Lopressor patient counseling information
Clinical data | |
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Trade names | Lopressor, Toprol-xl |
AHFS/Drugs.com | Monograph |
MedlinePlus | a682864 |
[[Regulation of therapeutic goods |Template:Engvar data]] |
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Pregnancy category | |
Routes of administration | Oral, IV |
ATC code | |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Bioavailability | 12% |
Metabolism | Hepatic via CYP2D6, CYP3A4 |
Elimination half-life | 3-7 hours |
Excretion | Renal |
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CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
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ChemSpider | |
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KEGG | |
ChEBI | |
ChEMBL | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C15H25NO3 |
Molar mass | 267.364 g/mol |
3D model (JSmol) | |
Melting point | 120 °C (248 °F) |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Zaghw, M.D. [2]
Information for Patients
Take Lopressor regularly and continuously, as directed, with or immediately following meals.
If a dose should be missed, the patient should take only the next scheduled dose (without doubling it).
Patients should not discontinue Lopressor without consulting the physician.
Avoid operating automobiles and machinery or engaging in other tasks requiring alertness until the patient’s response to therapy with Lopressor has been determined.
Contact the physician if any difficulty in breathing occurs.
Inform the physician or dentist before any type of surgery that he or she is taking Lopressor.[1]
References
Adapted from the FDA Package Insert.
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