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| __NOTOC__
| | #REDIRECT [[Ticagrelor#Contraindications]] |
| {{Ticagrelor}}
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| {{CMG}}; {{AE}} {{JH}}
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| ==Contraindications==
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| ====History of Intracranial Hemorrhage====
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| BRILINTA is contraindicated in patients with a history of [[intracranial hemorrhage|intracranial hemorrhage (ICH)]] because of a high risk of recurrent [[ICH]] in this population ''[see [[Ticagrelor clinical studies|Clinical Studies]]]''.
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| ====Active Bleeding====
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| BRILINTA is contraindicated in patients with active pathological bleeding such as peptic ulcer or [[intracranial hemorrhage]] [see Warnings and Precautions (5.1) and Adverse Reactions (6.1)].
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| ====Severe Hepatic Impairment====
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| BRILINTA is contraindicated in patients with severe hepatic impairment because of a probable increase in exposure, and it has not been studied in these patients. Severe hepatic impairment increases the risk of bleeding because of reduced synthesis of coagulation proteins [see Clinical Pharmacology (12.3)].
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| ====Hypersensitivity====
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| BRILINTA is contraindicated in patients with hypersensitivity (e.g. [[angioedema]]) to ticagrelor or any component of the product [see Adverse Reactions (6.2)].<ref name="dailymed.nlm.nih.gov">{{Cite web | last = | first = | title = BRILINTA (TICAGRELOR) TABLET [ASTRAZENECA LP] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f7b3f443-e83d-4bf2-0e96-023448fed9a8 | publisher = | date = | accessdate = }}</ref>
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| ==References==
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| {{Reflist}}
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| [[Category:ADP receptor inhibitors]]
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| [[Category:Cardiovascular Drugs]]
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| [[Category:Drugs]]
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