Metoprolol Tartrate description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Metoprolol Tartrate

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

BOXED WARNING


Ischemic Heart Disease:

METOPROLOL TARTRATE DESCRIPTION


Metoprolol Tartrate





CLINICAL PHARMACOLOGY
















PHARMACOKINETICS













INDICATIONS & USAGE

Hypertension


Angina Pectoris


Myocardial Infarction
DOSAGE AND ADMINISTRATIONCONTRAINDICATIONSWARNINGSDOSAGE AND ADMINISTRATION

METOPROLOL TARTRATE CONTRAINDICATIONS

Hypertension and Angina
WARNINGS




Myocardial Infarction
WARNINGS

WARNINGS

Hypertension and Angina

Cardiac Failure


In Patients Without a History of Cardiac Failure


Bronchospastic Diseases
PATIENTS WITH BRONCHOSPASTIC DISEASES SHOULD, IN GENERAL, NOT RECEIVE BETA BLOCKERS, including Metoprolol tartrate. Because of its relative beta1 selectivity, however, metoprolol may be used with caution in patients with bronchospastic disease who do not respond to, or cannot tolerate, other antihypertensive treatment. Since beta1 selectivity is not absolute, a beta2-stimulating agent should be administered concomitantly, and the lowest possible dose of metoprolol tartrate should be used. In these circumstances it would be prudent initially to administer metoprolol 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 (seeDOSAGE AND ADMINISTRATION).


Major Surgery



Diabetes and Hypoglycemia


Pheochromocytoma


Thyrotoxicosis


Myocardial Infarction

Cardiac Failure



Bradycardia


AV Block



Hypotension
above

Bronchospastic Diseases
PATIENTS WITH BRONCHOSPASTIC DISEASES SHOULD, IN GENERAL, NOT RECEIVE BETA BLOCKERS, including Metoprolol tartrate. Because of its relative beta1 selectivity, metoprolol may be used with extreme caution in patients with bronchospastic disease. Because it is unknown to what extent beta2-stimulating agents may exacerbate myocardial ischemia and the extent of infarction, these agents should not be used prophylactically. If bronchospasm not related to congestive heart failure occurs, metoprolol should be discontinued. A theophylline derivative or a beta2 agonist may be administered cautiously, depending on the clinical condition of the patient. Both theophylline derivatives and beta2 agonists may produce serious cardiac arrhythmias.


PRECAUTIONS

General


INFORMATION FOR PATIENTS




DRUG INTERACTIONS




Risk of Anaphylactic Reaction


General Anesthetics
WARNINGS, Major Surgery

CYP2D6 Inhibitors
Pharmacokinetics

Clonidine



CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY





PREGNANCY



NURSING MOTHERS



PEDIATRIC USE



GERIATRIC USE




METOPROLOL TARTRATE ADVERSE REACTIONS

Hypertension and Angina

Central Nervous System:
Cardiovascular:CONTRAINDICATIONSWARNINGSPRECAUTIONS
Respiratory:WARNINGS
Gastrointestinal:
Hypersensitive Reactions:
Miscellaneous:



Myocardial Infarction
Central Nervous System:

Cardiovascular:
metoprololPlaceboRespiratory:
Gastrointestinal:
Dermatologic:
Miscellaneous:

Potential Adverse Reactions

Central Nervous System:
Cardiovascular:CONTRAINDICATIONS
Hematologic:
Hypersensitive Reactions:
Postmarketing Experience


OVERDOSAGE


Acute Toxicity



Signs and Symptoms


Treatment

WARNINGS, Myocardial Infarction

Elimination of the Drug:
Bradycardia:
Hypotension:
Bronchospasm:
Cardiac Failure:

DOSAGE & ADMINISTRATION

Hypertension



Angina Pectoris

WARNINGS

Myocardial Infarction

Early Treatment


Late Treatment
WARNINGS

Late Treatment


HOW SUPPLIED

















STORAGE AND HANDLING



PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Metoprolol Tartrate

Metoprolol Tartrate

Metoprolol Tartrate

Metoprolol Tartrate TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-831(NDC:57664-167)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
METOPROLOL TARTRATE METOPROLOL 100 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
HYPROMELLOSES
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol
POLYSORBATE 20
povidone
SODIUM STARCH GLYCOLATE TYPE A POTATO
talc
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
white 14 mm 167 BULLET

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-831-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074644 2011-12-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.