase 3 | 5,364 participants (Actual) | Interventional | 2006-09-30 | Terminated (stopped due to Insufficient evidence of the clinical effectiveness of cangrelor) | ||
PPD Trial Pilot Study: Plavix, Prasugrel and Drug Eluting Stents[NCT01103843] | 1,000 participants (Anticipated) | Interventional | 2010-04-30 | Recruiting | |||
Pharmacist-led Intervention to Reduce Potentially Inappropriate Prescription in Elderly and Polypharmacy Patients at Primary Care Setting (PHARM-PC) Cluster Randomized Trial[NCT02224833] | 549 participants (Actual) | Interventional | 2015-01-31 | Completed | |||
Prevention of Adverse Drug Events (ADEs) in Hospitalised Older Patients Using STOPP/START Criteria[NCT01467050] | Phase 4 | 732 participants (Actual) | Interventional | 2011-06-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Clinical Events Committee (CEC)-adjudicated results (modified intent-to-treat [mITT] population) (NCT01156571)
Timeframe: 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Treatment Arm | 257 |
Clopidogrel Treatment Arm | 322 |
GUSTO = Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries trial (NCT01156571)
Timeframe: 48 hours after randomization
Intervention | participants (Number) | ||||||
---|---|---|---|---|---|---|---|
GUSTO severe/life threatening | GUSTO moderate | GUSTO severe or moderate | TIMI major | TIMI minor | TIMI major or minor | Any blood transfusion | |
Cangrelor Treatment Arm | 9 | 22 | 31 | 5 | 9 | 14 | 25 |
Clopidogrel Treatment Arm | 6 | 13 | 19 | 5 | 3 | 8 | 16 |
CEC-adjudicated results (mITT population) (NCT01156571)
Timeframe: 48 hours after randomization
Intervention | participants (Number) | |||
---|---|---|---|---|
Stent Thrombosis | Death | MI (myocardial infarction) | IDR (ischemia-driven revascularization) | |
Cangrelor Treatment Arm | 46 | 18 | 207 | 28 |
Clopidogrel Treatment Arm | 74 | 18 | 255 | 38 |
(a patient could have multiple procedural events) (NCT00305162)
Timeframe: during index PCI
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 127 |
Clopidogrel Arm | 141 |
Major bleeding (non-CABG-related) - Safety population (NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 151 |
Clopidogrel Arm | 120 |
excludes ACUITY major bleeding for which the only qualifying event was hematoma >/= 5 cm (NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 78 |
Clopidogrel Arm | 65 |
(excluding STEMI) (NCT00305162)
Timeframe: randomization through 1 year after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 116 |
Clopidogrel Arm | 120 |
(NCT00305162)
Timeframe: randomization through 30 days after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 34 |
Clopidogrel Arm | 29 |
(composite incidence) (NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 285 |
Clopidogrel Arm | 261 |
(composite incidence) (NCT00305162)
Timeframe: randomization through 30 days after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 321 |
Clopidogrel Arm | 298 |
(composite incidence) (NCT00305162)
Timeframe: randomization through 30 days after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 343 |
Clopidogrel Arm | 327 |
(composite incidence) (NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 290 |
Clopidogrel Arm | 276 |
Major bleeding (non-CABG-related) - Safety population (NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 10 |
Clopidogrel Arm | 11 |
(NCT00305162)
Timeframe: randomization through 30 days after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 44 |
Clopidogrel Arm | 52 |
(NCT00305162)
Timeframe: randomization through 30 days after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 297 |
Clopidogrel Arm | 276 |
(NCT00305162)
Timeframe: randomization through 30 days after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 5 |
Clopidogrel Arm | 7 |
Major bleeding (non-CABG-related) - Safety population (NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 19 |
Clopidogrel Arm | 14 |
(NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 8 |
Clopidogrel Arm | 5 |
(NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) |
---|---|
Cangrelor Arm | 13 |
Clopidogrel Arm | 23 |
"Stroke is defined as a sudden, focal neurological defect resulting from a cerebrovascular cause that is not reversible within 24 hours and not due to a readily identifiable cause such as a tumor or trauma. All suspected strokes were reviewed and adjudicated by the Clinical Events Committee (CEC) who considered all clinically relevant information and imaging studies to classify all strokes as:~primary hemorrhagic - stroke with focal collections of intracranial blood~ischemic cerebral infarction - stroke without focal collections of intracranial blood~infarction with hemorrhagic conversion - cerebral infarction with blood thought to represent hemorrhagic conversion and not primary bleeding~uncertain - no imaging or autopsy data are available." (NCT00305162)
Timeframe: randomization through 48 hours after randomization
Intervention | participants (Number) | |||
---|---|---|---|---|
primary hemorrhagic | infarction with hemorrhagic conversion | cerebral infarction | uncertain type | |
Cangrelor Arm | 1 | 0 | 5 | 0 |
Clopidogrel Arm | 0 | 0 | 7 | 0 |
Major bleeding (non-CABG-related) - Safety population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 145 |
Clopidogrel | 91 |
Major bleeding (non-CABG-related) - Safety population excludes ACUITY major bleeding for which the only qualifying event was hematoma >/= 5 cm. (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 43 |
Clopidogrel | 29 |
mITT population (NCT00385138)
Timeframe: randomization through 1 year post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 94 |
Clopidogrel | 113 |
mITT population (NCT00385138)
Timeframe: randomization through 30 days post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 35 |
Clopidogrel | 45 |
mITT population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 6 |
Clopidogrel | 18 |
mITT population (NCT00385138)
Timeframe: randomization through 30 days post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 213 |
Clopidogrel | 233 |
mITT population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 180 |
Clopidogrel | 204 |
mITT population (NCT00385138)
Timeframe: randomization through 30 days post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 227 |
Clopidogrel | 249 |
mITT population; (composite incidence) (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 185 |
Clopidogrel | 210 |
Major bleeding (non-CABG-related) - Safety population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 9 |
Clopidogrel | 6 |
mITT population (NCT00385138)
Timeframe: randomization through 30 days post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 37 |
Clopidogrel | 46 |
mITT population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 19 |
Clopidogrel | 24 |
mITT population (NCT00385138)
Timeframe: randomization through 30 days post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 189 |
Clopidogrel | 201 |
mITT population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 177 |
Clopidogrel | 191 |
mITT population A patient could have multiple procedural events. (NCT00385138)
Timeframe: During index PCI
Intervention | participants (Number) |
---|---|
Cangrelor | 122 |
Clopidogrel | 142 |
mITT population (NCT00385138)
Timeframe: randomization through 30 days post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 15 |
Clopidogrel | 28 |
mITT population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 5 |
Clopidogrel | 16 |
mITT (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 7 |
Clopidogrel | 5 |
mITT population (NCT00385138)
Timeframe: randomization through 30 days post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 6 |
Clopidogrel | 5 |
Major bleeding (non-CABG-related) - Safety population (NCT00385138)
Timeframe: randomization through 48 hours post randomization
Intervention | participants (Number) |
---|---|
Cangrelor | 4 |
Clopidogrel | 9 |
5 reviews available for ticlopidine and Adverse Drug Event
Article | Year |
---|---|
[Management of the bleeding risk associated with antiplatelet agents].
Topics: Adenosine; Aspirin; Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Hemorrhage; Humans | 2017 |
[Antiplatelet therapy in atherosclerosis of various localizations: acute and stable States].
Topics: Acute Coronary Syndrome; Aspirin; Atherosclerosis; Drug Therapy, Combination; Drug-Related Side Effe | 2014 |
Ongoing challenges in drug interaction safety: from exposure to pharmacogenomics.
Topics: Administration, Oral; Camptothecin; Clopidogrel; Drug Evaluation; Drug Interactions; Drug-Related Si | 2010 |
Implications of pharmacogenetic testing for patients taking warfarin or clopidogrel.
Topics: Anticoagulants; Clopidogrel; Cytochrome P-450 Enzyme System; Drug-Related Side Effects and Adverse R | 2011 |
The safety of clopidogrel.
Topics: Acute Coronary Syndrome; Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Hemorrhage; H | 2011 |
2 trials available for ticlopidine and Adverse Drug Event
Article | Year |
---|---|
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Characteristics of dyspnoea and associated clinical outcomes in the CHAMPION PHOENIX study.
Topics: Adenosine Monophosphate; Aged; Clopidogrel; Coronary Occlusion; Double-Blind Method; Drug-Related Si | 2017 |
Switching directly to prasugrel from clopidogrel results in greater inhibition of platelet aggregation in aspirin-treated subjects.
Topics: Adenosine Diphosphate; Adult; Aspirin; Clopidogrel; Drug-Related Side Effects and Adverse Reactions; | 2008 |
29 other studies available for ticlopidine and Adverse Drug Event
Article | Year |
---|---|
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
Topics: Adverse Drug Reaction Reporting Systems; Artificial Intelligence; Computers; Databases, Factual; Dru | 2004 |
FDA-approved drug labeling for the study of drug-induced liver injury.
Topics: Animals; Benchmarking; Biomarkers, Pharmacological; Chemical and Drug Induced Liver Injury; Drug Des | 2011 |
In vitro inhibition of the bile salt export pump correlates with risk of cholestatic drug-induced liver injury in humans.
Topics: Animals; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters | 2012 |
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
Topics: Animals; Anti-Infective Agents; Anti-Inflammatory Agents; Chemical and Drug Induced Liver Injury; Da | 2011 |
Preclinical strategy to reduce clinical hepatotoxicity using in vitro bioactivation data for >200 compounds.
Topics: Chemical and Drug Induced Liver Injury; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme | 2012 |
Systemic Barriers and Potential Concerns from Reporting Serious Adverse Drug Reactions.
Topics: Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Humans; Immunotherapy; Thalidomide; Ti | 2022 |
Systemic Barriers and Potential Concerns from Reporting Serious Adverse Drug Reactions.
Topics: Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Humans; Immunotherapy; Thalidomide; Ti | 2022 |
Systemic Barriers and Potential Concerns from Reporting Serious Adverse Drug Reactions.
Topics: Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Humans; Immunotherapy; Thalidomide; Ti | 2022 |
Systemic Barriers and Potential Concerns from Reporting Serious Adverse Drug Reactions.
Topics: Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Humans; Immunotherapy; Thalidomide; Ti | 2022 |
Association of CYP2C19*2 polymorphism with clopidogrel response and 1-year major adverse cardiovascular events in a multiethnic population with drug-eluting stents.
Topics: Alleles; Cardiovascular Diseases; Clopidogrel; Cohort Studies; Cytochrome P-450 CYP2C19; Drug-Elutin | 2017 |
Intramuscular hematoma with motor weakness after trigger point injection: A case report.
Topics: Aged; Biopsy, Fine-Needle; Buttocks; Clopidogrel; Drug-Related Side Effects and Adverse Reactions; F | 2017 |
Bleeding outcomes associated with coronary artery bypass graft surgery and recent clopidogrel exposure.
Topics: Causality; Clopidogrel; Comorbidity; Coronary Artery Bypass; Drug-Related Side Effects and Adverse R | 2013 |
Sex differences in spontaneous reports on adverse bleeding events of antithrombotic treatment.
Topics: Adolescent; Adult; Adverse Drug Reaction Reporting Systems; Aged; Aspirin; Child; Child, Preschool; | 2014 |
[Drug-drug interactions in nursing home patients].
Topics: Anti-Inflammatory Agents, Non-Steroidal; Antiparkinson Agents; Clopidogrel; Databases, Factual; Dopa | 2014 |
Exploring consumer opinions on the presentation of side-effects information in Australian Consumer Medicine Information leaflets.
Topics: Aged; Antihypertensive Agents; Attitude; Clopidogrel; Cognition; Drug-Related Side Effects and Adver | 2016 |
Physician perspectives of CYP2C19 and clopidogrel drug-gene interaction active clinical decision support alerts.
Topics: Adult; Adverse Drug Reaction Reporting Systems; Clopidogrel; Cytochrome P-450 CYP2C19; Decision Supp | 2016 |
Antiplatelet Therapy of Cilostazol or Sarpogrelate with Aspirin and Clopidogrel after Percutaneous Coronary Intervention: A Retrospective Cohort Study Using the Korean National Health Insurance Claim Database.
Topics: Aspirin; Cilostazol; Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Hemorrhage; Human | 2016 |
Efficacy and safety of optimized antithrombotic therapy with aspirin, clopidogrel and enoxaparin in patients with non-ST segment elevation acute coronary syndromes in clinical practice.
Topics: Acute Coronary Syndrome; Aged; Aspirin; Clopidogrel; Drug Evaluation; Drug Therapy, Combination; Dru | 2009 |
Treatment of multilesion coronary artery disease with simultaneous drug-eluting and bare-metal stent implantation: clinical follow up and angiographic mid-term results.
Topics: Abciximab; Adult; Aged; Aged, 80 and over; Angioplasty, Balloon, Coronary; Antibodies, Monoclonal; A | 2009 |
Safety of intravenous thrombolysis for acute ischemic stroke in patients receiving antiplatelet therapy at stroke onset.
Topics: Acute Disease; Adolescent; Adult; Aged; Aged, 80 and over; Aspirin; Brain Ischemia; Cerebral Hemorrh | 2010 |
Lack of complications in skin surgery of patients receiving clopidogrel as compared with patients taking aspirin, warfarin, and controls.
Topics: Aged; Anticoagulants; Aspirin; Case-Control Studies; Clopidogrel; Dermatologic Surgical Procedures; | 2010 |
Low risk of intracranial and systemic hemorrhages in patients on dual antiplatelet treatment beyond 1 month following neuroendovascular angioplasty and/or stent placement.
Topics: Angioplasty; Aspirin; Blood Vessel Prosthesis; Clopidogrel; Combined Modality Therapy; Comorbidity; | 2012 |
[Individual pharmacotherapy safety in the assessment of cytochrome P-450 3A4 (CYP3A4) isoenzyme activity].
Topics: Atorvastatin; Clinical Trials as Topic; Clopidogrel; Cytochrome P-450 CYP3A; Cytochrome P-450 CYP3A | 2010 |
[Active pharmacosurveillance of patients affiliated to the Colombian general social security/health system].
Topics: Adverse Drug Reaction Reporting Systems; Calcium Channel Blockers; Clopidogrel; Colombia; Diphosphon | 2010 |
Drug interaction study between bupropion and ticlopidine in male CF-1 mice.
Topics: Animals; Area Under Curve; Aryl Hydrocarbon Hydroxylases; Brain; Bupropion; Cytochrome P-450 CYP2B6; | 2011 |
Clinical update on nursing home medicine: 2011.
Topics: Anti-Ulcer Agents; Anticoagulants; Atrial Fibrillation; Clopidogrel; Clostridioides difficile; Delir | 2011 |
Preemptive genotyping trialed to prevent adverse drug reactions.
Topics: Clinical Trials as Topic; Clopidogrel; Drug-Related Side Effects and Adverse Reactions; Genetic Test | 2011 |
In vitro evaluation of the potential for drug-induced toxicity based on (35)S-labeled glutathione adduct formation and daily dose.
Topics: Diclofenac; Drug Administration Schedule; Drug-Related Side Effects and Adverse Reactions; Glutathio | 2012 |
Clopidogrel increases bleeding complications in patients undergoing heart rhythm device procedures.
Topics: Cardiac Resynchronization Therapy; Case-Control Studies; Clopidogrel; Comorbidity; Drug-Related Side | 2012 |
Incidence of side-effects of ticlopidine after sirolimus-eluting stent implantation.
Topics: Aged; Blood Vessel Prosthesis Implantation; Chemical and Drug Induced Liver Injury; Coronary Thrombo | 2007 |
Admissions to a medical intensive care unit related to adverse drug reactions.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Clopidogrel; Drug-Related Side Effects and Adverse | 2007 |
STOPP (Screening Tool of Older Person's Prescriptions) and START (Screening Tool to Alert doctors to Right Treatment). Consensus validation.
Topics: Abbreviations as Topic; Age Factors; Aged; Analgesics; Anti-Inflammatory Agents, Non-Steroidal; Aspi | 2008 |
STOPP (Screening Tool of Older Person's Prescriptions) and START (Screening Tool to Alert doctors to Right Treatment). Consensus validation.
Topics: Abbreviations as Topic; Age Factors; Aged; Analgesics; Anti-Inflammatory Agents, Non-Steroidal; Aspi | 2008 |
STOPP (Screening Tool of Older Person's Prescriptions) and START (Screening Tool to Alert doctors to Right Treatment). Consensus validation.
Topics: Abbreviations as Topic; Age Factors; Aged; Analgesics; Anti-Inflammatory Agents, Non-Steroidal; Aspi | 2008 |
STOPP (Screening Tool of Older Person's Prescriptions) and START (Screening Tool to Alert doctors to Right Treatment). Consensus validation.
Topics: Abbreviations as Topic; Age Factors; Aged; Analgesics; Anti-Inflammatory Agents, Non-Steroidal; Aspi | 2008 |