Brilinta tablet: Difference between revisions
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|hasBlackBoxWarning=Yes | |||
|blackBoxWarningTitle=WARNING: (A) BLEEDING RISK, (B) ASPIRIN DOSE AND BRILINTA EFFECTIVENESS | |||
|blackBoxWarningBody= A. BLEEDING RISK | |||
* BRILINTA, like other antiplatelet agents, can cause significant, sometimes fatal bleeding. | |||
* Do not use BRILINTA in patients with active pathological bleeding or a history of intracranial hemorrhage. | |||
* Do not start BRILINTA in patients planned to undergo urgent coronary artery bypass graft surgery (CABG). When possible, discontinue BRILINTA at least 5 days prior to any surgery. | |||
* 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 BRILINTA. | |||
* If possible, manage bleeding without discontinuing BRILINTA. Stopping BRILINTA increases the risk of subsequent cardiovascular events. | |||
B. ASPIRIN DOSE AND BRILINTA EFFECTIVENESS | |||
Maintenance doses of aspirin above 100 mg reduce the effectiveness of BRILINTA and should be avoided. After any initial dose, use with aspirin 75-100 mg per day. | |||
|hasUsageInfo=In Progress | |hasUsageInfo=In Progress | ||
}} | }} |
Revision as of 20:18, 19 March 2014
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]{{{authorTag}}}
For information about {{{genericName}}}, click here.
Disclaimer
Overview
Brilinta tablet is a P2Y12 platelet inhibitor drug that is FDA approved for the treatment of {{{indication}}}. Adverse reactions include {{{adverseReactions}}}.
Adult Indications and Dosage
Pediatric Indications and Dosage
Contraindications
Warnings
Adverse Reactions
Drug Interactions
Use in Specific Populations
Routes and Preparations
IV Compatibility
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Information
Patient Information from FDA
Patient Information from NLM
Look-Alike Drug Names
Price
Drug Shortage
Black Box Warning
Below is the code to be placed on the Black Box Warning Microchapter:
__NOTOC__
{{Labeltemplate}}
{{CMG}}
{{BlackBoxTemplate|blackBoxWarningTitle=WARNING: (A) BLEEDING RISK, (B) ASPIRIN DOSE AND BRILINTA EFFECTIVENESS|blackBoxWarningBody=A. BLEEDING RISK
- BRILINTA, like other antiplatelet agents, can cause significant, sometimes fatal bleeding.
- Do not use BRILINTA in patients with active pathological bleeding or a history of intracranial hemorrhage.
- Do not start BRILINTA in patients planned to undergo urgent coronary artery bypass graft surgery (CABG). When possible, discontinue BRILINTA at least 5 days prior to any surgery.
- 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 BRILINTA.
- If possible, manage bleeding without discontinuing BRILINTA. Stopping BRILINTA increases the risk of subsequent cardiovascular events.
B. ASPIRIN DOSE AND BRILINTA EFFECTIVENESS
Maintenance doses of aspirin above 100 mg reduce the effectiveness of BRILINTA and should be avoided. After any initial dose, use with aspirin 75-100 mg per day.}}
Use in Specific Populations
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===Pregnancy===
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There is no FDA guidance on usage of {{BASEPAGENAME}} in women who are pregnant.
:'''[[Pregnancy category#Australia|Pregnancy Category (AUS)]]'''
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of {{BASEPAGENAME}} in women who are pregnant.
===Labor and Delivery===
There is no FDA guidance on use of {{BASEPAGENAME}} during labor and delivery.
===Nursing Mothers===
There is no FDA guidance on the use of {{BASEPAGENAME}} in women who are nursing.
===Pediatric Use===
There is no FDA guidance on the use of {{BASEPAGENAME}} in pediatric settings.
===Geriatic Use===
There is no FDA guidance on the use of {{BASEPAGENAME}} in geriatric settings.
===Gender===
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===Race===
There is no FDA guidance on the use of {BASEPAGENAME}} with respect to specific racial populations.
===Renal Impairment===
There is no FDA guidance on the use of {{BASEPAGENAME}} in patients with renal impairment.
===Hepatic Impairment===
There is no FDA guidance on the use of {{BASEPAGENAME}} in patients with hepatic impairment.
===Females of Reproductive Potential and Males===
There is no FDA guidance on the use of {{BASEPAGENAME}} in women of reproductive potentials and males.
===Immunocompromised Patients===
There is no FDA guidance one the use of {{BASEPAGENAME}} in patients who are immunocompromised.
{{DrugReflist}}
Overdose
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===Overdose===
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{{DrugReflist}}Pharmacology
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===Mechanism of Action===
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===Structure===
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===Pharmacodynamics===
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===Pharmacokinetics===
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===Nonclinical Toxicology===
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