Label Changes for:

Lopressor (metoprolol tartrate) Injection, Solution

July 2008

Changes have been made to the WARNINGS and ADVERSE REACTIONS sections of the safety label.


Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER) -- July 2008

 

The detailed view includes drug products with safety labeling changes to the BOXED WARNING, CONTRAINDICATIONS, WARNINGS, PRECAUTIONS, ADVERSE REACTIONS, or PATIENT PACKAGE INSERT/MEDICATION GUIDE sections. Deletions or editorial revisions made to these sections are not included in this summary.


Summary View

 

Sections Modified Summary of Changes to Contraindications and Warnings

WARNINGS

  • Hypertension and Angina
    • Bronchospastic Diseases
  • Major Surgery
  • Myocardial Infarction
    • Bronchospastic Diseases

ADVERSE REACTIONS

  • Postmarketing Experience (section added)

WARNINGS

Hypertension and Angina

Bronchospastic Diseases

PATIENTS WITH BRONCHOSPASTIC DISEASES SHOULD, IN GENERAL, NOT RECEIVE BETA BLOCKERS, including Lopressor...

Major Surgery

The necessity or desirability of withdrawing beta-blocking therapy, including Lopressor, prior to major surgery is controversial; the impaired ability of the heart to respond to reflex adrenergic stimuli may augment the risks of general anesthesia and surgical procedures...

Myocardial Infarction/Bronchospastic Diseases

PATIENTS WITH BRONCHOSPASTIC DISEASES SHOULD, IN GENERAL, NOT RECEIVE BETA BLOCKERS, including Lopressor...

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