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100 mg per 5 mL (20 mg/mL) Oral Solution (colorless) (only for opioid tolerant adults) is supplied as a clear, colorless solution. Each 1 mL of clear, colorless oral solution contains 20 mg of morphine sulfate, USP (equivalent to 15 mg morphine). NDC 0054-0404-41: Bottle of 15 mL with an Oral Syringe.
Morphine Sulfate Injection is an opioid agonist, indicated for the management of pain severe enough to require use of an opioid analgesic by intravenous Patient-Controlled Analgesia (PCA) with a compatible PCA pump, or for controlled continuous intravenous infusion, and for which alternative treatments are inadequate.
Cautionary and advisory labels. Label . 2 Warning: This medicine may make you sleepy. If this happens, do not drive or use tools or machines. ... (Schedule 5 (CD Inv)) Morphine sulfate 10mg/5ml oral solution A A H Pharmaceuticals Ltd Show Cautionary and advisory labels. Label . 2 Warning: This medicine may make you sleepy.
15 de abr. de 2024 · Morphine Injection Prescribing Information. Package insert / product label. Generic name: morphine sulfate. Dosage form: injection, solution. Drug class: Opioids (narcotic analgesics) J Code (medical billing code): J2274 (Per 10 mg, injection) Medically reviewed by Drugs.com. Last updated on Apr 15, 2024.
13 de oct. de 2023 · Morphine may impair the mental and/or physical abilities required for the performance of potentially hazardous tasks, such as driving a car or operating machinery. Morphine in combination with other narcotic analgesics, phenothiazines, sedative-hypnotics, and alcohol have additive depressant effects. Patients should not drive or operate machinery.
Morphine | C17H19NO3 | CID 5288826 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, ... We are requiring changes to the labels of all opioid drugs to warn about these risks.
Use of Morphine Sulfate Oral Solution in this age group is supported by clinical evidence in adults and supportive data from an open-label, safety and pharmacokinetic study in pediatric patients 2 through 17 years of age with post-operative acute pain.
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