Država: Sjedinjene Američke Države
Jezik: engleski
Izvor: NLM (National Library of Medicine)
ATROPINE SULFATE (UNII: 03J5ZE7KA5) (ATROPINE - UNII:7C0697DR9I)
Hospira, Inc.
ATROPINE SULFATE
ATROPINE SULFATE 0.1 mg in 1 mL
INTRAVENOUS
PRESCRIPTION DRUG
Atropine Sulfate Injection, USP, is indicated for temporary blockade of severe or life threatening muscarinic effects, e.g., as an antisialagogue, an antivagal agent, an antidote for organophosphorus or muscarinic mushroom poisoning, and to treat bradyasystolic cardiac arrest. None. Animal reproduction studies have not been conducted with atropine. It also is not known whether atropine can cause fetal harm when given to a pregnant woman or can affect reproduction capacity. Trace amounts of atropine was found in breast milk. The clinical impact of this is not known. Recommendations for use in pediatric patients are not based on clinical trials. An evaluation of current literature revealed no clinical experience identifying differences in response between elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disea
Atropine Sulfate Injection, USP, 0.1 mg/mL, is a clear and colorless solution available in 5 mL and 10 mL single-dose glass vials. Each vial is co-packaged with an injector, which together make a LifeShield™ Abboject™ Glass Syringe. It is supplied in the following presentations: Store at 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F). [See USP Controlled Room Temperature.]
New Drug Application
ATROPINE SULFATE- ATROPINE SULFATE INJECTION, SOLUTION HOSPIRA, INC. ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE ATROPINE SULFATE INJECTION SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR ATROPINE SULFATE INJECTION. ATROPINE SULFATE INJECTION, FOR INTRAVENOUS USE INITIAL U.S. APPROVAL: 1960 INDICATIONS AND USAGE Atropine is a muscarinic antagonist indicated for temporary blockade of severe or life threatening muscarinic effects. (1) DOSAGE AND ADMINISTRATION For intravenous administration. (2.1, 2.3) Titrate according to heart rate, PR interval, blood pressure and symptoms. (2.1) Adult dosage - - - Patients with Coronary Artery Disease: Total dose should not exceed 0.03 mg/kg to 0.04 mg/kg. (5.1) DOSAGE FORMS AND STRENGTHS 0.1 mg/mL injection in LifeShield™ Abboject™ Glass Syringe (3) CONTRAINDICATIONS None. (4) WARNINGS AND PRECAUTIONS Tachycardia (5.1) Glaucoma (5.2) Pyloric obstruction (5.3) Worsening urinary retention (5.4) Viscid bronchial plugs (5.5) ADVERSE REACTIONS Most adverse reactions are directly related to atropine's antimuscarinic action. Dryness of the mouth, blurred vision, photophobia and tachycardia commonly occur with chronic administration of therapeutic doses. (6) TO REPORT SUSPECTED ADVERSE REACTIONS, CONTACT HOSPIRA, INC. AT 1-800-441-4100, OR FDA AT 1-800-FDA- 1088 OR _WWW.FDA.GOV/MEDWATCH_. DRUG INTERACTIONS _Mexiletine:_ Decreases rate of mexiletine absorption. (7.1) REVISED: 3/2018 FULL PRESCRIBING INFORMATION: CONTENTS* 1 INDICATIONS AND USAGE 2 DOSAGE AND ADMINISTRATION 2.1 General Administration 2.2 Adult Dosage 2.3 Pediatric Dosage 3 DOSAGE FORMS AND STRENGTHS 4 CONTRAINDICATIONS Antisialagogue or for antivagal effects: Initial single dose of 0.5 mg to 1 mg. (2.2) Antidote for organophosphorus or muscarinic mushroom poisoning: Initial single dose of 2 mg to 3 mg, repeated every 20–30 minutes. (2.2) Bradyasystolic cardiac arrest: 1 mg dose, repeated every 3–5 minutes if asystole persists. (2. Pročitajte cijeli dokument