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Prasugrel: Drug information

Prasugrel: Drug information
2024© UpToDate, Inc. and its affiliates and/or licensors. All Rights Reserved.
For additional information see "Prasugrel: Patient drug information"

For abbreviations, symbols, and age group definitions show table
ALERT: US Boxed Warning
Bleeding risk:

Prasugrel can cause significant, sometimes fatal, bleeding. Do not use prasugrel in patients with active pathological bleeding or a history of transient ischemic attack (TIA) or stroke.

In patients ≥75 years, prasugrel is generally not recommended because of the increased risk of fatal and intracranial bleeding and uncertain benefit, except in high-risk situations (patients with diabetes or a history of myocardial infarction [MI]) in which its effect appears to be greater and its use may be considered.

Do not start prasugrel in patients likely to undergo urgent coronary artery bypass graft (CABG) surgery. When possible, discontinue prasugrel at least 7 days prior to any surgery.

Additional risk factors for bleeding include body weight <60 kg, propensity to bleed, and concomitant use of medications that increase the risk of bleeding (eg, warfarin, heparin, fibrinolytic therapy, long-term use of nonsteroidal anti-inflammatory drugs [NSAIDs]).

Suspect bleeding in any patient who is hypotensive and has recently undergone coronary angiography, percutaneous coronary intervention (PCI), CABG, or other surgical procedures in the setting of prasugrel.

If possible, manage bleeding without discontinuing prasugrel. Discontinuing prasugrel, particularly in the first few weeks after acute coronary syndrome (ACS), increases the risk of subsequent cardiovascular events.

Brand Names: US
  • Effient
Brand Names: Canada
  • JAMP Prasugrel
Pharmacologic Category
  • Antiplatelet Agent;
  • Antiplatelet Agent, Thienopyridine;
  • P2Y12 Antagonist
Dosing: Adult

Dosage guidance:

Safety: Avoid use in patients with active bleeding or a history of stroke or transient ischemic attack. In patients who require concomitant therapeutic anticoagulation, antiplatelet selection and/or duration of therapy may differ in order to balance risks for thrombosis and bleeding (Ref).

Acute coronary syndrome managed by percutaneous coronary intervention

Acute coronary syndrome (non-ST-elevation myocardial infarction, unstable angina, or ST-elevation myocardial infarction) managed by percutaneous coronary intervention:

Note: For ST-elevation myocardial infarction managed with primary percutaneous coronary intervention (PCI), administer as early as possible after diagnosis. For non-ST-elevation acute coronary syndromes, administer after angiography once clinician decides to perform PCI; if PCI is not performed, use an alternative P2Y12 inhibitor (Ref).

Loading dose: Oral: 60 mg once before PCI in combination with aspirin and a parenteral anticoagulant; followed by maintenance dosing. If coronary angiography is planned soon after diagnosis, it is reasonable to delay the initial loading dose until after coronary anatomy is known (Ref).

Maintenance dose:

Oral: ≥60 kg: 10 mg once daily in combination with aspirin beginning the day after PCI (Ref).

East Asian descent: After 30 days, consider reducing to 5 mg once daily in patients of East Asian descent in order to decrease bleeding risk. Note: Patients of East Asian descent display a greater antiplatelet response compared to white patients. A reduced dose of prasugrel (5 mg once daily) after 30 days had a similar reduction in thrombotic events and fewer bleeding events compared to continuation of a higher maintenance dose (10 mg once daily) (Ref).

Oral: <60 kg: 5 mg once daily in combination with aspirin beginning the day after PCI (Ref). An alternative P2Y12 inhibitor may be considered if bleeding is major concern (Ref).

Duration of therapy:

Preferred approach: Continue prasugrel plus aspirin (dual antiplatelet therapy [DAPT]) for ≥12 months unless major bleeding is a concern. For patients at high risk of bleeding or who experience overt bleeding, DAPT for 6 months may be reasonable. If there have been no major bleeding complications after 12 months, continuation of DAPT may be considered. Reevaluate the need for DAPT at regular intervals based on bleeding and thrombotic risks. When DAPT is complete, discontinue prasugrel and continue aspirin indefinitely for secondary prevention (Ref).

Alternative approach in select patients to minimize bleeding events: Prasugrel in combination with aspirin (DAPT) should be continued for 1 to 3 months after PCI, then discontinue aspirin and continue prasugrel monotherapy. When prasugrel is discontinued, restart aspirin for secondary prevention (Ref).

Transitioning between P2Y12 inhibitors:

Note: This provides general guidance on transitioning between P2Y12 inhibitors.

Transitioning from another P2Y12 inhibitor to prasugrel:

Transitioning from clopidogrel:

≤30 days after acute coronary syndrome (ACS) or PCI: Give prasugrel 60 mg loading dose once (irrespective of timing of previous clopidogrel dose), followed the next day by 10 mg once daily (≥60 kg) or 5 mg once daily (<60 kg) (Ref).

>30 days after ACS or PCI: Give prasugrel 10 mg once daily (≥60 kg) or 5 mg once daily (<60 kg) beginning 24 hours after the last dose of clopidogrel (Ref).

Transitioning from ticagrelor: Give prasugrel 60 mg loading dose 12 to 24 hours after the last dose of ticagrelor, followed the next day by 10 mg once daily (≥60 kg) or 5 mg once daily (<60 kg) (Ref).

Dosage adjustment for concomitant therapy: Significant drug interactions exist, requiring dose/frequency adjustment or avoidance. Consult drug interactions database for more information.

Dosing: Kidney Impairment: Adult

No dosage adjustment necessary; use caution in moderate to severe impairment (patients are generally at higher risk of bleeding).

Hemodialysis: Not dialyzable (Ref).

Dosing: Hepatic Impairment: Adult

Mild to moderate hepatic impairment (Child-Pugh class A and B): No dosage adjustment necessary for mild-to-moderate hepatic impairment.

Severe hepatic impairment (Child-Pugh class C): There are no dosage adjustments provided in the manufacturer's labeling (has not been studied); use caution (patients are generally at higher risk of bleeding).

Dosing: Older Adult

Patients ≥75 years of age: Use is generally not recommended; may be considered in high-risk situations (eg, patients with diabetes or history of myocardial infarction).

Acute coronary syndrome (non-ST-elevation myocardial infarction, unstable angina, or ST-elevation myocardial infarction) managed by percutaneous coronary intervention:

Patients ≥75 years of age:

Loading dose: See adult dosing

Maintenance dose: Oral: 5 mg once daily in combination with aspirin beginning the day after PCI. An alternative P2Y12 inhibitor may be considered if bleeding is a major concern (Ref).

Adverse Reactions

The following adverse drug reactions and incidences are derived from product labeling unless otherwise specified.

1% to 10%:

Cardiovascular: Hypertension (8%), hypotension (4%), atrial fibrillation (3%), bradycardia (3%), peripheral edema (3%)

Central nervous system: Headache (6%), dizziness (4%), fatigue (4%), noncardiac chest pain (3%)

Dermatologic: Skin rash (3%)

Endocrine & metabolic: Hypercholesterolemia (≤7%), hyperlipidemia (≤7%)

Gastrointestinal: Nausea (5%), diarrhea (2%), gastrointestinal hemorrhage (2%)

Hematologic & oncologic: Leukopenia (3%), anemia (2%), major hemorrhage (2%), minor hemorrhage (2%), major hemorrhage (life-threatening: 1%)

Neuromuscular & skeletal: Back pain (5%), limb pain (3%)

Respiratory: Epistaxis (6%), dyspnea (5%), cough (4%)

Miscellaneous: Fever (3%)

<1%, postmarketing, and/or case reports: Abnormal hepatic function tests, anaphylaxis, angioedema, hematoma, hemoptysis, hemorrhage (requiring inotropes or transfusion), hypersensitivity reaction, intracranial hemorrhage (symptomatic), re-operation due to bleeding, thrombocytopenia, thrombotic thrombocytopenic purpura

Contraindications

Hypersensitivity (eg, anaphylaxis) to prasugrel or any component of the formulation; active pathological bleeding (eg, peptic ulcer, intracranial hemorrhage); prior transient ischemic attack or stroke.

Canadian labeling: Additional contraindications (not in US labeling): Severe hepatic impairment (Child-Pugh Class C).

Warnings/Precautions

Concerns related to adverse effects:

• Bleeding: [US Boxed Warning]: May cause significant, sometimes fatal, bleeding. Do not use prasugrel in patients with active pathological bleeding or a history of TIA or stroke. Additional risk factors for bleeding include body weight <60 kg, propensity to bleed (eg, recent trauma, recent surgery, recent or recurrent GI bleeding, active peptic ulcer disease, severe hepatic impairment, or moderate to severe renal impairment), and concomitant use of medications that increase the risk of bleeding (eg, warfarin, heparin, fibrinolytic therapy, long-term use of NSAIDs). Suspect bleeding in any patient who is hypotensive and has recently undergone coronary angiography, PCI, CABG, or other surgical procedures in the setting of prasugrel. If possible, manage bleeding without discontinuing prasugrel. Discontinuing prasugrel, particularly in the first few weeks after ACS, increases the risk of subsequent cardiovascular events. Management of bleeding episodes includes the use of PRBCs and platelet transfusion.

• Hypersensitivity: Hypersensitivity, including angioedema, has been reported, including in patients with a previous history of thienopyridine hypersensitivity. Because of structural similarities, cross-reactivity is possible among the thienopyridines (clopidogrel, prasugrel, and ticlopidine); use with caution or avoid in patients with previous history of thienopyridine hypersensitivity. Use of prasugrel is contraindicated in patients with hypersensitivity (eg, anaphylaxis) to prasugrel.

• Thrombotic thrombocytopenic purpura (TTP): Cases of TTP (usually occurring within the first 2 weeks of therapy), resulting in some fatalities, have been reported with prasugrel; urgent plasmapheresis is required.

Disease-related concerns:

• GI disease: Use with caution in patients with recent or recurrent GI bleeding or active peptic ulcer disease (patients are generally at higher risk of bleeding).

• Hepatic impairment: Use with caution in patients with severe hepatic impairment (patients are generally at higher risk of bleeding).

• Renal impairment: Use with caution in patients with moderate to severe renal impairment (patients are generally at higher risk of bleeding).

Special populations:

• Older adult: [US Boxed Warning]: In patients ≥75 years, use is generally not recommended due to increased risk of fatal and intracranial bleeding and uncertain benefit, except in high-risk situations (patients with diabetes or a history of MI) in which its effect appears to be greater and its use may be considered.

• Lower GI bleed patients: An individualized and multidisciplinary approach should be utilized to determine therapy discontinuation and management in patients with acute lower GI bleed (LGIB) who are on antiplatelet medications; risk of ongoing bleeding should be weighed with risk of thromboembolic events. In patients receiving dual antiplatelet therapy (aspirin plus P2Y12 receptor blocker [eg, clopidogrel, prasugrel, ticagrelor, ticlopidine]) or P2Y12 inhibitor monotherapy, the P2Y12 inhibitor should generally be resumed as soon as possible and at least within 7 days, taking into account control of bleeding and cardiovascular risk (aspirin should not be discontinued) (Strate 2016).

• Low-weight patients: In patients weighing <60 kg, risk of bleeding increased; consider lower maintenance dose.

• Surgical patients: [US Boxed Warning]: Do not initiate therapy in patients likely to undergo urgent CABG surgery; when possible, discontinue ≥7 days prior to any surgery; increased risk of bleeding. Patient-specific situations should be discussed with a cardiologist, interventional cardiologist, and a cardiac surgeon (ACC/AHA [Grines 2007]; ACC/AHA [Hillis 2011]; ACC/AHA [Lawton 2022]). In patients undergoing noncardiac surgery, the risks and benefits of prasugrel should be evaluated between the surgeon and the cardiology team. Elective noncardiac surgery should not be performed in patients in whom dual antiplatelet therapy (DAPT) will need to be discontinued perioperatively within 30 days following bare metal stent placement or within 3 months of drug-eluting stent placement. In patients undergoing urgent noncardiac surgery during the first 4 to 6 weeks after BMS or DES placement, continue DAPT. In patients undergoing noncardiac surgery that requires discontinuation of prasugrel, hold for 7 days preoperatively, continue aspirin and restart prasugrel as soon as possible (eg, ≤24 hours) after surgery based on bleeding and thrombotic risks (ACC/AHA [Fleisher 2014]; ACC/AHA [Lawton 2022]; ACC/AHA [Levine 2016]; ACCP [Douketis 2022]).

Other warnings/precautions:

• Discontinuation of therapy: For patients who undergo percutaneous coronary intervention with stenting, premature interruption of therapy may result in increased risk of myocardial infarction, stent thrombosis, stroke, or death. If therapy must be held temporarily (eg, bleeding, surgery), restart as soon as possible unless the reason for discontinuation is a stroke or TIA where subsequent use is contraindicated. Duration of therapy is determined by the type of stent placed (bare metal or drug eluting), whether an acute coronary syndrome event was ongoing at the time of placement, as well as risks for bleeding and thrombosis (ACC/AHA [Lawton 2022]).

Dosage Forms: US

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Tablet, Oral:

Effient: 5 mg, 10 mg

Generic: 5 mg, 10 mg

Generic Equivalent Available: US

Yes

Pricing: US

Tablets (Effient Oral)

5 mg (per each): $22.18

10 mg (per each): $22.18

Tablets (Prasugrel HCl Oral)

5 mg (per each): $16.51

10 mg (per each): $16.50 - $16.51

Disclaimer: A representative AWP (Average Wholesale Price) price or price range is provided as reference price only. A range is provided when more than one manufacturer's AWP price is available and uses the low and high price reported by the manufacturers to determine the range. The pricing data should be used for benchmarking purposes only, and as such should not be used alone to set or adjudicate any prices for reimbursement or purchasing functions or considered to be an exact price for a single product and/or manufacturer. Medi-Span expressly disclaims all warranties of any kind or nature, whether express or implied, and assumes no liability with respect to accuracy of price or price range data published in its solutions. In no event shall Medi-Span be liable for special, indirect, incidental, or consequential damages arising from use of price or price range data. Pricing data is updated monthly.

Dosage Forms: Canada

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Tablet, Oral:

Generic: 10 mg

Administration: Adult

Oral: Administer without regard to meals. In an emergent primary PCI setting, crushing the tablets (using a commercially available syringe crusher) and mixing with 25 mL of water led to faster absorption and a quicker, more potent antiplatelet effect seen as early as 30 minutes (Ref). In addition, according to the manufacturer, tablets may be chewed and swallowed (bitter to taste) or crushed and mixed in food or liquid (eg, applesauce, juice, water) and immediately administered by mouth or gastric tube. Administration via an enteral tube that bypasses the acidic environment of the stomach may result in reduced bioavailability of prasugrel (data on file, Daiichi Sankyo-Lilly 2012).

Medication Guide and/or Vaccine Information Statement (VIS)

An FDA-approved patient medication guide, which is available with the product information and at https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/022307s018lbl.pdf#page=21, must be dispensed with this medication.

Use: Labeled Indications

Acute coronary syndrome managed by percutaneous coronary intervention: To reduce the rate of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndrome who are to be managed with percutaneous coronary intervention for unstable angina, non-ST-elevation myocardial infarction (MI), or ST-elevation MI.

Medication Safety Issues
Sound-alike/look-alike issues:

Prasugrel may be confused with pravastatin, propranolol

Older Adult: High-Risk Medication:

Beers Criteria: Prasugrel is identified in the Beers Criteria as a potentially inappropriate medication to be used with caution, especially in patients 75 years and older due to increased risk of bleeding compared with clopidogrel; however, cardiovascular benefit in certain older adults may offset risk. Consider a lower dose (5 mg/day) if used in patients 75 years and older (Beers Criteria [AGS 2023]).

Metabolism/Transport Effects

Substrate of CYP2B6 (minor), CYP3A4 (minor); Note: Assignment of Major/Minor substrate status based on clinically relevant drug interaction potential

Drug Interactions

Note: Interacting drugs may not be individually listed below if they are part of a group interaction (eg, individual drugs within “CYP3A4 Inducers [Strong]” are NOT listed). For a complete list of drug interactions by individual drug name and detailed management recommendations, use the drug interactions program by clicking on the “Launch drug interactions program” link above.

Abrocitinib: Agents with Antiplatelet Properties may enhance the antiplatelet effect of Abrocitinib. Management: Do not use antiplatelet drugs with abrocitinib during the first 3 months of abrocitinib therapy. The abrocitinib prescribing information lists this combination as contraindicated. This does not apply to low dose aspirin (81 mg/day or less). Risk X: Avoid combination

Acalabrutinib: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Agents with Antiplatelet Properties (e.g., P2Y12 inhibitors, NSAIDs, SSRIs, etc.): May enhance the antiplatelet effect of other Agents with Antiplatelet Properties. Risk C: Monitor therapy

Anagrelide: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Anticoagulants: Agents with Antiplatelet Properties may enhance the anticoagulant effect of Anticoagulants. Risk C: Monitor therapy

Apixaban: Antiplatelet Agents (P2Y12 Inhibitors) may enhance the adverse/toxic effect of Apixaban. Specifically, the risk for bleeding may be increased. Management: Carefully consider risks and benefits of this combination and monitor closely; Canadian labeling recommends avoiding prasugrel or ticagrelor. Risk D: Consider therapy modification

Bemiparin: Agents with Antiplatelet Properties may enhance the anticoagulant effect of Bemiparin. Management: Avoid concomitant use of bemiparin with antiplatelet agents. If concomitant use is unavoidable, monitor closely for signs and symptoms of bleeding. Risk D: Consider therapy modification

Cangrelor: May diminish the antiplatelet effect of Prasugrel. More specifically, while the use of Cangrelor is expected to increase total platelet inhibition in patients who have previously received Prasugrel, Cangrelor is expected to decrease binding of Prasugrel metabolites to P2Y12 receptors and thus reduce the extent of irreversible platelet inhibition. Management: Avoid administration of prasugrel until cangrelor is discontinued. Risk D: Consider therapy modification

Caplacizumab: Agents with Antiplatelet Properties may enhance the adverse/toxic effect of Caplacizumab. Specifically, the risk of bleeding may be increased. Management: Avoid coadministration of caplacizumab with antiplatelets if possible. If coadministration is required, monitor closely for signs and symptoms of bleeding. Interrupt use of caplacizumab if clinically significant bleeding occurs. Risk D: Consider therapy modification

Cephalothin: Agents with Antiplatelet Properties may enhance the adverse/toxic effect of Cephalothin. Specifically, the risk for bleeding may be increased. Risk C: Monitor therapy

Collagenase (Systemic): Agents with Antiplatelet Properties may enhance the adverse/toxic effect of Collagenase (Systemic). Specifically, the risk of injection site bruising and or bleeding may be increased. Risk C: Monitor therapy

Dabigatran Etexilate: Agents with Antiplatelet Properties may enhance the anticoagulant effect of Dabigatran Etexilate. Agents with Antiplatelet Properties may increase the serum concentration of Dabigatran Etexilate. This mechanism applies specifically to clopidogrel. Management: Carefully consider risks and benefits of this combination and monitor closely; Canadian labeling recommends avoiding prasugrel or ticagrelor. Risk C: Monitor therapy

Dabigatran Etexilate: Antiplatelet Agents (P2Y12 Inhibitors) may enhance the adverse/toxic effect of Dabigatran Etexilate. Specifically, the risk of bleeding may be increased. Risk C: Monitor therapy

Dasatinib: May enhance the anticoagulant effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Deoxycholic Acid: Agents with Antiplatelet Properties may enhance the adverse/toxic effect of Deoxycholic Acid. Specifically, the risk for bleeding or bruising in the treatment area may be increased. Risk C: Monitor therapy

Diamorphine: May diminish the antiplatelet effect of Antiplatelet Agents (P2Y12 Inhibitors). Diamorphine may decrease the serum concentration of Antiplatelet Agents (P2Y12 Inhibitors). Risk C: Monitor therapy

Edoxaban: Antiplatelet Agents (P2Y12 Inhibitors) may enhance the adverse/toxic effect of Edoxaban. Specifically, the risk of bleeding may be increased. Management: Carefully consider the anticipated risks and benefits of this combination. If combined, increased monitoring for bleeding is recommended. Risk D: Consider therapy modification

Enoxaparin: Agents with Antiplatelet Properties may enhance the anticoagulant effect of Enoxaparin. Management: Discontinue antiplatelet agents prior to initiating enoxaparin whenever possible. If concomitant administration is unavoidable, monitor closely for signs and symptoms of bleeding. Risk D: Consider therapy modification

FentaNYL: May diminish the antiplatelet effect of Antiplatelet Agents (P2Y12 Inhibitors). FentaNYL may decrease the serum concentration of Antiplatelet Agents (P2Y12 Inhibitors). Risk C: Monitor therapy

Heparin: Agents with Antiplatelet Properties may enhance the anticoagulant effect of Heparin. Management: Decrease the dose of heparin or agents with antiplatelet properties if coadministration is required. Risk D: Consider therapy modification

Herbal Products with Anticoagulant/Antiplatelet Effects (eg, Alfalfa, Anise, Bilberry): May enhance the adverse/toxic effect of Agents with Antiplatelet Properties. Bleeding may occur. Risk C: Monitor therapy

Ibritumomab Tiuxetan: Agents with Antiplatelet Properties may enhance the adverse/toxic effect of Ibritumomab Tiuxetan. Both agents may contribute to impaired platelet function and an increased risk of bleeding. Risk C: Monitor therapy

Ibrutinib: May enhance the adverse/toxic effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Icosapent Ethyl: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Inotersen: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Lecanemab: May enhance the adverse/toxic effect of Agents with Antiplatelet Properties. Specifically, the risk of hemorrhage may be increased. Risk C: Monitor therapy

Limaprost: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Lipid Emulsion (Fish Oil Based): May enhance the adverse/toxic effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Morphine (Systemic): May diminish the antiplatelet effect of Antiplatelet Agents (P2Y12 Inhibitors). Morphine (Systemic) may decrease the serum concentration of Antiplatelet Agents (P2Y12 Inhibitors). Management: Consider alternative anti-ischemic/analgesic therapies (eg, beta-blockers, nitroglycerin) in patients with acute coronary syndromes treated with a P2Y12 inhibitor when possible. The risks associated with other opioids are unknown. Risk D: Consider therapy modification

Multivitamins/Fluoride (with ADE): May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Multivitamins/Minerals (with ADEK, Folate, Iron): May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Multivitamins/Minerals (with AE, No Iron): May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Obinutuzumab: Agents with Antiplatelet Properties may enhance the adverse/toxic effect of Obinutuzumab. Specifically, the risk of serious bleeding-related events may be increased. Risk C: Monitor therapy

Omega-3 Fatty Acids: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Pentosan Polysulfate Sodium: May enhance the adverse/toxic effect of Agents with Antiplatelet Properties. Specifically, the risk of bleeding may be increased by concurrent use of these agents. Risk C: Monitor therapy

Pentoxifylline: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Pirtobrutinib: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Prostacyclin Analogues: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Rivaroxaban: Antiplatelet Agents (P2Y12 Inhibitors) may enhance the adverse/toxic effect of Rivaroxaban. Specifically, the risk of bleeding may be increased. Management: Carefully consider risks and benefits of this combination and monitor closely; Canadian labeling recommends avoiding prasugrel or ticagrelor. Risk D: Consider therapy modification

Selective Serotonin Reuptake Inhibitors: May enhance the antiplatelet effect of Antiplatelet Agents (P2Y12 Inhibitors). Risk C: Monitor therapy

Selumetinib: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Serotonin/Norepinephrine Reuptake Inhibitors: May enhance the antiplatelet effect of Antiplatelet Agents (P2Y12 Inhibitors). Risk C: Monitor therapy

Telotristat Ethyl: May decrease serum concentrations of the active metabolite(s) of Prasugrel. Risk C: Monitor therapy

Thrombolytic Agents: Agents with Antiplatelet Properties may enhance the anticoagulant effect of Thrombolytic Agents. Risk C: Monitor therapy

Ticagrelor: Antiplatelet Agents (P2Y12 Inhibitors) may enhance the antiplatelet effect of Ticagrelor. Risk X: Avoid combination

Tipranavir: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Urokinase: Agents with Antiplatelet Properties may enhance the anticoagulant effect of Urokinase. Risk X: Avoid combination

Vitamin E (Systemic): May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Volanesorsen: May enhance the antiplatelet effect of Therapeutic Antiplatelets. Risk C: Monitor therapy

Zanubrutinib: May enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy

Pregnancy Considerations

Outcome data related to maternal use of prasugrel during pregnancy are limited (Pop 2020; Tello-Montoliu 2013).

Breastfeeding Considerations

It is not known if prasugrel is excreted in breast milk.

According to the manufacturer, the decision to breastfeed during therapy should consider the risk of infant exposure, the benefits of breastfeeding to the infant, and benefits of treatment to the mother.

Monitoring Parameters

Hemoglobin and hematocrit periodically.

Mechanism of Action

Prasugrel, an inhibitor of platelet activation and aggregation, is a prodrug that is metabolized to both active (R-138727) and inactive metabolites. The active metabolite irreversibly blocks the P2Y12 component of ADP receptors on the platelet, which prevents activation of the GPIIb/IIIa receptor complex, thereby reducing platelet activation and aggregation

Pharmacokinetics (Adult Data Unless Noted)

Onset of action: Inhibition of platelet aggregation (IPA): Dose dependent: 60 mg loading dose: <30 minutes; median time to reach ≥20% IPA: 30 minutes (Brandt 2007).

Peak effect: Time to maximal IPA: Dose-dependent: Note: Degree of IPA based on adenosine diphosphate (ADP) concentration used during light aggregometry: 60 mg loading dose: Occurs ~4 hours post administration; Mean IPA (ADP 5 micromole/L): ~84.1%; Mean IPA (ADP 20 micromole/L): ~78.8% (Brandt 2007).

Duration of effect: Platelet aggregation gradually returns to baseline values over 5 to 9 days after discontinuation; reflective of new platelet production.

Absorption: Rapid; ≥79%.

Distribution: Active metabolite: Vd: 44 to 68 L.

Protein binding: Active metabolite: ~98%.

Metabolism: Rapid intestinal and serum metabolism via esterase-mediated hydrolysis to a thiolactone intermediate (inactive), which is then converted, via CYP450-mediated (primarily CYP3A4 and CYP2B6) oxidation, to an active metabolite (R-138727) (Farid 2007; Riley 2008).

Half-life elimination: Active metabolite: ~7 hours (range 2 to 15 hours).

Time to peak, plasma: Active metabolite: ~30 minutes; With high-fat/high-calorie meal: 1.5 hours.

Excretion: Urine (~68% inactive metabolites); feces (27% inactive metabolites).

Pharmacokinetics: Additional Considerations (Adult Data Unless Noted)

Altered kidney function: In patients with ESRD, both Cmax and AUC0-t last of the active metabolite were approximately half that in healthy patients and in patients with moderate renal impairment.

Older adult: The AUC of active metabolite was 19% higher in patients 75 years and older than in patients younger than 75 years.

Race/ethnicity: The AUC of active metabolite was approximately 19% higher in Chinese, Japanese, and Korean subjects than in white subjects.

Body weight: The AUC of the active metabolite is approximately 30% to 40% higher in subjects with a body weight of less than 60 kg compared to those weighing 60 kg or more.

Brand Names: International
International Brand Names by Country
For country code abbreviations (show table)

  • (AR) Argentina: Effient | Fluidin | Nefagrel | Trocal;
  • (AT) Austria: Efient | Prasugrel aristo | Prasugrel hcs | Prasugrel ratiopharm | Prasugrel sandoz | Prasulan;
  • (AU) Australia: Effient | Prasugrel SCP;
  • (BD) Bangladesh: Apagrel | Appras | Asurel | Efigrel | Efirel | Hemagrel | Opagrel | Prapid | Prasulet | Prasurel | Prasuva;
  • (BE) Belgium: Efient;
  • (BG) Bulgaria: Bewim | Efient | Fluidoro | Prasugrel teva | Tosynal;
  • (BR) Brazil: Effient;
  • (CH) Switzerland: Efient | Prasugrel mepha;
  • (CO) Colombia: Effient | Perkunal;
  • (CZ) Czech Republic: Efient | Eliskardia;
  • (DE) Germany: Efient | Prasillt | Prasugrel accord | Prasugrel AL | Prasugrel aristo | Prasugrel beta | Prasugrel biomo | Prasugrel Glenmark | Prasugrel heumann | Prasugrel ratiopharm | Prasugrelhydrobromid Zentiva | Prasuhexal;
  • (DO) Dominican Republic: Prasusafe | Sugrel;
  • (EC) Ecuador: Perkunal | Rozolex;
  • (EE) Estonia: Efient;
  • (ES) Spain: Efient | Prasugrel combix | Prasugrel krka | Prasugrel qualigen | Prasugrel ratiopharm | Prasugrel stada | Prasugrel teva;
  • (FI) Finland: Efient;
  • (FR) France: Efient | Prasugrel arrow | Prasugrel biogaran | Prasugrel cristers | Prasugrel eg | Prasugrel krka | Prasugrel mylan | Prasugrel teva | Prasugrel zentiva lab;
  • (GB) United Kingdom: Efient | Prasugrel;
  • (GR) Greece: Efient | Prasugrel vocate;
  • (HK) Hong Kong: Effient;
  • (HU) Hungary: Bewim | Efient | Eliskardia;
  • (ID) Indonesia: Effient;
  • (IE) Ireland: Efient | Prasugrel accord | Prasugrel krka | Prasugrel mylan | Prasugrel rowex;
  • (IN) India: Apagrel | Aplet | Effient | Efiplat | Pangrel | Pasugen | Prasact | Prasita | Prasudin | Prasudoc | Prasugrin | Prasulet | Prasumax | Prasurel | Prasusafe | Prasutab | Prasuten | Prasuvas | Prasuvix | Prax | Prethromb | Redigrel | Troyplatt;
  • (IT) Italy: Efient | Prasugrel mylan | Prasugrel teva;
  • (JO) Jordan: Effient | Lexar;
  • (JP) Japan: Effient;
  • (KE) Kenya: Pragrel | Prasu | Prasusafe;
  • (KR) Korea, Republic of: Effient;
  • (KW) Kuwait: Lexar;
  • (LB) Lebanon: Effient;
  • (LT) Lithuania: Efient | Eliskardia;
  • (LU) Luxembourg: Efient;
  • (LV) Latvia: Efient | Eliskardia;
  • (MA) Morocco: Batens;
  • (MX) Mexico: Effient;
  • (MY) Malaysia: Effient;
  • (NL) Netherlands: Efient | Prasugrel | Prasugrel mylan | Prasugrel teva;
  • (NO) Norway: Efient | Prasugrel krka;
  • (NZ) New Zealand: Effient | Prasugrel;
  • (PE) Peru: Effient;
  • (PH) Philippines: Effient;
  • (PK) Pakistan: Atcogrel | Bestegrel | Effin | Persiva | Prag | Pragi | Prasubar | Prasug | Prasulet | Prasumac | Prezent | Prisa | Samig | Superplat;
  • (PL) Poland: Bewim | Efient;
  • (PR) Puerto Rico: Prasugrel;
  • (PT) Portugal: Efient | Prasugrel;
  • (PY) Paraguay: Agreplac;
  • (RO) Romania: Efient;
  • (RU) Russian Federation: Antagrex | Effient;
  • (SE) Sweden: Efient | Prasugrel ebb | Prasugrel krka | Prasugrel mylan;
  • (SG) Singapore: Effient;
  • (SI) Slovenia: Efient | Eliskardia | Prasugrel | Tosynal;
  • (SK) Slovakia: Bewim | Efient | Sigrada;
  • (TH) Thailand: Effient;
  • (TR) Turkey: Effient;
  • (TW) Taiwan: Efient;
  • (UA) Ukraine: Sagrada;
  • (UG) Uganda: Prasusafe;
  • (UY) Uruguay: Glitax | Perkunal | Sugrel;
  • (VE) Venezuela, Bolivarian Republic of: Effient | Perkunal;
  • (VN) Viet Nam: Razugrel;
  • (ZA) South Africa: Efient
  1. 2023 American Geriatrics Society Beers Criteria Update Expert Panel. American Geriatrics Society 2023 updated AGS Beers Criteria for potentially inappropriate medication use in older adults. J Am Geriatr Soc. 2023;71(7):2052-2081. doi:10.1111/jgs.18372 [PubMed 37139824]
  2. Amsterdam EA, Wenger NK, Brindis RG, et al; American College of Cardiology; American Heart Association Task Force on Practice Guidelines; Society for Cardiovascular Angiography and Interventions; Society of Thoracic Surgeons; American Association for Clinical Chemistry. 2014 AHA/ACC guideline for the management of patients with non-ST-elevation acute coronary syndromes: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines [published correction appears in J Am Coll Cardiol. 2014;64(24):2713-2714]. J Am Coll Cardiol. 2014;64(24):e139-e228. doi:10.1016/j.jacc.2014.09.017 [PubMed 25260718]
  3. Anderson JL, Adams CD, Antman EM, et al; American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. 2012 ACCF/AHA focused update incorporated into the ACCF/AHA 2007 guidelines for the management of patients with unstable angina/non-ST-elevation myocardial infarction: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation. 2013;127(23):e663-e828. doi:10.1161/CIR.0b013e31828478ac [PubMed 23630129]
  4. Angiolillo DJ, Curzen N, Gurbel P, et al. Pharmacodynamic evaluation of switching from ticagrelor to prasugrel in patients with stable coronary artery disease: results of the SWAP-2 study (switching anti platelet-2). J Am Coll Cardiol. 2014;63(15):1500-1509. doi:10.1016/j.jacc.2013.11.032 [PubMed 24333493]
  5. Angiolillo DJ, Rollini F, Storey RF, et al. International expert consensus on switching platelet P2Y(12) receptor-inhibiting therapies. Circulation. 2017;136(20):1955-1975. doi:10.1161/CIRCULATIONAHA.117.031164 [PubMed 29084738]
  6. Angiolillo DJ, Saucedo JF, Deraad R, et al; SWAP Investigators. Increased platelet inhibition after switching from maintenance clopidogrel to prasugrel in patients with acute coronary syndromes: results of the SWAP (Switching Anti Platelet) study. J Am Coll Cardiol. 2010;56(13):1017-1023. doi:10.1016/j.jacc.2010.02.072 [PubMed 20846599]
  7. Brandt JT, Payne CD, Wiviott SD, et al, “A Comparison of Prasugrel and Clopidogrel Loading Doses on Platelet Function: Magnitude of Platelet Inhibition is Related to Active Metabolite Formation,” Am Heart J, 2007, 153(1):66.e9-16. [PubMed 17174640]
  8. Cutlip D, Lincoff AM. Acute non-ST-elevation acute coronary syndromes: Early antiplatelet therapy. Post TW, ed. UpToDate. Waltham, MA: UpToDate Inc. http://www.uptodate.com. Accessed July 21, 2021.
  9. Douketis JD, Spyropoulos AC, Murad MH, et al. Perioperative management of antithrombotic therapy: an American College of Chest Physicians clinical practice guideline. Chest. 2022;162(5):e207-e243. doi:10.1016/j.chest.2022.07.025 [PubMed 35964704]
  10. Effient (prasugrel) [prescribing information]. South Plainfield, NJ: Cosette Pharmaceuticals Inc; February 2022.
  11. Erlinge D, Ten Berg J, Foley D, et al. Reduction in platelet reactivity with prasugrel 5 mg in low-body-weight patients is noninferior to prasugrel 10 mg in higher-body-weight patients: results from the FEATHER trial. J Am Coll Cardiol. 2012;60(20):2032-2040. doi:10.1016/j.jacc.2012.08.964 [PubMed 23083774]
  12. Farid NA, Smith RL, Gillespie TA, et al. The disposition of prasugrel, a novel thienopyridine, in humans. Drug Metab Dispos. 2007; 35(5):1096-1104. [PubMed 17403916]
  13. Ferraris VA, Saha SP, Oestreich JH, et al, “2012 Update to the Society of Thoracic Surgeons Guideline on Use of Antiplatelet Drugs in Patients Having Cardiac and Noncardiac Operations,” Ann Thorac Surg, 2012, 94(5):1761-81. [PubMed 23098967]
  14. Fleisher LA, Fleischmann KE, Auerbach AD, et al. 2014 ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;130(24):e278-e333. [PubMed 25085961]
  15. Frontera JA, Lewin JJ 3rd, Rabinstein AA, et al; Guideline for reversal of antithrombotics in intracranial hemorrhage: a statement for healthcare professionals from the Neurocritical Care Society and Society of Critical Care Medicine. Neurocrit Care. 2016;24(1):6-46. [PubMed 26714677]
  16. Grines CL, Bonow RO, Casey DE, et al. AHA/ACC/SCAI/ACS/ADA Science Advisory, Prevention of premature discontinuation of dual antiplatelet therapy in patients with coronary artery stents. A science advisory from the American Heart Association, American College of Cardiology, Society of Cardiovascular Angiography and Interventions, American College of Surgeons, and American Dental Association with representation from The American College Of Physicians. Circulation. 2007;115(6):813-818. Available at http://www.acc.org/qualityandscience/clinical/pdfs/Final_Dual_Antiplatelet_Statement_010507.pdf [PubMed 17224480]
  17. Guyatt GH, Akl EA, Crowther M, et al, “Executive Summary: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines,” Chest, 2012, 141(2 Suppl):7-47. [PubMed 22315257]
  18. Hillis LD, Smith PK, Anderson JL, et al, “2011 ACCF/AHA Guideline for Coronary Artery Bypass Graft Surgery: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines,” Circulation, 2011, 124(23):2610-42. [PubMed 22064600]
  19. JAMP Prasugrel (prasugrel) [product monograph]. Boucherville, Quebec, Canada: JAMP Pharma Corporation; July 2020.
  20. Kim HS, Kang J, Hwang D, et al; HOST-REDUCE-POLYTECH-ACS investigators. Prasugrel-based de-escalation of dual antiplatelet therapy after percutaneous coronary intervention in patients with acute coronary syndrome (HOST-REDUCE-POLYTECH-ACS): an open-label, multicentre, non-inferiority randomised trial. Lancet. 2020;396(10257):1079-1089. doi:10.1016/S0140-6736(20)31791-8 [PubMed 32882163]
  21. Kumbhani DJ, Cannon CP, Beavers CJ, et al. 2020 ACC expert consensus decision pathway for anticoagulant and antiplatelet therapy in patients with atrial fibrillation or venous thromboembolism undergoing percutaneous coronary intervention or with atherosclerotic cardiovascular disease: a report of the American College of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol. 2021;77(5):629-658. doi:10.1016/j.jacc.2020.09.011 [PubMed 33250267]
  22. Lawton JS, Tamis-Holland JE, Bangalore S, et al. 2021 ACC/AHA/SCAI guideline for coronary artery revascularization: a report of the American College of Cardiology/American Heart Association joint committee on clinical practice guidelines. J Am Coll Cardiol. 2022;79(2):e21-e129. doi:10.1016/j.jacc.2021.09.006 [PubMed 34895950]
  23. Levine GN, Bates ER, Bittl JA, et al. 2016 ACC/AHA guideline focused update on duration of dual antiplatelet therapy in patients with coronary artery disease: A report of the American College of Cardiology/American Heart Association task force on clinical practice guidelines. J Am Coll Cardiol. 2016;68(10):1082-1115. doi:10.1016/j.jacc.2016.03.513 [PubMed 27036918]
  24. Levine GN, Bates ER, Blankenship JC, et al, “2011 ACCF/AHA/SCAI Guideline for Percutaneous Coronary Intervention: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Society for Cardiovascular Angiography and Interventions,” Circulation, 2011, 124(23):e574-651. [PubMed 22064601]
  25. Levine GN, Jeong YH, Goto S, et al. Expert consensus document: World Heart Federation expert consensus statement on antiplatelet therapy in East Asian patients with ACS or undergoing PCI. Nat Rev Cardiol. 2014;11(10):597-606. doi:10.1038/nrcardio.2014.104 [PubMed 25154978]
  26. Mauri L, Kereiakes DJ, Yeh RW, et al; DAPT Study Investigators. Twelve or 30 months of dual antiplatelet therapy after drug-eluting stents. N Engl J Med. 2014;371(23):2155-2166. doi:10.1056/NEJMoa1409312 [PubMed 25399658]
  27. Menichelli M, Neumann FJ, Ndrepepa G, et al. Age- and weight-adapted dose of prasugrel versus standard dose of ticagrelor in patients with acute coronary syndromes: results from a randomized trial. Ann Intern Med. 2020;173(6):436-444. doi:10.7326/M20-1806 [PubMed 32687741]
  28. Montalescot G, Bolognese L, Dudek D, et al; ACCOAST Investigators. Pretreatment with prasugrel in non-ST-segment elevation acute coronary syndromes. N Engl J Med. 2013;369(11):999-1010. doi:10.1056/NEJMoa1308075 [PubMed 23991622]
  29. O'Donoghue ML, Murphy SA, Sabatine MS. The safety and efficacy of aspirin discontinuation on a background of a P2Y12 inhibitor in patients after percutaneous coronary intervention: a systematic review and meta-analysis. Circulation. 2020;142(6):538-545. doi:10.1161/CIRCULATIONAHA.120.046251 [PubMed 32551860]
  30. O'Gara PT, Kushner FG, Ascheim DD, et al; American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. 2013 ACCF/AHA guideline for the management of ST-elevation myocardial infarction: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines [published correction appears in Circulation. 2013;128(25):e481]. Circulation. 2013;127(4):e362-e425. [PubMed 23247304]
  31. Payne CD, Li YG, Brandt JT, et al. Switching directly to prasugrel from clopidogrel results in greater inhibition of platelet aggregation in aggregation in aspirin-treated subjects. Platelets. 2008;19(4):275-281. doi:10.1080/09537100801891640 [PubMed 18569863]
  32. Pop R, Cebula H, Lambert A, et al. Treatment with flow diverter stent during pregnancy. Neuroradiology. 2020;62(11):1507-1510. doi:10.1007/s00234-020-02474-0 [PubMed 32572512]
  33. Refer to manufacturer's labeling.
  34. Riesmeyer JS, Salazar DE, Weerakkody GJ, et al, "Relationship Between Exposure to Prasugrel Active Metabolite and Clinical Outcomes in the TRITON-TIMI 38 Substudy," J Clin Pharmacol, 2012, 52(6):789-97. [PubMed 21628601]
  35. Riley AB, Tafreshi MJ, Haber SL. Prasugrel: a novel antiplatelet agent. Am J Health Syst Pharm. 2008;65(11):1019-1028. [PubMed 18499874]
  36. Roe MT, Armstrong PW, Fox KA, et al, “Prasugrel versus Clopidogrel for Acute Coronary Syndromes Without Revascularization,” N Engl J Med, 2012, 367(14):1297-309. [PubMed 22920930]
  37. Rollini F, Franchi F, Hu J, et al. Crushed prasugrel tablets in patients with STEMI undergoing primary percutaneous coronary intervention: The CRUSH study. J Am Coll Cardiol. 2016;67(17):1994-2004. doi:10.1016/j.jacc.2016.02.045 [PubMed 27012781]
  38. Small DS, Kothare P, Yuen E, et al. The pharmacokinetics and pharmacodynamics of prasugrel in healthy Chinese, Japanese, and Korean subjects compared with healthy Caucasian subjects. Eur J Clin Pharmacol. 2010;66(2):127-135. doi:10.1007/s00228-009-0737-1 [PubMed 19888568]
  39. Strate LL, Gralnek IM. ACG clinical guideline: management of patients with acute lower gastrointestinal bleeding. Am J Gastroenterol. 2016;111(4):459-474. doi:10.1038/ajg.2016.41 [PubMed 26925883]
  40. Tello-Montoliu A, Seecheran NA, Angiolillo DJ. Successful pregnancy and delivery on prasugrel treatment: considerations for the use of dual antiplatelet therapy during pregnancy in clinical practice. J Thromb Thrombolysis. 2013;36(3):348-351. doi:10.1007/s11239-012-0830-7 [PubMed 23143651]
  41. Vogel RF, Delewi R, Angiolillo DJ, et al. Pharmacodynamic effects of pre-hospital administered crushed prasugrel in patients with ST-segment elevation myocardial infarction. JACC Cardiovasc Interv. 2021;14(12):1323-1333. doi:10.1016/j.jcin.2021.04.022 [PubMed 34167672]
  42. Wiviott SD, Braunwald E, McCabe CH, et al; TRITON-TIMI 38 Investigators. Prasugrel versus clopidogrel in patients with acute coronary syndromes. N Engl J Med. 2007;357(20):2001-2015. [PubMed 17982182]
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