Lopressor/warnings: Difference between revisions

Jump to navigation Jump to search
VisualWikitext
m (Gerald Chi moved page Metoprolol warnings and precautions to Lopressor warnings and precautions without leaving a redirect)
(←Redirected page to Metoprolol tartrate#Warnings)
 
(23 intermediate revisions by 3 users not shown)
Line 1: Line 1:
__NOTOC__
#REDIRECT [[Metoprolol tartrate#Warnings]]
{{Metoprolol}}
{{CMG}}
 
{|
| [[File:Metop01.png|800px|thumb]]
|}
 
==Warnings==
 
===Hypertension and Angina===
 
===Cardiac Failure===
 
[[Sympathetic]] stimulation is a vital component supporting circulatory function in [[congestive heart failure]], and [[beta blockade]] carries the potential hazard of further depressing myocardial [[contractility]] and precipitating more severe failure.
 
====In Patients Without a History of Cardiac Failure====
 
Continued depression of the myocardium with [[beta-blocking agents]] over a period of time can, in some cases, lead to [[cardiac failure]]. At the first sign or symptom of impending [[cardiac failure]], fully digitalize patients and/or give a [[diuretic]]. The response should be observed closely. If [[cardiac failure]] continues, despite adequate [[digitalization]] and [[diuretic]] therapy, withdraw Lopressor.
 
===Bronchospastic Diseases===
 
PATIENTS WITH [[BRONCHOSPASTIC DISEASES]] SHOULD, IN GENERAL, NOT RECEIVE BETA BLOCKERS, including Lopressor.
 
Because of its relative [[beta-1]] selectivity, however, Lopressor may be used with caution in patients with [[bronchospastic disease]] who do not respond to, or cannot tolerate, other [[antihypertensive]] treatment. Since [[beta-1]] selectivity is not absolute, a [[beta2]]-stimulating agent should be administered concomitantly, and the lowest possible dose of Lopressor should be used. In these circumstances it would be prudent initially to administer Lopressor in smaller doses three times daily, instead of larger doses two times daily, to avoid the higher plasma levels associated with the longer dosing interval (see DOSAGE AND ADMINISTRATION).
 
===Major Surgery===
 
Chronically administered [[beta-blocking therapy]] should not be routinely withdrawn prior to major surgery; however, the impaired ability of the heart to respond to reflex [[adrenergic]] stimuli may augment the risks of [[general anesthesia]] and surgical procedures.
 
===Diabetes and Hypoglycemia===
 
[[Beta blockers]] may mask [[tachycardia]] occurring with [[hypoglycemia]], but other manifestations such as [[dizziness]] and [[sweating]] may not be significantly affected.
 
===Pheochromocytoma===
 
If Lopressor is used in the setting of [[pheochromocytoma]], it should be given in combination with an [[alpha blocker]], and only after the [[alpha blocker]] has been initiated.
 
Administration of [[beta blocker]]s alone in the setting of [[pheochromocytoma]] has been associated with a paradoxical increase in [[blood pressure]] due to the attenuation of beta-mediated [[vasodilatation]] in [[skeletal muscle]].
 
===Thyrotoxicosis===
 
[[Beta-adrenergic blockade]] may mask certain clinical signs (e.g., [[tachycardia]]) of [[hyperthyroidism]]. Avoid abrupt withdrawal of [[beta blockade]], which might precipitate a [[thyroid storm]].
 
===Myocardial Infarction===
 
====Cardiac Failure====
 
 
[[Sympathetic]] stimulation is a vital component supporting circulatory function, and [[beta blockade]] carries the potential hazard of depressing [[myocardial contractility]] and precipitating or exacerbating minimal [[cardiac failure]].
 
During treatment with Lopressor, monitor the hemodynamic status of the patient. If [[heart failure]] occurs or persists despite appropriate treatment, discontinue Lopressor.
 
===Bradycardia===
 
Lopressor produces a decrease in sinus [[heart rate]] in most patients; this decrease is greatest among patients with high initial heart rates and least among patients with low initial heart rates. [[Acute myocardial infarction]] (particularly inferior infarction) may in itself produce significant lowering of the sinus rate. If the sinus rate decreases to <40 beats/min, particularly if associated with evidence of lowered [[cardiac output]], [[atropine]] (0.25-0.5 mg) should be administered intravenously. If treatment with [[atropine]] is not successful, discontinue Lopressor and consider cautious administration of [[isoproterenol]] or installation of a [[cardiac pacemaker]].
 
===AV Block===
 
Lopressor slows AV conduction and may produce significant [[First degree AV block|first]]- ([[PR interval]] ≥0.24 sec), [[Second degree AV block|second]]-, or [[Third degree AV block|third-degree heart block]]. [[Acute myocardial infarction]] also produces [[heart block]].
 
If heart block occurs, discontinue Lopressor and administer [[atropine]] (0.25-0.5 mg) intravenously. If treatment with [[atropine]] is not successful, consider administration of [[isoproterenol]] or installation of a [[cardiac pacemaker]].
 
===Hypotension===
 
If [[hypotension]] ([[systolic blood pressure]] ≤90 mmHg) occurs, discontinue Lopressor, and assess the hemodynamic status of the patient and the extent of myocardial damage. Invasive monitoring of [[central venous pressure|central venous]], [[pulmonary capillary wedge pressure|pulmonary capillary wedge]], and [[arterial pressure]]s may be required. Institute appropriate therapy with fluids, positive [[inotropic agent]]s, [[balloon counterpulsation]], or other treatment modalities. If [[hypotension]] is associated with [[sinus bradycardia]] or [[AV block]], direct treatment at reversing these (see above).
 
==Precautions==
 
===General===
 
Start at a low dose and uptitrate slowly in patients with impaired [[Liver function tests|hepatic function]].
 
====Information for Patients====
 
Advise patients to 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.
 
Advise patients to:
 
* 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.
 
====Carcinogenesis, Mutagenesis, Impairment of Fertility====
 
Long-term studies in animals have been conducted to evaluate carcinogenic potential. In a 2-year study in rats at three oral dosage levels of up to 800 mg/kg per day, there was no increase in the development of spontaneously occurring benign or malignant neoplasms of any type. The only histologic changes that appeared to be drug related were an increased incidence of generally mild focal accumulation of foamy macrophages in pulmonary alveoli and a slight increase in biliary hyperplasia. In a 21-month study in Swiss albino mice at three oral dosage levels of up to 750 mg/kg per day, benign lung tumors (small adenomas) occurred more frequently in female mice receiving the highest dose than in untreated control animals. There was no increase in malignant or total (benign plus malignant) lung tumors, or in the overall incidence of tumors or malignant tumors. This 21-month study was repeated in CD-1 mice, and no statistically or biologically significant differences were observed between treated and control mice of either sex for any type of tumor.
 
All mutagenicity tests performed (a dominant lethal study in mice, chromosome studies in somatic cells, a Salmonella/mammalian-microsome mutagenicity test, and a nucleus anomaly test in somatic interphase nuclei) were negative.
 
Reproduction toxicity studies in mice, rats and rabbits did not indicate teratogenic potential for metoprolol tartrate. Embryotoxicity and/or fetotoxicity in rats and rabbits were noted starting at doses of 50 mg/kg in rats and 25 mg/kg in rabbits, as demonstrated by increases in preimplantation loss, decreases in the number of viable fetuses per dose, and/or decreases in neonatal survival. High doses were associated with some maternal toxicity, and growth delay of the offspring in utero, which was reflected in minimally lower weights at birth. The oral NOAELs for embryo-fetal development in mice, rats, and rabbits were considered to be 25, 200, and 12.5 mg/kg. This corresponds to dose levels that are approximately 0.3, 4, and 0.5 times, respectively, when based on surface area, the maximum human oral dose (8 mg/kg/day) of metoprolol tartrate. Metoprolol tartrate has been associated with reversible adverse effects on spermatogenesis starting at oral dose levels of 3.5 mg/kg in rats (a dose that is only 0.1-times the human dose, when based on surface area), although other studies have shown no effect of metoprolol tartrate on reproductive performance in male rats.<ref name="dailymed.nlm.nih.gov">{{Cite web  | last =  | first =  | title = LOPRESSOR (METOPROLOL TARTRATE) TABLET [NOVARTIS PHARMACEUTICALS CORPORATION] | url =http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb05420c-fd24-4672-9f62-fdd313819287 | publisher =  | date =  | accessdate = }}</ref>
 
==References==
 
{{Reflist}}
 
{{FDA}}
 
[[Category:Drugs]]
[[Category:Cardiovascular Drugs]]
[[Category:Beta blockers]]

Latest revision as of 03:51, 22 July 2014

Redirect to:

Retrieved from "https://www.wikidoc.org/index.php?title=Lopressor/warnings&oldid=998887"